Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

2 structures for Q03014

Entry ID Method Resolution Chain Position Source
2E1O NMR - A 138-194 PDB
AF-Q03014-F1 Predicted AlphaFoldDB

219 variants for Q03014

Variant ID(s) Position Change Description Diseaes Association Provenance
CA212069963
rs890175536
2 Q>R No ClinGen
TOPMed
rs1564728388
CA377810847
4 P>L No ClinGen
Ensembl
CA377810842
rs1455869041
4 P>S No ClinGen
gnomAD
CA377810851
rs1589621587
5 H>P No ClinGen
Ensembl
CA212069965
rs1014685241
6 P>R No ClinGen
TOPMed
CA377810863
rs1190097525
7 G>R No ClinGen
TOPMed
CA212069967
rs546230628
8 P>L No ClinGen
1000Genomes
gnomAD
rs546230628
CA377810870
8 P>Q No ClinGen
1000Genomes
gnomAD
rs1231813088
CA377810883
10 A>V No ClinGen
gnomAD
rs1183185221
CA377810889
11 G>A No ClinGen
gnomAD
rs1423720818
CA377810890
12 A>T No ClinGen
gnomAD
CA377810898
rs1355791757
13 V>L No ClinGen
gnomAD
CA377810896
rs1355791757
13 V>M No ClinGen
gnomAD
CA377810904
rs1168959334
CA377810903
14 G>R No ClinGen
gnomAD
TCGA novel
rs748494650
CA5604578
15 V>G Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
gnomAD
NCI-TCGA
CA212069968
rs973237946
15 V>L No ClinGen
TOPMed
CA377810915
rs1335185921
16 P>L No ClinGen
gnomAD
rs1335185921
CA377810917
16 P>Q No ClinGen
gnomAD
CA212069970
rs867687942
19 A>E No ClinGen
Ensembl
rs867687942
CA377810935
19 A>G No ClinGen
Ensembl
rs1218689152
CA377810932
19 A>P No ClinGen
TOPMed
rs1218689152
CA377810931
19 A>T No ClinGen
TOPMed
rs1245578903
CA377810941
20 P>L No ClinGen
gnomAD
rs1194519827
CA377810948
22 P>T No ClinGen
gnomAD
CA377810967
rs1470860448
25 Q>P No ClinGen
TOPMed
rs749396288
CA5604581
26 P>A No ClinGen
ExAC
gnomAD
rs917914135
CA212069973
26 P>R No ClinGen
TOPMed
gnomAD
CA377810978
rs1240771743
27 A>T No ClinGen
gnomAD
CA377810995
rs1188874146
29 P>L No ClinGen
TOPMed
gnomAD
CA377810994
rs1188874146
29 P>R No ClinGen
TOPMed
gnomAD
CA377810999
rs1295181822
30 T>K No ClinGen
TOPMed
gnomAD
CA377811001
rs1295181822
30 T>M No ClinGen
TOPMed
gnomAD
CA377811002
rs1391782171
31 P>T No ClinGen
gnomAD
rs949426439
CA212069974
33 Y>C No ClinGen
TOPMed
CA377811017
rs1474310402
33 Y>H No ClinGen
gnomAD
TCGA novel 33 Y>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA5604582
rs770977782
34 I>M No ClinGen
ExAC
gnomAD
rs1156313218
CA377811036
35 E>D No ClinGen
TOPMed
CA212069975
rs943618846
36 D>N No ClinGen
gnomAD
rs1184570903
CA377811071
41 G>E No ClinGen
TOPMed
CA377811078
rs1338751519
42 P>L No ClinGen
TOPMed
gnomAD
CA5604586
rs771793065
44 A>V No ClinGen
ExAC
TOPMed
gnomAD
rs1298618123
CA377811096
45 P>L No ClinGen
gnomAD
CA5604587
rs775302104
48 A>T No ClinGen
ExAC
TOPMed
gnomAD
CA377811111
rs1253856328
48 A>V No ClinGen
gnomAD
CA5604588
rs760441003
50 T>K No ClinGen
ExAC
TOPMed
gnomAD
TCGA novel 50 T>R Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1208900235
CA377811134
52 P>L No ClinGen
TOPMed
gnomAD
rs1208900235
CA377811133
52 P>Q No ClinGen
TOPMed
gnomAD
rs776542212
CA5604590
53 S>F No ClinGen
ExAC
gnomAD
rs932231605
CA212069978
54 P>L No ClinGen
TOPMed
gnomAD
CA377811150
rs1170180635
55 N>S No ClinGen
TOPMed
gnomAD
rs1418617550
CA377811165
57 S>F No ClinGen
TOPMed
rs764744029
CA5604592
59 T>I No ClinGen
ExAC
TOPMed
gnomAD
rs1427205880
