P17706
Gene name |
PTPN2 (PTPT) |
Protein name |
Tyrosine-protein phosphatase non-receptor type 2 |
Names |
T-cell protein-tyrosine phosphatase, TCPTP |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:5771 |
EC number |
3.1.3.48: Phosphoric monoester hydrolases |
Protein Class |
TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 61F (PTHR46047) |

Descriptions
T cell protein tyrosine phosphatase(Tyrosine-protein phosphatase non-receptor type 2, TCPTP) is a regulator of diverse physiological processes such as cell growth, gene expression, differentiation, cytoskeletal dynamics, and cell motility. Alternative mRNA splicing results in variation in the sequence at the extreme C terminus of TCPTP and generates a 45-kDa form (TC45) that is targeted to the nucleus and a 48-kDa variant (TC48) associated with membranes of the endoplasmic reticulum. Analysis of the time course of limited trypsinolysis revealed that proteolytic activation occurred following cleavage of a protease-sensitive region (residues 353–387) located at the C terminus of TC45.
Autoinhibitory domains (AIDs)
Target domain |
1-288 (Catalytic domain) |
Relief mechanism |
Cleavage |
Assay |
Deletion assay |
Accessory elements
No accessory elements
Autoinhibited structure

Activated structure

269 variants for P17706
Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
---|---|---|---|---|---|
CA8898923 rs771614274 |
2 | P>H | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898924 rs771614274 |
2 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA402035792 rs771614274 |
2 | P>R | No |
ClinGen ExAC TOPMed gnomAD |
|
rs867096066 CA296791307 |
2 | P>S | No |
ClinGen TOPMed |
|
CA402035787 rs1276711486 |
3 | T>I | No |
ClinGen TOPMed gnomAD |
|
rs1276711486 CA402035788 |
3 | T>S | No |
ClinGen TOPMed gnomAD |
|
rs1385843772 CA402035791 |
3 | T>S | No |
ClinGen TOPMed |
|
CA296791299 rs945467973 |
4 | T>A | No |
ClinGen TOPMed |
|
rs747486746 CA402035782 |
4 | T>I | No |
ClinGen ExAC gnomAD |
|
CA8898922 rs747486746 |
4 | T>N | No |
ClinGen ExAC gnomAD |
|
CA402035783 rs747486746 |
4 | T>S | No |
ClinGen ExAC gnomAD |
|
CA8898921 rs778310630 |
6 | E>K | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898920 rs758737273 |
6 | E>V | No |
ClinGen ExAC gnomAD |
|
rs150641661 CA402035757 |
8 | E>D | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs1337353757 CA402035762 |
8 | E>K | No |
ClinGen TOPMed gnomAD |
|
CA402035763 rs1337353757 |
8 | E>Q | No |
ClinGen TOPMed gnomAD |
|
rs1451616383 CA402035758 |
8 | E>V | No |
ClinGen gnomAD |
|
rs1598913685 CA402035750 |
9 | F>C | No |
ClinGen Ensembl |
|
rs1598913694 CA402035753 |
9 | F>V | No |
ClinGen Ensembl |
|
CA402035740 rs1568185242 |
10 | E>D | No |
ClinGen Ensembl |
|
rs1395399977 CA402035734 |
11 | E>D | No |
ClinGen TOPMed gnomAD |
|
rs200164592 CA402035739 |
11 | E>K | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs200164592 CA8898918 |
11 | E>Q | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
CA296791270 rs867997369 |
12 | L>F | No |
ClinGen Ensembl |
|
CA402035729 rs1445972788 |
12 | L>S | No |
ClinGen gnomAD |
|
CA8898916 rs369944958 |
14 | T>A | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA402035716 rs1184779249 |
14 | T>N | No |
ClinGen gnomAD |
|
rs1184779249 CA402035715 |
14 | T>S | No |
ClinGen gnomAD |
|
CA402035706 rs1466257016 |
15 | Q>H | No |
ClinGen TOPMed |
|
rs1236087183 CA402035705 |
16 | R>C | No |
ClinGen gnomAD |
|
CA402035700 rs1206823913 |
16 | R>H | No |
ClinGen TOPMed gnomAD |
|
CA402035702 rs1206823913 |
16 | R>L | No |
ClinGen TOPMed gnomAD |
|
CA402035698 rs1438599484 |
17 | R>G | No |
ClinGen gnomAD |
|
CA402035696 rs1272652429 |
17 | R>H | No |
ClinGen TOPMed gnomAD |
|
CA402035682 rs1203075385 |
19 | Q>* | No |
ClinGen gnomAD |
|
rs562857102 CA8898915 |
20 | P>Q | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs562857102 CA402035673 |
