Mutagenetix > Incidental Mutation

Incidental Mutation 'R2128:Adgrv1'

227765

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

040131-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2128 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

81095068-81633154 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 81557080 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Tyrosine at position 1537 (F1537Y)

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: F1537Y

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

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: F1537Y

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: ENSMUST00000109565
AA Change: F817Y

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000105193
Gene: ENSMUSG00000069170
AA Change: F817Y

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000125663

Predicted Effect

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156627

Meta Mutation Damage Score

0.5712

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a 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
1700113H08Rik	A	G	10: 87,230,204 (GRCm38)	E249G	possibly damaging	Het
2610028H24Rik	A	G	10: 76,457,515 (GRCm38)	M136V	possibly damaging	Het
4930523C07Rik	A	T	1: 160,075,375 (GRCm38)	K72*	probably null	Het
Abca6	A	G	11: 110,219,649 (GRCm38)	I558T	probably benign	Het
Acot10	T	C	15: 20,666,626 (GRCm38)	T10A	probably benign	Het
Adgrl4	T	A	3: 151,500,201 (GRCm38)	D233E	probably benign	Het
Akap2	A	G	4: 57,854,890 (GRCm38)	Y134C	probably benign	Het
Aqp3	T	A	4: 41,098,061 (GRCm38)	I17F	probably benign	Het
Arap1	T	A	7: 101,409,320 (GRCm38)	L1375H	probably damaging	Het
Aspm	T	C	1: 139,457,635 (GRCm38)	V339A	probably benign	Het
Atp13a3	G	A	16: 30,354,276 (GRCm38)	A261V	probably damaging	Het
Casp8ap2	T	C	4: 32,640,142 (GRCm38)	Y399H	probably benign	Het
Cept1	A	G	3: 106,512,879 (GRCm38)	V213A	probably damaging	Het
Cit	A	G	5: 115,985,507 (GRCm38)	D1469G	possibly damaging	Het
Cnga2	A	G	X: 72,007,788 (GRCm38)	Y182C	possibly damaging	Het
Cox20	A	G	1: 178,321,947 (GRCm38)	I54V	probably benign	Het
Dhx8	C	A	11: 101,738,409 (GRCm38)	D261E	probably benign	Het
Dnah2	A	T	11: 69,458,185 (GRCm38)	I2486N	probably benign	Het
Dnah5	A	G	15: 28,408,321 (GRCm38)	Q3484R	probably benign	Het
Drd1	T	C	13: 54,053,553 (GRCm38)	Y207C	probably damaging	Het
Dtl	C	T	1: 191,558,110 (GRCm38)	V222I	probably damaging	Het
Dync1h1	T	C	12: 110,640,882 (GRCm38)	Y2636H	probably damaging	Het
Endog	C	A	2: 30,172,036 (GRCm38)	D154E	probably benign	Het
Epc1	A	T	18: 6,462,954 (GRCm38)	V14E	probably damaging	Het
Ercc4	C	A	16: 13,147,934 (GRCm38)	T810K	probably damaging	Het
Fam43b	T	A	4: 138,395,988 (GRCm38)	N7I	possibly damaging	Het
Fgd1	T	C	X: 151,086,217 (GRCm38)		probably null	Het
Filip1	G	T	9: 79,819,330 (GRCm38)	T669N	probably damaging	Het
Fndc1	A	G	17: 7,778,665 (GRCm38)		probably benign	Het
Foxk1	C	A	5: 142,435,188 (GRCm38)	S189*	probably null	Het
Gatm	T	C	2: 122,600,536 (GRCm38)	N274S	probably damaging	Het
Gdf9	A	G	11: 53,437,507 (GRCm38)	Y430C	probably damaging	Het
Gga1	C	T	15: 78,888,448 (GRCm38)	P260S	probably damaging	Het
Gm11595	A	T	11: 99,772,501 (GRCm38)	C118S	unknown	Het
Gm382	G	T	X: 127,062,651 (GRCm38)	V820L	possibly damaging	Het
Gzmk	T	A	13: 113,172,014 (GRCm38)	I179F	probably damaging	Het
Hsp90b1	T	C	10: 86,695,706 (GRCm38)	D421G	probably damaging	Het
Hus1	A	G	11: 9,006,011 (GRCm38)	M174T	probably damaging	Het
Ifngr2	T	A	16: 91,562,873 (GRCm38)	Y289*	probably null	Het
Il6st	T	A	13: 112,504,175 (GRCm38)	H828Q	probably benign	Het
Impg2	T	A	16: 56,218,379 (GRCm38)	Y127N	probably damaging	Het
Irf3	T	A	7: 45,001,744 (GRCm38)	W345R	probably damaging	Het
Kif1b	G	A	4: 149,187,640 (GRCm38)	S1568L	possibly damaging	Het
Klhl42	A	G	6: 147,101,753 (GRCm38)	T342A	probably benign	Het
Kndc1	G	T	7: 139,930,112 (GRCm38)	R1289L	probably damaging	Het
Knl1	A	T	2: 119,071,819 (GRCm38)	T1334S	possibly damaging	Het
L3mbtl3	G	T	10: 26,313,868 (GRCm38)	D499E	unknown	Het
Ldhd	T	A	8: 111,627,048 (GRCm38)	M478L	probably benign	Het
Loxl4	C	G	19: 42,603,963 (GRCm38)	E385D	probably damaging	Het
Lrriq1	G	A	10: 103,214,857 (GRCm38)	T678I	probably benign	Het
Macf1	T	A	4: 123,492,774 (GRCm38)	I1017F	probably benign	Het
Madcam1	A	G	10: 79,665,572 (GRCm38)	E157G	possibly damaging	Het
Mamdc4	T	C	2: 25,569,258 (GRCm38)	D195G	probably damaging	Het
Mctp1	A	G	13: 76,824,822 (GRCm38)	D648G	probably damaging	Het
Mycbp2	T	C	14: 103,201,230 (GRCm38)	M2072V	probably benign	Het
Nck1	A	G	9: 100,497,547 (GRCm38)		probably null	Het
Ndufaf4	G	T	4: 24,898,608 (GRCm38)	D55Y	probably damaging	Het
Nek11	A	T	9: 105,300,361 (GRCm38)	D230E	probably benign	Het
Nit2	T	C	16: 57,161,196 (GRCm38)	K67E	possibly damaging	Het
Olfr2	T	C	7: 107,001,248 (GRCm38)	D204G	probably damaging	Het
Olfr290	T	C	7: 84,916,493 (GRCm38)	F238S	probably damaging	Het
Olfr527	C	T	7: 140,336,429 (GRCm38)	T189M	probably damaging	Het
Olfr802	A	T	10: 129,682,532 (GRCm38)	V69E	possibly damaging	Het
Pccb	G	C	9: 100,985,831 (GRCm38)	D347E	probably damaging	Het
Plcl1	T	A	1: 55,697,838 (GRCm38)	F779L	probably damaging	Het
Prune2	C	A	19: 17,122,422 (GRCm38)	D1763E	probably benign	Het
Pwwp2a	A	G	11: 43,705,318 (GRCm38)	S437G	probably benign	Het
Rabgap1l	A	T	1: 160,738,957 (GRCm38)	D90E	probably benign	Het
Rapgef4	T	A	2: 72,226,553 (GRCm38)	I552N	possibly damaging	Het
Scn7a	A	T	2: 66,697,986 (GRCm38)	I720K	probably damaging	Het
Scn9a	T	A	2: 66,526,654 (GRCm38)	N1101I	probably damaging	Het
Siglec1	A	T	2: 131,080,497 (GRCm38)	Y553N	probably damaging	Het
Slc22a23	A	G	13: 34,203,970 (GRCm38)	L381P	possibly damaging	Het
Slc7a11	T	A	3: 50,384,109 (GRCm38)	T284S	probably damaging	Het
Slc8a2	T	A	7: 16,140,492 (GRCm38)		probably null	Het
Snx29	T	A	16: 11,400,971 (GRCm38)	S224T	probably damaging	Het
Stox1	T	C	10: 62,664,535 (GRCm38)	T749A	probably benign	Het
Tg	A	G	15: 66,694,894 (GRCm38)	I1264V	probably benign	Het
Tmem110	T	C	14: 30,866,624 (GRCm38)	Y103H	probably damaging	Het
Top2a	A	C	11: 99,009,807 (GRCm38)	V609G	probably damaging	Het
Trmt44	G	A	5: 35,574,832 (GRCm38)	P72S	probably benign	Het
Ttll3	G	C	6: 113,412,934 (GRCm38)	S760T	probably benign	Het
Ttn	G	A	2: 76,833,897 (GRCm38)		probably benign	Het
Ttn	T	C	2: 76,748,678 (GRCm38)	D23957G	probably damaging	Het
Ubxn1	T	G	19: 8,872,070 (GRCm38)	V59G	probably benign	Het
Ubxn4	T	C	1: 128,244,510 (GRCm38)	S14P	probably benign	Het
Uso1	T	A	5: 92,195,370 (GRCm38)	M771K	probably benign	Het
Utp20	A	G	10: 88,814,055 (GRCm38)	F431S	probably damaging	Het
Vmn1r206	T	C	13: 22,620,612 (GRCm38)	S142G	probably benign	Het
Vmn2r19	A	G	6: 123,308,330 (GRCm38)		probably null	Het
Vps36	G	T	8: 22,218,289 (GRCm38)		probably null	Het
Wnt3	A	G	11: 103,812,648 (GRCm38)	H319R	possibly damaging	Het
Zbtb26	G	T	2: 37,436,551 (GRCm38)	Q158K	probably benign	Het
Zfp648	T	C	1: 154,204,607 (GRCm38)	S171P	probably benign	Het

