Mutagenetix > Incidental Mutation

Incidental Mutation 'R6244:Adgrv1'

505480

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

044435-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6244 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

81243187-81781273 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 81255050 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 211 (T211I)

Ref Sequence

ENSEMBL: ENSMUSP00000153419 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000095585] [ENSMUST00000128120] [ENSMUST00000224088]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000095585
AA Change: T6191I

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

SMART Domains

Protein: ENSMUSP00000093245
Gene: ENSMUSG00000069170
AA Change: T6191I

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 benign
Transcript: ENSMUST00000125698

SMART Domains

Protein: ENSMUSP00000120136
Gene: ENSMUSG00000069170

Domain	Start	End	E-Value	Type
Pfam:Calx-beta	1	47	2e-9	PFAM
Pfam:Calx-beta	79	180	4e-11	PFAM
Pfam:Calx-beta	194	304	9.2e-4	PFAM
Pfam:Calx-beta	354	425	2.9e-3	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000128120
AA Change: T211I

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

SMART Domains

Protein: ENSMUSP00000122358
Gene: ENSMUSG00000069170
AA Change: T211I

Domain	Start	End	E-Value	Type
Pfam:7tm_2	1	161	4.4e-8	PFAM
low complexity region	247	260	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156631

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181043

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000181508

Predicted Effect

probably damaging
Transcript: ENSMUST00000224088
AA Change: T211I

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225082

Meta Mutation Damage Score

0.3651

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.3%
20x: 95.1%

Validation Efficiency

96% (82/85)

