Mutagenetix > Incidental Mutation

Incidental Mutation 'R5441:Or10g1'

427201

Institutional Source

Beutler Lab

Gene Symbol

Or10g1

Ensembl Gene

ENSMUSG00000063106

Gene Name

olfactory receptor family 10 subfamily G member 1

Synonyms

MOR223-6, GA_x6K02T2RJGY-583652-584608, Olfr1510

MMRRC Submission

043006-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5441 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

52647346-52648384 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 52647414 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Methionine at position 305 (K305M)

Ref Sequence

ENSEMBL: ENSMUSP00000150294 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000079459] [ENSMUST00000215928]

AlphaFold

E9PZZ6

Predicted Effect

probably benign
Transcript: ENSMUST00000079459
AA Change: K305M

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000078424
Gene: ENSMUSG00000063106
AA Change: K305M

Domain	Start	End	E-Value	Type
Pfam:7tm_4	35	311	8.1e-50	PFAM
Pfam:7tm_1	45	293	1.8e-20	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206257

Predicted Effect

probably benign
Transcript: ENSMUST00000215928
AA Change: K305M

PolyPhen 2 Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)

Meta Mutation Damage Score

0.0947

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 95.1%

Validation Efficiency

98% (56/57)

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: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	A	G	1: 71,334,215 (GRCm39)	Y1096H	probably damaging	Het
Aspa	A	T	11: 73,196,420 (GRCm39)	F261I	probably damaging	Het
Atm	C	A	9: 53,427,767 (GRCm39)	G448*	probably null	Het
Atmin	T	A	8: 117,684,696 (GRCm39)	D785E	probably damaging	Het
Car1	G	C	3: 14,841,364 (GRCm39)	R90G	probably damaging	Het
Cdh11	T	C	8: 103,374,178 (GRCm39)	D520G	probably benign	Het
Cers5	T	A	15: 99,649,119 (GRCm39)	K50*	probably null	Het
Chad	A	T	11: 94,459,118 (GRCm39)	D340V	probably benign	Het
Cspg5	T	C	9: 110,075,711 (GRCm39)	I68T	probably benign	Het
Fcgbpl1	C	T	7: 27,856,339 (GRCm39)	T2042M	probably damaging	Het
Fcrla	T	A	1: 170,752,991 (GRCm39)		probably benign	Het
Fer1l4	T	A	2: 155,865,177 (GRCm39)	D1608V	probably benign	Het
Fzd5	T	A	1: 64,774,576 (GRCm39)	Q395L	probably benign	Het
Gm7664	T	A	13: 62,676,464 (GRCm39)		probably benign	Het
Hk3	T	C	13: 55,162,869 (GRCm39)	E2G	probably damaging	Het
Hmcn2	G	A	2: 31,296,428 (GRCm39)	E2677K	possibly damaging	Het
Hydin	T	C	8: 111,291,741 (GRCm39)	L3411P	possibly damaging	Het
Ltbr	G	A	6: 125,289,757 (GRCm39)	R146W	probably damaging	Het
Lysmd2	C	T	9: 75,533,254 (GRCm39)	H70Y	possibly damaging	Het
Msi2	A	G	11: 88,370,818 (GRCm39)		probably benign	Het
Msi2	G	A	11: 88,608,921 (GRCm39)		probably benign	Het
Napsa	T	A	7: 44,230,817 (GRCm39)		probably benign	Het
Nlrp4a	T	A	7: 26,153,578 (GRCm39)	L710M	probably damaging	Het
Or12d13	T	C	17: 37,647,159 (GRCm39)		probably null	Het
Or5m13	T	A	2: 85,748,934 (GRCm39)	F222I	probably benign	Het
Or6ae1	T	C	7: 139,742,564 (GRCm39)	T100A	probably benign	Het
Or9a2	C	T	6: 41,748,782 (GRCm39)	M150I	probably benign	Het
Plbd2	T	A	5: 120,637,147 (GRCm39)	Y105F	probably benign	Het
Plppr5	A	T	3: 117,456,120 (GRCm39)	I214F	possibly damaging	Het
Pramel34	A	T	5: 93,784,456 (GRCm39)	M139K	possibly damaging	Het
Ptcd3	A	G	6: 71,858,505 (GRCm39)	V655A	possibly damaging	Het
Ptpn14	T	C	1: 189,530,767 (GRCm39)	L78P	probably damaging	Het
Ralgapa1	A	C	12: 55,766,408 (GRCm39)	D1295E	probably damaging	Het
Rnf213	G	A	11: 119,299,846 (GRCm39)	D192N	probably damaging	Het
Ropn1	A	G	16: 34,487,167 (GRCm39)	I34M	probably damaging	Het
Rpe65	G	T	3: 159,310,038 (GRCm39)	G104C	probably damaging	Het
Scgb2b27	T	C	7: 33,712,582 (GRCm39)		probably benign	Het
Sh3bgr	T	C	16: 96,007,117 (GRCm39)	I29T	possibly damaging	Het
Smg1	T	C	7: 117,794,304 (GRCm39)		probably benign	Het
Stim2	T	A	5: 54,232,712 (GRCm39)	C68*	probably null	Het
Syne2	G	A	12: 76,035,917 (GRCm39)	V3736I	possibly damaging	Het
Tbx19	T	C	1: 164,981,249 (GRCm39)	N82D	probably damaging	Het
Tdp1	T	A	12: 99,876,544 (GRCm39)	V353D	probably damaging	Het
Tg	T	A	15: 66,568,369 (GRCm39)	I1352K	possibly damaging	Het
Thsd4	T	C	9: 59,887,066 (GRCm39)	T919A	probably damaging	Het
Tmprss11f	A	T	5: 86,676,062 (GRCm39)	M373K	probably damaging	Het
Tmprss15	T	A	16: 78,868,335 (GRCm39)		probably null	Het
Tpd52	A	T	3: 9,068,466 (GRCm39)	Y16*	probably null	Het
Ube2o	G	A	11: 116,435,268 (GRCm39)	R507C	probably damaging	Het
Unc93b1	T	C	19: 3,993,703 (GRCm39)	F382L	probably benign	Het
Vav2	A	T	2: 27,160,122 (GRCm39)		probably benign	Het
Vmn1r207	T	C	13: 22,910,686 (GRCm39)		noncoding transcript	Het
Zan	T	A	5: 137,435,013 (GRCm39)	I2127F	unknown	Het
Zfp748	C	A	13: 67,688,737 (GRCm39)	C841F	probably damaging	Het
Zic4	C	A	9: 91,266,253 (GRCm39)	P299Q	probably damaging	Het