20 | P>R | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs1361746465 CA402035674 |
20 | P>S | No |
ClinGen TOPMed gnomAD |
|
rs756085499 CA8898914 |
21 | L>V | No |
ClinGen ExAC gnomAD |
|
CA402035666 rs1281057841 |
22 | Y>H | No |
ClinGen gnomAD |
|
rs1457235029 CA402035654 |
23 | L>F | No |
ClinGen TOPMed |
|
rs748912308 CA8898897 |
24 | E>A | No |
ClinGen ExAC gnomAD |
|
CA402035632 rs1285609315 |
25 | I>V | No |
ClinGen TOPMed |
|
rs779572195 CA8898896 |
26 | R>L | No |
ClinGen ExAC gnomAD |
|
CA296769472 rs950185463 |
27 | N>S | No |
ClinGen TOPMed |
|
CA402035602 rs1266017550 |
29 | S>F | No |
ClinGen gnomAD |
|
CA8898895 rs755572904 |
30 | H>N | No |
ClinGen ExAC TOPMed gnomAD |
|
rs917217934 CA296769459 |
30 | H>R | No |
ClinGen gnomAD |
|
CA296769452 rs950936929 |
31 | D>G | No |
ClinGen Ensembl |
|
CA296769442 rs1027932038 |
32 | Y>C | No |
ClinGen TOPMed gnomAD |
|
CA402035576 rs1375809882 |
33 | P>L | No |
ClinGen gnomAD |
|
rs750374603 CA8898894 |
35 | R>S | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898893 rs537221478 |
36 | V>M | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs1291106111 CA402035550 |
38 | K>Q | No |
ClinGen gnomAD |
|
CA402035535 rs1432117963 |
39 | F>L | No |
ClinGen TOPMed gnomAD |
|
CA402035536 rs1432117963 |
39 | F>L | No |
ClinGen TOPMed gnomAD |
|
rs1172950151 CA402035529 |
40 | P>L | No |
ClinGen gnomAD |
|
rs1318954462 CA402035522 |
41 | E>D | No |
ClinGen gnomAD |
|
rs763765476 CA8898891 |
44 | N>D | No |
ClinGen ExAC gnomAD |
|
rs763765476 CA8898890 |
44 | N>Y | No |
ClinGen ExAC gnomAD |
|
CA776261315 rs1191212687 |
48 | Y>* | No |
ClinGen TOPMed |
|
rs759832705 CA8898889 |
48 | Y>F | No |
ClinGen ExAC gnomAD |
|
CA296757886 rs913379921 |
55 | D>G | No |
ClinGen Ensembl |
|
CA296757885 rs996337306 |
63 | N>S | No |
ClinGen TOPMed gnomAD |
|
rs1455114748 CA402035103 |
72 | S>N | No |
ClinGen gnomAD |
|
CA402035090 rs1201944113 |
74 | V>L | No |
ClinGen TOPMed |
|
rs902050146 CA296757882 |
76 | I>T | No |
ClinGen TOPMed |
|
CA8898848 rs752113628 |
77 | E>Q | No |
ClinGen ExAC gnomAD |
|
rs953123344 CA296757878 |
79 | A>G | No |
ClinGen TOPMed |
|
rs74163638 CA8898845 |
82 | S>G | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA402035035 rs74163638 |
82 | S>R | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA296757874 rs943757284 |
83 | Y>H | No |
ClinGen TOPMed |
|
rs1267220108 CA402035008 |
86 | T>P | No |
ClinGen gnomAD |
|
CA402034951 rs1568124158 |
92 | N>K | No |
ClinGen Ensembl |
|
rs774373051 CA8898818 |
94 | C>S | No |
ClinGen ExAC gnomAD |
|
rs768576389 CA8898817 |
97 | F>L | No |
ClinGen ExAC gnomAD |
|
CA296755265 rs889010899 |
99 | L>F | No |
ClinGen TOPMed gnomAD |
|
rs1432576957 CA402034891 |
101 | V>I | No |
ClinGen gnomAD |
|
CA402034860 rs1408071596 |
105 | K>Q | No |
ClinGen gnomAD |
|
CA402034850 rs1336909079 |
106 | T>S | No |
ClinGen gnomAD |
|
rs1413571843 CA402034835 |
108 | A>S | No |
ClinGen TOPMed gnomAD |
|
CA402034813 rs1475479415 |
111 | M>I | No |
ClinGen gnomAD |
|
rs779886860 CA8898815 |
111 | M>R | No |
ClinGen ExAC |
|
rs1169141526 CA402034818 |
111 | M>V | No |
ClinGen gnomAD |
|
CA8898814 rs771096169 COSM1387818 |
114 | R>C | large_intestine [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
CA8898813 COSM986672 rs145657672 |
114 | R>H | endometrium [Cosmic] | No |
ClinGen cosmic curated ESP ExAC TOPMed gnomAD |
CA8898812 rs777852241 |
115 | I>T | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1188747865 CA402034780 |
117 | E>* | No |
ClinGen gnomAD |
|
rs758414586 CA296755255 |
120 | S>* | No |
ClinGen ExAC gnomAD |
|
CA8898811 rs758414586 |
120 | S>L | No |
ClinGen ExAC gnomAD |
|
CA402034736 rs1290556737 |
121 | V>A | No |
ClinGen gnomAD |
|
CA402034723 rs1400499894 |
123 | C>Y | No |
ClinGen TOPMed gnomAD |
|