CA377811182
60 S>N No ClinGen
gnomAD
rs750063118
CA377811194
CA5604593
62 V>L No ClinGen
ExAC
TOPMed
gnomAD
CA377811203
rs1321412297
63 S>F No ClinGen
gnomAD
CA5604596
rs142036619
64 P>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5604597
rs142036619
64 P>L No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5604598
rs142036619
64 P>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs766112006
CA5604595
64 P>S No ClinGen
ExAC
gnomAD
CA377811211
rs1244380185
65 Y>F No ClinGen
TOPMed
CA377811207
rs1332097827
65 Y>H No ClinGen
gnomAD
CA377811214
rs1225884461
66 R>G No ClinGen
gnomAD
CA212069982
rs868255183
66 R>Q No ClinGen
gnomAD
rs754315134
CA212069983
67 T>A No ClinGen
ExAC
TOPMed
gnomAD
rs757308946
CA5604600
67 T>I No ClinGen
ExAC
TOPMed
gnomAD
CA5604599
rs754315134
67 T>S No ClinGen
ExAC
TOPMed
gnomAD
rs757308946
CA377811220
67 T>S No ClinGen
ExAC
TOPMed
gnomAD
CA5604603
rs745904454
68 P>L No ClinGen
ExAC
gnomAD
CA5604602
rs745904454
68 P>R No ClinGen
ExAC
gnomAD
CA377811233
rs1204238532
70 Y>D No ClinGen
gnomAD
rs780241760
CA5604604
71 E>G No ClinGen
ExAC
gnomAD
rs746868626
CA5604605
72 P>H No ClinGen
ExAC
gnomAD
rs1442714190
CA377811256
73 T>M No ClinGen
gnomAD
TCGA novel 75 I>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1589621770
CA377811275
76 H>P No ClinGen
Ensembl
rs1248379400
CA377811289
78 A>V No ClinGen
TOPMed
TCGA novel 79 F>L Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA377811303
rs1320151050
80 S>L No ClinGen
TOPMed
rs1480129873
CA377811309
81 H>P No ClinGen
gnomAD
CA377811311
rs1589621781
81 H>Q No ClinGen
Ensembl
CA377811317
rs1159967487
82 H>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA377811325
rs1365657343
83 S>F No ClinGen
gnomAD
rs1451879808
CA377811326
84 A>T No ClinGen
gnomAD
rs1391826173
CA377811334
85 A>T No ClinGen
gnomAD
TCGA novel 86 A>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs769590079
CA377811350
88 A>S No ClinGen
ExAC
gnomAD
CA5604609
rs769590079
88 A>T No ClinGen
ExAC
gnomAD
CA377811357
rs1345400029
89 A>V No ClinGen
gnomAD
CA377811364
rs1418387
90 A>G No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1418387
CA5604610
90 A>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA377811369
rs1308497933
91 Y>C No ClinGen
gnomAD
CA212069989
rs867605493
COSM1741957
92 G>R Variant assessed as Somatic; 0.0 impact. urinary_tract [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs751190903
CA5604613
93 P>S No ClinGen
ExAC
TOPMed
gnomAD
rs867066260
CA212069990
94 G>S No ClinGen
Ensembl
rs1290819766
CA377811390
95 G>C No ClinGen
gnomAD
CA377811391
rs1483331825
95 G>D No ClinGen
gnomAD
CA377811403
rs1348962571
97 G>R No ClinGen
TOPMed
rs370000570
CA212069991
99 P>L No ClinGen
ESP
TOPMed
gnomAD
rs754334398
CA5604616
99 P>T No ClinGen
ExAC
gnomAD
CA377811419
rs1386125639
100 L>V No ClinGen
gnomAD
CA377811428
rs1422263508
101 Y>S No ClinGen
TOPMed
rs1426832512
CA377811436
102 P>L No ClinGen
TOPMed
gnomAD
rs1192192366
CA377811433
102 P>S No ClinGen
TOPMed
CA377811450
rs1365407216
104 P>Q No ClinGen
gnomAD
CA377811447
rs1162031192
104 P>S No ClinGen
TOPMed
gnomAD
CA377811461
rs1430945151
106 T>M No ClinGen
gnomAD
rs779264732
CA5604618
107 V>M No ClinGen
ExAC
gnomAD
CA212069992
rs994627049
