Mutagenetix > Incidental Mutation

Incidental Mutation 'R1450:Csmd1'

162151

Institutional Source

Beutler Lab

Gene Symbol

Csmd1

Ensembl Gene

ENSMUSG00000060924

Gene Name

CUB and Sushi multiple domains 1

Synonyms

MMRRC Submission

039505-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1450 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

15942537-17585602 bp(-) (GRCm39)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

T to G at 15995180 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000080751 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000082104] [ENSMUST00000082104]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000082104

SMART Domains

Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
CUB	32	140	1.46e-26	SMART
CCP	145	202	1.01e-11	SMART
CUB	208	312	1.05e-27	SMART
CCP	349	406	1.28e-8	SMART
CUB	411	522	2.34e-25	SMART
CCP	527	580	1.22e-14	SMART
CUB	584	692	1.61e-37	SMART
CCP	697	754	4.41e-12	SMART
CUB	758	866	6.55e-38	SMART
CCP	873	926	2.53e-12	SMART
CUB	930	1040	8.94e-22	SMART
CCP	1045	1100	7.06e-11	SMART
CUB	1104	1212	3.14e-26	SMART
CCP	1217	1273	1.18e-12	SMART
CUB	1277	1386	9.72e-32	SMART
CCP	1391	1447	2.06e-12	SMART
CUB	1451	1559	1.68e-35	SMART
CCP	1564	1621	2.53e-12	SMART
CUB	1625	1733	4.24e-14	SMART
CCP	1741	1798	9.46e-12	SMART
CUB	1802	1910	4.23e-32	SMART
CCP	1915	1970	8.23e-12	SMART
CUB	1974	2082	8.59e-33	SMART
CCP	2087	2142	6.09e-15	SMART
CUB	2146	2253	2.36e-30	SMART
CCP	2258	2315	1.1e-12	SMART
CUB	2320	2430	4.3e-24	SMART
CCP	2432	2490	2.94e-8	SMART
CCP	2495	2552	2.03e-11	SMART
CCP	2557	2617	1.22e-5	SMART
CCP	2622	2675	2.72e-12	SMART
CCP	2680	2733	5.86e-17	SMART
CCP	2738	2791	6.09e-15	SMART
CCP	2796	2854	9.1e-14	SMART
CCP	2859	2912	3.96e-14	SMART
CCP	2920	2973	4.41e-12	SMART
CCP	2978	3032	2.94e-8	SMART
CCP	3037	3092	6.59e-11	SMART
CCP	3097	3150	4.12e-12	SMART
CCP	3155	3208	7.92e-14	SMART
CCP	3216	3270	2.8e-14	SMART
CCP	3275	3330	3.78e-11	SMART
transmembrane domain	3487	3509	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000082104

SMART Domains

Protein: ENSMUSP00000080751
Gene: ENSMUSG00000060924

Domain	Start	End	E-Value	Type
signal peptide	1	29	N/A	INTRINSIC
CUB	32	140	1.46e-26	SMART
CCP	145	202	1.01e-11	SMART
CUB	208	312	1.05e-27	SMART
CCP	349	406	1.28e-8	SMART
CUB	411	522	2.34e-25	SMART
CCP	527	580	1.22e-14	SMART
CUB	584	692	1.61e-37	SMART
CCP	697	754	4.41e-12	SMART
CUB	758	866	6.55e-38	SMART
CCP	873	926	2.53e-12	SMART
CUB	930	1040	8.94e-22	SMART
CCP	1045	1100	7.06e-11	SMART
CUB	1104	1212	3.14e-26	SMART
CCP	1217	1273	1.18e-12	SMART
CUB	1277	1386	9.72e-32	SMART
CCP	1391	1447	2.06e-12	SMART
CUB	1451	1559	1.68e-35	SMART
CCP	1564	1621	2.53e-12	SMART
CUB	1625	1733	4.24e-14	SMART
CCP	1741	1798	9.46e-12	SMART
CUB	1802	1910	4.23e-32	SMART
CCP	1915	1970	8.23e-12	SMART
CUB	1974	2082	8.59e-33	SMART
CCP	2087	2142	6.09e-15	SMART
CUB	2146	2253	2.36e-30	SMART
CCP	2258	2315	1.1e-12	SMART
CUB	2320	2430	4.3e-24	SMART
CCP	2432	2490	2.94e-8	SMART
CCP	2495	2552	2.03e-11	SMART
CCP	2557	2617	1.22e-5	SMART
CCP	2622	2675	2.72e-12	SMART
CCP	2680	2733	5.86e-17	SMART
CCP	2738	2791	6.09e-15	SMART
CCP	2796	2854	9.1e-14	SMART
CCP	2859	2912	3.96e-14	SMART
CCP	2920	2973	4.41e-12	SMART
CCP	2978	3032	2.94e-8	SMART
CCP	3037	3092	6.59e-11	SMART
CCP	3097	3150	4.12e-12	SMART
CCP	3155	3208	7.92e-14	SMART
CCP	3216	3270	2.8e-14	SMART
CCP	3275	3330	3.78e-11	SMART
transmembrane domain	3487	3509	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125551

Meta Mutation Damage Score

0.9494

Coding Region Coverage

1x: 98.8%
3x: 97.7%
10x: 94.0%
20x: 84.8%

Validation Efficiency

96% (73/76)

MGI Phenotype

PHENOTYPE: Mice exhibit normal pre-pulse inhibition, social interaction, sucrose preference and d-amphetamine sensitivity. [provided by MGI curators]

