Mutagenetix > Incidental Mutation

Incidental Mutation 'R0973:Csmd2'

236720

Institutional Source

Beutler Lab

Gene Symbol

Csmd2

Ensembl Gene

ENSMUSG00000028804

Gene Name

CUB and Sushi multiple domains 2

Synonyms

MMRRC Submission

039102-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.150) question?

Stock #

R0973 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

127987857-128567656 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 128496188 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 2239 (I2239F)

Ref Sequence

ENSEMBL: ENSMUSP00000138958 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000184063]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000148247

Predicted Effect

possibly damaging
Transcript: ENSMUST00000184063
AA Change: I2239F

PolyPhen 2 Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)

Meta Mutation Damage Score

0.4754

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.6%
20x: 96.0%

Validation Efficiency

93% (38/41)

Allele List at MGI

Other mutations in this stock

Total: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700056E22Rik	C	T	1: 184,033,505 (GRCm38)	S119N	probably benign	Het
4930503L19Rik	T	A	18: 70,467,926 (GRCm38)		probably null	Het
5430419D17Rik	T	C	7: 131,238,182 (GRCm38)	L611P	probably damaging	Het
Adam18	T	C	8: 24,647,853 (GRCm38)	T324A	probably benign	Het
Adamts20	T	A	15: 94,286,371 (GRCm38)	Q1517L	probably benign	Het
AI429214	A	G	8: 36,994,319 (GRCm38)	Q207R	probably benign	Het
Arhgef7	A	G	8: 11,819,659 (GRCm38)	T432A	possibly damaging	Het
Atad2b	A	G	12: 5,031,784 (GRCm38)	N1231S	probably benign	Het
Atp13a1	T	C	8: 69,802,144 (GRCm38)		probably null	Het
Atp6v0a1	T	A	11: 101,055,491 (GRCm38)	L770*	probably null	Het
Atp8b3	T	C	10: 80,534,198 (GRCm38)	N127S	probably damaging	Het
B3gnt5	T	A	16: 19,770,010 (GRCm38)	D326E	probably damaging	Het
Birc6	T	A	17: 74,565,861 (GRCm38)	S372T	probably damaging	Het
Btbd9	T	A	17: 30,299,633 (GRCm38)	D451V	probably damaging	Het
Cd46	T	C	1: 195,041,992 (GRCm38)	*366W	probably null	Het
Cdh18	T	A	15: 23,473,995 (GRCm38)	D650E	probably damaging	Het
Cenpc1	A	T	5: 86,037,908 (GRCm38)	V248E	probably damaging	Het
Cep152	A	G	2: 125,594,899 (GRCm38)	S574P	probably benign	Het
Chd2	A	G	7: 73,478,664 (GRCm38)	S858P	probably damaging	Het
Cib4	T	C	5: 30,488,594 (GRCm38)	D110G	probably damaging	Het
Col9a2	T	A	4: 121,039,788 (GRCm38)		probably null	Het
Csmd3	C	A	15: 47,659,089 (GRCm38)	G2728V	probably damaging	Het
Cxcl1	A	T	5: 90,891,767 (GRCm38)	K85*	probably null	Het
Cyp2d11	A	G	15: 82,389,529 (GRCm38)	L416P	possibly damaging	Het
Daam1	A	C	12: 71,915,784 (GRCm38)	K90T	unknown	Het
Depdc5	T	A	5: 32,986,966 (GRCm38)	M1435K	possibly damaging	Het
Diexf	A	T	1: 193,114,703 (GRCm38)	N573K	probably damaging	Het
Dip2c	G	A	13: 9,576,908 (GRCm38)	A632T	probably damaging	Het
Dld	A	T	12: 31,334,054 (GRCm38)	I350N	probably damaging	Het
Dmtf1	T	A	5: 9,127,987 (GRCm38)	I391F	possibly damaging	Het
Dnah14	T	C	1: 181,752,145 (GRCm38)	V3081A	probably damaging	Het
Efemp1	A	G	11: 28,854,538 (GRCm38)	E22G	probably damaging	Het
Ephb6	A	G	6: 41,614,104 (GRCm38)	D65G	probably damaging	Het
Fsip2	A	T	2: 82,977,092 (GRCm38)	T1252S	probably benign	Het
Gm13084	T	C	4: 143,811,858 (GRCm38)	Y181C	probably damaging	Het
Gm4847	A	G	1: 166,630,255 (GRCm38)	S510P	probably benign	Het
Golga4	T	C	9: 118,537,273 (GRCm38)	I365T	probably damaging	Het
Gp2	A	T	7: 119,454,543 (GRCm38)	L65Q	probably damaging	Het
