Mutagenetix > Incidental Mutation

Incidental Mutation 'R8301:Cacna1s'

656513

Institutional Source

Beutler Lab

Gene Symbol

Cacna1s

Ensembl Gene

ENSMUSG00000026407

Gene Name

calcium channel, voltage-dependent, L type, alpha 1S subunit

Synonyms

sj, mdg, muscle dysgenesis, DHPR alpha1s, Cav1.1, Cchl1a3, fmd

MMRRC Submission

067789-MU

Accession Numbers

Genbank: NM_001081023; MGI: 88294

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R8301 (G1)

Quality Score

200.009

Status

Validated

Chromosome

Chromosomal Location

136052750-136119822 bp(+) (GRCm38)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to A at 136073441 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000125262 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000112064] [ENSMUST00000112068] [ENSMUST00000160641] [ENSMUST00000161865]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000112064

SMART Domains

Protein: ENSMUSP00000107695
Gene: ENSMUSG00000026407

Domain	Start	End	E-Value	Type
Pfam:Ion_trans	50	345	4.3e-68	PFAM
Pfam:Ion_trans	431	672	4.5e-56	PFAM
Pfam:PKD_channel	516	667	1.9e-7	PFAM
low complexity region	675	685	N/A	INTRINSIC
low complexity region	740	756	N/A	INTRINSIC
Pfam:Ion_trans	798	1076	2.6e-65	PFAM
Pfam:Ion_trans	1117	1392	1.2e-71	PFAM
Pfam:PKD_channel	1126	1387	8.4e-13	PFAM
Pfam:GPHH	1394	1463	2.3e-38	PFAM
Ca_chan_IQ	1515	1548	3.71e-14	SMART
low complexity region	1657	1669	N/A	INTRINSIC
Pfam:CAC1F_C	1756	1845	2.8e-8	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000112068

SMART Domains

Protein: ENSMUSP00000107699
Gene: ENSMUSG00000026407

Domain	Start	End	E-Value	Type
Pfam:Ion_trans	88	333	9.1e-57	PFAM
PDB:4DEY\|B	334	417	1e-20	PDB
Pfam:Ion_trans	466	660	3.7e-46	PFAM
Pfam:PKD_channel	513	667	6.7e-7	PFAM
low complexity region	675	685	N/A	INTRINSIC
low complexity region	740	756	N/A	INTRINSIC
low complexity region	804	818	N/A	INTRINSIC
Pfam:Ion_trans	834	1064	3.9e-53	PFAM
Pfam:Ion_trans	1152	1361	6.7e-66	PFAM
Pfam:PKD_channel	1201	1368	8.4e-10	PFAM
Blast:EFh	1382	1410	5e-8	BLAST
Ca_chan_IQ	1496	1529	3.71e-14	SMART
low complexity region	1638	1650	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000160641

SMART Domains

Protein: ENSMUSP00000125278
Gene: ENSMUSG00000026407

Domain	Start	End	E-Value	Type
Pfam:Ion_trans	88	333	9.3e-57	PFAM
PDB:4DEY\|B	334	417	1e-20	PDB
Pfam:Ion_trans	466	660	3.8e-46	PFAM
Pfam:PKD_channel	513	667	6.7e-7	PFAM
low complexity region	675	685	N/A	INTRINSIC
low complexity region	740	756	N/A	INTRINSIC
low complexity region	804	818	N/A	INTRINSIC
Pfam:Ion_trans	834	1064	4e-53	PFAM
Pfam:PKD_channel	1126	1387	6.1e-12	PFAM
Pfam:Ion_trans	1152	1380	9e-65	PFAM
Blast:EFh	1401	1429	5e-8	BLAST
Ca_chan_IQ	1515	1548	3.71e-14	SMART
low complexity region	1657	1669	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000161865

