ORTHOLOGY: K04853
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Entry
K04853 KO
Name
CACNA1F, CAV1.4
Definition
voltage-dependent calcium channel L type alpha-1F
Pathway
ko04010
MAPK signaling pathway
ko04020
Calcium signaling pathway
ko04022
cGMP-PKG signaling pathway
ko04024
cAMP signaling pathway
ko04260
Cardiac muscle contraction
ko04261
Adrenergic signaling in cardiomyocytes
ko04270
Vascular smooth muscle contraction
ko04723
Retrograde endocannabinoid signaling
ko04725
Cholinergic synapse
ko04726
Serotonergic synapse
ko04727
GABAergic synapse
ko04911
Insulin secretion
ko04912
GnRH signaling pathway
ko04921
Oxytocin signaling pathway
ko04924
Renin secretion
ko04925
Aldosterone synthesis and secretion
ko04927
Cortisol synthesis and secretion
ko04929
GnRH secretion
ko04934
Cushing syndrome
ko04935
Growth hormone synthesis, secretion and action
ko05010
Alzheimer disease
ko05020
Prion disease
ko05022
Pathways of neurodegeneration - multiple diseases
ko05410
Hypertrophic cardiomyopathy
ko05412
Arrhythmogenic right ventricular cardiomyopathy
ko05414
Dilated cardiomyopathy
Disease
H00481
Cone-rod dystrophy and cone dystrophy
H00690
Aland Island eye disease
H00787
Congenital stationary night blindness
Brite
KEGG Orthology (KO) [BR:
ko00001
]
09130 Environmental Information Processing
09132 Signal transduction
04010 MAPK signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04020 Calcium signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04024 cAMP signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04022 cGMP-PKG signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09150 Organismal Systems
09152 Endocrine system
04911 Insulin secretion
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04929 GnRH secretion
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04912 GnRH signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04921 Oxytocin signaling pathway
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04935 Growth hormone synthesis, secretion and action
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04924 Renin secretion
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04925 Aldosterone synthesis and secretion
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04927 Cortisol synthesis and secretion
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09153 Circulatory system
04260 Cardiac muscle contraction
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04261 Adrenergic signaling in cardiomyocytes
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04270 Vascular smooth muscle contraction
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09156 Nervous system
04727 GABAergic synapse
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04725 Cholinergic synapse
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04726 Serotonergic synapse
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
04723 Retrograde endocannabinoid signaling
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09160 Human Diseases
09164 Neurodegenerative disease
05010 Alzheimer disease
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
05020 Prion disease
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
05022 Pathways of neurodegeneration - multiple diseases
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09166 Cardiovascular disease
05410 Hypertrophic cardiomyopathy
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
05412 Arrhythmogenic right ventricular cardiomyopathy
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
05414 Dilated cardiomyopathy
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09167 Endocrine and metabolic disease
04934 Cushing syndrome
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04040 Ion channels
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
Ion channels [BR:
ko04040
]
Voltage-gated cation channels
Calcium channel, voltage-gated (Cav)
