Protein Cacnb2

URN urn:agi-llid:783
Connectivity 16
Name Cacnb2
Description calcium channel, voltage-dependent, beta 2 subunit
Notes This gene encodes a subunit of a voltage-dependent calcium channel protein which is a member of the voltage-gated calcium channel superfamily. The gene product was originally identified as an antigen target in Lambert-Eaton myasthenic syndrome which is an autoimmune disorder. Mutations in this gene are associated with Brugada symdrome. Alternatively spliced variants have been identified for this gene. [provided by RefSeq]

Pathway calcium/calmodulin dependent kinase 2 signaling pathway
calcium-calmodulin dependent kinase 2 signaling pathway

GO Molecular Function calcium channel regulator activity
calcium ion binding
ion channel activity
voltage-gated ion channel activity
calcium channel activity
voltage-gated calcium channel activity
dihydropyridine-sensitive calcium channel activity
high voltage-gated calcium channel activity

GO Cellular Component membrane
plasma membrane
voltage-gated calcium channel complex
integral to plasma membrane
sarcolemma

GO Biological Process transport
visual perception
synaptic transmission
neuromuscular junction development
ion transport
calcium ion transport

Ariadne Ontology Voltage-dependent Ca++ import

Group Voltage-dependent Ca++ import
transport
visual perception
synaptic transmission
neuromuscular junction development
ion transport
calcium ion transport
calcium channel regulator activity
calcium ion binding
ion channel activity
voltage-gated ion channel activity
calcium channel activity
voltage-gated calcium channel activity
dihydropyridine-sensitive calcium channel activity
high voltage-gated calcium channel activity
membrane
plasma membrane
voltage-gated calcium channel complex
integral to plasma membrane
sarcolemma

MedScan ID 783

Hugo ID 1402

Human chromosome position 10p12

LocusLink ID 783
12296
116600

Alias MYSB
CAVB2
CACNLB2
FLJ23743
RP11-383B4.2
voltage-dependent L-type calcium channel subunit beta-2
CAB2
lambert-Eaton myasthenic syndrome antigen B
myasthenic (Lambert-Eaton) syndrome antigen B
calcium channel voltage-dependent subunit beta 2
Cchb2
AW060387
Cavbeta2
MGC129334
MGC129335
RP23-56A7.2
OTTMUSP00000012041
calcium channel beta 2 subunit
BC056183
Cacnb2
calcium channel, voltage-dependent, beta 2 subunit
cDNA sequence BC056183
Dihydropyridine-sensitive L-type, calcium channel beta-2 subunit
OTTHUMP00000019254
OTTHUMP00000019255
OTTHUMP00000019256
OTTHUMP00000196786

