Mutagenetix > Incidental Mutations

Incidental Mutation 'R2063:Adgrv1'

228882

Institutional Source

Beutler Lab

Gene Symbol

Adgrv1

Ensembl Gene

ENSMUSG00000069170

Gene Name

adhesion G protein-coupled receptor V1

Synonyms

Mass1, Mgr1, VLGR1, Gpr98

MMRRC Submission

040068-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2063 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

81095068-81633154 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 81561469 bp

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 1135 (K1135R)

Ref Sequence

ENSEMBL: ENSMUSP00000093245 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095585] [ENSMUST00000109565] [ENSMUST00000126444]

Predicted Effect

possibly damaging
Transcript: ENSMUST00000095585
AA Change: K1135R

PolyPhen 2 Score 0.807 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: K1135R

Domain	Start	End	E-Value	Type
Calx_beta	20	116	1.53e-1	SMART
Calx_beta	132	236	1.58e-2	SMART
Calx_beta	251	362	2.33e-2	SMART
Pfam:Calx-beta	380	489	1.1e-3	PFAM
Pfam:Calx-beta	507	616	2.5e-2	PFAM
Pfam:Calx-beta	667	747	9.1e-4	PFAM
Calx_beta	764	862	1.55e-1	SMART
Calx_beta	877	980	1.07e-1	SMART
Calx_beta	994	1094	6.45e-5	SMART
Pfam:Calx-beta	1108	1208	7.4e-4	PFAM
Pfam:Laminin_G_3	1331	1492	4.4e-24	PFAM
Pfam:Calx-beta	1498	1542	6.5e-3	PFAM
Pfam:Calx-beta	1557	1662	1e-6	PFAM
Calx_beta	1706	1805	1.34e-11	SMART
Calx_beta	1846	1948	1.04e-2	SMART
Calx_beta	1962	2075	1.59e-3	SMART
Calx_beta	2103	2202	1.59e-4	SMART
Calx_beta	2218	2320	1.74e-3	SMART
Pfam:Calx-beta	2467	2539	2.1e-4	PFAM
Calx_beta	2576	2672	1.24e-6	SMART
Calx_beta	2687	2786	1.12e-1	SMART
Calx_beta	2810	2921	2.21e-2	SMART
Calx_beta	2945	3044	6.69e-12	SMART
Pfam:Calx-beta	3063	3168	1.2e-5	PFAM
Pfam:Calx-beta	3198	3252	1.2e-1	PFAM
Pfam:EPTP	3391	3434	2.8e-10	PFAM
Pfam:Calx-beta	3577	3623	6.5e-8	PFAM
Pfam:Calx-beta	3637	3737	6e-4	PFAM
Pfam:Calx-beta	3781	3872	6.9e-3	PFAM
Calx_beta	3919	4003	1.18e-2	SMART
Calx_beta	4017	4120	5.44e-2	SMART
Pfam:Calx-beta	4193	4236	2.3e-2	PFAM
Calx_beta	4251	4351	1.43e-20	SMART
Calx_beta	4384	4484	9.46e-3	SMART
Pfam:Calx-beta	4498	4608	2e-2	PFAM
Pfam:Calx-beta	4659	4729	5.1e-2	PFAM
Calx_beta	4989	5089	5.7e-6	SMART
Pfam:Calx-beta	5229	5326	1.9e-6	PFAM
Pfam:Calx-beta	5489	5592	7.2e-5	PFAM
low complexity region	5637	5648	N/A	INTRINSIC
GPS	5845	5895	9.48e-3	SMART
Pfam:7tm_2	5902	6141	2.3e-16	PFAM
low complexity region	6227	6240	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000109565
AA Change: K415R

PolyPhen 2 Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000105193
Gene: ENSMUSG00000069170
AA Change: K415R

Domain	Start	End	E-Value	Type
Calx_beta	44	142	1.55e-1	SMART
Calx_beta	157	260	1.07e-1	SMART
Calx_beta	274	374	6.45e-5	SMART
Pfam:Calx-beta	388	488	4.8e-4	PFAM
Pfam:Laminin_G_3	611	772	3.4e-24	PFAM
Pfam:Calx-beta	778	822	4.4e-3	PFAM
Pfam:Calx-beta	837	942	6.6e-7	PFAM
Calx_beta	986	1085	1.34e-11	SMART
Calx_beta	1126	1228	1.04e-2	SMART
Calx_beta	1242	1355	1.59e-3	SMART
Calx_beta	1383	1482	1.59e-4	SMART
Calx_beta	1498	1600	1.74e-3	SMART
Pfam:Calx-beta	1747	1819	1.4e-4	PFAM
Calx_beta	1856	1952	1.24e-6	SMART
Calx_beta	1967	2066	1.12e-1	SMART
Calx_beta	2090	2201	2.21e-2	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125663

Predicted Effect

possibly damaging
Transcript: ENSMUST00000126444
AA Change: K1135R

PolyPhen 2 Score 0.476 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000123552
Gene: ENSMUSG00000069170
AA Change: K1135R

