Mutagenetix > Incidental Mutation

Incidental Mutation 'R1539:Adgrv1'

171598

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

039578-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1539 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

81243187-81781273 bp(-) (GRCm39)

Type of Mutation

splice site (1754 bp from exon)

DNA Base Change (assembly)

T to A at 81652097 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000105193 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000095585
AA Change: E2969V

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: E2969V

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 null
Transcript: ENSMUST00000109565

SMART Domains

Protein: ENSMUSP00000105193
Gene: ENSMUSG00000069170

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: ENSMUST00000129725

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156627

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224788

Coding Region Coverage

1x: 99.0%
3x: 97.9%
10x: 94.9%
20x: 88.0%

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: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adh7	A	C	3: 137,929,716 (GRCm39)	T131P	possibly damaging	Het
Agxt	G	A	1: 93,065,701 (GRCm39)	G190D	probably damaging	Het
AI182371	A	G	2: 34,978,815 (GRCm39)	I193T	probably damaging	Het
Akna	T	A	4: 63,297,547 (GRCm39)	T836S	probably benign	Het
Alox12	T	C	11: 70,144,069 (GRCm39)		probably null	Het
Anapc2	C	A	2: 25,163,075 (GRCm39)	T104K	probably benign	Het
Ank1	T	C	8: 23,583,935 (GRCm39)	L346P	probably damaging	Het
Ankfn1	A	T	11: 89,332,217 (GRCm39)	I443N	probably damaging	Het
Arhgef17	G	A	7: 100,539,680 (GRCm39)	T1066I	probably damaging	Het
Atg2a	C	A	19: 6,296,801 (GRCm39)		probably null	Het
Bpifb5	T	A	2: 154,065,776 (GRCm39)	H24Q	probably benign	Het
Brd9	A	G	13: 74,092,862 (GRCm39)	E283G	probably damaging	Het
Cadm2	C	A	16: 66,581,727 (GRCm39)	V184F	probably damaging	Het
Casr	A	G	16: 36,315,499 (GRCm39)	V857A	probably benign	Het
Ccdc18	A	T	5: 108,339,843 (GRCm39)	Q796L	probably damaging	Het
Cep290	T	C	10: 100,332,690 (GRCm39)	V263A	probably benign	Het
Clec10a	A	T	11: 70,060,645 (GRCm39)	N167Y	probably damaging	Het
Cog1	A	G	11: 113,543,058 (GRCm39)	I189V	possibly damaging	Het
Commd2	A	G	3: 57,554,269 (GRCm39)	I144T	probably benign	Het
Cse1l	A	G	2: 166,768,292 (GRCm39)	T197A	probably benign	Het
Csmd3	A	T	15: 47,683,794 (GRCm39)	S1783R	probably benign	Het
Cxxc1	T	C	18: 74,352,278 (GRCm39)	V334A	possibly damaging	Het
Dennd2d	A	G	3: 106,394,236 (GRCm39)	I39V	probably benign	Het
Dgkz	G	A	2: 91,768,405 (GRCm39)	P734S	probably damaging	Het
Diaph3	T	C	14: 86,893,916 (GRCm39)	D31G	probably damaging	Het
Dlec1	T	C	9: 118,956,518 (GRCm39)	S731P	probably benign	Het
Dmac2l	G	A	12: 69,787,845 (GRCm39)	D94N	probably benign	Het
Dnah11	T	C	12: 117,894,991 (GRCm39)	R3619G	probably benign	Het
Doc2b	A	G	11: 75,662,783 (GRCm39)	L405P	probably damaging	Het
Dock3	A	T	9: 106,829,563 (GRCm39)	I1117N	probably damaging	Het
Dock3	G	A	9: 106,874,112 (GRCm39)	A453V	probably benign	Het
Ece2	T	A	16: 20,461,263 (GRCm39)	I474N	probably damaging	Het
Etv4	A	T	11: 101,662,513 (GRCm39)		probably null	Het
Fam171b	A	T	2: 83,710,442 (GRCm39)	M705L	probably benign	Het
Frem2	T	C	3: 53,561,631 (GRCm39)	K959E	probably benign	Het
Fyn	T	C	10: 39,408,066 (GRCm39)	M251T	possibly damaging	Het
Galnt13	G	A	2: 54,747,869 (GRCm39)	G250E	probably damaging	Het
Ggh	T	C	4: 20,054,204 (GRCm39)		probably null	Het
Glcci1	A	G	6: 8,591,620 (GRCm39)	E222G	probably damaging	Het
Gm1968	G	A	16: 29,777,659 (GRCm39)		noncoding transcript	Het
