Mutagenetix > Incidental Mutations

Incidental Mutation 'R5034:Csmd2'

389432

Institutional Source

Beutler Lab

Gene Symbol

Csmd2

Ensembl Gene

ENSMUSG00000028804

Gene Name

CUB and Sushi multiple domains 2

Synonyms

MMRRC Submission

042625-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.136) question?

Stock #

R5034 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

127987857-128567656 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 128059108 bp

Zygosity

Heterozygous

Amino Acid Change

Alanine to Threonine at position 117 (A117T)

Ref Sequence

ENSEMBL: ENSMUSP00000138958 (fasta)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129619

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000144298

Predicted Effect

probably damaging
Transcript: ENSMUST00000184063
AA Change: A117T

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

Meta Mutation Damage Score

0.3048

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.7%
20x: 93.6%

Validation Efficiency

97% (67/69)

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9030624J02Rik	T	C	7: 118,791,388	V368A	probably damaging	Het
Acaca	T	A	11: 84,245,264	S482T	probably benign	Het
Adam6b	G	T	12: 113,490,927	G455C	probably damaging	Het
Ahsg	C	A	16: 22,898,900	P237Q	probably damaging	Het
Asxl2	A	G	12: 3,502,193	S1312G	probably damaging	Het
Brinp3	C	T	1: 146,727,720		probably benign	Het
Col12a1	T	C	9: 79,657,367	H1677R	probably damaging	Het
Cops7a	A	G	6: 124,962,620		probably null	Het
Csmd3	T	C	15: 47,629,287	R3153G	possibly damaging	Het
Dctn4	A	G	18: 60,552,884	N342D	probably benign	Het
Dennd5a	A	T	7: 109,899,797	I953N	probably damaging	Het
Dmwd	T	C	7: 19,080,294	S290P	probably damaging	Het
Dsc1	T	A	18: 20,095,027	Y424F	possibly damaging	Het
Far2	C	A	6: 148,173,441	L391M	probably benign	Het
Foxd3	G	A	4: 99,657,090	G156S	probably damaging	Het
Galk2	A	T	2: 125,929,575	E173D	probably benign	Het
Hcar1	T	C	5: 123,879,669		probably benign	Het
Hsd17b11	C	T	5: 104,018,221	V91M	possibly damaging	Het
Ighv1-77	C	T	12: 115,861,874	C115Y	probably damaging	Het
Ighv9-2	A	G	12: 114,109,405	F9S	probably damaging	Het
Kdm6b	A	G	11: 69,401,910		probably benign	Het
Kif21a	T	A	15: 90,968,358	R890W	probably null	Het
Lin9	T	A	1: 180,669,198	L351I	probably benign	Het
Magel2	A	T	7: 62,379,868	H840L	unknown	Het
Mrgpra4	A	G	7: 47,981,569	F95L	probably benign	Het
Myo7b	A	G	18: 31,971,387	L1436P	probably damaging	Het
Nf1	C	T	11: 79,444,150	P943S	probably damaging	Het
Obscn	T	A	11: 59,061,676	R4153*	probably null	Het
Olfr1026	C	A	2: 85,923,547	S93Y	probably damaging	Het
Oosp2	T	C	19: 11,651,535	I67M	probably damaging	Het
Pcdh9	T	A	14: 93,326,849	D1023V	probably benign	Het
Pcdhb14	T	C	18: 37,448,806	S322P	probably damaging	Het
Pde2a	A	G	7: 101,502,024	D285G	probably benign	Het
Pde5a	G	C	3: 122,852,586	G809R	probably damaging	Het
Pde5a	G	T	3: 122,852,587	G809V	probably damaging	Het
Pphln1	T	C	15: 93,452,129	V120A	probably benign	Het
Rictor	T	C	15: 6,768,095	S311P	probably damaging	Het
Rilpl1	T	C	5: 124,493,824	D153G	probably damaging	Het
Rmdn3	G	T	2: 119,147,577	A181E	probably damaging	Het
Rnf213	G	A	11: 119,410,807	V369M	probably damaging	Het
Scyl1	T	A	19: 5,759,994	R601S	probably benign	Het
Sdcbp	G	A	4: 6,393,118		probably null	Het
Sept8	A	G	11: 53,534,438	T53A	probably damaging	Het
Sfpq	A	G	4: 127,023,669		probably benign	Het
Slc35b3	A	G	13: 38,943,158	Y163H	probably damaging	Het
Sra1	A	G	18: 36,678,995		probably null	Het
Sspo	A	T	6: 48,480,823	N3231Y	possibly damaging	Het
Tcf3	A	G	10: 80,417,543	V218A	possibly damaging	Het
Tgm3	T	C	2: 130,037,484	V332A	possibly damaging	Het
Tmprss11f	C	T	5: 86,591,384		probably benign	Het
Trbv4	A	G	6: 41,059,690	T50A	probably benign	Het
Trdv2-2	C	A	14: 53,961,425	Y57*	probably null	Het
Trim50	T	C	5: 135,367,293	V365A	possibly damaging	Het
Ubash3b	T	C	9: 41,029,740	Q245R	probably benign	Het
Ulk3	T	A	9: 57,593,764	V338E	possibly damaging	Het
Usf3	A	C	16: 44,216,399	K414T	probably damaging	Het
Usp48	C	T	4: 137,606,757	R161*	probably null	Het
Vps18	A	T	2: 119,293,306	D238V	probably benign	Het
Zfp354c	T	C	11: 50,815,039	E403G	probably benign	Het
Zscan18	A	G	7: 12,774,145	V476A	probably damaging	Het