109 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA212069993
rs1026326163
113 A>S No ClinGen
gnomAD
CA5604620
rs540724252
113 A>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA5604622
rs747172564
115 L>F No ClinGen
ExAC
TOPMed
gnomAD
CA212069994
rs993173166
116 R>C No ClinGen
TOPMed
gnomAD
rs1206459587
CA377811521
116 R>P No ClinGen
TOPMed
gnomAD
rs1024947210
CA377811527
117 H>L No ClinGen
TOPMed
gnomAD
CA212069995
rs1024947210
117 H>P No ClinGen
TOPMed
gnomAD
CA377811536
rs987560198
CA212069996
118 D>E No ClinGen
TOPMed
gnomAD
CA377811542
rs1243872043
119 P>L No ClinGen
gnomAD
CA377811546
rs1298456522
120 L>P No ClinGen
TOPMed
rs1384927212
CA377811548
121 G>S No ClinGen
gnomAD
CA5604633
rs777102021
123 P>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs762070983
CA5604634
124 L>P No ClinGen
ExAC
gnomAD
CA5604635
rs765838543
128 P>L No ClinGen
ExAC
gnomAD
rs1413060810
CA377811609
128 P>S No ClinGen
TOPMed
CA5604636
rs750824236
129 F>L No ClinGen
ExAC
gnomAD
rs1325695460
CA377811627
131 Q>E No ClinGen
gnomAD
rs538680375
CA5604637
132 R>K No ClinGen
1000Genomes
ExAC
gnomAD
CA5604638
rs150804177
133 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA377811652
rs1564729118
135 H>Y No ClinGen
Ensembl
rs1240715324
CA377811668
137 R>K No ClinGen
TOPMed
gnomAD
rs1200714119
CA377811714
144 F>I No ClinGen
gnomAD
CA377811727
rs1271715312
145 S>C No ClinGen
gnomAD
CA377811735
rs1293929865
146 N>K No ClinGen
gnomAD
rs781261088
CA5604642
147 D>E No ClinGen
ExAC
TOPMed
gnomAD
rs867064568
CA212070245
147 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
rs571252950
CA5604643
148 Q>* No ClinGen
1000Genomes
ExAC
gnomAD
rs777779960
CA5604645
150 I>V No ClinGen
ExAC
gnomAD
rs751797640
CA5604648
151 E>D No ClinGen
ExAC
TOPMed
gnomAD
CA5604647
rs770598208
151 E>Q No ClinGen
ExAC
gnomAD
rs745348021
TCGA novel
CA5604649
154 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
gnomAD
NCI-TCGA
rs1458326195
CA377811786
154 K>T No ClinGen
TOPMed
CA377811791
rs1343529616
155 K>E No ClinGen
gnomAD
rs1274323168
CA377811809
157 E>G No ClinGen
gnomAD
rs771813965
CA5604650
157 E>K No ClinGen
ExAC
gnomAD
rs765458169
CA5604653
159 Q>R No ClinGen
ExAC
TOPMed
gnomAD
CA377811838
rs1162165582
161 Y>C No ClinGen
TOPMed
CA377811851
rs1223732746
163 S>Y No ClinGen
gnomAD
rs755049912
CA5604658
165 P>L No ClinGen
ExAC
gnomAD
rs751698879
CA5604657
165 P>S No ClinGen
ExAC
gnomAD
TCGA novel 168 K>M Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA5604660
rs752804342
168 K>R No ClinGen
ExAC
gnomAD
CA212070246
rs17851141
171 A>T No ClinGen
Ensembl
CA5604661
rs755960214
173 M>R No ClinGen
ExAC
gnomAD
CA5604662
rs777393392
175 Q>H No ClinGen
ExAC
gnomAD
CA377811936
rs1292554684
177 S>R No ClinGen
Ensembl
rs753656580
CA5604663
178 E>G No ClinGen
ExAC
gnomAD
CA212070247
rs979370507
178 E>Q No ClinGen
Ensembl
TCGA novel 188 R>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 193 R>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
TCGA novel 197 Q>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs749658938
CA5604691
197 Q>H No ClinGen
ExAC
gnomAD
CA377812110
rs1589623553
198 E>K No ClinGen
Ensembl
rs1465729223
CA377812124
199 N>K No ClinGen
TOPMed
gnomAD
CA377812127
rs780836792
200 P>S No ClinGen
ExAC