Gm3604	T	A	13: 62,519,414 (GRCm39)	I52F	possibly damaging	Het
Gm43302	T	C	5: 105,422,635 (GRCm39)	I466V	probably benign	Het
Gm9789	T	C	16: 88,955,034 (GRCm39)	S48P	unknown	Het
Gpat3	A	T	5: 101,031,254 (GRCm39)	Y136F	probably benign	Het
Gpr171	T	C	3: 59,005,142 (GRCm39)	D211G	possibly damaging	Het
Grep1	T	A	17: 23,936,118 (GRCm39)		probably benign	Het
Hs3st1	T	C	5: 39,771,791 (GRCm39)	K284R	probably benign	Het
Htr2a	C	T	14: 74,882,608 (GRCm39)	A198V	possibly damaging	Het
Ice1	C	A	13: 70,754,023 (GRCm39)	D688Y	probably damaging	Het
Jade1	T	C	3: 41,559,431 (GRCm39)	M504T	probably benign	Het
Lrp1	T	C	10: 127,420,250 (GRCm39)		probably null	Het
Lsr	A	T	7: 30,671,517 (GRCm39)	I72N	possibly damaging	Het
Magel2	G	A	7: 62,028,557 (GRCm39)	R487H	possibly damaging	Het
Mertk	A	G	2: 128,624,446 (GRCm39)	D619G	probably benign	Het
Myo1b	A	T	1: 51,838,722 (GRCm39)	V245E	probably damaging	Het
Myrip	T	A	9: 120,253,689 (GRCm39)	L254Q	probably benign	Het
Nav3	A	G	10: 109,603,031 (GRCm39)	S1173P	probably damaging	Het
Ncoa7	T	C	10: 30,647,725 (GRCm39)	Y17C	probably damaging	Het
Ncor2	T	C	5: 125,187,003 (GRCm39)	E7G	probably benign	Het
Ninl	A	G	2: 150,817,867 (GRCm39)	V99A	probably damaging	Het
Noct	G	T	3: 51,155,333 (GRCm39)	E34*	probably null	Het
Notch1	A	T	2: 26,362,125 (GRCm39)	Y1043*	probably null	Het
Or10v1	T	C	19: 11,873,855 (GRCm39)	S157P	possibly damaging	Het
Or13a21	T	A	7: 139,999,326 (GRCm39)	Y120F	probably benign	Het
Or2d3	A	G	7: 106,490,483 (GRCm39)	Y278H	probably damaging	Het
Or6c88	G	A	10: 129,406,640 (GRCm39)	G39R	probably damaging	Het
Pde7b	C	A	10: 20,355,432 (GRCm39)	R104L	possibly damaging	Het
Pkn1	C	A	8: 84,396,966 (GRCm39)	R890L	possibly damaging	Het
Podn	A	T	4: 107,878,764 (GRCm39)	Y368N	probably damaging	Het
Polr1b	G	A	2: 128,960,019 (GRCm39)		probably null	Het
Ppp1r3c	A	T	19: 36,711,361 (GRCm39)	F136L	probably benign	Het
Ppp2ca	T	A	11: 52,011,800 (GRCm39)	F260Y	probably damaging	Het
Prss39	A	G	1: 34,537,616 (GRCm39)	S27G	possibly damaging	Het
Ptch1	A	G	13: 63,689,101 (GRCm39)	V340A	probably benign	Het
Ranbp17	T	C	11: 33,247,394 (GRCm39)	I246V	probably damaging	Het
Rilpl1	T	A	5: 124,653,618 (GRCm39)	D181V	probably damaging	Het
Sdk1	T	A	5: 142,080,354 (GRCm39)	V1282D	probably damaging	Het
Sh3rf2	T	C	18: 42,282,887 (GRCm39)	S514P	probably damaging	Het
Slc35f2	A	T	9: 53,716,992 (GRCm39)	I252F	possibly damaging	Het
Slc7a1	A	G	5: 148,272,403 (GRCm39)	Y425H	possibly damaging	Het
Spaca4	G	T	7: 45,374,984 (GRCm39)		probably benign	Het
Spata31d1b	T	C	13: 59,863,733 (GRCm39)	S294P	possibly damaging	Het
Ssh1	T	G	5: 114,090,064 (GRCm39)	T342P	probably damaging	Het
Stk10	T	A	11: 32,483,440 (GRCm39)	S13T	possibly damaging	Het
Tbx1	G	T	16: 18,402,843 (GRCm39)	D214E	probably benign	Het
Tdp1	A	G	12: 99,878,571 (GRCm39)	E453G	probably damaging	Het
Tlr1	T	C	5: 65,084,319 (GRCm39)	Y86C	probably damaging	Het
Tmem241	A	T	18: 12,176,297 (GRCm39)	C124S	possibly damaging	Het
Trp63	A	G	16: 25,703,599 (GRCm39)	M516V	probably benign	Het
Ttc28	T	C	5: 111,248,677 (GRCm39)	V210A	possibly damaging	Het
Tut1	C	T	19: 8,942,850 (GRCm39)	R646W	probably benign	Het
Ubald1	C	T	16: 4,694,261 (GRCm39)	E49K	possibly damaging	Het
Usp28	T	C	9: 48,949,096 (GRCm39)	Y897H	probably benign	Het
Vmn2r27	A	C	6: 124,168,730 (GRCm39)	F800C	probably damaging	Het
Vmn2r83	T	A	10: 79,327,759 (GRCm39)	M789K	probably damaging	Het
Vwa8	A	G	14: 79,300,002 (GRCm39)	D945G	probably benign	Het
Wdhd1	T	A	14: 47,482,507 (GRCm39)	K947N	possibly damaging	Het
Wdr12	A	T	1: 60,123,007 (GRCm39)		probably null	Het
Xrra1	A	T	7: 99,520,564 (GRCm39)	E57V	probably damaging	Het

