Pou3f4 (POU domain, class 3, transcription factor 4) - Rat Genome Database

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Gene: Pou3f4 (POU domain, class 3, transcription factor 4) Mus musculus
Analyze
Symbol: Pou3f4
Name: POU domain, class 3, transcription factor 4
RGD ID: 62240
MGI Page MGI
Description: Enables RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in cochlea morphogenesis and negative regulation of mesenchymal cell apoptotic process. Acts upstream of or within forebrain neuron differentiation; inner ear development; and sensory perception of sound. Predicted to be located in nucleoplasm. Is expressed in several structures, including brain; cranium; ear; embryo ectoderm; and foregut-midgut junction. Human ortholog(s) of this gene implicated in X-linked deafness 2. Orthologous to human POU3F4 (POU class 3 homeobox 4).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: Br; brain-4 class III POU-domain protein; brain-specific homeobox/POU domain protein 4; BRN; Brn-4; Brn4; oct-9; octamer-binding protein 9; octamer-binding transcription factor 9; Otf; OTF-9; Otf9; RP23-57B14.1; sex linked fidget; Slf
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X109,857,985 - 109,862,714 (+)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX109,857,886 - 109,860,813 (+)EnsemblGRCm39 Ensembl
GRCm38X110,814,379 - 110,819,108 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX110,814,280 - 110,817,207 (+)EnsemblGRCm38mm10GRCm38
MGSCv37X108,009,804 - 108,010,889 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X107,017,184 - 107,018,269 (+)NCBIMGSCv36mm8
CeleraX97,632,784 - 97,633,869 (+)NCBICelera
Cytogenetic MapXE1NCBI
cM MapX48.2NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
nucleoplasm  (IEA)

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal bony labyrinth  (IAGP)
abnormal cochlea morphology  (IAGP)
abnormal gait  (IAGP)
abnormal internal auditory canal morphology  (IAGP)
abnormal lateral semicircular canal morphology  (IAGP)
abnormal oval window morphology  (IAGP)
abnormal pinna reflex  (IAGP)
abnormal Reissner membrane morphology  (IAGP)
abnormal scala tympani morphology  (IAGP)
abnormal spiral ligament fibrocyte morphology  (IAGP)
abnormal spiral limbus morphology  (IAGP)
abnormal stapes crus morpholgy  (IAGP)
abnormal stapes footplate morphology  (IAGP)
abnormal stapes morphology  (IAGP)
abnormal stria vascularis morphology  (IAGP)
abnormal subarcuate fossa morphology  (IAGP)
abnormal superior semicircular canal morphology  (IAGP)
abnormal temporal bone morphology  (IAGP)
abnormal type I spiral ligament fibrocytes  (IAGP)
abnormal type II spiral ligament fibrocytes  (IAGP)
abnormal vestibular system physiology  (IAGP)
absent linear vestibular evoked potential  (IAGP)
absent startle reflex  (IAGP)
circling  (IAGP)
cochlear outer hair cell degeneration  (IAGP)
conductive hearing loss  (IAGP)
deafness  (IAGP)
decreased cochlea coiling  (IAGP)
decreased endocochlear potential  (IAGP)
detached Reissner membrane  (IAGP)
dilated endolymphatic duct  (IAGP)
distended Reissner membrane  (IAGP)
head bobbing  (IAGP)
head shaking  (IEA)
head tossing  (IAGP)
impaired hearing  (IAGP)
impaired swimming  (IAGP)
increased circulating potassium level  (IAGP)
increased or absent threshold for auditory brainstem response  (IAGP)
sensorineural hearing loss  (IAGP)
short vibrissae  (IAGP)
small scala tympani  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation. de Kok YJ, etal., Hum Mutat. 1997;10(3):207-11.
2. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. de Kok YJ, etal., Science. 1995 Feb 3;267(5198):685-8.
3. Electronic Transfer of Homolog Data MGD and Homologene mouse data transfer
4. MGDs mouse GO annotations MGD data from the GO Consortium
5. MGD IEA MGD IEA
6. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y, etal., Nature. 2002 Dec 5;420(6915):563-73.
7. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
8. Mouse MP Annotation Import Pipeline RGD automated import pipeline
9. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
10. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1565620   PMID:7911044   PMID:8075499   PMID:8276396   PMID:8276397   PMID:8543156   PMID:8703082   PMID:8827514   PMID:8900043   PMID:8934515   PMID:9105675   PMID:9118797  
PMID:9247261   PMID:9584121   PMID:9620855   PMID:9653165   PMID:9667433   PMID:9870661   PMID:9889200   PMID:10349636   PMID:10367888   PMID:10407036   PMID:10464101   PMID:10587581  
PMID:10588713   PMID:10868931   PMID:10903178   PMID:11042159   PMID:11071765   PMID:11076861   PMID:11124115   PMID:11152636   PMID:11217851   PMID:11356266   PMID:11834725   PMID:12049785  
PMID:12062767   PMID:12130536   PMID:12231626   PMID:12397111   PMID:12477932   PMID:12933680   PMID:14681479   PMID:15031110   PMID:15456859   PMID:15574296   PMID:15618518   PMID:15655183  
PMID:15872005   PMID:15882093   PMID:15999533   PMID:16141072   PMID:16141073   PMID:16235133   PMID:16407553   PMID:16602821   PMID:17141158   PMID:17360442   PMID:17609113   PMID:17953485  
PMID:17988662   PMID:18231833   PMID:18250082   PMID:18287559   PMID:18353863   PMID:18554416   PMID:18778483   PMID:19030180   PMID:19386638   PMID:19476657   PMID:19487809   PMID:19502415  
PMID:19696885   PMID:20059953   PMID:20211142   PMID:20346939   PMID:20377917   PMID:20524937   PMID:20932939   PMID:21144821   PMID:21209840   PMID:21267068   PMID:21658586   PMID:21766338  
PMID:21852533   PMID:21856296   PMID:21873635   PMID:21880149   PMID:22243746   PMID:22988430   PMID:22992956   PMID:23093780   PMID:23233153   PMID:23606270   PMID:23606368   PMID:23674600  
PMID:23843306   PMID:23979167   PMID:24146773   PMID:24236044   PMID:24727668   PMID:24952961   PMID:25178196   PMID:25259580   PMID:25299585   PMID:25343275   PMID:25915623   PMID:26554594  
PMID:26901059   PMID:27026076   PMID:27993987   PMID:29513653   PMID:30796806   PMID:31994726   PMID:32170006   PMID:33938018   PMID:34003106   PMID:34184034   PMID:34201511   PMID:34392304  
PMID:36899442   PMID:37720106   PMID:38577978  


