Mutagenetix > Incidental Mutation

Incidental Mutation 'R1866:Sdk2'

265984

Institutional Source

Beutler Lab

Gene Symbol

Sdk2

Ensembl Gene

ENSMUSG00000041592

Gene Name

sidekick cell adhesion molecule 2

Synonyms

5330435L01Rik, 4632412F08Rik

MMRRC Submission

039889-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.100) question?

Stock #

R1866 (G1)

Quality Score

189

Status

Not validated

Chromosome

Chromosomal Location

113776374-114067046 bp(-) (GRCm38)

Type of Mutation

synonymous

DNA Base Change (assembly)

C to T at 113838646 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000038972 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000041627] [ENSMUST00000041627]

AlphaFold

Q6V4S5

Predicted Effect

silent
Transcript: ENSMUST00000041627

SMART Domains

Protein: ENSMUSP00000038972
Gene: ENSMUSG00000041592

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
IGc2	43	102	4.67e-4	SMART
IG	123	208	6.07e-3	SMART
IG	225	309	1.4e-7	SMART
IGc2	325	391	6.21e-9	SMART
IGc2	418	486	8.57e-12	SMART
IG	506	591	2.37e-5	SMART
FN3	594	678	1.91e-7	SMART
FN3	694	780	2.42e-9	SMART
FN3	796	884	3.45e-5	SMART
FN3	899	981	2.36e-12	SMART
FN3	997	1084	1.64e-6	SMART
FN3	1101	1188	8.83e-12	SMART
FN3	1204	1289	3.62e-8	SMART
FN3	1305	1388	1.74e-10	SMART
FN3	1404	1489	8.23e-12	SMART
FN3	1506	1612	3.62e-8	SMART
FN3	1628	1713	1.15e-10	SMART
FN3	1728	1815	2.17e-11	SMART
FN3	1829	1913	5.04e-7	SMART
transmembrane domain	1935	1957	N/A	INTRINSIC
low complexity region	2138	2153	N/A	INTRINSIC

Predicted Effect

silent
Transcript: ENSMUST00000041627

SMART Domains

Protein: ENSMUSP00000038972
Gene: ENSMUSG00000041592

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
IGc2	43	102	4.67e-4	SMART
IG	123	208	6.07e-3	SMART
IG	225	309	1.4e-7	SMART
IGc2	325	391	6.21e-9	SMART
IGc2	418	486	8.57e-12	SMART
IG	506	591	2.37e-5	SMART
FN3	594	678	1.91e-7	SMART
FN3	694	780	2.42e-9	SMART
FN3	796	884	3.45e-5	SMART
FN3	899	981	2.36e-12	SMART
FN3	997	1084	1.64e-6	SMART
FN3	1101	1188	8.83e-12	SMART
FN3	1204	1289	3.62e-8	SMART
FN3	1305	1388	1.74e-10	SMART
FN3	1404	1489	8.23e-12	SMART
FN3	1506	1612	3.62e-8	SMART
FN3	1628	1713	1.15e-10	SMART
FN3	1728	1815	2.17e-11	SMART
FN3	1829	1913	5.04e-7	SMART
transmembrane domain	1935	1957	N/A	INTRINSIC
low complexity region	2138	2153	N/A	INTRINSIC

