HOXB1 (homeobox B1) - Rat Genome Database

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Gene: HOXB1 (homeobox B1) Homo sapiens
Analyze
Symbol: HOXB1
Name: homeobox B1
RGD ID: 1321119
HGNC Page HGNC
Description: Enables DNA-binding transcription activator activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein domain specific binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be part of chromatin. Predicted to be active in nucleus.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: HCFP3; homeo box 2I; homeobox protein Hox-2I; homeobox protein Hox-B1; Hox-2.9; HOX2; HOX2I; MGC116843; MGC116844; MGC116845
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1748,528,526 - 48,531,011 (-)EnsemblGRCh38hg38GRCh38
GRCh381748,528,526 - 48,531,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371746,605,888 - 46,608,373 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361743,961,806 - 43,963,271 (-)NCBINCBI36hg18NCBI36
Build 341743,961,812 - 43,963,271NCBI
Celera1743,060,953 - 43,062,427 (-)NCBI
Cytogenetic Map17q21.32NCBI
HuRef1741,976,125 - 41,977,599 (-)NCBIHuRef
CHM1_11746,672,595 - 46,674,060 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References

Additional References at PubMed
PMID:123121   PMID:1358459   PMID:1973146   PMID:2574852   PMID:2576652   PMID:7913891   PMID:8570656   PMID:8646877   PMID:8890171   PMID:9482740   PMID:9556594   PMID:10052460  
PMID:10331985   PMID:10373562   PMID:10671062   PMID:11069920   PMID:11091361   PMID:11278854   PMID:11585930   PMID:11840501   PMID:11857506   PMID:11972344   PMID:12477932   PMID:12487626  
PMID:17167333   PMID:17713478   PMID:18029348   PMID:19274049   PMID:19477923   PMID:20195514   PMID:20371328   PMID:20678259   PMID:21433221   PMID:21873635   PMID:21980499   PMID:22770981  
PMID:26496426   PMID:26565624   PMID:27144914   PMID:27640920   PMID:28473536   PMID:29923154   PMID:31182584   PMID:32102121   PMID:32296183  


Genomics

Comparative Map Data
HOXB1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1748,528,526 - 48,531,011 (-)EnsemblGRCh38hg38GRCh38
GRCh381748,528,526 - 48,531,011 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371746,605,888 - 46,608,373 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361743,961,806 - 43,963,271 (-)NCBINCBI36hg18NCBI36
Build 341743,961,812 - 43,963,271NCBI
Celera1743,060,953 - 43,062,427 (-)NCBI
Cytogenetic Map17q21.32NCBI
HuRef1741,976,125 - 41,977,599 (-)NCBIHuRef
CHM1_11746,672,595 - 46,674,060 (-)NCBICHM1_1
Hoxb1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391196,256,572 - 96,259,080 (+)NCBIGRCm39mm39
GRCm39 Ensembl1196,256,578 - 96,259,082 (+)Ensembl
GRCm381196,365,746 - 96,368,254 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1196,365,752 - 96,368,256 (+)EnsemblGRCm38mm10GRCm38
MGSCv371196,227,072 - 96,229,567 (+)NCBIGRCm37mm9NCBIm37
MGSCv361196,181,848 - 96,183,766 (+)NCBImm8
Celera11106,016,588 - 106,019,083 (+)NCBICelera
Cytogenetic Map11DNCBI
cM Map1159.86NCBI
Hoxb1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21081,331,507 - 81,332,928 (+)NCBImRatBN7.2
mRatBN7.2 Ensembl1081,331,507 - 81,332,836 (+)Ensembl
Rnor_6.01084,214,358 - 84,215,812 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1084,214,358 - 84,215,687 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01084,017,011 - 84,018,433 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41085,098,903 - 85,100,308 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11085,102,648 - 85,114,602 (+)NCBI
Celera1080,097,554 - 80,099,008 (+)NCBICelera
Cytogenetic Map10q26NCBI
Hoxb1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495545112,707,462 - 12,709,899 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495545112,707,560 - 12,708,950 (+)NCBIChiLan1.0ChiLan1.0
HOXB1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1179,190,137 - 9,191,696 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl179,190,137 - 9,191,696 (+)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0179,005,745 - 9,008,230 (+)NCBIMhudiblu_PPA_v0panPan3
HOXB1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1924,791,848 - 24,795,443 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl924,792,889 - 24,794,302 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha924,256,127 - 24,259,664 (-)NCBI
ROS_Cfam_1.0925,586,553 - 25,590,090 (-)NCBI
UMICH_Zoey_3.1924,354,782 - 24,358,319 (-)NCBI
UNSW_CanFamBas_1.0924,615,222 - 24,618,759 (-)NCBI
UU_Cfam_GSD_1.0924,743,539 - 24,747,076 (-)NCBI
Hoxb1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440560224,218,714 - 24,222,497 (-)NCBI
SpeTri2.0NW_00493649012,853,983 - 12,855,428 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
HOXB1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl1224,784,953 - 24,786,377 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.11224,784,953 - 24,786,377 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21224,742,328 - 24,743,755 (-)NCBISscrofa10.2Sscrofa10.2susScr3
HOXB1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11668,940,726 - 68,945,153 (-)NCBIChlSab1.1chlSab2
ChlSab1.1 Ensembl1668,941,746 - 68,943,111 (-)EnsemblChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366607739,995,445 - 39,997,937 (-)NCBIVero_WHO_p1.0
Hoxb1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247955,032,495 - 5,033,789 (-)NCBIHetGla_female_1.0hetGla2

