Mutagenetix > Incidental Mutation

Incidental Mutation 'R0532:Adgrv1'

49276

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

038724-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0532 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

81243187-81781273 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 81727015 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Leucine at position 446 (V446L)

Ref Sequence

ENSEMBL: ENSMUSP00000121899 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095585] [ENSMUST00000126444] [ENSMUST00000128585] [ENSMUST00000146749]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000095585
AA Change: V446L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: V446L

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 damaging
Transcript: ENSMUST00000126444
AA Change: V446L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000123552
Gene: ENSMUSG00000069170
AA Change: V446L

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

probably damaging
Transcript: ENSMUST00000128585
AA Change: V446L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000121899
Gene: ENSMUSG00000069170
AA Change: V446L

Domain	Start	End	E-Value	Type
Blast:Calx_beta	20	116	5e-59	BLAST
Pfam:Calx-beta	132	236	4e-11	PFAM
Pfam:Calx-beta	250	362	4.1e-9	PFAM
low complexity region	531	550	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000132045

Predicted Effect

probably benign
Transcript: ENSMUST00000146749

SMART Domains

Protein: ENSMUSP00000114579
Gene: ENSMUSG00000069170

Domain	Start	End	E-Value	Type
Blast:Calx_beta	20	116	1e-60	BLAST
Pfam:Calx-beta	132	236	3.1e-11	PFAM
Pfam:Calx-beta	250	362	3.1e-9	PFAM
Blast:Calx_beta	378	413	5e-14	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156627

Meta Mutation Damage Score

0.1427

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.5%
20x: 93.2%

Validation Efficiency

100% (90/90)