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: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
6430550D23Rik	T	C	2: 155,845,150 (GRCm39)	H113R	possibly damaging	Het
Adgrf3	A	T	5: 30,402,531 (GRCm39)	M499K	probably benign	Het
Adss2	C	T	1: 177,604,395 (GRCm39)	E153K	probably benign	Het
Ago4	C	A	4: 126,405,280 (GRCm39)	G431V	possibly damaging	Het
Araf	G	T	X: 20,726,339 (GRCm39)	R601L	probably damaging	Homo
Atp2b4	T	A	1: 133,654,299 (GRCm39)	I769F	probably damaging	Het
Atp9a	T	C	2: 168,531,272 (GRCm39)		probably null	Het
Bltp1	T	C	3: 37,011,148 (GRCm39)	V1782A	probably benign	Het
Brap	C	A	5: 121,803,372 (GRCm39)	D173E	probably benign	Het
Brca2	G	T	5: 150,490,443 (GRCm39)	R3035L	probably benign	Het
Ccdc8	C	A	7: 16,730,176 (GRCm39)	P555Q	probably benign	Het
Ccser2	A	G	14: 36,662,675 (GRCm39)	S170P	probably benign	Het
Celsr2	T	C	3: 108,300,444 (GRCm39)	H860R	probably damaging	Het
Cenpc1	C	A	5: 86,194,244 (GRCm39)	R174M	probably damaging	Het
Cfap57	T	G	4: 118,436,607 (GRCm39)	I930L	probably damaging	Het
Cx3cr1	C	T	9: 119,880,760 (GRCm39)	R214H	probably damaging	Het
Cyp4f14	T	A	17: 33,125,291 (GRCm39)	H429L	probably benign	Het
D5Ertd579e	A	G	5: 36,772,620 (GRCm39)	F592L	probably damaging	Het
Ddb1	A	G	19: 10,603,287 (GRCm39)	E865G	probably damaging	Het
Ddx50	A	T	10: 62,457,345 (GRCm39)		probably null	Het
Dpp6	A	G	5: 27,254,626 (GRCm39)	T14A	probably damaging	Het
Echs1	C	A	7: 139,692,982 (GRCm39)	Q51H	possibly damaging	Het
Ecm2	A	T	13: 49,683,783 (GRCm39)	D587V	probably damaging	Het
Ect2l	A	T	10: 18,016,145 (GRCm39)	Y666N	possibly damaging	Het
Epha2	G	A	4: 141,044,223 (GRCm39)	G342S	probably benign	Het
Fbxo33	C	A	12: 59,252,865 (GRCm39)	K211N	probably benign	Het
Fchsd2	A	G	7: 100,908,983 (GRCm39)		probably null	Het
Fen1	A	G	19: 10,178,051 (GRCm39)	V131A	probably damaging	Het
Fetub	C	T	16: 22,751,081 (GRCm39)	R143C	probably damaging	Het
Flnb	A	G	14: 7,892,092 (GRCm38)	E587G	probably damaging	Het
Foxd3	A	G	4: 99,545,477 (GRCm39)	T206A	possibly damaging	Het
Fut1	A	G	7: 45,268,730 (GRCm39)	E228G	possibly damaging	Het
Galnt13	T	C	2: 54,823,560 (GRCm39)	F379L	probably damaging	Het
Gcnt2	A	C	13: 41,014,717 (GRCm39)	E296A	probably damaging	Het
Gm7145	T	A	1: 117,913,870 (GRCm39)	C251S	probably damaging	Het
Gpam	G	A	19: 55,059,417 (GRCm39)	P810L	probably damaging	Het
Il1rl2	T	A	1: 40,366,726 (GRCm39)	L87M	possibly damaging	Het
Itgae	A	G	11: 73,036,427 (GRCm39)	S1122G	probably damaging	Het
Kcnh7	T	A	2: 63,012,570 (GRCm39)	D46V	probably damaging	Het
Kcnn3	T	G	3: 89,552,830 (GRCm39)	Y511*	probably null	Het
Kdm3b	T	A	18: 34,926,058 (GRCm39)	I66N	probably damaging	Het
Klk1b27	A	T	7: 43,703,974 (GRCm39)	H39L	probably benign	Het
Kmo	C	T	1: 175,487,261 (GRCm39)	T404I	possibly damaging	Het
Krt222	C	T	11: 99,125,884 (GRCm39)		probably null	Het
Magi3	G	C	3: 103,923,013 (GRCm39)	H1235D	probably benign	Het
Mapk8ip1	C	A	2: 92,219,589 (GRCm39)	G81C	probably damaging	Het
Med15	G	A	16: 17,470,609 (GRCm39)	Q583*	probably null	Het
Mroh2a	T	C	1: 88,184,476 (GRCm39)	V1453A	probably benign	Het
Myh13	A	G	11: 67,253,327 (GRCm39)	M1488V	probably benign	Het
Naip2	A	T	13: 100,288,645 (GRCm39)	F1193L	probably damaging	Het
Nop58	T	A	1: 59,742,014 (GRCm39)	M181K	probably damaging	Het
Npepps	A	T	11: 97,104,616 (GRCm39)	V796D	probably damaging	Het
Nr1d1	A	G	11: 98,661,363 (GRCm39)	F301S	probably damaging	Het
Nynrin	G	A	14: 56,105,485 (GRCm39)	V832I	probably damaging	Het
Or13a28	C	A	7: 140,218,346 (GRCm39)	S244Y	probably damaging	Het
Or1j14	T	A	2: 36,418,353 (GRCm39)	C310S	probably benign	Het
Or2ak7	A	T	11: 58,574,830 (GRCm39)	T44S	possibly damaging	Het
Or4e1	T	A	14: 52,701,352 (GRCm39)	Y38F	probably damaging	Het
Or8k1	T	A	2: 86,047,566 (GRCm39)	T163S	possibly damaging	Het
Phrf1	T	A	7: 140,817,586 (GRCm39)	C132S	probably damaging	Het
Plekhn1	T	C	4: 156,315,015 (GRCm39)		probably null	Het
Polr2a	G	A	11: 69,635,052 (GRCm39)	T569M	probably damaging	Het
Prr29	A	G	11: 106,267,458 (GRCm39)		probably null	Het
Rsf1	CG	CGACGGCGGAG	7: 97,229,115 (GRCm39)		probably benign	Homo
Sc5d	T	C	9: 42,166,717 (GRCm39)	E274G	probably benign	Het
Serpina1d	A	T	12: 103,731,087 (GRCm39)		probably null	Het
Serpinb11	T	A	1: 107,299,972 (GRCm39)	I106N	probably damaging	Het
Setd2	G	A	9: 110,377,733 (GRCm39)	R516K	probably damaging	Het
Sirt2	G	T	7: 28,487,222 (GRCm39)	C291F	probably damaging	Het
Stac3	T	C	10: 127,344,044 (GRCm39)	V314A	probably damaging	Het
Stat6	C	T	10: 127,493,581 (GRCm39)		probably null	Het
Strn3	A	G	12: 51,656,890 (GRCm39)	V712A	probably damaging	Het
Tmc5	G	T	7: 118,233,437 (GRCm39)	G84C	possibly damaging	Het
Tnik	C	A	3: 28,704,328 (GRCm39)	L996I	probably damaging	Het
Trim30d	G	T	7: 104,136,817 (GRCm39)	T129K	probably damaging	Het
Triml1	G	T	8: 43,591,793 (GRCm39)	Y188*	probably null	Het
Trpc7	A	G	13: 56,921,705 (GRCm39)	Y760H	probably damaging	Het
Uaca	G	A	9: 60,777,326 (GRCm39)	R571Q	probably damaging	Het
Ubash3a	A	T	17: 31,458,246 (GRCm39)	Q575L	possibly damaging	Het
Usp49	T	A	17: 47,983,827 (GRCm39)	C61*	probably null	Het
Vmn2r18	A	T	5: 151,508,116 (GRCm39)	V336E	probably damaging	Het
Vwa8	T	C	14: 79,324,102 (GRCm39)	V1135A	probably benign	Het
Zcchc4	T	C	5: 52,940,503 (GRCm39)	V24A	probably benign	Het
Zfp354c	A	G	11: 50,705,798 (GRCm39)	Y426H	probably benign	Het