K04853 CACNA1F, CAV1.4; voltage-dependent calcium channel L type alpha-1F
BRITE hierarchy
Other DBs
GO:
0005245
TC:
1.A.1.11.11
Genes
HSA:
778
(CACNA1F)
PTR:
740711
(CACNA1F)
PPS:
100988624
(CACNA1F)
GGO:
101131714
(CACNA1F)
PON:
100431752
(CACNA1F)
NLE:
100590475
(CACNA1F)
MCC:
715787
(CACNA1F)
MCF:
102119841
(CACNA1F)
CSAB:
103231971
(CACNA1F)
RRO:
104661816
(CACNA1F)
RBB:
108521361
CJC:
100386041
(CACNA1F)
SBQ:
101034685
(CACNA1F)
MMU:
54652
(Cacna1f)
MCAL:
110286673
(Cacna1f)
MPAH:
110313596
(Cacna1f)
RNO:
114493
(Cacna1f)
MUN:
110561910
(Cacna1f)
CGE:
100757994
(Cacna1f)
NGI:
103741673
(Cacna1f)
HGL:
101722090
(Cacna1f)
CCAN:
109697195
(Cacna1f)
OCU:
100357261
(CACNA1F)
TUP:
102482779
(CACNA1F)
CFA:
480915
(CACNA1F)
VVP:
112907237
(CACNA1F)
AML:
100468661
(CACNA1F)
UMR:
103667625
(CACNA1F)
UAH:
113265950
(CACNA1F)
ORO:
101364481
(CACNA1F)
ELK:
111150407
FCA:
101080870
(CACNA1F)
PTG:
102950547
(CACNA1F)
PPAD:
109248097
(CACNA1F)
AJU:
106988999
(CACNA1F)
BTA:
509779
(CACNA1F)
BOM:
102286805
(CACNA1F)
BIU:
109554975
(CACNA1F)
BBUB:
102407399
(CACNA1F)
CHX:
102189746
(CACNA1F)
OAS:
101104552
(CACNA1F)
SSC:
100514745
(CACNA1F)
CFR:
102504151
(CACNA1F)
CDK:
105103284
(CACNA1F)
BACU:
102998540
(CACNA1F)
LVE:
103082192
(CACNA1F)
OOR:
101281199
(CACNA1F)
DLE:
111169490
(CACNA1F)
PCAD:
102992313
(CACNA1F)
ECB:
100062861
(CACNA1F)
EPZ:
103543955
(CACNA1F)
EAI:
106826963
(CACNA1F)
MYB:
102260789
(CACNA1F)
MYD:
102771414
(CACNA1F)
MNA:
107541372
(CACNA1F)
HAI:
109374806
(CACNA1F)
DRO:
112322357
(CACNA1F)
PALE:
102893611
(CACNA1F)
RAY:
107514999
(CACNA1F)
MJV:
108404213
(CACNA1F)
LAV:
100674649
(CACNA1F)
TMU:
101340818
MDO:
100019531
(CACNA1F)
SHR:
100927554
(CACNA1F)
PCW:
110201034
(CACNA1F)
OAA:
100075939
(CACNA1F)
LSR:
110482322
FAB:
101817703
PHI:
102111116
(CACNA1F)
FPG:
101922071
FCH:
102046341
CLV:
102089966
AAM:
106493905
(CACNA1F)
ASN:
102368804
(CACNA1F)
AMJ:
102563169
(CACNA1F)
CPIC:
101934179
(CACNA1F)
ACS:
100565753
(cacna1f)
PVT:
110078615
(CACNA1F)
PBI:
103051695
(CACNA1F)
PMUR:
107284195
(CACNA1F)
PMUA:
114587594
(CACNA1F)
GJA:
107117359
XLA:
100462913
(cacna1f.L)
XTR:
100485906
(cacna1f)
NPR:
108788491
DRE:
559964
(cacna1fb)
793708
(cacna1fa)
SRX:
107723069
107731232
107745766
107756819
SANH:
107668072
107695300
SGH:
107548248
107549945
107550115
CCAR:
109065543
109087149
IPU:
108265065
108265094
(cacna1f)
PHYP:
113528653
113533319
AMEX:
103033957
103034295
EEE:
113578747
(cacna1f)
113579098
TRU:
101077620
(cacna1f)
101079199
TNG:
GSTEN00023513G001
GSTEN00026488G001
LCO:
104933125
104935494
MZE:
101480057
ONL:
100700615
100706871
OLA:
101171727
101171913
XMA:
102223947
102230940
XCO:
114141072
114141251
PRET:
103460216
103467718
CVG:
107095949
(cacna1f)
107099706
NFU:
107390498
(cacna1f)
107391407
KMR:
108228711
108232078
ALIM:
106519282
(cacna1f)
106523414
106533880
AOCE:
111580242
CSEM:
103384398
103385395
(cacna1f)
POV:
109642986
109643812
LCF:
108882181
108890565
SDU:
111234857
111235435
SLAL:
111654197
111669629
HCQ:
109510493
109512986
(cacna1f)
BPEC:
110154433
110164475
(cacna1f)
MALB:
109953071
SASA:
106572493
OTW:
112221526
SALP:
111966955
ELS:
105008776
105022404
SFM:
108918279
108934768
PKI:
111847817
111857113
LCM:
102353236
(CACNA1F)
» show all
Taxonomy
UniProt
Reference
PMID:
25468907
Authors
Lee A, Wang S, Williams B, Hagen J, Scheetz TE, Haeseleer F
Title
Characterization of Cav1.4 complexes (alpha11.4, beta2, and alpha2delta4) in HEK293T cells and in the retina.
Journal
J Biol Chem 290:1505-21 (2015)
DOI:
10.1074/jbc.M114.607465
Sequence
[hsa:
778
]
Reference
PMID:
9662399
Authors
Strom TM, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, Wutz K, Gutwillinger N, Ruther K, Drescher B, Sauer C, Zrenner E, Meitinger T, Rosenthal A, Meindl A
Title
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Journal
Nat Genet 19:260-3 (1998)
DOI:
10.1038/940
Sequence
[hsa:
778
]
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