Mutagenetix > Incidental Mutation

Incidental Mutation 'R1709:Adgrv1'

190357

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

039742-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1709 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

81243187-81781273 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 81741179 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 95 (V95E)

Ref Sequence

ENSEMBL: ENSMUSP00000114579 (fasta)

Gene Model

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

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000095585
AA Change: V95E

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

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: V95E

Domain	Start	End	E-Value	Type
Calx_beta	20	116	1.53e-1	SMART
Calx_beta	132	236	1.58e-2	SMART
Calx_beta	251	362	2.33e-2	SMART
Pfam:Calx-beta	380	489	1.1e-3	PFAM
Pfam:Calx-beta	507	616	2.5e-2	PFAM
Pfam:Calx-beta	667	747	9.1e-4	PFAM
Calx_beta	764	862	1.55e-1	SMART
Calx_beta	877	980	1.07e-1	SMART
Calx_beta	994	1094	6.45e-5	SMART
Pfam:Calx-beta	1108	1208	7.4e-4	PFAM
Pfam:Laminin_G_3	1331	1492	4.4e-24	PFAM
Pfam:Calx-beta	1498	1542	6.5e-3	PFAM
Pfam:Calx-beta	1557	1662	1e-6	PFAM
Calx_beta	1706	1805	1.34e-11	SMART
Calx_beta	1846	1948	1.04e-2	SMART
Calx_beta	1962	2075	1.59e-3	SMART
Calx_beta	2103	2202	1.59e-4	SMART
Calx_beta	2218	2320	1.74e-3	SMART
Pfam:Calx-beta	2467	2539	2.1e-4	PFAM
Calx_beta	2576	2672	1.24e-6	SMART
Calx_beta	2687	2786	1.12e-1	SMART
Calx_beta	2810	2921	2.21e-2	SMART
Calx_beta	2945	3044	6.69e-12	SMART
Pfam:Calx-beta	3063	3168	1.2e-5	PFAM
Pfam:Calx-beta	3198	3252	1.2e-1	PFAM
Pfam:EPTP	3391	3434	2.8e-10	PFAM
Pfam:Calx-beta	3577	3623	6.5e-8	PFAM
Pfam:Calx-beta	3637	3737	6e-4	PFAM
Pfam:Calx-beta	3781	3872	6.9e-3	PFAM
Calx_beta	3919	4003	1.18e-2	SMART
Calx_beta	4017	4120	5.44e-2	SMART
Pfam:Calx-beta	4193	4236	2.3e-2	PFAM
Calx_beta	4251	4351	1.43e-20	SMART
Calx_beta	4384	4484	9.46e-3	SMART
Pfam:Calx-beta	4498	4608	2e-2	PFAM
Pfam:Calx-beta	4659	4729	5.1e-2	PFAM
Calx_beta	4989	5089	5.7e-6	SMART
Pfam:Calx-beta	5229	5326	1.9e-6	PFAM
Pfam:Calx-beta	5489	5592	7.2e-5	PFAM
low complexity region	5637	5648	N/A	INTRINSIC
GPS	5845	5895	9.48e-3	SMART
Pfam:7tm_2	5902	6141	2.3e-16	PFAM
low complexity region	6227	6240	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000126444
AA Change: V95E

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

SMART Domains

Protein: ENSMUSP00000123552
Gene: ENSMUSG00000069170
AA Change: V95E

Domain	Start	End	E-Value	Type
Blast:Calx_beta	20	116	1e-56	BLAST
Pfam:Calx-beta	132	236	7.6e-11	PFAM
Pfam:Calx-beta	250	362	7.9e-9	PFAM
Blast:Calx_beta	378	489	9e-6	BLAST
low complexity region	531	550	N/A	INTRINSIC
Blast:Calx_beta	764	862	2e-59	BLAST
Blast:Calx_beta	877	980	1e-63	BLAST
Pfam:Calx-beta	994	1094	2.1e-15	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000128585
AA Change: V95E