Other mutations in Adgrv1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Adgrv1	APN	13	81,553,527 (GRCm39)	critical splice acceptor site	probably null
IGL00090:Adgrv1	APN	13	81,726,220 (GRCm39)	missense	probably damaging	1.00
IGL00091:Adgrv1	APN	13	81,726,220 (GRCm39)	missense	probably damaging	1.00
IGL00332:Adgrv1	APN	13	81,620,996 (GRCm39)	splice site	probably benign
IGL00471:Adgrv1	APN	13	81,657,661 (GRCm39)	missense	probably damaging	0.99
IGL00476:Adgrv1	APN	13	81,637,193 (GRCm39)	missense	probably damaging	0.98
IGL00508:Adgrv1	APN	13	81,654,306 (GRCm39)	missense	probably damaging	1.00
IGL00727:Adgrv1	APN	13	81,672,803 (GRCm39)	missense	probably damaging	0.98
IGL00781:Adgrv1	APN	13	81,726,349 (GRCm39)	missense	probably benign	0.19
IGL00816:Adgrv1	APN	13	81,545,322 (GRCm39)	missense	probably benign	0.01
IGL00844:Adgrv1	APN	13	81,688,238 (GRCm39)	missense	probably damaging	1.00
IGL00923:Adgrv1	APN	13	81,530,410 (GRCm39)	missense	probably damaging	0.99
IGL01113:Adgrv1	APN	13	81,637,147 (GRCm39)	missense	probably benign	0.00
IGL01143:Adgrv1	APN	13	81,567,470 (GRCm39)	missense	probably benign	0.00
IGL01151:Adgrv1	APN	13	81,553,518 (GRCm39)	missense	probably benign	0.00
IGL01153:Adgrv1	APN	13	81,567,247 (GRCm39)	missense	probably benign	0.01
IGL01363:Adgrv1	APN	13	81,705,184 (GRCm39)	missense	probably damaging	1.00
IGL01419:Adgrv1	APN	13	81,705,277 (GRCm39)	missense	probably damaging	0.99
IGL01545:Adgrv1	APN	13	81,614,303 (GRCm39)	missense	possibly damaging	0.46
IGL01701:Adgrv1	APN	13	81,567,750 (GRCm39)	missense	possibly damaging	0.55
IGL01796:Adgrv1	APN	13	81,715,461 (GRCm39)	missense	probably benign	0.01
IGL01816:Adgrv1	APN	13	81,677,168 (GRCm39)	missense	probably benign	0.00
IGL01871:Adgrv1	APN	13	81,620,513 (GRCm39)	critical splice donor site	probably null
IGL01955:Adgrv1	APN	13	81,330,902 (GRCm39)	missense	probably damaging	1.00
IGL01956:Adgrv1	APN	13	81,594,549 (GRCm39)	missense	possibly damaging	0.63
IGL01988:Adgrv1	APN	13	81,705,428 (GRCm39)	missense	probably damaging	0.99
IGL01990:Adgrv1	APN	13	81,705,115 (GRCm39)	missense	probably damaging	1.00
IGL02007:Adgrv1	APN	13	81,716,862 (GRCm39)	splice site	probably benign
IGL02016:Adgrv1	APN	13	81,545,572 (GRCm39)	missense	probably damaging	1.00
IGL02095:Adgrv1	APN	13	81,727,909 (GRCm39)	missense	possibly damaging	0.63
IGL02174:Adgrv1	APN	13	81,575,783 (GRCm39)	missense	probably benign	0.34
IGL02270:Adgrv1	APN	13	81,707,314 (GRCm39)	splice site	probably null
IGL02328:Adgrv1	APN	13	81,726,294 (GRCm39)	missense	probably damaging	1.00
IGL02350:Adgrv1	APN	13	81,418,974 (GRCm39)	missense	probably benign	0.00
IGL02357:Adgrv1	APN	13	81,418,974 (GRCm39)	missense	probably benign	0.00
IGL02373:Adgrv1	APN	13	81,607,832 (GRCm39)	missense	possibly damaging	0.90
IGL02402:Adgrv1	APN	13	81,707,543 (GRCm39)	missense	probably benign	0.18
IGL02407:Adgrv1	APN	13	81,627,789 (GRCm39)	missense	probably damaging	1.00
IGL02508:Adgrv1	APN	13	81,583,675 (GRCm39)	splice site	probably benign
IGL02603:Adgrv1	APN	13	81,637,071 (GRCm39)	missense	possibly damaging	0.93
IGL02648:Adgrv1	APN	13	81,659,738 (GRCm39)	missense	probably benign	0.35
IGL02720:Adgrv1	APN	13	81,726,991 (GRCm39)	missense	probably damaging	0.99
IGL02870:Adgrv1	APN	13	81,711,851 (GRCm39)	missense	probably benign	0.13
IGL02896:Adgrv1	APN	13	81,668,858 (GRCm39)	missense	probably damaging	1.00
IGL02931:Adgrv1	APN	13	81,727,833 (GRCm39)	missense	probably damaging	1.00
IGL02952:Adgrv1	APN	13	81,581,755 (GRCm39)	missense	probably benign	0.00
IGL02961:Adgrv1	APN	13	81,671,731 (GRCm39)	missense	probably damaging	1.00
IGL02999:Adgrv1	APN	13	81,726,973 (GRCm39)	missense	probably benign	0.12
IGL03067:Adgrv1	APN	13	81,590,599 (GRCm39)	missense	probably damaging	1.00
IGL03106:Adgrv1	APN	13	81,621,018 (GRCm39)	missense	probably benign	0.00
IGL03108:Adgrv1	APN	13	81,707,648 (GRCm39)	missense	probably damaging	1.00
IGL03119:Adgrv1	APN	13	81,581,819 (GRCm39)	missense	probably benign	0.02
IGL03119:Adgrv1	APN	13	81,530,492 (GRCm39)	missense	probably damaging	1.00
IGL03169:Adgrv1	APN	13	81,652,019 (GRCm39)	missense	probably damaging	1.00
IGL03186:Adgrv1	APN	13	81,581,737 (GRCm39)	missense	possibly damaging	0.80
IGL03196:Adgrv1	APN	13	81,594,597 (GRCm39)	missense	probably benign	0.02
IGL03207:Adgrv1	APN	13	81,255,017 (GRCm39)	splice site	probably null
IGL03343:Adgrv1	APN	13	81,431,507 (GRCm39)	missense	probably damaging	1.00
IGL03348:Adgrv1	APN	13	81,647,177 (GRCm39)	missense	possibly damaging	0.54
IGL03349:Adgrv1	APN	13	81,629,455 (GRCm39)	missense	probably benign	0.09
IGL03373:Adgrv1	APN	13	81,711,751 (GRCm39)	missense	probably damaging	0.99
IGL03381:Adgrv1	APN	13	81,666,086 (GRCm39)	missense	probably damaging	0.99
abetting	UTSW	13	81,727,679 (GRCm39)	missense	probably damaging	1.00
beatle	UTSW	13	81,727,713 (GRCm39)	nonsense	probably null
Escape	UTSW	13	81,583,824 (GRCm39)	missense	probably benign	0.02
