Mutagenetix > Incidental Mutation

Incidental Mutation 'R6020:Ush2a'

482051

Institutional Source

Beutler Lab

Gene Symbol

Ush2a

Ensembl Gene

ENSMUSG00000026609

Gene Name

usherin

Synonyms

A930011D15Rik, LOC381317, A930037M10Rik, LOC269160, Usherin, MUSH2A

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.699) question?

Stock #

R6020 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

188262023-188965041 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 188728096 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000050454 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060479]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000060479

SMART Domains

Protein: ENSMUSP00000050454
Gene: ENSMUSG00000026609

Domain	Start	End	E-Value	Type
transmembrane domain	9	31	N/A	INTRINSIC
Pfam:Laminin_G_3	128	283	6.5e-16	PFAM
LamNT	310	513	6.79e-9	SMART
EGF_Lam	515	569	1.58e-3	SMART
EGF_Lam	572	635	5.69e-10	SMART
EGF_Lam	638	688	4.38e-11	SMART
EGF_Lam	691	741	3.56e-11	SMART
EGF_Lam	744	789	7.93e-9	SMART
EGF_Lam	792	841	3.37e-12	SMART
EGF_Lam	844	894	2.01e-10	SMART
EGF_Lam	897	945	5.43e-16	SMART
EGF_Lam	948	996	7.88e-4	SMART
EGF_Lam	999	1047	2.96e-8	SMART
FN3	1051	1130	1e-1	SMART
FN3	1145	1224	2.06e-3	SMART
FN3	1239	1342	8.69e-11	SMART
FN3	1356	1447	5.32e-6	SMART
FN3	1461	1570	2.63e1	SMART
LamG	1531	1672	5.39e-19	SMART
LamG	1727	1862	2.33e-23	SMART
FN3	1861	1931	9.15e1	SMART
FN3	1945	2032	2.24e-4	SMART
FN3	2047	2120	1.13e0	SMART
FN3	2134	2218	3.4e-4	SMART
FN3	2232	2306	1.59e-4	SMART
FN3	2320	2412	1.12e-4	SMART
FN3	2423	2510	8.9e-8	SMART
FN3	2524	2600	1.95e-4	SMART
FN3	2612	2701	4.67e-2	SMART
FN3	2715	2792	1.17e-7	SMART
FN3	2809	2902	1.12e-4	SMART
FN3	2913	2997	5.36e-2	SMART
FN3	3011	3089	2.46e-1	SMART
FN3	3101	3477	2.85e1	SMART
FN3	3491	3568	4e-1	SMART
FN3	3582	3659	5.87e-8	SMART
FN3	3673	3750	1.75e-6	SMART
FN3	3764	3845	9.62e-4	SMART
FN3	3859	3943	2.41e-4	SMART
FN3	3954	4044	5.11e-8	SMART
FN3	4058	4133	1.06e0	SMART
FN3	4147	4241	7.87e-9	SMART
FN3	4255	4334	1.15e-1	SMART
FN3	4348	4422	6.39e-9	SMART
FN3	4435	4510	6.91e-5	SMART
FN3	4521	4610	2.28e-5	SMART
FN3	4626	4713	1.71e0	SMART
FN3	4724	4805	1.3e0	SMART
FN3	4817	4909	3.62e-8	SMART
transmembrane domain	5032	5054	N/A	INTRINSIC