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 95.3%
20x: 92.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains two immunoglobulin domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. This protein, and a homologous mouse sequence, are very similar to the Drosophila sidekick gene product but the specific function of this superfamily member is not yet known. Evidence for alternative splicing at this gene locus has been observed but the full-length nature of additional variants has not yet been determined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired interconnectvity between VG3 amacrine cells and W3B retinal ganglion cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 92 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apba1	A	T	19: 23,892,831 (GRCm38)	E9V	probably benign	Het
Armc8	T	A	9: 99,536,280 (GRCm38)	T32S	probably benign	Het
Atr	T	A	9: 95,870,605 (GRCm38)		probably null	Het
Blm	A	G	7: 80,494,114 (GRCm38)	L859P	probably benign	Het
Cacna2d3	A	T	14: 28,969,214 (GRCm38)	F51L	probably damaging	Het
Cdcp2	A	G	4: 107,107,000 (GRCm38)	N349S	probably damaging	Het
Cfap57	G	A	4: 118,599,927 (GRCm38)	H442Y	possibly damaging	Het
Chrm3	A	G	13: 9,878,481 (GRCm38)	L173P	probably damaging	Het
Cpb1	C	G	3: 20,263,756 (GRCm38)	M201I	probably benign	Het
Dgcr8	A	T	16: 18,258,314 (GRCm38)	N2K	probably damaging	Het
Dnah3	A	T	7: 119,928,856 (GRCm38)		probably null	Het
Dnah6	T	A	6: 73,100,088 (GRCm38)	Q2398L	probably benign	Het
Dpep2	A	T	8: 105,989,448 (GRCm38)		probably null	Het
E430018J23Rik	A	G	7: 127,393,331 (GRCm38)	W36R	probably damaging	Het
Eif2ak4	C	A	2: 118,472,661 (GRCm38)	T1504K	probably damaging	Het
Exoc6b	A	G	6: 84,851,914 (GRCm38)	V496A	probably damaging	Het
Fam174a	A	C	1: 95,313,895 (GRCm38)	S27R	probably benign	Het
Fat2	T	A	11: 55,292,014 (GRCm38)	Q1339L	probably benign	Het
Fkbpl	T	A	17: 34,645,823 (GRCm38)	D188E	possibly damaging	Het
Focad	A	G	4: 88,407,165 (GRCm38)	D89G	possibly damaging	Het
Fstl4	C	A	11: 53,186,398 (GRCm38)	Q661K	probably benign	Het
Gck	T	C	11: 5,903,253 (GRCm38)	Y289C	probably benign	Het
Gm156	A	G	6: 129,775,380 (GRCm38)		probably null	Het
Gm16181	T	A	17: 35,223,937 (GRCm38)		probably benign	Het
Herc1	G	A	9: 66,450,791 (GRCm38)	G2385S	probably damaging	Het
Igfn1	T	C	1: 135,974,868 (GRCm38)		probably null	Het
Il12b	T	C	11: 44,408,526 (GRCm38)	W141R	probably damaging	Het
Itga6	T	A	2: 71,834,070 (GRCm38)	S517T	probably benign	Het
Kank1	A	G	19: 25,411,449 (GRCm38)	S801G	probably benign	Het
Lctl	A	G	9: 64,131,721 (GRCm38)	D205G	probably damaging	Het
Lhx3	A	C	2: 26,203,974 (GRCm38)	V79G	probably damaging	Het
Lrrc9	T	C	12: 72,497,138 (GRCm38)	I1127T	probably damaging	Het
Ltbp3	A	T	19: 5,747,849 (GRCm38)	E505D	probably benign	Het
Man1c1	G	C	4: 134,703,438 (GRCm38)	P11R	probably damaging	Het
Map6	A	G	7: 99,315,876 (GRCm38)	S291G	probably damaging	Het
Mapk7	A	G	11: 61,489,413 (GRCm38)	F671L	probably benign	Het
Mau2	A	G	8: 70,031,492 (GRCm38)	W149R	probably damaging	Het
Mb21d2	C	T	16: 28,828,515 (GRCm38)	V236I	possibly damaging	Het
Mc5r	C	G	18: 68,338,670 (GRCm38)		probably null	Het
Mical1	C	A	10: 41,485,470 (GRCm38)	P797Q	probably benign	Het