lento	UTSW	13	81,419,016 (GRCm39)	missense	probably damaging	1.00
Metronome	UTSW	13	81,583,678 (GRCm39)	critical splice donor site	probably null
Murderous	UTSW	13	81,251,443 (GRCm39)	missense	possibly damaging	0.94
Nome	UTSW	13	81,539,886 (GRCm39)	missense	probably benign	0.00
Propulsion	UTSW	13	81,623,166 (GRCm39)	missense	probably benign	0.06
revulsion	UTSW	13	81,743,301 (GRCm39)	missense	probably damaging	1.00
Saturnv	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
Thrust	UTSW	13	81,522,375 (GRCm39)	missense	probably benign	0.01
Velocity	UTSW	13	81,545,473 (GRCm39)	missense	probably benign	0.00
Wilting	UTSW	13	81,640,620 (GRCm39)	missense	probably benign	0.02
Withering	UTSW	13	81,642,776 (GRCm39)	missense	probably damaging	1.00
F2404:Adgrv1	UTSW	13	81,568,125 (GRCm39)	missense	probably benign	0.13
G1patch:Adgrv1	UTSW	13	81,641,329 (GRCm39)	missense	probably damaging	1.00
G1patch:Adgrv1	UTSW	13	81,585,676 (GRCm39)	missense	probably damaging	0.99
I2288:Adgrv1	UTSW	13	81,585,643 (GRCm39)	missense	probably damaging	1.00
I2289:Adgrv1	UTSW	13	81,585,643 (GRCm39)	missense	probably damaging	1.00
PIT4377001:Adgrv1	UTSW	13	81,677,104 (GRCm39)	missense	probably damaging	1.00
PIT4504001:Adgrv1	UTSW	13	81,707,471 (GRCm39)	missense	probably damaging	0.99
R0017:Adgrv1	UTSW	13	81,727,065 (GRCm39)	missense	probably benign	0.13
R0017:Adgrv1	UTSW	13	81,727,065 (GRCm39)	missense	probably benign	0.13
R0058:Adgrv1	UTSW	13	81,330,791 (GRCm39)	missense	possibly damaging	0.65
R0058:Adgrv1	UTSW	13	81,330,791 (GRCm39)	missense	possibly damaging	0.65
R0083:Adgrv1	UTSW	13	81,726,523 (GRCm39)	unclassified	probably benign
R0087:Adgrv1	UTSW	13	81,535,070 (GRCm39)	missense	probably damaging	1.00
R0108:Adgrv1	UTSW	13	81,726,523 (GRCm39)	unclassified	probably benign
R0131:Adgrv1	UTSW	13	81,651,114 (GRCm39)	unclassified	probably benign
R0218:Adgrv1	UTSW	13	81,255,017 (GRCm39)	splice site	probably null
R0325:Adgrv1	UTSW	13	81,688,134 (GRCm39)	missense	probably damaging	1.00
R0326:Adgrv1	UTSW	13	81,623,112 (GRCm39)	missense	possibly damaging	0.46
R0395:Adgrv1	UTSW	13	81,534,072 (GRCm39)	missense	probably benign	0.00
R0441:Adgrv1	UTSW	13	81,545,345 (GRCm39)	nonsense	probably null
R0466:Adgrv1	UTSW	13	81,714,415 (GRCm39)	missense	probably benign	0.00
R0487:Adgrv1	UTSW	13	81,637,154 (GRCm39)	missense	probably damaging	1.00
R0501:Adgrv1	UTSW	13	81,707,269 (GRCm39)	missense	probably damaging	1.00
R0522:Adgrv1	UTSW	13	81,676,561 (GRCm39)	splice site	probably benign
R0532:Adgrv1	UTSW	13	81,727,015 (GRCm39)	missense	probably damaging	1.00
R0542:Adgrv1	UTSW	13	81,721,437 (GRCm39)	missense	probably damaging	1.00
R0681:Adgrv1	UTSW	13	81,676,649 (GRCm39)	missense	probably damaging	1.00
R0689:Adgrv1	UTSW	13	81,623,224 (GRCm39)	missense	possibly damaging	0.47
R0732:Adgrv1	UTSW	13	81,651,123 (GRCm39)	missense	possibly damaging	0.86
R0746:Adgrv1	UTSW	13	81,718,675 (GRCm39)	missense	probably benign	0.10
R0763:Adgrv1	UTSW	13	81,647,244 (GRCm39)	missense	probably damaging	0.98
R0846:Adgrv1	UTSW	13	81,627,861 (GRCm39)	nonsense	probably null
R0962:Adgrv1	UTSW	13	81,553,465 (GRCm39)	missense	probably benign	0.01
R1146:Adgrv1	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
R1146:Adgrv1	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
R1172:Adgrv1	UTSW	13	81,705,182 (GRCm39)	missense	probably damaging	0.98
R1178:Adgrv1	UTSW	13	81,588,156 (GRCm39)	splice site	probably benign
R1310:Adgrv1	UTSW	13	81,714,496 (GRCm39)	missense	probably benign	0.09
R1386:Adgrv1	UTSW	13	81,676,984 (GRCm39)	missense	probably benign	0.17
R1387:Adgrv1	UTSW	13	81,641,295 (GRCm39)	missense	possibly damaging	0.62
R1395:Adgrv1	UTSW	13	81,534,907 (GRCm39)	missense	probably benign	0.05
R1412:Adgrv1	UTSW	13	81,243,569 (GRCm39)	missense	probably damaging	1.00
R1448:Adgrv1	UTSW	13	81,581,632 (GRCm39)	missense	probably benign	0.08
R1470:Adgrv1	UTSW	13	81,530,417 (GRCm39)	missense	probably benign	0.03
R1470:Adgrv1	UTSW	13	81,530,417 (GRCm39)	missense	probably benign	0.03
R1485:Adgrv1	UTSW	13	81,727,738 (GRCm39)	missense	probably damaging	1.00
R1507:Adgrv1	UTSW	13	81,620,699 (GRCm39)	critical splice acceptor site	probably null
R1513:Adgrv1	UTSW	13	81,705,076 (GRCm39)	missense	probably damaging	1.00
R1513:Adgrv1	UTSW	13	81,741,167 (GRCm39)	missense	probably damaging	1.00
R1579:Adgrv1	UTSW	13	81,711,898 (GRCm39)	missense	probably damaging	1.00
R1580:Adgrv1	UTSW	13	81,614,279 (GRCm39)	critical splice donor site	probably null
R1611:Adgrv1	UTSW	13	81,707,236 (GRCm39)	missense	probably damaging	1.00
R1615:Adgrv1	UTSW	13	81,572,407 (GRCm39)	missense	probably benign	0.41
R1651:Adgrv1	UTSW	13	81,635,972 (GRCm39)	missense	probably benign	0.19
R1660:Adgrv1	UTSW	13	81,624,750 (GRCm39)	missense	probably benign	0.00
R1679:Adgrv1	UTSW	13	81,707,671 (GRCm39)	missense	probably damaging	1.00
R1709:Adgrv1	UTSW	13	81,741,179 (GRCm39)	missense	probably damaging	1.00
