Mutagenetix > Incidental Mutation

Incidental Mutation 'R1858:Sdk2'

265974

Institutional Source

Beutler Lab

Gene Symbol

Sdk2

Ensembl Gene

ENSMUSG00000041592

Gene Name

sidekick cell adhesion molecule 2

Synonyms

5330435L01Rik, 4632412F08Rik

MMRRC Submission

039882-MU

Accession Numbers

Essential gene?

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

Stock #

R1858 (G1)

Quality Score

168

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: 96.7%
10x: 94.8%
20x: 91.0%

Validation Efficiency

97% (112/116)

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: 110 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A830018L16Rik	C	A	1: 11,974,953 (GRCm38)	A443E	unknown	Het
Acacb	A	T	5: 114,196,709 (GRCm38)	Y613F	probably benign	Het
Adam23	A	C	1: 63,557,456 (GRCm38)	I566L	probably benign	Het
Adar	G	T	3: 89,739,282 (GRCm38)	R338L	probably benign	Het
Akap14	C	T	X: 37,157,126 (GRCm38)	A476T	probably damaging	Het
Amotl1	T	A	9: 14,575,401 (GRCm38)	Q399L	probably benign	Het
Ankrd16	T	G	2: 11,778,596 (GRCm38)	L3R	probably benign	Het
Arfgap1	G	C	2: 180,974,088 (GRCm38)	G187R	probably damaging	Het
Arhgap19	A	T	19: 41,779,153 (GRCm38)	V399D	probably benign	Het
Arl4d	A	G	11: 101,666,752 (GRCm38)	T35A	probably damaging	Het
Atr	T	A	9: 95,865,097 (GRCm38)	I144N	probably damaging	Het
Bptf	A	G	11: 107,073,301 (GRCm38)	M1574T	probably benign	Het
Cacna1h	T	A	17: 25,380,807 (GRCm38)	D1684V	probably damaging	Het
Celsr1	C	A	15: 86,032,759 (GRCm38)	V338F	probably damaging	Het
Cep164	T	C	9: 45,823,640 (GRCm38)		probably benign	Het
Clock	C	A	5: 76,240,909 (GRCm38)	G390C	possibly damaging	Het
Col6a6	A	G	9: 105,781,102 (GRCm38)	F637S	probably damaging	Het
Crebrf	T	A	17: 26,742,963 (GRCm38)	Y345N	probably benign	Het
Cul1	A	G	6: 47,525,524 (GRCm38)		probably null	Het
Cyb5r4	C	T	9: 87,041,279 (GRCm38)	S185L	probably benign	Het
Cyp3a57	T	C	5: 145,381,249 (GRCm38)	Y347H	probably damaging	Het
Dgkq	G	T	5: 108,653,731 (GRCm38)	T487K	probably benign	Het
Dmkn	T	C	7: 30,764,565 (GRCm38)	V143A	probably benign	Het
Dmp1	A	T	5: 104,207,630 (GRCm38)	E32V	possibly damaging	Het
Dsc3	T	C	18: 19,965,716 (GRCm38)	D802G	probably damaging	Het
Dse	T	C	10: 34,153,229 (GRCm38)	T622A	probably benign	Het
Dusp27	T	C	1: 166,100,846 (GRCm38)	Y399C	possibly damaging	Het
Dyrk1b	A	T	7: 28,182,646 (GRCm38)		probably null	Het
Ehd2	T	C	7: 15,952,188 (GRCm38)	T320A	probably benign	Het
Eif3a	A	C	19: 60,782,197 (GRCm38)	L71V	probably damaging	Het
Eif4e1b	A	G	13: 54,787,278 (GRCm38)		probably null	Het
Fam131b	A	G	6: 42,318,980 (GRCm38)	F161L	probably damaging	Het
Fam171b	A	T	2: 83,853,381 (GRCm38)	M81L	probably benign	Het
Gal3st4	T	C	5: 138,270,788 (GRCm38)		probably null	Het
Gdf11	A	T	10: 128,886,446 (GRCm38)	V180E	probably damaging	Het
Gm4758	A	T	16: 36,308,087 (GRCm38)	I15F	probably damaging	Het
Gm4981	A	G	10: 58,235,780 (GRCm38)	V204A	probably benign	Het
Grin3a	T	A	4: 49,792,437 (GRCm38)	Y432F	probably benign	Het
Hif1a	C	A	12: 73,944,155 (GRCm38)	H708N	probably benign	Het
Hmcn2	G	T	2: 31,415,283 (GRCm38)		probably null	Het
Hrasls	G	A	16: 29,217,718 (GRCm38)	G36D	probably damaging	Het
Hs3st6	T	A	17: 24,757,999 (GRCm38)	M151K	possibly damaging	Het
Hyal2	T	A	9: 107,572,338 (GRCm38)	L431Q	probably benign	Het
Hyal6	A	T	6: 24,740,858 (GRCm38)	T337S	probably benign	Het
Igsf5	A	T	16: 96,386,629 (GRCm38)		probably null	Het
Kif13a	G	A	13: 46,864,838 (GRCm38)		probably benign	Het
Krtap19-3	G	A	16: 88,877,990 (GRCm38)		probably benign	Het
Lgalsl	T	C	11: 20,829,420 (GRCm38)	D75G	probably benign	Het
Lrrc56	A	G	7: 141,207,508 (GRCm38)	M353V	probably benign	Het
Ltbp2	T	A	12: 84,830,781 (GRCm38)	K337*	probably null	Het
Mdn1	C	T	4: 32,730,881 (GRCm38)	H2917Y	probably benign	Het
