Homo sapiens Gene: FAM9B
Summary
InnateDB Gene IDBG-42388.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM9B
Gene Name family with sequence similarity 9, member B
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000177138
Encoded Proteins
family with sequence similarity 9, member B
family with sequence similarity 9, member B
family with sequence similarity 9, member B
family with sequence similarity 9, member B
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:9024232-9164639
Strand Reverse strand
Band p22.31
Transcripts
ENST00000327220 ENSP00000318716
ENST00000362066 ENSP00000354770
ENST00000428477 ENSP00000412606
ENST00000461107
ENST00000472522 ENSP00000431456
ENST00000494744
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 7 experimentally validated interaction(s) in this database.
Experimentally validated
Total 7 [view]
Protein-Protein 7 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
Cellular Component
GO:0005634 nucleus
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.733351
RefSeq NM_205849 XM_005274456
HUGO
OMIM
CCDS CCDS14132
HPRD 15955
IMGT
EMBL
GenPept
RNA Seq Atlas