Mnx1	G	A	5: 29,474,045 (GRCm38)	R347C	unknown	Het
Mslnl	G	A	17: 25,742,934 (GRCm38)	V128M	probably damaging	Het
Nlrp2	G	T	7: 5,327,716 (GRCm38)	C560*	probably null	Het
Npat	T	A	9: 53,563,116 (GRCm38)	L736H	probably damaging	Het
Nup155	T	A	15: 8,115,526 (GRCm38)	V147E	probably damaging	Het
Nxpe2	A	G	9: 48,326,821 (GRCm38)	F45L	probably benign	Het
Obscn	T	C	11: 59,060,915 (GRCm38)	D4370G	probably benign	Het
Olfr1000	T	A	2: 85,608,844 (GRCm38)	H22L	probably benign	Het
Olfr1047	A	C	2: 86,228,728 (GRCm38)	M81R	probably damaging	Het
Olfr1252	T	C	2: 89,721,206 (GRCm38)	K302E	probably benign	Het
Olfr1260	T	C	2: 89,978,327 (GRCm38)	L183S	probably damaging	Het
Olfr1425	A	G	19: 12,073,819 (GRCm38)	V271A	probably benign	Het
Olfr1532-ps1	A	G	7: 106,915,066 (GRCm38)	I289M	probably damaging	Het
Olfr658	A	G	7: 104,644,797 (GRCm38)	S190P	probably benign	Het
Pcx	T	C	19: 4,621,221 (GRCm38)	I1157T	possibly damaging	Het
Pias2	T	A	18: 77,152,716 (GRCm38)	S589R	probably benign	Het
Plcb1	T	C	2: 135,344,173 (GRCm38)	F687L	probably benign	Het
Plk5	G	T	10: 80,360,569 (GRCm38)		probably null	Het
Pnpla2	T	A	7: 141,455,416 (GRCm38)	Y44N	probably damaging	Het
Ppp1r12a	T	A	10: 108,262,431 (GRCm38)	D337E	possibly damaging	Het
Prl2c5	G	T	13: 13,190,773 (GRCm38)		probably null	Het
Prom2	T	C	2: 127,536,594 (GRCm38)	D460G	probably damaging	Het
Pros1	A	G	16: 62,928,135 (GRCm38)	H657R	possibly damaging	Het
Prune2	A	G	19: 17,123,492 (GRCm38)	E2120G	probably damaging	Het
Rap2a	T	A	14: 120,478,935 (GRCm38)	L70Q	probably damaging	Het
Rbl2	A	T	8: 91,112,529 (GRCm38)	E858D	probably benign	Het
Rbm48	T	C	5: 3,595,997 (GRCm38)	Y69C	probably damaging	Het
Rgs12	T	A	5: 34,965,674 (GRCm38)	I267N	probably damaging	Het
Rpusd2	G	T	2: 119,035,247 (GRCm38)	A142S	probably benign	Het
Rspo2	A	T	15: 43,075,936 (GRCm38)	W153R	probably damaging	Het
Serinc5	T	A	13: 92,706,263 (GRCm38)	M407K	probably damaging	Het
Slain2	T	C	5: 72,957,322 (GRCm38)	S299P	probably damaging	Het
Slc17a4	A	G	13: 23,900,545 (GRCm38)	Y419H	possibly damaging	Het
Slc1a6	T	A	10: 78,791,349 (GRCm38)	D173E	probably damaging	Het
Slc22a19	A	T	19: 7,711,141 (GRCm38)	I18N	probably damaging	Het
Slc37a3	A	T	6: 39,359,968 (GRCm38)	F91L	probably damaging	Het
Spag5	C	A	11: 78,304,455 (GRCm38)	T196K	possibly damaging	Het
Susd2	G	T	10: 75,639,732 (GRCm38)	A326D	probably damaging	Het
Syna	G	T	5: 134,559,915 (GRCm38)	A60D	probably damaging	Het
Tchh	A	T	3: 93,447,760 (GRCm38)	E1502D	unknown	Het
Tecta	T	C	9: 42,392,024 (GRCm38)	H104R	probably damaging	Het
Tmed1	T	C	9: 21,509,091 (GRCm38)	D102G	probably damaging	Het
Trip12	T	C	1: 84,745,060 (GRCm38)	D128G	probably damaging	Het
Uroc1	A	G	6: 90,361,524 (GRCm38)	M656V	probably benign	Het
Usp47	T	A	7: 112,101,870 (GRCm38)	V1096D	possibly damaging	Het
Utp20	T	A	10: 88,762,770 (GRCm38)	K115*	probably null	Het
Vmn2r19	G	T	6: 123,331,638 (GRCm38)		probably null	Het
Vmn2r86	A	T	10: 130,446,386 (GRCm38)	V787D	probably damaging	Het
Vmn2r87	A	T	10: 130,472,572 (GRCm38)	I599N	possibly damaging	Het
Vwf	A	G	6: 125,667,529 (GRCm38)	D2449G	possibly damaging	Het
Zbtb7c	T	A	18: 76,136,906 (GRCm38)	C22S	probably benign	Het
Zc3h7a	A	G	16: 11,147,304 (GRCm38)	I655T	possibly damaging	Het

