Homo sapiens Gene: ATOH7
Summary
InnateDB Gene IDBG-75985.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ATOH7
Gene Name atonal homolog 7 (Drosophila)
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000179774
Encoded Proteins
atonal homolog 7 (Drosophila)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This intronless gene encodes a member of the basic helix-loop-helix family of transcription factors, with similarity to Drosophila atonal gene that controls photoreceptor development. Studies in mice suggest that this gene plays a central role in retinal ganglion cell and optic nerve formation. Mutations in this gene are associated with nonsyndromic congenital retinal nonattachment. [provided by RefSeq, Dec 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:68230624-68232103
Strand Reverse strand
Band q21.3
Transcripts
ENST00000373673 ENSP00000362777
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0046983 protein dimerization activity
Biological Process
GO:0003407 neural retina development
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007623 circadian rhythm
GO:0009649 entrainment of circadian clock
GO:0021554 optic nerve development
GO:0030154 cell differentiation
Cellular Component
GO:0005634 nucleus
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q8N100
TrEMBL F1T0H4
UniProt Splice Variant
Entrez Gene 220202
UniGene Hs.175396 Hs.606763 Hs.737072
RefSeq NM_145178
HUGO HGNC:13907
OMIM 609875
CCDS CCDS7276
HPRD
IMGT
EMBL AB593108 AB593109 AF418922 BC032621 BK000277 CH471083
GenPept AAH32621 AAL11911 BAJ84048 BAJ84049 DAA01057 EAW54269
RNA Seq Atlas 220202