Other mutations in Adgrv1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00090:Adgrv1	APN	13	81,553,527 (GRCm39)	critical splice acceptor site	probably null
IGL00090:Adgrv1	APN	13	81,726,220 (GRCm39)	missense	probably damaging	1.00
IGL00091:Adgrv1	APN	13	81,726,220 (GRCm39)	missense	probably damaging	1.00
IGL00332:Adgrv1	APN	13	81,620,996 (GRCm39)	splice site	probably benign
IGL00471:Adgrv1	APN	13	81,657,661 (GRCm39)	missense	probably damaging	0.99
IGL00476:Adgrv1	APN	13	81,637,193 (GRCm39)	missense	probably damaging	0.98
IGL00508:Adgrv1	APN	13	81,654,306 (GRCm39)	missense	probably damaging	1.00
IGL00727:Adgrv1	APN	13	81,672,803 (GRCm39)	missense	probably damaging	0.98
IGL00781:Adgrv1	APN	13	81,726,349 (GRCm39)	missense	probably benign	0.19
IGL00816:Adgrv1	APN	13	81,545,322 (GRCm39)	missense	probably benign	0.01
IGL00844:Adgrv1	APN	13	81,688,238 (GRCm39)	missense	probably damaging	1.00
IGL00923:Adgrv1	APN	13	81,530,410 (GRCm39)	missense	probably damaging	0.99
IGL01113:Adgrv1	APN	13	81,637,147 (GRCm39)	missense	probably benign	0.00
IGL01143:Adgrv1	APN	13	81,567,470 (GRCm39)	missense	probably benign	0.00
IGL01151:Adgrv1	APN	13	81,553,518 (GRCm39)	missense	probably benign	0.00
IGL01153:Adgrv1	APN	13	81,567,247 (GRCm39)	missense	probably benign	0.01
IGL01363:Adgrv1	APN	13	81,705,184 (GRCm39)	missense	probably damaging	1.00
IGL01419:Adgrv1	APN	13	81,705,277 (GRCm39)	missense	probably damaging	0.99
IGL01545:Adgrv1	APN	13	81,614,303 (GRCm39)	missense	possibly damaging	0.46
IGL01701:Adgrv1	APN	13	81,567,750 (GRCm39)	missense	possibly damaging	0.55
IGL01796:Adgrv1	APN	13	81,715,461 (GRCm39)	missense	probably benign	0.01
IGL01816:Adgrv1	APN	13	81,677,168 (GRCm39)	missense	probably benign	0.00
IGL01871:Adgrv1	APN	13	81,620,513 (GRCm39)	critical splice donor site	probably null
IGL01955:Adgrv1	APN	13	81,330,902 (GRCm39)	missense	probably damaging	1.00
IGL01956:Adgrv1	APN	13	81,594,549 (GRCm39)	missense	possibly damaging	0.63
IGL01988:Adgrv1	APN	13	81,705,428 (GRCm39)	missense	probably damaging	0.99
IGL01990:Adgrv1	APN	13	81,705,115 (GRCm39)	missense	probably damaging	1.00
IGL02007:Adgrv1	APN	13	81,716,862 (GRCm39)	splice site	probably benign
IGL02016:Adgrv1	APN	13	81,545,572 (GRCm39)	missense	probably damaging	1.00
IGL02095:Adgrv1	APN	13	81,727,909 (GRCm39)	missense	possibly damaging	0.63
IGL02174:Adgrv1	APN	13	81,575,783 (GRCm39)	missense	probably benign	0.34
IGL02270:Adgrv1	APN	13	81,707,314 (GRCm39)	splice site	probably null
IGL02328:Adgrv1	APN	13	81,726,294 (GRCm39)	missense	probably damaging	1.00
IGL02350:Adgrv1	APN	13	81,418,974 (GRCm39)	missense	probably benign	0.00
IGL02357:Adgrv1	APN	13	81,418,974 (GRCm39)	missense	probably benign	0.00
IGL02373:Adgrv1	APN	13	81,607,832 (GRCm39)	missense	possibly damaging	0.90
IGL02402:Adgrv1	APN	13	81,707,543 (GRCm39)	missense	probably benign	0.18
IGL02407:Adgrv1	APN	13	81,627,789 (GRCm39)	missense	probably damaging	1.00
IGL02508:Adgrv1	APN	13	81,583,675 (GRCm39)	splice site	probably benign
IGL02603:Adgrv1	APN	13	81,637,071 (GRCm39)	missense	possibly damaging	0.93
IGL02648:Adgrv1	APN	13	81,659,738 (GRCm39)	missense	probably benign	0.35
IGL02720:Adgrv1	APN	13	81,726,991 (GRCm39)	missense	probably damaging	0.99