SMART Domains

Protein: ENSMUSP00000125262
Gene: ENSMUSG00000026407

Domain	Start	End	E-Value	Type
Pfam:Ion_trans	3	98	1.1e-21	PFAM
Pfam:Ion_trans	184	425	3.3e-56	PFAM
Pfam:PKD_channel	267	420	1.8e-7	PFAM
low complexity region	428	438	N/A	INTRINSIC
low complexity region	493	509	N/A	INTRINSIC
Pfam:Ion_trans	551	829	1.9e-65	PFAM
Pfam:Ion_trans	870	1126	5.4e-72	PFAM
Pfam:PKD_channel	954	1121	7.2e-10	PFAM
Pfam:GPHH	1128	1197	1.8e-38	PFAM
Ca_chan_IQ	1249	1282	3.71e-14	SMART
low complexity region	1391	1403	N/A	INTRINSIC

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (71/71)

MGI Phenotype

Strain: 1856326
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the five subunits of the slowly inactivating L-type voltage-dependent calcium channel in skeletal muscle cells. Mutations in this gene have been associated with hypokalemic periodic paralysis, thyrotoxic periodic paralysis and malignant hyperthermia susceptibility. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous mutants show edema and failure of myoblast differentiation by day 13 of embryonic development and die perinatally. All muscles degenerate and additional secondary anomalies of the skeleton, short jaw, and cleft palate are seen. [provided by MGI curators]

Allele List at MGI

All alleles(4) : Targeted(3) Spontaneous(1)

