Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | CACNA1H | contributors: mct - updated : 08-12-2016 |
HGNC name | calcium channel, voltage-dependent, alpha 1H subunit |
HGNC id | 1395 |
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RNA |
TRANSCRIPTS | type | messenger |
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text | alternative splice isoform of CACNA1G |
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EXPRESSION |
Type | widely |
constitutive of |
expressed in | (based on citations) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
organ(s) |
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tissue |
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cells |
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cell lineage
cell lines
| fluid/secretion
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at STAGE |
PROTEIN |
PHYSICAL PROPERTIES
STRUCTURE
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motifs/domains
| |
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conjugated | GlycoP |
HOMOLOGY |
interspecies | ortholog to rattus cacna1h |
ortholog to murine Cacna1h |
Homologene |
FAMILY | calcium channel alpha-1 subunit family |
CATEGORY | transport channel |
SUBCELLULAR LOCALIZATION | plasma membrane |
basic FUNCTION |
CELLULAR PROCESS |
PHYSIOLOGICAL PROCESS |
text | substrate for CaMKII |
PATHWAY |
metabolism |
signaling |
a component |
INTERACTION |
DNA |
RNA |
small molecule | metal binding, |
CA2+ |
protein |
cell & other |
REGULATION |
ASSOCIATED DISORDERS |
corresponding disease(s) | ECA6 |
Susceptibility | to childhood absence epilepsy (see ECA4) |
Variant & Polymorphism SNP | increasing the risk of childhood absence epilepsy |
ANIMAL & CELL MODELS |