Domain	Start	End	E-Value	Type
Blast:Calx_beta	20	116	1e-56	BLAST
Pfam:Calx-beta	132	236	7.6e-11	PFAM
Pfam:Calx-beta	250	362	7.9e-9	PFAM
Blast:Calx_beta	378	489	9e-6	BLAST
low complexity region	531	550	N/A	INTRINSIC
Blast:Calx_beta	764	862	2e-59	BLAST
Blast:Calx_beta	877	980	1e-63	BLAST
Pfam:Calx-beta	994	1094	2.1e-15	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156627

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.4%
20x: 95.5%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the G-protein coupled receptor superfamily. The encoded protein contains a 7-transmembrane receptor domain, binds calcium and is expressed in the central nervous system. Mutations in this gene are associated with Usher syndrome 2 and familial febrile seizures. Several alternatively spliced transcripts have been described. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a spontaneous and a targeted mutation exhibit high sensitivity to audiogenic seizures. Targeted mutant mice lack the ankle links that connect growing stereocilia in the developing cochlear hair cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933436I01Rik	T	A	X: 67,920,702	I184L	probably benign	Het
9530002B09Rik	T	A	4: 122,689,322		probably benign	Het
Abca15	A	T	7: 120,360,904	T637S	possibly damaging	Het
Afap1l1	A	T	18: 61,739,122		probably null	Het
AI467606	A	G	7: 127,092,837	S195G	probably damaging	Het
Alox12e	G	A	11: 70,316,002	R620W	probably damaging	Het
Ascc2	A	T	11: 4,681,496	M646L	probably benign	Het
Ccnt1	A	T	15: 98,551,942	H156Q	probably benign	Het
Cic	T	A	7: 25,273,451	V869E	probably damaging	Het
Cpsf2	A	G	12: 101,983,463	D118G	probably damaging	Het
Csnk1g1	A	G	9: 66,002,230	S210G	probably damaging	Het
Cyp2c40	T	A	19: 39,786,780	M343L	probably benign	Het
Cyp4a12b	A	T	4: 115,433,503	D274V	possibly damaging	Het
Dnaaf3	T	C	7: 4,523,799	I426M	possibly damaging	Het
Dnah3	C	T	7: 119,951,909	M3062I	probably damaging	Het
Dtx2	C	T	5: 136,030,577	S493F	probably damaging	Het
Elavl2	A	T	4: 91,253,450	S278R	possibly damaging	Het
Emilin2	T	C	17: 71,274,955	S259G	probably benign	Het
Endov	T	C	11: 119,499,582	F12S	probably damaging	Het
Faim2	G	A	15: 99,514,433	T140I	probably damaging	Het
Fbxo21	T	C	5: 117,976,966	S56P	probably benign	Het
Fgb	C	A	3: 83,049,689	D25Y	probably benign	Het
Foxj2	A	T	6: 122,840,241	H509L	probably benign	Het
Fth1	T	A	19: 9,984,212	L49Q	probably damaging	Het
Gbp11	C	A	5: 105,328,584	E220*	probably null	Het
Gm12695	T	C	4: 96,769,726	T69A	probably benign	Het
Gm1527	C	A	3: 28,926,647	T632N	probably benign	Het
Gm4787	A	T	12: 81,378,920	S155T	probably benign	Het
Gm9573	T	A	17: 35,621,405		probably benign	Het
Gtf2f2	A	G	14: 75,917,696	S142P	possibly damaging	Het
Helb	T	C	10: 120,105,766	Y339C	probably benign	Het
Hs3st4	A	G	7: 124,397,013	I301V	probably benign	Het
Hunk	A	G	16: 90,493,480	D382G	probably damaging	Het
Ifnb1	T	A	4: 88,522,759	I6F	possibly damaging	Het