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310003L06Rik	A	T	5: 87,972,505 (GRCm38)	I374F	probably benign	Het
Ak9	G	A	10: 41,424,716 (GRCm38)	V1108I		Het
Aldh16a1	C	T	7: 45,141,982 (GRCm38)	A790T	possibly damaging	Het
Anks1	A	T	17: 28,059,580 (GRCm38)		probably benign	Het
Antxr2	T	G	5: 97,977,679 (GRCm38)	T240P	probably benign	Het
Arfgef1	A	T	1: 10,179,833 (GRCm38)	M945K	probably damaging	Het
Arhgef17	T	C	7: 100,879,659 (GRCm38)	T1591A	probably benign	Het
Aurka	A	G	2: 172,356,930 (GRCm38)	S374P	probably damaging	Het
Bccip	T	C	7: 133,719,204 (GRCm38)	S236P	probably benign	Het
Calm1	A	G	12: 100,205,685 (GRCm38)	E132G	probably benign	Het
Casz1	A	G	4: 148,946,043 (GRCm38)	D1173G	probably damaging	Het
Cdh17	A	G	4: 11,795,659 (GRCm38)	D413G	probably damaging	Het
Cfap57	A	G	4: 118,593,074 (GRCm38)	I617T	possibly damaging	Het
Creb5	A	G	6: 53,681,033 (GRCm38)	D116G	possibly damaging	Het
Csnka2ip	A	C	16: 64,478,991 (GRCm38)	S337A	unknown	Het
Ddx60	A	G	8: 62,000,597 (GRCm38)	E1250G	probably benign	Het
Dlgap2	T	A	8: 14,823,577 (GRCm38)	S727T	probably benign	Het
Dpy19l1	T	C	9: 24,485,111 (GRCm38)		probably benign	Het
Ebf2	A	G	14: 67,238,982 (GRCm38)	T134A	possibly damaging	Het
Echdc2	A	T	4: 108,172,909 (GRCm38)	M136L	probably benign	Het
Enpp2	A	G	15: 54,851,407 (GRCm38)	F598S	probably benign	Het
Extl3	A	C	14: 65,076,284 (GRCm38)	L483R	probably damaging	Het
Gcat	T	C	15: 79,035,889 (GRCm38)	V227A	possibly damaging	Het
Hsf2	A	G	10: 57,505,346 (GRCm38)	D344G	probably damaging	Het
Ighm	C	T	12: 113,421,545 (GRCm38)	G265D		Het
Igsf9b	T	G	9: 27,334,739 (GRCm38)		probably benign	Het
Ints6	A	G	14: 62,702,453 (GRCm38)	V596A	probably benign	Het
Ints8	T	C	4: 11,246,120 (GRCm38)	E182G	probably damaging	Het
Iqgap2	A	G	13: 95,682,151 (GRCm38)		probably null	Het
Kalrn	G	T	16: 34,357,100 (GRCm38)	Q250K	probably benign	Het
Lrrc1	T	A	9: 77,544,488 (GRCm38)	N46Y	probably damaging	Het
Myl10	G	C	5: 136,697,971 (GRCm38)	V70L	probably benign	Het
Naa50	A	G	16: 44,157,131 (GRCm38)	N74S	probably benign	Het
Neb	T	C	2: 52,288,835 (GRCm38)	N1303S	probably benign	Het
Nfs1	A	T	2: 156,134,493 (GRCm38)	C160*	probably null	Het
Olfr472	A	G	7: 107,903,626 (GRCm38)	K303R	probably benign	Het
Olfr591	T	G	7: 103,173,073 (GRCm38)	K188T	probably damaging	Het
Olfr740	T	A	14: 50,453,564 (GRCm38)	S171T	probably benign	Het
Olfr809	T	C	10: 129,776,840 (GRCm38)	S309P	probably benign	Het
Orm2	T	C	4: 63,363,026 (GRCm38)	F67S	possibly damaging	Het
Pex5	A	G	6: 124,405,183 (GRCm38)	S180P	probably benign	Het
Phf14	G	C	6: 11,992,062 (GRCm38)	G746R	probably damaging	Het
Pkm	T	A	9: 59,668,631 (GRCm38)	V110E	probably damaging	Het
Plekha6	T	G	1: 133,264,687 (GRCm38)	N78K	probably damaging	Het
Plxna2	G	A	1: 194,790,175 (GRCm38)	V1076I	probably benign	Het
Polq	C	A	16: 37,061,819 (GRCm38)	D1448E	probably damaging	Het
Pot1b	T	C	17: 55,687,895 (GRCm38)	T256A	probably benign	Het
Prkch	C	T	12: 73,702,764 (GRCm38)	T377I	possibly damaging	Het
Prl3c1	A	C	13: 27,199,185 (GRCm38)		probably benign	Het
Prl7b1	A	C	13: 27,602,772 (GRCm38)	V158G	possibly damaging	Het
Prss22	T	C	17: 23,993,981 (GRCm38)	S261G	probably damaging	Het
Psd	T	C	19: 46,321,102 (GRCm38)		probably benign	Het
Psg18	A	T	7: 18,353,377 (GRCm38)	Y119N	probably damaging	Het
Rbm6	T	G	9: 107,852,794 (GRCm38)	R218S	probably damaging	Het
Rnf213	T	A	11: 119,434,742 (GRCm38)	S1491T		Het
Rsf1	T	C	7: 97,661,925 (GRCm38)	S621P		Het
Runx1	C	A	16: 92,605,656 (GRCm38)	*466L	probably null	Het
Samd4	A	G	14: 47,016,678 (GRCm38)	I200V	probably benign	Het
Sdsl	C	T	5: 120,459,519 (GRCm38)	C241Y	probably benign	Het
Selenon	T	C	4: 134,551,414 (GRCm38)		probably benign	Het
Setx	C	T	2: 29,145,690 (GRCm38)	P729L	possibly damaging	Het
Sf1	C	T	19: 6,368,366 (GRCm38)	Q55*	probably null	Het
Slc12a5	A	T	2: 164,993,691 (GRCm38)	N833I	probably damaging	Het
Slc1a4	T	C	11: 20,332,286 (GRCm38)	R63G	probably damaging	Het
Tmeff2	G	T	1: 51,181,837 (GRCm38)	A324S	probably benign	Het
Tmem217	A	G	17: 29,526,492 (GRCm38)	I88T	possibly damaging	Het
Tnfsf8	A	T	4: 63,860,878 (GRCm38)	I61N	probably benign	Het
Tpbgl	G	T	7: 99,625,567 (GRCm38)	A361E	probably damaging	Het
Trhde	T	A	10: 114,487,006 (GRCm38)	E667V	probably benign	Het
Unc13b	A	G	4: 43,263,568 (GRCm38)	T1598A	probably benign	Het
Vmn2r73	A	T	7: 85,858,302 (GRCm38)	C601S	probably benign	Het
Zfp873	C	A	10: 82,060,879 (GRCm38)	H481Q	probably damaging	Het