Organism Homo sapiens
Mus musculus
Rattus norvegicus

GenBank ID NC_000010
NM_201596
NP_963890
NM_201593
NP_963887
NM_201597
NP_963891
NM_201571
NP_963865
NM_201572
NP_963866
NM_000724
NP_000715
NM_201590
NP_963884
NM_201570
NP_963864
NT_008705
NW_924584
NW_001837931
AC_000053
AC_000142
NM_001167945
AL139814
CAH71349
CAH71350
CAH71351
CAH71352
CAH71353
CAO03603
CAO03604
CAO03605
CAO03606
AL162054
AL353603
AL360231
CAH70125
CAH70126
AL390783
CAH70065
CAH70066
CAO03475
AL450364
CAI14731
CAI14732
CAI14733
CAI14734
CAI14735
CAO03634
CAO03635
CAO03636
CAO03637
AL450384
CAH73206
CAH73207
CAH73208
CAH73209
CAH73210
AY027898
AAK16994
CH471072
EAW86193
EAW86194
EAW86195
EAW86196
EAW86197
AB208917
BAD92154
AF137376
AAD33729
AF137377
AAD33730
AF285239
AAG01473
AF423189
AAL16948
AF423190
AAL16949
AF423191
AAL16950
AF423192
AAL16951
AF465485
AAL73495
AK021994
AK022426
AK128769
AK293837
BAH11608
AK293937
BAH11631
AK295113
BAH11979
AK296471
BAH12366
AK299873
BAH13158
AK307526
AK307800
AK310943
AK311694
AL119895
AL599294
AL600557
AY393858
AAQ97606
AY393859
AAQ97607
AY393860
AAQ97608
AY393861
AAQ97609
AY393862
AAQ97610
AY393863
AAQ97611
AY675091
AAV49501
AY675092
AAV49502
BC136409
AAI36410
BM312516
DB235418
DC307859
DC352526
S60415
AAB51370
U95019
AAB53332
AAB27916
Q08289
Q59H42
Q5QJ99
Q5QJA0
Q5UM67
Q5UM68
Q5VVH1
Q6TME0
Q6TME1
Q6TME2
Q6TME3
NC_000068
NM_023116
NP_075605
NT_039202
NW_001030686
AC_000024
AB109465
BAD01474
AL928632
CAM20243
AL929165
AL935312
CAM26080
CH466542
EDL08067
EDL08068
EDL08069
EDL08070
EDL08071
EDL08072
EDL08073
AK020806
BAB32216
AK034054
BAC28562
AK044560
AK046048
AK078220
BAC37179
AK082315
AK143332
AM259383
CAJ90741
BC048944
BC056183
BC109156
AAI09157
BC109157
AAI09158
FM872406
CAS06709
FM872407
CAS06710
FM872408
CAS06711
L20343
Q32MF3
Q8CC27
NC_005116
NM_053851
NP_446303
NW_047496
NW_001084730
AC_000085
CH473990
EDL78736
EDL78737
EDL78738
EDL78739
EDL78740
EDL78741
EDL78742
EDL78743
EDL78744
AF394941
AAL47074
AF423193
AAL16952
AY190119
AAO38996
AY190120
AAO38997
M80545
AAK14821
Q8VGC3

OMIM ID 600003
611876

Mouse chromosome position 2 14.5 cM

GO ID 0005262
0005245
0005244
0006816
0006811
0007528
0007268
0006810
0007601
0005887
0042383
0005891
0005246
0008331
0005216
0016020
0005886
0015270
0005509

Rat chromosome position 17q12.3

Swiss-Prot Accession Q59H42
Q08289
Q5VVH1
A6PVM7
Q5QJ99
Q5VWV7
Q6TME3
Q5QJA0
Q5UM67
Q5UM68
Q6TME0
Q6TME1
Q6TME2
Q32MF3
Q8CC27
Q8VGC3
Q811Q6
Q811Q7
Q91ZJ8
Q9QUU7
A2ASJ8
Q8C5J5
Q9CTQ6
A6PVM5
A6PVM8
O00304
Q5VVG9
Q5VVH0
Q5VWV6
Q8WX81
Q96NZ3
Q96NZ4
Q96NZ5
Q9BWU2
Q9HD32
Q9Y340
Q9Y341

PIR ID A42044
A48895

Unigene ID Hs.59093
Mm.313930
Rn.10739

KEGG ID hsa:783
mmu:12296
rno:116600

Swiss-Prot ID CACB2_RAT
CACB2_MOUSE
CACB2_HUMAN
A6PVM7_HUMAN
Q32MF3_MOUSE
Q5VWV7_HUMAN
Q5VVH1_HUMAN
Q5QJ99_HUMAN
Q59H42_HUMAN
Q6TME3_HUMAN
Q6TME2_HUMAN
A6PVM5_HUMAN
A6PVM8_HUMAN
Q5VVG9_HUMAN
Q5VWV6_HUMAN

Cell Localization Cell membrane
sarcolemma
Plasma membrane

IPI ID IPI00421663
IPI00421664
IPI00421665
IPI00421666
IPI00950751
IPI00228423
IPI00420994
IPI00420995
IPI00420996
IPI00000867
IPI00218399
IPI00218400
IPI00218401
IPI00218402
IPI00218404
IPI00218405
IPI00409678
IPI00853583
IPI00872366
IPI00902807
IPI00479687
IPI00757117
IPI00758114
IPI00567533
IPI00421662

Homologene ID 75191

RGD ID 67385

MGI ID 894644