Other mutations in Adgrv1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Adgrv1	APN	13	81,405,408 (GRCm38)	critical splice acceptor site	probably null
IGL00090:Adgrv1	APN	13	81,578,101 (GRCm38)	missense	probably damaging	1.00
IGL00091:Adgrv1	APN	13	81,578,101 (GRCm38)	missense	probably damaging	1.00
IGL00332:Adgrv1	APN	13	81,472,877 (GRCm38)	splice site	probably benign
IGL00471:Adgrv1	APN	13	81,509,542 (GRCm38)	missense	probably damaging	0.99
IGL00476:Adgrv1	APN	13	81,489,074 (GRCm38)	missense	probably damaging	0.98
IGL00508:Adgrv1	APN	13	81,506,187 (GRCm38)	missense	probably damaging	1.00
IGL00727:Adgrv1	APN	13	81,524,684 (GRCm38)	missense	probably damaging	0.98
IGL00781:Adgrv1	APN	13	81,578,230 (GRCm38)	missense	probably benign	0.19
IGL00816:Adgrv1	APN	13	81,397,203 (GRCm38)	missense	probably benign	0.01
IGL00844:Adgrv1	APN	13	81,540,119 (GRCm38)	missense	probably damaging	1.00
IGL00923:Adgrv1	APN	13	81,382,291 (GRCm38)	missense	probably damaging	0.99
IGL01113:Adgrv1	APN	13	81,489,028 (GRCm38)	missense	probably benign	0.00
IGL01143:Adgrv1	APN	13	81,419,351 (GRCm38)	missense	probably benign	0.00
IGL01151:Adgrv1	APN	13	81,405,399 (GRCm38)	missense	probably benign	0.00
IGL01153:Adgrv1	APN	13	81,419,128 (GRCm38)	missense	probably benign	0.01
IGL01363:Adgrv1	APN	13	81,557,065 (GRCm38)	missense	probably damaging	1.00
IGL01419:Adgrv1	APN	13	81,557,158 (GRCm38)	missense	probably damaging	0.99
IGL01545:Adgrv1	APN	13	81,466,184 (GRCm38)	missense	possibly damaging	0.46
IGL01701:Adgrv1	APN	13	81,419,631 (GRCm38)	missense	possibly damaging	0.55
IGL01796:Adgrv1	APN	13	81,567,342 (GRCm38)	missense	probably benign	0.01
IGL01816:Adgrv1	APN	13	81,529,049 (GRCm38)	missense	probably benign	0.00
IGL01871:Adgrv1	APN	13	81,472,394 (GRCm38)	critical splice donor site	probably null
IGL01955:Adgrv1	APN	13	81,182,783 (GRCm38)	missense	probably damaging	1.00
IGL01956:Adgrv1	APN	13	81,446,430 (GRCm38)	missense	possibly damaging	0.63
IGL01988:Adgrv1	APN	13	81,557,309 (GRCm38)	missense	probably damaging	0.99
IGL01990:Adgrv1	APN	13	81,556,996 (GRCm38)	missense	probably damaging	1.00
IGL02007:Adgrv1	APN	13	81,568,743 (GRCm38)	splice site	probably benign
IGL02016:Adgrv1	APN	13	81,397,453 (GRCm38)	missense	probably damaging	1.00
IGL02095:Adgrv1	APN	13	81,579,790 (GRCm38)	missense	possibly damaging	0.63
IGL02174:Adgrv1	APN	13	81,427,664 (GRCm38)	missense	probably benign	0.34
IGL02270:Adgrv1	APN	13	81,559,195 (GRCm38)	splice site	probably null
IGL02328:Adgrv1	APN	13	81,578,175 (GRCm38)	missense	probably damaging	1.00
IGL02350:Adgrv1	APN	13	81,270,855 (GRCm38)	missense	probably benign	0.00
IGL02357:Adgrv1	APN	13	81,270,855 (GRCm38)	missense	probably benign	0.00
IGL02373:Adgrv1	APN	13	81,459,713 (GRCm38)	missense	possibly damaging	0.90
IGL02402:Adgrv1	APN	13	81,559,424 (GRCm38)	missense	probably benign	0.18
IGL02407:Adgrv1	APN	13	81,479,670 (GRCm38)	missense	probably damaging	1.00
IGL02508:Adgrv1	APN	13	81,435,556 (GRCm38)	splice site	probably benign
IGL02603:Adgrv1	APN	13	81,488,952 (GRCm38)	missense	possibly damaging	0.93
IGL02648:Adgrv1	APN	13	81,511,619 (GRCm38)	missense	probably benign	0.35
IGL02720:Adgrv1	APN	13	81,578,872 (GRCm38)	missense	probably damaging	0.99
IGL02870:Adgrv1	APN	13	81,563,732 (GRCm38)	missense	probably benign	0.13
IGL02896:Adgrv1	APN	13	81,520,739 (GRCm38)	missense	probably damaging	1.00
IGL02931:Adgrv1	APN	13	81,579,714 (GRCm38)	missense	probably damaging	1.00
IGL02952:Adgrv1	APN	13	81,433,636 (GRCm38)	missense	probably benign	0.00
IGL02961:Adgrv1	APN	13	81,523,612 (GRCm38)	missense	probably damaging	1.00
IGL02999:Adgrv1	APN	13	81,578,854 (GRCm38)	missense	probably benign	0.12
IGL03067:Adgrv1	APN	13	81,442,480 (GRCm38)	missense	probably damaging	1.00
IGL03106:Adgrv1	APN	13	81,472,899 (GRCm38)	missense	probably benign	0.00
IGL03108:Adgrv1	APN	13	81,559,529 (GRCm38)	missense	probably damaging	1.00
IGL03119:Adgrv1	APN	13	81,433,700 (GRCm38)	missense	probably benign	0.02
IGL03119:Adgrv1	APN	13	81,382,373 (GRCm38)	missense	probably damaging	1.00
IGL03169:Adgrv1	APN	13	81,503,900 (GRCm38)	missense	probably damaging	1.00
IGL03186:Adgrv1	APN	13	81,433,618 (GRCm38)	missense	possibly damaging	0.80