Il10	T	C	1: 131,020,033	L41P	probably damaging	Het
Il2rg	A	G	X: 101,267,810	L57P	possibly damaging	Het
Invs	T	A	4: 48,396,287	L320Q	probably damaging	Het
Itpr3	G	A	17: 27,098,076	M768I	probably benign	Het
Krt90	T	C	15: 101,558,359	E263G	probably benign	Het
Lama2	C	T	10: 27,164,926	C1467Y	probably damaging	Het
Med24	A	G	11: 98,715,646	L330P	probably damaging	Het
Mrto4	T	C	4: 139,349,023	K86E	probably benign	Het
Mtcl1	T	C	17: 66,346,355	R1065G	probably damaging	Het
Mtmr14	G	A	6: 113,240,361	G38D	probably damaging	Het
Mtus1	T	C	8: 41,082,708	E657G	probably damaging	Het
Myo5c	A	T	9: 75,281,868	Q1020L	probably benign	Het
Nav1	C	T	1: 135,449,004	R1694Q	probably damaging	Het
Nckap1	T	C	2: 80,570,150	K69R	probably damaging	Het
Nlrp1b	T	C	11: 71,161,086	N1012D	probably benign	Het
Ntrk2	A	C	13: 58,859,297	K238Q	probably damaging	Het
Oas1g	T	C	5: 120,885,883	E121G	probably damaging	Het
Olfr324	A	G	11: 58,597,570	N58S	probably damaging	Het
Olfr667	T	C	7: 104,916,775	N174D	probably benign	Het
Pcdh8	A	T	14: 79,768,211	S912R	probably damaging	Het
Pfpl	C	T	19: 12,429,873	S496L	probably damaging	Het
Phc2	T	C	4: 128,747,136	F672S	probably damaging	Het
Pkhd1l1	A	T	15: 44,550,752	H2805L	possibly damaging	Het
Pla2g4a	T	C	1: 149,840,676	N678S	possibly damaging	Het
Plxnb3	T	A	X: 73,771,751	Y1845*	probably null	Het
Polr1a	T	G	6: 71,936,285		probably null	Het
Prl3d3	A	C	13: 27,162,321	E180D	probably benign	Het
Prl7a2	T	A	13: 27,660,887	Y172F	probably damaging	Het
Prpf3	A	T	3: 95,844,239	D383E	probably benign	Het
Psmc4	A	T	7: 28,048,897	L73H	probably damaging	Het
Rapgef3	C	A	15: 97,766,961	G7V	probably damaging	Het
Rasl12	G	A	9: 65,410,824	G157R	probably damaging	Het
Rnf38	A	C	4: 44,149,098	V83G	probably damaging	Het
Rnls	A	C	19: 33,202,544	S51A	probably benign	Het
Siglecf	A	G	7: 43,352,380	T205A	possibly damaging	Het
Skint1	T	A	4: 112,025,533	V258D	probably benign	Het
Slc12a5	C	T	2: 164,997,147	R1072W	probably damaging	Het
Spata13	GTTAGGCT	GT	14: 60,760,871		probably benign	Het
Specc1	T	G	11: 62,118,296	S293A	probably benign	Het
Speer2	T	G	16: 69,860,497	Q86P	probably benign	Het
Tbc1d15	T	C	10: 115,229,173	D169G	probably benign	Het
Tbx20	C	A	9: 24,769,771	E142*	probably null	Het
Tcp1	T	A	17: 12,920,812	L199H	probably damaging	Het
Tex26	A	T	5: 149,439,739	R5W	probably damaging	Het
Tg	C	A	15: 66,828,553	A120E	probably damaging	Het
Thrap3	T	C	4: 126,175,396	Y654C	possibly damaging	Het
Tmem57	A	T	4: 134,828,279	N294K	possibly damaging	Het
Troap	T	C	15: 99,082,463	L508P	probably benign	Het
Ubap2	C	T	4: 41,199,872	A752T	probably benign	Het
Ush1c	T	C	7: 46,229,481	Y74C	probably damaging	Het
Vmn1r55	A	G	7: 5,147,049	V125A	possibly damaging	Het
Vmn2r120	T	A	17: 57,524,553	H412L	possibly damaging	Het
Vps54	C	T	11: 21,277,955	T176I	probably damaging	Het
Wdr95	T	C	5: 149,579,162		probably null	Het
Zfp81	T	C	17: 33,335,304	T179A	probably benign	Het