R1735:Adgrv1	UTSW	13	81,636,066 (GRCm39)	missense	possibly damaging	0.62
R1762:Adgrv1	UTSW	13	81,654,265 (GRCm39)	missense	probably benign	0.08
R1830:Adgrv1	UTSW	13	81,637,196 (GRCm39)	missense	possibly damaging	0.65
R1836:Adgrv1	UTSW	13	81,652,232 (GRCm39)	missense	probably benign	0.01
R1843:Adgrv1	UTSW	13	81,692,652 (GRCm39)	missense	probably damaging	1.00
R1863:Adgrv1	UTSW	13	81,711,685 (GRCm39)	missense	probably damaging	1.00
R1895:Adgrv1	UTSW	13	81,522,368 (GRCm39)	missense	probably damaging	1.00
R1907:Adgrv1	UTSW	13	81,740,670 (GRCm39)	splice site	probably benign
R1928:Adgrv1	UTSW	13	81,668,905 (GRCm39)	missense	probably benign	0.00
R1938:Adgrv1	UTSW	13	81,539,876 (GRCm39)	missense	probably damaging	0.99
R1944:Adgrv1	UTSW	13	81,659,030 (GRCm39)	missense	probably damaging	1.00
R1946:Adgrv1	UTSW	13	81,522,368 (GRCm39)	missense	probably damaging	1.00
R1984:Adgrv1	UTSW	13	81,671,868 (GRCm39)	missense	probably damaging	1.00
R2027:Adgrv1	UTSW	13	81,743,301 (GRCm39)	missense	probably damaging	1.00
R2063:Adgrv1	UTSW	13	81,709,588 (GRCm39)	missense	possibly damaging	0.81
R2116:Adgrv1	UTSW	13	81,677,132 (GRCm39)	missense	probably benign	0.11
R2117:Adgrv1	UTSW	13	81,640,656 (GRCm39)	missense	probably benign	0.00
R2125:Adgrv1	UTSW	13	81,568,069 (GRCm39)	missense	probably benign	0.02
R2125:Adgrv1	UTSW	13	81,567,654 (GRCm39)	missense	probably benign	0.00
R2127:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2128:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2129:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2130:Adgrv1	UTSW	13	81,729,846 (GRCm39)	missense	possibly damaging	0.61
R2135:Adgrv1	UTSW	13	81,672,676 (GRCm39)	critical splice donor site	probably null
R2138:Adgrv1	UTSW	13	81,593,439 (GRCm39)	missense	probably benign	0.00
R2166:Adgrv1	UTSW	13	81,716,762 (GRCm39)	missense	probably damaging	1.00
R2171:Adgrv1	UTSW	13	81,419,037 (GRCm39)	missense	probably damaging	1.00
R2191:Adgrv1	UTSW	13	81,714,409 (GRCm39)	missense	possibly damaging	0.90
R2256:Adgrv1	UTSW	13	81,654,259 (GRCm39)	missense	probably benign
R2260:Adgrv1	UTSW	13	81,716,493 (GRCm39)	missense	probably damaging	0.97
R2323:Adgrv1	UTSW	13	81,743,298 (GRCm39)	missense	probably damaging	1.00
R2432:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R2910:Adgrv1	UTSW	13	81,705,238 (GRCm39)	missense	possibly damaging	0.61
R2920:Adgrv1	UTSW	13	81,596,984 (GRCm39)	missense	probably benign	0.01
R2989:Adgrv1	UTSW	13	81,729,866 (GRCm39)	missense	probably damaging	1.00
R3402:Adgrv1	UTSW	13	81,691,661 (GRCm39)	missense	probably damaging	1.00
R3692:Adgrv1	UTSW	13	81,672,719 (GRCm39)	missense	possibly damaging	0.91
R3711:Adgrv1	UTSW	13	81,567,594 (GRCm39)	missense	probably benign	0.02
R3732:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3732:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3733:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3773:Adgrv1	UTSW	13	81,647,162 (GRCm39)	missense	probably damaging	0.98
R3791:Adgrv1	UTSW	13	81,741,221 (GRCm39)	missense	probably damaging	1.00
R3794:Adgrv1	UTSW	13	81,431,486 (GRCm39)	start codon destroyed	probably damaging	1.00
R3848:Adgrv1	UTSW	13	81,588,191 (GRCm39)	missense	probably damaging	0.97
R3880:Adgrv1	UTSW	13	81,583,824 (GRCm39)	missense	probably benign	0.02
R3925:Adgrv1	UTSW	13	81,726,891 (GRCm39)	missense	possibly damaging	0.89
R3934:Adgrv1	UTSW	13	81,623,166 (GRCm39)	missense	probably benign	0.06
R3942:Adgrv1	UTSW	13	81,330,908 (GRCm39)	missense	probably damaging	1.00
R4002:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R4003:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R4194:Adgrv1	UTSW	13	81,647,115 (GRCm39)	missense	probably damaging	0.98
R4308:Adgrv1	UTSW	13	81,588,311 (GRCm39)	missense	probably damaging	0.96
R4368:Adgrv1	UTSW	13	81,641,029 (GRCm39)	missense	unknown
R4388:Adgrv1	UTSW	13	81,729,828 (GRCm39)	missense	probably damaging	0.98
R4421:Adgrv1	UTSW	13	81,714,421 (GRCm39)	missense	probably damaging	1.00
R4468:Adgrv1	UTSW	13	81,522,375 (GRCm39)	missense	probably benign	0.01
R4483:Adgrv1	UTSW	13	81,567,349 (GRCm39)	missense	probably benign	0.01
R4487:Adgrv1	UTSW	13	81,588,185 (GRCm39)	missense	probably damaging	0.99
R4566:Adgrv1	UTSW	13	81,567,927 (GRCm39)	missense	probably damaging	1.00
R4615:Adgrv1	UTSW	13	81,642,688 (GRCm39)	splice site	probably null
R4647:Adgrv1	UTSW	13	81,676,914 (GRCm39)	nonsense	probably null
R4657:Adgrv1	UTSW	13	81,553,483 (GRCm39)	missense	probably benign	0.01
R4723:Adgrv1	UTSW	13	81,581,644 (GRCm39)	missense	probably benign	0.02
R4765:Adgrv1	UTSW	13	81,255,038 (GRCm39)	missense	probably damaging	0.99
R4783:Adgrv1	UTSW	13	81,243,564 (GRCm39)	missense	probably damaging	0.99
R4796:Adgrv1	UTSW	13	81,303,350 (GRCm39)	nonsense	probably null
R4816:Adgrv1	UTSW	13	81,676,793 (GRCm39)	missense	probably damaging	1.00
R4833:Adgrv1	UTSW	13	81,708,963 (GRCm39)	missense	possibly damaging	0.81