IGL03196:Adgrv1	APN	13	81,446,478 (GRCm38)	missense	probably benign	0.02
IGL03207:Adgrv1	APN	13	81,106,898 (GRCm38)	splice site	probably null
IGL03343:Adgrv1	APN	13	81,283,388 (GRCm38)	missense	probably damaging	1.00
IGL03348:Adgrv1	APN	13	81,499,058 (GRCm38)	missense	possibly damaging	0.54
IGL03349:Adgrv1	APN	13	81,481,336 (GRCm38)	missense	probably benign	0.09
IGL03373:Adgrv1	APN	13	81,563,632 (GRCm38)	missense	probably damaging	0.99
IGL03381:Adgrv1	APN	13	81,517,967 (GRCm38)	missense	probably damaging	0.99
abetting	UTSW	13	81,579,560 (GRCm38)	missense	probably damaging	1.00
beatle	UTSW	13	81,579,594 (GRCm38)	nonsense	probably null
Escape	UTSW	13	81,435,705 (GRCm38)	missense	probably benign	0.02
lento	UTSW	13	81,270,897 (GRCm38)	missense	probably damaging	1.00
Metronome	UTSW	13	81,435,559 (GRCm38)	critical splice donor site	probably null
Murderous	UTSW	13	81,103,324 (GRCm38)	missense	possibly damaging	0.94
Nome	UTSW	13	81,391,767 (GRCm38)	missense	probably benign	0.00
Propulsion	UTSW	13	81,475,047 (GRCm38)	missense	probably benign	0.06
revulsion	UTSW	13	81,595,182 (GRCm38)	missense	probably damaging	1.00
Saturnv	UTSW	13	81,531,676 (GRCm38)	missense	probably damaging	1.00
Thrust	UTSW	13	81,374,256 (GRCm38)	missense	probably benign	0.01
Velocity	UTSW	13	81,397,354 (GRCm38)	missense	probably benign	0.00
Wilting	UTSW	13	81,492,501 (GRCm38)	missense	probably benign	0.02
Withering	UTSW	13	81,494,657 (GRCm38)	missense	probably damaging	1.00
F2404:Adgrv1	UTSW	13	81,420,006 (GRCm38)	missense	probably benign	0.13
G1patch:Adgrv1	UTSW	13	81,493,210 (GRCm38)	missense	probably damaging	1.00
G1patch:Adgrv1	UTSW	13	81,437,557 (GRCm38)	missense	probably damaging	0.99
I2288:Adgrv1	UTSW	13	81,437,524 (GRCm38)	missense	probably damaging	1.00
I2289:Adgrv1	UTSW	13	81,437,524 (GRCm38)	missense	probably damaging	1.00
PIT4377001:Adgrv1	UTSW	13	81,528,985 (GRCm38)	missense	probably damaging	1.00
PIT4504001:Adgrv1	UTSW	13	81,559,352 (GRCm38)	missense	probably damaging	0.99
R0017:Adgrv1	UTSW	13	81,578,946 (GRCm38)	missense	probably benign	0.13
R0017:Adgrv1	UTSW	13	81,578,946 (GRCm38)	missense	probably benign	0.13
R0058:Adgrv1	UTSW	13	81,182,672 (GRCm38)	missense	possibly damaging	0.65
R0058:Adgrv1	UTSW	13	81,182,672 (GRCm38)	missense	possibly damaging	0.65
R0083:Adgrv1	UTSW	13	81,578,404 (GRCm38)	unclassified	probably benign
R0087:Adgrv1	UTSW	13	81,386,951 (GRCm38)	missense	probably damaging	1.00
R0108:Adgrv1	UTSW	13	81,578,404 (GRCm38)	unclassified	probably benign
R0131:Adgrv1	UTSW	13	81,502,995 (GRCm38)	unclassified	probably benign
R0218:Adgrv1	UTSW	13	81,106,898 (GRCm38)	splice site	probably null
R0325:Adgrv1	UTSW	13	81,540,015 (GRCm38)	missense	probably damaging	1.00
R0326:Adgrv1	UTSW	13	81,474,993 (GRCm38)	missense	possibly damaging	0.46
R0395:Adgrv1	UTSW	13	81,385,953 (GRCm38)	missense	probably benign	0.00
R0441:Adgrv1	UTSW	13	81,397,226 (GRCm38)	nonsense	probably null
R0466:Adgrv1	UTSW	13	81,566,296 (GRCm38)	missense	probably benign	0.00
R0487:Adgrv1	UTSW	13	81,489,035 (GRCm38)	missense	probably damaging	1.00
R0501:Adgrv1	UTSW	13	81,559,150 (GRCm38)	missense	probably damaging	1.00
R0522:Adgrv1	UTSW	13	81,528,442 (GRCm38)	splice site	probably benign
R0532:Adgrv1	UTSW	13	81,578,896 (GRCm38)	missense	probably damaging	1.00
R0542:Adgrv1	UTSW	13	81,573,318 (GRCm38)	missense	probably damaging	1.00
R0681:Adgrv1	UTSW	13	81,528,530 (GRCm38)	missense	probably damaging	1.00
R0689:Adgrv1	UTSW	13	81,475,105 (GRCm38)	missense	possibly damaging	0.47
R0732:Adgrv1	UTSW	13	81,503,004 (GRCm38)	missense	possibly damaging	0.86
R0746:Adgrv1	UTSW	13	81,570,556 (GRCm38)	missense	probably benign	0.10
R0763:Adgrv1	UTSW	13	81,499,125 (GRCm38)	missense	probably damaging	0.98
R0846:Adgrv1	UTSW	13	81,479,742 (GRCm38)	nonsense	probably null
R0962:Adgrv1	UTSW	13	81,405,346 (GRCm38)	missense	probably benign	0.01
R1146:Adgrv1	UTSW	13	81,531,676 (GRCm38)	missense	probably damaging	1.00
R1146:Adgrv1	UTSW	13	81,531,676 (GRCm38)	missense	probably damaging	1.00
R1172:Adgrv1	UTSW	13	81,557,063 (GRCm38)	missense	probably damaging	0.98
R1178:Adgrv1	UTSW	13	81,440,037 (GRCm38)	splice site	probably benign
R1310:Adgrv1	UTSW	13	81,566,377 (GRCm38)	missense	probably benign	0.09
