HOXB8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Homeobox protein Hox-B8 is a protein that in humans is encoded by the HOXB8 gene.[5][6][7]

AliasesHOXB8, HOX2, HOX2D, Hox-2.4, homeobox B8
End48,615,292 bp[1]
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HOXB8
Identifiers
AliasesHOXB8, HOX2, HOX2D, Hox-2.4, homeobox B8
External IDsOMIM: 142963; MGI: 96189; HomoloGene: 7768; GeneCards: HOXB8; OMA:HOXB8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_024016

NM_010461

RefSeq (protein)

NP_076921

NP_034591

Location (UCSC)Chr 17: 48.61 – 48.62 MbChr 11: 96.17 – 96.18 Mb
PubMed search[3][4]
Wikidata
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Function

This gene is a member of the Antp homeobox family and encodes a nuclear protein with a homeobox DNA-binding domain. It is included in a cluster of Homeobox B genes located on chromosome 17. The encoded protein functions as a sequence-specific transcription factor that is involved in development. Increased expression of this gene is associated with colorectal cancer. Mice that have had the murine ortholog (see Homology (biology) § Orthology) of this gene knocked out exhibit an excessive pathologic grooming behavior. This behavior is similar to the hair-pulling behavior of humans suffering from trichotillomania (TTM).[7]

Transplantation of normal (wild-type) bone marrow into a Hoxb8 mutant mouse results in a reduction of compulsive grooming.[8]

See also

References

Further reading

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