Other mutations in Cacna1s

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00336:Cacna1s	APN	1	136,084,273 (GRCm38)	nonsense	probably null
IGL00517:Cacna1s	APN	1	136,087,339 (GRCm38)	missense	probably damaging	1.00
IGL01316:Cacna1s	APN	1	136,118,964 (GRCm38)	missense	probably benign	0.01
IGL01348:Cacna1s	APN	1	136,075,152 (GRCm38)	missense	possibly damaging	0.95
IGL01739:Cacna1s	APN	1	136,097,132 (GRCm38)	critical splice donor site	probably null
IGL01773:Cacna1s	APN	1	136,118,753 (GRCm38)	missense	probably benign	0.32
IGL02056:Cacna1s	APN	1	136,119,000 (GRCm38)	missense	probably benign
IGL02262:Cacna1s	APN	1	136,108,129 (GRCm38)	missense	probably damaging	0.98
IGL02324:Cacna1s	APN	1	136,075,176 (GRCm38)	splice site	probably benign
IGL02352:Cacna1s	APN	1	136,093,252 (GRCm38)	splice site	probably benign
IGL02359:Cacna1s	APN	1	136,093,252 (GRCm38)	splice site	probably benign
IGL02370:Cacna1s	APN	1	136,085,347 (GRCm38)	missense	probably damaging	1.00
IGL02377:Cacna1s	APN	1	136,068,994 (GRCm38)	missense	probably damaging	1.00
IGL02474:Cacna1s	APN	1	136,118,380 (GRCm38)	missense	probably benign
IGL02606:Cacna1s	APN	1	136,079,519 (GRCm38)	missense	probably damaging	0.99
IGL02833:Cacna1s	APN	1	136,071,005 (GRCm38)	missense	probably benign	0.03
IGL02974:Cacna1s	APN	1	136,092,617 (GRCm38)	missense	possibly damaging	0.78
IGL03064:Cacna1s	APN	1	136,111,993 (GRCm38)	missense	probably damaging	1.00
IGL03093:Cacna1s	APN	1	136,116,064 (GRCm38)	missense	probably benign	0.00
IGL03286:Cacna1s	APN	1	136,077,659 (GRCm38)	missense	probably benign
brookstone	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
flyfish	UTSW	1	136,116,061 (GRCm38)	missense	probably benign	0.21
forelle	UTSW	1	136,095,858 (GRCm38)	missense	probably damaging	0.99
river	UTSW	1	136,105,844 (GRCm38)	missense	possibly damaging	0.88
stream	UTSW	1	136,105,814 (GRCm38)	missense	probably damaging	1.00
BB009:Cacna1s	UTSW	1	136,084,359 (GRCm38)	missense	probably damaging	0.99
BB019:Cacna1s	UTSW	1	136,084,359 (GRCm38)	missense	probably damaging	0.99
G1Funyon:Cacna1s	UTSW	1	136,073,441 (GRCm38)	unclassified	probably benign
N/A:Cacna1s	UTSW	1	136,073,509 (GRCm38)	missense	probably benign	0.00
R0030:Cacna1s	UTSW	1	136,094,989 (GRCm38)	critical splice donor site	probably null
R0030:Cacna1s	UTSW	1	136,094,989 (GRCm38)	critical splice donor site	probably null
R0097:Cacna1s	UTSW	1	136,100,622 (GRCm38)	missense	possibly damaging	0.79
R0097:Cacna1s	UTSW	1	136,100,622 (GRCm38)	missense	possibly damaging	0.79
R0240:Cacna1s	UTSW	1	136,073,496 (GRCm38)	unclassified	probably benign
R0255:Cacna1s	UTSW	1	136,118,806 (GRCm38)	missense	possibly damaging	0.93
R0302:Cacna1s	UTSW	1	136,100,604 (GRCm38)	missense	probably benign	0.01
R0319:Cacna1s	UTSW	1	136,070,717 (GRCm38)	missense	probably damaging	0.99
R0411:Cacna1s	UTSW	1	136,113,303 (GRCm38)	missense	probably damaging	1.00
