KEGG   Homo sapiens (human): 786
Entry
786               CDS       T01001                                 
Symbol
CACNG1, CACNLG
Name
(RefSeq) calcium voltage-gated channel auxiliary subunit gamma 1
  KO
K04866  voltage-dependent calcium channel gamma-1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04010  MAPK signaling pathway
hsa04260  Cardiac muscle contraction
hsa04261  Adrenergic signaling in cardiomyocytes
hsa04921  Oxytocin signaling pathway
hsa05410  Hypertrophic cardiomyopathy
hsa05412  Arrhythmogenic right ventricular cardiomyopathy
hsa05414  Dilated cardiomyopathy
Network
nt06528  Calcium signaling
  Element
N01637  Ca2+ entry, Voltage-gated Ca2+ channel
N01638  Skeletal-type VGCC-RYR signaling
N01639  Cardiac-type VGCC-RYR signaling
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04010 MAPK signaling pathway
    786 (CACNG1)
 09150 Organismal Systems
  09152 Endocrine system
   04921 Oxytocin signaling pathway
    786 (CACNG1)
  09153 Circulatory system
   04260 Cardiac muscle contraction
    786 (CACNG1)
   04261 Adrenergic signaling in cardiomyocytes
    786 (CACNG1)
 09160 Human Diseases
  09166 Cardiovascular disease
   05410 Hypertrophic cardiomyopathy
    786 (CACNG1)
   05412 Arrhythmogenic right ventricular cardiomyopathy
    786 (CACNG1)
   05414 Dilated cardiomyopathy
    786 (CACNG1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:hsa04040]
    786 (CACNG1)
Ion channels [BR:hsa04040]
 Voltage-gated cation channels
  Calcium channel, voltage-gated (Cav)
   786 (CACNG1)
SSDB
Motif
Pfam: Claudin_2 PMP22_Claudin LapA_dom Claudin_3 UL45 TMD0_ABC DUF981 T4SS_pilin Acyl_transf_3
Other DBs
NCBI-GeneID: 786
NCBI-ProteinID: NP_000718
OMIM: 114209
HGNC: 1405
Ensembl: ENSG00000108878
UniProt: Q06432
LinkDB
Position
17:67044554..67056797
AA seq 222 aa
MSQTKMLKVRVTLFCILAGIVLAMTAVVTDHWAVLSPHMEHHNTTCEAAHFGLWRICTKR
IPMDDSKTCGPITLPGEKNCSYFRHFNPGESSEIFEFTTQKEYSISAAAIAIFSLGFIIL
GSLCVLLSLGKKRDYLLRPASMFYAFAGLCILVSVEVMRQSVKRMIDSEDTVWIEYYYSW
SFACACAAFILLFLGGLALLLFSLPRMPRNPWESCMDAEPEH
NT seq 669 nt   +upstreamnt  +downstreamnt
atgtcccagaccaaaatgctgaaggtccgcgtgaccctcttctgcatcctggcaggcatc
gtgctggccatgacagccgtggtaaccgaccactgggctgtgctgagcccccacatggag
caccacaacactacctgcgaggcggcccacttcggcctctggcggatttgtaccaagcgc
atccccatggacgacagcaagacctgcgggcccatcaccctgcccggggagaagaactgt
tcctacttcaggcattttaaccccggcgagagctcggagatcttcgaattcaccactcag
aaggagtacagcatctcggcagccgccatcgccatcttcagccttggcttcatcatcctg
ggcagcctctgtgtcctcctgtccctcgggaagaagagggactatctgctgcgacccgcg
tccatgttctatgcctttgcaggtctctgcatcctcgtctcggtggaggtcatgcggcag
tcggtgaagcgcatgattgacagtgaggacaccgtctggatcgagtactattactcctgg
tcctttgcctgcgcctgtgccgccttcatcctcctctttctcggcggtctcgccctcctg
ctgttctccctgcctcgaatgccccggaacccatgggagtcctgcatggatgctgagccc
gagcactaa

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