R4841:Adgrv1	UTSW	13	81,651,120 (GRCm39)	critical splice donor site	probably null
R4871:Adgrv1	UTSW	13	81,681,241 (GRCm39)	intron	probably benign
R4897:Adgrv1	UTSW	13	81,709,704 (GRCm39)	splice site	probably null
R4906:Adgrv1	UTSW	13	81,418,857 (GRCm39)	splice site	probably null
R4917:Adgrv1	UTSW	13	81,658,996 (GRCm39)	missense	probably benign	0.30
R4996:Adgrv1	UTSW	13	81,726,853 (GRCm39)	missense	probably benign	0.01
R5030:Adgrv1	UTSW	13	81,607,948 (GRCm39)	missense	probably benign	0.43
R5044:Adgrv1	UTSW	13	81,637,050 (GRCm39)	missense	probably benign	0.01
R5052:Adgrv1	UTSW	13	81,676,940 (GRCm39)	missense	probably damaging	0.97
R5093:Adgrv1	UTSW	13	81,740,704 (GRCm39)	missense	probably damaging	1.00
R5095:Adgrv1	UTSW	13	81,243,606 (GRCm39)	missense	probably benign	0.00
R5119:Adgrv1	UTSW	13	81,567,546 (GRCm39)	missense	possibly damaging	0.93
R5133:Adgrv1	UTSW	13	81,587,560 (GRCm39)	missense	probably damaging	1.00
R5141:Adgrv1	UTSW	13	81,419,037 (GRCm39)	missense	probably damaging	1.00
R5164:Adgrv1	UTSW	13	81,583,793 (GRCm39)	missense	probably benign	0.00
R5180:Adgrv1	UTSW	13	81,431,535 (GRCm39)	start gained	probably benign
R5203:Adgrv1	UTSW	13	81,659,024 (GRCm39)	missense	possibly damaging	0.91
R5241:Adgrv1	UTSW	13	81,637,048 (GRCm39)	nonsense	probably null
R5280:Adgrv1	UTSW	13	81,545,584 (GRCm39)	missense	possibly damaging	0.95
R5289:Adgrv1	UTSW	13	81,669,203 (GRCm39)	missense	probably benign	0.04
R5304:Adgrv1	UTSW	13	81,726,372 (GRCm39)	missense	possibly damaging	0.93
R5310:Adgrv1	UTSW	13	81,624,809 (GRCm39)	missense	possibly damaging	0.95
R5338:Adgrv1	UTSW	13	81,677,165 (GRCm39)	missense	possibly damaging	0.80
R5352:Adgrv1	UTSW	13	81,642,776 (GRCm39)	missense	probably damaging	1.00
R5402:Adgrv1	UTSW	13	81,607,834 (GRCm39)	missense	probably benign	0.25
R5418:Adgrv1	UTSW	13	81,567,427 (GRCm39)	missense	probably benign	0.01
R5460:Adgrv1	UTSW	13	81,572,377 (GRCm39)	missense	possibly damaging	0.95
R5510:Adgrv1	UTSW	13	81,593,363 (GRCm39)	missense	probably damaging	1.00
R5521:Adgrv1	UTSW	13	81,567,508 (GRCm39)	missense	probably benign	0.01
R5538:Adgrv1	UTSW	13	81,581,808 (GRCm39)	missense	probably benign	0.02
R5561:Adgrv1	UTSW	13	81,624,683 (GRCm39)	missense	probably damaging	0.99
R5584:Adgrv1	UTSW	13	81,553,386 (GRCm39)	missense	probably damaging	1.00
R5608:Adgrv1	UTSW	13	81,303,395 (GRCm39)	missense	probably damaging	1.00
R5610:Adgrv1	UTSW	13	81,669,236 (GRCm39)	missense	probably damaging	1.00
R5619:Adgrv1	UTSW	13	81,620,619 (GRCm39)	missense	probably damaging	1.00
R5751:Adgrv1	UTSW	13	81,670,355 (GRCm39)	missense	probably damaging	1.00
R5832:Adgrv1	UTSW	13	81,251,421 (GRCm39)	missense	possibly damaging	0.95
R5885:Adgrv1	UTSW	13	81,572,390 (GRCm39)	missense	probably benign	0.15
R5930:Adgrv1	UTSW	13	81,545,570 (GRCm39)	missense	probably benign	0.06
R5937:Adgrv1	UTSW	13	81,255,194 (GRCm39)	missense	probably damaging	0.96
R5943:Adgrv1	UTSW	13	81,534,985 (GRCm39)	missense	probably damaging	0.98
R5951:Adgrv1	UTSW	13	81,590,620 (GRCm39)	missense	probably damaging	1.00
R5977:Adgrv1	UTSW	13	81,583,678 (GRCm39)	critical splice donor site	probably null
R5995:Adgrv1	UTSW	13	81,614,378 (GRCm39)	missense	probably benign	0.03
R6017:Adgrv1	UTSW	13	81,545,542 (GRCm39)	nonsense	probably null
R6024:Adgrv1	UTSW	13	81,624,624 (GRCm39)	missense	probably benign	0.26
R6049:Adgrv1	UTSW	13	81,545,473 (GRCm39)	missense	probably benign	0.00
R6108:Adgrv1	UTSW	13	81,539,814 (GRCm39)	missense	probably damaging	0.99
R6130:Adgrv1	UTSW	13	81,575,864 (GRCm39)	missense	probably damaging	0.99
R6132:Adgrv1	UTSW	13	81,654,195 (GRCm39)	missense	probably benign	0.04
R6149:Adgrv1	UTSW	13	81,330,893 (GRCm39)	missense	probably damaging	1.00
R6169:Adgrv1	UTSW	13	81,567,378 (GRCm39)	missense	probably benign	0.00
R6175:Adgrv1	UTSW	13	81,534,124 (GRCm39)	missense	probably damaging	1.00
R6184:Adgrv1	UTSW	13	81,581,957 (GRCm39)	missense	probably benign	0.01
R6190:Adgrv1	UTSW	13	81,672,898 (GRCm39)	splice site	probably null
R6190:Adgrv1	UTSW	13	81,607,882 (GRCm39)	splice site	probably null
R6215:Adgrv1	UTSW	13	81,727,713 (GRCm39)	nonsense	probably null
R6216:Adgrv1	UTSW	13	81,672,590 (GRCm39)	splice site	probably null
R6238:Adgrv1	UTSW	13	81,614,402 (GRCm39)	missense	probably benign	0.07
R6244:Adgrv1	UTSW	13	81,255,050 (GRCm39)	missense	probably damaging	1.00
R6298:Adgrv1	UTSW	13	81,539,886 (GRCm39)	missense	probably benign	0.00
R6316:Adgrv1	UTSW	13	81,647,187 (GRCm39)	missense	possibly damaging	0.63
R6336:Adgrv1	UTSW	13	81,534,100 (GRCm39)	missense	probably benign	0.09
R6358:Adgrv1	UTSW	13	81,562,702 (GRCm39)	missense	probably damaging	0.99
R6421:Adgrv1	UTSW	13	81,656,855 (GRCm39)	missense	possibly damaging	0.69
R6466:Adgrv1	UTSW	13	81,723,220 (GRCm39)	splice site	probably null
R6467:Adgrv1	UTSW	13	81,592,657 (GRCm39)	missense	probably benign	0.01
R6510:Adgrv1	UTSW	13	81,707,609 (GRCm39)	missense	possibly damaging	0.88