R0413:Cacna1s	UTSW	1	136,098,209 (GRCm38)	missense	probably benign	0.00
R0482:Cacna1s	UTSW	1	136,113,394 (GRCm38)	missense	probably benign
R0491:Cacna1s	UTSW	1	136,089,008 (GRCm38)	splice site	probably benign
R0518:Cacna1s	UTSW	1	136,076,859 (GRCm38)	missense	probably benign
R0717:Cacna1s	UTSW	1	136,098,291 (GRCm38)	missense	probably damaging	1.00
R0725:Cacna1s	UTSW	1	136,098,526 (GRCm38)	splice site	probably benign
R0815:Cacna1s	UTSW	1	136,112,957 (GRCm38)	missense	possibly damaging	0.95
R1384:Cacna1s	UTSW	1	136,094,971 (GRCm38)	missense	probably benign	0.02
R1518:Cacna1s	UTSW	1	136,098,551 (GRCm38)	missense	probably damaging	1.00
R1548:Cacna1s	UTSW	1	136,110,937 (GRCm38)	missense	probably damaging	1.00
R1725:Cacna1s	UTSW	1	136,098,623 (GRCm38)	missense	probably damaging	1.00
R1728:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1729:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1730:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1739:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1762:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1783:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1784:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1785:Cacna1s	UTSW	1	136,118,716 (GRCm38)	missense	probably benign
R1800:Cacna1s	UTSW	1	136,076,854 (GRCm38)	missense	probably benign
R1924:Cacna1s	UTSW	1	136,089,017 (GRCm38)	splice site	probably null
R1969:Cacna1s	UTSW	1	136,119,095 (GRCm38)	missense	probably benign	0.42
R2072:Cacna1s	UTSW	1	136,079,504 (GRCm38)	missense	probably benign
R2380:Cacna1s	UTSW	1	136,095,848 (GRCm38)	missense	probably damaging	1.00
R3110:Cacna1s	UTSW	1	136,075,093 (GRCm38)	nonsense	probably null
R3112:Cacna1s	UTSW	1	136,075,093 (GRCm38)	nonsense	probably null
R3151:Cacna1s	UTSW	1	136,105,794 (GRCm38)	missense	probably damaging	1.00
R3696:Cacna1s	UTSW	1	136,105,814 (GRCm38)	missense	probably damaging	1.00
R3722:Cacna1s	UTSW	1	136,069,042 (GRCm38)	missense	possibly damaging	0.77
R3804:Cacna1s	UTSW	1	136,107,018 (GRCm38)	missense	possibly damaging	0.85
R3813:Cacna1s	UTSW	1	136,085,347 (GRCm38)	missense	probably damaging	1.00
R3905:Cacna1s	UTSW	1	136,084,269 (GRCm38)	missense	probably damaging	0.99
R3907:Cacna1s	UTSW	1	136,084,269 (GRCm38)	missense	probably damaging	0.99
R3909:Cacna1s	UTSW	1	136,084,269 (GRCm38)	missense	probably damaging	0.99
R4170:Cacna1s	UTSW	1	136,108,195 (GRCm38)	missense	probably damaging	1.00
R4329:Cacna1s	UTSW	1	136,119,033 (GRCm38)	missense	probably benign	0.00
R4485:Cacna1s	UTSW	1	136,076,852 (GRCm38)	missense	probably damaging	1.00
R4581:Cacna1s	UTSW	1	136,070,970 (GRCm38)	splice site	probably null
R4719:Cacna1s	UTSW	1	136,118,652 (GRCm38)	splice site	probably benign
R4816:Cacna1s	UTSW	1	136,115,269 (GRCm38)	missense	possibly damaging	0.89
R4909:Cacna1s	UTSW	1	136,079,604 (GRCm38)	missense	probably damaging	0.99
