Mutagenetix > Incidental Mutation

Incidental Mutation 'R7395:Adgrv1'

573772

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

045477-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7395 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

81243187-81781273 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 81707467 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Arginine at position 1313 (H1313R)

Ref Sequence

ENSEMBL: ENSMUSP00000093245 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000095585
AA Change: H1313R

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

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: H1313R

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

possibly damaging
Transcript: ENSMUST00000109565
AA Change: H593R

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000105193
Gene: ENSMUSG00000069170
AA Change: H593R

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

probably benign
Transcript: ENSMUST00000126444

SMART Domains

Protein: ENSMUSP00000123552
Gene: ENSMUSG00000069170

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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

99% (92/93)

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: 94 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3830403N18Rik	G	T	X: 55,184,140 (GRCm39)		probably null	Het
4930433I11Rik	A	T	7: 40,639,102 (GRCm39)	T13S	probably damaging	Het
Abca13	A	G	11: 9,241,658 (GRCm39)	I1174V	probably benign	Het
Acoxl	G	A	2: 127,726,336 (GRCm39)	V237M	probably damaging	Het
Adam33	A	C	2: 130,903,089 (GRCm39)	W52G	probably benign	Het
Ap3d1	T	C	10: 80,566,716 (GRCm39)	T89A	probably benign	Het
Armc8	T	C	9: 99,415,185 (GRCm39)	E165G	probably damaging	Het
Atp6v1c1	T	C	15: 38,691,949 (GRCm39)	*383Q	probably null	Het
Atp8b4	A	T	2: 126,217,614 (GRCm39)	L634Q	possibly damaging	Het
B3glct	A	G	5: 149,649,069 (GRCm39)		probably null	Het
Bhlhe40	TG	TGG	6: 108,641,818 (GRCm39)	254	probably null	Het
Bicd2	A	G	13: 49,531,706 (GRCm39)	D316G	possibly damaging	Het
Bop1	A	T	15: 76,338,041 (GRCm39)	S610T	probably damaging	Het
Car11	T	A	7: 45,350,745 (GRCm39)	Y80*	probably null	Het
Ccdc121rt2	A	T	5: 112,598,035 (GRCm39)	E194V	possibly damaging	Het
Ccdc96	T	C	5: 36,642,609 (GRCm39)	I205T	probably benign	Het
Ces2a	A	G	8: 105,466,273 (GRCm39)	E390G	probably benign	Het
Cfap54	C	A	10: 92,720,565 (GRCm39)	V2630L	unknown	Het
Chek2	G	T	5: 111,019,974 (GRCm39)		probably null	Het
Cntn3	C	T	6: 102,314,355 (GRCm39)		probably null	Het
Cpne3	A	T	4: 19,528,239 (GRCm39)	D339E	probably damaging	Het
Crocc2	C	T	1: 93,143,829 (GRCm39)	Q1403*	probably null	Het
Crppa	A	T	12: 36,551,994 (GRCm39)	I283F	possibly damaging	Het
Csnka2ip	G	A	16: 64,299,803 (GRCm39)	T187I		Het
Ctu1	A	G	7: 43,326,019 (GRCm39)	H226R	possibly damaging	Het
Cubn	G	T	2: 13,291,875 (GRCm39)	Q3317K	probably damaging	Het
Cyp17a1	A	G	19: 46,659,134 (GRCm39)	L169P	probably benign	Het
Dcc	T	A	18: 71,507,640 (GRCm39)	K911*	probably null	Het
Dcun1d2	G	A	8: 13,328,675 (GRCm39)	R75*	probably null	Het
Defb19	A	T	2: 152,421,943 (GRCm39)		probably null	Het
Dffb	A	T	4: 154,053,570 (GRCm39)	S257R	probably damaging	Het
Dip2c	A	C	13: 9,664,413 (GRCm39)	N942T	probably damaging	Het
Dnah3	T	A	7: 119,565,474 (GRCm39)	I169F		Het
Dnah3	T	C	7: 119,660,183 (GRCm39)	M830V	probably benign	Het
Dnajc5g	G	A	5: 31,269,009 (GRCm39)	S130N	possibly damaging	Het
Dscaml1	C	A	9: 45,613,703 (GRCm39)	Q939K	possibly damaging	Het
Evpl	G	C	11: 116,117,905 (GRCm39)	N761K	possibly damaging	Het
Fbxw8	A	T	5: 118,206,280 (GRCm39)	I556N	probably damaging	Het
Fry	G	T	5: 150,304,348 (GRCm39)	M579I	possibly damaging	Het