Ibtk	T	C	9: 85,743,577 (GRCm38)	Y40C	probably damaging	Het
Ice1	C	A	13: 70,602,427 (GRCm38)	V1847L	probably benign	Het
Ift172	C	T	5: 31,265,355 (GRCm38)	R917H	probably benign	Het
Itgae	C	T	11: 73,138,509 (GRCm38)	Q1037*	probably null	Het
Kbtbd7	A	G	14: 79,427,430 (GRCm38)	E234G	possibly damaging	Het
Khsrp	T	C	17: 57,025,576 (GRCm38)	T235A	probably benign	Het
Klk13	T	C	7: 43,721,158 (GRCm38)		probably null	Het
Lrfn5	G	A	12: 61,843,437 (GRCm38)	G504D	probably damaging	Het
Macf1	A	G	4: 123,476,000 (GRCm38)	V91A	possibly damaging	Het
Map6	G	A	7: 99,336,743 (GRCm38)	G821D	possibly damaging	Het
Mark1	A	C	1: 184,921,604 (GRCm38)	V167G	probably damaging	Het
Mrgprf	T	A	7: 145,308,256 (GRCm38)	L185Q	probably damaging	Het
Mtor	T	A	4: 148,550,188 (GRCm38)	V2422D	probably damaging	Het
Myh13	T	A	11: 67,332,520 (GRCm38)	I222N	probably damaging	Het
Myh7b	G	A	2: 155,620,427 (GRCm38)	C350Y	probably benign	Het
Nfix	G	A	8: 84,726,526 (GRCm38)	R300C	probably damaging	Het
Olfm3	C	A	3: 115,101,986 (GRCm38)	S172R	probably benign	Het
Olfr1168	A	T	2: 88,184,978 (GRCm38)	T34S	probably benign	Het
Olfr1231	A	T	2: 89,303,184 (GRCm38)	I136N	probably damaging	Het
Olfr342	A	G	2: 36,528,008 (GRCm38)	I199V	probably benign	Het
Olfr70	A	G	4: 43,696,706 (GRCm38)	S156P	probably damaging	Het
Olfr912	T	A	9: 38,581,283 (GRCm38)	V2D	possibly damaging	Het
Pacs1	A	T	19: 5,143,829 (GRCm38)	D557E	probably damaging	Het
Pde1c	A	G	6: 56,361,815 (GRCm38)	F11L	probably benign	Het
Phactr2	T	C	10: 13,247,139 (GRCm38)	D343G	possibly damaging	Het
Piezo2	T	C	18: 63,015,802 (GRCm38)	Y2659C	probably damaging	Het
Pkd2l2	A	G	18: 34,428,252 (GRCm38)	T438A	probably damaging	Het
Pld2	T	C	11: 70,557,081 (GRCm38)	W857R	probably damaging	Het
Plxnb1	T	C	9: 109,102,142 (GRCm38)	V410A	possibly damaging	Het
Ptger2	A	G	14: 44,989,500 (GRCm38)	Y179C	probably damaging	Het
Ptpro	T	A	6: 137,443,594 (GRCm38)	V1007D	probably damaging	Het
Rcan1	A	T	16: 92,393,520 (GRCm38)	M177K	probably benign	Het
Rilpl1	A	G	5: 124,501,888 (GRCm38)	I122T	possibly damaging	Het
Rilpl1	A	G	5: 124,501,871 (GRCm38)	S156P	probably benign	Het
Rims4	C	T	2: 163,863,929 (GRCm38)	V262M	possibly damaging	Het
Rpa1	C	T	11: 75,312,973 (GRCm38)		probably null	Het
Saxo2	A	G	7: 82,634,870 (GRCm38)	V260A	probably benign	Het
Sel1l	T	C	12: 91,824,860 (GRCm38)	Y309C	probably damaging	Het
Setd1b	GCCCCCCC	GCCCCCCCCCCCCC	5: 123,160,703 (GRCm38)		probably benign	Het
Slc33a1	A	G	3: 63,943,304 (GRCm38)	F533S	probably benign	Het
Slc38a4	C	T	15: 97,005,858 (GRCm38)	V421M	probably benign	Het
Snx14	A	G	9: 88,400,721 (GRCm38)		probably null	Het
Spef2	A	G	15: 9,716,396 (GRCm38)	F368S	probably damaging	Het
Sri	A	T	5: 8,059,381 (GRCm38)	Q55L	probably damaging	Het
Stat4	A	G	1: 52,096,820 (GRCm38)	I429M	probably damaging	Het
Stkld1	A	T	2: 26,951,450 (GRCm38)	Q469L	probably benign	Het
Tm9sf1	T	C	14: 55,642,935 (GRCm38)	T2A	possibly damaging	Het
Tmco5	A	G	2: 116,883,218 (GRCm38)	T122A	probably benign	Het
Tmem59l	G	A	8: 70,486,060 (GRCm38)	P124S	possibly damaging	Het
Tmem81	G	A	1: 132,507,924 (GRCm38)	R156Q	probably damaging	Het
Trpv6	T	A	6: 41,625,188 (GRCm38)	T396S	probably benign	Het
Usp24	T	A	4: 106,371,079 (GRCm38)	Y780*	probably null	Het
Vmn1r120	A	G	7: 21,053,016 (GRCm38)	C257R	probably damaging	Het
Vmn2r53	A	G	7: 12,601,392 (GRCm38)	F114L	probably damaging	Het
Vwf	A	G	6: 125,643,006 (GRCm38)	E1549G	probably damaging	Het
Zfp626	G	A	7: 27,818,482 (GRCm38)	R296H	probably damaging	Het

