Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02301:Vmn1r-ps123'

290287

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn1r-ps123

Ensembl Gene

ENSMUSG00000079064

Gene Name

vomeronasal 1 receptor, pseudogene 123

Synonyms

Gm11044

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.156) question?

Stock #

IGL02301

Quality Score

Status

Chromosome

Chromosomal Location

23180434-23180670 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to C at 23180527 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000110449

SMART Domains

Protein: ENSMUSP00000106079
Gene: ENSMUSG00000079064

Domain	Start	End	E-Value	Type
Pfam:V1R	1	107	7.4e-10	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Akap8l	A	G	17: 32,551,900 (GRCm39)		probably benign	Het
Alk	T	C	17: 72,181,171 (GRCm39)	Q1373R	probably damaging	Het
Atf7ip2	T	G	16: 10,028,911 (GRCm39)	S148A	probably benign	Het
Bpi	C	T	2: 158,116,734 (GRCm39)	S377F	probably damaging	Het
Ccni	A	T	5: 93,336,034 (GRCm39)	C122S	possibly damaging	Het
Cd5l	A	G	3: 87,273,300 (GRCm39)	R90G	probably benign	Het
Ceacam3	C	T	7: 16,897,026 (GRCm39)	S664F	probably damaging	Het
Clca3a2	A	T	3: 144,512,133 (GRCm39)	D534E	probably damaging	Het
Ep400	A	T	5: 110,822,826 (GRCm39)	S2524R	probably damaging	Het
Fhdc1	G	A	3: 84,352,042 (GRCm39)	A1061V	possibly damaging	Het
Gart	A	G	16: 91,418,725 (GRCm39)		probably benign	Het
Gsdmc4	A	G	15: 63,767,113 (GRCm39)	V219A	probably benign	Het
Hus1	T	C	11: 8,946,915 (GRCm39)	T261A	probably benign	Het
Lman2l	A	G	1: 36,482,624 (GRCm39)	I84T	probably damaging	Het
Megf8	G	A	7: 25,037,325 (GRCm39)	V742M	probably damaging	Het
Myo1d	A	G	11: 80,567,679 (GRCm39)	V267A	probably benign	Het
Notch2	A	G	3: 98,048,870 (GRCm39)	T1803A	probably benign	Het
Or1e17	T	A	11: 73,831,894 (GRCm39)	M274K	possibly damaging	Het
Or4f54	T	A	2: 111,123,042 (GRCm39)	M143K	probably benign	Het
Or6c70	A	G	10: 129,709,948 (GRCm39)	F226S	probably damaging	Het
Pate11	T	C	9: 36,388,483 (GRCm39)		probably benign	Het
Pde5a	G	A	3: 122,554,534 (GRCm39)	R208Q	probably damaging	Het
Pla2r1	T	C	2: 60,282,780 (GRCm39)	N745S	probably benign	Het
Ptgdr2	T	A	19: 10,917,573 (GRCm39)	I30N	possibly damaging	Het
Rap1gap2	G	A	11: 74,298,195 (GRCm39)	T415I	probably damaging	Het
Slc6a6	T	C	6: 91,703,037 (GRCm39)	Y137H	probably benign	Het
Sptbn1	A	T	11: 30,092,129 (GRCm39)	D532E	probably damaging	Het
Stk39	T	C	2: 68,042,306 (GRCm39)	D543G	probably damaging	Het
Trpc4	G	A	3: 54,198,653 (GRCm39)	V526M	probably damaging	Het
Trrap	A	G	5: 144,714,727 (GRCm39)	I100V	probably benign	Het
Vwa5b2	G	A	16: 20,423,540 (GRCm39)	G1151D	probably damaging	Het
Zfp358	T	A	8: 3,546,858 (GRCm39)	I480N	probably benign	Het
Zfp423	T	C	8: 88,508,202 (GRCm39)	D714G	probably damaging	Het

Other mutations in Vmn1r-ps123

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R4876:Vmn1r-ps123	UTSW	13	23,180,535 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16