Human (GRCh37.p13)
Description

family with sequence similarity 50, member A [Source:HGNC Symbol;Acc:18786]

Gene Synonyms

9F, DXS9928E, HXC-26, HXC26, XAP5

Location

Chromosome X: 153,672,473-153,679,002 forward strand.

GRCh37:CM000685.1

View alleles of this gene on alternative sequences

About this gene

This gene has 7 transcripts (splice variants), 1 gene allele, 1 paralogue and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000393600.3FAM50A-0011352339aaENSP00000377225.3
 
Protein coding
CCDS14751B0S8I6 Q14320 Q6PJH5
NM_004699.3GENCODE basic
ENST00000158526.9FAM50A-0021240260aaENSP00000158526.9
 
Protein coding
B0S8I6 -CDS 3' incomplete
ENST00000464419.1FAM50A-0051470No protein-
 
Retained intron
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ENST00000481619.1FAM50A-007763No protein-
 
Retained intron
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ENST00000478509.1FAM50A-004682No protein-
 
Retained intron
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ENST00000490480.1FAM50A-003346No protein-
 
Retained intron
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ENST00000494278.1FAM50A-006294No protein-
 
Retained intron
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