TAF12 (TATA-box binding protein associated factor 12) - Rat Genome Database
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Gene: TAF12 (TATA-box binding protein associated factor 12) Homo sapiens
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Symbol: TAF12
Name: TATA-box binding protein associated factor 12
RGD ID: 1348553
Description: Exhibits DNA binding activity; transcription coactivator activity; and transcription factor binding activity. Contributes to RNA polymerase II general transcription initiation factor activity and histone acetyltransferase activity. Involved in histone H3 acetylation; positive regulation of DNA-binding transcription factor activity; and transcription initiation from RNA polymerase II promoter. Localizes to nucleoplasm.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 20kDa; TAF2J; TAFII-20/TAFII-15; TAFII20; TAFII20/TAFII15; TATA box binding protein (TBP)-associated factor, RNA polymerase II, J, 20kD; TATA box binding protein associated factor 12; transcription initiation factor TFIID 20/15 kDa subunits; transcription initiation factor TFIID subunit 12
Orthologs:
Mus musculus (house mouse) : Taf12 (TATA-box binding protein associated factor 12)  MGI  Alliance
Rattus norvegicus (Norway rat) : Taf12 (TATA-box binding protein associated factor 12)  Alliance
Pan paniscus (bonobo/pygmy chimpanzee) : TAF12 (TATA-box binding protein associated factor 12)
Canis lupus familiaris (dog) : TAF12 (TATA-box binding protein associated factor 12)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Taf12 (TATA-box binding protein associated factor 12)
Sus scrofa (pig) : TAF12 (TATA-box binding protein associated factor 12)
Chlorocebus sabaeus (African green monkey) : TAF12 (TATA-box binding protein associated factor 12)
Heterocephalus glaber (naked mole-rat) : Taf12 (TATA-box binding protein associated factor 12)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl128,589,323 - 28,643,085 (-)EnsemblGRCh38hg38GRCh38
GRCh38128,602,850 - 28,648,707 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37128,929,608 - 28,975,416 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36128,802,200 - 28,842,172 (-)NCBINCBI36hg18NCBI36
Build 34128,750,228 - 28,790,201NCBI
Celera127,325,365 - 27,365,501 (-)NCBI
Cytogenetic Map1p35.3NCBI
HuRef127,182,618 - 27,222,688 (-)NCBIHuRef
CHM1_1129,045,214 - 29,085,178 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:1939271   PMID:2449431   PMID:7667268   PMID:7729427   PMID:7835343   PMID:7836461   PMID:7933101   PMID:8121496   PMID:8598932   PMID:8647459   PMID:8663456   PMID:8680883  
PMID:8764009   PMID:8764062   PMID:8849451   PMID:8889548   PMID:8946909   PMID:9045704   PMID:9054383   PMID:9133630   PMID:9311784   PMID:9405375   PMID:9603525   PMID:9674425  
PMID:9885574   PMID:10594036   PMID:11406595   PMID:11438666   PMID:11564863   PMID:11564872   PMID:11689552   PMID:12237304   PMID:12477932   PMID:12601814   PMID:12660246   PMID:14580349  
PMID:15489334   PMID:15601843   PMID:15637059   PMID:15735663   PMID:15932940   PMID:16494529   PMID:16710414   PMID:17158164   PMID:17264123   PMID:17268553   PMID:17884155   PMID:17967894  
PMID:18029348   PMID:18838386   PMID:19114550   PMID:19240132   PMID:19322201   PMID:19635797   PMID:20850016   PMID:21873635   PMID:22323595   PMID:23426901   PMID:25416956   PMID:25965574  
PMID:26186194   PMID:26496610   PMID:26638075   PMID:26673895   PMID:27551064   PMID:27601583   PMID:27703004   PMID:28514442   PMID:29111974   PMID:29316427   PMID:29509190   PMID:30415952  
PMID:30804502   PMID:31753913   PMID:32296183  