Other mutations in Sdk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00972:Sdk2	APN	11	113,854,384 (GRCm38)	missense	possibly damaging	0.86
IGL01063:Sdk2	APN	11	113,830,842 (GRCm38)	missense	probably damaging	1.00
IGL01291:Sdk2	APN	11	113,843,080 (GRCm38)	missense	probably benign
IGL01316:Sdk2	APN	11	113,867,965 (GRCm38)	missense	probably benign	0.09
IGL01614:Sdk2	APN	11	113,793,858 (GRCm38)	missense	probably damaging	1.00
IGL01998:Sdk2	APN	11	113,838,532 (GRCm38)	missense	probably damaging	0.98
IGL02014:Sdk2	APN	11	113,838,494 (GRCm38)	missense	probably damaging	1.00
IGL02095:Sdk2	APN	11	113,834,830 (GRCm38)	missense	probably damaging	1.00
IGL02115:Sdk2	APN	11	113,834,813 (GRCm38)	splice site	probably benign
IGL02543:Sdk2	APN	11	113,868,921 (GRCm38)	missense	possibly damaging	0.90
IGL02976:Sdk2	APN	11	113,851,842 (GRCm38)	missense	probably damaging	1.00
IGL03001:Sdk2	APN	11	113,821,626 (GRCm38)	missense	probably benign	0.00
IGL03122:Sdk2	APN	11	113,842,068 (GRCm38)	missense	probably damaging	1.00
IGL03183:Sdk2	APN	11	113,850,984 (GRCm38)	missense	probably benign	0.19
IGL03222:Sdk2	APN	11	113,838,431 (GRCm38)	missense	probably benign	0.01
IGL03310:Sdk2	APN	11	113,793,325 (GRCm38)	missense	possibly damaging	0.77
Curtailed	UTSW	11	113,851,800 (GRCm38)	missense	probably damaging	1.00
Trimmed	UTSW	11	113,856,696 (GRCm38)	nonsense	probably null
ANU05:Sdk2	UTSW	11	113,843,080 (GRCm38)	missense	probably benign
BB008:Sdk2	UTSW	11	113,893,441 (GRCm38)	missense	possibly damaging	0.79
BB018:Sdk2	UTSW	11	113,893,441 (GRCm38)	missense	possibly damaging	0.79
R0008:Sdk2	UTSW	11	113,856,755 (GRCm38)	missense	probably damaging	1.00
R0008:Sdk2	UTSW	11	113,856,755 (GRCm38)	missense	probably damaging	1.00
R0088:Sdk2	UTSW	11	113,827,086 (GRCm38)	missense	possibly damaging	0.74
R0096:Sdk2	UTSW	11	113,903,144 (GRCm38)	splice site	probably benign
R0386:Sdk2	UTSW	11	113,893,464 (GRCm38)	missense	probably damaging	0.96
R0396:Sdk2	UTSW	11	113,829,967 (GRCm38)	missense	probably benign	0.04
R0409:Sdk2	UTSW	11	113,850,891 (GRCm38)	splice site	probably benign
R0416:Sdk2	UTSW	11	113,803,203 (GRCm38)	missense	probably damaging	1.00
R0456:Sdk2	UTSW	11	113,791,466 (GRCm38)	missense	possibly damaging	0.93
R0544:Sdk2	UTSW	11	113,781,010 (GRCm38)	missense	probably damaging	1.00
R0691:Sdk2	UTSW	11	113,794,920 (GRCm38)	splice site	probably null
R0711:Sdk2	UTSW	11	113,903,144 (GRCm38)	splice site	probably benign
R0717:Sdk2	UTSW	11	113,832,326 (GRCm38)	missense	probably damaging	1.00
R0780:Sdk2	UTSW	11	113,893,508 (GRCm38)	missense	probably benign	0.07
R0831:Sdk2	UTSW	11	113,832,258 (GRCm38)	missense	probably damaging	0.96
R0853:Sdk2	UTSW	11	113,821,415 (GRCm38)	missense	probably benign	0.00
R0865:Sdk2	UTSW	11	113,850,922 (GRCm38)	missense	probably benign	0.12
R0930:Sdk2	UTSW	11	113,838,445 (GRCm38)	missense	probably benign	0.01
R0964:Sdk2	UTSW	11	113,806,417 (GRCm38)	splice site	probably benign
R1051:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1052:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1054:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1055:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1077:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1079:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1115:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1186:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1187:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1337:Sdk2	UTSW	11	113,832,331 (GRCm38)	missense	possibly damaging	0.79