Other mutations in Csmd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00519:Csmd2	APN	4	128483473	missense	probably benign	0.03
IGL01098:Csmd2	APN	4	128059052	missense	probably damaging	0.99
IGL01114:Csmd2	APN	4	128369130	missense	probably benign	0.04
IGL01364:Csmd2	APN	4	128414288	missense	probably benign	0.01
IGL01530:Csmd2	APN	4	128414301	missense	possibly damaging	0.66
IGL01582:Csmd2	APN	4	128563305	nonsense	probably null
IGL01670:Csmd2	APN	4	128513371	splice site	probably benign
IGL01707:Csmd2	APN	4	128383005	missense	possibly damaging	0.81
IGL01810:Csmd2	APN	4	128480845	splice site	probably benign
IGL01837:Csmd2	APN	4	128419570	missense	possibly damaging	0.92
IGL01924:Csmd2	APN	4	128559947	missense	unknown
IGL02013:Csmd2	APN	4	128321323	missense	possibly damaging	0.47
IGL02020:Csmd2	APN	4	128559879	missense	probably damaging	1.00
IGL02037:Csmd2	APN	4	128477470	splice site	probably benign
IGL02303:Csmd2	APN	4	128369008	missense	probably benign	0.01
IGL02317:Csmd2	APN	4	128463727	splice site	probably benign
IGL02322:Csmd2	APN	4	128463727	splice site	probably benign
IGL02338:Csmd2	APN	4	128395066	missense	possibly damaging	0.79
IGL02412:Csmd2	APN	4	128513372	splice site	probably benign
IGL02428:Csmd2	APN	4	128474816	missense	possibly damaging	0.82
IGL02491:Csmd2	APN	4	128534257	missense	probably benign
IGL02701:Csmd2	APN	4	128496141	missense	probably benign	0.17
IGL02801:Csmd2	APN	4	128552075	splice site	probably null
IGL02818:Csmd2	APN	4	128209728	missense	probably damaging	1.00
IGL02863:Csmd2	APN	4	128521884	missense	probably benign	0.00
IGL02876:Csmd2	APN	4	128321335	nonsense	probably null
IGL02977:Csmd2	APN	4	128493276	nonsense	probably null
IGL03006:Csmd2	APN	4	128480765	splice site	probably benign
IGL03032:Csmd2	APN	4	128519041	missense	probably benign	0.03
IGL03148:Csmd2	APN	4	128384269	missense	probably damaging	1.00
IGL03157:Csmd2	APN	4	128414299	nonsense	probably null
IGL03245:Csmd2	APN	4	128509122	missense	probably benign	0.12
IGL03376:Csmd2	APN	4	128517671	missense	probably benign	0.03
IGL03014:Csmd2	UTSW	4	128296429	missense	probably benign	0.01
R0109:Csmd2	UTSW	4	128544743	missense	probably benign	0.03
R0112:Csmd2	UTSW	4	128496029	missense	probably damaging	1.00
R0157:Csmd2	UTSW	4	128521911	missense	probably benign	0.02
R0390:Csmd2	UTSW	4	128133673	intron	probably benign
R0441:Csmd2	UTSW	4	128520230	missense	probably benign	0.00
R0519:Csmd2	UTSW	4	128487005	missense	possibly damaging	0.95
