Mutagenetix > Incidental Mutations

Incidental Mutation 'R0090:Olfr376'

20161

Institutional Source

Beutler Lab

Gene Symbol

Olfr376

Ensembl Gene

ENSMUSG00000063881

Gene Name

olfactory receptor 376

Synonyms

GA_x6K02T2P1NL-3535075-3536028, MOR135-12

MMRRC Submission

038377-MU

Accession Numbers

Is this an essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0090 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

73371246-73377836 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 73375576 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 276 (V276I)

Ref Sequence

ENSEMBL: ENSMUSP00000126073 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078952] [ENSMUST00000120401] [ENSMUST00000170592]

Predicted Effect

probably benign
Transcript: ENSMUST00000078952
AA Change: V279I

PolyPhen 2 Score 0.018 (Sensitivity: 0.95; Specificity: 0.80)

SMART Domains

Protein: ENSMUSP00000077977
Gene: ENSMUSG00000063881
AA Change: V279I

Domain	Start	End	E-Value	Type
Pfam:7tm_4	37	314	3e-59	PFAM
Pfam:7TM_GPCR_Srsx	41	311	7.4e-8	PFAM
Pfam:7tm_1	47	296	2.7e-27	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000120401
AA Change: V276I

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000113236
Gene: ENSMUSG00000063881
AA Change: V276I

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	38	308	1.1e-7	PFAM
Pfam:7tm_1	44	293	7.2e-36	PFAM
Pfam:7tm_4	142	286	1.4e-46	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000170592
AA Change: V276I

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)

SMART Domains

Protein: ENSMUSP00000126073
Gene: ENSMUSG00000063881
AA Change: V276I

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	38	308	1.1e-7	PFAM
Pfam:7tm_1	44	293	7.2e-36	PFAM
Pfam:7tm_4	142	286	1.4e-46	PFAM

Meta Mutation Damage Score

0.1814

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 95.7%
20x: 91.4%

Validation Efficiency

99% (90/91)

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: 89 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010315B03Rik	T	C	9: 124,295,159		probably benign	Het
4933427I04Rik	A	G	4: 123,860,982	T230A	possibly damaging	Het
9230110C19Rik	T	A	9: 8,027,183	N118I	probably benign	Het
Acsm1	T	C	7: 119,662,189		probably benign	Het
Acta1	T	C	8: 123,893,657	N14S	probably damaging	Het
Aff4	A	G	11: 53,392,782	T362A	probably benign	Het
Aggf1	A	G	13: 95,364,959	I305T	probably benign	Het
Ap4b1	A	G	3: 103,820,429	D325G	possibly damaging	Het
Ap4e1	C	T	2: 127,064,985	T1055I	possibly damaging	Het
Arhgef2	A	T	3: 88,639,348	Q496L	probably damaging	Het
Arhgef28	A	G	13: 98,075,110	F122L	probably damaging	Het
Baiap3	G	A	17: 25,250,070		probably benign	Het
Casp8ap2	T	A	4: 32,640,327	H460Q	probably damaging	Het
Casz1	A	G	4: 148,933,411	T386A	probably benign	Het
Cd53	A	T	3: 106,767,409	V114E	possibly damaging	Het
Celsr2	A	G	3: 108,393,327		probably benign	Het
Chaf1b	G	T	16: 93,887,124	A88S	possibly damaging	Het
Cldn10	A	T	14: 118,874,200	Y194F	probably damaging	Het
Clec2e	A	C	6: 129,095,218		probably null	Het
Cmpk2	A	T	12: 26,478,022	T413S	probably benign	Het
Col9a1	T	A	1: 24,223,562		probably null	Het
Dchs1	G	T	7: 105,755,932	Q2468K	probably benign	Het
Ddx60	A	G	8: 61,942,293	D88G	probably damaging	Het
Dnah8	A	G	17: 30,784,090	R3588G	probably benign	Het
Ect2	T	C	3: 27,115,476	T774A	probably benign	Het
Ect2	C	T	3: 27,138,502	E431K	probably null	Het
Ern1	A	G	11: 106,405,823	V767A	probably damaging	Het
Fbln1	A	C	15: 85,224,288	E75A	possibly damaging	Het
Fgf5	C	T	5: 98,261,987	R132*	probably null	Het
Folh1	T	C	7: 86,725,868		probably benign	Het
Gdf15	A	T	8: 70,629,684	H257Q	probably damaging	Het
Ghitm	T	C	14: 37,122,219	T322A	probably benign	Het
Gm13212	A	T	4: 145,622,625	K211*	probably null	Het
Gm5709	A	G	3: 59,618,771		noncoding transcript	Het
Hbb-y	C	T	7: 103,852,743		probably null	Het
Hmcn2	A	T	2: 31,426,198	D3771V	probably damaging	Het
Hspa12a	T	C	19: 58,799,509	D627G	probably benign	Het
Idh2	T	C	7: 80,097,914	E286G	probably damaging	Het
Idh3b	C	A	2: 130,280,979	A297S	probably benign	Het
Igsf3	A	G	3: 101,435,652	E535G	probably damaging	Het
Ilf3	T	A	9: 21,395,414	D314E	probably damaging	Het
Itgb8	A	G	12: 119,202,563	S78P	probably benign	Het
Itih5	G	A	2: 10,164,684	V31I	probably benign	Het
Kcnj2	T	C	11: 111,073,027	V415A	probably benign	Het
Kin	A	G	2: 10,085,773	Q53R	possibly damaging	Het
Krt78	A	T	15: 101,947,837	M513K	probably benign	Het
Krtap4-8	A	T	11: 99,780,486		probably benign	Het
Ltbr	T	C	6: 125,309,449		probably benign	Het
Mgat4a	G	A	1: 37,490,333	T146I	probably damaging	Het
Mrps2	G	C	2: 28,468,256	W19C	probably damaging	Het
Mthfs	T	C	9: 89,211,291	S33P	probably damaging	Het
Myh6	T	C	14: 54,958,704	D546G	probably damaging	Het
Nanos3	C	T	8: 84,176,134	R133Q	probably damaging	Het
Ndst2	T	C	14: 20,727,267	T553A	probably damaging	Het
Nlrp12	T	C	7: 3,240,034	E616G	probably damaging	Het
Nrde2	T	C	12: 100,129,286		probably benign	Het
Nup210l	G	A	3: 90,211,779	V1832I	probably benign	Het
Olfr1283	A	T	2: 111,369,294	I221F	probably damaging	Het
Pcm1	A	T	8: 41,256,041	E9D	probably damaging	Het
Pear1	A	T	3: 87,754,342	D541E	possibly damaging	Het
Peg10	A	G	6: 4,756,063		probably benign	Het
Prss1	G	A	6: 41,461,232	R31Q	probably benign	Het
Ptpn13	T	C	5: 103,569,503	V1837A	probably damaging	Het
Rasgrp3	A	G	17: 75,498,461	D149G	probably damaging	Het
Reg3d	A	T	6: 78,378,483	H8Q	possibly damaging	Het
Rhox4f	A	C	X: 37,607,469	V15G	probably benign	Het
Sacs	T	A	14: 61,205,440	L1645H	probably damaging	Het
Slc16a5	A	T	11: 115,464,925	S71C	probably damaging	Het
Slc9a3	A	G	13: 74,158,728	E324G	probably damaging	Het
Smgc	T	C	15: 91,859,762	V574A	possibly damaging	Het
Stac3	C	T	10: 127,503,930		probably benign	Het
Supv3l1	A	G	10: 62,429,706	L685P	probably benign	Het
Taar2	G	A	10: 23,941,495	R311H	probably benign	Het
Tas2r125	G	T	6: 132,910,398	A250S	probably benign	Het
Tdrd6	C	T	17: 43,628,241	V639I	probably benign	Het
Thap12	T	G	7: 98,715,893	W423G	probably damaging	Het
Tmem245	T	C	4: 56,899,410	I217V	probably benign	Het
Trip12	T	A	1: 84,732,136		probably benign	Het
Tshz3	T	C	7: 36,768,892	V102A	probably benign	Het
Ubap1	T	C	4: 41,379,826	S347P	probably damaging	Het
Usp10	C	T	8: 119,953,196	Q612*	probably null	Het
Vmn2r72	T	C	7: 85,754,876	I36V	probably benign	Het
Vps37a	T	C	8: 40,526,989	I63T	possibly damaging	Het
Whrn	C	A	4: 63,432,732	R9L	possibly damaging	Het
Xrcc1	T	C	7: 24,570,217	Y401H	probably damaging	Het
Ylpm1	GCCTAAGCAGCAACCTAAG	GCCTAAG	12: 85,029,040		probably benign	Het
Zfhx3	G	A	8: 108,950,057	D2580N	possibly damaging	Het
Zfhx4	A	G	3: 5,243,625	N637S	probably damaging	Het
Zyg11a	A	T	4: 108,201,347		probably benign	Het