R1430:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1433:Sdk2	UTSW	11	113,795,045 (GRCm38)	missense	probably damaging	0.99
R1464:Sdk2	UTSW	11	113,830,080 (GRCm38)	missense	possibly damaging	0.86
R1464:Sdk2	UTSW	11	113,830,080 (GRCm38)	missense	possibly damaging	0.86
R1497:Sdk2	UTSW	11	113,893,575 (GRCm38)	splice site	probably benign
R1514:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1529:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1596:Sdk2	UTSW	11	113,838,609 (GRCm38)	splice site	probably benign
R1680:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1680:Sdk2	UTSW	11	113,791,436 (GRCm38)	missense	possibly damaging	0.47
R1770:Sdk2	UTSW	11	113,793,741 (GRCm38)	missense	probably benign	0.05
R1858:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1874:Sdk2	UTSW	11	113,834,956 (GRCm38)	missense	probably benign	0.00
R1899:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1905:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1907:Sdk2	UTSW	11	113,838,646 (GRCm38)	synonymous	silent
R1913:Sdk2	UTSW	11	113,856,726 (GRCm38)	missense	possibly damaging	0.77
R1964:Sdk2	UTSW	11	113,781,017 (GRCm38)	nonsense	probably null
R2055:Sdk2	UTSW	11	113,850,954 (GRCm38)	missense	probably damaging	1.00
R2059:Sdk2	UTSW	11	113,854,332 (GRCm38)	missense	probably damaging	1.00
R2093:Sdk2	UTSW	11	113,943,122 (GRCm38)	missense	probably damaging	1.00
R2256:Sdk2	UTSW	11	113,830,794 (GRCm38)	missense	probably benign	0.44
R3720:Sdk2	UTSW	11	113,800,244 (GRCm38)	missense	probably damaging	1.00
R3795:Sdk2	UTSW	11	113,856,696 (GRCm38)	nonsense	probably null
R4037:Sdk2	UTSW	11	113,795,055 (GRCm38)	missense	probably damaging	1.00
R4171:Sdk2	UTSW	11	113,866,989 (GRCm38)	splice site	probably null
R4717:Sdk2	UTSW	11	113,854,369 (GRCm38)	missense	probably damaging	0.96
R4758:Sdk2	UTSW	11	113,827,054 (GRCm38)	missense	possibly damaging	0.87
R4857:Sdk2	UTSW	11	113,821,382 (GRCm38)	nonsense	probably null
R4924:Sdk2	UTSW	11	113,857,758 (GRCm38)	missense	probably damaging	1.00
R5015:Sdk2	UTSW	11	113,793,761 (GRCm38)	missense	probably damaging	1.00
R5171:Sdk2	UTSW	11	113,850,982 (GRCm38)	missense	probably benign	0.01
R5239:Sdk2	UTSW	11	113,868,033 (GRCm38)	missense	probably damaging	1.00
R5243:Sdk2	UTSW	11	113,825,086 (GRCm38)	missense	possibly damaging	0.76
R5279:Sdk2	UTSW	11	113,867,031 (GRCm38)	missense	probably benign	0.31
R5535:Sdk2	UTSW	11	113,943,158 (GRCm38)	missense	possibly damaging	0.80
R5634:Sdk2	UTSW	11	113,851,714 (GRCm38)	missense	probably damaging	1.00
R5637:Sdk2	UTSW	11	113,833,179 (GRCm38)	missense	probably damaging	1.00
R5726:Sdk2	UTSW	11	113,851,800 (GRCm38)	missense	probably damaging	1.00
R5793:Sdk2	UTSW	11	113,868,952 (GRCm38)	missense	possibly damaging	0.46
R5798:Sdk2	UTSW	11	113,827,116 (GRCm38)	missense	probably damaging	1.00
R5834:Sdk2	UTSW	11	113,854,273 (GRCm38)	missense	probably damaging	1.00
R5863:Sdk2	UTSW	11	113,834,984 (GRCm38)	missense	probably damaging	0.98
R5869:Sdk2	UTSW	11	113,851,882 (GRCm38)	missense	probably damaging	0.96
R5875:Sdk2	UTSW	11	113,830,059 (GRCm38)	missense	probably benign	0.00
R5953:Sdk2	UTSW	11	113,793,744 (GRCm38)	missense	probably damaging	1.00
R5991:Sdk2	UTSW	11	113,943,254 (GRCm38)	missense	probably damaging	0.97