Ggt7	A	T	2: 155,337,800 (GRCm39)	M488K	probably benign	Het
Gnpnat1	T	A	14: 45,619,038 (GRCm39)	H107L	probably benign	Het
Golga2	C	A	2: 32,195,599 (GRCm39)	P798Q	possibly damaging	Het
Gpr35	G	A	1: 92,910,929 (GRCm39)	A214T	probably damaging	Het
Greb1	A	T	12: 16,759,431 (GRCm39)		probably null	Het
Hdac10	G	A	15: 89,012,487 (GRCm39)	T32I	probably benign	Het
Hkdc1	G	A	10: 62,221,478 (GRCm39)	T860I	probably damaging	Het
Icam5	C	A	9: 20,946,738 (GRCm39)	P422Q	possibly damaging	Het
Ist1	A	C	8: 110,404,159 (GRCm39)	S238A	probably benign	Het
Lrig2	T	C	3: 104,404,836 (GRCm39)	N91D	probably benign	Het
Mapt	A	C	11: 104,218,949 (GRCm39)	D352A	probably damaging	Het
Micall2	G	A	5: 139,702,124 (GRCm39)	P373L	possibly damaging	Het
Mocs1	A	G	17: 49,761,585 (GRCm39)	S560G	possibly damaging	Het
Mpo	A	G	11: 87,691,950 (GRCm39)	D461G	probably damaging	Het
Myo1a	G	T	10: 127,546,309 (GRCm39)	V271L	probably damaging	Het
Ncoa1	G	A	12: 4,345,188 (GRCm39)	P720S	not run	Het
Ncr1	T	A	7: 4,341,150 (GRCm39)	I47N	probably damaging	Het
Ndufb6	G	A	4: 40,277,730 (GRCm39)	R66C	probably damaging	Het
Obox5	A	T	7: 15,492,668 (GRCm39)	S208C	probably damaging	Het
Or10q1	T	C	19: 13,726,502 (GRCm39)	S11P	probably damaging	Het
Or2n1d	A	T	17: 38,646,755 (GRCm39)	K236*	probably null	Het
Or5p75-ps1	T	A	7: 108,107,611 (GRCm39)	F116Y	unknown	Het
Or7d9	T	A	9: 20,197,826 (GRCm39)	M285K	probably damaging	Het
Padi4	A	C	4: 140,488,983 (GRCm39)	V152G	probably damaging	Het
Pdzd7	A	T	19: 45,025,450 (GRCm39)	D348E	probably damaging	Het
Pdzph1	T	A	17: 59,186,154 (GRCm39)	K1212N	possibly damaging	Het
Piezo2	C	T	18: 63,160,634 (GRCm39)	G2341R	probably damaging	Het
Plb1	A	G	5: 32,511,028 (GRCm39)	K1298E	probably benign	Het
Prr14l	A	G	5: 32,985,982 (GRCm39)	L1171P	probably benign	Het
Rab11fip5	T	C	6: 85,318,850 (GRCm39)	T680A	probably benign	Het
Rev1	A	T	1: 38,127,146 (GRCm39)	N371K	possibly damaging	Het
Rsf1	CGGCGGCGG	CGGCGGCGGGGGCGGCGG	7: 97,229,133 (GRCm39)		probably benign	Het
Ryr2	A	G	13: 11,799,997 (GRCm39)	C917R	probably damaging	Het
Sall1	A	T	8: 89,757,549 (GRCm39)	S852T	possibly damaging	Het
Serpine2	A	G	1: 79,779,272 (GRCm39)	F296L	probably damaging	Het
Slc12a6	A	T	2: 112,182,887 (GRCm39)	N754I	probably damaging	Het
Slc39a6	A	T	18: 24,718,332 (GRCm39)	L575Q	probably damaging	Het
Smarcc2	T	A	10: 128,321,475 (GRCm39)	L890Q	probably damaging	Het
Smg5	T	A	3: 88,268,378 (GRCm39)	V1006D	probably damaging	Het
Ssh2	T	C	11: 77,283,899 (GRCm39)	V51A	probably damaging	Het
St14	T	C	9: 31,008,195 (GRCm39)	K547E	probably benign	Het
Stag1	T	G	9: 100,678,781 (GRCm39)	V234G	probably damaging	Het
Stag3	A	T	5: 138,280,207 (GRCm39)	Q24L	probably benign	Het
Stra6	T	C	9: 58,048,380 (GRCm39)	Y158H	probably damaging	Het
Tcstv1a	A	T	13: 120,355,666 (GRCm39)		probably null	Het
Tmem196	G	A	12: 119,975,002 (GRCm39)	C62Y	probably damaging	Het
Tmem265	T	A	7: 127,164,039 (GRCm39)	F84L		Het
Tph1	C	T	7: 46,306,627 (GRCm39)		probably null	Het
Ttn	A	G	2: 76,776,834 (GRCm39)	I1522T	unknown	Het
Ulk4	T	A	9: 121,084,178 (GRCm39)	Q129L	probably benign	Het
Usp17la	T	A	7: 104,510,792 (GRCm39)	S466T	probably benign	Het
Vmn2r31	A	T	7: 7,387,744 (GRCm39)	V609E	probably damaging	Het
Vmn2r52	C	T	7: 9,904,744 (GRCm39)	C365Y	probably benign	Het
Zbtb4	A	T	11: 69,666,937 (GRCm39)	T81S	possibly damaging	Het
Zfp605	A	T	5: 110,259,885 (GRCm39)		probably benign	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
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
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'- AAAGGGTCACGTGGGTTTC -3'
(R):5'- GAAGATGTCCTCTCAGAAGACGAC -3'

Sequencing Primer
(F):5'- CTCCATAGTAGATGCTACCATGACTG -3'
(R):5'- GACGACATGTCTTACATCACCAG -3'

Posted On

2019-09-13