Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03070:Vmn2r72'

417495

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn2r72

Ensembl Gene

ENSMUSG00000051877

Gene Name

vomeronasal 2, receptor 72

Synonyms

Vmn2r72-ps, EG244114

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.113) question?

Stock #

IGL03070

Quality Score

Status

Chromosome

Chromosomal Location

85737784-85754981 bp(-) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

C to T at 85752041 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000133014 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000063425]

AlphaFold

D3Z4N8

Predicted Effect

probably benign
Transcript: ENSMUST00000063425

SMART Domains

Protein: ENSMUSP00000133014
Gene: ENSMUSG00000051877

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	82	469	2.3e-28	PFAM
Pfam:NCD3G	512	564	1.2e-18	PFAM
Pfam:7tm_3	594	832	4e-53	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 26 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam3	T	C	8: 24,703,784 (GRCm38)	E404G	probably damaging	Het
Arid1a	A	G	4: 133,694,753 (GRCm38)	S778P	unknown	Het
Asah2	A	T	19: 32,006,344 (GRCm38)	Y567N	probably damaging	Het
Crb1	G	T	1: 139,241,258 (GRCm38)	H841N	possibly damaging	Het
Ehbp1l1	A	G	19: 5,715,953 (GRCm38)	V1454A	probably benign	Het
Eif3d	A	G	15: 77,959,643 (GRCm38)	L501P	probably damaging	Het
Fbxo4	A	T	15: 3,977,862 (GRCm38)	S107T	possibly damaging	Het
Galnt10	T	C	11: 57,725,582 (GRCm38)	Y108H	probably damaging	Het
Hspbap1	T	A	16: 35,818,726 (GRCm38)	D263E	probably damaging	Het
Kpna3	T	C	14: 61,370,782 (GRCm38)		probably benign	Het
Miox	A	G	15: 89,336,084 (GRCm38)	T160A	possibly damaging	Het
Mlxipl	G	A	5: 135,132,453 (GRCm38)	V409M	possibly damaging	Het
Mrps21	A	T	3: 95,870,585 (GRCm38)		probably benign	Het
Muc6	A	G	7: 141,644,567 (GRCm38)		probably benign	Het
Mup6	A	T	4: 60,003,999 (GRCm38)	I31F	probably damaging	Het
Or52s1	A	G	7: 103,212,697 (GRCm38)	H279R	probably benign	Het
Pabir1	A	C	19: 24,476,952 (GRCm38)	D135E	probably damaging	Het
Pgr	T	A	9: 8,903,664 (GRCm38)	I562N	possibly damaging	Het
Prag1	T	A	8: 36,103,549 (GRCm38)	W429R	probably benign	Het
Prrc2c	G	T	1: 162,677,409 (GRCm38)	P2621Q	probably damaging	Het
Psip1	T	G	4: 83,465,081 (GRCm38)	K232N	probably damaging	Het
Ryr1	T	C	7: 29,070,659 (GRCm38)	Y2663C	probably damaging	Het
Trhr2	T	A	8: 122,358,603 (GRCm38)	Q214L	probably benign	Het
Txndc11	A	T	16: 11,075,287 (GRCm38)	Y860N	probably damaging	Het
Uqcc6	A	T	10: 82,620,116 (GRCm38)		probably benign	Het
Yif1a	T	A	19: 5,088,729 (GRCm38)	H4Q	possibly damaging	Het