R6018:Sdk2	UTSW	11	113,830,063 (GRCm38)	missense	probably benign	0.00
R6116:Sdk2	UTSW	11	113,854,364 (GRCm38)	missense	probably damaging	0.99
R6328:Sdk2	UTSW	11	113,793,755 (GRCm38)	missense	probably damaging	1.00
R6348:Sdk2	UTSW	11	113,893,508 (GRCm38)	missense	probably benign	0.07
R6383:Sdk2	UTSW	11	113,832,265 (GRCm38)	missense	probably damaging	1.00
R6824:Sdk2	UTSW	11	113,867,934 (GRCm38)	missense	probably benign	0.43
R6835:Sdk2	UTSW	11	113,830,048 (GRCm38)	missense	probably damaging	0.98
R6853:Sdk2	UTSW	11	113,780,929 (GRCm38)	missense	probably damaging	0.99
R6912:Sdk2	UTSW	11	113,903,120 (GRCm38)	missense	probably benign	0.03
R7000:Sdk2	UTSW	11	113,803,169 (GRCm38)	missense	probably damaging	1.00
R7099:Sdk2	UTSW	11	113,834,905 (GRCm38)	missense	probably damaging	0.98
R7102:Sdk2	UTSW	11	113,842,690 (GRCm38)	nonsense	probably null
R7177:Sdk2	UTSW	11	113,829,969 (GRCm38)	missense	possibly damaging	0.91
R7381:Sdk2	UTSW	11	113,838,489 (GRCm38)	missense	probably damaging	0.98
R7412:Sdk2	UTSW	11	113,868,083 (GRCm38)	splice site	probably null
R7504:Sdk2	UTSW	11	113,867,967 (GRCm38)	missense	possibly damaging	0.50
R7552:Sdk2	UTSW	11	113,873,213 (GRCm38)	missense	possibly damaging	0.63
R7604:Sdk2	UTSW	11	113,829,969 (GRCm38)	missense	possibly damaging	0.91
R7647:Sdk2	UTSW	11	113,793,737 (GRCm38)	missense	probably damaging	1.00
R7897:Sdk2	UTSW	11	113,873,201 (GRCm38)	missense	possibly damaging	0.50
R7931:Sdk2	UTSW	11	113,893,441 (GRCm38)	missense	possibly damaging	0.79
R7998:Sdk2	UTSW	11	113,859,938 (GRCm38)	missense	probably benign	0.18
R8052:Sdk2	UTSW	11	113,854,351 (GRCm38)	missense	probably damaging	1.00
R8053:Sdk2	UTSW	11	113,854,351 (GRCm38)	missense	probably damaging	1.00
R8084:Sdk2	UTSW	11	113,827,089 (GRCm38)	missense	possibly damaging	0.67
R8136:Sdk2	UTSW	11	113,851,713 (GRCm38)	missense	probably damaging	1.00
R8151:Sdk2	UTSW	11	113,872,857 (GRCm38)	missense	possibly damaging	0.84
R8394:Sdk2	UTSW	11	113,838,716 (GRCm38)	missense	probably benign
R8715:Sdk2	UTSW	11	113,780,902 (GRCm38)	missense	probably damaging	1.00
R8774:Sdk2	UTSW	11	113,839,343 (GRCm38)	missense	probably damaging	1.00
R8774-TAIL:Sdk2	UTSW	11	113,839,343 (GRCm38)	missense	probably damaging	1.00
R8804:Sdk2	UTSW	11	113,873,152 (GRCm38)	nonsense	probably null
R9136:Sdk2	UTSW	11	113,806,377 (GRCm38)	missense	probably damaging	1.00
R9147:Sdk2	UTSW	11	113,823,400 (GRCm38)	missense	probably benign	0.18
R9300:Sdk2	UTSW	11	113,825,030 (GRCm38)	missense	possibly damaging	0.63
R9354:Sdk2	UTSW	11	113,834,931 (GRCm38)	missense	probably benign	0.00
R9450:Sdk2	UTSW	11	113,806,279 (GRCm38)	missense	probably benign
R9462:Sdk2	UTSW	11	113,869,918 (GRCm38)	missense	possibly damaging	0.56
R9616:Sdk2	UTSW	11	113,800,235 (GRCm38)	missense	probably benign	0.05
R9678:Sdk2	UTSW	11	113,794,963 (GRCm38)	nonsense	probably null
RF002:Sdk2	UTSW	11	113,885,252 (GRCm38)	missense	probably benign	0.00
V1662:Sdk2	UTSW	11	113,834,908 (GRCm38)	missense	probably damaging	1.00
Z1176:Sdk2	UTSW	11	113,851,836 (GRCm38)	missense	probably damaging	0.97
Z1176:Sdk2	UTSW	11	113,839,322 (GRCm38)	missense	probably benign	0.41
Z1177:Sdk2	UTSW	11	113,859,956 (GRCm38)	missense	probably benign
Z1177:Sdk2	UTSW	11	113,839,320 (GRCm38)	missense	probably damaging	1.00
Z1177:Sdk2	UTSW	11	113,838,659 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

Posted On

2015-02-05