Allele List at MGI

All alleles(1) : Targeted, knock-out(1)

Other mutations in this stock

Total: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca13	A	T	11: 9,380,531 (GRCm39)		probably benign	Het
Adh4	C	T	3: 138,129,935 (GRCm39)	P254S	probably damaging	Het
Amfr	T	C	8: 94,714,375 (GRCm39)	T223A	probably benign	Het
Ank2	T	C	3: 126,750,951 (GRCm39)	T412A	possibly damaging	Het
Bag6	T	A	17: 35,360,934 (GRCm39)	D422E	probably benign	Het
Ccdc185	T	G	1: 182,575,129 (GRCm39)	Q520P	possibly damaging	Het
Cfap276	T	A	3: 108,449,799 (GRCm39)		probably null	Het
Clock	G	A	5: 76,410,578 (GRCm39)	Q98*	probably null	Het
Cngb3	A	T	4: 19,395,922 (GRCm39)		probably benign	Het
Cubn	A	G	2: 13,365,130 (GRCm39)	L1636P	probably damaging	Het
Dennd4a	A	G	9: 64,818,947 (GRCm39)	I1701V	probably benign	Het
Dgcr2	T	C	16: 17,674,678 (GRCm39)	H243R	possibly damaging	Het
Dimt1	A	G	13: 107,084,151 (GRCm39)	N46S	probably benign	Het
Dnah9	T	C	11: 65,818,612 (GRCm39)	Y58C	probably damaging	Het
Dsg1b	T	A	18: 20,542,241 (GRCm39)	V916E	probably damaging	Het
Dst	T	C	1: 34,227,476 (GRCm39)	S1690P	probably damaging	Het
Dst	T	A	1: 34,251,340 (GRCm39)	I2131K	probably damaging	Het
Epb41l1	T	C	2: 156,353,745 (GRCm39)		probably benign	Het
Fem1a	T	C	17: 56,564,579 (GRCm39)	V224A	probably damaging	Het
Got2	C	T	8: 96,598,614 (GRCm39)	E203K	probably benign	Het
Hcar2	A	T	5: 124,002,813 (GRCm39)	I230N	probably damaging	Het
Herc3	A	T	6: 58,853,500 (GRCm39)	K554*	probably null	Het
Hfm1	A	G	5: 107,066,324 (GRCm39)	F35L	probably damaging	Het
Hmcn1	A	G	1: 150,528,257 (GRCm39)		probably benign	Het
Hoxa13	C	G	6: 52,260,647 (GRCm38)		probably benign	Het
Hoxa13	G	C	6: 52,260,648 (GRCm38)		probably benign	Het
Hs2st1	C	T	3: 144,140,479 (GRCm39)		probably benign	Het
Igfbp5	T	A	1: 72,913,048 (GRCm39)	D84V	probably benign	Het
Ints3	C	A	3: 90,340,135 (GRCm39)	L41F	probably damaging	Het
Ipo5	T	C	14: 121,181,805 (GRCm39)	V966A	probably benign	Het
Kif26a	C	T	12: 112,140,286 (GRCm39)	T505M	probably damaging	Het
Kpna2	A	G	11: 106,888,135 (GRCm39)	S2P	probably benign	Het
Lct	A	G	1: 128,235,640 (GRCm39)	S456P	probably damaging	Het
Lonrf2	G	A	1: 38,852,357 (GRCm39)	P165S	probably benign	Het
Lrrc7	T	G	3: 157,892,681 (GRCm39)	I323L	possibly damaging	Het
Ly6g	A	G	15: 75,030,482 (GRCm39)	K77R	probably benign	Het
Maea	T	C	5: 33,523,144 (GRCm39)		probably null	Het
Marco	A	T	1: 120,404,474 (GRCm39)		probably benign	Het
Mcmbp	G	T	7: 128,317,655 (GRCm39)		probably benign	Het
Mtcl3	A	T	10: 29,023,736 (GRCm39)	N361I	probably damaging	Het
Mtr	T	A	13: 12,208,619 (GRCm39)	R1017W	probably damaging	Het
Myo15a	T	A	11: 60,386,308 (GRCm39)	I1811N	probably damaging	Het
Nbeal2	G	A	9: 110,462,740 (GRCm39)		probably benign	Het
Nlrp10	A	G	7: 108,524,595 (GRCm39)	V295A	probably damaging	Het
Or10ak7	T	C	4: 118,791,707 (GRCm39)	T111A	probably benign	Het
Or51ac3	A	G	7: 103,213,658 (GRCm39)	V276A	probably benign	Het
Or5e1	A	T	7: 108,354,719 (GRCm39)	I219F	probably damaging	Het
Pde4b	A	T	4: 102,458,832 (GRCm39)	Q496L	probably damaging	Het
Peg12	C	A	7: 62,113,324 (GRCm39)	G258*	probably null	Het
Pigc	A	G	1: 161,798,822 (GRCm39)	Y268C	probably benign	Het
Pnisr	G	T	4: 21,874,912 (GRCm39)		probably null	Het
Poteg	T	C	8: 27,937,871 (GRCm39)	F5S	probably benign	Het
Prss40	T	A	1: 34,595,178 (GRCm39)	I101F	probably benign	Het
Ptges3l	T	A	11: 101,312,731 (GRCm39)	D113V	possibly damaging	Het
Raver2	T	C	4: 100,993,349 (GRCm39)	S510P	possibly damaging	Het
Rgr	A	T	14: 36,766,641 (GRCm39)	C94*	probably null	Het
Rp1l1	T	A	14: 64,265,599 (GRCm39)	I395N	probably benign	Het
Sesn3	T	A	9: 14,227,520 (GRCm39)	H168Q	possibly damaging	Het
Sox30	C	A	11: 45,908,098 (GRCm39)	P755Q	probably damaging	Het
Stac3	T	C	10: 127,340,754 (GRCm39)	F173S	probably damaging	Het
Synj2	C	A	17: 6,077,599 (GRCm39)		probably benign	Het
Tars3	A	T	7: 65,297,244 (GRCm39)	I120L	probably benign	Het
Tas2r124	A	G	6: 132,732,019 (GRCm39)	I109M	probably damaging	Het
Tm4sf19	A	T	16: 32,226,781 (GRCm39)	H190L	probably damaging	Het
Tmem143	T	G	7: 45,556,532 (GRCm39)	V179G	probably damaging	Het
Ubr4	T	C	4: 139,195,339 (GRCm39)	F1187S	probably damaging	Het
Ubtfl1	A	G	9: 18,321,209 (GRCm39)	R246G	possibly damaging	Het
Zdhhc5	A	G	2: 84,532,733 (GRCm39)	F57S	probably damaging	Het
Zfp40	A	T	17: 23,394,232 (GRCm39)	M717K	probably benign	Het