Other mutations in Csmd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00519:Csmd2	APN	4	128,483,473 (GRCm38)	missense	probably benign	0.03
IGL01098:Csmd2	APN	4	128,059,052 (GRCm38)	missense	probably damaging	0.99
IGL01114:Csmd2	APN	4	128,369,130 (GRCm38)	missense	probably benign	0.04
IGL01364:Csmd2	APN	4	128,414,288 (GRCm38)	missense	probably benign	0.01
IGL01530:Csmd2	APN	4	128,414,301 (GRCm38)	missense	possibly damaging	0.66
IGL01582:Csmd2	APN	4	128,563,305 (GRCm38)	nonsense	probably null
IGL01670:Csmd2	APN	4	128,513,371 (GRCm38)	splice site	probably benign
IGL01707:Csmd2	APN	4	128,383,005 (GRCm38)	missense	possibly damaging	0.81
IGL01810:Csmd2	APN	4	128,480,845 (GRCm38)	splice site	probably benign
IGL01837:Csmd2	APN	4	128,419,570 (GRCm38)	missense	possibly damaging	0.92
IGL01924:Csmd2	APN	4	128,559,947 (GRCm38)	missense	unknown
IGL02013:Csmd2	APN	4	128,321,323 (GRCm38)	missense	possibly damaging	0.47
IGL02020:Csmd2	APN	4	128,559,879 (GRCm38)	missense	probably damaging	1.00
IGL02037:Csmd2	APN	4	128,477,470 (GRCm38)	splice site	probably benign
IGL02303:Csmd2	APN	4	128,369,008 (GRCm38)	missense	probably benign	0.01
IGL02317:Csmd2	APN	4	128,463,727 (GRCm38)	splice site	probably benign
IGL02322:Csmd2	APN	4	128,463,727 (GRCm38)	splice site	probably benign
IGL02338:Csmd2	APN	4	128,395,066 (GRCm38)	missense	possibly damaging	0.79
IGL02412:Csmd2	APN	4	128,513,372 (GRCm38)	splice site	probably benign
IGL02428:Csmd2	APN	4	128,474,816 (GRCm38)	missense	possibly damaging	0.82
IGL02491:Csmd2	APN	4	128,534,257 (GRCm38)	missense	probably benign
IGL02701:Csmd2	APN	4	128,496,141 (GRCm38)	missense	probably benign	0.17
IGL02801:Csmd2	APN	4	128,552,075 (GRCm38)	splice site	probably null
IGL02818:Csmd2	APN	4	128,209,728 (GRCm38)	missense	probably damaging	1.00
IGL02863:Csmd2	APN	4	128,521,884 (GRCm38)	missense	probably benign	0.00
IGL02876:Csmd2	APN	4	128,321,335 (GRCm38)	nonsense	probably null
IGL02977:Csmd2	APN	4	128,493,276 (GRCm38)	nonsense	probably null
IGL03006:Csmd2	APN	4	128,480,765 (GRCm38)	splice site	probably benign
IGL03032:Csmd2	APN	4	128,519,041 (GRCm38)	missense	probably benign	0.03
IGL03148:Csmd2	APN	4	128,384,269 (GRCm38)	missense	probably damaging	1.00
IGL03157:Csmd2	APN	4	128,414,299 (GRCm38)	nonsense	probably null
IGL03245:Csmd2	APN	4	128,509,122 (GRCm38)	missense	probably benign	0.12
IGL03376:Csmd2	APN	4	128,517,671 (GRCm38)	missense	probably benign	0.03
IGL03014:Csmd2	UTSW	4	128,296,429 (GRCm38)	missense	probably benign	0.01
R0109:Csmd2	UTSW	4	128,544,743 (GRCm38)	missense	probably benign	0.03
R0112:Csmd2	UTSW	4	128,496,029 (GRCm38)	missense	probably damaging	1.00
