Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01650:Vmn2r44'

102821

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Vmn2r44

Ensembl Gene

ENSMUSG00000094098

Gene Name

vomeronasal 2, receptor 44

Synonyms

EG434113

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01650

Quality Score

Status

Chromosome

Chromosomal Location

8366502-8383354 bp(-) (GRCm38)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

C to A at 8380104 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000132467 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166499]

AlphaFold

L7N2E1

Predicted Effect

probably null
Transcript: ENSMUST00000166499

SMART Domains

Protein: ENSMUSP00000132467
Gene: ENSMUSG00000094098

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:ANF_receptor	73	469	2.5e-34	PFAM
Pfam:NCD3G	512	565	3.8e-20	PFAM
Pfam:7tm_3	598	833	5.7e-55	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	G	A	3: 36,992,673		probably benign	Het
Agbl1	A	G	7: 76,420,319	D281G	probably damaging	Het
Arhgap28	T	C	17: 67,873,132	E236G	probably damaging	Het
Btbd3	A	T	2: 138,284,105	D334V	probably damaging	Het
Cabp4	T	C	19: 4,139,324	E78G	probably benign	Het
Clcn4	T	C	7: 7,284,281		probably benign	Het
Col14a1	A	G	15: 55,406,693	Y600C	unknown	Het
Cpne4	A	G	9: 104,901,511	D167G	probably damaging	Het
Eif3a	T	A	19: 60,773,996	I450F	probably damaging	Het
Enpp2	T	A	15: 54,919,933	Y10F	probably benign	Het
Fam227a	A	T	15: 79,634,073	H339Q	possibly damaging	Het
Far2	C	A	6: 148,173,487	T406K	possibly damaging	Het
Fmo1	A	G	1: 162,833,584	S377P	probably benign	Het
Fsip2	G	A	2: 82,991,086	S5721N	probably benign	Het
Gatb	T	C	3: 85,613,484	I300T	possibly damaging	Het
Gpam	T	C	19: 55,081,700	N375D	probably benign	Het
Gsdma	G	T	11: 98,673,687	D331Y	probably damaging	Het
Kif13b	T	C	14: 64,765,145	V1073A	probably benign	Het
Mfsd4b1	T	A	10: 40,003,119	M261L	probably benign	Het
Nav1	A	T	1: 135,454,760	D1321E	probably damaging	Het
Olfr1312	A	G	2: 112,042,375	I219T	possibly damaging	Het
Olfr592	A	G	7: 103,187,079	I159M	probably benign	Het
Olfr813	T	A	10: 129,857,067	L183Q	probably damaging	Het
Olfr816	A	G	10: 129,911,681	V199A	probably benign	Het
Olfr951	G	T	9: 39,393,956	S55I	probably damaging	Het
Ppp1r10	G	T	17: 35,931,161	R857L	unknown	Het
Prune2	T	A	19: 17,168,292	I2752N	possibly damaging	Het
Pxdn	T	C	12: 30,002,401	I859T	probably benign	Het
Ros1	T	C	10: 52,154,979	D510G	probably damaging	Het
Sema3g	C	A	14: 31,221,787	P208H	probably benign	Het
Smcr8	T	C	11: 60,778,184	F53L	probably damaging	Het
Tnfsf13b	A	T	8: 10,031,411	I219F	probably damaging	Het
Vmn1r62	T	C	7: 5,676,025	V235A	probably damaging	Het
Zkscan7	A	G	9: 122,894,827	D287G	probably benign	Het

Other mutations in Vmn2r44

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01723:Vmn2r44	APN	7	8377916	missense	probably damaging	0.97
IGL01767:Vmn2r44	APN	7	8380238	missense	probably benign	0.00
IGL02161:Vmn2r44	APN	7	8377815	missense	possibly damaging	0.94
IGL02299:Vmn2r44	APN	7	8377816	missense	probably benign
IGL02418:Vmn2r44	APN	7	8377865	missense	probably damaging	1.00
IGL02829:Vmn2r44	APN	7	8377880	missense	possibly damaging	0.94
IGL02851:Vmn2r44	APN	7	8383051	missense	probably damaging	1.00
IGL03080:Vmn2r44	APN	7	8383245	utr 5 prime	probably benign
R1471:Vmn2r44	UTSW	7	8377883	missense	probably damaging	0.99
R1789:Vmn2r44	UTSW	7	8380123	missense	possibly damaging	0.64
R1932:Vmn2r44	UTSW	7	8367982	missense	probably benign	0.04
R2354:Vmn2r44	UTSW	7	8370640	missense	probably damaging	0.99
R4009:Vmn2r44	UTSW	7	8377988	missense	possibly damaging	0.82
R4130:Vmn2r44	UTSW	7	8367919	missense	probably damaging	1.00
R4790:Vmn2r44	UTSW	7	8367950	missense	probably damaging	1.00
R4854:Vmn2r44	UTSW	7	8380301	missense	possibly damaging	0.94
R4887:Vmn2r44	UTSW	7	8377986	missense	probably benign	0.19
R4888:Vmn2r44	UTSW	7	8377986	missense	probably benign	0.19
R5484:Vmn2r44	UTSW	7	8380124	missense	possibly damaging	0.69
R6110:Vmn2r44	UTSW	7	8378006	missense	probably damaging	1.00
R6357:Vmn2r44	UTSW	7	8370658	missense	probably benign	0.01
R6526:Vmn2r44	UTSW	7	8378099	missense	probably benign	0.01
R7083:Vmn2r44	UTSW	7	8378370	missense	probably benign	0.44
R7087:Vmn2r44	UTSW	7	8378367	missense	probably benign	0.02
R7115:Vmn2r44	UTSW	7	8367528	nonsense	probably null
R7125:Vmn2r44	UTSW	7	8367942	missense	probably damaging	1.00
R7258:Vmn2r44	UTSW	7	8377849	missense	probably damaging	1.00
R7359:Vmn2r44	UTSW	7	8367539	missense	probably benign	0.30
R7494:Vmn2r44	UTSW	7	8383123	nonsense	probably null
R7766:Vmn2r44	UTSW	7	8368220	missense	probably damaging	1.00
R7777:Vmn2r44	UTSW	7	8378315	missense	possibly damaging	0.81
R8184:Vmn2r44	UTSW	7	8368228	nonsense	probably null
R8674:Vmn2r44	UTSW	7	8377823	missense	probably damaging	1.00
R8752:Vmn2r44	UTSW	7	8367806	missense	probably damaging	1.00
R8897:Vmn2r44	UTSW	7	8378243	missense	probably damaging	1.00
R8915:Vmn2r44	UTSW	7	8367651	missense	probably damaging	1.00
R8928:Vmn2r44	UTSW	7	8378102	missense	probably damaging	1.00
R9163:Vmn2r44	UTSW	7	8368092	missense	probably benign	0.00
Z1177:Vmn2r44	UTSW	7	8367977	missense	probably damaging	0.99

Posted On

2014-01-21