Mutagenetix > Incidental Mutation

Incidental Mutation 'R5934:Or10v1'

462139

Institutional Source

Beutler Lab

Gene Symbol

Or10v1

Ensembl Gene

ENSMUSG00000060878

Gene Name

olfactory receptor family 10 subfamily V member 1

Synonyms

Olfr1420, GA_x6K02T2RE5P-2247227-2248156, MOR266-4

MMRRC Submission

044128-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.112) question?

Stock #

R5934 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

11873387-11874316 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 11874293 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 303 (R303G)

Ref Sequence

ENSEMBL: ENSMUSP00000149208 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072784] [ENSMUST00000217281]

AlphaFold

Q8VF55

Predicted Effect

probably benign
Transcript: ENSMUST00000072784
AA Change: R303G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000072563
Gene: ENSMUSG00000060878
AA Change: R303G

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	5.3e-54	PFAM
Pfam:7tm_1	41	291	3.4e-23	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000215766

Predicted Effect

probably benign
Transcript: ENSMUST00000217281
AA Change: R303G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.3%
20x: 95.3%

Validation Efficiency

MGI Phenotype

FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb4	T	C	5: 8,980,806 (GRCm39)	V596A	probably benign	Het
Acot11	C	T	4: 106,617,327 (GRCm39)	G240R	probably damaging	Het
Afg1l	G	A	10: 42,194,682 (GRCm39)	T370M	probably damaging	Het
Aldh2	T	C	5: 121,717,678 (GRCm39)	T118A	probably benign	Het
Apcdd1	C	T	18: 63,084,940 (GRCm39)	A379V	possibly damaging	Het
Atp1a3	T	C	7: 24,678,299 (GRCm39)		probably benign	Het
Calhm5	A	G	10: 33,968,198 (GRCm39)	V285A	possibly damaging	Het
Cd96	G	T	16: 45,938,266 (GRCm39)	D66E	probably benign	Het
Cdh5	T	A	8: 104,864,900 (GRCm39)	V506E	probably benign	Het
Cep70	T	C	9: 99,136,318 (GRCm39)	I7T	probably benign	Het
Ckb	A	T	12: 111,636,663 (GRCm39)	V237D	probably damaging	Het
Col6a6	C	T	9: 105,644,274 (GRCm39)	D1306N	probably damaging	Het
Cysltr2	T	C	14: 73,266,931 (GRCm39)	K260E	probably benign	Het
Ddhd2	A	G	8: 26,243,140 (GRCm39)	S19P	probably damaging	Het
Dnah17	G	T	11: 117,931,928 (GRCm39)	D3681E	probably benign	Het
Dop1a	T	A	9: 86,424,495 (GRCm39)	Y2068*	probably null	Het
Fryl	T	C	5: 73,248,060 (GRCm39)	Y1019C	probably damaging	Het
Fsip2	G	A	2: 82,817,092 (GRCm39)	C4275Y	possibly damaging	Het
Gapdh	A	G	6: 125,139,664 (GRCm39)	V202A	probably damaging	Het
Gmeb2	T	C	2: 180,897,367 (GRCm39)	I250M	possibly damaging	Het
Gpr88	C	T	3: 116,045,958 (GRCm39)	G118R	probably damaging	Het
Hdhd3	C	A	4: 62,417,607 (GRCm39)	V190L	possibly damaging	Het
Heg1	C	T	16: 33,547,289 (GRCm39)	T461M	probably damaging	Het
Hspg2	A	G	4: 137,246,083 (GRCm39)	Y989C	probably damaging	Het
Ift74	A	T	4: 94,520,971 (GRCm39)	M175L	probably benign	Het
Kcnh3	G	A	15: 99,124,414 (GRCm39)	R101Q	possibly damaging	Het
Kif20b	G	T	19: 34,918,721 (GRCm39)	V702F	probably benign	Het
Klhl1	A	G	14: 96,360,651 (GRCm39)		probably null	Het
Lrrk2	T	C	15: 91,618,249 (GRCm39)	V916A	probably benign	Het
Macir	A	T	1: 97,573,655 (GRCm39)	C137S	possibly damaging	Het
Mpp4	A	T	1: 59,160,535 (GRCm39)	D589E	probably damaging	Het
Msl2	T	C	9: 100,979,017 (GRCm39)	C464R	probably damaging	Het
Mucl2	A	T	15: 103,927,832 (GRCm39)	S42T	probably benign	Het
Musk	T	A	4: 58,373,613 (GRCm39)	L838Q	probably damaging	Het
Nos1	A	G	5: 118,074,510 (GRCm39)	H1052R	probably damaging	Het
Or10d4b	C	T	9: 39,534,479 (GRCm39)	T20I	probably damaging	Het
Or1j20	T	A	2: 36,760,280 (GRCm39)	I234N	probably benign	Het
Or2at1	A	T	7: 99,416,596 (GRCm39)	I76F	probably damaging	Het
Or4d2	T	C	11: 87,784,049 (GRCm39)	R234G	possibly damaging	Het
Or52e15	C	A	7: 104,645,385 (GRCm39)	C242F	probably damaging	Het
Or56a5	G	A	7: 104,792,867 (GRCm39)	S211F	probably benign	Het
Or5w8	T	C	2: 87,687,585 (GRCm39)	V22A	probably benign	Het
Or8u8	T	A	2: 86,012,446 (GRCm39)	Q3L	probably benign	Het
Pard3	T	G	8: 128,115,819 (GRCm39)	L636R	probably damaging	Het
Pigr	A	T	1: 130,772,264 (GRCm39)	S161C	probably damaging	Het
Polr1e	T	C	4: 45,029,369 (GRCm39)	S325P	probably damaging	Het
Prrc2a	A	T	17: 35,369,060 (GRCm39)	V1992E	probably damaging	Het
Psma5-ps	T	C	10: 85,150,145 (GRCm39)		noncoding transcript	Het
Ptpdc1	T	C	13: 48,739,845 (GRCm39)	K468E	probably benign	Het
Rab22a	A	G	2: 173,503,297 (GRCm39)	T37A	probably damaging	Het
Rai14	T	A	15: 10,575,245 (GRCm39)	K571I	probably damaging	Het
Reck	G	A	4: 43,930,979 (GRCm39)	G660D	probably damaging	Het
Rgs4	T	C	1: 169,572,807 (GRCm39)	D43G	possibly damaging	Het
Ryr2	A	T	13: 11,599,040 (GRCm39)	D4645E	probably damaging	Het
Sf3b3	A	G	8: 111,550,102 (GRCm39)	S639P	probably damaging	Het
Slc27a4	G	T	2: 29,701,672 (GRCm39)	R430L	probably damaging	Het
Slfn1	T	A	11: 83,012,770 (GRCm39)	Y295*	probably null	Het
Slfn5	C	T	11: 82,847,418 (GRCm39)	S101L	probably damaging	Het
Sult1d1	CCATG	CCATGGCATG	5: 87,707,629 (GRCm39)		probably null	Het
Tchh	A	T	3: 93,351,419 (GRCm39)	Q286H	unknown	Het
Tmem184c	A	T	8: 78,331,352 (GRCm39)	Y172*	probably null	Het
Tsc22d1	T	G	14: 76,656,266 (GRCm39)	M833R	possibly damaging	Het
Ugt1a7c	G	T	1: 88,023,601 (GRCm39)	L253F	probably damaging	Het
Usp19	C	T	9: 108,369,766 (GRCm39)		probably benign	Het
Xirp2	T	A	2: 67,355,148 (GRCm39)	I3303K	possibly damaging	Het
Zfp574	G	A	7: 24,779,757 (GRCm39)	A260T	probably benign	Het
Zswim6	A	G	13: 107,880,642 (GRCm39)		noncoding transcript	Het