Other mutations in Csmd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00095:Csmd1	APN	8	16,059,297 (GRCm39)	splice site	probably benign
IGL00433:Csmd1	APN	8	16,281,387 (GRCm39)	missense	probably damaging	1.00
IGL00500:Csmd1	APN	8	15,971,139 (GRCm39)	missense	probably damaging	1.00
IGL00666:Csmd1	APN	8	16,240,004 (GRCm39)	missense	probably damaging	1.00
IGL00913:Csmd1	APN	8	16,121,301 (GRCm39)	missense	probably benign	0.00
IGL01012:Csmd1	APN	8	15,967,341 (GRCm39)	missense	probably benign	0.00
IGL01123:Csmd1	APN	8	17,584,944 (GRCm39)	missense	possibly damaging	0.96
IGL01348:Csmd1	APN	8	15,960,596 (GRCm39)	missense	probably damaging	0.99
IGL01444:Csmd1	APN	8	16,250,069 (GRCm39)	missense	probably benign	0.00
IGL01530:Csmd1	APN	8	15,953,195 (GRCm39)	missense	probably damaging	0.99
IGL01548:Csmd1	APN	8	16,338,660 (GRCm39)	nonsense	probably null
IGL01814:Csmd1	APN	8	16,551,389 (GRCm39)	missense	probably damaging	1.00
IGL01889:Csmd1	APN	8	16,048,857 (GRCm39)	missense	probably damaging	1.00
IGL02055:Csmd1	APN	8	16,119,015 (GRCm39)	missense	probably damaging	0.99
IGL02066:Csmd1	APN	8	15,976,594 (GRCm39)	missense	probably damaging	1.00
IGL02097:Csmd1	APN	8	16,261,773 (GRCm39)	missense	probably null	0.17
IGL02112:Csmd1	APN	8	16,131,719 (GRCm39)	missense	probably benign	0.18
IGL02161:Csmd1	APN	8	16,408,426 (GRCm39)	missense	probably damaging	0.97
IGL02189:Csmd1	APN	8	16,321,620 (GRCm39)	missense	probably damaging	0.99
IGL02272:Csmd1	APN	8	16,249,907 (GRCm39)	missense	probably damaging	0.99
IGL02292:Csmd1	APN	8	16,261,884 (GRCm39)	missense	probably damaging	1.00
IGL02385:Csmd1	APN	8	15,953,275 (GRCm39)	missense	probably benign	0.08
IGL02424:Csmd1	APN	8	16,142,340 (GRCm39)	missense	probably benign	0.22
IGL02492:Csmd1	APN	8	16,052,597 (GRCm39)	missense	probably benign	0.13
IGL02507:Csmd1	APN	8	17,584,992 (GRCm39)	utr 5 prime	probably benign
IGL02513:Csmd1	APN	8	16,049,869 (GRCm39)	splice site	probably benign
IGL02727:Csmd1	APN	8	16,281,341 (GRCm39)	missense	probably damaging	1.00
IGL02728:Csmd1	APN	8	16,049,779 (GRCm39)	critical splice donor site	probably null
IGL02852:Csmd1	APN	8	15,945,728 (GRCm39)	missense	probably damaging	0.99
IGL02935:Csmd1	APN	8	16,273,348 (GRCm39)	missense	probably damaging	1.00
IGL02945:Csmd1	APN	8	16,321,584 (GRCm39)	missense	possibly damaging	0.92
IGL02959:Csmd1	APN	8	15,960,465 (GRCm39)	missense	probably damaging	0.99
IGL03113:Csmd1	APN	8	16,078,712 (GRCm39)	missense	probably benign
IGL03129:Csmd1	APN	8	16,011,521 (GRCm39)	missense	probably damaging	0.99
IGL03131:Csmd1	APN	8	16,138,231 (GRCm39)	missense	probably damaging	1.00
IGL03275:Csmd1	APN	8	16,207,106 (GRCm39)	missense	probably benign	0.00
IGL03297:Csmd1	APN	8	16,059,432 (GRCm39)	nonsense	probably null
ikura	UTSW	8	16,281,285 (GRCm39)	missense	probably damaging	1.00
I2289:Csmd1	UTSW	8	15,962,381 (GRCm39)	missense	probably benign	0.10
IGL03055:Csmd1	UTSW	8	16,145,515 (GRCm39)	missense	probably damaging	1.00
IGL03097:Csmd1	UTSW	8	15,995,127 (GRCm39)	missense	probably damaging	1.00
PIT4260001:Csmd1	UTSW	8	16,120,327 (GRCm39)	missense	probably damaging	1.00
PIT4378001:Csmd1	UTSW	8	15,945,728 (GRCm39)	missense	probably damaging	0.99
PIT4520001:Csmd1	UTSW	8	15,956,023 (GRCm39)	missense	probably benign	0.01
R0037:Csmd1	UTSW	8	15,967,248 (GRCm39)	missense	probably damaging	0.97
R0095:Csmd1	UTSW	8	16,283,065 (GRCm39)	missense	probably damaging	1.00