Other mutations in Or10g1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01564:Or10g1	APN	14	52,648,299 (GRCm39)	missense	probably benign	0.04
IGL02097:Or10g1	APN	14	52,647,511 (GRCm39)	missense	probably benign
R0282:Or10g1	UTSW	14	52,647,720 (GRCm39)	missense	possibly damaging	0.94
R1449:Or10g1	UTSW	14	52,648,024 (GRCm39)	missense	probably damaging	1.00
R2113:Or10g1	UTSW	14	52,647,753 (GRCm39)	missense	probably damaging	1.00
R2870:Or10g1	UTSW	14	52,648,318 (GRCm39)	missense	probably benign
R2870:Or10g1	UTSW	14	52,648,318 (GRCm39)	missense	probably benign
R2872:Or10g1	UTSW	14	52,648,318 (GRCm39)	missense	probably benign
R2872:Or10g1	UTSW	14	52,648,318 (GRCm39)	missense	probably benign
R2873:Or10g1	UTSW	14	52,648,318 (GRCm39)	missense	probably benign
R3409:Or10g1	UTSW	14	52,647,818 (GRCm39)	missense	possibly damaging	0.64
R3411:Or10g1	UTSW	14	52,647,818 (GRCm39)	missense	possibly damaging	0.64
R4480:Or10g1	UTSW	14	52,647,765 (GRCm39)	missense	probably damaging	1.00
R5292:Or10g1	UTSW	14	52,647,902 (GRCm39)	missense	possibly damaging	0.90
R5297:Or10g1	UTSW	14	52,647,675 (GRCm39)	missense	probably damaging	1.00
R5749:Or10g1	UTSW	14	52,647,961 (GRCm39)	missense	probably damaging	1.00
R5872:Or10g1	UTSW	14	52,648,225 (GRCm39)	missense	probably damaging	1.00
R5941:Or10g1	UTSW	14	52,647,525 (GRCm39)	missense	probably benign	0.01
R7209:Or10g1	UTSW	14	52,647,550 (GRCm39)	missense	possibly damaging	0.80
R7379:Or10g1	UTSW	14	52,647,718 (GRCm39)	missense	probably benign	0.08
R7463:Or10g1	UTSW	14	52,648,168 (GRCm39)	missense	probably benign	0.00
R7692:Or10g1	UTSW	14	52,647,945 (GRCm39)	missense	probably damaging	1.00
R8894:Or10g1	UTSW	14	52,647,465 (GRCm39)	missense	probably damaging	1.00
R9286:Or10g1	UTSW	14	52,648,075 (GRCm39)	nonsense	probably null
R9394:Or10g1	UTSW	14	52,647,570 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAAGCATCTTCTCCTCTCAGG -3'
(R):5'- ATCTCACTGTGGTCACCGTC -3'

Sequencing Primer
(F):5'- CCTCTCAGGAAGTCGTTAGATG -3'
(R):5'- ACTGTGGTCACCGTCTACTATG -3'

Posted On

2016-09-01