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.8%
20x: 93.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that contains laminin EGF motifs, a pentaxin domain, and many fibronectin type III motifs. The protein is found in the basement membrane, and may be important in development and homeostasis of the inner ear and retina. Mutations within this gene have been associated with Usher syndrome type IIa and retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
PHENOTYPE: Mice homozygous for a knock-out allele display progressive retinal photoreceptor degeneration along with significantly reduced a- and b-wave amplitudes, and a moderate but nonprogressive high-frequency hearing loss associated with widespread loss of outer hair cells in the basal turn of the cochlea. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	C	A	11: 110,145,613 (GRCm38)	V557F	possibly damaging	Het
Abi3	A	T	11: 95,842,025 (GRCm38)	L41*	probably null	Het
Actn1	C	A	12: 80,174,455 (GRCm38)		probably null	Het
Adamts15	G	T	9: 30,902,062 (GRCm38)	R936S	probably benign	Het
Angel2	T	C	1: 190,932,871 (GRCm38)	S22P	probably benign	Het
Ank2	T	G	3: 126,946,821 (GRCm38)		probably benign	Het
Astn1	A	G	1: 158,509,993 (GRCm38)	D423G	probably damaging	Het
Casp9	A	G	4: 141,796,538 (GRCm38)	D78G	probably damaging	Het
Cbr4	A	G	8: 61,487,853 (GRCm38)	D2G	probably benign	Het
Ccdc8	T	A	7: 16,996,581 (GRCm38)	L665H	probably damaging	Het
Cdh23	T	A	10: 60,331,326 (GRCm38)	N1847I	probably damaging	Het
Cnst	T	C	1: 179,609,875 (GRCm38)	W335R	probably benign	Het
Ddr2	T	A	1: 170,005,102 (GRCm38)	I130F	probably benign	Het
Dnah2	C	T	11: 69,500,839 (GRCm38)	A677T	probably benign	Het
Dzip3	C	A	16: 48,951,842 (GRCm38)	W488L	probably damaging	Het
Ephb3	T	G	16: 21,222,013 (GRCm38)	I637S	probably damaging	Het
Etv3	A	G	3: 87,529,364 (GRCm38)	D142G	probably benign	Het
Fabp5	C	T	3: 10,016,089 (GRCm38)	T126I	probably benign	Het
Fam13b	A	C	18: 34,494,774 (GRCm38)	Y125D	probably damaging	Het
Fsip2	C	A	2: 82,992,127 (GRCm38)	P6068Q	probably damaging	Het
Gm11232	A	G	4: 71,756,668 (GRCm38)	F199S	possibly damaging	Het
Gm340	G	A	19: 41,583,547 (GRCm38)	G247D	possibly damaging	Het
Gm5493	A	G	17: 22,748,061 (GRCm38)	K57E	probably benign	Het
Gm7334	A	G	17: 50,699,237 (GRCm38)	M184V	probably benign	Het
Gm9894	T	C	13: 67,763,835 (GRCm38)		noncoding transcript	Het
Gpd2	T	A	2: 57,364,513 (GRCm38)	N674K	probably benign	Het
H2-M10.6	A	G	17: 36,813,067 (GRCm38)	Y141C	probably damaging	Het
Heatr5a	C	T	12: 51,884,327 (GRCm38)	E1796K	probably benign	Het
Hexim2	A	G	11: 103,138,292 (GRCm38)	T57A	probably benign	Het
Hrg	A	T	16: 22,954,518 (GRCm38)	N134Y	probably damaging	Het
Hsd17b12	T	C	2: 94,033,977 (GRCm38)	T262A	probably damaging	Het
Irak3	G	T	10: 120,143,137 (GRCm38)	P470T	probably damaging	Het
Itgbl1	A	T	14: 123,846,565 (GRCm38)	D285V	probably damaging	Het
Kcp	A	T	6: 29,502,864 (GRCm38)	V164E	probably benign	Het
Klhdc7b	T	A	15: 89,388,386 (GRCm38)	M1157K	probably damaging	Het
Mdc1	G	A	17: 35,848,633 (GRCm38)	G635D	probably benign	Het
Mdc1	A	G	17: 35,857,572 (GRCm38)	K1690R	probably benign	Het
Mpp3	A	T	11: 102,018,539 (GRCm38)		probably benign	Het
Ncor2	G	T	5: 125,020,011 (GRCm38)	H2285N	probably benign	Het
Neb	T	A	2: 52,257,827 (GRCm38)	T2727S	probably benign	Het
Nkx6-2	T	C	7: 139,581,567 (GRCm38)	D234G	possibly damaging	Het
Nlrp9c	T	C	7: 26,384,725 (GRCm38)	I476M	probably benign	Het
Nrsn1	T	G	13: 25,253,372 (GRCm38)	Q191P	probably damaging	Het
Olfr116	A	T	17: 37,623,967 (GRCm38)	S223T	possibly damaging	Het
Olfr390	C	T	11: 73,787,552 (GRCm38)	L205F	probably benign	Het
Olfr610	T	A	7: 103,506,799 (GRCm38)	H49L	probably benign	Het
Patl1	T	G	19: 11,937,354 (GRCm38)	L623R	probably damaging	Het
Pdc	T	C	1: 150,333,366 (GRCm38)	I200T	probably benign	Het
Pdzk1	A	G	3: 96,868,426 (GRCm38)	D370G	probably benign	Het
Pglyrp3	A	T	3: 92,031,534 (GRCm38)	I339F	probably damaging	Het
Plxnb1	T	C	9: 109,116,611 (GRCm38)	V2070A	probably damaging	Het
Poln	G	A	5: 34,109,431 (GRCm38)	R461C	probably damaging	Het
Prl2b1	C	A	13: 27,383,508 (GRCm38)	V218L	probably damaging	Het
Pygl	T	C	12: 70,216,654 (GRCm38)	D55G	probably damaging	Het
Rif1	C	G	2: 52,095,844 (GRCm38)	L614V	probably damaging	Het
Rnd2	C	T	11: 101,468,999 (GRCm38)	L57F	probably damaging	Het
RP24-351P7.8	T	C	7: 11,610,301 (GRCm38)	F62S	probably damaging	Het
Rsrp1	T	C	4: 134,924,381 (GRCm38)	F152S	probably damaging	Het
Sim2	T	C	16: 94,097,251 (GRCm38)	S115P	probably damaging	Het
Slc17a1	T	A	13: 23,875,610 (GRCm38)	I108K	possibly damaging	Het
Slc30a8	A	G	15: 52,325,658 (GRCm38)	D223G	probably damaging	Het
Slc39a4	A	T	15: 76,616,142 (GRCm38)	N69K	probably benign	Het
Slc51a	T	G	16: 32,479,766 (GRCm38)	T58P	probably damaging	Het
Slc7a14	T	C	3: 31,224,112 (GRCm38)	H448R	probably benign	Het
Smc3	G	A	19: 53,625,163 (GRCm38)		probably null	Het
Sox6	A	T	7: 115,486,628 (GRCm38)	D659E	probably damaging	Het
Stard9	GCCC	GCC	2: 120,693,715 (GRCm38)		probably null	Het
Tsr1	C	T	11: 74,900,293 (GRCm38)		probably null	Het
Ttc12	T	C	9: 49,443,122 (GRCm38)	K565E	probably damaging	Het
Ube4b	A	T	4: 149,368,311 (GRCm38)	V386E	probably benign	Het
Usp5	C	A	6: 124,817,613 (GRCm38)		probably benign	Het
Vmn1r216	T	C	13: 23,099,935 (GRCm38)	F263L	probably benign	Het
Vmn2r88	T	A	14: 51,418,149 (GRCm38)	L606*	probably null	Het
Wee2	T	A	6: 40,449,620 (GRCm38)		probably null	Het
Zfhx3	T	C	8: 108,792,527 (GRCm38)	Y94H	probably damaging	Het
Zfp385c	G	A	11: 100,632,768 (GRCm38)	P120L	probably benign	Het