R0113:Csmd1	UTSW	8	16,034,849 (GRCm39)	missense	probably damaging	1.00
R0129:Csmd1	UTSW	8	16,129,956 (GRCm39)	missense	possibly damaging	0.95
R0144:Csmd1	UTSW	8	16,441,838 (GRCm39)	missense	probably benign	0.16
R0166:Csmd1	UTSW	8	16,283,036 (GRCm39)	missense	probably benign	0.29
R0227:Csmd1	UTSW	8	16,441,836 (GRCm39)	missense	probably benign	0.05
R0279:Csmd1	UTSW	8	16,273,249 (GRCm39)	missense	probably damaging	0.99
R0280:Csmd1	UTSW	8	16,321,616 (GRCm39)	missense	probably damaging	1.00
R0312:Csmd1	UTSW	8	16,034,760 (GRCm39)	missense	probably damaging	1.00
R0355:Csmd1	UTSW	8	15,968,330 (GRCm39)	missense	probably damaging	0.97
R0367:Csmd1	UTSW	8	15,967,270 (GRCm39)	missense	probably damaging	1.00
R0395:Csmd1	UTSW	8	16,396,652 (GRCm39)	missense	probably damaging	0.99
R0413:Csmd1	UTSW	8	16,760,530 (GRCm39)	missense	probably damaging	0.97
R0457:Csmd1	UTSW	8	16,551,407 (GRCm39)	critical splice acceptor site	probably null
R0463:Csmd1	UTSW	8	15,971,759 (GRCm39)	missense	probably damaging	0.99
R0482:Csmd1	UTSW	8	16,283,115 (GRCm39)	missense	probably damaging	1.00
R0501:Csmd1	UTSW	8	17,077,339 (GRCm39)	missense	probably damaging	0.97
R0505:Csmd1	UTSW	8	16,042,758 (GRCm39)	missense	probably damaging	1.00
R0507:Csmd1	UTSW	8	16,235,358 (GRCm39)	splice site	probably benign
R0511:Csmd1	UTSW	8	15,982,529 (GRCm39)	missense	possibly damaging	0.80
R0555:Csmd1	UTSW	8	16,235,287 (GRCm39)	missense	probably benign
R0580:Csmd1	UTSW	8	15,960,528 (GRCm39)	missense	probably damaging	1.00
R0610:Csmd1	UTSW	8	15,968,208 (GRCm39)	missense	possibly damaging	0.95
R0634:Csmd1	UTSW	8	16,276,405 (GRCm39)	missense	probably damaging	1.00
R0666:Csmd1	UTSW	8	16,119,063 (GRCm39)	missense	possibly damaging	0.88
R0674:Csmd1	UTSW	8	16,050,550 (GRCm39)	missense	probably benign	0.03
R0675:Csmd1	UTSW	8	16,208,145 (GRCm39)	missense	probably benign	0.01
R0763:Csmd1	UTSW	8	17,077,300 (GRCm39)	missense	possibly damaging	0.67
R0781:Csmd1	UTSW	8	15,971,174 (GRCm39)	missense	probably benign	0.35
R0862:Csmd1	UTSW	8	16,240,040 (GRCm39)	missense	probably damaging	0.99
R0864:Csmd1	UTSW	8	16,240,040 (GRCm39)	missense	probably damaging	0.99
R0925:Csmd1	UTSW	8	16,760,634 (GRCm39)	missense	probably benign	0.29
R0926:Csmd1	UTSW	8	16,083,590 (GRCm39)	splice site	probably null
R1005:Csmd1	UTSW	8	16,338,707 (GRCm39)	missense	probably damaging	0.99
R1073:Csmd1	UTSW	8	16,408,477 (GRCm39)	splice site	probably benign
R1185:Csmd1	UTSW	8	16,408,362 (GRCm39)	missense	probably damaging	0.96
R1185:Csmd1	UTSW	8	16,408,362 (GRCm39)	missense	probably damaging	0.96
R1185:Csmd1	UTSW	8	16,408,362 (GRCm39)	missense	probably damaging	0.96
R1256:Csmd1	UTSW	8	16,129,978 (GRCm39)	missense	probably damaging	1.00
R1294:Csmd1	UTSW	8	16,748,052 (GRCm39)	missense	probably damaging	0.99
R1375:Csmd1	UTSW	8	16,513,095 (GRCm39)	splice site	probably null
R1447:Csmd1	UTSW	8	15,975,306 (GRCm39)	nonsense	probably null
R1470:Csmd1	UTSW	8	16,207,218 (GRCm39)	splice site	probably benign
R1580:Csmd1	UTSW	8	15,975,299 (GRCm39)	missense	probably damaging	1.00
R1591:Csmd1	UTSW	8	15,950,710 (GRCm39)	missense	probably damaging	0.99
R1658:Csmd1	UTSW	8	16,131,739 (GRCm39)	missense	possibly damaging	0.69
R1678:Csmd1	UTSW	8	15,968,252 (GRCm39)	missense	possibly damaging	0.58
R1717:Csmd1	UTSW	8	17,266,708 (GRCm39)	missense	possibly damaging	0.58
R1735:Csmd1	UTSW	8	15,982,610 (GRCm39)	missense	probably damaging	0.99
