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GENE INFORMATION

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Gene name

OTX2

Synonyms

Description

orthodenticle homeobox 2 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the bicoid subfamily of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and plays a role in brain, craniofacial, and sensory organ development. The encoded protein also influences the proliferation and differentiation of dopaminergic neuronal progenitor cells during mitosis. Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6). This gene is also suspected of having an oncogenic role in medulloblastoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Pseudogenes of this gene are known to exist on chromosomes two and nine. [provided by RefSeq, Jul 2012]

Chromosome

14 (Chromosome progress)

Cytoband

q22.3

Chromosome location (bp)

57267426 - 57277197

Ensembl

ENSG00000165588 (version 69.37)

Entrez gene

5015

UniProt

P32243

neXtProt

NX_P32243

Antibodypedia

OTX2 antibodies
 

PROTEIN VIEW

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OTX2-001
 
OTX2-002
 
OTX2-003
 
OTX2-004
 
OTX2-006
 
OTX2-007
 
 
 
 
 

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)

OTX2-001 ENSP00000343819
ENST00000339475
P32243
Show all »
Show » Show » 297 32.4 No 0
OTX2-002 ENSP00000452336
ENST00000555006
P32243
Show all »
Show » Show » 289 31.6 No 0
OTX2-003 ENSP00000451272
ENST00000555804
G3V3J3
Show all »
Show » 163 18.1 No 0
OTX2-004 ENSP00000450468
ENST00000554559
F1T0C9
Show all »
Show » 35 3.8 No 0
OTX2-006 ENSP00000451357
ENST00000554845
G3V3P9
Show all »
Show » Show » 239 26 No 0
OTX2-007 ENSP00000386185
ENST00000408990
P32243
Show all »
Show » Show » 289 31.6 No 0