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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: Predicted to be involved in meiotic cell cycle and spermatid development. Predicted to localize to the synaptonemal complex.
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
GRCh38 EnsemblX13,035,617 - 13,044,682 (-)Ensembl
GRCh38X13,035,617 - 13,044,793 (-)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

Expression

RNA-SEQ Expression

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

RGD Object Information
RGD ID: 1345371
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-12-25
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.