Other mutations in Or10v1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02419:Or10v1	APN	19	11,874,186 (GRCm39)	missense	probably benign	0.06
IGL02703:Or10v1	APN	19	11,873,606 (GRCm39)	missense	possibly damaging	0.96
IGL02948:Or10v1	APN	19	11,874,145 (GRCm39)	nonsense	probably null
R1514:Or10v1	UTSW	19	11,873,978 (GRCm39)	missense	probably benign
R1539:Or10v1	UTSW	19	11,873,855 (GRCm39)	missense	possibly damaging	0.88
R1852:Or10v1	UTSW	19	11,874,249 (GRCm39)	missense	probably damaging	1.00
R1903:Or10v1	UTSW	19	11,873,913 (GRCm39)	missense	probably benign	0.24
R2061:Or10v1	UTSW	19	11,873,921 (GRCm39)	missense	probably damaging	0.98
R3768:Or10v1	UTSW	19	11,873,676 (GRCm39)	missense	probably damaging	0.99
R3977:Or10v1	UTSW	19	11,873,880 (GRCm39)	missense	probably damaging	1.00
R4479:Or10v1	UTSW	19	11,873,922 (GRCm39)	missense	probably damaging	0.99
R4592:Or10v1	UTSW	19	11,874,126 (GRCm39)	missense	probably benign
R6058:Or10v1	UTSW	19	11,873,388 (GRCm39)	start codon destroyed	probably null	1.00
R6536:Or10v1	UTSW	19	11,873,760 (GRCm39)	missense	probably benign	0.05
R7752:Or10v1	UTSW	19	11,873,898 (GRCm39)	missense	probably benign	0.01
R7901:Or10v1	UTSW	19	11,873,898 (GRCm39)	missense	probably benign	0.01
R8250:Or10v1	UTSW	19	11,873,741 (GRCm39)	missense	probably damaging	1.00
R9434:Or10v1	UTSW	19	11,873,393 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TCGTAGTGGTCCTCCTACAGTATG -3'
(R):5'- CACATGTCTCTATGTGCTGAGG -3'

Sequencing Primer
(F):5'- CAGAATGGTGTCTGTGGTC -3'
(R):5'- AGAATTGAACCTGGATCCTCTGG -3'

Posted On

2017-02-28