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

SMART Domains

Protein: ENSMUSP00000121899
Gene: ENSMUSG00000069170
AA Change: V95E

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

Predicted Effect

probably damaging
Transcript: ENSMUST00000146749
AA Change: V95E

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

SMART Domains

Protein: ENSMUSP00000114579
Gene: ENSMUSG00000069170
AA Change: V95E

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

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.4%
20x: 92.9%

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
Aacs	A	G	5: 125,566,942 (GRCm39)	K152E	probably benign	Het
Adgrd1	T	C	5: 129,256,292 (GRCm39)	V641A	possibly damaging	Het
Agbl5	G	A	5: 31,063,585 (GRCm39)	C872Y	probably damaging	Het
Aldh1a7	G	T	19: 20,693,316 (GRCm39)	T201K	probably damaging	Het
Aox1	C	T	1: 58,116,633 (GRCm39)	A788V	probably benign	Het
Apob	T	C	12: 8,059,306 (GRCm39)	V2563A	probably damaging	Het
Atcay	G	A	10: 81,049,065 (GRCm39)	T179I	probably damaging	Het
Atf5	A	T	7: 44,462,707 (GRCm39)	L139Q	probably benign	Het
Atp13a3	T	C	16: 30,134,659 (GRCm39)	T1205A	probably benign	Het
Atr	C	T	9: 95,753,129 (GRCm39)	T656I	probably benign	Het
Bloc1s3	T	C	7: 19,241,453 (GRCm39)	E25G	possibly damaging	Het
Brap	T	C	5: 121,803,353 (GRCm39)		probably null	Het
C6	G	T	15: 4,820,452 (GRCm39)	A488S	probably benign	Het
Ccin	T	C	4: 43,984,133 (GRCm39)	F180S	probably damaging	Het
Cd207	T	C	6: 83,649,818 (GRCm39)	I256V	possibly damaging	Het
Cdc42bpa	G	T	1: 179,894,789 (GRCm39)	C323F	probably damaging	Het
Cfap57	T	C	4: 118,428,901 (GRCm39)	T1022A	probably benign	Het
Cmtr2	A	T	8: 110,948,581 (GRCm39)	Q297L	probably benign	Het
Coro7	A	T	16: 4,452,305 (GRCm39)		probably null	Het
Cpsf2	T	A	12: 101,965,801 (GRCm39)	Y589N	probably damaging	Het
Cpxm2	T	C	7: 131,661,563 (GRCm39)	Y408C	probably damaging	Het
Crocc	A	G	4: 140,753,410 (GRCm39)		probably null	Het
Cryzl1	A	C	16: 91,509,124 (GRCm39)	F59C	probably damaging	Het
Csmd2	T	C	4: 128,389,988 (GRCm39)	V2241A	probably damaging	Het
Cxcl15	C	A	5: 90,949,275 (GRCm39)	H147N	unknown	Het
Dennd4a	A	G	9: 64,796,887 (GRCm39)	T860A	possibly damaging	Het
Dnah10	C	T	5: 124,837,155 (GRCm39)	P966L	probably damaging	Het
Dpp9	T	A	17: 56,501,431 (GRCm39)	M594L	probably benign	Het
Dspp	C	A	5: 104,323,590 (GRCm39)	N244K	probably damaging	Het
Efcab8	T	A	2: 153,656,290 (GRCm39)		probably null	Het
Elapor2	C	T	5: 9,490,726 (GRCm39)	R579*	probably null	Het
Fabp3	C	T	4: 130,206,180 (GRCm39)	T57I	probably benign	Het
Fbxw17	A	G	13: 50,585,693 (GRCm39)	M299V	probably benign	Het
Fbxw7	T	A	3: 84,883,659 (GRCm39)	I530N	probably damaging	Het
Gp2	C	A	7: 119,050,808 (GRCm39)	D308Y	probably null	Het
Gpd2	G	A	2: 57,247,667 (GRCm39)	V537M	probably damaging	Het
Gpr18	T	A	14: 122,149,404 (GRCm39)	Y207F	probably damaging	Het
Grip1	A	T	10: 119,733,620 (GRCm39)	D20V	probably damaging	Het
Gzmf	A	C	14: 56,444,397 (GRCm39)	F59V	probably damaging	Het
H3c1	T	A	13: 23,945,964 (GRCm39)	I125F	probably damaging	Het
Igfn1	T	C	1: 135,883,311 (GRCm39)	I2732V	probably benign	Het
Ipo8	A	T	6: 148,684,226 (GRCm39)	D855E	probably benign	Het
Klrk1	A	T	6: 129,591,682 (GRCm39)		probably null	Het
Megf11	A	G	9: 64,602,694 (GRCm39)	Y876C	probably damaging	Het
Mettl8	G	T	2: 70,812,495 (GRCm39)	Q12K	probably benign	Het
