Homo sapiens (human): 10368
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Entry
10368 CDS
T01001
Symbol
CACNG3
Name
(RefSeq) calcium voltage-gated channel auxiliary subunit gamma 3
KO
K04868
voltage-dependent calcium channel gamma-3
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
10368 (CACNG3)
09150 Organismal Systems
09152 Endocrine system
04921 Oxytocin signaling pathway
10368 (CACNG3)
09153 Circulatory system
04260 Cardiac muscle contraction
10368 (CACNG3)
04261 Adrenergic signaling in cardiomyocytes
10368 (CACNG3)
09160 Human Diseases
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
10368 (CACNG3)
05412 Arrhythmogenic right ventricular cardiomyopathy
10368 (CACNG3)
05414 Dilated cardiomyopathy
10368 (CACNG3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels [BR:
hsa04040
]
10368 (CACNG3)
Ion channels [BR:
hsa04040
]
Voltage-gated cation channels
Calcium channel, voltage-gated (Cav)
10368 (CACNG3)
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SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
PMP22_Claudin
Claudin_2
Motif
Other DBs
NCBI-GeneID:
10368
NCBI-ProteinID:
NP_006530
OMIM:
606403
HGNC:
1407
Ensembl:
ENSG00000006116
UniProt:
O60359
LinkDB
All DBs
Position
16:24256335..24362412
Genome browser
AA seq
315 aa
AA seq
DB search
MRMCDRGIQMLITTVGAFAAFSLMTIAVGTDYWLYSRGVCRTKSTSDNETSRKNEEVMTH
SGLWRTCCLEGAFRGVCKKIDHFPEDADYEQDTAEYLLRAVRASSVFPILSVTLLFFGGL
CVAASEFHRSRHNVILSAGIFFVSAGLSNIIGIIVYISANAGDPGQRDSKKSYSYGWSFY
FGAFSFIIAEIVGVVAVHIYIEKHQQLRAKSHSEFLKKSTFARLPPYRYRFRRRSSSRST
EPRSRDLSPISKGFHTIPSTDISMFTLSRDPSKITMGTLLNSDRDHAFLQFHNSTPKEFK
ESLHNNPANRRTTPV
NT seq
948 nt
NT seq
+upstream
nt +downstream
nt
atgaggatgtgtgacagaggtatccagatgttgatcaccactgtaggagcctttgccgct
tttagtttaatgaccattgcagtgggcacggactactggttatattccagaggtgtgtgc
aggactaaatctacaagtgataatgaaaccagcaggaagaatgaagaagtaatgacccat
tcggggctgtggaggacctgctgcctagaaggggctttccgaggcgtgtgcaagaaaatc
gatcacttccctgaagatgctgactacgaacaggacacagccgaatatctcctgcgagct
gtgagggcctccagtgtcttccccatcctcagtgtcacgctgctgttcttcggcgggctc
tgcgtggcagccagtgagttccaccgcagcagacacaacgtcattctcagcgcgggcatc
ttttttgtctctgcagggttaagcaacatcattggcatcatagtttatatatcagccaac
gccggagaccccgggcagcgtgactccaaaaaaagttactcctatggttggtccttttat
ttcggagccttctctttcatcatcgcagaaattgtaggagtggttgccgtgcacatctat
attgaaaaacatcagcagttacgagccaaatcccactcggagttcctgaagaaatctact
tttgcccgcctcccaccctacaggtatcgattccggaggcggtcaagttctcgctccacc
gagcccagatcccgagacctgtcccccatcagcaaaggcttccacaccatcccttccact
gacatctcgatgttcaccctctcccgggacccctcaaagatcaccatggggaccctcctc
aactccgaccgggaccacgcttttctacagttccacaattccacacccaaagagttcaaa
gagtcactgcataataatccggccaacaggcgcaccacgcccgtctga
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