Other mutations in Vmn2r72

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00931:Vmn2r72	APN	7	85,749,646 (GRCm38)	missense	probably benign	0.01
IGL01019:Vmn2r72	APN	7	85,738,334 (GRCm38)	missense	probably benign	0.26
IGL01445:Vmn2r72	APN	7	85,749,646 (GRCm38)	missense	probably benign	0.06
IGL02076:Vmn2r72	APN	7	85,738,367 (GRCm38)	missense	probably damaging	1.00
IGL02082:Vmn2r72	APN	7	85,738,166 (GRCm38)	missense	probably benign	0.00
IGL02086:Vmn2r72	APN	7	85,738,166 (GRCm38)	missense	probably benign	0.00
IGL02089:Vmn2r72	APN	7	85,738,166 (GRCm38)	missense	probably benign	0.00
IGL02125:Vmn2r72	APN	7	85,750,711 (GRCm38)	missense	probably benign	0.00
IGL02146:Vmn2r72	APN	7	85,737,962 (GRCm38)	missense	probably damaging	1.00
IGL02272:Vmn2r72	APN	7	85,750,693 (GRCm38)	missense	probably benign
IGL02514:Vmn2r72	APN	7	85,738,699 (GRCm38)	missense	possibly damaging	0.90
IGL02662:Vmn2r72	APN	7	85,738,183 (GRCm38)	missense	probably benign	0.26
IGL02697:Vmn2r72	APN	7	85,738,671 (GRCm38)	missense	probably benign	0.36
IGL02733:Vmn2r72	APN	7	85,751,813 (GRCm38)	missense	probably benign	0.05
IGL03150:Vmn2r72	APN	7	85,751,176 (GRCm38)	missense	probably damaging	1.00
IGL03159:Vmn2r72	APN	7	85,754,954 (GRCm38)	missense	probably benign	0.05
IGL03333:Vmn2r72	APN	7	85,750,867 (GRCm38)	missense	probably benign	0.10
R0081:Vmn2r72	UTSW	7	85,751,836 (GRCm38)	missense	probably benign	0.01
R0090:Vmn2r72	UTSW	7	85,754,876 (GRCm38)	missense	probably benign
R0655:Vmn2r72	UTSW	7	85,738,111 (GRCm38)	nonsense	probably null
R0778:Vmn2r72	UTSW	7	85,749,739 (GRCm38)	missense	probably benign	0.00
R1169:Vmn2r72	UTSW	7	85,751,309 (GRCm38)	missense	probably benign	0.01
R1172:Vmn2r72	UTSW	7	85,751,944 (GRCm38)	missense	probably damaging	1.00
R1173:Vmn2r72	UTSW	7	85,751,944 (GRCm38)	missense	probably damaging	1.00
R1175:Vmn2r72	UTSW	7	85,751,944 (GRCm38)	missense	probably damaging	1.00
R1248:Vmn2r72	UTSW	7	85,749,188 (GRCm38)	missense	probably benign	0.02
R1302:Vmn2r72	UTSW	7	85,738,257 (GRCm38)	missense	probably damaging	1.00
R1506:Vmn2r72	UTSW	7	85,749,211 (GRCm38)	missense	probably benign
R1632:Vmn2r72	UTSW	7	85,751,792 (GRCm38)	missense	probably benign	0.13
R1775:Vmn2r72	UTSW	7	85,738,170 (GRCm38)	missense	probably benign	0.01
R1962:Vmn2r72	UTSW	7	85,749,161 (GRCm38)	missense	probably benign	0.00
R2201:Vmn2r72	UTSW	7	85,738,236 (GRCm38)	missense	probably benign	0.12
R2290:Vmn2r72	UTSW	7	85,738,341 (GRCm38)	missense	probably damaging	1.00
R2327:Vmn2r72	UTSW	7	85,738,256 (GRCm38)	missense	probably damaging	1.00
R2424:Vmn2r72	UTSW	7	85,750,953 (GRCm38)	missense	probably damaging	1.00
R2655:Vmn2r72	UTSW	7	85,751,269 (GRCm38)	missense	possibly damaging	0.95
R2860:Vmn2r72	UTSW	7	85,750,836 (GRCm38)	missense	probably damaging	0.99
R2861:Vmn2r72	UTSW	7	85,750,836 (GRCm38)	missense	probably damaging	0.99
R2862:Vmn2r72	UTSW	7	85,750,836 (GRCm38)	missense	probably damaging	0.99
R3009:Vmn2r72	UTSW	7	85,749,642 (GRCm38)	missense	probably benign	0.00
R3797:Vmn2r72	UTSW	7	85,738,077 (GRCm38)	missense	probably benign	0.44
R3798:Vmn2r72	UTSW	7	85,738,077 (GRCm38)	missense	probably benign	0.44
R3902:Vmn2r72	UTSW	7	85,749,735 (GRCm38)	missense	possibly damaging	0.52
R3959:Vmn2r72	UTSW	7	85,751,131 (GRCm38)	missense	probably benign	0.36