R1750:Csmd1	UTSW	8	15,967,303 (GRCm39)	missense	probably damaging	0.99
R1753:Csmd1	UTSW	8	16,207,134 (GRCm39)	nonsense	probably null
R1822:Csmd1	UTSW	8	16,273,340 (GRCm39)	missense	probably damaging	1.00
R1875:Csmd1	UTSW	8	15,979,101 (GRCm39)	missense	probably damaging	0.99
R1909:Csmd1	UTSW	8	15,956,116 (GRCm39)	missense	probably damaging	1.00
R1912:Csmd1	UTSW	8	16,284,012 (GRCm39)	critical splice donor site	probably null
R1993:Csmd1	UTSW	8	16,396,698 (GRCm39)	missense	probably damaging	0.99
R2067:Csmd1	UTSW	8	15,950,782 (GRCm39)	missense	probably benign
R2094:Csmd1	UTSW	8	16,129,992 (GRCm39)	missense	probably damaging	0.99
R2119:Csmd1	UTSW	8	17,266,749 (GRCm39)	missense	probably damaging	0.98
R2127:Csmd1	UTSW	8	15,967,392 (GRCm39)	missense	probably damaging	1.00
R2138:Csmd1	UTSW	8	15,979,088 (GRCm39)	missense	probably damaging	0.96
R2216:Csmd1	UTSW	8	17,077,355 (GRCm39)	critical splice acceptor site	probably null
R2220:Csmd1	UTSW	8	16,042,641 (GRCm39)	missense	possibly damaging	0.94
R2380:Csmd1	UTSW	8	16,240,101 (GRCm39)	missense	probably damaging	1.00
R2471:Csmd1	UTSW	8	16,261,776 (GRCm39)	missense	probably damaging	1.00
R2984:Csmd1	UTSW	8	16,003,782 (GRCm39)	missense	probably damaging	1.00
R3001:Csmd1	UTSW	8	16,246,184 (GRCm39)	missense	probably damaging	0.98
R3002:Csmd1	UTSW	8	16,246,184 (GRCm39)	missense	probably damaging	0.98
R3003:Csmd1	UTSW	8	16,246,184 (GRCm39)	missense	probably damaging	0.98
R3103:Csmd1	UTSW	8	15,967,405 (GRCm39)	missense	probably damaging	1.00
R3104:Csmd1	UTSW	8	17,077,247 (GRCm39)	missense	probably damaging	1.00
R3620:Csmd1	UTSW	8	16,042,684 (GRCm39)	missense	probably benign	0.29
R3621:Csmd1	UTSW	8	16,042,684 (GRCm39)	missense	probably benign	0.29
R3748:Csmd1	UTSW	8	15,956,071 (GRCm39)	missense	probably damaging	0.99
R3780:Csmd1	UTSW	8	16,252,000 (GRCm39)	missense	probably damaging	1.00
R3815:Csmd1	UTSW	8	16,052,522 (GRCm39)	missense	probably damaging	1.00
R3816:Csmd1	UTSW	8	16,052,522 (GRCm39)	missense	probably damaging	1.00
R3818:Csmd1	UTSW	8	16,052,522 (GRCm39)	missense	probably damaging	1.00
R3819:Csmd1	UTSW	8	16,052,522 (GRCm39)	missense	probably damaging	1.00
R3850:Csmd1	UTSW	8	16,129,936 (GRCm39)	missense	probably benign	0.00
R3945:Csmd1	UTSW	8	15,960,619 (GRCm39)	splice site	probably null
R3980:Csmd1	UTSW	8	15,956,056 (GRCm39)	nonsense	probably null
R4061:Csmd1	UTSW	8	15,995,158 (GRCm39)	missense	probably benign	0.00
R4086:Csmd1	UTSW	8	16,042,738 (GRCm39)	missense	probably damaging	0.99
R4087:Csmd1	UTSW	8	16,042,738 (GRCm39)	missense	probably damaging	0.99
R4089:Csmd1	UTSW	8	16,042,738 (GRCm39)	missense	probably damaging	0.99
R4183:Csmd1	UTSW	8	15,960,464 (GRCm39)	missense	probably damaging	0.99
R4226:Csmd1	UTSW	8	16,050,490 (GRCm39)	missense	probably damaging	0.99
R4454:Csmd1	UTSW	8	15,995,011 (GRCm39)	missense	probably damaging	0.99
R4533:Csmd1	UTSW	8	15,981,037 (GRCm39)	splice site	probably null
R4544:Csmd1	UTSW	8	16,760,652 (GRCm39)	missense	possibly damaging	0.93
R4547:Csmd1	UTSW	8	16,441,811 (GRCm39)	missense	possibly damaging	0.48
R4612:Csmd1	UTSW	8	15,971,908 (GRCm39)	splice site	probably null
R4620:Csmd1	UTSW	8	16,052,694 (GRCm39)	critical splice acceptor site	probably null
R4627:Csmd1	UTSW	8	16,747,933 (GRCm39)	missense	probably benign	0.00
R4633:Csmd1	UTSW	8	16,052,620 (GRCm39)	missense	probably damaging	0.99