Position Markers
RH71278  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371746,606,907 - 46,607,086UniSTSGRCh37
Build 361743,961,906 - 43,962,085RGDNCBI36
Celera1743,061,053 - 43,061,232RGD
Cytogenetic Map17q21.3UniSTS
HuRef1741,976,225 - 41,976,404UniSTS
GeneMap99-GB4 RH Map17338.99UniSTS
HOXB1_2983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371746,606,666 - 46,607,285UniSTSGRCh37
Build 361743,961,665 - 43,962,284RGDNCBI36
Celera1743,060,812 - 43,061,431RGD
HuRef1741,975,984 - 41,976,603UniSTS
Hoxb1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371746,606,959 - 46,607,736UniSTSGRCh37
Celera1743,061,105 - 43,061,882UniSTS
HuRef1741,976,277 - 41,977,054UniSTS
UniSTS:481565  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371746,606,859 - 46,608,272UniSTSGRCh37
Celera1743,061,005 - 43,062,427UniSTS
HuRef1741,976,177 - 41,977,599UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1064
Count of miRNA genes:629
Interacting mature miRNAs:707
Transcripts:ENST00000239174, ENST00000577092
Prediction methods:Miranda, 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.


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 adipose tissue appendage
High
Medium 1 8 2 1
Low 6 1 1 1 8 1 227 1 5 52 417 15 113
Below cutoff 1231 744 373 79 435 48 1997 696 766 201 489 593 35 422 1214

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000239174   ⟹   ENSP00000355140
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1748,528,526 - 48,531,011 (-)Ensembl
RefSeq Acc Id: ENST00000577092   ⟹   ENSP00000459066
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1748,529,497 - 48,530,910 (-)Ensembl
RefSeq Acc Id: NM_002144   ⟹   NP_002135
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381748,528,526 - 48,531,011 (-)NCBI
GRCh371746,606,807 - 46,608,272 (-)ENTREZGENE
Build 361743,961,806 - 43,963,271 (-)NCBI Archive
HuRef1741,976,125 - 41,977,599 (-)ENTREZGENE
CHM1_11746,672,595 - 46,674,060 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_002135   ⟸   NM_002144
- UniProtKB: P14653 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000459066   ⟸   ENST00000577092
RefSeq Acc Id: ENSP00000355140   ⟸   ENST00000239174
Protein Domains
Homeobox