Other mutations in Adgrv1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Adgrv1	APN	13	81405408	critical splice acceptor site	probably null
IGL00090:Adgrv1	APN	13	81578101	missense	probably damaging	1.00
IGL00091:Adgrv1	APN	13	81578101	missense	probably damaging	1.00
IGL00332:Adgrv1	APN	13	81472877	splice site	probably benign
IGL00471:Adgrv1	APN	13	81509542	missense	probably damaging	0.99
IGL00476:Adgrv1	APN	13	81489074	missense	probably damaging	0.98
IGL00508:Adgrv1	APN	13	81506187	missense	probably damaging	1.00
IGL00727:Adgrv1	APN	13	81524684	missense	probably damaging	0.98
IGL00781:Adgrv1	APN	13	81578230	missense	probably benign	0.19
IGL00816:Adgrv1	APN	13	81397203	missense	probably benign	0.01
IGL00844:Adgrv1	APN	13	81540119	missense	probably damaging	1.00
IGL00923:Adgrv1	APN	13	81382291	missense	probably damaging	0.99
IGL01113:Adgrv1	APN	13	81489028	missense	probably benign	0.00
IGL01143:Adgrv1	APN	13	81419351	missense	probably benign	0.00
IGL01151:Adgrv1	APN	13	81405399	missense	probably benign	0.00
IGL01153:Adgrv1	APN	13	81419128	missense	probably benign	0.01
IGL01363:Adgrv1	APN	13	81557065	missense	probably damaging	1.00
IGL01419:Adgrv1	APN	13	81557158	missense	probably damaging	0.99
IGL01545:Adgrv1	APN	13	81466184	missense	possibly damaging	0.46
IGL01701:Adgrv1	APN	13	81419631	missense	possibly damaging	0.55
IGL01796:Adgrv1	APN	13	81567342	missense	probably benign	0.01
IGL01816:Adgrv1	APN	13	81529049	missense	probably benign	0.00
IGL01871:Adgrv1	APN	13	81472394	critical splice donor site	probably null
IGL01955:Adgrv1	APN	13	81182783	missense	probably damaging	1.00
IGL01956:Adgrv1	APN	13	81446430	missense	possibly damaging	0.63
IGL01988:Adgrv1	APN	13	81557309	missense	probably damaging	0.99
IGL01990:Adgrv1	APN	13	81556996	missense	probably damaging	1.00
IGL02007:Adgrv1	APN	13	81568743	splice site	probably benign
IGL02016:Adgrv1	APN	13	81397453	missense	probably damaging	1.00
IGL02095:Adgrv1	APN	13	81579790	missense	possibly damaging	0.63
IGL02174:Adgrv1	APN	13	81427664	missense	probably benign	0.34
IGL02270:Adgrv1	APN	13	81559195	unclassified	probably null
IGL02328:Adgrv1	APN	13	81578175	missense	probably damaging	1.00
IGL02350:Adgrv1	APN	13	81270855	missense	probably benign	0.00
IGL02357:Adgrv1	APN	13	81270855	missense	probably benign	0.00
IGL02373:Adgrv1	APN	13	81459713	missense	possibly damaging	0.90
IGL02402:Adgrv1	APN	13	81559424	missense	probably benign	0.18
IGL02407:Adgrv1	APN	13	81479670	missense	probably damaging	1.00
IGL02508:Adgrv1	APN	13	81435556	splice site	probably benign
IGL02603:Adgrv1	APN	13	81488952	missense	possibly damaging	0.93
IGL02648:Adgrv1	APN	13	81511619	missense	probably benign	0.35
IGL02720:Adgrv1	APN	13	81578872	missense	probably damaging	0.99
IGL02870:Adgrv1	APN	13	81563732	missense	probably benign	0.13
IGL02896:Adgrv1	APN	13	81520739	missense	probably damaging	1.00
IGL02931:Adgrv1	APN	13	81579714	missense	probably damaging	1.00
IGL02952:Adgrv1	APN	13	81433636	missense	probably benign	0.00
IGL02961:Adgrv1	APN	13	81523612	missense	probably damaging	1.00
IGL02999:Adgrv1	APN	13	81578854	missense	probably benign	0.12
IGL03067:Adgrv1	APN	13	81442480	missense	probably damaging	1.00
IGL03106:Adgrv1	APN	13	81472899	missense	probably benign	0.00
IGL03108:Adgrv1	APN	13	81559529	missense	probably damaging	1.00
IGL03119:Adgrv1	APN	13	81382373	missense	probably damaging	1.00
IGL03119:Adgrv1	APN	13	81433700	missense	probably benign	0.02
IGL03169:Adgrv1	APN	13	81503900	missense	probably damaging	1.00
IGL03186:Adgrv1	APN	13	81433618	missense	possibly damaging	0.80
IGL03196:Adgrv1	APN	13	81446478	missense	probably benign	0.02
IGL03207:Adgrv1	APN	13	81106898	splice site	probably null
IGL03343:Adgrv1	APN	13	81283388	missense	probably damaging	1.00
IGL03348:Adgrv1	APN	13	81499058	missense	possibly damaging	0.54
IGL03349:Adgrv1	APN	13	81481336	missense	probably benign	0.09
IGL03373:Adgrv1	APN	13	81563632	missense	probably damaging	0.99