Genomics

Comparative Map Data
Pou3f4
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X109,857,985 - 109,862,714 (+)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX109,857,886 - 109,860,813 (+)EnsemblGRCm39 Ensembl
GRCm38X110,814,379 - 110,819,108 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX110,814,280 - 110,817,207 (+)EnsemblGRCm38mm10GRCm38
MGSCv37X108,009,804 - 108,010,889 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X107,017,184 - 107,018,269 (+)NCBIMGSCv36mm8
CeleraX97,632,784 - 97,633,869 (+)NCBICelera
Cytogenetic MapXE1NCBI
cM MapX48.2NCBI
POU3F4
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X83,508,290 - 83,512,127 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblX83,508,290 - 83,512,127 (+)EnsemblGRCh38hg38GRCh38
GRCh37X82,763,298 - 82,767,135 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X82,649,941 - 82,651,431 (+)NCBINCBI36Build 36hg18NCBI36
Build 34X82,569,445 - 82,570,920NCBI
CeleraX83,000,650 - 83,002,156 (+)NCBICelera
Cytogenetic MapXq21.1NCBI
HuRefX76,337,125 - 76,338,589 (+)NCBIHuRef
CHM1_1X82,657,165 - 82,658,671 (+)NCBICHM1_1
T2T-CHM13v2.0X81,941,865 - 81,945,703 (+)NCBIT2T-CHM13v2.0
Pou3f4
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8X79,974,808 - 79,976,085 (+)NCBIGRCr8
mRatBN7.2X75,858,646 - 75,859,923 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 EnsemblX75,858,646 - 75,859,923 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_UtxX77,428,273 - 77,429,550 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0X80,870,563 - 80,871,840 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0X78,451,380 - 78,452,657 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0X82,143,789 - 82,145,066 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 EnsemblX82,143,789 - 82,145,066 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0X82,301,578 - 82,302,855 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X99,214,446 - 99,215,723 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1X99,287,906 - 99,289,156 (+)NCBI
CeleraX77,112,524 - 77,113,801 (+)NCBICelera
Cytogenetic MapXq31NCBI
Pou3f4
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049555292,726,133 - 2,727,218 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049555292,726,121 - 2,727,311 (+)NCBIChiLan1.0ChiLan1.0
POU3F4
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2X82,964,178 - 82,968,669 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1X82,967,786 - 82,972,282 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0X72,563,887 - 72,568,233 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1X82,666,699 - 82,668,337 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX82,666,757 - 82,667,842 (+)Ensemblpanpan1.1panPan2
POU3F4
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X64,427,161 - 64,428,825 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX64,427,325 - 64,428,410 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX55,185,767 - 55,187,326 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0X65,745,624 - 65,747,183 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 EnsemblX65,745,693 - 65,746,778 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1X63,406,449 - 63,408,008 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0X65,024,007 - 65,025,564 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0X64,613,109 - 64,614,668 (+)NCBIUU_Cfam_GSD_1.0
Pou3f4
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X58,133,789 - 58,135,350 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365474,454,297 - 4,455,382 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365474,454,239 - 4,455,460 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
POU3F4
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX66,765,105 - 66,766,190 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X66,765,044 - 66,766,642 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X76,477,799 - 76,479,225 (+)NCBISscrofa10.2Sscrofa10.2susScr3
POU3F4
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X72,379,656 - 72,381,186 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 EnsemblX72,379,979 - 72,381,064 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660678,524,912 - 8,526,260 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Pou3f4
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248525,037,373 - 5,040,139 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248525,036,585 - 5,040,160 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in Pou3f4
148 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:170
Count of miRNA genes:152
Interacting mature miRNAs:160
Transcripts:ENSMUST00000078229
Prediction methods:Miranda, Pita, Rnahybrid, Targetscan
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.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
4141630Gct6_mgranulosa cell tumorigenesis 6 (mouse)Not determined47179121129764756Mouse
13208552Wght12_mweight 12 (mouse)X94043606149782996Mouse
4141803Lmr30_mleishmaniasis resistance 30 (mouse)Not determined85062606119062720Mouse
13208556Lgth14_mbody length 14 (mouse)X94043606149782996Mouse
11075102Modc2_mmodifier of Odc2 (mouse)X80189914114190059Mouse
13824980Ferq1_mgenetic fertility QTL 1 (mouse)X54045360148782996Mouse
1357823Spha3_msperm head anomaly 3 (mouse)Not determinedX102055848162758941Mouse
1357433Dbts2_mdiabetes 2 (mouse)Not determinedX7226295150107038Mouse
4141665Mhysq2_mmale hybrid sterility QTL 2 (mouse)Not determined71453852139203212Mouse