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: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921524L21Rik	A	T	18: 6,638,618 (GRCm39)	E339V	possibly damaging	Het
9230009I02Rik	A	T	11: 50,982,405 (GRCm39)		noncoding transcript	Het
9230112D13Rik	A	T	14: 34,234,054 (GRCm39)	I79K	unknown	Het
Adam25	C	T	8: 41,208,987 (GRCm39)	T751I	probably benign	Het
Afap1	C	A	5: 36,125,944 (GRCm39)	A313D	possibly damaging	Het
Akap6	A	G	12: 52,934,766 (GRCm39)	T753A	probably benign	Het
Aldh16a1	G	T	7: 44,792,262 (GRCm39)	T730N	probably damaging	Het
Amfr	A	T	8: 94,725,736 (GRCm39)	M215K	probably damaging	Het
Apob	A	G	12: 8,066,188 (GRCm39)	R4386G	possibly damaging	Het
Arhgap45	A	T	10: 79,857,917 (GRCm39)	M217L	possibly damaging	Het
Baiap2l2	C	T	15: 79,168,276 (GRCm39)	E49K	possibly damaging	Het
Baz1a	C	T	12: 54,981,605 (GRCm39)	E350K	possibly damaging	Het
Bbx	A	T	16: 50,086,647 (GRCm39)	V83D	probably damaging	Het
Btaf1	T	C	19: 36,928,586 (GRCm39)		probably benign	Het
Cacna2d1	G	A	5: 16,567,271 (GRCm39)	E942K	probably benign	Het
Cad	T	C	5: 31,219,531 (GRCm39)		probably benign	Het
Ccdc96	A	G	5: 36,643,710 (GRCm39)	K572R	probably benign	Het
Cdc5l	G	A	17: 45,726,610 (GRCm39)	R321W	probably damaging	Het
Cep164	G	A	9: 45,721,124 (GRCm39)	R93*	probably null	Het
Cir1	A	G	2: 73,140,799 (GRCm39)		probably null	Het
Crocc	A	G	4: 140,757,558 (GRCm39)	S912P	possibly damaging	Het
Cwf19l2	T	C	9: 3,431,057 (GRCm39)	L463P	probably benign	Het
Cyp3a59	C	T	5: 146,033,463 (GRCm39)	Q200*	probably null	Het
Cyp4b1	G	T	4: 115,484,073 (GRCm39)	P303T	probably damaging	Het
Dcbld1	C	A	10: 52,193,173 (GRCm39)	T306K	probably benign	Het
Dgat2	A	G	7: 98,818,988 (GRCm39)	V56A	possibly damaging	Het
Dnajc16	A	C	4: 141,516,320 (GRCm39)	L16R	probably damaging	Het
Dnmt1	A	C	9: 20,829,852 (GRCm39)		probably benign	Het
Dus3l	A	G	17: 57,076,308 (GRCm39)	I528V	probably damaging	Het
Egflam	T	C	15: 7,263,718 (GRCm39)	D744G	probably benign	Het
Epb41	A	C	4: 131,706,106 (GRCm39)		probably benign	Het
Eri2	C	T	7: 119,385,206 (GRCm39)	V432I	probably benign	Het
Esyt2	A	G	12: 116,320,818 (GRCm39)		probably benign	Het
Extl3	A	T	14: 65,315,122 (GRCm39)	M20K	probably benign	Het
Fam32a	A	G	8: 72,976,063 (GRCm39)	Y103C	probably damaging	Het
Fat4	T	C	3: 39,035,870 (GRCm39)	V3174A	probably benign	Het
Fbxo40	T	A	16: 36,789,984 (GRCm39)	E375D	possibly damaging	Het
Frrs1	A	G	3: 116,676,813 (GRCm39)	T182A	probably benign	Het
Fry	A	G	5: 150,357,172 (GRCm39)		probably benign	Het
Fry	T	C	5: 150,402,226 (GRCm39)		probably benign	Het
Fsip2	A	G	2: 82,808,129 (GRCm39)	I1483V	probably benign	Het
Glra3	T	A	8: 56,578,111 (GRCm39)	D389E	probably benign	Het
Gpr3	A	T	4: 132,937,796 (GRCm39)	I292N	probably damaging	Het
Grina	T	C	15: 76,133,045 (GRCm39)	M230T	probably damaging	Het
Igkv11-125	G	A	6: 67,890,603 (GRCm39)	W16*	probably null	Het
Il18r1	T	C	1: 40,514,061 (GRCm39)	V89A	probably damaging	Het
Ino80	T	C	2: 119,212,464 (GRCm39)	E1286G	possibly damaging	Het
Iqch	G	A	9: 63,415,514 (GRCm39)		probably benign	Het
Itpr2	G	T	6: 146,013,898 (GRCm39)	Q2666K	probably damaging	Het
Kcnh3	A	G	15: 99,130,844 (GRCm39)	D487G	probably damaging	Het
Kdm1a	A	G	4: 136,288,377 (GRCm39)	L402P	probably damaging	Het
Klhl10	T	G	11: 100,337,937 (GRCm39)		probably benign	Het
Krt39	T	C	11: 99,405,617 (GRCm39)	T428A	possibly damaging	Het
Mapk3	G	A	7: 126,362,558 (GRCm39)		probably benign	Het
Med13l	T	A	5: 118,897,188 (GRCm39)	S2089T	possibly damaging	Het
Mex3c	G	A	18: 73,723,124 (GRCm39)	D406N	possibly damaging	Het
Mki67	G	A	7: 135,299,893 (GRCm39)	R1714*	probably null	Het
Mmp9	C	A	2: 164,791,740 (GRCm39)	S211*	probably null	Het
Nat8f2	G	T	6: 85,844,784 (GRCm39)	Q193K	probably benign	Het
Omt2a	C	A	9: 78,220,187 (GRCm39)	A71S	possibly damaging	Het
Or10ak11	T	G	4: 118,686,897 (GRCm39)	T247P	probably damaging	Het
Or5ac22	T	C	16: 59,134,964 (GRCm39)	K269E	probably benign	Het
Pdgfra	G	A	5: 75,331,434 (GRCm39)	V315I	probably benign	Het
Pdgfrb	A	G	18: 61,216,337 (GRCm39)	D1065G	probably damaging	Het
Pfas	A	T	11: 68,893,455 (GRCm39)		probably benign	Het
Pramel5	T	C	4: 143,999,310 (GRCm39)	E259G	probably benign	Het
Prpf6	A	G	2: 181,264,004 (GRCm39)	Y222C	possibly damaging	Het
Rbck1	C	A	2: 152,166,250 (GRCm39)	Q229H	probably damaging	Het
Rdm1	T	A	11: 101,526,661 (GRCm39)	C278S	probably benign	Het
Sall1	T	C	8: 89,759,819 (GRCm39)	D95G	probably benign	Het
Scn1a	T	A	2: 66,148,167 (GRCm39)	D1126V	probably damaging	Het
Scn4a	C	T	11: 106,221,226 (GRCm39)	G811D	probably benign	Het
Sh2b1	A	G	7: 126,071,444 (GRCm39)	I247T	probably benign	Het
Shprh	C	A	10: 11,038,556 (GRCm39)	T437K	possibly damaging	Het
Slc13a4	A	T	6: 35,264,339 (GRCm39)		probably null	Het
Slc16a1	C	A	3: 104,560,734 (GRCm39)	Y346*	probably null	Het
Slc25a38	G	T	9: 119,949,772 (GRCm39)	A163S	probably damaging	Het
Slc6a12	G	A	6: 121,333,877 (GRCm39)	V238I	probably damaging	Het
Slc8b1	C	A	5: 120,657,736 (GRCm39)	D66E	probably damaging	Het
Snapin	A	G	3: 90,396,893 (GRCm39)	L106P	probably damaging	Het
Tas2r122	G	A	6: 132,688,791 (GRCm39)	S34F	possibly damaging	Het
Tiam2	A	G	17: 3,471,921 (GRCm39)	K521R	probably damaging	Het
Tmem81	C	G	1: 132,435,567 (GRCm39)	I124M	probably damaging	Het
Ttc3	T	C	16: 94,188,189 (GRCm39)		probably benign	Het
Uba1y	T	C	Y: 820,911 (GRCm39)	F31L	probably benign	Het
Ucp3	A	G	7: 100,131,186 (GRCm39)		probably benign	Het
Vcan	T	C	13: 89,851,891 (GRCm39)	E1023G	probably damaging	Het
Vmn2r45	A	G	7: 8,474,820 (GRCm39)	I736T	probably damaging	Het
Vps36	T	C	8: 22,708,261 (GRCm39)	F342L	probably benign	Het
Zc3hc1	A	G	6: 30,374,929 (GRCm39)		probably benign	Het
Zmym4	G	A	4: 126,792,194 (GRCm39)	Q596*	probably null	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
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
R1539:Adgrv1	UTSW	13	81,652,097 (GRCm39)	splice site	probably null
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'- TTCGCATGGAGACGTGTACAGGAC -3'
(R):5'- AAGCCAAATGACAAGCCCTATGGAG -3'

Sequencing Primer
(F):5'- tgacagggtgaagcacag -3'
(R):5'- GTTGACACAATGCTGAGCTG -3'

Posted On

2013-06-12