R4917:Cacna1s	UTSW	1	136,101,564 (GRCm38)	critical splice donor site	probably null
R5296:Cacna1s	UTSW	1	136,095,785 (GRCm38)	missense	probably benign	0.11
R5411:Cacna1s	UTSW	1	136,105,811 (GRCm38)	missense	probably benign	0.09
R5503:Cacna1s	UTSW	1	136,086,742 (GRCm38)	missense	probably damaging	1.00
R5533:Cacna1s	UTSW	1	136,098,375 (GRCm38)	critical splice donor site	probably null
R5714:Cacna1s	UTSW	1	136,112,066 (GRCm38)	missense	probably benign	0.44
R5775:Cacna1s	UTSW	1	136,108,122 (GRCm38)	missense	probably damaging	1.00
R5814:Cacna1s	UTSW	1	136,107,142 (GRCm38)	missense	probably benign	0.31
R5820:Cacna1s	UTSW	1	136,079,604 (GRCm38)	missense	probably damaging	1.00
R5822:Cacna1s	UTSW	1	136,112,078 (GRCm38)	missense	probably damaging	1.00
R5877:Cacna1s	UTSW	1	136,100,667 (GRCm38)	missense	probably damaging	0.99
R5923:Cacna1s	UTSW	1	136,076,822 (GRCm38)	missense	possibly damaging	0.79
R6021:Cacna1s	UTSW	1	136,106,487 (GRCm38)	missense	probably benign	0.15
R6037:Cacna1s	UTSW	1	136,070,967 (GRCm38)	missense	possibly damaging	0.90
R6037:Cacna1s	UTSW	1	136,070,967 (GRCm38)	missense	possibly damaging	0.90
R6056:Cacna1s	UTSW	1	136,105,836 (GRCm38)	missense	probably damaging	1.00
R6143:Cacna1s	UTSW	1	136,076,758 (GRCm38)	missense	probably damaging	0.99
R6222:Cacna1s	UTSW	1	136,104,622 (GRCm38)	missense	probably benign	0.00
R6237:Cacna1s	UTSW	1	136,105,844 (GRCm38)	missense	possibly damaging	0.88
R6274:Cacna1s	UTSW	1	136,089,045 (GRCm38)	missense	probably benign	0.02
R6609:Cacna1s	UTSW	1	136,113,391 (GRCm38)	missense	probably benign	0.30
R6626:Cacna1s	UTSW	1	136,094,965 (GRCm38)	missense	probably damaging	1.00
R6838:Cacna1s	UTSW	1	136,084,437 (GRCm38)	missense	possibly damaging	0.91
R6848:Cacna1s	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
R6849:Cacna1s	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
R6850:Cacna1s	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
R6851:Cacna1s	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
R6868:Cacna1s	UTSW	1	136,092,694 (GRCm38)	missense	probably benign	0.01
R6879:Cacna1s	UTSW	1	136,115,959 (GRCm38)	missense	probably benign	0.12
R6893:Cacna1s	UTSW	1	136,077,693 (GRCm38)	missense	probably benign	0.05
R7017:Cacna1s	UTSW	1	136,095,858 (GRCm38)	missense	probably damaging	0.99
R7228:Cacna1s	UTSW	1	136,071,059 (GRCm38)	missense	possibly damaging	0.90
R7283:Cacna1s	UTSW	1	136,073,708 (GRCm38)	missense	probably damaging	1.00
R7357:Cacna1s	UTSW	1	136,071,021 (GRCm38)	missense	probably damaging	0.99
R7385:Cacna1s	UTSW	1	136,092,633 (GRCm38)	missense	probably damaging	0.99
R7421:Cacna1s	UTSW	1	136,086,802 (GRCm38)	missense	probably damaging	1.00
R7505:Cacna1s	UTSW	1	136,085,449 (GRCm38)	nonsense	probably null
R7519:Cacna1s	UTSW	1	136,070,756 (GRCm38)	missense	probably damaging	0.99