R3974:Vmn2r72	UTSW	7	85,749,809 (GRCm38)	missense	probably damaging	1.00
R4399:Vmn2r72	UTSW	7	85,738,500 (GRCm38)	missense	probably damaging	1.00
R4421:Vmn2r72	UTSW	7	85,738,500 (GRCm38)	missense	probably damaging	1.00
R4426:Vmn2r72	UTSW	7	85,737,828 (GRCm38)	nonsense	probably null
R4522:Vmn2r72	UTSW	7	85,751,926 (GRCm38)	missense	probably benign	0.44
R4523:Vmn2r72	UTSW	7	85,751,926 (GRCm38)	missense	probably benign	0.44
R4533:Vmn2r72	UTSW	7	85,751,926 (GRCm38)	missense	probably benign	0.44
R4691:Vmn2r72	UTSW	7	85,737,911 (GRCm38)	nonsense	probably null
R4781:Vmn2r72	UTSW	7	85,737,861 (GRCm38)	missense	probably benign	0.14
R4863:Vmn2r72	UTSW	7	85,750,598 (GRCm38)	missense	possibly damaging	0.91
R4952:Vmn2r72	UTSW	7	85,751,109 (GRCm38)	missense	probably benign
R4991:Vmn2r72	UTSW	7	85,751,130 (GRCm38)	missense	probably damaging	0.99
R4995:Vmn2r72	UTSW	7	85,738,485 (GRCm38)	missense	probably damaging	1.00
R5095:Vmn2r72	UTSW	7	85,737,853 (GRCm38)	missense	probably damaging	0.98
R5174:Vmn2r72	UTSW	7	85,737,840 (GRCm38)	missense	probably benign	0.00
R5276:Vmn2r72	UTSW	7	85,738,254 (GRCm38)	missense	possibly damaging	0.90
R5395:Vmn2r72	UTSW	7	85,750,897 (GRCm38)	missense	possibly damaging	0.71
R5560:Vmn2r72	UTSW	7	85,751,942 (GRCm38)	missense	probably damaging	0.96
R5933:Vmn2r72	UTSW	7	85,737,850 (GRCm38)	missense	probably benign	0.05
R6033:Vmn2r72	UTSW	7	85,737,929 (GRCm38)	missense	probably damaging	1.00
R6033:Vmn2r72	UTSW	7	85,737,929 (GRCm38)	missense	probably damaging	1.00
R6354:Vmn2r72	UTSW	7	85,750,539 (GRCm38)	critical splice donor site	probably null
R6362:Vmn2r72	UTSW	7	85,751,174 (GRCm38)	missense	probably damaging	1.00
R6594:Vmn2r72	UTSW	7	85,749,684 (GRCm38)	missense	probably benign	0.32
R6794:Vmn2r72	UTSW	7	85,737,996 (GRCm38)	missense	probably damaging	1.00
R7113:Vmn2r72	UTSW	7	85,749,803 (GRCm38)	splice site	probably null
R7189:Vmn2r72	UTSW	7	85,754,917 (GRCm38)	missense	probably benign	0.36
R7266:Vmn2r72	UTSW	7	85,738,274 (GRCm38)	nonsense	probably null
R7323:Vmn2r72	UTSW	7	85,750,563 (GRCm38)	missense	probably benign
R7426:Vmn2r72	UTSW	7	85,751,140 (GRCm38)	missense	probably benign
R7606:Vmn2r72	UTSW	7	85,751,154 (GRCm38)	missense	possibly damaging	0.91
R7651:Vmn2r72	UTSW	7	85,751,938 (GRCm38)	missense	probably damaging	1.00
R7688:Vmn2r72	UTSW	7	85,754,890 (GRCm38)	missense	probably benign	0.32
R7753:Vmn2r72	UTSW	7	85,750,626 (GRCm38)	missense	probably damaging	1.00
R7843:Vmn2r72	UTSW	7	85,749,630 (GRCm38)	missense	probably benign	0.01
R8157:Vmn2r72	UTSW	7	85,751,233 (GRCm38)	missense	probably benign	0.09
R8254:Vmn2r72	UTSW	7	85,751,019 (GRCm38)	missense	probably damaging	1.00
R8389:Vmn2r72	UTSW	7	85,751,960 (GRCm38)	missense	probably damaging	0.99
R8444:Vmn2r72	UTSW	7	85,738,175 (GRCm38)	missense	probably benign
R8989:Vmn2r72	UTSW	7	85,754,926 (GRCm38)	missense	probably benign	0.10
R9015:Vmn2r72	UTSW	7	85,749,180 (GRCm38)	missense	probably benign	0.01
R9080:Vmn2r72	UTSW	7	85,738,256 (GRCm38)	missense	probably damaging	1.00
R9269:Vmn2r72	UTSW	7	85,751,203 (GRCm38)	missense	probably benign	0.03
R9317:Vmn2r72	UTSW	7	85,754,814 (GRCm38)	missense	probably benign	0.04
R9509:Vmn2r72	UTSW	7	85,754,867 (GRCm38)	missense	probably benign
Z1176:Vmn2r72	UTSW	7	85,749,191 (GRCm38)	missense	probably damaging	0.99

Posted On

2016-08-02