TOPMed
gnomAD
CA5604707
rs780836792
200 P>T No ClinGen
ExAC
TOPMed
gnomAD
rs139182180
CA5604708
202 S>N No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA5604709
rs757653686
203 N>S No ClinGen
ExAC
gnomAD
rs757653686
CA5604710
203 N>T No ClinGen
ExAC
gnomAD
TCGA novel 206 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs770553856 207 E>missing Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
rs1300666221
CA377812178
207 E>Q No ClinGen
TOPMed
rs1224472544
CA377812181
207 E>V No ClinGen
TOPMed
rs746224197
CA5604712
208 L>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1280797145
CA377812188
209 E>* No ClinGen
TOPMed
gnomAD
rs1330004120
CA377812192
209 E>G No ClinGen
gnomAD
rs1280797145
CA377812189
209 E>Q No ClinGen
TOPMed
gnomAD
rs1348222290
CA377812207
211 L>S No ClinGen
gnomAD
rs1375795368
CA377812223
213 S>I No ClinGen
TOPMed
rs1375795368
CA377812221
213 S>N No ClinGen
TOPMed
rs747061001
CA5604716
213 S>R No ClinGen
ExAC
gnomAD
CA5604717
rs149951495
214 S>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs777011688
CA5604718
215 C>S No ClinGen
ExAC
gnomAD
rs1301655370
CA377812240
216 D>Y No ClinGen
gnomAD
rs1347616290
CA377812271
220 D>Y No ClinGen
gnomAD
rs1159187572
CA377812283
221 L>F No ClinGen
TOPMed
CA5604719
rs762086181
223 S>G No ClinGen
ExAC
TOPMed
gnomAD
rs1365794476
CA377812318
225 Q>H No ClinGen
gnomAD
rs1468837966
CA377812363
228 G>D No ClinGen
TOPMed
gnomAD
rs909818705
CA212070418
228 G>S No ClinGen
Ensembl
rs939992398
CA212070419
229 A>T No ClinGen
Ensembl
rs775389812
CA212070420
230 S>A No ClinGen
Ensembl
rs1366647435
CA377812403
231 L>S No ClinGen
gnomAD
rs772927960
CA5604721
232 D>N No ClinGen
ExAC
TOPMed
gnomAD
rs772927960
CA377812415
232 D>Y No ClinGen
ExAC
TOPMed
gnomAD
rs762793686
CA5604722
233 S>I No ClinGen
ExAC
gnomAD
CA5604725
RCV000950750
rs184882393
234 S>C No ClinGen
ClinVar
1000Genomes
ExAC
TOPMed
dbSNP
gnomAD
rs751457715
CA5604724
234 S>P No ClinGen
ExAC
gnomAD
rs755816063
CA5604728
236 C>Y No ClinGen
ExAC
TOPMed
gnomAD
CA5604729
rs777471219
237 S>L No ClinGen
ExAC
TOPMed
gnomAD
CA212070421
rs201876873
238 P>L No ClinGen
Ensembl
CA377812535
rs1264817116
240 P>S No ClinGen
gnomAD
CA377812552
rs1488175634
241 A>V No ClinGen
gnomAD
rs758719291
CA5604731
243 Q>* No ClinGen
ExAC
gnomAD
rs1252818021
CA377812578
243 Q>L No ClinGen
gnomAD
rs1217153454
CA377812595
244 E>G No ClinGen
TOPMed
rs780435092
CA5604732
246 L>I No ClinGen
ExAC
gnomAD
rs200052261
COSM921488
CA5604733
249 E>D Variant assessed as Somatic; 0.0 impact. liver endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs1386188015
CA377812670
250 I>M No ClinGen
gnomAD
rs1286564454
CA377812711
256 Q>R No ClinGen
TOPMed
TCGA novel 259 D>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1227981903
CA377812741
260 I>T No ClinGen
TOPMed
CA377812763
rs1368365223
263 D>G No ClinGen
gnomAD
CA5604736
rs374722314
264 K>E No ClinGen
ESP
ExAC
TOPMed
gnomAD
TCGA novel 264 K>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs368062383
CA212070422
265 S>R No ClinGen
ESP
rs1394138052
COSM3978903
CA377812800
268 N>S lung [Cosmic] No ClinGen
cosmic curated
TOPMed
rs773419319
CA5604738
271 G>L No ClinGen
ExAC
TOPMed
gnomAD
rs1445495335
CA377812817
271 G>R No ClinGen
gnomAD

