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Gene: FAM9C (family with sequence similarity 9 member C) Homo sapiens
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Symbol: FAM9C
Name: family with sequence similarity 9 member C
Description: 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]
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: family with sequence similarity 9, member C; testis expressed 39C; TEX39C
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X13,035,617 - 13,044,798 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X13,053,736 - 13,062,917 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X12,963,658 - 12,972,721 (-)NCBINCBI36hg18NCBI36
Build 34X12,813,488 - 12,822,378NCBI
CeleraX17,171,404 - 17,180,585 (-)NCBI
Cytogenetic MapXp22.2NCBI
HuRefX10,816,570 - 10,825,752 (-)NCBIHuRef
CHM1_1X13,084,293 - 13,093,476 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM9C
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1345371
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-06-18
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.