Genomics

Comparative Map Data
TAF12
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl128,589,323 - 28,643,085 (-)EnsemblGRCh38hg38GRCh38
GRCh38128,602,850 - 28,648,707 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37128,929,608 - 28,975,416 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36128,802,200 - 28,842,172 (-)NCBINCBI36hg18NCBI36
Build 34128,750,228 - 28,790,201NCBI
Celera127,325,365 - 27,365,501 (-)NCBI
Cytogenetic Map1p35.3NCBI
HuRef127,182,618 - 27,222,688 (-)NCBIHuRef
CHM1_1129,045,214 - 29,085,178 (-)NCBICHM1_1
Taf12
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394132,001,667 - 132,020,640 (+)NCBI
GRCm384132,274,355 - 132,293,329 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4132,274,375 - 132,295,766 (+)EnsemblGRCm38mm10GRCm38
MGSCv374131,830,290 - 131,849,244 (+)NCBIGRCm37mm9NCBIm37
MGSCv364131,546,489 - 131,565,403 (+)NCBImm8
Celera4130,435,455 - 130,454,533 (+)NCBICelera
Cytogenetic Map4D2.3NCBI
Taf12
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.05150,459,701 - 150,476,521 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5150,459,713 - 150,475,186 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05154,126,851 - 154,143,964 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera5142,905,400 - 142,920,328 (+)NCBICelera
Cytogenetic Map5q36NCBI
TAF12
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1128,907,540 - 28,948,322 (-)NCBIpanpan1.1PanPan1.1panPan2
Mhudiblu_PPA_v0127,874,675 - 27,914,672 (-)NCBIMhudiblu_PPA_v0panPan3
TAF12
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1 Ensembl271,865,289 - 71,898,236 (+)EnsemblCanFam3.1canFam3CanFam3.1
CanFam3.1271,865,274 - 71,898,236 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Taf12
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
SpeTri2.0NW_00493647412,695,508 - 12,719,384 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TAF12
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl685,618,688 - 85,643,076 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1685,618,679 - 85,643,087 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2679,432,412 - 79,441,136 (-)NCBISscrofa10.2Sscrofa10.2susScr3
TAF12
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1 Ensembl20104,164,907 - 104,200,272 (+)Ensembl
ChlSab1.120104,164,912 - 104,199,925 (+)NCBI
Taf12
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476412,401,152 - 12,444,978 (-)NCBI

Position Markers
SHGC-30964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37128,929,663 - 28,929,787UniSTSGRCh37
Build 36128,802,250 - 28,802,374RGDNCBI36
Celera127,325,420 - 27,325,544RGD
Cytogenetic Map1p35.3UniSTS
HuRef127,182,673 - 27,182,797UniSTS
TNG Radiation Hybrid Map113365.0UniSTS
GeneMap99-GB4 RH Map190.53UniSTS
Whitehead-RH Map192.3UniSTS
NCBI RH Map1142.5UniSTS
RH67949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37128,929,760 - 28,929,994UniSTSGRCh37
GRCh37114,992,510 - 14,992,744UniSTSGRCh37
Build 36114,865,097 - 14,865,331RGDNCBI36
Celera113,475,466 - 13,475,700RGD
Celera127,325,517 - 27,325,751UniSTS
Cytogenetic Map1p35.3UniSTS
Cytogenetic Map1p36.21UniSTS
HuRef127,182,770 - 27,183,004UniSTS
HuRef113,512,315 - 13,512,549UniSTS
GeneMap99-GB4 RH Map171.55UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR26Bhsa-miR-26b-5pMirecordsexternal_info{changed}NA20831567

Predicted Target Of
Summary Value
Count of predictions:835
Count of miRNA genes:514
Interacting mature miRNAs:554
Transcripts:ENST00000263974, ENST00000373824, ENST00000471683, ENST00000495422
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1886 2122 1374 297 1604 186 4038 1466 1805 323 1413 1548 128 1 1170 2477 6 2
Low 553 869 352 327 347 279 319 731 1929 96 47 65 47 34 311
Below cutoff

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001135218 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_005644 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017002186 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449360 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024449368 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AK310097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL360012 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL513497 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY206865 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC011986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BE787487 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM676557 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BT007031 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX095156 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471059 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CX865268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  D50544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KT584524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U57693 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X84002 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000263974   ⟹   ENSP00000263974
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl128,603,101 - 28,643,005 (-)Ensembl
RefSeq Acc Id: ENST00000373824   ⟹   ENSP00000362930
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl128,602,850 - 28,643,066 (-)Ensembl
RefSeq Acc Id: ENST00000471683
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl128,589,323 - 28,618,030 (-)Ensembl
RefSeq Acc Id: ENST00000495422
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl128,613,247 - 28,643,085 (-)Ensembl
RefSeq Acc Id: NM_001135218   ⟹   NP_001128690
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,602,850 - 28,643,067 (-)NCBI
GRCh37128,929,608 - 28,975,416 (-)NCBI
HuRef127,182,618 - 27,222,688 (-)ENTREZGENE
CHM1_1129,045,214 - 29,085,178 (-)NCBI
Sequence:
RefSeq Acc Id: NM_005644   ⟹   NP_005635
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,602,850 - 28,643,067 (-)NCBI
GRCh37128,929,608 - 28,975,416 (-)NCBI
Build 36128,802,200 - 28,842,172 (-)NCBI Archive
HuRef127,182,618 - 27,222,688 (-)ENTREZGENE
CHM1_1129,045,214 - 29,085,178 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017002186   ⟹   XP_016857675
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,603,096 - 28,648,707 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449360   ⟹   XP_024305128
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,603,096 - 28,643,102 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024449368   ⟹   XP_024305136
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,603,096 - 28,643,102 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_005635   ⟸   NM_005644
- UniProtKB: Q16514 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: NP_001128690   ⟸   NM_001135218
- UniProtKB: Q16514 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016857675   ⟸   XM_017002186
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_024305128   ⟸   XM_024449360
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024305136   ⟸   XM_024449368
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: ENSP00000362930   ⟸   ENST00000373824
RefSeq Acc Id: ENSP00000263974   ⟸   ENST00000263974
Protein Domains
Histone-fold