Other mutations in Ush2a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00155:Ush2a	APN	1	188,864,678 (GRCm38)	missense	probably benign	0.00
IGL00391:Ush2a	APN	1	188,916,061 (GRCm38)	missense	probably damaging	1.00
IGL00429:Ush2a	APN	1	188,400,114 (GRCm38)	nonsense	probably null
IGL00484:Ush2a	APN	1	188,782,513 (GRCm38)	missense	probably benign	0.00
IGL00519:Ush2a	APN	1	188,444,668 (GRCm38)	missense	probably benign	0.03
IGL00567:Ush2a	APN	1	188,964,917 (GRCm38)	missense	probably damaging	1.00
IGL00823:Ush2a	APN	1	188,911,443 (GRCm38)	missense	possibly damaging	0.61
IGL00940:Ush2a	APN	1	188,357,961 (GRCm38)	nonsense	probably null
IGL00951:Ush2a	APN	1	188,263,465 (GRCm38)	missense	probably benign	0.33
IGL00956:Ush2a	APN	1	188,753,522 (GRCm38)	missense	probably damaging	0.99
IGL01096:Ush2a	APN	1	188,678,377 (GRCm38)	missense	probably damaging	1.00
IGL01108:Ush2a	APN	1	188,862,825 (GRCm38)	missense	probably benign	0.00
IGL01315:Ush2a	APN	1	188,633,614 (GRCm38)	missense	possibly damaging	0.51
IGL01318:Ush2a	APN	1	188,814,353 (GRCm38)	missense	probably benign	0.00
IGL01324:Ush2a	APN	1	188,848,992 (GRCm38)	missense	probably benign	0.38
IGL01326:Ush2a	APN	1	188,263,321 (GRCm38)	nonsense	probably null
IGL01384:Ush2a	APN	1	188,553,228 (GRCm38)	missense	possibly damaging	0.65
IGL01466:Ush2a	APN	1	188,911,622 (GRCm38)	missense	probably benign	0.00
IGL01518:Ush2a	APN	1	188,399,785 (GRCm38)	missense	probably benign	0.01
IGL01585:Ush2a	APN	1	188,430,727 (GRCm38)	missense	probably damaging	1.00
IGL01595:Ush2a	APN	1	188,654,724 (GRCm38)	critical splice donor site	probably null
IGL01657:Ush2a	APN	1	188,826,461 (GRCm38)	missense	probably benign	0.03
IGL01797:Ush2a	APN	1	188,263,509 (GRCm38)	missense	probably damaging	1.00
IGL01802:Ush2a	APN	1	188,436,957 (GRCm38)	missense	probably damaging	0.99
IGL01836:Ush2a	APN	1	188,759,863 (GRCm38)	splice site	probably benign
IGL01938:Ush2a	APN	1	188,797,845 (GRCm38)	missense	probably damaging	1.00
IGL01976:Ush2a	APN	1	188,911,241 (GRCm38)	missense	probably benign	0.04
IGL02023:Ush2a	APN	1	188,733,514 (GRCm38)	missense	probably benign	0.03
IGL02126:Ush2a	APN	1	188,263,391 (GRCm38)	missense	probably benign	0.01
IGL02133:Ush2a	APN	1	188,443,343 (GRCm38)	missense	probably damaging	1.00
IGL02147:Ush2a	APN	1	188,864,703 (GRCm38)	missense	probably benign
IGL02275:Ush2a	APN	1	188,263,269 (GRCm38)	missense	possibly damaging	0.67
IGL02314:Ush2a	APN	1	188,633,629 (GRCm38)	missense	probably benign	0.00
IGL02353:Ush2a	APN	1	188,728,438 (GRCm38)	missense	probably benign	0.04
IGL02360:Ush2a	APN	1	188,728,438 (GRCm38)	missense	probably benign	0.04
IGL02367:Ush2a	APN	1	188,784,746 (GRCm38)	missense	probably benign
IGL02402:Ush2a	APN	1	188,267,108 (GRCm38)	missense	probably benign	0.02
IGL02410:Ush2a	APN	1	188,915,997 (GRCm38)	missense	probably damaging	1.00
IGL02490:Ush2a	APN	1	188,810,364 (GRCm38)	missense	probably damaging	1.00
IGL02500:Ush2a	APN	1	188,822,696 (GRCm38)	missense	probably damaging	1.00
IGL02511:Ush2a	APN	1	188,743,687 (GRCm38)	critical splice donor site	probably null
IGL02517:Ush2a	APN	1	188,915,998 (GRCm38)	missense	probably damaging	1.00
IGL02536:Ush2a	APN	1	188,957,266 (GRCm38)	critical splice acceptor site	probably null
IGL02585:Ush2a	APN	1	188,728,333 (GRCm38)	missense	probably benign	0.00
IGL02610:Ush2a	APN	1	188,444,466 (GRCm38)	missense	probably damaging	0.98
IGL02677:Ush2a	APN	1	188,734,685 (GRCm38)	missense	probably damaging	1.00
IGL02691:Ush2a	APN	1	188,734,752 (GRCm38)	missense	probably damaging	1.00
IGL02740:Ush2a	APN	1	188,648,388 (GRCm38)	missense	possibly damaging	0.68
IGL02744:Ush2a	APN	1	188,358,717 (GRCm38)	splice site	probably null
IGL02749:Ush2a	APN	1	188,946,958 (GRCm38)	missense	probably damaging	0.99
IGL02806:Ush2a	APN	1	188,810,357 (GRCm38)	nonsense	probably null
IGL02870:Ush2a	APN	1	188,678,358 (GRCm38)	missense	probably benign	0.42
IGL02894:Ush2a	APN	1	188,451,846 (GRCm38)	missense	probably damaging	1.00
IGL02904:Ush2a	APN	1	188,906,506 (GRCm38)	missense	probably benign	0.06
IGL03000:Ush2a	APN	1	188,549,856 (GRCm38)	missense	possibly damaging	0.81
IGL03015:Ush2a	APN	1	188,436,950 (GRCm38)	missense	probably benign	0.01
IGL03036:Ush2a	APN	1	188,864,621 (GRCm38)	missense	possibly damaging	0.80
IGL03057:Ush2a	APN	1	188,797,838 (GRCm38)	missense	probably damaging	1.00
IGL03230:Ush2a	APN	1	188,466,193 (GRCm38)	missense	probably benign	0.09
