CACNA1C
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Homo sapiens |
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CACNA1C is differentially expressed in 228 experiments: 159 organism parts: bone marrow, liver, ... (157 more);, 189 disease states: normal, astrocytoma, ... (187 more);, 64 cell types 260 cell lines 20 compound treatments and 70 other conditions. |
| Synonyms |
TS, CACNL1A1, CCHL1A1, Cav1.2, CACN2, CACH2 |
| Orthologs |
CACNA1C
(Bos taurus)
Cacna1c
(Rattus norvegicus)
F1NJQ0_CHICK
(Gallus gallus)
Cacna1c
(Mus musculus)
CACNA1C
(Danio rerio)
F6X5E1_CIOIN
(Ciona intestinalis)
Ca-alpha1D
(Drosophila melanogaster)
CACNA1C
(Xenopus laevis)
A0ZSX7_CANFA
(Canis familiaris)
(Compare orthologs)
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| Gene Ontology Term |
plasma membrane, protein binding, visual learning, ion transport, membrane, ion channel activity, voltage-gated calcium channel activity, protein domain specific binding, membrane fraction, sarcolemma, glucose homeostasis, adult walking behavior, smooth muscle contraction, regulation of organ growth, protein phosphatase 2A binding, synaptic transmission, cellular calcium ion homeostasis, postsynaptic density, dendrite, voltage-gated ion channel activity, integral to membrane, transmembrane transport, calcium ion transport, voltage-gated calcium channel complex, Z disc, neuronal cell body, T-tubule, caveolar macromolecular signaling complex, calcium ion-dependent exocytosis, smooth muscle contraction involved in micturition, regulation of blood pressure, insulin secretion, regulation of calcium ion transport via voltage-gated calcium channel activity, growth hormone secretion, dendritic shaft, regulation of vasoconstriction, calcium ion transmembrane transport |
| Gene Ontology ID |
GO:0016020, GO:0016021, GO:0007268, GO:0008542, GO:0005891, GO:0042383, GO:0007628, GO:0042593, GO:0030425, GO:0005624, GO:0014069, GO:0005515, GO:0006939, GO:0006874, GO:0005886, GO:0055085, GO:0006811, GO:0006816, GO:0019904, GO:0005216, GO:0005244, GO:0005245, GO:0043025, GO:0051721, GO:0046620, GO:0030018, GO:0008217, GO:0060083, GO:0002095, GO:0051925, GO:0019229, GO:0043198, GO:0030073, GO:0030315, GO:0030252, GO:0017156, GO:0070588 |
| InterPro Term |
VDCC_L_a1su, VDCC_a1su_IQ, VDCC_L_a1csu, VDCCAlpha1, PKD1_2_channel, Ion_trans |
| InterPro ID |
IPR005821, IPR005446, IPR005451, IPR013122, IPR014873, IPR002077 |
| Ensembl Family |
ENSFM00500000269632 |
| RefSeq ID |
NM_001129846, NM_001129844, NM_001129843, NM_001129842, NM_001129841, NM_001129840, NM_001129838, NM_001129839, NM_001129836, NM_001129837, NM_001129830, NM_001129831, NM_001129834, NM_001129835, NM_001129832, NM_001129833, NM_001129827, NM_001129829, NP_001123299, NP_001123318, NP_001123315, NP_001123314, NP_001123316, NP_001123311, NP_001123310, NP_001123313, NP_001123312, NP_001123309, NP_001123308, NP_001123307, NP_001123306, NP_001123305, NP_001123304, NP_001123303, NP_001123302, NP_001123301, NM_001167623, NM_001167624, NM_001167625, NM_000719, NP_001161095, NP_001161096, NP_001161097, NP_000710 |
| Description |
calcium channel, voltage-dependent, L type, alpha 1C subunit [Source:HGNC Symbol;Acc:1390] |
| EMBL-Bank ID |
AC007618, AJ537510, AC005866, AC005344, AC005342, AC005414, AC005293, AC006051, AY562395, AJ536834, AF070589 |
| UniGene ID |
Hs.697137, Hs.690010 |
| Ensembl Protein ID |
ENSP00000385896, ENSP00000385724, ENSP00000329877, ENSP00000323129, ENSP00000341092, ENSP00000266376, ENSP00000336982, ENSP00000382504, ENSP00000382506, ENSP00000382500, ENSP00000382526, ENSP00000382510, ENSP00000382515, ENSP00000382512, ENSP00000382557, ENSP00000382552, ENSP00000382563, ENSP00000382537, ENSP00000382530, ENSP00000382547, ENSP00000382546, ENSP00000382549, ENSP00000382542, ENSP00000437936, ENSP00000445849 |
| UniProt Accession |
Q13936, Q5V9X9, Q86XX0, Q86XX1, O95234, F5GY28, E9PDI6, E9PDJ1, E9PDJ0, F5H0X0, F5H638, F5H522 |
| Ensembl Gene ID |
ENSG00000151067 |
| HGNC Symbol |
CACNA1C |
| Gene-Disease Assocation |
BRUGADA SYNDROME 3, TIMOTHY SYNDROME; TS |
| Entrez Gene ID |
775 |
| Ensembl Family Description |
VOLTAGE DEPENDENT L TYPE CALCIUM CHANNEL SUBUNIT ALPHA CALCIUM CHANNEL L TYPE ALPHA 1 POLYPEPTIDE VOLTAGE GATED CALCIUM CHANNEL SUBUNIT ALPHA CAV1 |
| Ensembl Transcript ID |
ENST00000491104, ENST00000543114, ENST00000327702, ENST00000347598, ENST00000399597, ENST00000399595, ENST00000399591, ENST00000465278, ENST00000406454, ENST00000465934, ENST00000399655, ENST00000399644, ENST00000399649, ENST00000399641, ENST00000399617, ENST00000399603, ENST00000399606, ENST00000399601, ENST00000399638, ENST00000399637, ENST00000399634, ENST00000399629, ENST00000399621, ENST00000496818, ENST00000492150, ENST00000481826, ENST00000335762, ENST00000402845, ENST00000322367, ENST00000483136, ENST00000344100, ENST00000480911 |
| Design Element |
L04569_at, Z26256_at, ENST00000480911, ENST00000465278, 33623_g_at, ENST00000399644, ENST00000465934, ENST00000481826, ENST00000399649, ENST00000399601, ENST00000399603, ENST00000399641, ENST00000399606, ENST00000483136, M92269_f_at, ENST00000543114, Hs.66147.0.A1_3p_at, ENST00000406454, ENST00000496818, 242973_at, ENST00000399634, ENST00000399638, 38002_s_at, 208020_s_at, ENST00000399637, 38001_at, ENST00000322367, 211592_s_at, ENST00000492150, ENST00000399629, 76029_at, ENST00000399621, ENST00000335762, 55902_at, ENST00000344100, Hs.118262.0.A1_3p_at, ENST00000399591, ENST00000402845, ENST00000399595, ENST00000491104, ENST00000399597, ENST00000399655, g4502524_3p_a_at, ENST00000399617, 238636_at, g463081_3p_a_at, ENST00000327702, Z34822_f_at, ENST00000347598 |
| Search EB-eye |
ENSG00000151067
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