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Gene: C9orf131 (chromosome 9 open reading frame 131) Homo sapiens
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Symbol: C9orf131
Name: chromosome 9 open reading frame 131
Description: ASSOCIATED WITH anauxetic dysplasia 1; distal spinal muscular atrophy 2; Hyperphosphatasia with Mental Retardation Syndrome 2; INTERACTS WITH (-)-epigallocatechin 3-gallate; aflatoxin B1; benzo[a]pyrene
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FLJ00273; hypothetical protein LOC138724; MGC41945; uncharacterized protein C9orf131
Orthologs:
Mus musculus (house mouse) : 1700022I11Rik (RIKEN cDNA 1700022I11 gene)  MGI  Alliance
Rattus norvegicus (Norway rat) : LOC100360821 (rCG55159-like)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : LOC106147709 (chromosome unknown open reading frame, human C9orf131)
Pan paniscus (bonobo/pygmy chimpanzee) : C9H9orf131 (chromosome 9 C9orf131 homolog)
Canis lupus familiaris (dog) : C11H9orf131 (chromosome 11 C9orf131 homolog)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : CUNH9orf131 (chromosome unknown C9orf131 homolog)
Sus scrofa (pig) : C1H9orf131 (chromosome 1 C9orf131 homolog)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38935,041,095 - 35,045,991 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37935,041,102 - 35,045,988 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36935,031,102 - 35,035,988 (+)NCBINCBI36hg18NCBI36
Celera934,973,075 - 34,977,961 (+)NCBI
Cytogenetic Map9p13.3NCBI
HuRef934,996,685 - 35,001,571 (+)NCBIHuRef
CHM1_1935,040,928 - 35,045,824 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on C9orf131
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604527
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-11-26
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.