IGL03278:Ush2a	APN	1	188,849,116 (GRCm38)	missense	probably damaging	1.00
BB003:Ush2a	UTSW	1	188,728,600 (GRCm38)	missense	probably benign
BB013:Ush2a	UTSW	1	188,728,600 (GRCm38)	missense	probably benign
PIT4283001:Ush2a	UTSW	1	188,436,867 (GRCm38)	missense	probably benign	0.01
R0003:Ush2a	UTSW	1	188,578,491 (GRCm38)	missense	probably damaging	0.99
R0030:Ush2a	UTSW	1	188,822,657 (GRCm38)	missense	possibly damaging	0.51
R0035:Ush2a	UTSW	1	188,356,888 (GRCm38)	missense	probably benign
R0038:Ush2a	UTSW	1	188,626,612 (GRCm38)	missense	probably benign	0.00
R0038:Ush2a	UTSW	1	188,626,612 (GRCm38)	missense	probably benign	0.00
R0067:Ush2a	UTSW	1	188,964,846 (GRCm38)	missense	probably damaging	0.99
R0067:Ush2a	UTSW	1	188,964,846 (GRCm38)	missense	probably damaging	0.99
R0103:Ush2a	UTSW	1	188,319,070 (GRCm38)	missense	possibly damaging	0.81
R0103:Ush2a	UTSW	1	188,319,070 (GRCm38)	missense	possibly damaging	0.81
R0122:Ush2a	UTSW	1	188,948,455 (GRCm38)	missense	possibly damaging	0.65
R0206:Ush2a	UTSW	1	188,531,761 (GRCm38)	missense	probably damaging	0.99
R0208:Ush2a	UTSW	1	188,531,761 (GRCm38)	missense	probably damaging	0.99
R0230:Ush2a	UTSW	1	188,850,104 (GRCm38)	missense	probably damaging	1.00
R0269:Ush2a	UTSW	1	188,810,176 (GRCm38)	missense	probably benign	0.33
R0319:Ush2a	UTSW	1	188,948,374 (GRCm38)	splice site	probably benign
R0358:Ush2a	UTSW	1	188,537,780 (GRCm38)	missense	possibly damaging	0.83
R0379:Ush2a	UTSW	1	188,451,819 (GRCm38)	missense	probably damaging	1.00
R0427:Ush2a	UTSW	1	188,400,281 (GRCm38)	missense	probably damaging	1.00
R0437:Ush2a	UTSW	1	188,911,031 (GRCm38)	missense	probably benign	0.00
R0462:Ush2a	UTSW	1	188,910,939 (GRCm38)	missense	probably benign
R0510:Ush2a	UTSW	1	188,734,663 (GRCm38)	splice site	probably benign
R0531:Ush2a	UTSW	1	188,443,181 (GRCm38)	missense	probably benign	0.18
R0541:Ush2a	UTSW	1	188,714,466 (GRCm38)	splice site	probably benign
R0549:Ush2a	UTSW	1	188,946,953 (GRCm38)	missense	probably damaging	0.99
R0562:Ush2a	UTSW	1	188,356,847 (GRCm38)	missense	probably damaging	1.00
R0636:Ush2a	UTSW	1	188,822,738 (GRCm38)	missense	probably benign
R0662:Ush2a	UTSW	1	188,351,093 (GRCm38)	missense	probably benign	0.26
R0685:Ush2a	UTSW	1	188,400,278 (GRCm38)	missense	probably damaging	1.00
R0718:Ush2a	UTSW	1	188,797,830 (GRCm38)	missense	probably damaging	1.00
R0725:Ush2a	UTSW	1	188,951,525 (GRCm38)	missense	probably damaging	1.00
R0735:Ush2a	UTSW	1	188,864,693 (GRCm38)	missense	probably benign	0.04
R0744:Ush2a	UTSW	1	188,814,406 (GRCm38)	splice site	probably benign
R0765:Ush2a	UTSW	1	188,948,574 (GRCm38)	missense	possibly damaging	0.67
R0862:Ush2a	UTSW	1	188,542,818 (GRCm38)	nonsense	probably null
R1067:Ush2a	UTSW	1	188,550,207 (GRCm38)	missense	probably benign	0.35
R1072:Ush2a	UTSW	1	188,728,717 (GRCm38)	missense	possibly damaging	0.91
R1099:Ush2a	UTSW	1	188,864,639 (GRCm38)	missense	probably damaging	1.00
R1099:Ush2a	UTSW	1	188,648,348 (GRCm38)	missense	probably benign	0.06
R1104:Ush2a	UTSW	1	188,916,256 (GRCm38)	missense	probably benign
R1106:Ush2a	UTSW	1	188,910,983 (GRCm38)	missense	possibly damaging	0.82
R1124:Ush2a	UTSW	1	188,753,536 (GRCm38)	missense	probably damaging	0.99
R1168:Ush2a	UTSW	1	188,678,411 (GRCm38)	missense	probably benign	0.01
R1199:Ush2a	UTSW	1	188,759,795 (GRCm38)	missense	probably benign	0.00
R1215:Ush2a	UTSW	1	188,957,282 (GRCm38)	missense	possibly damaging	0.66
R1307:Ush2a	UTSW	1	188,451,840 (GRCm38)	missense	probably damaging	1.00
R1307:Ush2a	UTSW	1	188,357,967 (GRCm38)	missense	probably damaging	1.00
R1311:Ush2a	UTSW	1	188,947,145 (GRCm38)	missense	possibly damaging	0.86
R1388:Ush2a	UTSW	1	188,523,318 (GRCm38)	splice site	probably benign
R1416:Ush2a	UTSW	1	188,436,883 (GRCm38)	missense	probably damaging	1.00
R1424:Ush2a	UTSW	1	188,542,878 (GRCm38)	critical splice donor site	probably null
R1459:Ush2a	UTSW	1	188,862,851 (GRCm38)	missense	probably benign	0.05
R1470:Ush2a	UTSW	1	188,400,206 (GRCm38)	missense	probably benign	0.00
R1470:Ush2a	UTSW	1	188,400,206 (GRCm38)	missense	probably benign	0.00
R1477:Ush2a	UTSW	1	188,849,076 (GRCm38)	missense	probably benign	0.05
R1484:Ush2a	UTSW	1	188,810,337 (GRCm38)	nonsense	probably null
R1490:Ush2a	UTSW	1	188,359,841 (GRCm38)	missense	probably benign	0.24
R1510:Ush2a	UTSW	1	188,648,304 (GRCm38)	missense	probably damaging	1.00
R1522:Ush2a	UTSW	1	188,797,814 (GRCm38)	missense	possibly damaging	0.94
R1606:Ush2a	UTSW	1	188,759,766 (GRCm38)	missense	probably benign	0.17