IGL03381:Adgrv1	APN	13	81517967	missense	probably damaging	0.99
beatle	UTSW	13	81579594	nonsense	probably null
Escape	UTSW	13	81435705	missense	probably benign	0.02
lento	UTSW	13	81270897	missense	probably damaging	1.00
Metronome	UTSW	13	81435559	critical splice donor site	probably null
Nome	UTSW	13	81391767	missense	probably benign	0.00
Propulsion	UTSW	13	81475047	missense	probably benign	0.06
revulsion	UTSW	13	81595182	missense	probably damaging	1.00
Saturnv	UTSW	13	81531676	missense	probably damaging	1.00
Thrust	UTSW	13	81374256	missense	probably benign	0.01
Velocity	UTSW	13	81397354	missense	probably benign	0.00
Wilting	UTSW	13	81492501	missense	probably benign	0.02
Withering	UTSW	13	81494657	missense	probably damaging	1.00
F2404:Adgrv1	UTSW	13	81420006	missense	probably benign	0.13
I2288:Adgrv1	UTSW	13	81437524	missense	probably damaging	1.00
I2289:Adgrv1	UTSW	13	81437524	missense	probably damaging	1.00
PIT4377001:Adgrv1	UTSW	13	81528985	missense	probably damaging	1.00
PIT4504001:Adgrv1	UTSW	13	81559352	missense	probably damaging	0.99
R0017:Adgrv1	UTSW	13	81578946	missense	probably benign	0.13
R0017:Adgrv1	UTSW	13	81578946	missense	probably benign	0.13
R0058:Adgrv1	UTSW	13	81182672	missense	possibly damaging	0.65
R0058:Adgrv1	UTSW	13	81182672	missense	possibly damaging	0.65
R0083:Adgrv1	UTSW	13	81578404	unclassified	probably benign
R0087:Adgrv1	UTSW	13	81386951	missense	probably damaging	1.00
R0108:Adgrv1	UTSW	13	81578404	unclassified	probably benign
R0131:Adgrv1	UTSW	13	81502995	unclassified	probably benign
R0218:Adgrv1	UTSW	13	81106898	splice site	probably null
R0325:Adgrv1	UTSW	13	81540015	missense	probably damaging	1.00
R0326:Adgrv1	UTSW	13	81474993	missense	possibly damaging	0.46
R0395:Adgrv1	UTSW	13	81385953	missense	probably benign	0.00
R0441:Adgrv1	UTSW	13	81397226	nonsense	probably null
R0466:Adgrv1	UTSW	13	81566296	missense	probably benign	0.00
R0487:Adgrv1	UTSW	13	81489035	missense	probably damaging	1.00
R0501:Adgrv1	UTSW	13	81559150	missense	probably damaging	1.00
R0522:Adgrv1	UTSW	13	81528442	splice site	probably benign
R0532:Adgrv1	UTSW	13	81578896	missense	probably damaging	1.00
R0542:Adgrv1	UTSW	13	81573318	missense	probably damaging	1.00
R0681:Adgrv1	UTSW	13	81528530	missense	probably damaging	1.00
R0689:Adgrv1	UTSW	13	81475105	missense	possibly damaging	0.47
R0732:Adgrv1	UTSW	13	81503004	missense	possibly damaging	0.86
R0746:Adgrv1	UTSW	13	81570556	missense	probably benign	0.10
R0763:Adgrv1	UTSW	13	81499125	missense	probably damaging	0.98
R0846:Adgrv1	UTSW	13	81479742	nonsense	probably null
R0962:Adgrv1	UTSW	13	81405346	missense	probably benign	0.01
R1146:Adgrv1	UTSW	13	81531676	missense	probably damaging	1.00
R1146:Adgrv1	UTSW	13	81531676	missense	probably damaging	1.00
R1172:Adgrv1	UTSW	13	81557063	missense	probably damaging	0.98
R1178:Adgrv1	UTSW	13	81440037	splice site	probably benign
R1310:Adgrv1	UTSW	13	81566377	missense	probably benign	0.09
R1386:Adgrv1	UTSW	13	81528865	missense	probably benign	0.17
R1387:Adgrv1	UTSW	13	81493176	missense	possibly damaging	0.62
R1395:Adgrv1	UTSW	13	81386788	missense	probably benign	0.05
R1412:Adgrv1	UTSW	13	81095450	missense	probably damaging	1.00
R1448:Adgrv1	UTSW	13	81433513	missense	probably benign	0.08
R1470:Adgrv1	UTSW	13	81382298	missense	probably benign	0.03
R1470:Adgrv1	UTSW	13	81382298	missense	probably benign	0.03
R1485:Adgrv1	UTSW	13	81579619	missense	probably damaging	1.00
R1507:Adgrv1	UTSW	13	81472580	critical splice acceptor site	probably null
R1513:Adgrv1	UTSW	13	81556957	missense	probably damaging	1.00
R1513:Adgrv1	UTSW	13	81593048	missense	probably damaging	1.00
R1539:Adgrv1	UTSW	13	81503978	unclassified	probably null
R1579:Adgrv1	UTSW	13	81563779	missense	probably damaging	1.00
R1580:Adgrv1	UTSW	13	81466160	critical splice donor site	probably null
R1611:Adgrv1	UTSW	13	81559117	missense	probably damaging	1.00
R1615:Adgrv1	UTSW	13	81424288	missense	probably benign	0.41