R4646:Csmd1	UTSW	8	15,982,511 (GRCm39)	missense	possibly damaging	0.87
R4648:Csmd1	UTSW	8	16,048,788 (GRCm39)	nonsense	probably null
R4668:Csmd1	UTSW	8	16,073,905 (GRCm39)	missense	possibly damaging	0.50
R4709:Csmd1	UTSW	8	16,760,522 (GRCm39)	critical splice donor site	probably null
R4709:Csmd1	UTSW	8	16,073,905 (GRCm39)	missense	possibly damaging	0.96
R4741:Csmd1	UTSW	8	15,960,447 (GRCm39)	missense	probably damaging	0.99
R4774:Csmd1	UTSW	8	16,059,369 (GRCm39)	missense	probably benign	0.11
R4793:Csmd1	UTSW	8	16,138,277 (GRCm39)	missense	probably damaging	1.00
R4829:Csmd1	UTSW	8	16,177,310 (GRCm39)	missense	probably damaging	1.00
R4888:Csmd1	UTSW	8	15,945,674 (GRCm39)	utr 3 prime	probably benign
R4896:Csmd1	UTSW	8	16,059,439 (GRCm39)	missense	probably benign	0.00
R4932:Csmd1	UTSW	8	16,073,779 (GRCm39)	missense	probably damaging	0.99
R4944:Csmd1	UTSW	8	16,048,772 (GRCm39)	missense	probably damaging	1.00
R4953:Csmd1	UTSW	8	16,249,931 (GRCm39)	missense	probably damaging	0.99
R4996:Csmd1	UTSW	8	15,960,452 (GRCm39)	missense	probably damaging	0.97
R5028:Csmd1	UTSW	8	16,039,090 (GRCm39)	missense	probably damaging	1.00
R5146:Csmd1	UTSW	8	16,246,204 (GRCm39)	missense	probably damaging	1.00
R5272:Csmd1	UTSW	8	16,249,958 (GRCm39)	missense	probably damaging	0.99
R5327:Csmd1	UTSW	8	17,266,728 (GRCm39)	missense	possibly damaging	0.94
R5399:Csmd1	UTSW	8	16,760,613 (GRCm39)	missense	probably damaging	1.00
R5411:Csmd1	UTSW	8	15,960,471 (GRCm39)	missense	probably damaging	1.00
R5462:Csmd1	UTSW	8	16,011,486 (GRCm39)	missense	probably benign	0.12
R5463:Csmd1	UTSW	8	16,034,860 (GRCm39)	missense	probably benign	0.34
R5497:Csmd1	UTSW	8	16,135,195 (GRCm39)	missense	probably benign	0.20
R5536:Csmd1	UTSW	8	16,338,674 (GRCm39)	missense	probably damaging	0.99
R5711:Csmd1	UTSW	8	16,003,703 (GRCm39)	missense	probably damaging	1.00
R5730:Csmd1	UTSW	8	16,235,206 (GRCm39)	nonsense	probably null
R5788:Csmd1	UTSW	8	16,251,980 (GRCm39)	missense	probably damaging	1.00
R5941:Csmd1	UTSW	8	15,982,471 (GRCm39)	missense	probably damaging	0.99
R5960:Csmd1	UTSW	8	16,121,430 (GRCm39)	missense	possibly damaging	0.68
R5961:Csmd1	UTSW	8	16,120,366 (GRCm39)	missense	probably damaging	0.99
R5969:Csmd1	UTSW	8	16,121,367 (GRCm39)	missense	probably benign	0.00
R5998:Csmd1	UTSW	8	15,960,443 (GRCm39)	missense	probably damaging	1.00
R6062:Csmd1	UTSW	8	16,142,319 (GRCm39)	missense	possibly damaging	0.68
R6109:Csmd1	UTSW	8	16,249,874 (GRCm39)	missense	possibly damaging	0.93
R6116:Csmd1	UTSW	8	16,261,864 (GRCm39)	missense	probably damaging	1.00
R6143:Csmd1	UTSW	8	16,138,315 (GRCm39)	missense	probably damaging	1.00
R6155:Csmd1	UTSW	8	15,953,231 (GRCm39)	missense	probably benign	0.01
R6197:Csmd1	UTSW	8	15,976,611 (GRCm39)	missense	probably benign	0.32
R6247:Csmd1	UTSW	8	16,246,249 (GRCm39)	missense	possibly damaging	0.91
R6304:Csmd1	UTSW	8	16,108,688 (GRCm39)	missense	probably damaging	1.00
R6317:Csmd1	UTSW	8	16,760,658 (GRCm39)	missense	possibly damaging	0.89
R6318:Csmd1	UTSW	8	15,953,212 (GRCm39)	missense	probably damaging	1.00
R6338:Csmd1	UTSW	8	15,982,492 (GRCm39)	missense	possibly damaging	0.75
R6369:Csmd1	UTSW	8	17,585,020 (GRCm39)	start gained	probably benign
R6447:Csmd1	UTSW	8	15,960,527 (GRCm39)	missense	probably damaging	1.00
R6454:Csmd1	UTSW	8	15,971,150 (GRCm39)	missense	probably damaging	0.99
R6494:Csmd1	UTSW	8	16,261,709 (GRCm39)	splice site	probably null