Markers in Region
Pou3f4  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X110,814,499 - 110,814,927UniSTSGRCm38
MGSCv37X108,009,838 - 108,010,266UniSTSGRCm37
CeleraX97,632,818 - 97,633,246UniSTS
Cytogenetic MapXE1UniSTS
cM MapX48.4UniSTS
cM MapX48.4UniSTS
Pou3f4  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X110,814,552 - 110,815,526UniSTSGRCm38
MGSCv37X108,009,891 - 108,010,865UniSTSGRCm37
CeleraX97,632,871 - 97,633,845UniSTS
Cytogenetic MapXE1UniSTS
cM MapX48.4UniSTS


Expression

RNA-SEQ Expression


Sequence


Ensembl Acc Id: ENSMUST00000078229   ⟹   ENSMUSP00000077354
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX109,857,886 - 109,860,813 (+)Ensembl
GRCm38.p6 EnsemblX110,814,280 - 110,817,207 (+)Ensembl
RefSeq Acc Id: NM_008901   ⟹   NP_032927
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39X109,857,985 - 109,862,714 (+)NCBI
GRCm38X110,814,379 - 110,819,108 (+)NCBI
MGSCv37X108,009,804 - 108,010,889 (+)RGD
CeleraX97,632,784 - 97,633,869 (+)RGD
cM MapX ENTREZGENE
Sequence:
Protein Sequences
Protein RefSeqs NP_032927 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAA39962 (Get FASTA)   NCBI Sequence Viewer  
  AAI38658 (Get FASTA)   NCBI Sequence Viewer  
  AAI45920 (Get FASTA)   NCBI Sequence Viewer  
  BAE34453 (Get FASTA)   NCBI Sequence Viewer  
  EDL14021 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSMUSP00000077354
  ENSMUSP00000077354.4
GenBank Protein P62515 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_032927   ⟸   NM_008901
- UniProtKB: P25216 (UniProtKB/Swiss-Prot),   P62515 (UniProtKB/Swiss-Prot),   A6H6L6 (UniProtKB/TrEMBL),   Q3TYV9 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSMUSP00000077354   ⟸   ENSMUST00000078229
Protein Domains
Homeobox   POU-specific

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P62515-F1-model_v2 AlphaFold P62515 1-361 view protein structure

Promoters
RGD ID:6846116
Promoter ID:MM_KWN:61600
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain,   MEF_B4,   MEF_B6
Transcripts:NM_008901
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X108,009,546 - 108,010,046 (+)MPROMDB
RGD ID:13681252
Promoter ID:EPDNEW_M24775
Type:initiation region
Name:Pou3f4_1
Description:Mus musculus POU domain, class 3, transcription factor 4 , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38X110,814,433 - 110,814,493EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene MGI:101894 AgrOrtholog
Ensembl Genes ENSMUSG00000056854 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSMUST00000078229 ENTREZGENE
  ENSMUST00000078229.5 UniProtKB/Swiss-Prot
Gene3D-CATH 1.10.260.40 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeodomain-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
InterPro Homeobox-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Lambda_DNA-bd_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU_domain_TF UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TF_POU_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:18994 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
MGD MGI:101894 ENTREZGENE
NCBI Gene 18994 ENTREZGENE
PANTHER POU DOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU DOMAIN, CLASS 3, TRANSCRIPTION FACTOR 4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Homeodomain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pou UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen Pou3f4 PhenoGen
PIRSF Transcription_factor_POU UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PRINTS POUDOMAIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE HOMEOBOX_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HOMEOBOX_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  POU UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46689 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47413 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A6H6L6 ENTREZGENE, UniProtKB/TrEMBL
  P25216 ENTREZGENE
  P62515 ENTREZGENE, UniProtKB/Swiss-Prot
  Q3TYV9 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary P25216 UniProtKB/Swiss-Prot