R1651:Adgrv1	UTSW	13	81487853	missense	probably benign	0.19
R1660:Adgrv1	UTSW	13	81476631	missense	probably benign	0.00
R1679:Adgrv1	UTSW	13	81559552	missense	probably damaging	1.00
R1709:Adgrv1	UTSW	13	81593060	missense	probably damaging	1.00
R1735:Adgrv1	UTSW	13	81487947	missense	possibly damaging	0.62
R1762:Adgrv1	UTSW	13	81506146	missense	probably benign	0.08
R1830:Adgrv1	UTSW	13	81489077	missense	possibly damaging	0.65
R1836:Adgrv1	UTSW	13	81504113	missense	probably benign	0.01
R1843:Adgrv1	UTSW	13	81544533	missense	probably damaging	1.00
R1863:Adgrv1	UTSW	13	81563566	missense	probably damaging	1.00
R1895:Adgrv1	UTSW	13	81374249	missense	probably damaging	1.00
R1907:Adgrv1	UTSW	13	81592551	splice site	probably benign
R1928:Adgrv1	UTSW	13	81520786	missense	probably benign	0.00
R1938:Adgrv1	UTSW	13	81391757	missense	probably damaging	0.99
R1944:Adgrv1	UTSW	13	81510911	missense	probably damaging	1.00
R1946:Adgrv1	UTSW	13	81374249	missense	probably damaging	1.00
R1984:Adgrv1	UTSW	13	81523749	missense	probably damaging	1.00
R2027:Adgrv1	UTSW	13	81595182	missense	probably damaging	1.00
R2116:Adgrv1	UTSW	13	81529013	missense	probably benign	0.11
R2117:Adgrv1	UTSW	13	81492537	missense	probably benign	0.00
R2125:Adgrv1	UTSW	13	81419535	missense	probably benign	0.00
R2125:Adgrv1	UTSW	13	81419950	missense	probably benign	0.02
R2127:Adgrv1	UTSW	13	81557080	missense	probably damaging	1.00
R2128:Adgrv1	UTSW	13	81557080	missense	probably damaging	1.00
R2129:Adgrv1	UTSW	13	81557080	missense	probably damaging	1.00
R2130:Adgrv1	UTSW	13	81581727	missense	possibly damaging	0.61
R2135:Adgrv1	UTSW	13	81524557	critical splice donor site	probably null
R2138:Adgrv1	UTSW	13	81445320	missense	probably benign	0.00
R2166:Adgrv1	UTSW	13	81568643	missense	probably damaging	1.00
R2171:Adgrv1	UTSW	13	81270918	missense	probably damaging	1.00
R2191:Adgrv1	UTSW	13	81566290	missense	possibly damaging	0.90
R2256:Adgrv1	UTSW	13	81506140	missense	probably benign
R2260:Adgrv1	UTSW	13	81568374	missense	probably damaging	0.97
R2323:Adgrv1	UTSW	13	81595179	missense	probably damaging	1.00
R2432:Adgrv1	UTSW	13	81540132	frame shift	probably null
R2910:Adgrv1	UTSW	13	81557119	missense	possibly damaging	0.61
R2920:Adgrv1	UTSW	13	81448865	missense	probably benign	0.01
R2989:Adgrv1	UTSW	13	81581747	missense	probably damaging	1.00
R3402:Adgrv1	UTSW	13	81543542	missense	probably damaging	1.00
R3692:Adgrv1	UTSW	13	81524600	missense	possibly damaging	0.91
R3711:Adgrv1	UTSW	13	81419475	missense	probably benign	0.02
R3732:Adgrv1	UTSW	13	81556956	missense	probably damaging	1.00
R3732:Adgrv1	UTSW	13	81556956	missense	probably damaging	1.00
R3733:Adgrv1	UTSW	13	81556956	missense	probably damaging	1.00
R3773:Adgrv1	UTSW	13	81499043	missense	probably damaging	0.98
R3791:Adgrv1	UTSW	13	81593102	missense	probably damaging	1.00
R3794:Adgrv1	UTSW	13	81283367	start codon destroyed	probably damaging	1.00
R3848:Adgrv1	UTSW	13	81440072	missense	probably damaging	0.97
R3880:Adgrv1	UTSW	13	81435705	missense	probably benign	0.02
R3925:Adgrv1	UTSW	13	81578772	missense	possibly damaging	0.89
R3934:Adgrv1	UTSW	13	81475047	missense	probably benign	0.06
R3942:Adgrv1	UTSW	13	81182789	missense	probably damaging	1.00
R4002:Adgrv1	UTSW	13	81540132	frame shift	probably null
R4003:Adgrv1	UTSW	13	81540132	frame shift	probably null
R4194:Adgrv1	UTSW	13	81498996	missense	probably damaging	0.98
R4308:Adgrv1	UTSW	13	81440192	missense	probably damaging	0.96
R4368:Adgrv1	UTSW	13	81492910	missense	unknown
R4388:Adgrv1	UTSW	13	81581709	missense	probably damaging	0.98
R4421:Adgrv1	UTSW	13	81566302	missense	probably damaging	1.00
R4468:Adgrv1	UTSW	13	81374256	missense	probably benign	0.01
R4483:Adgrv1	UTSW	13	81419230	missense	probably benign	0.01
R4487:Adgrv1	UTSW	13	81440066	missense	probably damaging	0.99
R4566:Adgrv1	UTSW	13	81419808	missense	probably damaging	1.00
R4615:Adgrv1	UTSW	13	81494569	splice site	probably null
