CACNA1B
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Homo sapiens |
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CACNA1B is differentially expressed in 172 experiments: 124 organism parts: lung, adipose tissue, ... (122 more);, 128 disease states: normal, Huntington's disease, ... (126 more);, 50 cell types 171 cell lines 12 compound treatments and 67 other conditions. |
| Synonyms |
CACNL1A5, CACNN, Cav2.2 |
| Orthologs |
CACNA1B
(Bos taurus)
CAC1B_CHICK
(Gallus gallus)
F6QCH7_CIOIN
(Ciona intestinalis)
Cacna1b
(Mus musculus)
cacna1ba
(Danio rerio)
Cacna1b
(Rattus norvegicus)
cacna1bb
(Danio rerio)
LOC100489231
(Xenopus laevis)
CACNA1B
(Canis familiaris)
(Compare orthologs)
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| InterPro ID |
IPR003915, IPR005821, IPR018249, IPR013122, IPR014873, IPR002077, IPR005447 |
| Gene Ontology Term |
plasma membrane, transport, protein binding, regulation of heart contraction, ion transport, membrane, locomotory behavior, ion channel activity, voltage-gated calcium channel activity, neurotransmitter secretion, ATP binding, synaptic transmission, dendrite, nucleotide binding, voltage-gated ion channel activity, integral to membrane, protein C-terminus binding, transmembrane transport, calcium ion transport, voltage-gated calcium channel complex, neuronal cell body, membrane depolarization, response to pain, regulation of blood pressure, regulation of calcium ion transport via voltage-gated calcium channel activity, calcium ion transmembrane transport |
| Gene Ontology ID |
GO:0016020, GO:0016021, GO:0008022, GO:0008016, GO:0007268, GO:0007269, GO:0005891, GO:0007626, GO:0030425, GO:0005524, GO:0005515, GO:0005886, GO:0055085, GO:0006811, GO:0006810, GO:0006816, GO:0005216, GO:0005244, GO:0005245, GO:0043025, GO:0000166, GO:0008217, GO:0048265, GO:0051925, GO:0051899, GO:0070588 |
| InterPro Term |
VDCC_a1su_IQ, PKD_2, VDCCAlpha1, PKD1_2_channel, EF_HAND_2, Ion_trans, VDCC_N_a1su |
| Ensembl Family |
ENSFM00600000921217 |
| Ensembl Family Description |
VOLTAGE DEPENDENT TYPE CALCIUM CHANNEL SUBUNIT ALPHA BRAIN CALCIUM CHANNEL CALCIUM CHANNEL L TYPE ALPHA 1 POLYPEPTIDE VOLTAGE GATED CALCIUM CHANNEL SUBUNIT ALPHA CAV2 |
| Description |
calcium channel, voltage-dependent, N type, alpha 1B subunit [Source:HGNC Symbol;Acc:1389] |
| EMBL-Bank ID |
M94172, M94173, AL591424, AF302780, AF302782, AF302779, AB209467, AF239237, AL772363, AF245660, AF245659, AF233289, AF237470, AF247811, U76666, AF238295, AF238296 |
| UniGene ID |
Hs.495522 |
| Ensembl Gene ID |
ENSG00000148408 |
| UniProt Accession |
Q00975, Q9HAT3, Q9HAT4, Q9HAT5, Q9HAT6, Q9HBI4, Q9HBI3, Q9HBG3, Q9HBG2, Q9HBH2, Q9HBH3, Q9HBH4, B1AQK6, B1AQK4, B1AQK7, Q59FJ3, Q5JRE4, F6RH32, E9PDR3, Q9HBG1 |
| Ensembl Protein ID |
ENSP00000413042, ENSP00000277550, ENSP00000277551, ENSP00000277549, ENSP00000360423, ENSP00000360406, ENSP00000360408, ENSP00000360418, ENSP00000360416, ENSP00000360414, ENSP00000441232 |
| HGNC Symbol |
CACNA1B |
| RefSeq ID |
NM_000718, NP_000709, NP_001230741, NM_001243812 |
| Entrez Gene ID |
774 |
| Ensembl Transcript ID |
ENST00000545473, ENST00000277551, ENST00000277550, ENST00000277549, ENST00000413253, ENST00000371355, ENST00000371357, ENST00000371363, ENST00000371365, ENST00000371367, ENST00000371372 |
| Design Element |
ENST00000413253, 56074_at, M94172_s_at, g4502522_3p_a_at, ENST00000371372, ENST00000277549, 33960_s_at, gnf1h05247_x_at, ENST00000371367, Hs.99163.0.A1_3p_at, ENST00000371357, 235781_at, ENST00000545473, ENST00000371355, ENST00000277551, ENST00000371363, ENST00000277550, 207162_s_at, ENST00000371365 |
| Search EB-eye |
ENSG00000148408
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