Mutagenetix > Incidental Mutation

Incidental Mutation 'R7073:Adgrv1'

549059

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

045169-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7073 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

81095068-81633154 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 81561474 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Aspartic acid at position 1133 (E1133D)

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: E1133D

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

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: E1133D

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: E413D

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000105193
Gene: ENSMUSG00000069170
AA Change: E413D

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 damaging
Transcript: ENSMUST00000126444
AA Change: E1133D

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000123552
Gene: ENSMUSG00000069170
AA Change: E1133D

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: 99.7%
20x: 99.0%

Validation Efficiency

MGI Phenotype

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

Allele List at MGI

Other mutations in this stock

Total: 80 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankrd13b	A	T	11: 77,472,509 (GRCm38)	D505E	probably benign	Het
Ano1	C	T	7: 144,638,552 (GRCm38)	E361K	probably damaging	Het
Arap3	T	A	18: 37,974,442 (GRCm38)	K1341*	probably null	Het
Arhgef17	A	C	7: 100,929,991 (GRCm38)	Y583*	probably null	Het
Ash1l	G	A	3: 88,985,340 (GRCm38)	E1509K	probably damaging	Het
B430305J03Rik	T	G	3: 61,364,260 (GRCm38)	R21S	unknown	Het
Bbof1	A	G	12: 84,426,835 (GRCm38)	E313G	probably damaging	Het
Catsperb	C	T	12: 101,509,238 (GRCm38)	T347I	probably benign	Het
Ccdc24	G	T	4: 117,872,004 (GRCm38)	A92D	probably damaging	Het
Ccdc63	T	C	5: 122,111,010 (GRCm38)	T419A	probably benign	Het
Ccdc7a	C	T	8: 128,892,385 (GRCm38)	V893I	possibly damaging	Het
Ccdc88b	G	T	19: 6,853,962 (GRCm38)	D537E	probably benign	Het
Cd276	T	C	9: 58,537,332 (GRCm38)	S119G	probably damaging	Het
Cdkn3	T	C	14: 46,767,190 (GRCm38)	Y70H	possibly damaging	Het
Cdo1	G	A	18: 46,728,199 (GRCm38)		probably benign	Het
Cdr2	A	T	7: 120,982,024 (GRCm38)	F10Y	probably damaging	Het
Cep290	A	T	10: 100,539,003 (GRCm38)	K1370N	possibly damaging	Het
Crb1	T	A	1: 139,248,311 (GRCm38)	I645F	probably damaging	Het
Cul7	T	C	17: 46,658,731 (GRCm38)	W975R	probably damaging	Het
Ddx39b	A	C	17: 35,252,850 (GRCm38)	E324A	probably benign	Het
Diaph1	T	G	18: 37,889,814 (GRCm38)		probably null	Het
Dnah2	G	A	11: 69,430,492 (GRCm38)	R3917*	probably null	Het
Dnph1	T	A	17: 46,496,889 (GRCm38)	L27Q	probably damaging	Het
Duox2	A	G	2: 122,289,307 (GRCm38)	F880S	probably damaging	Het
Ell2	C	A	13: 75,761,887 (GRCm38)	L119M	probably damaging	Het
Enpep	A	T	3: 129,312,670 (GRCm38)	Y302*	probably null	Het
Ergic2	G	T	6: 148,195,209 (GRCm38)	H186Q	probably damaging	Het
Fam83b	T	C	9: 76,545,749 (GRCm38)	D12G	probably benign	Het
Fbxw16	A	T	9: 109,441,055 (GRCm38)	V206D	probably damaging	Het
Fhod1	A	T	8: 105,337,139 (GRCm38)	V278D	unknown	Het
Gba2	G	C	4: 43,573,753 (GRCm38)	Q180E	probably damaging	Het
Gm11127	A	T	17: 36,058,343 (GRCm38)	C7S	unknown	Het