R6519:Adgrv1	UTSW	13	81,715,462 (GRCm39)	missense	probably benign	0.01
R6521:Adgrv1	UTSW	13	81,581,771 (GRCm39)	missense	probably damaging	1.00
R6598:Adgrv1	UTSW	13	81,654,298 (GRCm39)	missense	probably damaging	1.00
R6605:Adgrv1	UTSW	13	81,636,081 (GRCm39)	missense	possibly damaging	0.80
R6626:Adgrv1	UTSW	13	81,666,245 (GRCm39)	missense	probably damaging	1.00
R6633:Adgrv1	UTSW	13	81,716,762 (GRCm39)	missense	probably damaging	1.00
R6721:Adgrv1	UTSW	13	81,629,634 (GRCm39)	missense	probably benign	0.00
R6725:Adgrv1	UTSW	13	81,585,676 (GRCm39)	missense	probably damaging	0.99
R6725:Adgrv1	UTSW	13	81,641,329 (GRCm39)	missense	probably damaging	1.00
R6796:Adgrv1	UTSW	13	81,620,597 (GRCm39)	missense	probably damaging	1.00
R6809:Adgrv1	UTSW	13	81,621,072 (GRCm39)	missense	probably benign	0.01
R6823:Adgrv1	UTSW	13	81,705,200 (GRCm39)	missense	probably damaging	1.00
R6876:Adgrv1	UTSW	13	81,303,273 (GRCm39)	critical splice donor site	probably null
R6878:Adgrv1	UTSW	13	81,581,613 (GRCm39)	missense	probably benign	0.06
R6887:Adgrv1	UTSW	13	81,676,820 (GRCm39)	missense	probably benign	0.01
R6888:Adgrv1	UTSW	13	81,656,788 (GRCm39)	missense	probably damaging	1.00
R6957:Adgrv1	UTSW	13	81,715,609 (GRCm39)	missense	probably benign	0.00
R6976:Adgrv1	UTSW	13	81,669,116 (GRCm39)	missense	probably damaging	1.00
R7003:Adgrv1	UTSW	13	81,670,223 (GRCm39)	critical splice donor site	probably null
R7007:Adgrv1	UTSW	13	81,684,483 (GRCm39)	missense	possibly damaging	0.80
R7073:Adgrv1	UTSW	13	81,709,593 (GRCm39)	missense	probably damaging	1.00
R7100:Adgrv1	UTSW	13	81,419,016 (GRCm39)	missense	probably damaging	1.00
R7107:Adgrv1	UTSW	13	81,726,261 (GRCm39)	missense	probably benign	0.13
R7123:Adgrv1	UTSW	13	81,740,693 (GRCm39)	missense	probably damaging	1.00
R7141:Adgrv1	UTSW	13	81,640,620 (GRCm39)	missense	probably benign	0.02
R7168:Adgrv1	UTSW	13	81,545,328 (GRCm39)	missense	possibly damaging	0.52
R7205:Adgrv1	UTSW	13	81,627,777 (GRCm39)	missense	probably benign	0.00
R7239:Adgrv1	UTSW	13	81,624,731 (GRCm39)	missense	possibly damaging	0.69
R7249:Adgrv1	UTSW	13	81,522,378 (GRCm39)	missense	probably damaging	1.00
R7313:Adgrv1	UTSW	13	81,668,634 (GRCm39)	missense	possibly damaging	0.95
R7376:Adgrv1	UTSW	13	81,666,245 (GRCm39)	missense	probably damaging	1.00
R7392:Adgrv1	UTSW	13	81,708,808 (GRCm39)	missense	probably damaging	1.00
R7395:Adgrv1	UTSW	13	81,707,467 (GRCm39)	missense	probably damaging	1.00
R7410:Adgrv1	UTSW	13	81,711,738 (GRCm39)	missense	probably benign	0.04
R7449:Adgrv1	UTSW	13	81,647,192 (GRCm39)	missense	probably damaging	0.99
R7496:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R7497:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R7498:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R7567:Adgrv1	UTSW	13	81,727,596 (GRCm39)	missense	probably damaging	1.00
R7567:Adgrv1	UTSW	13	81,581,648 (GRCm39)	missense	probably benign	0.00
R7614:Adgrv1	UTSW	13	81,668,780 (GRCm39)	missense	probably damaging	1.00
R7623:Adgrv1	UTSW	13	81,570,344 (GRCm39)	missense	possibly damaging	0.77
R7665:Adgrv1	UTSW	13	81,647,261 (GRCm39)	missense	probably damaging	1.00
R7685:Adgrv1	UTSW	13	81,251,443 (GRCm39)	missense	possibly damaging	0.94
R7788:Adgrv1	UTSW	13	81,721,433 (GRCm39)	missense	probably damaging	1.00
R7809:Adgrv1	UTSW	13	81,676,760 (GRCm39)	missense	possibly damaging	0.81
R7854:Adgrv1	UTSW	13	81,741,207 (GRCm39)	missense	probably damaging	1.00
R7894:Adgrv1	UTSW	13	81,715,570 (GRCm39)	missense	probably benign	0.00
R7948:Adgrv1	UTSW	13	81,707,707 (GRCm39)	missense	probably damaging	1.00
R7948:Adgrv1	UTSW	13	81,707,648 (GRCm39)	missense	probably damaging	1.00
R7949:Adgrv1	UTSW	13	81,303,353 (GRCm39)	missense	probably damaging	1.00
R7951:Adgrv1	UTSW	13	81,711,689 (GRCm39)	missense	probably damaging	1.00
R7968:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R7969:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R7973:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8007:Adgrv1	UTSW	13	81,431,585 (GRCm39)	missense	probably benign	0.04
R8018:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8044:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8050:Adgrv1	UTSW	13	81,561,296 (GRCm39)	missense	probably damaging	1.00
R8090:Adgrv1	UTSW	13	81,596,953 (GRCm39)	critical splice donor site	probably null
R8104:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8122:Adgrv1	UTSW	13	81,419,037 (GRCm39)	missense	probably damaging	1.00
R8122:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8123:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8125:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8126:Adgrv1	UTSW	13	81,588,344 (GRCm39)	missense	possibly damaging	0.79
R8212:Adgrv1	UTSW	13	81,670,240 (GRCm39)	missense	probably benign	0.01
R8221:Adgrv1	UTSW	13	81,677,033 (GRCm39)	missense	probably benign	0.00