CA402034700 rs1354030120 |
126 | Y>C | No |
ClinGen gnomAD |
|
rs1280858319 CA402034671 |
130 | D>G | No |
ClinGen gnomAD |
|
CA296753533 rs756443279 |
132 | Q>H | No |
ClinGen ExAC gnomAD |
|
CA8898781 rs750105074 |
135 | L>M | No |
ClinGen ExAC TOPMed gnomAD |
|
rs142645165 CA8898780 |
136 | F>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA402034606 rs1400124644 |
139 | T>A | No |
ClinGen gnomAD |
|
rs1352097620 CA402034591 |
141 | F>C | No |
ClinGen gnomAD |
|
CA402034584 rs1213254112 |
142 | S>T | No |
ClinGen TOPMed |
|
CA8898779 rs761548219 |
145 | L>F | No |
ClinGen ExAC TOPMed gnomAD |
|
rs148072900 CA8898777 |
146 | L>F | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA296753505 rs929363513 |
150 | V>A | No |
ClinGen TOPMed |
|
rs568984333 CA296753502 |
151 | K>N | No |
ClinGen 1000Genomes |
|
CA402034524 rs1160459981 |
151 | K>R | No |
ClinGen gnomAD |
|
CA402034519 rs1473036088 |
152 | S>A | No |
ClinGen gnomAD |
|
rs1411593047 CA402034516 |
152 | S>L | No |
ClinGen TOPMed gnomAD |
|
rs1189334871 CA402034514 |
153 | Y>H | No |
ClinGen TOPMed |
|
CA8898772 rs776397445 |
158 | L>V | No |
ClinGen ExAC gnomAD |
|
CA8898771 rs772328138 |
160 | Q>P | No |
ClinGen ExAC gnomAD |
|
rs143546199 CA296753490 |
161 | L>I | No |
ClinGen ESP TOPMed gnomAD |
|
rs1286069969 CA402034443 |
163 | N>K | No |
ClinGen gnomAD |
|
rs1417557137 CA402034437 |
164 | I>T | No |
ClinGen gnomAD |
|
rs1447598742 CA402034430 |
165 | N>S | No |
ClinGen TOPMed |
|
CA296750857 rs1026936564 |
166 | S>N | No |
ClinGen Ensembl |
|
rs1254988153 CA402032832 |
168 | E>K | No |
ClinGen gnomAD |
|
RCV000955616 CA8898744 rs78174797 |
171 | T>K | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
rs1251890800 CA402032794 |
173 | S>F | No |
ClinGen gnomAD |
|
CA296750853 rs1019476175 |
175 | F>L | No |
ClinGen Ensembl |
|
rs1203900630 CA402032759 |
177 | Y>C | No |
ClinGen gnomAD |
|
CA296750851 rs527692021 |
178 | T>A | No |
ClinGen TOPMed gnomAD |
|
rs1249657620 CA402032735 |
179 | T>A | No |
ClinGen TOPMed |
|
CA8898741 rs757973522 |
179 | T>S | No |
ClinGen ExAC gnomAD |
|
CA402032708 rs752299864 |
181 | P>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs752299864 CA8898740 |
181 | P>T | No |
ClinGen ExAC TOPMed gnomAD |
|
rs766175622 CA402032532 |
206 | N>K | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898736 rs753727316 |
206 | N>S | No |
ClinGen ExAC gnomAD |
|
rs1295244418 CA402032526 |
207 | P>L | No |
ClinGen gnomAD |
|
rs1368613939 CA402032529 |
207 | P>S | No |
ClinGen TOPMed gnomAD |
|
CA402032432 rs1324373480 |
209 | H>R | No |
ClinGen TOPMed |
|
CA402032420 rs1162194232 |
211 | P>S | No |
ClinGen gnomAD |
|
rs764438771 CA8898732 |
212 | A>V | No |
ClinGen ExAC TOPMed gnomAD |
|
rs893136826 CA296750787 |
213 | V>M | No |
ClinGen Ensembl |
|
rs1324789871 CA402032404 |
214 | I>F | No |
ClinGen TOPMed |
|
rs1180798384 CA402032393 |
215 | H>Q | No |
ClinGen gnomAD |
|
CA402032348 rs1248980805 |
222 | R>C | No |
ClinGen TOPMed gnomAD |
|
rs769957418 CA8898729 |
223 | S>C | No |
ClinGen ExAC gnomAD |
|
rs772643237 CA8898728 |
227 | S>C | No |
ClinGen ExAC gnomAD |
|
rs750274051 COSM1263355 CA296750761 |
229 | V>A | oesophagus [Cosmic] | No |
ClinGen cosmic curated Ensembl |
rs777208240 CA8898727 |
229 | V>I | No |
ClinGen ExAC gnomAD |
|
CA402032279 rs1331450260 |
233 | L>I | No |
ClinGen gnomAD |
|
RCV000883504 CA8898726 rs77573141 |
234 | V>I | No |
ClinGen ClinVar 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
rs1348743305 CA402032263 |
235 | L>F | No |
ClinGen gnomAD |
|
CA402032247 rs1188397881 |
236 | M>V | No |
ClinGen gnomAD |
|
rs778472790 CA8898700 |
238 | K>E | No |
ClinGen ExAC TOPMed gnomAD |
|
COSM228678 CA8898699 rs768294026 |
239 | G>R | skin [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
CA402032223 COSM228678 rs768294026 |