R1386:Adgrv1	UTSW	13	81,528,865 (GRCm38)	missense	probably benign	0.17
R1387:Adgrv1	UTSW	13	81,493,176 (GRCm38)	missense	possibly damaging	0.62
R1395:Adgrv1	UTSW	13	81,386,788 (GRCm38)	missense	probably benign	0.05
R1412:Adgrv1	UTSW	13	81,095,450 (GRCm38)	missense	probably damaging	1.00
R1448:Adgrv1	UTSW	13	81,433,513 (GRCm38)	missense	probably benign	0.08
R1470:Adgrv1	UTSW	13	81,382,298 (GRCm38)	missense	probably benign	0.03
R1470:Adgrv1	UTSW	13	81,382,298 (GRCm38)	missense	probably benign	0.03
R1485:Adgrv1	UTSW	13	81,579,619 (GRCm38)	missense	probably damaging	1.00
R1507:Adgrv1	UTSW	13	81,472,580 (GRCm38)	critical splice acceptor site	probably null
R1513:Adgrv1	UTSW	13	81,556,957 (GRCm38)	missense	probably damaging	1.00
R1513:Adgrv1	UTSW	13	81,593,048 (GRCm38)	missense	probably damaging	1.00
R1539:Adgrv1	UTSW	13	81,503,978 (GRCm38)	splice site	probably null
R1579:Adgrv1	UTSW	13	81,563,779 (GRCm38)	missense	probably damaging	1.00
R1580:Adgrv1	UTSW	13	81,466,160 (GRCm38)	critical splice donor site	probably null
R1611:Adgrv1	UTSW	13	81,559,117 (GRCm38)	missense	probably damaging	1.00
R1615:Adgrv1	UTSW	13	81,424,288 (GRCm38)	missense	probably benign	0.41
R1651:Adgrv1	UTSW	13	81,487,853 (GRCm38)	missense	probably benign	0.19
R1660:Adgrv1	UTSW	13	81,476,631 (GRCm38)	missense	probably benign	0.00
R1679:Adgrv1	UTSW	13	81,559,552 (GRCm38)	missense	probably damaging	1.00
R1709:Adgrv1	UTSW	13	81,593,060 (GRCm38)	missense	probably damaging	1.00
R1735:Adgrv1	UTSW	13	81,487,947 (GRCm38)	missense	possibly damaging	0.62
R1762:Adgrv1	UTSW	13	81,506,146 (GRCm38)	missense	probably benign	0.08
R1830:Adgrv1	UTSW	13	81,489,077 (GRCm38)	missense	possibly damaging	0.65
R1836:Adgrv1	UTSW	13	81,504,113 (GRCm38)	missense	probably benign	0.01
R1843:Adgrv1	UTSW	13	81,544,533 (GRCm38)	missense	probably damaging	1.00
R1863:Adgrv1	UTSW	13	81,563,566 (GRCm38)	missense	probably damaging	1.00
R1895:Adgrv1	UTSW	13	81,374,249 (GRCm38)	missense	probably damaging	1.00
R1907:Adgrv1	UTSW	13	81,592,551 (GRCm38)	splice site	probably benign
R1928:Adgrv1	UTSW	13	81,520,786 (GRCm38)	missense	probably benign	0.00
R1938:Adgrv1	UTSW	13	81,391,757 (GRCm38)	missense	probably damaging	0.99
R1944:Adgrv1	UTSW	13	81,510,911 (GRCm38)	missense	probably damaging	1.00
R1946:Adgrv1	UTSW	13	81,374,249 (GRCm38)	missense	probably damaging	1.00
R1984:Adgrv1	UTSW	13	81,523,749 (GRCm38)	missense	probably damaging	1.00
R2027:Adgrv1	UTSW	13	81,595,182 (GRCm38)	missense	probably damaging	1.00
R2063:Adgrv1	UTSW	13	81,561,469 (GRCm38)	missense	possibly damaging	0.81
R2116:Adgrv1	UTSW	13	81,529,013 (GRCm38)	missense	probably benign	0.11
R2117:Adgrv1	UTSW	13	81,492,537 (GRCm38)	missense	probably benign	0.00
R2125:Adgrv1	UTSW	13	81,419,950 (GRCm38)	missense	probably benign	0.02
R2125:Adgrv1	UTSW	13	81,419,535 (GRCm38)	missense	probably benign	0.00
R2127:Adgrv1	UTSW	13	81,557,080 (GRCm38)	missense	probably damaging	1.00
R2129:Adgrv1	UTSW	13	81,557,080 (GRCm38)	missense	probably damaging	1.00
R2130:Adgrv1	UTSW	13	81,581,727 (GRCm38)	missense	possibly damaging	0.61
R2135:Adgrv1	UTSW	13	81,524,557 (GRCm38)	critical splice donor site	probably null
R2138:Adgrv1	UTSW	13	81,445,320 (GRCm38)	missense	probably benign	0.00
R2166:Adgrv1	UTSW	13	81,568,643 (GRCm38)	missense	probably damaging	1.00
R2171:Adgrv1	UTSW	13	81,270,918 (GRCm38)	missense	probably damaging	1.00
R2191:Adgrv1	UTSW	13	81,566,290 (GRCm38)	missense	possibly damaging	0.90
R2256:Adgrv1	UTSW	13	81,506,140 (GRCm38)	missense	probably benign
R2260:Adgrv1	UTSW	13	81,568,374 (GRCm38)	missense	probably damaging	0.97
R2323:Adgrv1	UTSW	13	81,595,179 (GRCm38)	missense	probably damaging	1.00
R2432:Adgrv1	UTSW	13	81,540,132 (GRCm38)	frame shift	probably null
R2910:Adgrv1	UTSW	13	81,557,119 (GRCm38)	missense	possibly damaging	0.61
R2920:Adgrv1	UTSW	13	81,448,865 (GRCm38)	missense	probably benign	0.01
R2989:Adgrv1	UTSW	13	81,581,747 (GRCm38)	missense	probably damaging	1.00
R3402:Adgrv1	UTSW	13	81,543,542 (GRCm38)	missense	probably damaging	1.00
R3692:Adgrv1	UTSW	13	81,524,600 (GRCm38)	missense	possibly damaging	0.91
R3711:Adgrv1	UTSW	13	81,419,475 (GRCm38)	missense	probably benign	0.02
R3732:Adgrv1	UTSW	13	81,556,956 (GRCm38)	missense	probably damaging	1.00