R4647:Adgrv1	UTSW	13	81528795	nonsense	probably null
R4657:Adgrv1	UTSW	13	81405364	missense	probably benign	0.01
R4723:Adgrv1	UTSW	13	81433525	missense	probably benign	0.02
R4765:Adgrv1	UTSW	13	81106919	missense	probably damaging	0.99
R4783:Adgrv1	UTSW	13	81095445	missense	probably damaging	0.99
R4796:Adgrv1	UTSW	13	81155231	nonsense	probably null
R4816:Adgrv1	UTSW	13	81528674	missense	probably damaging	1.00
R4833:Adgrv1	UTSW	13	81560844	missense	possibly damaging	0.81
R4841:Adgrv1	UTSW	13	81503001	critical splice donor site	probably null
R4871:Adgrv1	UTSW	13	81533122	intron	probably benign
R4897:Adgrv1	UTSW	13	81561585	splice site	probably null
R4906:Adgrv1	UTSW	13	81270738	splice site	probably null
R4917:Adgrv1	UTSW	13	81510877	missense	probably benign	0.30
R4996:Adgrv1	UTSW	13	81578734	missense	probably benign	0.01
R5030:Adgrv1	UTSW	13	81459829	missense	probably benign	0.43
R5044:Adgrv1	UTSW	13	81488931	missense	probably benign	0.01
R5052:Adgrv1	UTSW	13	81528821	missense	probably damaging	0.97
R5093:Adgrv1	UTSW	13	81592585	missense	probably damaging	1.00
R5095:Adgrv1	UTSW	13	81095487	missense	probably benign	0.00
R5119:Adgrv1	UTSW	13	81419427	missense	possibly damaging	0.93
R5133:Adgrv1	UTSW	13	81439441	missense	probably damaging	1.00
R5141:Adgrv1	UTSW	13	81270918	missense	probably damaging	1.00
R5164:Adgrv1	UTSW	13	81435674	missense	probably benign	0.00
R5180:Adgrv1	UTSW	13	81283416	start gained	probably benign
R5203:Adgrv1	UTSW	13	81510905	missense	possibly damaging	0.91
R5241:Adgrv1	UTSW	13	81488929	nonsense	probably null
R5280:Adgrv1	UTSW	13	81397465	missense	possibly damaging	0.95
R5289:Adgrv1	UTSW	13	81521084	missense	probably benign	0.04
R5304:Adgrv1	UTSW	13	81578253	missense	possibly damaging	0.93
R5310:Adgrv1	UTSW	13	81476690	missense	possibly damaging	0.95
R5338:Adgrv1	UTSW	13	81529046	missense	possibly damaging	0.80
R5352:Adgrv1	UTSW	13	81494657	missense	probably damaging	1.00
R5402:Adgrv1	UTSW	13	81459715	missense	probably benign	0.25
R5418:Adgrv1	UTSW	13	81419308	missense	probably benign	0.01
R5460:Adgrv1	UTSW	13	81424258	missense	possibly damaging	0.95
R5510:Adgrv1	UTSW	13	81445244	missense	probably damaging	1.00
R5521:Adgrv1	UTSW	13	81419389	missense	probably benign	0.01
R5538:Adgrv1	UTSW	13	81433689	missense	probably benign	0.02
R5561:Adgrv1	UTSW	13	81476564	missense	probably damaging	0.99
R5584:Adgrv1	UTSW	13	81405267	missense	probably damaging	1.00
R5608:Adgrv1	UTSW	13	81155276	missense	probably damaging	1.00
R5610:Adgrv1	UTSW	13	81521117	missense	probably damaging	1.00
R5619:Adgrv1	UTSW	13	81472500	missense	probably damaging	1.00
R5751:Adgrv1	UTSW	13	81522236	missense	probably damaging	1.00
R5832:Adgrv1	UTSW	13	81103302	missense	possibly damaging	0.95
R5885:Adgrv1	UTSW	13	81424271	missense	probably benign	0.15
R5930:Adgrv1	UTSW	13	81397451	missense	probably benign	0.06
R5937:Adgrv1	UTSW	13	81107075	missense	probably damaging	0.96
R5943:Adgrv1	UTSW	13	81386866	missense	probably damaging	0.98
R5951:Adgrv1	UTSW	13	81442501	missense	probably damaging	1.00
R5977:Adgrv1	UTSW	13	81435559	critical splice donor site	probably null
R5995:Adgrv1	UTSW	13	81466259	missense	probably benign	0.03
R6017:Adgrv1	UTSW	13	81397423	nonsense	probably null
R6024:Adgrv1	UTSW	13	81476505	missense	probably benign	0.26
R6049:Adgrv1	UTSW	13	81397354	missense	probably benign	0.00
R6108:Adgrv1	UTSW	13	81391695	missense	probably damaging	0.99
R6130:Adgrv1	UTSW	13	81427745	missense	probably damaging	0.99
R6132:Adgrv1	UTSW	13	81506076	missense	probably benign	0.04
R6149:Adgrv1	UTSW	13	81182774	missense	probably damaging	1.00
R6169:Adgrv1	UTSW	13	81419259	missense	probably benign	0.00
R6175:Adgrv1	UTSW	13	81386005	missense	probably damaging	1.00
R6184:Adgrv1	UTSW	13	81433838	missense	probably benign	0.01
R6190:Adgrv1	UTSW	13	81459763	synonymous	probably null
R6190:Adgrv1	UTSW	13	81524779	splice site	probably null
R6215:Adgrv1	UTSW	13	81579594	nonsense	probably null
