Human (GRCh37.p13)
Description

family with sequence similarity 167, member A [Source:HGNC Symbol;Acc:15549]

Gene Synonyms

C8orf13, D8S265

Location

Chromosome 8: 11,278,972-11,332,224 reverse strand.

GRCh37:CM000670.1

About this gene

This gene has 7 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000284486.4FAM167A-0014094214aaENSP00000284486.4
 
Protein coding
CCDS5981E9PIY0 Q86Y02 Q96KS9
NM_053279.2GENCODE basic
ENST00000534308.1FAM167A-0081642214aaENSP00000432232.1
 
Protein coding
CCDS5981E9PIY0 Q86Y02 Q96KS9
-GENCODE basic
ENST00000528897.1FAM167A-0031620214aaENSP00000436655.1
 
Protein coding
CCDS5981E9PIY0 Q86Y02 Q96KS9
-GENCODE basic
ENST00000531804.1FAM167A-005112091aaENSP00000431951.1
 
Protein coding
E9PIY0 -CDS 3' incomplete
ENST00000531564.1FAM167A-0041325No protein-
 
Processed transcript
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ENST00000527445.1FAM167A-007801No protein-
 
Processed transcript
---
ENST00000528111.1FAM167A-006712No protein-
 
Processed transcript
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Retirement notice

Human only - retirement of this view

As of Ensembl release 93 this view will no longer be available for human, because we feel that the density of known human genetic variation is too great for the display to be informative in its current form.

Other species will not be affected, as they have less variation data.

For more information about the decision and on how to find variation data for a gene, please see our blog post.