Mutagenetix > Incidental Mutations

Incidental Mutation 'R5352:Vmn1r48'

423834

Institutional Source

Beutler Lab

Gene Symbol

Vmn1r48

Ensembl Gene

ENSMUSG00000057592

Gene Name

vomeronasal 1 receptor 48

Synonyms

V1ra3

MMRRC Submission

042931-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.109) question?

Stock #

R5352 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

90035933-90036841 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 90036147 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Glutamic Acid at position 232 (A232E)

Ref Sequence

ENSEMBL: ENSMUSP00000073121 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073415]

AlphaFold

Q9EQ52

Predicted Effect

probably benign
Transcript: ENSMUST00000073415
AA Change: A232E

PolyPhen 2 Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000073121
Gene: ENSMUSG00000057592
AA Change: A232E

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
Pfam:V1R	38	302	5.5e-131	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.9%

Validation Efficiency

100% (66/66)

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630010A05Rik	T	G	16: 14,618,701	L206*	probably null	Het
Adgrv1	T	C	13: 81,494,657	Y3218C	probably damaging	Het
Agtpbp1	G	A	13: 59,473,746	T41M	probably damaging	Het
Akap6	A	T	12: 52,796,097	E76V	probably damaging	Het
Ank2	C	A	3: 127,498,991		probably benign	Het
Atp6ap1l	A	C	13: 90,883,756	L269R	probably damaging	Het
Blk	A	G	14: 63,375,971	S363P	probably damaging	Het
Btnl9	T	C	11: 49,178,840	N204S	probably benign	Het
Cc2d2a	G	T	5: 43,706,213	W672C	probably damaging	Het
Ccnf	A	G	17: 24,243,273		probably null	Het
Cdc45	C	T	16: 18,795,897	R205H	probably damaging	Het
Chst1	A	G	2: 92,613,365	T61A	possibly damaging	Het
Col6a4	G	A	9: 106,061,544	T1325I	probably damaging	Het
Col7a1	A	C	9: 108,961,411	T976P	unknown	Het
Corin	C	T	5: 72,305,033	S811N	probably benign	Het
Dnal1	T	C	12: 84,136,548	V27A	possibly damaging	Het
Dupd1	G	A	14: 21,677,023	R186W	probably benign	Het
F830045P16Rik	T	A	2: 129,472,901	H152L	probably damaging	Het
Flnc	A	G	6: 29,449,318	S1405G	possibly damaging	Het
Foxj1	T	C	11: 116,334,079	N154S	possibly damaging	Het
Gm12183	T	C	11: 48,752,162		noncoding transcript	Het
Gm27047	G	A	6: 130,631,019		noncoding transcript	Het
Grm5	A	G	7: 88,074,850	I783V	probably damaging	Het
Hk1	A	T	10: 62,304,770	S113T	probably damaging	Het
Iqca	A	T	1: 90,130,196	N260K	probably benign	Het
Iws1	A	T	18: 32,083,404	K399M	probably damaging	Het
Kdm4d	A	G	9: 14,464,358	I68T	probably damaging	Het
Man2a1	T	C	17: 64,731,246	I75T	probably damaging	Het
Med13	T	A	11: 86,301,468	I824L	possibly damaging	Het
Meioc	A	T	11: 102,675,313	E585V	probably benign	Het
Mrgpre	A	C	7: 143,781,094	F224C	probably damaging	Het
Muc5b	T	A	7: 141,864,558	F3747Y	possibly damaging	Het
Nlrp4e	T	C	7: 23,353,173	V839A	probably benign	Het
Nup210	A	T	6: 91,069,316	V545E	probably damaging	Het
Ola1	T	C	2: 73,099,330	T310A	probably damaging	Het
Pdxdc1	T	C	16: 13,840,311	N516S	probably benign	Het
Phlpp1	A	G	1: 106,172,725	D241G	probably benign	Het
Ppp1r36	T	C	12: 76,428,083	V85A	probably damaging	Het
Rasa3	A	C	8: 13,631,778	L57R	possibly damaging	Het
Rp1	T	C	1: 4,347,098	S1264G	probably benign	Het
Rprd1b	A	G	2: 158,058,736	E247G	probably damaging	Het
Sag	G	T	1: 87,812,993	V46L	probably benign	Het
Sat2	A	T	11: 69,622,315	I17F	probably damaging	Het
Slc39a6	A	T	18: 24,601,036	Y199N	probably benign	Het
Slc9a3r2	C	T	17: 24,642,255	R66H	probably damaging	Het
Snx2	A	G	18: 53,197,925		probably null	Het
Thbs4	T	C	13: 92,763,590	D466G	probably damaging	Het
Tmem208	A	G	8: 105,328,431	D91G	probably damaging	Het
Tmf1	A	G	6: 97,176,809	L101P	probably damaging	Het
Tnni1	A	G	1: 135,805,592	T51A	probably benign	Het
Tor3a	T	G	1: 156,674,193	E38A	probably damaging	Het
Trim31	T	A	17: 36,899,918	D147E	possibly damaging	Het
Uhrf1bp1	G	A	17: 27,887,515	S1005N	probably benign	Het
Vmn1r89	T	G	7: 13,219,357	F7V	probably benign	Het
Zfp160	A	G	17: 21,026,852	T555A	probably benign	Het
Zfp981	C	A	4: 146,537,005	T129K	probably benign	Het
Zfpm2	T	A	15: 40,870,542	F106I	probably benign	Het

Other mutations in Vmn1r48

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01749:Vmn1r48	APN	6	90035952	missense	possibly damaging	0.82
IGL01833:Vmn1r48	APN	6	90036283	missense	probably damaging	0.99
R0052:Vmn1r48	UTSW	6	90036264	missense	possibly damaging	0.59
R3160:Vmn1r48	UTSW	6	90036378	missense	probably benign
R3162:Vmn1r48	UTSW	6	90036378	missense	probably benign
R5262:Vmn1r48	UTSW	6	90036034	missense	probably benign	0.03
R6901:Vmn1r48	UTSW	6	90036568	missense	possibly damaging	0.46
R7607:Vmn1r48	UTSW	6	90035980	missense	probably benign	0.01
R7877:Vmn1r48	UTSW	6	90036449	missense	probably benign	0.01
R8157:Vmn1r48	UTSW	6	90036012	missense	probably damaging	0.98
RF001:Vmn1r48	UTSW	6	90036204	missense	probably benign	0.01
Z1177:Vmn1r48	UTSW	6	90036274	missense	probably benign	0.22

Predicted Primers

PCR Primer
(F):5'- ACACAAAAGGGCTGACTGTG -3'
(R):5'- TGTCAATTAGCAGTCACCTCC -3'

Sequencing Primer
(F):5'- ACTGTGGCATAGATGTGCATCAC -3'
(R):5'- CCCAATTTGACCATGAATGACTTTC -3'

Posted On

2016-08-04