239 | G>R | skin [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
CA8898697 rs779521258 |
240 | D>Y | No |
ClinGen ExAC |
|
rs929466536 CA296749353 |
243 | N>K | No |
ClinGen Ensembl |
|
rs750290141 CA8898695 |
244 | I>T | No |
ClinGen ExAC gnomAD |
|
rs142941831 CA8898696 |
244 | I>V | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA402032177 rs1296589139 |
245 | K>I | No |
ClinGen gnomAD |
|
rs61731982 CA8898694 |
247 | V>M | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
CA296749346 rs918133281 |
249 | L>M | No |
ClinGen Ensembl |
|
CA296749343 rs756931750 |
250 | N>K | No |
ClinGen ExAC gnomAD |
|
CA8898693 rs756931750 |
250 | N>K | No |
ClinGen ExAC gnomAD |
|
CA296749335 rs1001108405 |
251 | M>I | No |
ClinGen Ensembl |
|
CA8898692 rs751393298 |
251 | M>L | No |
ClinGen ExAC gnomAD |
|
rs1394909927 CA402032121 |
254 | Y>H | No |
ClinGen gnomAD |
|
CA8898689 rs754009863 |
256 | M>L | No |
ClinGen ExAC TOPMed gnomAD |
|
rs754009863 CA8898690 |
256 | M>V | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898688 rs766526989 |
257 | G>C | No |
ClinGen ExAC gnomAD |
|
CA8898687 rs761265276 |
262 | P>S | No |
ClinGen ExAC gnomAD |
|
rs1474643355 CA402032061 |
263 | D>G | No |
ClinGen gnomAD |
|
CA8898684 rs199581316 |
270 | M>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs762152963 CA8898683 |
272 | I>V | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1207461588 CA402031974 |
276 | A>T | No |
ClinGen gnomAD |
|
CA402031952 rs1273897023 |
278 | C>Y | No |
ClinGen gnomAD |
|
CA296749303 rs201489635 |
279 | I>V | No |
ClinGen TOPMed gnomAD |
|
CA402031930 rs1324827128 |
281 | G>E | No |
ClinGen TOPMed |
|
CA8898681 rs768347316 |
281 | G>R | No |
ClinGen ExAC gnomAD |
|
rs748912257 CA8898680 |
284 | S>G | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1568101581 CA402031875 |
284 | S>R | No |
ClinGen Ensembl |
|
CA296749300 rs937963823 |
286 | Q>K | No |
ClinGen Ensembl |
|
rs967979446 CA296741439 |
287 | K>R | No |
ClinGen TOPMed |
|
CA8898664 rs531038472 |
288 | R>L | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA8898665 rs531038472 COSM1387814 |
288 | R>Q | large_intestine [Cosmic] | No |
ClinGen cosmic curated 1000Genomes ExAC gnomAD |
rs1568085594 CA402031206 |
289 | W>R | No |
ClinGen Ensembl |
|
rs767968416 CA8898663 |
290 | K>E | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1324580908 CA402031170 |
294 | K>E | No |
ClinGen gnomAD |
|
rs1023064878 CA296741425 |
294 | K>R | No |
ClinGen Ensembl |
|
rs1327473482 CA402031147 |
297 | L>V | No |
ClinGen TOPMed |
|
rs200711300 CA8898661 |
298 | S>A | No |
ClinGen ExAC TOPMed gnomAD |
|
rs764406914 CA8898660 |
298 | S>C | No |
ClinGen ExAC gnomAD |
|
rs200711300 CA402031140 |
298 | S>P | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1214528299 CA402031130 |
300 | A>P | No |
ClinGen TOPMed |
|
rs762619357 CA8898659 |
301 | F>S | No |
ClinGen ExAC gnomAD |
|
rs1272668578 CA402031090 |
306 | N>D | No |
ClinGen TOPMed |
|
rs202049574 CA296741405 |
310 | T>A | No |
ClinGen gnomAD |
|
rs202049574 CA402031057 |
310 | T>P | No |
ClinGen gnomAD |
|
CA8898657 rs769480553 |
311 | E>K | No |
ClinGen ExAC TOPMed gnomAD |
|
CA402031033 rs1478967579 |
313 | Y>C | No |
ClinGen gnomAD |
|
CA8898656 rs745424901 |
314 | N>S | No |
ClinGen ExAC gnomAD |
|
rs1269551755 CA402031014 |
316 | N>Y | No |
ClinGen gnomAD |
|
rs1007687769 CA296741380 |
317 | R>I | No |
ClinGen gnomAD |
|
rs1281520282 CA402030999 |
318 | I>K | No |
ClinGen TOPMed gnomAD |
|
rs1190838392 CA402030997 |
318 | I>M | No |
ClinGen TOPMed |
|
rs1281520282 CA402031000 |
318 | I>T | No |
ClinGen TOPMed gnomAD |
|
CA8898653 rs746902207 |
318 | I>V | No |
ClinGen ExAC gnomAD |
|
rs530108359 CA8898651 |
321 | E>K | No |
ClinGen 1000Genomes ExAC gnomAD |
|
rs530108359 CA8898652 |
321 | E>Q | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA8898649 rs749523806 |