No associated diseases with Q03014

4 regional properties for Q03014

Type Name Position InterPro Accession
domain Homeobox domain 135 - 199 IPR001356
conserved_site Homeobox, conserved site 170 - 193 IPR017970
domain Homeobox domain, metazoa 159 - 170 IPR020479-1
domain Homeobox domain, metazoa 174 - 193 IPR020479-2

Functions

Description
EC Number
Subcellular Localization
  • Nucleus
  • Nucleus, nuclear body
  • Cytoplasm
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

4 GO annotations of cellular component

Name Definition
chromatin The ordered and organized complex of DNA, protein, and sometimes RNA, that forms the chromosome.
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
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.
protein-DNA complex A macromolecular complex containing both protein and DNA molecules.

11 GO annotations of molecular function

Name Definition
DNA binding, bending The activity of binding selectively and non-covalently to and distorting the original structure of DNA, typically a straight helix, into a bend, or increasing the bend if the original structure was intrinsically bent due to its sequence.
DNA-binding transcription activator activity, RNA polymerase II-specific A DNA-binding transcription factor activity that activates or increases transcription of specific gene sets transcribed by RNA polymerase II.
DNA-binding transcription factor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that modulates the transcription of specific gene sets transcribed by RNA polymerase II.
DNA-binding transcription factor binding Binding to a DNA-binding transcription factor, a protein that interacts with a specific DNA sequence (sometimes referred to as a motif) within the regulatory region of a gene to modulate transcription.
DNA-binding transcription repressor activity, RNA polymerase II-specific A DNA-binding transcription factor activity that represses or decreases the transcription of specific gene sets transcribed by RNA polymerase II.
eukaryotic initiation factor 4E binding Binding to eukaryotic initiation factor 4E, a polypeptide factor involved in the initiation of ribosome-mediated translation.
protein homodimerization activity Binding to an identical protein to form a homodimer.
RNA polymerase II cis-regulatory region sequence-specific DNA binding Binding to a specific upstream regulatory DNA sequence (transcription factor recognition sequence or binding site) located in cis relative to the transcription start site (i.e., on the same strand of DNA) of a gene transcribed by RNA polymerase II.
sequence-specific DNA binding Binding to DNA of a specific nucleotide composition, e.g. GC-rich DNA binding, or with a specific sequence motif or type of DNA e.g. promotor binding or rDNA binding.
TBP-class protein binding Binding to a member of the class of TATA-binding proteins (TBP), including any of the TBP-related factors (TRFs).
transcription cis-regulatory region binding Binding to a specific sequence of DNA that is part of a regulatory region that controls transcription of that section of the DNA. The transcribed region might be described as a gene, cistron, or operon.