IGL02870:Adgrv1	APN	13	81,711,851 (GRCm39)	missense	probably benign	0.13
IGL02896:Adgrv1	APN	13	81,668,858 (GRCm39)	missense	probably damaging	1.00
IGL02931:Adgrv1	APN	13	81,727,833 (GRCm39)	missense	probably damaging	1.00
IGL02952:Adgrv1	APN	13	81,581,755 (GRCm39)	missense	probably benign	0.00
IGL02961:Adgrv1	APN	13	81,671,731 (GRCm39)	missense	probably damaging	1.00
IGL02999:Adgrv1	APN	13	81,726,973 (GRCm39)	missense	probably benign	0.12
IGL03067:Adgrv1	APN	13	81,590,599 (GRCm39)	missense	probably damaging	1.00
IGL03106:Adgrv1	APN	13	81,621,018 (GRCm39)	missense	probably benign	0.00
IGL03108:Adgrv1	APN	13	81,707,648 (GRCm39)	missense	probably damaging	1.00
IGL03119:Adgrv1	APN	13	81,581,819 (GRCm39)	missense	probably benign	0.02
IGL03119:Adgrv1	APN	13	81,530,492 (GRCm39)	missense	probably damaging	1.00
IGL03169:Adgrv1	APN	13	81,652,019 (GRCm39)	missense	probably damaging	1.00
IGL03186:Adgrv1	APN	13	81,581,737 (GRCm39)	missense	possibly damaging	0.80
IGL03196:Adgrv1	APN	13	81,594,597 (GRCm39)	missense	probably benign	0.02
IGL03207:Adgrv1	APN	13	81,255,017 (GRCm39)	splice site	probably null
IGL03343:Adgrv1	APN	13	81,431,507 (GRCm39)	missense	probably damaging	1.00
IGL03348:Adgrv1	APN	13	81,647,177 (GRCm39)	missense	possibly damaging	0.54
IGL03349:Adgrv1	APN	13	81,629,455 (GRCm39)	missense	probably benign	0.09
IGL03373:Adgrv1	APN	13	81,711,751 (GRCm39)	missense	probably damaging	0.99
IGL03381:Adgrv1	APN	13	81,666,086 (GRCm39)	missense	probably damaging	0.99
abetting	UTSW	13	81,727,679 (GRCm39)	missense	probably damaging	1.00
beatle	UTSW	13	81,727,713 (GRCm39)	nonsense	probably null
Escape	UTSW	13	81,583,824 (GRCm39)	missense	probably benign	0.02
lento	UTSW	13	81,419,016 (GRCm39)	missense	probably damaging	1.00
Metronome	UTSW	13	81,583,678 (GRCm39)	critical splice donor site	probably null
Murderous	UTSW	13	81,251,443 (GRCm39)	missense	possibly damaging	0.94
Nome	UTSW	13	81,539,886 (GRCm39)	missense	probably benign	0.00
Propulsion	UTSW	13	81,623,166 (GRCm39)	missense	probably benign	0.06
revulsion	UTSW	13	81,743,301 (GRCm39)	missense	probably damaging	1.00
Saturnv	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
Thrust	UTSW	13	81,522,375 (GRCm39)	missense	probably benign	0.01
Velocity	UTSW	13	81,545,473 (GRCm39)	missense	probably benign	0.00
Wilting	UTSW	13	81,640,620 (GRCm39)	missense	probably benign	0.02
Withering	UTSW	13	81,642,776 (GRCm39)	missense	probably damaging	1.00
F2404:Adgrv1	UTSW	13	81,568,125 (GRCm39)	missense	probably benign	0.13
G1patch:Adgrv1	UTSW	13	81,641,329 (GRCm39)	missense	probably damaging	1.00
G1patch:Adgrv1	UTSW	13	81,585,676 (GRCm39)	missense	probably damaging	0.99
I2288:Adgrv1	UTSW	13	81,585,643 (GRCm39)	missense	probably damaging	1.00
I2289:Adgrv1	UTSW	13	81,585,643 (GRCm39)	missense	probably damaging	1.00
PIT4377001:Adgrv1	UTSW	13	81,677,104 (GRCm39)	missense	probably damaging	1.00
PIT4504001:Adgrv1	UTSW	13	81,707,471 (GRCm39)	missense	probably damaging	0.99
R0017:Adgrv1	UTSW	13	81,727,065 (GRCm39)	missense	probably benign	0.13
R0017:Adgrv1	UTSW	13	81,727,065 (GRCm39)	missense	probably benign	0.13
R0058:Adgrv1	UTSW	13	81,330,791 (GRCm39)	missense	possibly damaging	0.65