327 | G>S | No |
ClinGen ExAC gnomAD |
|
rs1598742182 CA402030930 |
329 | R>* | No |
ClinGen Ensembl |
|
rs370657302 CA8898647 |
329 | R>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA8898646 rs750518471 |
330 | C>S | No |
ClinGen ExAC TOPMed gnomAD |
|
rs781301782 CA8898645 |
331 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1458373462 CA402030908 |
333 | L>V | No |
ClinGen TOPMed |
|
rs148776205 CA8898642 |
338 | Q>E | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs763240651 CA8898641 |
338 | Q>H | No |
ClinGen ExAC gnomAD |
|
CA402030851 rs1189050273 |
341 | M>T | No |
ClinGen TOPMed gnomAD |
|
CA296741338 rs934635618 |
341 | M>V | No |
ClinGen TOPMed |
|
rs764843165 CA8898639 |
343 | E>K | No |
ClinGen ExAC gnomAD |
|
rs1568084999 CA402030819 |
345 | S>T | No |
ClinGen Ensembl |
|
CA401966442 rs1172559636 |
348 | A>V | No |
ClinGen TOPMed |
|
CA401966440 rs1393218349 |
349 | L>V | No |
ClinGen gnomAD |
|
rs558014719 CA8898601 |
350 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
rs779158537 CA8898599 |
352 | R>C | No |
ClinGen ExAC gnomAD |
|
rs1485325592 CA401966397 |
353 | I>M | No |
ClinGen gnomAD |
|
rs376625912 CA296736382 |
353 | I>T | No |
ClinGen ESP TOPMed gnomAD |
|
CA401966391 rs754147924 |
354 | R>L | No |
ClinGen ExAC TOPMed gnomAD |
|
CA8898597 rs754147924 |
354 | R>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1469212865 CA401966380 |
356 | D>N | No |
ClinGen TOPMed gnomAD |
|
rs766193092 CA8898596 |
357 | R>K | No |
ClinGen ExAC TOPMed gnomAD |
|
rs1568075133 CA401966360 |
358 | K>E | No |
ClinGen Ensembl |
|
rs755807202 CA8898595 |
360 | T>A | No |
ClinGen ExAC gnomAD |
|
CA8898594 rs373011018 |
360 | T>S | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
rs767098194 CA8898593 |
361 | T>A | No |
ClinGen ExAC TOPMed gnomAD |
|
rs754659029 CA296736371 |
361 | T>I | No |
ClinGen Ensembl |
|
CA401966322 rs1598727976 |
362 | A>T | No |
ClinGen Ensembl |
|
CA401966308 rs1345870640 |
363 | Q>H | No |
ClinGen TOPMed |
|
CA8898592 rs761682597 |
364 | K>N | No |
ClinGen ExAC TOPMed gnomAD |
|
rs144276145 CA8898591 |
365 | V>M | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
rs775240072 CA8898588 |
370 | Q>K | No |
ClinGen ExAC gnomAD |
|
rs536642089 CA8898586 |
371 | R>G | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs536642089 CA8898587 |
371 | R>W | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
rs1451022700 CA401966188 |
375 | N>S | No |
ClinGen gnomAD |
|
CA8898584 rs753694114 |
377 | R>L | No |
ClinGen ExAC gnomAD |
|
CA296736352 rs753694114 |
377 | R>Q | No |
ClinGen ExAC gnomAD |
|
rs1568074907 CA401966157 |
378 | K>R | No |
ClinGen Ensembl |
|
CA296736349 rs1011286538 |
379 | R>T | No |
ClinGen Ensembl |
|
rs566280122 CA8898583 |
384 | Y>C | No |
ClinGen 1000Genomes ExAC gnomAD |
|
CA8898581 rs368834137 |
385 | W>R | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
CA8898580 rs780534824 |
387 | P>L | No |
ClinGen ExAC gnomAD |
|
CA8898579 rs780534824 |
387 | P>R | No |
ClinGen ExAC gnomAD |
|
rs755863299 CA8898578 |
388 | I>V | No |
ClinGen ExAC TOPMed gnomAD |
|
rs891105715 CA296736338 |
389 | L>F | No |
ClinGen TOPMed gnomAD |
|
CA8898576 rs767151704 |
390 | T>A | No |
ClinGen ExAC gnomAD |
|
rs1450842484 CA401965977 |
392 | M>V | No |
ClinGen TOPMed |
|
rs751031063 CA8898574 |
393 | G>E | No |
ClinGen ExAC gnomAD |
|
rs762765433 CA8898572 |
395 | M>I | No |
ClinGen ExAC gnomAD |
|
CA401965925 rs1168717190 |
395 | M>V | No |
ClinGen TOPMed |
|
CA296736323 rs937020466 |
396 | S>L | No |
ClinGen gnomAD |
|
rs767583744 CA296736320 |
397 | V>I | No |
ClinGen Ensembl |
|
CA8898570 rs764960685 |
400 | V>F | No |
ClinGen ExAC gnomAD |
|
rs1045651503 CA296736308 |
401 | G>A | No |
ClinGen Ensembl |
|
rs74163636 CA296736311 |
401 | G>C | No |
ClinGen gnomAD |
|
CA8898568 COSM986662 rs773354544 |