Promoters
RGD ID:7235467
Promoter ID:EPDNEW_H23479
Type:initiation region
Name:HOXB1_1
Description:homeobox B1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381748,531,001 - 48,531,061EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17q21.33-24.2(chr17:36449220-68170214)x3 copy number gain See cases [RCV000050957] Chr17:36449220..68170214 [GRCh38]
Chr17:48563237..65936105 [GRCh37]
Chr17:45918236..63677950 [NCBI36]
Chr17:17q21.33-24.2
pathogenic
NM_002144.4(HOXB1):c.619C>T (p.Arg207Cys) single nucleotide variant Hereditary congenital facial paresis 3 [RCV000029225] Chr17:48529834 [GRCh38]
Chr17:46607196 [GRCh37]
Chr17:17q21.32
pathogenic
GRCh38/hg38 17q23.2-25.3(chr17:36449220-83086677)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052483]|See cases [RCV000052483] Chr17:36449220..83086677 [GRCh38]
Chr17:58617905..81044553 [GRCh37]
Chr17:55972687..78637842 [NCBI36]
Chr17:17q23.2-25.3
pathogenic
GRCh38/hg38 17q21.31-21.33(chr17:44955325-49381173)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052480]|See cases [RCV000052480] Chr17:44955325..49381173 [GRCh38]
Chr17:43032693..47458535 [GRCh37]
Chr17:40388219..44813534 [NCBI36]
Chr17:17q21.31-21.33
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:48520885-49511208)x1 copy number loss See cases [RCV000053431] Chr17:48520885..49511208 [GRCh38]
Chr17:46598247..47588570 [GRCh37]
Chr17:43953246..44943569 [NCBI36]
Chr17:17q21.32-21.33
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:47986886-49329397)x1 copy number loss See cases [RCV000142900] Chr17:47986886..49329397 [GRCh38]
Chr17:46064252..47406759 [GRCh37]
Chr17:43419251..44761758 [NCBI36]
Chr17:17q21.32-21.33
pathogenic
GRCh38/hg38 17q21.32-21.33(chr17:48450628-49552921)x3 copy number gain See cases [RCV000143451] Chr17:48450628..49552921 [GRCh38]
Chr17:46527990..47630283 [GRCh37]
Chr17:43882989..44985282 [NCBI36]
Chr17:17q21.32-21.33
uncertain significance
GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3 copy number gain See cases [RCV000137437] Chr17:36449220..75053130 [GRCh38]
Chr17:57595736..73049225 [GRCh37]
Chr17:54950518..70560820 [NCBI36]
Chr17:17q23.1-25.1
pathogenic
NM_002144.4(HOXB1):c.170T>A (p.Phe57Tyr) single nucleotide variant not provided [RCV000352097] Chr17:48530735 [GRCh38]
Chr17:46608097 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_002144.4(HOXB1):c.620G>A (p.Arg207His) single nucleotide variant Hereditary congenital facial paresis 3 [RCV000585798] Chr17:48529833 [GRCh38]
Chr17:46607195 [GRCh37]
Chr17:17q21.32
pathogenic
NM_002144.4(HOXB1):c.66C>G (p.Tyr22Ter) single nucleotide variant Hereditary congenital facial paresis 3 [RCV000585800] Chr17:48530839 [GRCh38]
Chr17:46608201 [GRCh37]
Chr17:17q21.32
pathogenic
GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3 copy number gain See cases [RCV000447823] Chr17:42580684..81085615 [GRCh37]
Chr17:17q21.31-25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17q21.32-22(chr17:46481089-51396368)x1 copy number loss not provided [RCV000513510] Chr17:46481089..51396368 [GRCh37]
Chr17:17q21.32-22
likely pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_002144.4(HOXB1):c.871_872delinsAA (p.Ser291Asn) indel not provided [RCV000711985] Chr17:48529581..48529582 [GRCh38]
Chr17:46606943..46606944 [GRCh37]
Chr17:17q21.32
uncertain significance
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3
pathogenic
NM_002144.4(HOXB1):c.578-8G>A single nucleotide variant not provided [RCV000872925] Chr17:48529883 [GRCh38]
Chr17:46607245 [GRCh37]
Chr17:17q21.32
likely benign
NM_002144.4(HOXB1):c.484G>A (p.Glu162Lys) single nucleotide variant not provided [RCV000983909] Chr17:48530421 [GRCh38]
