Mutagenetix > Incidental Mutation

Incidental Mutation 'R6925:Olfr951'

541098

Institutional Source

Beutler Lab

Gene Symbol

Olfr951

Ensembl Gene

ENSMUSG00000094269

Gene Name

olfactory receptor 951

Synonyms

MOR171-49, MOR171-33P, GA_x6K02T2PVTD-33090395-33091330

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R6925 (G1)

Quality Score

220.009

Status

Validated

Chromosome

Chromosomal Location

39387410-39395633 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 39393861 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Histidine at position 20 (Q20H)

Ref Sequence

ENSEMBL: ENSMUSP00000150976 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078531] [ENSMUST00000216107]

AlphaFold

Q9EQ94

Predicted Effect

probably benign
Transcript: ENSMUST00000078531
AA Change: Q23H

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)

SMART Domains

Protein: ENSMUSP00000077615
Gene: ENSMUSG00000094269
AA Change: Q23H

Domain	Start	End	E-Value	Type
Pfam:7tm_4	34	311	2.5e-52	PFAM
Pfam:7tm_1	44	293	5e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000216107
AA Change: Q20H

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.0%

Validation Efficiency

100% (91/91)

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
5430419D17Rik	A	G	7: 131,222,707	Q177R	possibly damaging	Het
Acat1	A	T	9: 53,592,029	V170E	probably benign	Het
Atp2b2	T	A	6: 113,760,720	I902F	probably damaging	Het
Cacna1d	A	G	14: 30,051,637	V1697A	probably benign	Het
Ccdc14	T	A	16: 34,690,749	F31Y	probably benign	Het
Ccdc17	T	A	4: 116,598,210	V250E	probably damaging	Het
Cct7	A	G	6: 85,459,182	N25S	probably damaging	Het
Cep19	G	C	16: 32,103,942	G9R	probably damaging	Het
Ces5a	A	T	8: 93,523,057		probably null	Het
Chd1l	T	G	3: 97,582,826	E471A	probably damaging	Het
Chd6	A	G	2: 161,013,127	I787T	probably damaging	Het
Cntnap5c	A	C	17: 58,395,266	T1194P	probably benign	Het
Col6a3	T	A	1: 90,816,002	M208L	probably benign	Het
Coro7	A	T	16: 4,628,674		probably null	Het
Csrnp2	T	C	15: 100,481,958	K484R	probably benign	Het
Cyp2c39	T	A	19: 39,513,195	V64E	probably damaging	Het
Ddr2	T	C	1: 169,998,132	K300E	probably benign	Het
Ddx56	T	C	11: 6,263,980	E393G	probably damaging	Het
Diaph1	A	C	18: 37,853,679	Y1084*	probably null	Het
Disp1	A	T	1: 183,086,478	F1459L	probably benign	Het
Dnajc8	G	A	4: 132,544,113	A80T	probably damaging	Het
Elfn1	T	A	5: 139,971,685	M148K	probably benign	Het
Emcn	T	A	3: 137,419,002	I154N	probably damaging	Het
Enah	C	G	1: 181,905,898		probably null	Het
Enah	T	A	1: 181,905,899		probably null	Het
Ep300	C	A	15: 81,649,981	Q2080K	probably benign	Het
Epha2	T	A	4: 141,308,757	M168K	probably benign	Het
Ercc6	T	A	14: 32,562,608	I776N	probably damaging	Het
Fan1	T	A	7: 64,372,486	N340Y	probably damaging	Het
Fat4	G	T	3: 38,996,204		probably null	Het
G3bp1	A	G	11: 55,497,960	R333G	possibly damaging	Het
Gm3604	A	G	13: 62,369,390	F385L	probably benign	Het
Gm5800	T	C	14: 51,713,700	I147M	possibly damaging	Het
Hipk1	A	G	3: 103,778,245	F18S	unknown	Het
Ighv3-8	A	T	12: 114,322,330	C131S	probably benign	Het
Il23r	T	G	6: 67,423,493	T618P	probably damaging	Het
Il31ra	G	A	13: 112,527,529	T538I	possibly damaging	Het
Kcns2	A	G	15: 34,839,913	D474G	unknown	Het
Klc4	T	C	17: 46,636,229	T407A	possibly damaging	Het
Klra5	C	T	6: 129,911,457	S2N	probably benign	Het
Krt10	T	C	11: 99,388,851	Y161C	probably damaging	Het
Kxd1	A	T	8: 70,523,278	M1K	probably null	Het
Lgals1	A	C	15: 78,928,040	D27A	possibly damaging	Het
Lgr5	T	C	10: 115,466,346	S308G	probably benign	Het
Lrp1	G	A	10: 127,556,988	S2736L	probably benign	Het
Lrpap1	G	T	5: 35,102,536	H73N	probably benign	Het
Mcpt1	C	A	14: 56,019,065	T86K	probably damaging	Het
Megf6	A	T	4: 154,254,587	D527V	probably damaging	Het
Mical3	A	T	6: 120,959,390	S1392T	probably benign	Het
Mmp2	A	T	8: 92,839,382	D437V	probably damaging	Het
Mob4	T	A	1: 55,152,722	Y166*	probably null	Het
Mrap2	G	A	9: 87,182,474	M89I	possibly damaging	Het
Mug1	G	A	6: 121,881,787	A1155T	probably damaging	Het
Myh2	G	T	11: 67,193,218	A1556S	probably benign	Het
Nfatc3	A	G	8: 106,119,322	D1028G	probably benign	Het
Ngef	T	G	1: 87,503,263		probably null	Het
Nlrp1a	A	T	11: 71,092,513	L1209Q	probably null	Het
Npr2	C	T	4: 43,647,553	R819C	probably damaging	Het
Nsd2	A	T	5: 33,879,110	D646V	probably damaging	Het
Nsun7	A	G	5: 66,277,072	H252R	probably damaging	Het
Olfr267	A	T	4: 58,785,647	I25N	possibly damaging	Het
Olfr447	T	A	6: 42,911,857	C111*	probably null	Het
Olfr642	C	T	7: 104,049,740	V205I	probably benign	Het
Pcdhga2	A	T	18: 37,670,585	D494V	probably damaging	Het
Pcsk2	A	G	2: 143,813,747	E617G	probably damaging	Het
Pdc	T	C	1: 150,333,180	I138T	probably damaging	Het
Phc2	T	A	4: 128,748,134	S750T	probably damaging	Het
Pkd2l1	T	A	19: 44,191,508	N88Y	possibly damaging	Het
Plcl1	C	T	1: 55,406,598	R71*	probably null	Het
Prag1	C	A	8: 36,103,894	L544M	probably damaging	Het
Prkg2	A	G	5: 98,966,510		probably null	Het
Psd2	G	A	18: 35,979,711	S153N	probably damaging	Het
Rab11fip1	A	T	8: 27,152,972	S600T	probably damaging	Het
Rbms1	T	G	2: 60,762,304	T222P	probably benign	Het
Slfn8	A	T	11: 83,013,417	Y382*	probably null	Het
Socs4	T	A	14: 47,289,738	C43*	probably null	Het
Sorl1	T	A	9: 42,033,626	T868S	probably damaging	Het
St6gal1	A	G	16: 23,356,213	Y267C	probably damaging	Het
Syne1	A	G	10: 5,126,682	V6879A	probably benign	Het
Syne2	C	A	12: 75,854,132	H22N	possibly damaging	Het
Tmeff2	T	A	1: 50,928,021	L25Q	probably damaging	Het
Tmprss11g	G	T	5: 86,487,426	D396E	probably benign	Het
Tmprss11g	T	A	5: 86,487,436	H393L	probably benign	Het
Vmn2r23	A	G	6: 123,704,553	E140G	probably damaging	Het
Wapl	T	C	14: 34,677,363	S130P	probably benign	Het
Zeb2	T	A	2: 44,994,529	K982M	probably damaging	Het
Zfhx3	C	G	8: 108,956,821	H3631D	unknown	Het
Zfp719	T	C	7: 43,590,706	S573P	probably damaging	Het
Zfp979	A	T	4: 147,613,542	C237S	possibly damaging	Het

