FAM58A

GENE INFORMATION

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Gene name

FAM58A (HGNC Symbol)

Synonyms

FLJ21610, MGC29729

Description

Family with sequence similarity 58, member A (HGNC Symbol)

Entrez gene summary

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]

Chromosome

X

Cytoband

q28

Chromosome location (bp)

152853377 - 152865500

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000147382 (version 75.37)

Entrez gene

92002

UniProt

neXtProt

Antibodypedia

FAM58A antibodies
 

PROTEIN VIEW

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FAM58A-002
 
FAM58A-005
 
FAM58A-011
 
FAM58A-201
 
 
 
 
 

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)

FAM58A-002 ENSP00000402949
ENST00000440428
Show » 121 14.2 No 0
FAM58A-005 ENSP00000412865
ENST00000429336
Show » 94 11 No 0
FAM58A-011 ENSP00000466345
ENST00000482182
K7EM37
Show all »
Show » Show » 142 16.8 No 0
FAM58A-201 ENSP00000384396
ENST00000406277
J3QT30
Show all »
Show » Show » 246 28.2 No 0