Promoters
RGD ID:6854742
Promoter ID:EPDNEW_H536
Type:initiation region
Name:TAF12_1
Description:TATA-box binding protein associated factor 12
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H545  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38128,643,026 - 28,643,086EPDNEW
RGD ID:6786564
Promoter ID:HG_KWN:1652
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   Jurkat,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_001135218,   OTTHUMT00000010341,   OTTHUMT00000010368,   OTTHUMT00000010370,   UC009VTI.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36128,842,086 - 28,842,927 (+)MPROMDB
RGD ID:6809738
Promoter ID:HG_ACW:1273
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:TAF12.CAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 36128,847,616 - 28,848,116 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1p36.11-35.2(chr1:26963045-32279045)x3 copy number gain See cases [RCV000051801] Chr1:26963045..32279045 [GRCh38]
Chr1:27289536..32744646 [GRCh37]
Chr1:27162123..32517233 [NCBI36]
Chr1:1p36.11-35.2
pathogenic
GRCh38/hg38 1p35.3-35.1(chr1:28424867-33122854)x1 copy number loss See cases [RCV000135447] Chr1:28424867..33122854 [GRCh38]
Chr1:28751378..33588455 [GRCh37]
Chr1:28623965..33361042 [NCBI36]
Chr1:1p35.3-35.1
pathogenic
GRCh38/hg38 1p35.3(chr1:28298657-28634562)x1 copy number loss See cases [RCV000137656] Chr1:28298657..28634562 [GRCh38]
Chr1:28625168..28961074 [GRCh37]
Chr1:28497755..28833661 [NCBI36]
Chr1:1p35.3
uncertain significance
GRCh38/hg38 1p35.3(chr1:27919199-28607226)x3 copy number gain See cases [RCV000137584] Chr1:27919199..28607226 [GRCh38]
Chr1:28245710..28933738 [GRCh37]
Chr1:28118297..28806325 [NCBI36]
Chr1:1p35.3
uncertain significance
GRCh38/hg38 1p36.11-34.2(chr1:24381206-41401517)x3 copy number gain See cases [RCV000138891] Chr1:24381206..41401517 [GRCh38]
Chr1:24707696..41886350 [GRCh37]
Chr1:24580283..41658937 [NCBI36]
Chr1:1p36.11-34.2
pathogenic
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
GRCh37/hg19 1p35.3(chr1:28292253-28969539)x3 copy number gain See cases [RCV000240431] Chr1:28292253..28969539 [GRCh37]
Chr1:1p35.3
uncertain significance
GRCh37/hg19 1p35.3(chr1:28891341-28969495)x3 copy number gain See cases [RCV000447346] Chr1:28891341..28969495 [GRCh37]
Chr1:1p35.3
likely benign
GRCh37/hg19 1p35.3(chr1:28891341-28939710)x3 copy number gain See cases [RCV000446159] Chr1:28891341..28939710 [GRCh37]
Chr1:1p35.3
likely benign
GRCh37/hg19 1p35.3(chr1:28666901-28929761)x3 copy number gain See cases [RCV000448758] Chr1:28666901..28929761 [GRCh37]
Chr1:1p35.3
uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11545 AgrOrtholog
COSMIC TAF12 COSMIC
Ensembl Genes ENSG00000120656 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000263974 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000362930 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000263974 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000373824 ENTREZGENE, UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.20.10 UniProtKB/Swiss-Prot
GTEx ENSG00000120656 GTEx
HGNC ID HGNC:11545 ENTREZGENE
Human Proteome Map TAF12 Human Proteome Map
InterPro Histone-fold UniProtKB/Swiss-Prot
  TAF12 UniProtKB/Swiss-Prot
  TFIID_TAF12_dom UniProtKB/Swiss-Prot
KEGG Report hsa:6883 UniProtKB/Swiss-Prot
NCBI Gene 6883 ENTREZGENE
OMIM 600773 OMIM
PANTHER PTHR12264 UniProtKB/Swiss-Prot
Pfam TFIID_20kDa UniProtKB/Swiss-Prot
PharmGKB PA36320 PharmGKB
Superfamily-SCOP SSF47113 UniProtKB/Swiss-Prot
UniGene Hs.530251 ENTREZGENE
UniProt Q16514 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary D3DPM5 UniProtKB/Swiss-Prot
  Q15775 UniProtKB/Swiss-Prot
  Q5T077 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-11-24 TAF12  TATA-box binding protein associated factor 12  TAF12  TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 20kDa  Symbol and/or name change 5135510 APPROVED