21 GO annotations of biological process

Name Definition
anterior/posterior pattern specification The regionalization process in which specific areas of cell differentiation are determined along the anterior-posterior axis. The anterior-posterior axis is defined by a line that runs from the head or mouth of an organism to the tail or opposite end of the organism.
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.
cell differentiation The process in which relatively unspecialized cells, e.g. embryonic or regenerative cells, acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism's life history. Differentiation includes the processes involved in commitment of a cell to a specific fate and its subsequent development to the mature state.
DNA conformation change A cellular process that results in a change in the spatial configuration of a DNA molecule. A conformation change can bend DNA, or alter the, twist, writhe, or linking number of a DNA molecule.
mRNA export from nucleus The directed movement of mRNA from the nucleus to the cytoplasm.
negative regulation of angiogenesis Any process that stops, prevents, or reduces the frequency, rate or extent of angiogenesis.
negative regulation of cyclin-dependent protein serine/threonine kinase activity Any process that stops, prevents, or reduces the frequency, rate or extent of cyclin-dependent protein serine/threonine kinase activity.
negative regulation of DNA-templated transcription Any process that stops, prevents, or reduces the frequency, rate or extent of cellular DNA-templated transcription.
negative regulation of transcription by competitive promoter binding Any process that stops, prevents, or reduces the frequency, rate or extent of DNA-dependent transcription using a mechanism that involves direct competition for interaction with a promoter binding site.
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 transcription by transcription factor localization Any process that stops, prevents, or reduces the frequency, rate or extent of DNA-dependent transcription using a mechanism that involves the localization of a transcription factor.
negative regulation of vascular endothelial growth factor receptor signaling pathway Any process that stops, prevents, or reduces the frequency, rate or extent of vascular endothelial growth factor receptor signaling pathway activity.
poly(A)+ mRNA export from nucleus The directed movement of poly(A)+ mRNA out of the nucleus into the cytoplasm.
positive regulation of canonical Wnt signaling pathway Any process that increases the rate, frequency, or extent of the Wnt signaling pathway through beta-catenin, the series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell, followed by propagation of the signal via beta-catenin, and ending with a change in transcription of target genes.
positive regulation of DNA-templated transcription Any process that activates or increases the frequency, rate or extent of cellular DNA-templated transcription.
positive regulation of transcription by RNA polymerase II Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter.
positive regulation of Wnt signaling pathway Any process that activates or increases the frequency, rate or extent of Wnt signal transduction.
protein localization to nucleus A process in which a protein transports or maintains the localization of another protein to the nucleus.
regulation of leukocyte proliferation Any process that modulates the frequency, rate or extent of leukocyte proliferation.
regulation of transcription by RNA polymerase II Any process that modulates the frequency, rate or extent of transcription mediated by RNA polymerase II.
Wnt signaling pathway The series of molecular signals initiated by binding of a Wnt protein to a frizzled family receptor on the surface of the target cell and ending with a change in cell state.

8 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q6H6S3 HOX24 Homeobox-leucine zipper protein HOX24 Oryza sativa subsp japonica (Rice) PR
Q7XUJ5 HOX22 Homeobox-leucine zipper protein HOX22 Oryza sativa subsp japonica (Rice) PR
Q5VPE5 HOX28 Homeobox-leucine zipper protein HOX28 Oryza sativa subsp japonica (Rice) PR
A3BYC1 HOX25 Homeobox-leucine zipper protein HOX25 Oryza sativa subsp japonica (Rice) PR
P46603 HAT9 Homeobox-leucine zipper protein HAT9 Arabidopsis thaliana (Mouse-ear cress) PR
Q9FN29 ATHB-52 Homeobox-leucine zipper protein ATHB-52 Arabidopsis thaliana (Mouse-ear cress) PR
Q9M276 ATHB-12 Homeobox-leucine zipper protein ATHB-12 Arabidopsis thaliana (Mouse-ear cress) PR
Q9IAV3 hhex Hematopoietically-expressed homeobox protein hhex Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MQYPHPGPAA GAVGVPLYAP TPLLQPAHPT PFYIEDILGR GPAAPTPAPT LPSPNSSFTS
70 80 90 100 110 120
LVSPYRTPVY EPTPIHPAFS HHSAAALAAA YGPGGFGGPL YPFPRTVNDY THALLRHDPL
130 140 150 160 170 180
GKPLLWSPFL QRPLHKRKGG QVRFSNDQTI ELEKKFETQK YLSPPERKRL AKMLQLSERQ
190 200 210 220 230 240
VKTWFQNRRA KWRRLKQENP QSNKKEELES LDSSCDQRQD LPSEQNKGAS LDSSQCSPSP
250 260
ASQEDLESEI SEDSDQEVDI EGDKSYFNAG