Grhl3	G	A	4: 135,573,412 (GRCm38)	L5F	probably benign	Het
Ifit1bl1	C	T	19: 34,599,267 (GRCm38)		probably null	Het
Ift57	A	G	16: 49,763,867 (GRCm38)	T413A	probably benign	Het
Itga2	A	G	13: 114,859,613 (GRCm38)	F714S	probably damaging	Het
Jmy	A	G	13: 93,441,333 (GRCm38)	S776P	probably benign	Het
Kbtbd8	G	A	6: 95,121,833 (GRCm38)	A108T	probably damaging	Het
Kpna6	G	A	4: 129,654,346 (GRCm38)	A230V	probably damaging	Het
Lrfn1	C	T	7: 28,459,972 (GRCm38)	L439F	possibly damaging	Het
Lrrc1	T	A	9: 77,468,565 (GRCm38)	I147F	probably benign	Het
Lrrc7	C	T	3: 158,127,247 (GRCm38)	G1425R	probably damaging	Het
Madd	T	A	2: 91,162,509 (GRCm38)	I1022F	probably damaging	Het
Map2k2	A	T	10: 81,106,183 (GRCm38)	T13S	probably benign	Het
Mdc1	G	A	17: 35,854,068 (GRCm38)	V1459I	probably benign	Het
Mdh1b	G	A	1: 63,721,560 (GRCm38)	T114M	probably damaging	Het
Mfsd2a	T	C	4: 122,951,295 (GRCm38)	I208V	possibly damaging	Het
Mmrn1	T	A	6: 60,988,427 (GRCm38)	D1147E	probably damaging	Het
Nbeal2	T	A	9: 110,626,109 (GRCm38)	I2574F	probably damaging	Het
Nr1d1	T	G	11: 98,772,066 (GRCm38)	S34R	probably damaging	Het
Nr3c1	A	T	18: 39,486,396 (GRCm38)	D279E	probably benign	Het
Nrde2	T	C	12: 100,132,488 (GRCm38)	D640G	probably benign	Het
Odf4	A	G	11: 68,926,688 (GRCm38)	L58P	probably damaging	Het
Olfr1184	A	T	2: 88,487,307 (GRCm38)	I192F	probably benign	Het
Olfr1287	A	T	2: 111,449,286 (GRCm38)	I49F	probably benign	Het
Otud6b	A	C	4: 14,811,743 (GRCm38)	M300R	probably damaging	Het
Pamr1	T	A	2: 102,640,935 (GRCm38)	D534E	probably benign	Het
Pcdh7	T	A	5: 57,720,957 (GRCm38)	V618E	probably benign	Het
Pcgf6	A	C	19: 47,042,787 (GRCm38)	N266K	possibly damaging	Het
Plcz1	A	T	6: 140,023,123 (GRCm38)	Y196*	probably null	Het
Plxna1	A	T	6: 89,357,329 (GRCm38)	L106Q	probably damaging	Het
Qrich2	G	A	11: 116,446,875 (GRCm38)	A184V	probably damaging	Het
Rimkla	A	G	4: 119,468,078 (GRCm38)	L378S	probably benign	Het
Rufy1	G	T	11: 50,404,463 (GRCm38)	H472Q	probably benign	Het
Samd7	T	A	3: 30,756,482 (GRCm38)	M216K	probably benign	Het
Samd9l	A	T	6: 3,375,856 (GRCm38)	Y468*	probably null	Het
Scn2a	T	G	2: 65,728,443 (GRCm38)	L1194R	probably benign	Het
Sgo2a	T	A	1: 58,017,785 (GRCm38)	S1043T	possibly damaging	Het
Slc6a17	G	T	3: 107,471,439 (GRCm38)	H642Q	probably benign	Het
Smox	C	T	2: 131,522,111 (GRCm38)	A45V	possibly damaging	Het
St6galnac3	T	A	3: 153,411,637 (GRCm38)	T150S	possibly damaging	Het
Strip2	T	A	6: 29,941,912 (GRCm38)	I627N	possibly damaging	Het
Sv2c	A	T	13: 96,088,250 (GRCm38)	C184S	probably damaging	Het
Tm7sf2	A	T	19: 6,066,497 (GRCm38)		probably null	Het
Ttc28	T	C	5: 111,223,416 (GRCm38)	I608T	possibly damaging	Het
Vmn1r183	T	G	7: 24,055,501 (GRCm38)	L243R	probably damaging	Het
Vmn1r68	T	C	7: 10,527,851 (GRCm38)	T107A	probably benign	Het
Vnn3	G	A	10: 23,864,413 (GRCm38)	G205R	probably damaging	Het
Zfp516	T	A	18: 82,988,200 (GRCm38)		probably null	Het
Zpbp2	A	G	11: 98,552,509 (GRCm38)	D56G	probably damaging	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
R2128: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
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'- TAGCAGATGAATGGTTGTCATGGATAG -3'
(R):5'- CTGGGAGTATATATGCACACGC -3'

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

Posted On

2019-05-15