R1618:Ush2a	UTSW	1	188,814,224 (GRCm38)	missense	probably benign	0.29
R1636:Ush2a	UTSW	1	188,466,176 (GRCm38)	missense	possibly damaging	0.53
R1646:Ush2a	UTSW	1	188,415,821 (GRCm38)	missense	probably damaging	1.00
R1660:Ush2a	UTSW	1	188,916,064 (GRCm38)	missense	probably benign
R1676:Ush2a	UTSW	1	188,728,585 (GRCm38)	missense	probably damaging	1.00
R1704:Ush2a	UTSW	1	188,821,796 (GRCm38)	missense	probably damaging	1.00
R1705:Ush2a	UTSW	1	188,911,541 (GRCm38)	missense	probably benign	0.40
R1705:Ush2a	UTSW	1	188,874,869 (GRCm38)	missense	probably damaging	1.00
R1760:Ush2a	UTSW	1	188,910,983 (GRCm38)	missense	possibly damaging	0.82
R1776:Ush2a	UTSW	1	188,728,203 (GRCm38)	missense	possibly damaging	0.83
R1782:Ush2a	UTSW	1	188,911,185 (GRCm38)	missense	probably benign	0.06
R1794:Ush2a	UTSW	1	188,862,809 (GRCm38)	missense	probably benign	0.00
R1796:Ush2a	UTSW	1	188,910,827 (GRCm38)	missense	probably benign	0.11
R1804:Ush2a	UTSW	1	188,633,729 (GRCm38)	critical splice donor site	probably null
R1835:Ush2a	UTSW	1	188,451,818 (GRCm38)	missense	probably benign	0.13
R1871:Ush2a	UTSW	1	188,826,468 (GRCm38)	missense	probably benign	0.02
R1876:Ush2a	UTSW	1	188,678,289 (GRCm38)	missense	possibly damaging	0.51
R1887:Ush2a	UTSW	1	188,399,980 (GRCm38)	missense	probably benign	0.05
R1896:Ush2a	UTSW	1	188,550,009 (GRCm38)	missense	probably benign	0.00
R1907:Ush2a	UTSW	1	188,715,064 (GRCm38)	missense	probably benign	0.01
R1940:Ush2a	UTSW	1	188,951,561 (GRCm38)	missense	probably null	0.89
R1950:Ush2a	UTSW	1	188,755,185 (GRCm38)	missense	probably damaging	1.00
R1991:Ush2a	UTSW	1	188,578,532 (GRCm38)	splice site	probably benign
R2043:Ush2a	UTSW	1	188,916,256 (GRCm38)	missense	probably benign	0.00
R2046:Ush2a	UTSW	1	188,356,927 (GRCm38)	missense	probably benign	0.01
R2059:Ush2a	UTSW	1	188,381,549 (GRCm38)	critical splice donor site	probably null
R2239:Ush2a	UTSW	1	188,576,214 (GRCm38)	missense	probably benign
R2365:Ush2a	UTSW	1	188,378,991 (GRCm38)	missense	possibly damaging	0.68
R2395:Ush2a	UTSW	1	188,947,040 (GRCm38)	missense	probably damaging	1.00
R2425:Ush2a	UTSW	1	188,537,804 (GRCm38)	missense	possibly damaging	0.82
R2519:Ush2a	UTSW	1	188,267,107 (GRCm38)	missense	probably benign
R3039:Ush2a	UTSW	1	188,911,547 (GRCm38)	missense	probably damaging	0.99
R3434:Ush2a	UTSW	1	188,733,758 (GRCm38)	missense	probably damaging	1.00
R3711:Ush2a	UTSW	1	188,810,292 (GRCm38)	missense	probably benign	0.05
R3712:Ush2a	UTSW	1	188,810,292 (GRCm38)	missense	probably benign	0.05
R3732:Ush2a	UTSW	1	188,944,760 (GRCm38)	missense	probably benign	0.16
R3746:Ush2a	UTSW	1	188,810,292 (GRCm38)	missense	probably benign	0.05
R3747:Ush2a	UTSW	1	188,810,292 (GRCm38)	missense	probably benign	0.05
R3883:Ush2a	UTSW	1	188,263,382 (GRCm38)	missense	probably benign
R3911:Ush2a	UTSW	1	188,399,954 (GRCm38)	missense	probably benign	0.05
R3934:Ush2a	UTSW	1	188,263,511 (GRCm38)	critical splice donor site	probably null
R3946:Ush2a	UTSW	1	188,728,504 (GRCm38)	missense	probably benign	0.01
R3974:Ush2a	UTSW	1	188,381,501 (GRCm38)	missense	probably benign	0.06
R4158:Ush2a	UTSW	1	188,728,710 (GRCm38)	missense	probably damaging	1.00
R4159:Ush2a	UTSW	1	188,728,710 (GRCm38)	missense	probably damaging	1.00
R4161:Ush2a	UTSW	1	188,728,710 (GRCm38)	missense	probably damaging	1.00
R4162:Ush2a	UTSW	1	188,743,680 (GRCm38)	missense	probably benign	0.00
R4255:Ush2a	UTSW	1	188,759,843 (GRCm38)	nonsense	probably null
R4280:Ush2a	UTSW	1	188,578,461 (GRCm38)	missense	probably benign	0.16
R4387:Ush2a	UTSW	1	188,443,431 (GRCm38)	missense	probably benign	0.00
R4416:Ush2a	UTSW	1	188,356,874 (GRCm38)	missense	probably damaging	0.97
R4494:Ush2a	UTSW	1	188,553,276 (GRCm38)	missense	possibly damaging	0.50
R4505:Ush2a	UTSW	1	188,728,596 (GRCm38)	missense	possibly damaging	0.92
R4522:Ush2a	UTSW	1	188,864,625 (GRCm38)	missense	probably damaging	1.00
R4584:Ush2a	UTSW	1	188,451,798 (GRCm38)	missense	probably benign	0.00
R4599:Ush2a	UTSW	1	188,911,647 (GRCm38)	missense	probably benign	0.01
R4605:Ush2a	UTSW	1	188,910,801 (GRCm38)	missense	probably damaging	1.00
R4632:Ush2a	UTSW	1	188,395,874 (GRCm38)	missense	possibly damaging	0.82
R4688:Ush2a	UTSW	1	188,399,941 (GRCm38)	missense	probably benign	0.01
R4751:Ush2a	UTSW	1	188,850,087 (GRCm38)	missense	probably damaging	0.98
R4770:Ush2a	UTSW	1	188,549,879 (GRCm38)	missense	probably benign	0.25
R4771:Ush2a	UTSW	1	188,797,769 (GRCm38)	missense	possibly damaging	0.92