402 | A>T | endometrium [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
CA8898567 rs374559958 |
403 | F>I | No |
ClinGen ESP ExAC gnomAD |
|
CA401965756 rs1454835324 |
404 | V>F | No |
ClinGen gnomAD |
|
rs748317104 CA8898566 |
406 | W>R | No |
ClinGen ExAC gnomAD |
|
CA401965676 rs1373821237 |
408 | L>Q | No |
ClinGen gnomAD |
|
rs1192755703 CA401965667 |
409 | F>V | No |
ClinGen TOPMed gnomAD |
|
rs769245865 CA8898564 |
410 | F>S | No |
ClinGen ExAC gnomAD |
|
rs1258342176 CA401965599 |
412 | Q>* | No |
ClinGen gnomAD |
|
rs1285450753 CA401965597 |
412 | Q>P | No |
ClinGen Ensembl |
|
CA401965570 rs1568074548 |
413 | N>S | No |
ClinGen Ensembl |
|
rs1342999390 CA401965540 |
414 | A>G | No |
ClinGen gnomAD |
|
rs780589820 CA8898563 |
415 | L>I | No |
ClinGen ExAC gnomAD |
|
CA401965504 rs1278131043 |
416 | L>Y | No |
ClinGen gnomAD |
No associated diseases with P17706
6 regional properties for P17706
Type | Name | Position | InterPro Accession |
---|---|---|---|
domain | DRF autoregulatory | 1027 - 1041 | IPR010465 |
domain | Formin, FH3 domain | 246 - 444 | IPR010472 |
domain | Formin, GTPase-binding domain | 59 - 241 | IPR010473 |
domain | Diaphanous autoregulatory (DAD) domain | 1022 - 1054 | IPR014767 |
domain | Rho GTPase-binding/formin homology 3 (GBD/FH3) domain | 59 - 431 | IPR014768 |
domain | Formin, FH2 domain | 601 - 1044 | IPR015425 |
Functions
Description | ||
---|---|---|
EC Number | 3.1.3.48 | Phosphoric monoester hydrolases |
Subcellular Localization |
|
|
PANTHER Family | PTHR46047 | TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 61F |
PANTHER Subfamily | PTHR46047:SF1 | TYROSINE-PROTEIN PHOSPHATASE NON-RECEPTOR TYPE 2 |
PANTHER Protein Class |
protein phosphatase
protein modifying enzyme |
|
PANTHER Pathway Category | No pathway information available |
6 GO annotations of cellular component
Name | Definition |
---|---|
cytosol | The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes. |
endoplasmic reticulum | The irregular network of unit membranes, visible only by electron microscopy, that occurs in the cytoplasm of many eukaryotic cells. The membranes form a complex meshwork of tubular channels, which are often expanded into slitlike cavities called cisternae. The ER takes two forms, rough (or granular), with ribosomes adhering to the outer surface, and smooth (with no ribosomes attached). |
endoplasmic reticulum-Golgi intermediate compartment | A complex system of membrane-bounded compartments located between endoplasmic reticulum (ER) and the Golgi complex, with a distinctive membrane protein composition; involved in ER-to-Golgi and Golgi-to-ER transport. |
nucleoplasm | That part of the nuclear content other than the chromosomes or the nucleolus. |
nucleus | A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent. |
plasma membrane | The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins. |
6 GO annotations of molecular function
Name | Definition |
---|---|
integrin binding | Binding to an integrin. |
protein kinase binding | Binding to a protein kinase, any enzyme that catalyzes the transfer of a phosphate group, usually from ATP, to a protein substrate. |
protein tyrosine phosphatase activity | Catalysis of the reaction: protein tyrosine phosphate + H2O = protein tyrosine + phosphate. |
receptor tyrosine kinase binding | Binding to a receptor that possesses protein tyrosine kinase activity. |
STAT family protein binding | Binding to a member of the signal transducers and activators of transcription (STAT) protein family. STATs are, as the name indicates, both signal transducers and transcription factors. STATs are activated by cytokines and some growth factors and thus control important biological processes including cell growth, cell differentiation, apoptosis and immune responses. |