R3732:Adgrv1	UTSW	13	81,556,956 (GRCm38)	missense	probably damaging	1.00
R3733:Adgrv1	UTSW	13	81,556,956 (GRCm38)	missense	probably damaging	1.00
R3773:Adgrv1	UTSW	13	81,499,043 (GRCm38)	missense	probably damaging	0.98
R3791:Adgrv1	UTSW	13	81,593,102 (GRCm38)	missense	probably damaging	1.00
R3794:Adgrv1	UTSW	13	81,283,367 (GRCm38)	start codon destroyed	probably damaging	1.00
R3848:Adgrv1	UTSW	13	81,440,072 (GRCm38)	missense	probably damaging	0.97
R3880:Adgrv1	UTSW	13	81,435,705 (GRCm38)	missense	probably benign	0.02
R3925:Adgrv1	UTSW	13	81,578,772 (GRCm38)	missense	possibly damaging	0.89
R3934:Adgrv1	UTSW	13	81,475,047 (GRCm38)	missense	probably benign	0.06
R3942:Adgrv1	UTSW	13	81,182,789 (GRCm38)	missense	probably damaging	1.00
R4002:Adgrv1	UTSW	13	81,540,132 (GRCm38)	frame shift	probably null
R4003:Adgrv1	UTSW	13	81,540,132 (GRCm38)	frame shift	probably null
R4194:Adgrv1	UTSW	13	81,498,996 (GRCm38)	missense	probably damaging	0.98
R4308:Adgrv1	UTSW	13	81,440,192 (GRCm38)	missense	probably damaging	0.96
R4368:Adgrv1	UTSW	13	81,492,910 (GRCm38)	missense	unknown
R4388:Adgrv1	UTSW	13	81,581,709 (GRCm38)	missense	probably damaging	0.98
R4421:Adgrv1	UTSW	13	81,566,302 (GRCm38)	missense	probably damaging	1.00
R4468:Adgrv1	UTSW	13	81,374,256 (GRCm38)	missense	probably benign	0.01
R4483:Adgrv1	UTSW	13	81,419,230 (GRCm38)	missense	probably benign	0.01
R4487:Adgrv1	UTSW	13	81,440,066 (GRCm38)	missense	probably damaging	0.99
R4566:Adgrv1	UTSW	13	81,419,808 (GRCm38)	missense	probably damaging	1.00
R4615:Adgrv1	UTSW	13	81,494,569 (GRCm38)	splice site	probably null
R4647:Adgrv1	UTSW	13	81,528,795 (GRCm38)	nonsense	probably null
R4657:Adgrv1	UTSW	13	81,405,364 (GRCm38)	missense	probably benign	0.01
R4723:Adgrv1	UTSW	13	81,433,525 (GRCm38)	missense	probably benign	0.02
R4765:Adgrv1	UTSW	13	81,106,919 (GRCm38)	missense	probably damaging	0.99
R4783:Adgrv1	UTSW	13	81,095,445 (GRCm38)	missense	probably damaging	0.99
R4796:Adgrv1	UTSW	13	81,155,231 (GRCm38)	nonsense	probably null
R4816:Adgrv1	UTSW	13	81,528,674 (GRCm38)	missense	probably damaging	1.00
R4833:Adgrv1	UTSW	13	81,560,844 (GRCm38)	missense	possibly damaging	0.81
R4841:Adgrv1	UTSW	13	81,503,001 (GRCm38)	critical splice donor site	probably null
R4871:Adgrv1	UTSW	13	81,533,122 (GRCm38)	intron	probably benign
R4897:Adgrv1	UTSW	13	81,561,585 (GRCm38)	splice site	probably null
R4906:Adgrv1	UTSW	13	81,270,738 (GRCm38)	splice site	probably null
R4917:Adgrv1	UTSW	13	81,510,877 (GRCm38)	missense	probably benign	0.30
R4996:Adgrv1	UTSW	13	81,578,734 (GRCm38)	missense	probably benign	0.01
R5030:Adgrv1	UTSW	13	81,459,829 (GRCm38)	missense	probably benign	0.43
R5044:Adgrv1	UTSW	13	81,488,931 (GRCm38)	missense	probably benign	0.01
R5052:Adgrv1	UTSW	13	81,528,821 (GRCm38)	missense	probably damaging	0.97
R5093:Adgrv1	UTSW	13	81,592,585 (GRCm38)	missense	probably damaging	1.00
R5095:Adgrv1	UTSW	13	81,095,487 (GRCm38)	missense	probably benign	0.00
R5119:Adgrv1	UTSW	13	81,419,427 (GRCm38)	missense	possibly damaging	0.93
R5133:Adgrv1	UTSW	13	81,439,441 (GRCm38)	missense	probably damaging	1.00
R5141:Adgrv1	UTSW	13	81,270,918 (GRCm38)	missense	probably damaging	1.00
R5164:Adgrv1	UTSW	13	81,435,674 (GRCm38)	missense	probably benign	0.00
R5180:Adgrv1	UTSW	13	81,283,416 (GRCm38)	start gained	probably benign
R5203:Adgrv1	UTSW	13	81,510,905 (GRCm38)	missense	possibly damaging	0.91
R5241:Adgrv1	UTSW	13	81,488,929 (GRCm38)	nonsense	probably null
R5280:Adgrv1	UTSW	13	81,397,465 (GRCm38)	missense	possibly damaging	0.95
R5289:Adgrv1	UTSW	13	81,521,084 (GRCm38)	missense	probably benign	0.04
R5304:Adgrv1	UTSW	13	81,578,253 (GRCm38)	missense	possibly damaging	0.93
R5310:Adgrv1	UTSW	13	81,476,690 (GRCm38)	missense	possibly damaging	0.95
R5338:Adgrv1	UTSW	13	81,529,046 (GRCm38)	missense	possibly damaging	0.80
R5352:Adgrv1	UTSW	13	81,494,657 (GRCm38)	missense	probably damaging	1.00
R5402:Adgrv1	UTSW	13	81,459,715 (GRCm38)	missense	probably benign	0.25
R5418:Adgrv1	UTSW	13	81,419,308 (GRCm38)	missense	probably benign	0.01
R5460:Adgrv1	UTSW	13	81,424,258 (GRCm38)	missense	possibly damaging	0.95
R5510:Adgrv1	UTSW	13	81,445,244 (GRCm38)	missense	probably damaging	1.00