Chr17:46607783 [GRCh37]
Chr17:17q21.32
likely benign
NM_002144.4(HOXB1):c.283C>A (p.Pro95Thr) single nucleotide variant not provided [RCV000872417] Chr17:48530622 [GRCh38]
Chr17:46607984 [GRCh37]
Chr17:17q21.32
benign
NM_002144.4(HOXB1):c.834G>A (p.Glu278=) single nucleotide variant not provided [RCV000915181] Chr17:48529619 [GRCh38]
Chr17:46606981 [GRCh37]
Chr17:17q21.32
likely benign
NM_002144.4(HOXB1):c.764G>A (p.Arg255Gln) single nucleotide variant Hereditary congenital facial paresis 3 [RCV000785946] Chr17:48529689 [GRCh38]
Chr17:46607051 [GRCh37]
Chr17:17q21.32
uncertain significance
NM_002144.4(HOXB1):c.154C>T (p.Leu52=) single nucleotide variant not provided [RCV000871120] Chr17:48530751 [GRCh38]
Chr17:46608113 [GRCh37]
Chr17:17q21.32
benign
NM_002144.4(HOXB1):c.65ACAGCGCCC[3] (p.His25_Ala27dup) microsatellite not provided [RCV000870526] Chr17:48530822..48530823 [GRCh38]
Chr17:46608184..46608185 [GRCh37]
Chr17:17q21.32
benign
NM_002144.4(HOXB1):c.153G>A (p.Gly51=) single nucleotide variant not provided [RCV000917433] Chr17:48530752 [GRCh38]
Chr17:46608114 [GRCh37]
Chr17:17q21.32
likely benign
NM_002144.4(HOXB1):c.702G>A (p.Val234=) single nucleotide variant not provided [RCV000870749] Chr17:48529751 [GRCh38]
Chr17:46607113 [GRCh37]
Chr17:17q21.32
benign
NM_002144.4(HOXB1):c.246G>A (p.Ser82=) single nucleotide variant not provided [RCV000870963] Chr17:48530659 [GRCh38]
Chr17:46608021 [GRCh37]
Chr17:17q21.32
benign
NM_000070.3(CAPN3):c.468C>T (p.Ile156=) single nucleotide variant Hereditary congenital facial paresis 3 [RCV001703117]|not provided [RCV001692450]|not specified [RCV001529661] Chr17:48529659 [GRCh38]
Chr17:46607021 [GRCh37]
Chr17:17q21.32
benign
null single nucleotide variant not provided [RCV001637730] Chr17:48530596 [GRCh38]
Chr17:46607958 [GRCh37]
Chr17:17q21.32
benign
NM_001458.4(FLNC):c.5124G>A (p.Ala1708=) single nucleotide variant not provided [RCV001707876]|not specified [RCV001529963] Chr17:48530668 [GRCh38]
Chr17:46608030 [GRCh37]
Chr17:17q21.32
benign
NM_002144.4(HOXB1):c.793_794insGAGGT (p.Glu265fs) insertion Hereditary congenital facial paresis 3 [RCV001335911] Chr17:48529659..48529660 [GRCh38]
Chr17:46607021..46607022 [GRCh37]
Chr17:17q21.32
pathogenic
null single nucleotide variant not provided [RCV001693586] Chr17:48530455 [GRCh38]
Chr17:46607817 [GRCh37]
Chr17:17q21.32
benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:5111 AgrOrtholog
COSMIC HOXB1 COSMIC
Ensembl Genes ENSG00000120094 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000355140 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000459066 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000239174 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000577092 UniProtKB/Swiss-Prot
GTEx ENSG00000120094 GTEx
HGNC ID HGNC:5111 ENTREZGENE
Human Proteome Map HOXB1 Human Proteome Map
InterPro Homeobox-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Homeobox_metazoa UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:3211 UniProtKB/Swiss-Prot
NCBI Gene 3211 ENTREZGENE
OMIM 142968 OMIM
  614744 OMIM
Pfam Homeodomain UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA29387 PharmGKB
PRINTS HOMEOBOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE HOMEOBOX_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  HOMEOBOX_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART HOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF46689 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt HXB1_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q4VB01_HUMAN UniProtKB/TrEMBL
  Q9HB13_HUMAN UniProtKB/TrEMBL
UniProt Secondary Q4VB03 UniProtKB/Swiss-Prot