syntaxin binding | Binding to a syntaxin, a SNAP receptor involved in the docking of synaptic vesicles at the presynaptic zone of a synapse. |
32 GO annotations of biological process
Name | Definition |
---|---|
B cell differentiation | The process in which a precursor cell type acquires the specialized features of a B cell. A B cell is a lymphocyte of B lineage with the phenotype CD19-positive and capable of B cell mediated immunity. |
erythrocyte differentiation | The process in which a myeloid precursor cell acquires specializes features of an erythrocyte. |
glucose homeostasis | Any process involved in the maintenance of an internal steady state of glucose within an organism or cell. |
insulin receptor signaling pathway | The series of molecular signals generated as a consequence of the insulin receptor binding to insulin. |
negative regulation of cell population proliferation | Any process that stops, prevents or reduces the rate or extent of cell proliferation. |
negative regulation of chemotaxis | Any process that stops, prevents, or reduces the frequency, rate or extent of the directed movement of a motile cell or organism in response to a specific chemical concentration gradient. |
negative regulation of epidermal growth factor receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of epidermal growth factor receptor signaling pathway activity. |
negative regulation of ERK1 and ERK2 cascade | Any process that stops, prevents, or reduces the frequency, rate or extent of signal transduction mediated by the ERK1 and ERK2 cascade. |
negative regulation of inflammatory response | Any process that stops, prevents, or reduces the frequency, rate or extent of the inflammatory response. |
negative regulation of insulin receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of insulin receptor signaling. |
negative regulation of interferon-gamma-mediated signaling pathway | Any process that decreases the rate, frequency or extent of an interferon-gamma-mediated signaling pathway. |
negative regulation of interleukin-2-mediated signaling pathway | Any process that stops, prevents or reduces the frequency, rate or extent of interleukin-2-mediated signaling pathway. |
negative regulation of interleukin-4-mediated signaling pathway | Any process that stops, prevents or reduces the frequency, rate or extent of interleukin-4-mediated signaling pathway. |
negative regulation of interleukin-6-mediated signaling pathway | Any process that decreases the rate, frequency or extent of an interleukin-6-mediated signaling pathway. |
negative regulation of lipid storage | Any process that decreases the rate, frequency or extent of lipid storage. Lipid storage is the accumulation and maintenance in cells or tissues of lipids, compounds soluble in organic solvents but insoluble or sparingly soluble in aqueous solvents. Lipid reserves can be accumulated during early developmental stages for mobilization and utilization at later stages of development. |
negative regulation of macrophage colony-stimulating factor signaling pathway | Any process that stops, prevents or reduces the frequency, rate or extent of macrophage colony-stimulating factor signaling pathway. |
negative regulation of macrophage differentiation | Any process that stops, prevents, or reduces the frequency, rate or extent of macrophage differentiation. |
negative regulation of platelet-derived growth factor receptor-beta signaling pathway | Any process that stops, prevents or reduces the frequency, rate or extent of platelet-derived growth factor receptor-beta signaling pathway. |
negative regulation of positive thymic T cell selection | Any process that stops, prevents or reduces the frequency, rate or extent of positive thymic T cell selection. |
negative regulation of protein tyrosine kinase activity | Any process that decreases the rate, frequency, or extent of protein tyrosine kinase activity. |