R0743:Csmd2	UTSW	4	128113676	missense	probably benign	0.00
R0746:Csmd2	UTSW	4	128414297	missense	probably damaging	1.00
R0973:Csmd2	UTSW	4	128496188	missense	possibly damaging	0.91
R1019:Csmd2	UTSW	4	128522014	missense	probably benign	0.00
R1476:Csmd2	UTSW	4	128487001	missense	probably benign	0.08
R1641:Csmd2	UTSW	4	128483395	missense	possibly damaging	0.68
R1709:Csmd2	UTSW	4	128496195	missense	probably damaging	0.96
R2866:Csmd2	UTSW	4	128414392	critical splice donor site	probably null
R2870:Csmd2	UTSW	4	128557718	missense	unknown
R2870:Csmd2	UTSW	4	128557718	missense	unknown
R2871:Csmd2	UTSW	4	128557718	missense	unknown
R2871:Csmd2	UTSW	4	128557718	missense	unknown
R2872:Csmd2	UTSW	4	128557718	missense	unknown
R2872:Csmd2	UTSW	4	128557718	missense	unknown
R2873:Csmd2	UTSW	4	128557718	missense	unknown
R2893:Csmd2	UTSW	4	128538993	intron	probably null
R3796:Csmd2	UTSW	4	128517595	missense	probably benign	0.20
R3797:Csmd2	UTSW	4	128517595	missense	probably benign	0.20
R3798:Csmd2	UTSW	4	128517595	missense	probably benign	0.20
R3914:Csmd2	UTSW	4	128321324	missense	probably benign	0.07
R4198:Csmd2	UTSW	4	128510924	missense	probably benign	0.07
R4489:Csmd2	UTSW	4	128381945	missense	possibly damaging	0.68
R4571:Csmd2	UTSW	4	128480095	splice site	probably null
R4581:Csmd2	UTSW	4	128369088	missense	probably benign	0.02
R4599:Csmd2	UTSW	4	127988128	missense	probably benign	0.35
R4649:Csmd2	UTSW	4	128546073	missense	probably benign
R4706:Csmd2	UTSW	4	128544751	missense	probably benign
R4776:Csmd2	UTSW	4	128442892	missense	probably benign	0.09
R4838:Csmd2	UTSW	4	128517749	missense	probably benign
R4900:Csmd2	UTSW	4	128452525	missense	probably benign	0.03
R4999:Csmd2	UTSW	4	128521930	missense	probably benign	0.00
R5024:Csmd2	UTSW	4	128321348	missense	possibly damaging	0.94
R5152:Csmd2	UTSW	4	128552035	missense	probably benign	0.27
R5172:Csmd2	UTSW	4	128477397	missense	probably benign	0.10
R5231:Csmd2	UTSW	4	128546049	missense	probably benign	0.00
R5279:Csmd2	UTSW	4	128456914	missense	probably benign	0.30
R5287:Csmd2	UTSW	4	128486884	missense	probably benign	0.01
R5403:Csmd2	UTSW	4	128486884	missense	probably benign	0.01
R5410:Csmd2	UTSW	4	128548819	missense	probably benign
R5551:Csmd2	UTSW	4	128510948	missense	possibly damaging	0.83
R5566:Csmd2	UTSW	4	128462889	critical splice donor site	probably null
R5826:Csmd2	UTSW	4	128519199	splice site	probably null
R5907:Csmd2	UTSW	4	128197385	missense	probably damaging	0.99
R5913:Csmd2	UTSW	4	128551988	missense	probably benign	0.01
