Homo sapiens Gene: FAM126A
Summary
InnateDB Gene IDBG-9521.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM126A
Gene Name family with sequence similarity 126, member A
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000122591
Encoded Proteins
family with sequence similarity 126, member A
family with sequence similarity 126, member A
family with sequence similarity 126, member A
family with sequence similarity 126, member A
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:22889371-23014130
Strand Reverse strand
Band p15.3
Transcripts
ENST00000409923 ENSP00000386246
ENST00000409763 ENSP00000386624
ENST00000440481 ENSP00000397168
ENST00000432176 ENSP00000403396
ENST00000498833
ENST00000477349
ENST00000467005
ENST00000465661
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:0004871 signal transducer activity
Biological Process
GO:0007165 signal transduction
GO:0008150 biological_process
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.85603
RefSeq NM_032581 XM_005249894 XM_006715799
HUGO
OMIM
CCDS CCDS5377
HPRD 16837
IMGT
EMBL
GenPept
RNA Seq Atlas