R6216:Adgrv1	UTSW	13	81524471	intron	probably null
R6238:Adgrv1	UTSW	13	81466283	missense	probably benign	0.07
R6244:Adgrv1	UTSW	13	81106931	missense	probably damaging	1.00
R6298:Adgrv1	UTSW	13	81391767	missense	probably benign	0.00
R6316:Adgrv1	UTSW	13	81499068	missense	possibly damaging	0.63
R6336:Adgrv1	UTSW	13	81385981	missense	probably benign	0.09
R6358:Adgrv1	UTSW	13	81414583	missense	probably damaging	0.99
R6421:Adgrv1	UTSW	13	81508736	missense	possibly damaging	0.69
R6466:Adgrv1	UTSW	13	81575101	unclassified	probably null
R6467:Adgrv1	UTSW	13	81444538	missense	probably benign	0.01
R6510:Adgrv1	UTSW	13	81559490	missense	possibly damaging	0.88
R6519:Adgrv1	UTSW	13	81567343	missense	probably benign	0.01
R6521:Adgrv1	UTSW	13	81433652	missense	probably damaging	1.00
R6598:Adgrv1	UTSW	13	81506179	missense	probably damaging	1.00
R6605:Adgrv1	UTSW	13	81487962	missense	possibly damaging	0.80
R6626:Adgrv1	UTSW	13	81518126	missense	probably damaging	1.00
R6633:Adgrv1	UTSW	13	81568643	missense	probably damaging	1.00
R6721:Adgrv1	UTSW	13	81481515	missense	probably benign	0.00
R6725:Adgrv1	UTSW	13	81437557	missense	probably damaging	0.99
R6725:Adgrv1	UTSW	13	81493210	missense	probably damaging	1.00
R6796:Adgrv1	UTSW	13	81472478	missense	probably damaging	1.00
R6809:Adgrv1	UTSW	13	81472953	missense	probably benign	0.01
R6823:Adgrv1	UTSW	13	81557081	missense	probably damaging	1.00
R6876:Adgrv1	UTSW	13	81155154	critical splice donor site	probably null
R6878:Adgrv1	UTSW	13	81433494	missense	probably benign	0.06
R6887:Adgrv1	UTSW	13	81528701	missense	probably benign	0.01
R6888:Adgrv1	UTSW	13	81508669	missense	probably damaging	1.00
R6957:Adgrv1	UTSW	13	81567490	missense	probably benign	0.00
R6976:Adgrv1	UTSW	13	81520997	missense	probably damaging	1.00
R7003:Adgrv1	UTSW	13	81522104	critical splice donor site	probably null
R7007:Adgrv1	UTSW	13	81536364	missense	possibly damaging	0.80
R7073:Adgrv1	UTSW	13	81561474	missense	probably damaging	1.00
R7100:Adgrv1	UTSW	13	81270897	missense	probably damaging	1.00
R7107:Adgrv1	UTSW	13	81578142	missense	probably benign	0.13
R7123:Adgrv1	UTSW	13	81592574	missense	probably damaging	1.00
R7141:Adgrv1	UTSW	13	81492501	missense	probably benign	0.02
R7168:Adgrv1	UTSW	13	81397209	missense	possibly damaging	0.52
R7205:Adgrv1	UTSW	13	81479658	missense	probably benign	0.00
R7239:Adgrv1	UTSW	13	81476612	missense	possibly damaging	0.69
R7249:Adgrv1	UTSW	13	81374259	missense	probably damaging	1.00
R7313:Adgrv1	UTSW	13	81520515	missense	possibly damaging	0.95
R7376:Adgrv1	UTSW	13	81518126	missense	probably damaging	1.00
R7392:Adgrv1	UTSW	13	81560689	missense	probably damaging	1.00
R7395:Adgrv1	UTSW	13	81559348	missense	probably damaging	1.00
R7410:Adgrv1	UTSW	13	81563619	missense	probably benign	0.04
R7449:Adgrv1	UTSW	13	81499073	missense	probably damaging	0.99
R7496:Adgrv1	UTSW	13	81440225	missense	possibly damaging	0.79
R7497:Adgrv1	UTSW	13	81440225	missense	possibly damaging	0.79
R7498:Adgrv1	UTSW	13	81440225	missense	possibly damaging	0.79
R7567:Adgrv1	UTSW	13	81433529	missense	probably benign	0.00
R7567:Adgrv1	UTSW	13	81579477	missense	probably damaging	1.00
R7614:Adgrv1	UTSW	13	81520661	missense	probably damaging	1.00
R7623:Adgrv1	UTSW	13	81422225	missense	possibly damaging	0.77
R7665:Adgrv1	UTSW	13	81499142	missense	probably damaging	1.00
R7685:Adgrv1	UTSW	13	81103324	missense	possibly damaging	0.94
R7788:Adgrv1	UTSW	13	81573314	missense	probably damaging	1.00
R7809:Adgrv1	UTSW	13	81528641	missense	possibly damaging	0.81
X0054:Adgrv1	UTSW	13	81559270	missense	probably damaging	1.00
X0062:Adgrv1	UTSW	13	81386926	missense	probably damaging	0.99
X0067:Adgrv1	UTSW	13	81543392	missense	possibly damaging	0.51
Z1088:Adgrv1	UTSW	13	81476672	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CAGATGAATGGTTGTCATGGATAG -3'
(R):5'- CTGGGAGTATATATGCACACGC -3'

Sequencing Primer
(F):5'- AATGGTTGTCATGGATAGTTACTTAC -3'
(R):5'- TGTGCTGGAAACCATACTCG -3'

Posted On

2014-09-17