R4798:Ush2a	UTSW	1	188,743,545 (GRCm38)	missense	probably damaging	1.00
R4821:Ush2a	UTSW	1	188,753,651 (GRCm38)	missense	probably benign	0.32
R4857:Ush2a	UTSW	1	188,537,720 (GRCm38)	missense	probably benign	0.01
R4860:Ush2a	UTSW	1	188,553,275 (GRCm38)	missense	probably benign	0.07
R4860:Ush2a	UTSW	1	188,553,275 (GRCm38)	missense	probably benign	0.07
R4898:Ush2a	UTSW	1	188,626,608 (GRCm38)	missense	probably benign	0.37
R4993:Ush2a	UTSW	1	188,910,720 (GRCm38)	missense	probably benign	0.03
R5035:Ush2a	UTSW	1	188,910,808 (GRCm38)	missense	probably damaging	1.00
R5061:Ush2a	UTSW	1	188,957,274 (GRCm38)	missense	probably benign	0.03
R5150:Ush2a	UTSW	1	188,451,870 (GRCm38)	missense	possibly damaging	0.95
R5205:Ush2a	UTSW	1	188,874,936 (GRCm38)	missense	probably benign	0.21
R5212:Ush2a	UTSW	1	188,444,705 (GRCm38)	critical splice donor site	probably null
R5252:Ush2a	UTSW	1	188,821,717 (GRCm38)	missense	possibly damaging	0.83
R5260:Ush2a	UTSW	1	188,947,079 (GRCm38)	missense	possibly damaging	0.95
R5304:Ush2a	UTSW	1	188,356,798 (GRCm38)	missense	probably damaging	0.99
R5323:Ush2a	UTSW	1	188,821,677 (GRCm38)	critical splice acceptor site	probably null
R5330:Ush2a	UTSW	1	188,728,381 (GRCm38)	missense	probably benign	0.00
R5331:Ush2a	UTSW	1	188,728,381 (GRCm38)	missense	probably benign	0.00
R5332:Ush2a	UTSW	1	188,351,079 (GRCm38)	missense	probably damaging	1.00
R5371:Ush2a	UTSW	1	188,443,070 (GRCm38)	missense	probably benign	0.00
R5374:Ush2a	UTSW	1	188,755,206 (GRCm38)	missense	probably benign
R5377:Ush2a	UTSW	1	188,912,123 (GRCm38)	missense	probably benign	0.00
R5525:Ush2a	UTSW	1	188,753,606 (GRCm38)	missense	probably benign	0.01
R5558:Ush2a	UTSW	1	188,797,827 (GRCm38)	missense	possibly damaging	0.47
R5562:Ush2a	UTSW	1	188,576,217 (GRCm38)	missense	probably damaging	1.00
R5595:Ush2a	UTSW	1	188,906,498 (GRCm38)	missense	possibly damaging	0.95
R5620:Ush2a	UTSW	1	188,759,823 (GRCm38)	missense	possibly damaging	0.82
R5714:Ush2a	UTSW	1	188,400,257 (GRCm38)	missense	probably benign	0.00
R5743:Ush2a	UTSW	1	188,436,962 (GRCm38)	missense	probably benign	0.01
R5779:Ush2a	UTSW	1	188,443,510 (GRCm38)	critical splice donor site	probably null
R5795:Ush2a	UTSW	1	188,443,397 (GRCm38)	missense	probably benign	0.34
R5897:Ush2a	UTSW	1	188,821,738 (GRCm38)	missense	probably damaging	1.00
R5918:Ush2a	UTSW	1	188,356,814 (GRCm38)	missense	probably benign	0.26
R6000:Ush2a	UTSW	1	188,267,026 (GRCm38)	nonsense	probably null
R6014:Ush2a	UTSW	1	188,850,040 (GRCm38)	missense	probably damaging	0.98
R6017:Ush2a	UTSW	1	188,957,514 (GRCm38)	critical splice donor site	probably null
R6039:Ush2a	UTSW	1	188,319,020 (GRCm38)	missense	possibly damaging	0.76
R6039:Ush2a	UTSW	1	188,319,020 (GRCm38)	missense	possibly damaging	0.76
R6050:Ush2a	UTSW	1	188,957,324 (GRCm38)	missense	probably benign	0.06
R6083:Ush2a	UTSW	1	188,267,023 (GRCm38)	missense	probably damaging	1.00
R6091:Ush2a	UTSW	1	188,399,803 (GRCm38)	missense	probably damaging	1.00
R6120:Ush2a	UTSW	1	188,358,603 (GRCm38)	missense	probably benign	0.04
R6135:Ush2a	UTSW	1	188,912,106 (GRCm38)	missense	possibly damaging	0.68
R6141:Ush2a	UTSW	1	188,357,963 (GRCm38)	missense	possibly damaging	0.71
R6157:Ush2a	UTSW	1	188,728,270 (GRCm38)	missense	probably benign	0.00
R6180:Ush2a	UTSW	1	188,399,871 (GRCm38)	nonsense	probably null
R6191:Ush2a	UTSW	1	188,263,101 (GRCm38)	nonsense	probably null
R6217:Ush2a	UTSW	1	188,743,454 (GRCm38)	splice site	probably null
R6263:Ush2a	UTSW	1	188,358,642 (GRCm38)	missense	probably damaging	1.00
R6294:Ush2a	UTSW	1	188,536,370 (GRCm38)	missense	possibly damaging	0.49
R6320:Ush2a	UTSW	1	188,356,846 (GRCm38)	missense	probably benign	0.01
R6321:Ush2a	UTSW	1	188,849,046 (GRCm38)	nonsense	probably null
R6347:Ush2a	UTSW	1	188,910,887 (GRCm38)	missense	probably benign
R6382:Ush2a	UTSW	1	188,814,302 (GRCm38)	missense	probably benign	0.01
R6408:Ush2a	UTSW	1	188,267,032 (GRCm38)	nonsense	probably null
R6418:Ush2a	UTSW	1	188,628,566 (GRCm38)	missense	probably damaging	1.00
R6500:Ush2a	UTSW	1	188,841,527 (GRCm38)	missense	probably benign	0.00
R6504:Ush2a	UTSW	1	188,911,247 (GRCm38)	missense	probably benign	0.00
R6534:Ush2a	UTSW	1	188,451,802 (GRCm38)	nonsense	probably null
R6594:Ush2a	UTSW	1	188,910,798 (GRCm38)	missense	possibly damaging	0.93
R6612:Ush2a	UTSW	1	188,911,397 (GRCm38)	missense	possibly damaging	0.91
R6645:Ush2a	UTSW	1	188,523,331 (GRCm38)	missense	probably damaging	0.99