R0157:Csmd2	UTSW	4	128,521,911 (GRCm38)	missense	probably benign	0.02
R0390:Csmd2	UTSW	4	128,133,673 (GRCm38)	intron	probably benign
R0441:Csmd2	UTSW	4	128,520,230 (GRCm38)	missense	probably benign	0.00
R0519:Csmd2	UTSW	4	128,487,005 (GRCm38)	missense	possibly damaging	0.95
R0743:Csmd2	UTSW	4	128,113,676 (GRCm38)	missense	probably benign	0.00
R0746:Csmd2	UTSW	4	128,414,297 (GRCm38)	missense	probably damaging	1.00
R1019:Csmd2	UTSW	4	128,522,014 (GRCm38)	missense	probably benign	0.00
R1476:Csmd2	UTSW	4	128,487,001 (GRCm38)	missense	probably benign	0.08
R1641:Csmd2	UTSW	4	128,483,395 (GRCm38)	missense	possibly damaging	0.68
R1709:Csmd2	UTSW	4	128,496,195 (GRCm38)	missense	probably damaging	0.96
R2866:Csmd2	UTSW	4	128,414,392 (GRCm38)	critical splice donor site	probably null
R2870:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2870:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2871:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2871:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2872:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2872:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2873:Csmd2	UTSW	4	128,557,718 (GRCm38)	missense	unknown
R2893:Csmd2	UTSW	4	128,538,993 (GRCm38)	splice site	probably null
R3796:Csmd2	UTSW	4	128,517,595 (GRCm38)	missense	probably benign	0.20
R3797:Csmd2	UTSW	4	128,517,595 (GRCm38)	missense	probably benign	0.20
R3798:Csmd2	UTSW	4	128,517,595 (GRCm38)	missense	probably benign	0.20
R3914:Csmd2	UTSW	4	128,321,324 (GRCm38)	missense	probably benign	0.07
R4198:Csmd2	UTSW	4	128,510,924 (GRCm38)	missense	probably benign	0.07
R4489:Csmd2	UTSW	4	128,381,945 (GRCm38)	missense	possibly damaging	0.68
R4571:Csmd2	UTSW	4	128,480,095 (GRCm38)	splice site	probably null
R4581:Csmd2	UTSW	4	128,369,088 (GRCm38)	missense	probably benign	0.02
R4599:Csmd2	UTSW	4	127,988,128 (GRCm38)	missense	probably benign	0.35
R4649:Csmd2	UTSW	4	128,546,073 (GRCm38)	missense	probably benign
R4706:Csmd2	UTSW	4	128,544,751 (GRCm38)	missense	probably benign
R4776:Csmd2	UTSW	4	128,442,892 (GRCm38)	missense	probably benign	0.09
R4838:Csmd2	UTSW	4	128,517,749 (GRCm38)	missense	probably benign
R4900:Csmd2	UTSW	4	128,452,525 (GRCm38)	missense	probably benign	0.03
R4999:Csmd2	UTSW	4	128,521,930 (GRCm38)	missense	probably benign	0.00
R5024:Csmd2	UTSW	4	128,321,348 (GRCm38)	missense	possibly damaging	0.94
R5034:Csmd2	UTSW	4	128,059,108 (GRCm38)	missense	probably damaging	0.98
R5152:Csmd2	UTSW	4	128,552,035 (GRCm38)	missense	probably benign	0.27
R5172:Csmd2	UTSW	4	128,477,397 (GRCm38)	missense	probably benign	0.10