negative regulation of T cell receptor signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of signaling pathways initiated by the cross-linking of an antigen receptor on a T cell. |
negative regulation of transcription by RNA polymerase II | Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II. |
negative regulation of tumor necrosis factor-mediated signaling pathway | Any process that decreases the rate or extent of the tumor necrosis factor-mediated signaling pathway. The tumor necrosis factor-mediated signaling pathway is the series of molecular signals generated as a consequence of tumor necrosis factor binding to a cell surface receptor. |
negative regulation of type I interferon-mediated signaling pathway | Any process that decreases the rate, frequency or extent of a type I interferon-mediated signaling pathway. |
negative regulation of tyrosine phosphorylation of STAT protein | Any process that stops, prevents, or reduces the frequency, rate or extent of the introduction of a phosphate group to a tyrosine residue of a STAT (Signal Transducer and Activator of Transcription) protein. |
peptidyl-tyrosine dephosphorylation | The removal of phosphoric residues from peptidyl-O-phospho-tyrosine to form peptidyl-tyrosine. |
positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway | Any process that activates or increases the frequency, rate or extent of an endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway. |
positive regulation of gluconeogenesis | Any process that activates or increases the frequency, rate or extent of gluconeogenesis. |
positive regulation of PERK-mediated unfolded protein response | Any process that activates or increases the frequency, rate or extent of the PERK-mediated unfolded protein response. |
regulation of hepatocyte growth factor receptor signaling pathway | Any process that modulates the frequency, rate or extent of hepatocyte growth factor receptor signaling pathway. |
regulation of interferon-gamma-mediated signaling pathway | Any process that modulates the rate, frequency or extent of an interferon-gamma-mediated signaling pathway. |
T cell differentiation | The process in which a precursor cell type acquires characteristics of a more mature T-cell. A T cell is a type of lymphocyte whose definin characteristic is the expression of a T cell receptor complex. |
6 homologous proteins in AiPD
UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
---|---|---|---|---|
P18031 | PTPN1 | Tyrosine-protein phosphatase non-receptor type 1 | Homo sapiens (Human) | PR |
P35821 | Ptpn1 | Tyrosine-protein phosphatase non-receptor type 1 | Mus musculus (Mouse) | PR |
Q06180 | Ptpn2 | Tyrosine-protein phosphatase non-receptor type 2 | Mus musculus (Mouse) | SS |
P20417 | Ptpn1 | Tyrosine-protein phosphatase non-receptor type 1 | Rattus norvegicus (Rat) | PR |
A1L1L3 | Ptpn20 | Tyrosine-protein phosphatase non-receptor type 20 | Rattus norvegicus (Rat) | PR |
P35233 | Ptpn2 | Tyrosine-protein phosphatase non-receptor type 2 | Rattus norvegicus (Rat) | SS |
10 | 20 | 30 | 40 | 50 | 60 |
MPTTIEREFE | ELDTQRRWQP | LYLEIRNESH | DYPHRVAKFP | ENRNRNRYRD | VSPYDHSRVK |
70 | 80 | 90 | 100 | 110 | 120 |
LQNAENDYIN | ASLVDIEEAQ | RSYILTQGPL | PNTCCHFWLM | VWQQKTKAVV | MLNRIVEKES |
130 | 140 | 150 | 160 | 170 | 180 |
VKCAQYWPTD | DQEMLFKETG | FSVKLLSEDV | KSYYTVHLLQ | LENINSGETR | TISHFHYTTW |
190 | 200 | 210 | 220 | 230 | 240 |
PDFGVPESPA | SFLNFLFKVR | ESGSLNPDHG | PAVIHCSAGI | GRSGTFSLVD | TCLVLMEKGD |
250 | 260 | 270 | 280 | 290 | 300 |
DINIKQVLLN | MRKYRMGLIQ | TPDQLRFSYM | AIIEGAKCIK | GDSSIQKRWK | ELSKEDLSPA |
310 | 320 | 330 | 340 | 350 | 360 |
FDHSPNKIMT | EKYNGNRIGL | EEEKLTGDRC | TGLSSKMQDT | MEENSESALR | KRIREDRKAT |
370 | 380 | 390 | 400 | 410 | |
TAQKVQQMKQ | RLNENERKRK | RWLYWQPILT | KMGFMSVILV | GAFVGWTLFF | QQNAL |