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Gene: Cnnm4 (cyclin and CBS domain divalent metal cation transport mediator 4) Rattus norvegicus
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Symbol: Cnnm4
Name: cyclin and CBS domain divalent metal cation transport mediator 4
Description: Predicted to have magnesium ion transmembrane transporter activity and sodium ion transmembrane transporter activity. Predicted to be involved in enamel mineralization; magnesium ion homeostasis; and magnesium ion transport. Localizes to the dendrite and neuronal cell body. Orthologous to human CNNM4 (cyclin and CBS domain divalent metal cation transport mediator 4); INTERACTS WITH acrylamide; bisphenol A; calcium atom.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: ancient conserved domain-containing protein 4; cyclin M4; cyclin-M4; LOC363216; metal transporter CNNM4
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.0943,049,587 - 43,088,690 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0942,703,466 - 42,742,596 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4935,410,644 - 35,448,730 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1935,406,796 - 35,457,552 (+)NCBI
Celera936,478,287 - 36,517,394 (+)NCBICelera
Cytogenetic Map9q21NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 5.0)

Additional Information

External Database Links
Nomenclature History
 
More on Cnnm4
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1305571
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2019-07-09
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.