R5521:Adgrv1	UTSW	13	81,419,389 (GRCm38)	missense	probably benign	0.01
R5538:Adgrv1	UTSW	13	81,433,689 (GRCm38)	missense	probably benign	0.02
R5561:Adgrv1	UTSW	13	81,476,564 (GRCm38)	missense	probably damaging	0.99
R5584:Adgrv1	UTSW	13	81,405,267 (GRCm38)	missense	probably damaging	1.00
R5608:Adgrv1	UTSW	13	81,155,276 (GRCm38)	missense	probably damaging	1.00
R5610:Adgrv1	UTSW	13	81,521,117 (GRCm38)	missense	probably damaging	1.00
R5619:Adgrv1	UTSW	13	81,472,500 (GRCm38)	missense	probably damaging	1.00
R5751:Adgrv1	UTSW	13	81,522,236 (GRCm38)	missense	probably damaging	1.00
R5832:Adgrv1	UTSW	13	81,103,302 (GRCm38)	missense	possibly damaging	0.95
R5885:Adgrv1	UTSW	13	81,424,271 (GRCm38)	missense	probably benign	0.15
R5930:Adgrv1	UTSW	13	81,397,451 (GRCm38)	missense	probably benign	0.06
R5937:Adgrv1	UTSW	13	81,107,075 (GRCm38)	missense	probably damaging	0.96
R5943:Adgrv1	UTSW	13	81,386,866 (GRCm38)	missense	probably damaging	0.98
R5951:Adgrv1	UTSW	13	81,442,501 (GRCm38)	missense	probably damaging	1.00
R5977:Adgrv1	UTSW	13	81,435,559 (GRCm38)	critical splice donor site	probably null
R5995:Adgrv1	UTSW	13	81,466,259 (GRCm38)	missense	probably benign	0.03
R6017:Adgrv1	UTSW	13	81,397,423 (GRCm38)	nonsense	probably null
R6024:Adgrv1	UTSW	13	81,476,505 (GRCm38)	missense	probably benign	0.26
R6049:Adgrv1	UTSW	13	81,397,354 (GRCm38)	missense	probably benign	0.00
R6108:Adgrv1	UTSW	13	81,391,695 (GRCm38)	missense	probably damaging	0.99
R6130:Adgrv1	UTSW	13	81,427,745 (GRCm38)	missense	probably damaging	0.99
R6132:Adgrv1	UTSW	13	81,506,076 (GRCm38)	missense	probably benign	0.04
R6149:Adgrv1	UTSW	13	81,182,774 (GRCm38)	missense	probably damaging	1.00
R6169:Adgrv1	UTSW	13	81,419,259 (GRCm38)	missense	probably benign	0.00
R6175:Adgrv1	UTSW	13	81,386,005 (GRCm38)	missense	probably damaging	1.00
R6184:Adgrv1	UTSW	13	81,433,838 (GRCm38)	missense	probably benign	0.01
R6190:Adgrv1	UTSW	13	81,524,779 (GRCm38)	splice site	probably null
R6190:Adgrv1	UTSW	13	81,459,763 (GRCm38)	splice site	probably null
R6215:Adgrv1	UTSW	13	81,579,594 (GRCm38)	nonsense	probably null
R6216:Adgrv1	UTSW	13	81,524,471 (GRCm38)	splice site	probably null
R6238:Adgrv1	UTSW	13	81,466,283 (GRCm38)	missense	probably benign	0.07
R6244:Adgrv1	UTSW	13	81,106,931 (GRCm38)	missense	probably damaging	1.00
R6298:Adgrv1	UTSW	13	81,391,767 (GRCm38)	missense	probably benign	0.00
R6316:Adgrv1	UTSW	13	81,499,068 (GRCm38)	missense	possibly damaging	0.63
R6336:Adgrv1	UTSW	13	81,385,981 (GRCm38)	missense	probably benign	0.09
R6358:Adgrv1	UTSW	13	81,414,583 (GRCm38)	missense	probably damaging	0.99
R6421:Adgrv1	UTSW	13	81,508,736 (GRCm38)	missense	possibly damaging	0.69
R6466:Adgrv1	UTSW	13	81,575,101 (GRCm38)	splice site	probably null
R6467:Adgrv1	UTSW	13	81,444,538 (GRCm38)	missense	probably benign	0.01
R6510:Adgrv1	UTSW	13	81,559,490 (GRCm38)	missense	possibly damaging	0.88
R6519:Adgrv1	UTSW	13	81,567,343 (GRCm38)	missense	probably benign	0.01
R6521:Adgrv1	UTSW	13	81,433,652 (GRCm38)	missense	probably damaging	1.00
R6598:Adgrv1	UTSW	13	81,506,179 (GRCm38)	missense	probably damaging	1.00
R6605:Adgrv1	UTSW	13	81,487,962 (GRCm38)	missense	possibly damaging	0.80
R6626:Adgrv1	UTSW	13	81,518,126 (GRCm38)	missense	probably damaging	1.00
R6633:Adgrv1	UTSW	13	81,568,643 (GRCm38)	missense	probably damaging	1.00
R6721:Adgrv1	UTSW	13	81,481,515 (GRCm38)	missense	probably benign	0.00
R6725:Adgrv1	UTSW	13	81,437,557 (GRCm38)	missense	probably damaging	0.99
R6725:Adgrv1	UTSW	13	81,493,210 (GRCm38)	missense	probably damaging	1.00
R6796:Adgrv1	UTSW	13	81,472,478 (GRCm38)	missense	probably damaging	1.00
R6809:Adgrv1	UTSW	13	81,472,953 (GRCm38)	missense	probably benign	0.01
R6823:Adgrv1	UTSW	13	81,557,081 (GRCm38)	missense	probably damaging	1.00
R6876:Adgrv1	UTSW	13	81,155,154 (GRCm38)	critical splice donor site	probably null
R6878:Adgrv1	UTSW	13	81,433,494 (GRCm38)	missense	probably benign	0.06
R6887:Adgrv1	UTSW	13	81,528,701 (GRCm38)	missense	probably benign	0.01
R6888:Adgrv1	UTSW	13	81,508,669 (GRCm38)	missense	probably damaging	1.00
R6957:Adgrv1	UTSW	13	81,567,490 (GRCm38)	missense	probably benign	0.00
R6976:Adgrv1	UTSW	13	81,520,997 (GRCm38)	missense	probably damaging	1.00
