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Gene: C2CD6 (C2 calcium dependent domain containing 6) Homo sapiens
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Symbol: C2CD6
Name: C2 calcium dependent domain containing 6
RGD ID: 1345082
Description: An autosomal recessive form of juvenile amyotrophic lateral sclerosis was originally mapped to a region of chromosome 2 that includes this gene. The encoded protein contains a calcium-dependent membrane targeting C2 domain. This domain is often found in proteins that are involved in membrane trafficking and signal transduction. [provided by RefSeq, Jun 2016]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ALS2CR11; amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 11; amyotrophic lateral sclerosis 2 chromosomal region candidate gene 11 protein; amyotrophic lateral sclerosis 2 chromosome region candidate 11; amyotrophic lateral sclerosis 2 chromosome region, candidate 11; C2 calcium-dependent domain-containing protein 6; DKFZp686H0636; FLJ25351; FLJ40332; testicular tissue protein Li 16
Orthologs:
Mus musculus (house mouse) : C2cd6 (C2 calcium dependent domain containing 6)  MGI  Alliance
Rattus norvegicus (Norway rat) : C2cd6 (C2 calcium dependent domain containing 6)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : C2cd6 (C2 calcium dependent domain containing 6)
Pan paniscus (bonobo/pygmy chimpanzee) : C2CD6 (C2 calcium dependent domain containing 6)
Canis lupus familiaris (dog) : C2CD6 (C2 calcium dependent domain containing 6)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : C2cd6 (C2 calcium dependent domain containing 6)
Sus scrofa (pig) : C2CD6 (C2 calcium dependent domain containing 6)
Chlorocebus sabaeus (African green monkey) : C2CD6 (C2 calcium dependent domain containing 6)
Heterocephalus glaber (naked mole-rat) : C2cd6 (C2 calcium dependent domain containing 6)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2201,487,421 - 201,619,178 (-)EnsemblGRCh38hg38GRCh38
GRCh382201,487,421 - 201,619,182 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372202,352,144 - 202,483,905 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362202,060,393 - 202,192,146 (-)NCBINCBI36hg18NCBI36
Build 342202,177,656 - 202,309,404NCBI
Celera2196,104,082 - 196,235,806 (-)NCBI
Cytogenetic Map2q33.1NCBI
HuRef2194,200,052 - 194,332,020 (-)NCBIHuRef
CHM1_12202,358,246 - 202,490,417 (-)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 C2CD6
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1345082
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.