Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01301:Vmn1r18'

73258

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn1r18

Ensembl Gene

ENSMUSG00000091382

Gene Name

vomeronasal 1 receptor 18

Synonyms

V1rc26

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.055) question?

Stock #

IGL01301

Quality Score

Status

Chromosome

Chromosomal Location

57366653-57367552 bp(-) (GRCm39)

Type of Mutation

utr 3 prime

DNA Base Change (assembly)

T to C at 57366652 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000154497 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164732] [ENSMUST00000228574]

AlphaFold

Q8R2C8

Predicted Effect

probably benign
Transcript: ENSMUST00000164732

SMART Domains

Protein: ENSMUSP00000129827
Gene: ENSMUSG00000091382

Domain	Start	End	E-Value	Type
Pfam:V1R	29	293	1.1e-59	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000228574

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1600012H06Rik	C	T	17: 15,164,181 (GRCm39)		probably null	Het
Acacb	A	T	5: 114,384,559 (GRCm39)	I2238L	probably benign	Het
Aldh1l2	T	C	10: 83,358,710 (GRCm39)	Y95C	probably damaging	Het
Asxl2	A	G	12: 3,551,425 (GRCm39)	T1056A	probably damaging	Het
B4galnt1	A	G	10: 127,005,648 (GRCm39)	T250A	possibly damaging	Het
Cela3b	A	T	4: 137,151,154 (GRCm39)		probably null	Het
Chst3	T	C	10: 60,021,654 (GRCm39)	T398A	probably damaging	Het
Cngb3	A	G	4: 19,425,625 (GRCm39)	T478A	probably damaging	Het
Cyp4a10	T	C	4: 115,375,652 (GRCm39)	L45P	probably damaging	Het
Defb21	A	G	2: 152,416,671 (GRCm39)	E49G	possibly damaging	Het
Dnajc1	T	C	2: 18,313,645 (GRCm39)	T159A	probably damaging	Het
Dnmbp	A	G	19: 43,890,793 (GRCm39)	S325P	probably benign	Het
Fam91a1	T	C	15: 58,314,720 (GRCm39)	F534L	probably damaging	Het
Fermt2	T	C	14: 45,702,320 (GRCm39)	E488G	probably damaging	Het
Filip1	T	C	9: 79,726,462 (GRCm39)	D719G	possibly damaging	Het
Gad1-ps	A	G	10: 99,281,013 (GRCm39)		noncoding transcript	Het
Glra3	C	A	8: 56,393,997 (GRCm39)	A36E	probably benign	Het
Gm9884	T	A	1: 25,869,729 (GRCm39)		probably benign	Het
Hectd2	T	C	19: 36,546,770 (GRCm39)		probably benign	Het
Hnrnpm	C	T	17: 33,888,142 (GRCm39)		probably null	Het
Lrrk2	T	A	15: 91,651,542 (GRCm39)	Y1733N	probably damaging	Het
Mindy1	T	C	3: 95,195,701 (GRCm39)	L148P	probably damaging	Het
Mkrn2	C	A	6: 115,588,750 (GRCm39)	Y164*	probably null	Het
Msra	T	C	14: 64,447,884 (GRCm39)	Y135C	probably damaging	Het
Ndst3	C	T	3: 123,342,565 (GRCm39)	A749T	probably damaging	Het
Ngdn	G	T	14: 55,254,571 (GRCm39)	A41S	probably benign	Het
Nlrp12	A	T	7: 3,288,722 (GRCm39)	S597T	probably damaging	Het
Or5b99	A	T	19: 12,976,781 (GRCm39)	I144F	probably damaging	Het
Pabpc6	A	G	17: 9,886,899 (GRCm39)	S551P	probably benign	Het
Plekhg5	C	T	4: 152,197,010 (GRCm39)	A752V	probably benign	Het
Prpf4b	T	C	13: 35,068,274 (GRCm39)	S368P	probably benign	Het
Pus7	A	G	5: 23,951,422 (GRCm39)		probably null	Het
Rad23b	T	C	4: 55,366,774 (GRCm39)		probably benign	Het
Rgs13	T	C	1: 144,047,152 (GRCm39)		probably benign	Het
Sfpq	T	C	4: 126,920,553 (GRCm39)		probably benign	Het
Slc9a9	T	A	9: 94,937,512 (GRCm39)	S455T	probably benign	Het
Slco1a1	A	G	6: 141,878,256 (GRCm39)		probably benign	Het
Tmem26	A	T	10: 68,614,436 (GRCm39)	N284Y	probably damaging	Het
Tmem87a	T	C	2: 120,211,250 (GRCm39)	I232V	probably benign	Het
Trpm2	A	G	10: 77,759,818 (GRCm39)	L1106P	probably damaging	Het
Zfp213	G	T	17: 23,780,391 (GRCm39)	A43D	probably benign	Het
Zfp365	A	G	10: 67,745,184 (GRCm39)	V198A	probably damaging	Het
Zfp395	T	A	14: 65,632,200 (GRCm39)		probably null	Het
Zfp618	G	A	4: 63,051,063 (GRCm39)	V615M	probably damaging	Het

Other mutations in Vmn1r18

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01129:Vmn1r18	APN	6	57,367,482 (GRCm39)	missense	probably benign	0.03
IGL01996:Vmn1r18	APN	6	57,367,001 (GRCm39)	missense	possibly damaging	0.80
IGL02017:Vmn1r18	APN	6	57,366,741 (GRCm39)	missense	probably benign	0.01
R1908:Vmn1r18	UTSW	6	57,367,026 (GRCm39)	missense	possibly damaging	0.77
R4200:Vmn1r18	UTSW	6	57,367,101 (GRCm39)	missense	probably benign	0.01
R4288:Vmn1r18	UTSW	6	57,367,392 (GRCm39)	missense	probably damaging	1.00
R4667:Vmn1r18	UTSW	6	57,367,069 (GRCm39)	missense	probably benign	0.11
R6029:Vmn1r18	UTSW	6	57,367,451 (GRCm39)	missense	possibly damaging	0.88
R6767:Vmn1r18	UTSW	6	57,367,206 (GRCm39)	missense	probably damaging	1.00
R7174:Vmn1r18	UTSW	6	57,366,609 (GRCm39)	splice site	probably null
R7229:Vmn1r18	UTSW	6	57,367,083 (GRCm39)	missense	probably benign	0.14
R7332:Vmn1r18	UTSW	6	57,367,503 (GRCm39)	missense	probably benign	0.06
R7425:Vmn1r18	UTSW	6	57,367,551 (GRCm39)	start codon destroyed	probably null	1.00
R9428:Vmn1r18	UTSW	6	57,367,535 (GRCm39)	missense	possibly damaging	0.88
R9561:Vmn1r18	UTSW	6	57,367,202 (GRCm39)	missense	probably benign	0.01
R9685:Vmn1r18	UTSW	6	57,367,463 (GRCm39)	missense	possibly damaging	0.67

Posted On

2013-10-07