Homo sapiens Gene: FAM161A | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-53408.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | FAM161A | ||||||||||||||||||
Gene Name | family with sequence similarity 161, member A | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000170264 | ||||||||||||||||||
Encoded Proteins |
family with sequence similarity 161, member A
family with sequence similarity 161, member A
family with sequence similarity 161, member A
family with sequence similarity 161, member A
family with sequence similarity 161, member A
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Protein Structure | |||||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 2:61824854-61854143 | ||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||
Band | p15 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||||||||||||||
SwissProt | Q3B820 | ||||||||||||||||||
TrEMBL | F8W731 F8WCZ8 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 84140 | ||||||||||||||||||
UniGene | Hs.440466 | ||||||||||||||||||
RefSeq | NM_001201543 NM_032180 XM_006712113 XM_006712114 | ||||||||||||||||||
HUGO | HGNC:25808 | ||||||||||||||||||
OMIM | 613596 | ||||||||||||||||||
CCDS | CCDS42687 CCDS56120 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC107081 AK023367 AK296255 BC107162 BC107163 BX648834 BX649029 | ||||||||||||||||||
GenPept | BAB14544 BAG58969 | ||||||||||||||||||
RNA Seq Atlas | 84140 | ||||||||||||||||||