R7003:Adgrv1	UTSW	13	81,522,104 (GRCm38)	critical splice donor site	probably null
R7007:Adgrv1	UTSW	13	81,536,364 (GRCm38)	missense	possibly damaging	0.80
R7073:Adgrv1	UTSW	13	81,561,474 (GRCm38)	missense	probably damaging	1.00
R7100:Adgrv1	UTSW	13	81,270,897 (GRCm38)	missense	probably damaging	1.00
R7107:Adgrv1	UTSW	13	81,578,142 (GRCm38)	missense	probably benign	0.13
R7123:Adgrv1	UTSW	13	81,592,574 (GRCm38)	missense	probably damaging	1.00
R7141:Adgrv1	UTSW	13	81,492,501 (GRCm38)	missense	probably benign	0.02
R7168:Adgrv1	UTSW	13	81,397,209 (GRCm38)	missense	possibly damaging	0.52
R7205:Adgrv1	UTSW	13	81,479,658 (GRCm38)	missense	probably benign	0.00
R7239:Adgrv1	UTSW	13	81,476,612 (GRCm38)	missense	possibly damaging	0.69
R7249:Adgrv1	UTSW	13	81,374,259 (GRCm38)	missense	probably damaging	1.00
R7313:Adgrv1	UTSW	13	81,520,515 (GRCm38)	missense	possibly damaging	0.95
R7376:Adgrv1	UTSW	13	81,518,126 (GRCm38)	missense	probably damaging	1.00
R7392:Adgrv1	UTSW	13	81,560,689 (GRCm38)	missense	probably damaging	1.00
R7395:Adgrv1	UTSW	13	81,559,348 (GRCm38)	missense	probably damaging	1.00
R7410:Adgrv1	UTSW	13	81,563,619 (GRCm38)	missense	probably benign	0.04
R7449:Adgrv1	UTSW	13	81,499,073 (GRCm38)	missense	probably damaging	0.99
R7496:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R7497:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R7498:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R7567:Adgrv1	UTSW	13	81,579,477 (GRCm38)	missense	probably damaging	1.00
R7567:Adgrv1	UTSW	13	81,433,529 (GRCm38)	missense	probably benign	0.00
R7614:Adgrv1	UTSW	13	81,520,661 (GRCm38)	missense	probably damaging	1.00
R7623:Adgrv1	UTSW	13	81,422,225 (GRCm38)	missense	possibly damaging	0.77
R7665:Adgrv1	UTSW	13	81,499,142 (GRCm38)	missense	probably damaging	1.00
R7685:Adgrv1	UTSW	13	81,103,324 (GRCm38)	missense	possibly damaging	0.94
R7788:Adgrv1	UTSW	13	81,573,314 (GRCm38)	missense	probably damaging	1.00
R7809:Adgrv1	UTSW	13	81,528,641 (GRCm38)	missense	possibly damaging	0.81
R7854:Adgrv1	UTSW	13	81,593,088 (GRCm38)	missense	probably damaging	1.00
R7894:Adgrv1	UTSW	13	81,567,451 (GRCm38)	missense	probably benign	0.00
R7948:Adgrv1	UTSW	13	81,559,588 (GRCm38)	missense	probably damaging	1.00
R7948:Adgrv1	UTSW	13	81,559,529 (GRCm38)	missense	probably damaging	1.00
R7949:Adgrv1	UTSW	13	81,155,234 (GRCm38)	missense	probably damaging	1.00
R7951:Adgrv1	UTSW	13	81,563,570 (GRCm38)	missense	probably damaging	1.00
R7968:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R7969:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R7973:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8007:Adgrv1	UTSW	13	81,283,466 (GRCm38)	missense	probably benign	0.04
R8018:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8044:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8050:Adgrv1	UTSW	13	81,413,177 (GRCm38)	missense	probably damaging	1.00
R8090:Adgrv1	UTSW	13	81,448,834 (GRCm38)	critical splice donor site	probably null
R8104:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8122:Adgrv1	UTSW	13	81,270,918 (GRCm38)	missense	probably damaging	1.00
R8122:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8123:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8125:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8126:Adgrv1	UTSW	13	81,440,225 (GRCm38)	missense	possibly damaging	0.79
R8212:Adgrv1	UTSW	13	81,522,121 (GRCm38)	missense	probably benign	0.01
R8221:Adgrv1	UTSW	13	81,528,914 (GRCm38)	missense	probably benign	0.00
R8256:Adgrv1	UTSW	13	81,579,560 (GRCm38)	missense	probably damaging	1.00
R8270:Adgrv1	UTSW	13	81,503,044 (GRCm38)	missense	probably damaging	0.96
R8290:Adgrv1	UTSW	13	81,481,883 (GRCm38)	missense	probably benign	0.00
R8298:Adgrv1	UTSW	13	81,385,914 (GRCm38)	nonsense	probably null
R8317:Adgrv1	UTSW	13	81,575,117 (GRCm38)	missense	probably damaging	0.98
R8326:Adgrv1	UTSW	13	81,445,343 (GRCm38)	missense	probably damaging	1.00
R8327:Adgrv1	UTSW	13	81,445,343 (GRCm38)	missense	probably damaging	1.00
R8330:Adgrv1	UTSW	13	81,445,343 (GRCm38)	missense	probably damaging	1.00
R8332:Adgrv1	UTSW	13	81,445,343 (GRCm38)	missense	probably damaging	1.00
R8345:Adgrv1	UTSW	13	81,103,386 (GRCm38)	missense	probably damaging	1.00