R7675:Cacna1s	UTSW	1	136,110,874 (GRCm38)	missense	probably damaging	1.00
R7746:Cacna1s	UTSW	1	136,069,018 (GRCm38)	missense	probably damaging	0.99
R7779:Cacna1s	UTSW	1	136,119,029 (GRCm38)	missense	probably damaging	1.00
R7850:Cacna1s	UTSW	1	136,071,048 (GRCm38)	missense	probably damaging	1.00
R7932:Cacna1s	UTSW	1	136,084,359 (GRCm38)	missense	probably damaging	0.99
R7935:Cacna1s	UTSW	1	136,092,595 (GRCm38)	missense	possibly damaging	0.62
R7950:Cacna1s	UTSW	1	136,100,625 (GRCm38)	missense	probably benign	0.01
R7969:Cacna1s	UTSW	1	136,076,732 (GRCm38)	missense	probably damaging	1.00
R8083:Cacna1s	UTSW	1	136,095,791 (GRCm38)	missense	possibly damaging	0.91
R8101:Cacna1s	UTSW	1	136,118,665 (GRCm38)	missense	probably benign	0.02
R8123:Cacna1s	UTSW	1	136,108,179 (GRCm38)	missense	probably damaging	1.00
R8191:Cacna1s	UTSW	1	136,108,155 (GRCm38)	missense	probably damaging	1.00
R8194:Cacna1s	UTSW	1	136,077,692 (GRCm38)	missense	probably benign	0.33
R8251:Cacna1s	UTSW	1	136,086,723 (GRCm38)	missense	probably damaging	1.00
R8265:Cacna1s	UTSW	1	136,092,626 (GRCm38)	nonsense	probably null
R8310:Cacna1s	UTSW	1	136,087,337 (GRCm38)	missense	probably damaging	1.00
R8359:Cacna1s	UTSW	1	136,116,061 (GRCm38)	missense	probably benign	0.21
R8461:Cacna1s	UTSW	1	136,073,702 (GRCm38)	missense	possibly damaging	0.53
R8553:Cacna1s	UTSW	1	136,091,802 (GRCm38)	missense	possibly damaging	0.93
R8743:Cacna1s	UTSW	1	136,105,548 (GRCm38)	missense	probably damaging	1.00
R8766:Cacna1s	UTSW	1	136,075,143 (GRCm38)	missense	probably damaging	1.00
R8884:Cacna1s	UTSW	1	136,115,243 (GRCm38)	missense	probably benign	0.05
R8897:Cacna1s	UTSW	1	136,117,654 (GRCm38)	missense	probably benign	0.01
R8939:Cacna1s	UTSW	1	136,086,806 (GRCm38)	critical splice donor site	probably null
R8953:Cacna1s	UTSW	1	136,097,432 (GRCm38)	missense	possibly damaging	0.94
R9039:Cacna1s	UTSW	1	136,088,319 (GRCm38)	missense	probably benign
R9058:Cacna1s	UTSW	1	136,070,698 (GRCm38)	nonsense	probably null
R9137:Cacna1s	UTSW	1	136,069,006 (GRCm38)	missense	possibly damaging	0.89
R9332:Cacna1s	UTSW	1	136,092,714 (GRCm38)	nonsense	probably null
R9416:Cacna1s	UTSW	1	136,094,951 (GRCm38)	missense	possibly damaging	0.88
R9427:Cacna1s	UTSW	1	136,084,352 (GRCm38)	missense	probably benign	0.30
R9446:Cacna1s	UTSW	1	136,117,624 (GRCm38)	missense	probably benign	0.00
R9564:Cacna1s	UTSW	1	136,118,778 (GRCm38)	missense	probably benign
R9620:Cacna1s	UTSW	1	136,108,171 (GRCm38)	missense	probably damaging	1.00
X0025:Cacna1s	UTSW	1	136,115,970 (GRCm38)	missense	probably benign	0.00
Z1176:Cacna1s	UTSW	1	136,107,084 (GRCm38)	nonsense	probably null
Z1177:Cacna1s	UTSW	1	136,117,686 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GTCTCAGAAGGTACAGAGGTCC -3'
(R):5'- CCAAAGTTGTCGAAGTGGGTG -3'

Sequencing Primer
(F):5'- CCCTCTGGTTGTTCCTGAAGTATGAG -3'
(R):5'- CGAAGTGGGTGATGCCG -3'

Posted On

2020-12-09