Homo sapiens Gene: FAM9C
Summary
InnateDB Gene IDBG-44544.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM9C
Gene Name family with sequence similarity 9, member C
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000187268
Encoded Proteins
family with sequence similarity 9, member C
family with sequence similarity 9, member C
family with sequence similarity 9, member C
family with sequence similarity 9, member C
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex protein. [provided by RefSeq, Aug 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome X:13035618-13044682
Strand Reverse strand
Band p22.2
Transcripts
ENST00000333995 ENSP00000334430
ENST00000380625 ENSP00000369999
ENST00000438997 ENSP00000409506
ENST00000468287
ENST00000542843 ENSP00000439185
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
Biological Process
Cellular Component
GO:0005634 nucleus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt Q8IZT9
TrEMBL A0A024RBW5 G3V1I3
UniProt Splice Variant
Entrez Gene 171484
UniGene Hs.667546
RefSeq NM_174901 XM_005274462 XM_005274463
HUGO HGNC:18405
OMIM 300479
CCDS CCDS35203
HPRD
IMGT
EMBL AC139705 AF494345 AK313776 BC127957 BX647580 CH471074
GenPept AAI27958 AAN07164 BAG36514 CAI46094 EAW98815 EAW98816 EAW98817
RNA Seq Atlas 171484