R8398:Adgrv1	UTSW	13	81,182,678 (GRCm38)	missense	probably damaging	1.00
R8399:Adgrv1	UTSW	13	81,489,170 (GRCm38)	missense	possibly damaging	0.55
R8450:Adgrv1	UTSW	13	81,435,843 (GRCm38)	splice site	probably null
R8471:Adgrv1	UTSW	13	81,446,472 (GRCm38)	missense	probably benign	0.00
R8534:Adgrv1	UTSW	13	81,386,768 (GRCm38)	missense	probably benign	0.02
R8537:Adgrv1	UTSW	13	81,536,372 (GRCm38)	missense	probably damaging	1.00
R8703:Adgrv1	UTSW	13	81,528,673 (GRCm38)	missense	probably damaging	1.00
R8845:Adgrv1	UTSW	13	81,481,359 (GRCm38)	missense	possibly damaging	0.79
R8846:Adgrv1	UTSW	13	81,488,906 (GRCm38)	critical splice donor site	probably null
R8849:Adgrv1	UTSW	13	81,521,205 (GRCm38)	missense	probably benign
R8856:Adgrv1	UTSW	13	81,559,502 (GRCm38)	missense	probably benign	0.11
R8915:Adgrv1	UTSW	13	81,567,439 (GRCm38)	missense	probably damaging	1.00
R8963:Adgrv1	UTSW	13	81,419,469 (GRCm38)	missense	probably benign
R8994:Adgrv1	UTSW	13	81,405,338 (GRCm38)	frame shift	probably null
R8995:Adgrv1	UTSW	13	81,405,338 (GRCm38)	frame shift	probably null
R8996:Adgrv1	UTSW	13	81,405,338 (GRCm38)	frame shift	probably null
R8997:Adgrv1	UTSW	13	81,405,338 (GRCm38)	frame shift	probably null
R9022:Adgrv1	UTSW	13	81,155,193 (GRCm38)	missense	probably damaging	1.00
R9059:Adgrv1	UTSW	13	81,414,573 (GRCm38)	critical splice donor site	probably null
R9076:Adgrv1	UTSW	13	81,422,128 (GRCm38)	critical splice donor site	probably null
R9119:Adgrv1	UTSW	13	81,510,876 (GRCm38)	missense	probably damaging	0.97
R9137:Adgrv1	UTSW	13	81,540,014 (GRCm38)	missense	probably damaging	1.00
R9146:Adgrv1	UTSW	13	81,413,172 (GRCm38)	missense	probably benign	0.11
R9156:Adgrv1	UTSW	13	81,521,183 (GRCm38)	missense	probably benign	0.00
R9163:Adgrv1	UTSW	13	81,419,422 (GRCm38)	missense	probably benign	0.19
R9282:Adgrv1	UTSW	13	81,103,372 (GRCm38)	missense	probably damaging	1.00
R9286:Adgrv1	UTSW	13	81,446,401 (GRCm38)	missense	probably damaging	0.98
R9328:Adgrv1	UTSW	13	81,472,404 (GRCm38)	missense	probably damaging	1.00
R9329:Adgrv1	UTSW	13	81,499,122 (GRCm38)	missense	probably damaging	1.00
R9350:Adgrv1	UTSW	13	81,506,155 (GRCm38)	missense	probably damaging	1.00
R9377:Adgrv1	UTSW	13	81,557,158 (GRCm38)	missense	probably damaging	0.99
R9394:Adgrv1	UTSW	13	81,476,648 (GRCm38)	missense	possibly damaging	0.95
R9419:Adgrv1	UTSW	13	81,508,768 (GRCm38)	missense	probably benign	0.44
R9427:Adgrv1	UTSW	13	81,584,115 (GRCm38)	missense	probably benign	0.00
R9429:Adgrv1	UTSW	13	81,593,046 (GRCm38)	missense	probably damaging	0.99
R9429:Adgrv1	UTSW	13	81,419,349 (GRCm38)	missense	probably damaging	1.00
R9433:Adgrv1	UTSW	13	81,566,352 (GRCm38)	missense	probably benign	0.02
R9434:Adgrv1	UTSW	13	81,518,173 (GRCm38)	splice site	probably benign
R9513:Adgrv1	UTSW	13	81,382,353 (GRCm38)	missense	possibly damaging	0.95
R9515:Adgrv1	UTSW	13	81,543,378 (GRCm38)	missense	probably damaging	0.99
R9523:Adgrv1	UTSW	13	81,419,059 (GRCm38)	missense
R9525:Adgrv1	UTSW	13	81,445,334 (GRCm38)	missense	possibly damaging	0.77
R9576:Adgrv1	UTSW	13	81,543,489 (GRCm38)	missense	probably benign	0.06
R9612:Adgrv1	UTSW	13	81,492,963 (GRCm38)	missense	probably damaging	1.00
R9664:Adgrv1	UTSW	13	81,595,252 (GRCm38)	missense	probably damaging	1.00
R9664:Adgrv1	UTSW	13	81,522,169 (GRCm38)	missense	probably benign	0.01
R9702:Adgrv1	UTSW	13	81,536,364 (GRCm38)	missense	possibly damaging	0.80
R9717:Adgrv1	UTSW	13	81,520,781 (GRCm38)	missense	probably damaging	1.00
R9720:Adgrv1	UTSW	13	81,592,574 (GRCm38)	missense	probably damaging	1.00
X0054:Adgrv1	UTSW	13	81,559,270 (GRCm38)	missense	probably damaging	1.00
X0062:Adgrv1	UTSW	13	81,386,926 (GRCm38)	missense	probably damaging	0.99
X0067:Adgrv1	UTSW	13	81,543,392 (GRCm38)	missense	possibly damaging	0.51
Z1088:Adgrv1	UTSW	13	81,476,672 (GRCm38)	missense	probably damaging	1.00
Z1176:Adgrv1	UTSW	13	81,559,634 (GRCm38)	missense	possibly damaging	0.90
Z1177:Adgrv1	UTSW	13	81,419,256 (GRCm38)	missense	possibly damaging	0.54

Predicted Primers

PCR Primer
(F):5'- GGCTCCTACATACTTCAAACGC -3'
(R):5'- ATGTGAGGACCTATGAGCGC -3'

Sequencing Primer
(F):5'- CCTACATACTTCAAACGCTAGTTC -3'
(R):5'- GCAAGCTGACTCCCGAG -3'

Posted On

2014-09-17