R6658:Ush2a	UTSW	1	188,814,359 (GRCm38)	missense	possibly damaging	0.95
R6726:Ush2a	UTSW	1	188,753,684 (GRCm38)	missense	possibly damaging	0.85
R6755:Ush2a	UTSW	1	188,443,219 (GRCm38)	missense	possibly damaging	0.95
R6782:Ush2a	UTSW	1	188,356,834 (GRCm38)	missense	probably benign
R6817:Ush2a	UTSW	1	188,862,864 (GRCm38)	missense	probably benign	0.03
R6834:Ush2a	UTSW	1	188,356,792 (GRCm38)	missense	probably damaging	1.00
R6851:Ush2a	UTSW	1	188,533,205 (GRCm38)	missense	probably benign	0.06
R6853:Ush2a	UTSW	1	188,911,237 (GRCm38)	nonsense	probably null
R6867:Ush2a	UTSW	1	188,910,973 (GRCm38)	missense	probably damaging	1.00
R6889:Ush2a	UTSW	1	188,797,871 (GRCm38)	missense	probably damaging	1.00
R6931:Ush2a	UTSW	1	188,728,383 (GRCm38)	missense	probably benign	0.01
R6953:Ush2a	UTSW	1	188,263,145 (GRCm38)	missense	possibly damaging	0.94
R6966:Ush2a	UTSW	1	188,576,244 (GRCm38)	missense	probably damaging	1.00
R7109:Ush2a	UTSW	1	188,381,484 (GRCm38)	missense	probably benign	0.19
R7153:Ush2a	UTSW	1	188,728,484 (GRCm38)	missense	possibly damaging	0.93
R7176:Ush2a	UTSW	1	188,537,728 (GRCm38)	missense	probably benign	0.00
R7182:Ush2a	UTSW	1	188,753,543 (GRCm38)	missense	probably benign	0.01
R7201:Ush2a	UTSW	1	188,874,754 (GRCm38)	missense	probably benign
R7223:Ush2a	UTSW	1	188,810,217 (GRCm38)	missense	probably benign	0.09
R7231:Ush2a	UTSW	1	188,759,763 (GRCm38)	missense	possibly damaging	0.49
R7240:Ush2a	UTSW	1	188,911,661 (GRCm38)	missense	possibly damaging	0.83
R7263:Ush2a	UTSW	1	188,443,329 (GRCm38)	missense	possibly damaging	0.94
R7329:Ush2a	UTSW	1	188,553,198 (GRCm38)	missense	probably damaging	0.97
R7343:Ush2a	UTSW	1	188,415,746 (GRCm38)	missense	probably benign	0.00
R7352:Ush2a	UTSW	1	188,466,124 (GRCm38)	missense	probably benign	0.04
R7384:Ush2a	UTSW	1	188,400,163 (GRCm38)	missense	probably damaging	0.99
R7391:Ush2a	UTSW	1	188,962,008 (GRCm38)	small deletion	probably benign
R7394:Ush2a	UTSW	1	188,911,416 (GRCm38)	missense	possibly damaging	0.83
R7403:Ush2a	UTSW	1	188,633,727 (GRCm38)	missense	probably damaging	1.00
R7408:Ush2a	UTSW	1	188,733,529 (GRCm38)	missense	probably benign	0.00
R7453:Ush2a	UTSW	1	188,553,111 (GRCm38)	missense	probably damaging	1.00
R7496:Ush2a	UTSW	1	188,351,087 (GRCm38)	missense	possibly damaging	0.50
R7552:Ush2a	UTSW	1	188,267,044 (GRCm38)	missense	possibly damaging	0.65
R7556:Ush2a	UTSW	1	188,957,493 (GRCm38)	missense	probably benign	0.31
R7575:Ush2a	UTSW	1	188,822,688 (GRCm38)	missense	possibly damaging	0.90
R7578:Ush2a	UTSW	1	188,549,913 (GRCm38)	missense	probably damaging	1.00
R7584:Ush2a	UTSW	1	188,728,109 (GRCm38)	critical splice acceptor site	probably null
R7589:Ush2a	UTSW	1	188,542,849 (GRCm38)	missense	probably benign	0.00
R7602:Ush2a	UTSW	1	188,648,409 (GRCm38)	missense	probably damaging	1.00
R7670:Ush2a	UTSW	1	188,784,708 (GRCm38)	missense	possibly damaging	0.78
R7743:Ush2a	UTSW	1	188,810,179 (GRCm38)	missense	probably benign	0.05
R7753:Ush2a	UTSW	1	188,443,406 (GRCm38)	missense	probably benign	0.28
R7767:Ush2a	UTSW	1	188,553,260 (GRCm38)	missense	probably benign	0.01
R7784:Ush2a	UTSW	1	188,444,592 (GRCm38)	missense	possibly damaging	0.55
R7831:Ush2a	UTSW	1	188,759,841 (GRCm38)	missense	probably damaging	0.98
R7834:Ush2a	UTSW	1	188,733,440 (GRCm38)	nonsense	probably null
R7847:Ush2a	UTSW	1	188,430,808 (GRCm38)	missense	probably damaging	1.00
R7926:Ush2a	UTSW	1	188,728,600 (GRCm38)	missense	probably benign
R7969:Ush2a	UTSW	1	188,826,371 (GRCm38)	missense	probably benign	0.02
R7978:Ush2a	UTSW	1	188,399,938 (GRCm38)	missense	probably benign	0.00
R7990:Ush2a	UTSW	1	188,542,799 (GRCm38)	missense	probably benign	0.00
R8001:Ush2a	UTSW	1	188,911,064 (GRCm38)	missense	probably damaging	0.98
R8039:Ush2a	UTSW	1	188,957,373 (GRCm38)	missense	probably damaging	1.00
R8077:Ush2a	UTSW	1	188,542,828 (GRCm38)	missense	probably benign	0.01
R8165:Ush2a	UTSW	1	188,451,755 (GRCm38)	missense	possibly damaging	0.70
R8208:Ush2a	UTSW	1	188,874,793 (GRCm38)	missense	possibly damaging	0.95
R8220:Ush2a	UTSW	1	188,728,666 (GRCm38)	missense	probably damaging	1.00
R8270:Ush2a	UTSW	1	188,444,641 (GRCm38)	missense	probably benign	0.06
R8316:Ush2a	UTSW	1	188,446,702 (GRCm38)	missense	probably benign	0.01
R8347:Ush2a	UTSW	1	188,947,084 (GRCm38)	missense	probably benign	0.02
R8360:Ush2a	UTSW	1	188,466,271 (GRCm38)	missense	probably benign	0.01
R8362:Ush2a	UTSW	1	188,957,453 (GRCm38)	missense	probably damaging	0.96
R8386:Ush2a	UTSW	1	188,728,206 (GRCm38)	missense	possibly damaging	0.80