R8256:Adgrv1	UTSW	13	81,727,679 (GRCm39)	missense	probably damaging	1.00
R8270:Adgrv1	UTSW	13	81,651,163 (GRCm39)	missense	probably damaging	0.96
R8290:Adgrv1	UTSW	13	81,630,002 (GRCm39)	missense	probably benign	0.00
R8298:Adgrv1	UTSW	13	81,534,033 (GRCm39)	nonsense	probably null
R8317:Adgrv1	UTSW	13	81,723,236 (GRCm39)	missense	probably damaging	0.98
R8326:Adgrv1	UTSW	13	81,593,462 (GRCm39)	missense	probably damaging	1.00
R8327:Adgrv1	UTSW	13	81,593,462 (GRCm39)	missense	probably damaging	1.00
R8330:Adgrv1	UTSW	13	81,593,462 (GRCm39)	missense	probably damaging	1.00
R8332:Adgrv1	UTSW	13	81,593,462 (GRCm39)	missense	probably damaging	1.00
R8345:Adgrv1	UTSW	13	81,251,505 (GRCm39)	missense	probably damaging	1.00
R8398:Adgrv1	UTSW	13	81,330,797 (GRCm39)	missense	probably damaging	1.00
R8399:Adgrv1	UTSW	13	81,637,289 (GRCm39)	missense	possibly damaging	0.55
R8450:Adgrv1	UTSW	13	81,583,962 (GRCm39)	splice site	probably null
R8471:Adgrv1	UTSW	13	81,594,591 (GRCm39)	missense	probably benign	0.00
R8534:Adgrv1	UTSW	13	81,534,887 (GRCm39)	missense	probably benign	0.02
R8537:Adgrv1	UTSW	13	81,684,491 (GRCm39)	missense	probably damaging	1.00
R8703:Adgrv1	UTSW	13	81,676,792 (GRCm39)	missense	probably damaging	1.00
R8845:Adgrv1	UTSW	13	81,629,478 (GRCm39)	missense	possibly damaging	0.79
R8846:Adgrv1	UTSW	13	81,637,025 (GRCm39)	critical splice donor site	probably null
R8849:Adgrv1	UTSW	13	81,669,324 (GRCm39)	missense	probably benign
R8856:Adgrv1	UTSW	13	81,707,621 (GRCm39)	missense	probably benign	0.11
R8915:Adgrv1	UTSW	13	81,715,558 (GRCm39)	missense	probably damaging	1.00
R8963:Adgrv1	UTSW	13	81,567,588 (GRCm39)	missense	probably benign
R8994:Adgrv1	UTSW	13	81,553,457 (GRCm39)	frame shift	probably null
R8995:Adgrv1	UTSW	13	81,553,457 (GRCm39)	frame shift	probably null
R8996:Adgrv1	UTSW	13	81,553,457 (GRCm39)	frame shift	probably null
R8997:Adgrv1	UTSW	13	81,553,457 (GRCm39)	frame shift	probably null
R9022:Adgrv1	UTSW	13	81,303,312 (GRCm39)	missense	probably damaging	1.00
R9059:Adgrv1	UTSW	13	81,562,692 (GRCm39)	critical splice donor site	probably null
R9076:Adgrv1	UTSW	13	81,570,247 (GRCm39)	critical splice donor site	probably null
R9119:Adgrv1	UTSW	13	81,658,995 (GRCm39)	missense	probably damaging	0.97
R9137:Adgrv1	UTSW	13	81,688,133 (GRCm39)	missense	probably damaging	1.00
R9146:Adgrv1	UTSW	13	81,561,291 (GRCm39)	missense	probably benign	0.11
R9156:Adgrv1	UTSW	13	81,669,302 (GRCm39)	missense	probably benign	0.00
R9163:Adgrv1	UTSW	13	81,567,541 (GRCm39)	missense	probably benign	0.19
R9282:Adgrv1	UTSW	13	81,251,491 (GRCm39)	missense	probably damaging	1.00
R9286:Adgrv1	UTSW	13	81,594,520 (GRCm39)	missense	probably damaging	0.98
R9328:Adgrv1	UTSW	13	81,620,523 (GRCm39)	missense	probably damaging	1.00
R9329:Adgrv1	UTSW	13	81,647,241 (GRCm39)	missense	probably damaging	1.00
R9350:Adgrv1	UTSW	13	81,654,274 (GRCm39)	missense	probably damaging	1.00
R9377:Adgrv1	UTSW	13	81,705,277 (GRCm39)	missense	probably damaging	0.99
R9394:Adgrv1	UTSW	13	81,624,767 (GRCm39)	missense	possibly damaging	0.95
R9419:Adgrv1	UTSW	13	81,656,887 (GRCm39)	missense	probably benign	0.44
R9427:Adgrv1	UTSW	13	81,732,234 (GRCm39)	missense	probably benign	0.00
R9429:Adgrv1	UTSW	13	81,741,165 (GRCm39)	missense	probably damaging	0.99
R9429:Adgrv1	UTSW	13	81,567,468 (GRCm39)	missense	probably damaging	1.00
R9433:Adgrv1	UTSW	13	81,714,471 (GRCm39)	missense	probably benign	0.02
R9434:Adgrv1	UTSW	13	81,666,292 (GRCm39)	splice site	probably benign
R9513:Adgrv1	UTSW	13	81,530,472 (GRCm39)	missense	possibly damaging	0.95
R9515:Adgrv1	UTSW	13	81,691,497 (GRCm39)	missense	probably damaging	0.99
R9523:Adgrv1	UTSW	13	81,567,178 (GRCm39)	missense
R9525:Adgrv1	UTSW	13	81,593,453 (GRCm39)	missense	possibly damaging	0.77
R9576:Adgrv1	UTSW	13	81,691,608 (GRCm39)	missense	probably benign	0.06
R9612:Adgrv1	UTSW	13	81,641,082 (GRCm39)	missense	probably damaging	1.00
R9664:Adgrv1	UTSW	13	81,743,371 (GRCm39)	missense	probably damaging	1.00
R9664:Adgrv1	UTSW	13	81,670,288 (GRCm39)	missense	probably benign	0.01
R9702:Adgrv1	UTSW	13	81,684,483 (GRCm39)	missense	possibly damaging	0.80
R9717:Adgrv1	UTSW	13	81,668,900 (GRCm39)	missense	probably damaging	1.00
R9720:Adgrv1	UTSW	13	81,740,693 (GRCm39)	missense	probably damaging	1.00
X0054:Adgrv1	UTSW	13	81,707,389 (GRCm39)	missense	probably damaging	1.00
X0062:Adgrv1	UTSW	13	81,535,045 (GRCm39)	missense	probably damaging	0.99
X0067:Adgrv1	UTSW	13	81,691,511 (GRCm39)	missense	possibly damaging	0.51
Z1088:Adgrv1	UTSW	13	81,624,791 (GRCm39)	missense	probably damaging	1.00
Z1176:Adgrv1	UTSW	13	81,707,753 (GRCm39)	missense	possibly damaging	0.90
Z1177:Adgrv1	UTSW	13	81,567,375 (GRCm39)	missense	possibly damaging	0.54

Predicted Primers

PCR Primer
(F):5'- ACTTAATTCAACCACCTGTCGCAGC -3'
(R):5'- TAGATGCCAATGACGGTGCCCAAG -3'

Sequencing Primer
(F):5'- TCTCCCTATGAAGTATCTTACACAG -3'
(R):5'- GTGCCCAAGGCATGATTG -3'

Posted On

2014-04-13