R6614:Csmd1	UTSW	8	17,266,803 (GRCm39)	missense	probably damaging	1.00
R6736:Csmd1	UTSW	8	16,052,626 (GRCm39)	missense	probably damaging	0.99
R6769:Csmd1	UTSW	8	16,121,408 (GRCm39)	missense	possibly damaging	0.80
R6771:Csmd1	UTSW	8	16,121,408 (GRCm39)	missense	possibly damaging	0.80
R6804:Csmd1	UTSW	8	16,087,260 (GRCm39)	missense	probably damaging	1.00
R6818:Csmd1	UTSW	8	16,235,341 (GRCm39)	missense	probably damaging	1.00
R6863:Csmd1	UTSW	8	17,584,929 (GRCm39)	missense	possibly damaging	0.85
R6930:Csmd1	UTSW	8	16,142,409 (GRCm39)	missense	probably damaging	0.97
R6969:Csmd1	UTSW	8	17,266,805 (GRCm39)	missense	possibly damaging	0.94
R7112:Csmd1	UTSW	8	16,151,142 (GRCm39)	missense	probably damaging	1.00
R7124:Csmd1	UTSW	8	15,953,202 (GRCm39)	missense	probably damaging	1.00
R7167:Csmd1	UTSW	8	15,976,524 (GRCm39)	missense	probably benign
R7243:Csmd1	UTSW	8	15,965,357 (GRCm39)	missense	probably damaging	1.00
R7260:Csmd1	UTSW	8	16,050,574 (GRCm39)	missense	probably damaging	1.00
R7271:Csmd1	UTSW	8	17,077,295 (GRCm39)	missense	probably damaging	0.99
R7324:Csmd1	UTSW	8	16,108,721 (GRCm39)	missense	probably damaging	1.00
R7325:Csmd1	UTSW	8	16,108,721 (GRCm39)	missense	probably damaging	1.00
R7327:Csmd1	UTSW	8	16,108,721 (GRCm39)	missense	probably damaging	1.00
R7373:Csmd1	UTSW	8	16,042,713 (GRCm39)	missense	probably damaging	1.00
R7406:Csmd1	UTSW	8	16,338,707 (GRCm39)	missense	probably damaging	0.99
R7427:Csmd1	UTSW	8	16,073,864 (GRCm39)	missense	possibly damaging	0.91
R7428:Csmd1	UTSW	8	16,073,864 (GRCm39)	missense	possibly damaging	0.91
R7445:Csmd1	UTSW	8	16,208,268 (GRCm39)	missense	possibly damaging	0.61
R7458:Csmd1	UTSW	8	16,003,738 (GRCm39)	missense	probably damaging	1.00
R7476:Csmd1	UTSW	8	15,945,731 (GRCm39)	missense	probably damaging	1.00
R7527:Csmd1	UTSW	8	16,261,732 (GRCm39)	missense	probably damaging	1.00
R7544:Csmd1	UTSW	8	16,142,310 (GRCm39)	missense	probably damaging	1.00
R7583:Csmd1	UTSW	8	16,048,833 (GRCm39)	missense	probably damaging	0.96
R7603:Csmd1	UTSW	8	16,338,696 (GRCm39)	missense	probably damaging	1.00
R7607:Csmd1	UTSW	8	15,968,331 (GRCm39)	missense	possibly damaging	0.94
R7642:Csmd1	UTSW	8	16,135,192 (GRCm39)	missense	probably damaging	0.99
R7669:Csmd1	UTSW	8	15,967,273 (GRCm39)	missense	probably damaging	1.00
R7720:Csmd1	UTSW	8	15,981,108 (GRCm39)	missense	probably damaging	1.00
R7728:Csmd1	UTSW	8	16,281,285 (GRCm39)	missense	probably damaging	1.00
R7738:Csmd1	UTSW	8	16,151,004 (GRCm39)	missense	probably damaging	1.00
R7745:Csmd1	UTSW	8	15,982,461 (GRCm39)	critical splice donor site	probably null
R7879:Csmd1	UTSW	8	16,441,820 (GRCm39)	missense	probably benign	0.28
R7884:Csmd1	UTSW	8	16,011,418 (GRCm39)	missense	probably damaging	1.00
R7897:Csmd1	UTSW	8	17,584,935 (GRCm39)	missense	possibly damaging	0.96
R8111:Csmd1	UTSW	8	15,967,306 (GRCm39)	missense	probably benign
R8119:Csmd1	UTSW	8	17,077,310 (GRCm39)	missense	probably damaging	0.99
R8134:Csmd1	UTSW	8	15,982,550 (GRCm39)	missense	probably damaging	0.99
R8187:Csmd1	UTSW	8	16,177,188 (GRCm39)	missense	probably damaging	0.99
R8196:Csmd1	UTSW	8	16,059,468 (GRCm39)	missense	probably benign	0.18
R8231:Csmd1	UTSW	8	16,747,939 (GRCm39)	missense	possibly damaging	0.82
R8242:Csmd1	UTSW	8	16,760,670 (GRCm39)	missense	probably benign	0.42
R8274:Csmd1	UTSW	8	15,960,453 (GRCm39)	missense	possibly damaging	0.93
R8286:Csmd1	UTSW	8	16,039,188 (GRCm39)	missense	probably benign	0.18