R0058:Adgrv1	UTSW	13	81,330,791 (GRCm39)	missense	possibly damaging	0.65
R0083:Adgrv1	UTSW	13	81,726,523 (GRCm39)	unclassified	probably benign
R0087:Adgrv1	UTSW	13	81,535,070 (GRCm39)	missense	probably damaging	1.00
R0108:Adgrv1	UTSW	13	81,726,523 (GRCm39)	unclassified	probably benign
R0131:Adgrv1	UTSW	13	81,651,114 (GRCm39)	unclassified	probably benign
R0218:Adgrv1	UTSW	13	81,255,017 (GRCm39)	splice site	probably null
R0325:Adgrv1	UTSW	13	81,688,134 (GRCm39)	missense	probably damaging	1.00
R0326:Adgrv1	UTSW	13	81,623,112 (GRCm39)	missense	possibly damaging	0.46
R0395:Adgrv1	UTSW	13	81,534,072 (GRCm39)	missense	probably benign	0.00
R0441:Adgrv1	UTSW	13	81,545,345 (GRCm39)	nonsense	probably null
R0466:Adgrv1	UTSW	13	81,714,415 (GRCm39)	missense	probably benign	0.00
R0487:Adgrv1	UTSW	13	81,637,154 (GRCm39)	missense	probably damaging	1.00
R0501:Adgrv1	UTSW	13	81,707,269 (GRCm39)	missense	probably damaging	1.00
R0522:Adgrv1	UTSW	13	81,676,561 (GRCm39)	splice site	probably benign
R0532:Adgrv1	UTSW	13	81,727,015 (GRCm39)	missense	probably damaging	1.00
R0542:Adgrv1	UTSW	13	81,721,437 (GRCm39)	missense	probably damaging	1.00
R0681:Adgrv1	UTSW	13	81,676,649 (GRCm39)	missense	probably damaging	1.00
R0689:Adgrv1	UTSW	13	81,623,224 (GRCm39)	missense	possibly damaging	0.47
R0732:Adgrv1	UTSW	13	81,651,123 (GRCm39)	missense	possibly damaging	0.86
R0746:Adgrv1	UTSW	13	81,718,675 (GRCm39)	missense	probably benign	0.10
R0763:Adgrv1	UTSW	13	81,647,244 (GRCm39)	missense	probably damaging	0.98
R0846:Adgrv1	UTSW	13	81,627,861 (GRCm39)	nonsense	probably null
R0962:Adgrv1	UTSW	13	81,553,465 (GRCm39)	missense	probably benign	0.01
R1146:Adgrv1	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
R1146:Adgrv1	UTSW	13	81,679,795 (GRCm39)	missense	probably damaging	1.00
R1172:Adgrv1	UTSW	13	81,705,182 (GRCm39)	missense	probably damaging	0.98
R1178:Adgrv1	UTSW	13	81,588,156 (GRCm39)	splice site	probably benign
R1310:Adgrv1	UTSW	13	81,714,496 (GRCm39)	missense	probably benign	0.09
R1386:Adgrv1	UTSW	13	81,676,984 (GRCm39)	missense	probably benign	0.17
R1387:Adgrv1	UTSW	13	81,641,295 (GRCm39)	missense	possibly damaging	0.62
R1395:Adgrv1	UTSW	13	81,534,907 (GRCm39)	missense	probably benign	0.05
R1412:Adgrv1	UTSW	13	81,243,569 (GRCm39)	missense	probably damaging	1.00
R1448:Adgrv1	UTSW	13	81,581,632 (GRCm39)	missense	probably benign	0.08
R1470:Adgrv1	UTSW	13	81,530,417 (GRCm39)	missense	probably benign	0.03
R1470:Adgrv1	UTSW	13	81,530,417 (GRCm39)	missense	probably benign	0.03
R1485:Adgrv1	UTSW	13	81,727,738 (GRCm39)	missense	probably damaging	1.00
R1507:Adgrv1	UTSW	13	81,620,699 (GRCm39)	critical splice acceptor site	probably null
R1513:Adgrv1	UTSW	13	81,705,076 (GRCm39)	missense	probably damaging	1.00
R1513:Adgrv1	UTSW	13	81,741,167 (GRCm39)	missense	probably damaging	1.00
R1539:Adgrv1	UTSW	13	81,652,097 (GRCm39)	splice site	probably null
R1579:Adgrv1	UTSW	13	81,711,898 (GRCm39)	missense	probably damaging	1.00
R1580:Adgrv1	UTSW	13	81,614,279 (GRCm39)	critical splice donor site	probably null
R1611:Adgrv1	UTSW	13	81,707,236 (GRCm39)	missense	probably damaging	1.00
R1615:Adgrv1	UTSW	13	81,572,407 (GRCm39)	missense	probably benign	0.41
R1651:Adgrv1	UTSW	13	81,635,972 (GRCm39)	missense	probably benign	0.19