R5231:Csmd2	UTSW	4	128,546,049 (GRCm38)	missense	probably benign	0.00
R5279:Csmd2	UTSW	4	128,456,914 (GRCm38)	missense	probably benign	0.30
R5287:Csmd2	UTSW	4	128,486,884 (GRCm38)	missense	probably benign	0.01
R5403:Csmd2	UTSW	4	128,486,884 (GRCm38)	missense	probably benign	0.01
R5410:Csmd2	UTSW	4	128,548,819 (GRCm38)	missense	probably benign
R5551:Csmd2	UTSW	4	128,510,948 (GRCm38)	missense	possibly damaging	0.83
R5566:Csmd2	UTSW	4	128,462,889 (GRCm38)	critical splice donor site	probably null
R5826:Csmd2	UTSW	4	128,519,199 (GRCm38)	splice site	probably null
R5907:Csmd2	UTSW	4	128,197,385 (GRCm38)	missense	probably damaging	0.99
R5913:Csmd2	UTSW	4	128,551,988 (GRCm38)	missense	probably benign	0.01
R5970:Csmd2	UTSW	4	128,546,151 (GRCm38)	missense	probably benign	0.00
R5977:Csmd2	UTSW	4	128,059,034 (GRCm38)	missense	probably damaging	1.00
R6027:Csmd2	UTSW	4	128,559,946 (GRCm38)	missense	unknown
R6075:Csmd2	UTSW	4	128,486,865 (GRCm38)	missense	probably benign	0.15
R6129:Csmd2	UTSW	4	128,493,334 (GRCm38)	missense	possibly damaging	0.79
R6363:Csmd2	UTSW	4	128,400,379 (GRCm38)	missense	probably benign	0.00
R6366:Csmd2	UTSW	4	128,483,452 (GRCm38)	missense	probably benign	0.00
R6404:Csmd2	UTSW	4	128,521,950 (GRCm38)	missense	possibly damaging	0.90
R6437:Csmd2	UTSW	4	127,988,100 (GRCm38)	missense	probably benign	0.24
R6441:Csmd2	UTSW	4	128,394,964 (GRCm38)	missense	probably benign	0.03
R6643:Csmd2	UTSW	4	128,372,597 (GRCm38)	missense	probably benign	0.14
R6724:Csmd2	UTSW	4	128,563,371 (GRCm38)	missense	probably damaging	0.97
R6734:Csmd2	UTSW	4	128,463,813 (GRCm38)	missense	probably benign	0.00
R6750:Csmd2	UTSW	4	128,197,225 (GRCm38)	missense	possibly damaging	0.91
R6801:Csmd2	UTSW	4	128,383,950 (GRCm38)	missense	probably benign	0.11
R6842:Csmd2	UTSW	4	128,509,159 (GRCm38)	missense	possibly damaging	0.72
R6843:Csmd2	UTSW	4	128,463,794 (GRCm38)	missense	probably benign	0.27
R6868:Csmd2	UTSW	4	128,442,840 (GRCm38)	missense	probably benign
R6882:Csmd2	UTSW	4	128,449,269 (GRCm38)	missense	probably benign	0.01
R7019:Csmd2	UTSW	4	128,369,063 (GRCm38)	missense
R7028:Csmd2	UTSW	4	128,277,228 (GRCm38)	missense
R7096:Csmd2	UTSW	4	128,462,726 (GRCm38)	missense
R7122:Csmd2	UTSW	4	128,449,227 (GRCm38)	missense
R7125:Csmd2	UTSW	4	128,496,162 (GRCm38)	missense
R7197:Csmd2	UTSW	4	128,511,033 (GRCm38)	missense
R7234:Csmd2	UTSW	4	128,456,779 (GRCm38)	missense
R7299:Csmd2	UTSW	4	128,528,262 (GRCm38)	missense
R7301:Csmd2	UTSW	4	128,528,262 (GRCm38)	missense
R7319:Csmd2	UTSW	4	128,393,679 (GRCm38)	missense
R7331:Csmd2	UTSW	4	128,564,228 (GRCm38)	splice site	probably null
R7332:Csmd2	UTSW	4	128,419,567 (GRCm38)	missense