R8289:Csmd1	UTSW	8	16,108,716 (GRCm39)	missense	probably damaging	0.99
R8314:Csmd1	UTSW	8	16,208,258 (GRCm39)	missense	probably benign
R8323:Csmd1	UTSW	8	17,266,751 (GRCm39)	nonsense	probably null
R8387:Csmd1	UTSW	8	16,050,484 (GRCm39)	missense	possibly damaging	0.94
R8413:Csmd1	UTSW	8	15,950,676 (GRCm39)	missense	probably damaging	0.98
R8672:Csmd1	UTSW	8	15,976,598 (GRCm39)	missense	probably benign	0.01
R8765:Csmd1	UTSW	8	16,760,627 (GRCm39)	nonsense	probably null
R8789:Csmd1	UTSW	8	17,266,722 (GRCm39)	missense	probably damaging	0.99
R8828:Csmd1	UTSW	8	16,048,794 (GRCm39)	missense	probably benign	0.00
R8858:Csmd1	UTSW	8	16,120,318 (GRCm39)	missense	probably benign	0.10
R8878:Csmd1	UTSW	8	15,960,528 (GRCm39)	missense	probably damaging	1.00
R8911:Csmd1	UTSW	8	16,748,019 (GRCm39)	missense	probably damaging	0.99
R8966:Csmd1	UTSW	8	16,250,059 (GRCm39)	missense	probably damaging	1.00
R8978:Csmd1	UTSW	8	15,971,056 (GRCm39)	missense	probably benign	0.37
R8996:Csmd1	UTSW	8	15,971,105 (GRCm39)	missense	possibly damaging	0.54
R9045:Csmd1	UTSW	8	16,284,088 (GRCm39)	missense	probably damaging	0.99
R9084:Csmd1	UTSW	8	16,138,325 (GRCm39)	missense	probably benign
R9124:Csmd1	UTSW	8	16,034,806 (GRCm39)	missense	probably damaging	0.99
R9127:Csmd1	UTSW	8	16,273,286 (GRCm39)	missense	probably benign	0.31
R9146:Csmd1	UTSW	8	16,048,832 (GRCm39)	missense	probably benign	0.00
R9198:Csmd1	UTSW	8	15,962,430 (GRCm39)	missense	probably damaging	1.00
R9285:Csmd1	UTSW	8	15,956,088 (GRCm39)	missense	probably damaging	1.00
R9303:Csmd1	UTSW	8	16,011,532 (GRCm39)	missense	probably benign	0.31
R9305:Csmd1	UTSW	8	16,011,532 (GRCm39)	missense	probably benign	0.31
R9326:Csmd1	UTSW	8	16,049,803 (GRCm39)	missense	probably benign	0.21
R9356:Csmd1	UTSW	8	16,252,069 (GRCm39)	missense	probably damaging	1.00
R9385:Csmd1	UTSW	8	16,034,756 (GRCm39)	missense	probably benign	0.19
R9444:Csmd1	UTSW	8	16,208,250 (GRCm39)	missense	probably benign	0.30
R9476:Csmd1	UTSW	8	15,981,215 (GRCm39)	critical splice acceptor site	probably null
R9506:Csmd1	UTSW	8	16,250,023 (GRCm39)	missense	probably damaging	1.00
R9614:Csmd1	UTSW	8	16,208,239 (GRCm39)	missense	probably benign	0.00
R9668:Csmd1	UTSW	8	16,261,772 (GRCm39)	missense	probably benign	0.00
X0011:Csmd1	UTSW	8	16,246,277 (GRCm39)	missense	probably damaging	1.00
X0021:Csmd1	UTSW	8	16,235,270 (GRCm39)	missense	probably damaging	1.00
X0024:Csmd1	UTSW	8	16,087,232 (GRCm39)	missense	probably damaging	0.99
X0028:Csmd1	UTSW	8	15,965,333 (GRCm39)	missense	possibly damaging	0.79
Z1088:Csmd1	UTSW	8	16,239,992 (GRCm39)	missense	possibly damaging	0.50
Z1088:Csmd1	UTSW	8	16,142,272 (GRCm39)	missense	probably damaging	1.00
Z1088:Csmd1	UTSW	8	15,971,875 (GRCm39)	missense	possibly damaging	0.91
Z1088:Csmd1	UTSW	8	16,396,631 (GRCm39)	missense	probably damaging	0.99
Z1088:Csmd1	UTSW	8	16,250,072 (GRCm39)	missense	probably damaging	0.97
Z1176:Csmd1	UTSW	8	16,087,212 (GRCm39)	missense	probably damaging	1.00
Z1176:Csmd1	UTSW	8	16,048,814 (GRCm39)	missense	probably damaging	1.00
Z1177:Csmd1	UTSW	8	16,250,033 (GRCm39)	missense	probably damaging	1.00
Z1177:Csmd1	UTSW	8	16,034,708 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGATCCACTCCAGAGACCATTGGC -3'
(R):5'- GTTGCTGCATTACACACTGTGTCC -3'

Sequencing Primer
(F):5'- GCCAAGCACTCCCGGAC -3'
(R):5'- AAACACTGTGGGTCACTGC -3'

Posted On

2014-03-14