Other mutations in Olfr376

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01011:Olfr376	APN	11	73375007	missense	probably benign	0.03
IGL01462:Olfr376	APN	11	73374752	start codon destroyed	probably null	0.02
IGL01725:Olfr376	APN	11	73375156	missense	probably benign	0.39
IGL02225:Olfr376	APN	11	73375078	missense	probably damaging	0.98
R0006:Olfr376	UTSW	11	73375588	missense	possibly damaging	0.65
R0743:Olfr376	UTSW	11	73374889	missense	probably benign	0.03
R0884:Olfr376	UTSW	11	73374889	missense	probably benign	0.03
R1102:Olfr376	UTSW	11	73374874	missense	probably benign	0.00
R1582:Olfr376	UTSW	11	73375264	missense	probably damaging	1.00
R1765:Olfr376	UTSW	11	73375344	missense	probably damaging	1.00
R1929:Olfr376	UTSW	11	73375601	missense	probably damaging	1.00
R1941:Olfr376	UTSW	11	73375621	missense	probably damaging	1.00
R4738:Olfr376	UTSW	11	73375350	missense	possibly damaging	0.94
R4947:Olfr376	UTSW	11	73375417	nonsense	probably null
R5837:Olfr376	UTSW	11	73375648	missense	probably benign	0.02
R6440:Olfr376	UTSW	11	73375347	missense	probably benign	0.06
R6736:Olfr376	UTSW	11	73375576	missense	probably benign	0.18
R7254:Olfr376	UTSW	11	73375375	missense	probably benign
R7354:Olfr376	UTSW	11	73375375	missense	probably benign	0.01
R7437:Olfr376	UTSW	11	73375018	missense	probably benign	0.02
R7918:Olfr376	UTSW	11	73375097	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTCCTATGCACGAATTGTGTCCTCC -3'
(R):5'- TTCTGAGCCCTGCAAACACTGTCC -3'

Sequencing Primer
(F):5'- GAATTGTGTCCTCCATTCTCAAGG -3'
(R):5'- AGATGTGCTGTATCTATCACACC -3'

Posted On

2013-04-11