R7352:Csmd2	UTSW	4	128,557,636 (GRCm38)	missense
R7402:Csmd2	UTSW	4	128,322,096 (GRCm38)	missense
R7402:Csmd2	UTSW	4	128,322,095 (GRCm38)	missense
R7474:Csmd2	UTSW	4	128,546,127 (GRCm38)	missense
R7555:Csmd2	UTSW	4	128,452,458 (GRCm38)	missense
R7592:Csmd2	UTSW	4	128,463,798 (GRCm38)	missense
R7700:Csmd2	UTSW	4	128,545,756 (GRCm38)	splice site	probably null
R7714:Csmd2	UTSW	4	128,382,950 (GRCm38)	nonsense	probably null
R7734:Csmd2	UTSW	4	128,552,057 (GRCm38)	missense
R7735:Csmd2	UTSW	4	128,456,930 (GRCm38)	critical splice donor site	probably null
R7757:Csmd2	UTSW	4	128,483,456 (GRCm38)	missense
R7805:Csmd2	UTSW	4	128,419,573 (GRCm38)	missense
R7823:Csmd2	UTSW	4	128,209,905 (GRCm38)	missense
R7904:Csmd2	UTSW	4	128,419,553 (GRCm38)	missense
R7946:Csmd2	UTSW	4	128,520,265 (GRCm38)	missense
R7964:Csmd2	UTSW	4	128,523,510 (GRCm38)	missense
R7968:Csmd2	UTSW	4	128,197,325 (GRCm38)	missense
R8003:Csmd2	UTSW	4	128,539,187 (GRCm38)	nonsense	probably null
R8071:Csmd2	UTSW	4	128,393,538 (GRCm38)	missense
R8504:Csmd2	UTSW	4	128,546,690 (GRCm38)	missense
R8511:Csmd2	UTSW	4	128,368,899 (GRCm38)	missense
R8517:Csmd2	UTSW	4	128,552,686 (GRCm38)	missense
R8704:Csmd2	UTSW	4	128,197,354 (GRCm38)	missense
R8722:Csmd2	UTSW	4	128,551,950 (GRCm38)	unclassified	probably benign
R8729:Csmd2	UTSW	4	128,462,845 (GRCm38)	missense
R8801:Csmd2	UTSW	4	128,563,402 (GRCm38)	missense	probably damaging	0.97
R8803:Csmd2	UTSW	4	128,546,684 (GRCm38)	missense
R8839:Csmd2	UTSW	4	128,442,888 (GRCm38)	missense
R8867:Csmd2	UTSW	4	128,557,676 (GRCm38)	missense
R8913:Csmd2	UTSW	4	128,523,558 (GRCm38)	missense
R8928:Csmd2	UTSW	4	128,475,789 (GRCm38)	missense
R8974:Csmd2	UTSW	4	128,552,587 (GRCm38)	missense
R9001:Csmd2	UTSW	4	128,414,286 (GRCm38)	missense
R9132:Csmd2	UTSW	4	128,549,214 (GRCm38)	missense
R9245:Csmd2	UTSW	4	128,306,375 (GRCm38)	missense
R9249:Csmd2	UTSW	4	128,419,530 (GRCm38)	nonsense	probably null
R9254:Csmd2	UTSW	4	128,197,319 (GRCm38)	missense
R9265:Csmd2	UTSW	4	128,400,370 (GRCm38)	missense
R9407:Csmd2	UTSW	4	128,548,820 (GRCm38)	missense
R9432:Csmd2	UTSW	4	128,277,211 (GRCm38)	missense
R9559:Csmd2	UTSW	4	128,544,768 (GRCm38)	missense
R9673:Csmd2	UTSW	4	128,414,269 (GRCm38)	missense
R9735:Csmd2	UTSW	4	128,509,108 (GRCm38)	missense
R9749:Csmd2	UTSW	4	128,496,128 (GRCm38)	missense
R9803:Csmd2	UTSW	4	128,369,193 (GRCm38)	missense
Z1177:Csmd2	UTSW	4	128,530,797 (GRCm38)	missense

Predicted Primers

PCR Primer
(F):5'- ACTGAGGTTTTACGGGGAAG -3'
(R):5'- CCCTTCTTAGTCTGGACAGC -3'

Sequencing Primer
(F):5'- CTGAGGTTTTACGGGGAAGACATC -3'
(R):5'- CTTCTTAGTCTGGACAGCTTAGTTAG -3'

Posted On

2014-10-02