R1660:Adgrv1	UTSW	13	81,624,750 (GRCm39)	missense	probably benign	0.00
R1679:Adgrv1	UTSW	13	81,707,671 (GRCm39)	missense	probably damaging	1.00
R1709:Adgrv1	UTSW	13	81,741,179 (GRCm39)	missense	probably damaging	1.00
R1735:Adgrv1	UTSW	13	81,636,066 (GRCm39)	missense	possibly damaging	0.62
R1762:Adgrv1	UTSW	13	81,654,265 (GRCm39)	missense	probably benign	0.08
R1830:Adgrv1	UTSW	13	81,637,196 (GRCm39)	missense	possibly damaging	0.65
R1836:Adgrv1	UTSW	13	81,652,232 (GRCm39)	missense	probably benign	0.01
R1843:Adgrv1	UTSW	13	81,692,652 (GRCm39)	missense	probably damaging	1.00
R1863:Adgrv1	UTSW	13	81,711,685 (GRCm39)	missense	probably damaging	1.00
R1895:Adgrv1	UTSW	13	81,522,368 (GRCm39)	missense	probably damaging	1.00
R1907:Adgrv1	UTSW	13	81,740,670 (GRCm39)	splice site	probably benign
R1928:Adgrv1	UTSW	13	81,668,905 (GRCm39)	missense	probably benign	0.00
R1938:Adgrv1	UTSW	13	81,539,876 (GRCm39)	missense	probably damaging	0.99
R1944:Adgrv1	UTSW	13	81,659,030 (GRCm39)	missense	probably damaging	1.00
R1946:Adgrv1	UTSW	13	81,522,368 (GRCm39)	missense	probably damaging	1.00
R1984:Adgrv1	UTSW	13	81,671,868 (GRCm39)	missense	probably damaging	1.00
R2027:Adgrv1	UTSW	13	81,743,301 (GRCm39)	missense	probably damaging	1.00
R2063:Adgrv1	UTSW	13	81,709,588 (GRCm39)	missense	possibly damaging	0.81
R2116:Adgrv1	UTSW	13	81,677,132 (GRCm39)	missense	probably benign	0.11
R2117:Adgrv1	UTSW	13	81,640,656 (GRCm39)	missense	probably benign	0.00
R2125:Adgrv1	UTSW	13	81,568,069 (GRCm39)	missense	probably benign	0.02
R2125:Adgrv1	UTSW	13	81,567,654 (GRCm39)	missense	probably benign	0.00
R2127:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2128:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2129:Adgrv1	UTSW	13	81,705,199 (GRCm39)	missense	probably damaging	1.00
R2130:Adgrv1	UTSW	13	81,729,846 (GRCm39)	missense	possibly damaging	0.61
R2135:Adgrv1	UTSW	13	81,672,676 (GRCm39)	critical splice donor site	probably null
R2138:Adgrv1	UTSW	13	81,593,439 (GRCm39)	missense	probably benign	0.00
R2166:Adgrv1	UTSW	13	81,716,762 (GRCm39)	missense	probably damaging	1.00
R2171:Adgrv1	UTSW	13	81,419,037 (GRCm39)	missense	probably damaging	1.00
R2191:Adgrv1	UTSW	13	81,714,409 (GRCm39)	missense	possibly damaging	0.90
R2256:Adgrv1	UTSW	13	81,654,259 (GRCm39)	missense	probably benign
R2260:Adgrv1	UTSW	13	81,716,493 (GRCm39)	missense	probably damaging	0.97
R2323:Adgrv1	UTSW	13	81,743,298 (GRCm39)	missense	probably damaging	1.00
R2432:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R2910:Adgrv1	UTSW	13	81,705,238 (GRCm39)	missense	possibly damaging	0.61
R2920:Adgrv1	UTSW	13	81,596,984 (GRCm39)	missense	probably benign	0.01
R2989:Adgrv1	UTSW	13	81,729,866 (GRCm39)	missense	probably damaging	1.00
R3402:Adgrv1	UTSW	13	81,691,661 (GRCm39)	missense	probably damaging	1.00
R3692:Adgrv1	UTSW	13	81,672,719 (GRCm39)	missense	possibly damaging	0.91
R3711:Adgrv1	UTSW	13	81,567,594 (GRCm39)	missense	probably benign	0.02
R3732:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3732:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3733:Adgrv1	UTSW	13	81,705,075 (GRCm39)	missense	probably damaging	1.00
R3773:Adgrv1	UTSW	13	81,647,162 (GRCm39)	missense	probably damaging	0.98