R8401:Ush2a	UTSW	1	188,542,865 (GRCm38)	missense	probably benign	0.10
R8439:Ush2a	UTSW	1	188,850,057 (GRCm38)	missense	probably damaging	1.00
R8465:Ush2a	UTSW	1	188,415,678 (GRCm38)	missense	probably damaging	1.00
R8478:Ush2a	UTSW	1	188,443,232 (GRCm38)	missense	possibly damaging	0.83
R8540:Ush2a	UTSW	1	188,542,661 (GRCm38)	missense	probably benign	0.00
R8684:Ush2a	UTSW	1	188,911,023 (GRCm38)	missense	possibly damaging	0.45
R8685:Ush2a	UTSW	1	188,466,204 (GRCm38)	missense	probably damaging	1.00
R8699:Ush2a	UTSW	1	188,911,377 (GRCm38)	missense	probably damaging	1.00
R8720:Ush2a	UTSW	1	188,358,518 (GRCm38)	missense	probably benign	0.05
R8754:Ush2a	UTSW	1	188,848,965 (GRCm38)	nonsense	probably null
R8756:Ush2a	UTSW	1	188,911,944 (GRCm38)	missense	possibly damaging	0.91
R8788:Ush2a	UTSW	1	188,743,619 (GRCm38)	nonsense	probably null
R8803:Ush2a	UTSW	1	188,944,801 (GRCm38)	missense	probably benign
R8817:Ush2a	UTSW	1	188,263,034 (GRCm38)	start codon destroyed	probably benign	0.00
R8837:Ush2a	UTSW	1	188,753,650 (GRCm38)	missense	probably benign
R8880:Ush2a	UTSW	1	188,728,536 (GRCm38)	missense	probably benign	0.11
R8902:Ush2a	UTSW	1	188,443,084 (GRCm38)	missense	probably damaging	0.98
R8918:Ush2a	UTSW	1	188,537,820 (GRCm38)	missense	possibly damaging	0.85
R8940:Ush2a	UTSW	1	188,400,308 (GRCm38)	missense	probably benign	0.02
R8968:Ush2a	UTSW	1	188,395,759 (GRCm38)	missense	probably damaging	1.00
R8995:Ush2a	UTSW	1	188,444,653 (GRCm38)	missense	probably damaging	0.98
R9011:Ush2a	UTSW	1	188,906,479 (GRCm38)	missense	probably damaging	0.99
R9037:Ush2a	UTSW	1	188,263,290 (GRCm38)	missense	possibly damaging	0.51
R9063:Ush2a	UTSW	1	188,263,260 (GRCm38)	missense	probably benign	0.00
R9089:Ush2a	UTSW	1	188,755,177 (GRCm38)	nonsense	probably null
R9096:Ush2a	UTSW	1	188,466,136 (GRCm38)	missense	probably benign	0.00
R9118:Ush2a	UTSW	1	188,654,642 (GRCm38)	missense	probably damaging	0.98
R9174:Ush2a	UTSW	1	188,728,219 (GRCm38)	missense	probably damaging	0.99
R9210:Ush2a	UTSW	1	188,784,669 (GRCm38)	missense	probably null	0.01
R9242:Ush2a	UTSW	1	188,633,590 (GRCm38)	missense	probably damaging	1.00
R9321:Ush2a	UTSW	1	188,356,951 (GRCm38)	missense	probably damaging	0.97
R9338:Ush2a	UTSW	1	188,576,292 (GRCm38)	critical splice donor site	probably null
R9357:Ush2a	UTSW	1	188,874,950 (GRCm38)	missense	probably benign	0.01
R9358:Ush2a	UTSW	1	188,874,950 (GRCm38)	missense	probably benign	0.01
R9406:Ush2a	UTSW	1	188,263,449 (GRCm38)	missense	probably benign	0.00
R9407:Ush2a	UTSW	1	188,911,848 (GRCm38)	missense	probably damaging	1.00
R9428:Ush2a	UTSW	1	188,443,119 (GRCm38)	missense	probably damaging	1.00
R9456:Ush2a	UTSW	1	188,826,392 (GRCm38)	missense	probably benign	0.00
R9507:Ush2a	UTSW	1	188,864,740 (GRCm38)	nonsense	probably null
R9509:Ush2a	UTSW	1	188,916,243 (GRCm38)	missense	probably damaging	1.00
R9512:Ush2a	UTSW	1	188,910,963 (GRCm38)	missense	probably damaging	0.99
R9564:Ush2a	UTSW	1	188,536,354 (GRCm38)	missense	possibly damaging	0.90
R9612:Ush2a	UTSW	1	188,359,866 (GRCm38)	nonsense	probably null
R9670:Ush2a	UTSW	1	188,628,571 (GRCm38)	missense	probably benign	0.03
R9684:Ush2a	UTSW	1	188,399,881 (GRCm38)	missense	possibly damaging	0.67
R9798:Ush2a	UTSW	1	188,911,805 (GRCm38)	missense	possibly damaging	0.80
RF017:Ush2a	UTSW	1	188,263,469 (GRCm38)	missense	probably damaging	1.00
U24488:Ush2a	UTSW	1	188,430,766 (GRCm38)	missense	probably damaging	0.99
X0011:Ush2a	UTSW	1	188,318,969 (GRCm38)	missense	probably benign	0.00
X0024:Ush2a	UTSW	1	188,400,282 (GRCm38)	missense	probably damaging	1.00
X0026:Ush2a	UTSW	1	188,319,025 (GRCm38)	missense	possibly damaging	0.94
X0062:Ush2a	UTSW	1	188,549,854 (GRCm38)	missense	probably damaging	1.00
Y4340:Ush2a	UTSW	1	188,743,629 (GRCm38)	missense	possibly damaging	0.87
Y4341:Ush2a	UTSW	1	188,743,629 (GRCm38)	missense	possibly damaging	0.87
Z1088:Ush2a	UTSW	1	188,947,004 (GRCm38)	missense	probably benign	0.26
Z1088:Ush2a	UTSW	1	188,911,983 (GRCm38)	missense	probably benign
Z1176:Ush2a	UTSW	1	188,356,841 (GRCm38)	missense	probably damaging	1.00
Z1177:Ush2a	UTSW	1	188,912,210 (GRCm38)	missense	possibly damaging	0.77
Z1177:Ush2a	UTSW	1	188,733,544 (GRCm38)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CTCTGTTAGGAAAGAAAGAACAACC -3'
(R):5'- TGGAAGTGATAGGCCTTGTAAG -3'

Sequencing Primer
(F):5'- ACAACCTTAGAAATATTCAGCAAGG -3'
(R):5'- GACCACAGTATAGTTAGTGACTCGTC -3'

Posted On

2017-06-27