HMX2

GENE INFORMATION

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Gene name

HMX2 (HGNC Symbol)

Synonyms

NKX5-2

Description

H6 family homeobox 2 (HGNC Symbol)

Entrez gene summary

The protein encoded by this gene is a member of the NKL homeobox family of transcription factors. Members in this family are of ancient origin and play an important role in organ development during embryogenesis. A related mouse protein plays a role in patterning of inner ear structures. In humans, variations in a region containing this gene have been associated with inner ear malformations, vestibular dysfunction, and hearing loss. [provided by RefSeq, Aug 2012]

Chromosome

10

Cytoband

q26.13

Chromosome location (bp)

124907638 - 124910188

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000188816 (version 75.37)

Entrez gene

3167

UniProt

A2RU54 (UniProt - Evidence at transcript level)

neXtProt

NX_A2RU54

Antibodypedia

HMX2 antibodies
 

PROTEIN VIEW

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HMX2-001
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HMX2-001 ENSP00000341108
ENST00000339992
A2RU54
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