R3791:Adgrv1	UTSW	13	81,741,221 (GRCm39)	missense	probably damaging	1.00
R3794:Adgrv1	UTSW	13	81,431,486 (GRCm39)	start codon destroyed	probably damaging	1.00
R3848:Adgrv1	UTSW	13	81,588,191 (GRCm39)	missense	probably damaging	0.97
R3880:Adgrv1	UTSW	13	81,583,824 (GRCm39)	missense	probably benign	0.02
R3925:Adgrv1	UTSW	13	81,726,891 (GRCm39)	missense	possibly damaging	0.89
R3934:Adgrv1	UTSW	13	81,623,166 (GRCm39)	missense	probably benign	0.06
R3942:Adgrv1	UTSW	13	81,330,908 (GRCm39)	missense	probably damaging	1.00
R4002:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R4003:Adgrv1	UTSW	13	81,688,251 (GRCm39)	frame shift	probably null
R4194:Adgrv1	UTSW	13	81,647,115 (GRCm39)	missense	probably damaging	0.98
R4308:Adgrv1	UTSW	13	81,588,311 (GRCm39)	missense	probably damaging	0.96
R4368:Adgrv1	UTSW	13	81,641,029 (GRCm39)	missense	unknown
R4388:Adgrv1	UTSW	13	81,729,828 (GRCm39)	missense	probably damaging	0.98
R4421:Adgrv1	UTSW	13	81,714,421 (GRCm39)	missense	probably damaging	1.00
R4468:Adgrv1	UTSW	13	81,522,375 (GRCm39)	missense	probably benign	0.01
R4483:Adgrv1	UTSW	13	81,567,349 (GRCm39)	missense	probably benign	0.01
R4487:Adgrv1	UTSW	13	81,588,185 (GRCm39)	missense	probably damaging	0.99
R4566:Adgrv1	UTSW	13	81,567,927 (GRCm39)	missense	probably damaging	1.00
R4615:Adgrv1	UTSW	13	81,642,688 (GRCm39)	splice site	probably null
R4647:Adgrv1	UTSW	13	81,676,914 (GRCm39)	nonsense	probably null
R4657:Adgrv1	UTSW	13	81,553,483 (GRCm39)	missense	probably benign	0.01
R4723:Adgrv1	UTSW	13	81,581,644 (GRCm39)	missense	probably benign	0.02
R4765:Adgrv1	UTSW	13	81,255,038 (GRCm39)	missense	probably damaging	0.99
R4783:Adgrv1	UTSW	13	81,243,564 (GRCm39)	missense	probably damaging	0.99
R4796:Adgrv1	UTSW	13	81,303,350 (GRCm39)	nonsense	probably null
R4816:Adgrv1	UTSW	13	81,676,793 (GRCm39)	missense	probably damaging	1.00
R4833:Adgrv1	UTSW	13	81,708,963 (GRCm39)	missense	possibly damaging	0.81
R4841:Adgrv1	UTSW	13	81,651,120 (GRCm39)	critical splice donor site	probably null
R4871:Adgrv1	UTSW	13	81,681,241 (GRCm39)	intron	probably benign
R4897:Adgrv1	UTSW	13	81,709,704 (GRCm39)	splice site	probably null
R4906:Adgrv1	UTSW	13	81,418,857 (GRCm39)	splice site	probably null
R4917:Adgrv1	UTSW	13	81,658,996 (GRCm39)	missense	probably benign	0.30
R4996:Adgrv1	UTSW	13	81,726,853 (GRCm39)	missense	probably benign	0.01
R5030:Adgrv1	UTSW	13	81,607,948 (GRCm39)	missense	probably benign	0.43
R5044:Adgrv1	UTSW	13	81,637,050 (GRCm39)	missense	probably benign	0.01
R5052:Adgrv1	UTSW	13	81,676,940 (GRCm39)	missense	probably damaging	0.97
R5093:Adgrv1	UTSW	13	81,740,704 (GRCm39)	missense	probably damaging	1.00
R5095:Adgrv1	UTSW	13	81,243,606 (GRCm39)	missense	probably benign	0.00
R5119:Adgrv1	UTSW	13	81,567,546 (GRCm39)	missense	possibly damaging	0.93
R5133:Adgrv1	UTSW	13	81,587,560 (GRCm39)	missense	probably damaging	1.00
R5141:Adgrv1	UTSW	13	81,419,037 (GRCm39)	missense	probably damaging	1.00
R5164:Adgrv1	UTSW	13	81,583,793 (GRCm39)	missense	probably benign	0.00
R5180:Adgrv1	UTSW	13	81,431,535 (GRCm39)	start gained	probably benign
R5203:Adgrv1	UTSW	13	81,659,024 (GRCm39)	missense	possibly damaging	0.91
R5241:Adgrv1	UTSW	13	81,637,048 (GRCm39)	nonsense	probably null