R5970:Csmd2	UTSW	4	128546151	missense	probably benign	0.00
R5977:Csmd2	UTSW	4	128059034	missense	probably damaging	1.00
R6027:Csmd2	UTSW	4	128559946	missense	unknown
R6075:Csmd2	UTSW	4	128486865	missense	probably benign	0.15
R6129:Csmd2	UTSW	4	128493334	missense	possibly damaging	0.79
R6363:Csmd2	UTSW	4	128400379	missense	probably benign	0.00
R6366:Csmd2	UTSW	4	128483452	missense	probably benign	0.00
R6404:Csmd2	UTSW	4	128521950	missense	possibly damaging	0.90
R6437:Csmd2	UTSW	4	127988100	missense	probably benign	0.24
R6441:Csmd2	UTSW	4	128394964	missense	probably benign	0.03
R6643:Csmd2	UTSW	4	128372597	missense	probably benign	0.14
R6724:Csmd2	UTSW	4	128563371	missense	probably damaging	0.97
R6734:Csmd2	UTSW	4	128463813	missense	probably benign	0.00
R6750:Csmd2	UTSW	4	128197225	missense	possibly damaging	0.91
R6801:Csmd2	UTSW	4	128383950	missense	probably benign	0.11
R6842:Csmd2	UTSW	4	128509159	missense	possibly damaging	0.72
R6843:Csmd2	UTSW	4	128463794	missense	probably benign	0.27
R6868:Csmd2	UTSW	4	128442840	missense	probably benign
R6882:Csmd2	UTSW	4	128449269	missense	probably benign	0.01
R7019:Csmd2	UTSW	4	128369063	missense
R7028:Csmd2	UTSW	4	128277228	missense
R7096:Csmd2	UTSW	4	128462726	missense
R7122:Csmd2	UTSW	4	128449227	missense
R7125:Csmd2	UTSW	4	128496162	missense
R7197:Csmd2	UTSW	4	128511033	missense
R7234:Csmd2	UTSW	4	128456779	missense
R7299:Csmd2	UTSW	4	128528262	missense
R7301:Csmd2	UTSW	4	128528262	missense
R7319:Csmd2	UTSW	4	128393679	missense
R7331:Csmd2	UTSW	4	128564228	splice site	probably null
R7332:Csmd2	UTSW	4	128419567	missense
R7352:Csmd2	UTSW	4	128557636	missense
R7402:Csmd2	UTSW	4	128322095	missense
R7402:Csmd2	UTSW	4	128322096	missense
R7474:Csmd2	UTSW	4	128546127	missense
R7555:Csmd2	UTSW	4	128452458	missense
R7592:Csmd2	UTSW	4	128463798	missense
R7714:Csmd2	UTSW	4	128382950	nonsense	probably null
R7734:Csmd2	UTSW	4	128552057	missense
R7735:Csmd2	UTSW	4	128456930	critical splice donor site	probably null
R7757:Csmd2	UTSW	4	128483456	missense
R7805:Csmd2	UTSW	4	128419573	missense
R7823:Csmd2	UTSW	4	128209905	missense
R7904:Csmd2	UTSW	4	128419553	missense
R7987:Csmd2	UTSW	4	128419553	missense
R8003:Csmd2	UTSW	4	128539187	nonsense	probably null
Z1177:Csmd2	UTSW	4	128530797	missense

Predicted Primers

PCR Primer
(F):5'- TCACGTCCACACTGACCTTT -3'
(R):5'- CCCCGTAGAAAGGAAGGCAA -3'

Sequencing Primer
(F):5'- GTCCACACTGACCTTTTGCCC -3'
(R):5'- CTGGTAAGGTGCCCAATGCTTC -3'

Posted On

2016-06-06