Mrgprf	T	C	7: 144,861,954 (GRCm39)	F172S	probably benign	Het
Mycbp2	G	A	14: 103,461,852 (GRCm39)	T1432I	probably damaging	Het
Nek11	A	C	9: 105,225,260 (GRCm39)	L84R	probably damaging	Het
Nlrp1b	T	C	11: 71,092,099 (GRCm39)	E9G	probably benign	Het
Nrxn1	T	C	17: 90,344,615 (GRCm39)	I433V	probably damaging	Het
Nup153	A	G	13: 46,847,450 (GRCm39)	C660R	probably damaging	Het
Or1o11	T	A	17: 37,757,091 (GRCm39)	Y226*	probably null	Het
Or2a25	T	C	6: 42,889,078 (GRCm39)	V207A	possibly damaging	Het
Or4z4	G	T	19: 12,076,245 (GRCm39)	P253T	probably damaging	Het
Or5h26	T	A	16: 58,988,264 (GRCm39)	M81L	probably benign	Het
P2rx7	T	A	5: 122,808,528 (GRCm39)	N303K	possibly damaging	Het
Pank4	T	C	4: 155,054,504 (GRCm39)	L159P	probably damaging	Het
Pcdhb22	A	T	18: 37,651,553 (GRCm39)	H7L	probably benign	Het
Pdzd8	A	T	19: 59,289,771 (GRCm39)	I543N	probably benign	Het
Pramel25	T	C	4: 143,520,116 (GRCm39)	V120A	possibly damaging	Het
Prrc2b	C	A	2: 32,084,473 (GRCm39)	R313S	probably damaging	Het
Rbm12b1	T	C	4: 12,145,827 (GRCm39)	C600R	probably benign	Het
Rem1	G	A	2: 152,476,455 (GRCm39)	V238M	probably damaging	Het
Rfx6	T	A	10: 51,554,498 (GRCm39)	M113K	possibly damaging	Het
Rlf	A	T	4: 121,007,020 (GRCm39)	D653E	probably benign	Het
Rnf130	A	G	11: 49,978,213 (GRCm39)	D258G	possibly damaging	Het
Robo2	A	G	16: 73,753,411 (GRCm39)	V822A	possibly damaging	Het
Rps6kc1	G	T	1: 190,532,533 (GRCm39)	Q490K	possibly damaging	Het
Scn9a	T	C	2: 66,313,850 (GRCm39)	Y1945C	probably damaging	Het
Setd2	T	A	9: 110,378,925 (GRCm39)	D913E	probably benign	Het
Sfr1	G	T	19: 47,723,442 (GRCm39)	E315D	possibly damaging	Het
Smarca5	G	A	8: 81,435,849 (GRCm39)	R763*	probably null	Het
Sugct	A	C	13: 17,847,151 (GRCm39)	I44S	probably damaging	Het
Syce1l	A	G	8: 114,380,662 (GRCm39)		probably null	Het
Tbc1d8b	A	G	X: 138,634,829 (GRCm39)	I654V	probably benign	Het
Tcf23	T	A	5: 31,130,852 (GRCm39)	Y163*	probably null	Het
Terf2ip	TG	T	8: 112,738,238 (GRCm39)		probably null	Het
Tmem158	T	C	9: 123,088,950 (GRCm39)	S221G	possibly damaging	Het
Tnrc6a	A	G	7: 122,769,205 (GRCm39)	T332A	probably benign	Het
Trappc4	T	C	9: 44,318,508 (GRCm39)	T31A	probably benign	Het
Trim27	T	C	13: 21,372,235 (GRCm39)		probably null	Het
Ttyh2	T	A	11: 114,599,301 (GRCm39)	L330Q	probably damaging	Het
Tubgcp3	A	T	8: 12,689,532 (GRCm39)	L578*	probably null	Het
Txndc11	C	A	16: 10,946,565 (GRCm39)	E83*	probably null	Het
Utp20	T	C	10: 88,585,159 (GRCm39)	K2635R	probably benign	Het
V1ra8	C	T	6: 90,180,304 (GRCm39)	T169I	probably damaging	Het
Vcl	G	A	14: 21,069,441 (GRCm39)	V706I	probably benign	Het
Vmn2r106	A	T	17: 20,499,373 (GRCm39)	D179E	probably benign	Het
Vmn2r80	T	C	10: 79,030,223 (GRCm39)	M683T	probably benign	Het
Xirp2	A	G	2: 67,340,215 (GRCm39)	I819V	probably benign	Het
Zfp735	T	C	11: 73,602,589 (GRCm39)	F511S	probably benign	Het
Zfp831	T	C	2: 174,487,683 (GRCm39)	V786A	probably benign	Het
Zfp992	T	A	4: 146,550,949 (GRCm39)	H223Q	probably benign	Het
Zfyve19	A	C	2: 119,041,300 (GRCm39)	Q72P	probably damaging	Het

Other mutations in Adgrv1

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

Predicted Primers

PCR Primer
(F):5'- GGATTGTCACAGAAGCAGCCCTTG -3'
(R):5'- GACAGTGCCACTTGATCTGTACCC -3'

Sequencing Primer
(F):5'- TGTATCTACTAGCCAGGAGCAC -3'
(R):5'- CTTTCTTCTGGTTGCTCCAATGAG -3'

Posted On

2014-05-14