R5280:Adgrv1	UTSW	13	81,545,584 (GRCm39)	missense	possibly damaging	0.95
R5289:Adgrv1	UTSW	13	81,669,203 (GRCm39)	missense	probably benign	0.04
R5304:Adgrv1	UTSW	13	81,726,372 (GRCm39)	missense	possibly damaging	0.93
R5310:Adgrv1	UTSW	13	81,624,809 (GRCm39)	missense	possibly damaging	0.95
R5338:Adgrv1	UTSW	13	81,677,165 (GRCm39)	missense	possibly damaging	0.80
R5352:Adgrv1	UTSW	13	81,642,776 (GRCm39)	missense	probably damaging	1.00
R5402:Adgrv1	UTSW	13	81,607,834 (GRCm39)	missense	probably benign	0.25
R5418:Adgrv1	UTSW	13	81,567,427 (GRCm39)	missense	probably benign	0.01
R5460:Adgrv1	UTSW	13	81,572,377 (GRCm39)	missense	possibly damaging	0.95
R5510:Adgrv1	UTSW	13	81,593,363 (GRCm39)	missense	probably damaging	1.00
R5521:Adgrv1	UTSW	13	81,567,508 (GRCm39)	missense	probably benign	0.01
R5538:Adgrv1	UTSW	13	81,581,808 (GRCm39)	missense	probably benign	0.02
R5561:Adgrv1	UTSW	13	81,624,683 (GRCm39)	missense	probably damaging	0.99
R5584:Adgrv1	UTSW	13	81,553,386 (GRCm39)	missense	probably damaging	1.00
R5608:Adgrv1	UTSW	13	81,303,395 (GRCm39)	missense	probably damaging	1.00
R5610:Adgrv1	UTSW	13	81,669,236 (GRCm39)	missense	probably damaging	1.00
R5619:Adgrv1	UTSW	13	81,620,619 (GRCm39)	missense	probably damaging	1.00
R5751:Adgrv1	UTSW	13	81,670,355 (GRCm39)	missense	probably damaging	1.00
R5832:Adgrv1	UTSW	13	81,251,421 (GRCm39)	missense	possibly damaging	0.95
R5885:Adgrv1	UTSW	13	81,572,390 (GRCm39)	missense	probably benign	0.15
R5930:Adgrv1	UTSW	13	81,545,570 (GRCm39)	missense	probably benign	0.06
R5937:Adgrv1	UTSW	13	81,255,194 (GRCm39)	missense	probably damaging	0.96
R5943:Adgrv1	UTSW	13	81,534,985 (GRCm39)	missense	probably damaging	0.98
R5951:Adgrv1	UTSW	13	81,590,620 (GRCm39)	missense	probably damaging	1.00
R5977:Adgrv1	UTSW	13	81,583,678 (GRCm39)	critical splice donor site	probably null
R5995:Adgrv1	UTSW	13	81,614,378 (GRCm39)	missense	probably benign	0.03
R6017:Adgrv1	UTSW	13	81,545,542 (GRCm39)	nonsense	probably null
R6024:Adgrv1	UTSW	13	81,624,624 (GRCm39)	missense	probably benign	0.26
R6049:Adgrv1	UTSW	13	81,545,473 (GRCm39)	missense	probably benign	0.00
R6108:Adgrv1	UTSW	13	81,539,814 (GRCm39)	missense	probably damaging	0.99
R6130:Adgrv1	UTSW	13	81,575,864 (GRCm39)	missense	probably damaging	0.99
R6132:Adgrv1	UTSW	13	81,654,195 (GRCm39)	missense	probably benign	0.04
R6149:Adgrv1	UTSW	13	81,330,893 (GRCm39)	missense	probably damaging	1.00
R6169:Adgrv1	UTSW	13	81,567,378 (GRCm39)	missense	probably benign	0.00
R6175:Adgrv1	UTSW	13	81,534,124 (GRCm39)	missense	probably damaging	1.00
R6184:Adgrv1	UTSW	13	81,581,957 (GRCm39)	missense	probably benign	0.01
R6190:Adgrv1	UTSW	13	81,672,898 (GRCm39)	splice site	probably null
R6190:Adgrv1	UTSW	13	81,607,882 (GRCm39)	splice site	probably null
R6215:Adgrv1	UTSW	13	81,727,713 (GRCm39)	nonsense	probably null
R6216:Adgrv1	UTSW	13	81,672,590 (GRCm39)	splice site	probably null
R6238:Adgrv1	UTSW	13	81,614,402 (GRCm39)	missense	probably benign	0.07
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'- TGATCCAAATCGCTCACAGGAC -3'
(R):5'- TTTAGCTGAGCTGGCCAGATG -3'

Sequencing Primer
(F):5'- TCGCTCACAGGACAGAAAAG -3'
(R):5'- TGGCCAGATGACCTTTGACATAC -3'

Posted On

2018-02-28