Medag	A	G	5: 149,429,794 (GRCm38)	I151M	probably damaging	Het
Meiob	T	C	17: 24,823,570 (GRCm38)	V124A	probably damaging	Het
Mmp3	A	G	9: 7,451,799 (GRCm38)	H379R	probably benign	Het
Mpg	A	G	11: 32,231,957 (GRCm38)		probably null	Het
Ncoa6	G	T	2: 155,421,639 (GRCm38)	Q292K	probably benign	Het
Ndufaf6	G	T	4: 11,053,474 (GRCm38)	H277Q	probably benign	Het
Nlrp4c	A	G	7: 6,084,656 (GRCm38)	I763V	probably benign	Het
Nlrp5	A	T	7: 23,418,161 (GRCm38)	I437F	probably damaging	Het
Noc2l	G	A	4: 156,245,270 (GRCm38)	R435Q	probably damaging	Het
Nova2	T	C	7: 18,958,401 (GRCm38)	I485T	probably damaging	Het
Nrxn2	G	A	19: 6,488,795 (GRCm38)	V794I	probably benign	Het
Nup210l	A	G	3: 90,154,499 (GRCm38)	T662A	probably damaging	Het
Olfr1014	T	C	2: 85,777,238 (GRCm38)	L218P	probably damaging	Het
Olfr1367	A	G	13: 21,347,176 (GRCm38)	M83V	possibly damaging	Het
Olfr1368	A	T	13: 21,142,394 (GRCm38)	I221N	probably damaging	Het
Olfr1370	A	T	13: 21,072,471 (GRCm38)	F277I	probably damaging	Het
Olfr606	G	A	7: 103,452,125 (GRCm38)	V263I	probably benign	Het
Olfr612	G	A	7: 103,538,652 (GRCm38)	T194I	probably damaging	Het
Olfr78	A	C	7: 102,742,364 (GRCm38)	I213S	probably damaging	Het
Pelp1	G	A	11: 70,394,742 (GRCm38)	P767S	probably damaging	Het
Pfdn1	C	A	18: 36,451,100 (GRCm38)	M60I	probably benign	Het
Plcxd3	T	A	15: 4,516,611 (GRCm38)		probably benign	Het
Plekhg1	C	A	10: 3,945,917 (GRCm38)	D436E	possibly damaging	Het
Ppfibp1	G	A	6: 146,990,592 (GRCm38)	V117I	probably benign	Het
Prss44	A	G	9: 110,814,109 (GRCm38)	K24R	probably benign	Het
Ptger1	G	T	8: 83,668,478 (GRCm38)	G195W	probably benign	Het
Ptgs1	A	C	2: 36,242,770 (GRCm38)	D260A	probably benign	Het
Ptprd	T	A	4: 75,947,147 (GRCm38)	T1198S	probably damaging	Het
Qsox2	A	G	2: 26,214,062 (GRCm38)	S319P	probably damaging	Het
Rab35	A	G	5: 115,640,088 (GRCm38)	I38V	probably damaging	Het
Rapgef4	A	G	2: 72,031,064 (GRCm38)	I33V	possibly damaging	Het
Rbbp8nl	C	T	2: 180,282,213 (GRCm38)		probably benign	Het
Riok1	A	T	13: 38,058,718 (GRCm38)	K473*	probably null	Het
Rtca	C	T	3: 116,494,115 (GRCm38)	G288S	probably benign	Het
Sag	A	T	1: 87,814,848 (GRCm38)	D114V	probably benign	Het
Sec61g	A	G	11: 16,506,371 (GRCm38)		probably null	Het
Sf3a3	A	T	4: 124,729,495 (GRCm38)	I440F	probably damaging	Het
Sgta	T	C	10: 81,048,861 (GRCm38)	K205E	possibly damaging	Het
Slc36a4	A	G	9: 15,720,710 (GRCm38)	T61A	probably damaging	Het
Slc5a4a	T	C	10: 76,166,735 (GRCm38)	S242P	probably benign	Het
Srgap3	A	T	6: 112,771,518 (GRCm38)	L391Q	probably damaging	Het
Stard13	T	C	5: 151,095,438 (GRCm38)	Y60C	probably damaging	Het
Syt12	G	T	19: 4,447,797 (GRCm38)	H386N	probably damaging	Het
Thyn1	T	A	9: 27,003,774 (GRCm38)	M74K	probably benign	Het
Tmem130	C	A	5: 144,752,283 (GRCm38)		probably null	Het
Trim71	A	G	9: 114,562,948 (GRCm38)	V57A	possibly damaging	Het
Twf1	T	C	15: 94,585,547 (GRCm38)		probably benign	Het
Tyro3	T	A	2: 119,801,695 (GRCm38)	I81N	possibly damaging	Het
Unc13a	A	T	8: 71,652,399 (GRCm38)	C740S	probably damaging	Het
Vmn1r15	A	T	6: 57,258,631 (GRCm38)	K161N	probably benign	Het
Vmn1r16	A	T	6: 57,322,899 (GRCm38)	I246N	probably damaging	Het
Vmn1r42	A	G	6: 89,844,615 (GRCm38)	I324T	probably benign	Het
Vmn2r35	T	C	7: 7,816,806 (GRCm38)	Y155C	possibly damaging	Het
Wif1	T	A	10: 121,083,883 (GRCm38)		probably null	Het
Wscd2	G	A	5: 113,551,170 (GRCm38)	R79Q	possibly damaging	Het
Zan	G	T	5: 137,405,877 (GRCm38)		probably benign	Het
Zfp9	G	T	6: 118,465,060 (GRCm38)	H214N	probably benign	Het
Zfp985	A	T	4: 147,582,858 (GRCm38)	Y61F	probably benign	Het
Zscan30	A	G	18: 23,971,467 (GRCm38)		noncoding transcript	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
R1866: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