Other mutations in Olfr951

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01527:Olfr951	APN	9	39393818	missense	probably benign	0.01
IGL01650:Olfr951	APN	9	39393956	missense	probably damaging	0.99
IGL02134:Olfr951	APN	9	39394534	missense	probably damaging	0.99
IGL03113:Olfr951	APN	9	39394685	missense	probably damaging	1.00
R0127:Olfr951	UTSW	9	39393942	missense	probably benign	0.16
R1730:Olfr951	UTSW	9	39394222	missense	probably benign	0.01
R1783:Olfr951	UTSW	9	39394222	missense	probably benign	0.01
R1924:Olfr951	UTSW	9	39393867	missense	possibly damaging	0.93
R3785:Olfr951	UTSW	9	39394382	missense	probably benign	0.07
R3787:Olfr951	UTSW	9	39394382	missense	probably benign	0.07
R4607:Olfr951	UTSW	9	39394735	makesense	probably null
R4803:Olfr951	UTSW	9	39394636	missense	probably benign	0.26
R5314:Olfr951	UTSW	9	39394489	missense	probably damaging	1.00
R5338:Olfr951	UTSW	9	39394075	missense	probably damaging	1.00
R5360:Olfr951	UTSW	9	39394402	missense	probably benign	0.00
R5468:Olfr951	UTSW	9	39393961	missense	probably benign	0.33
R6590:Olfr951	UTSW	9	39394549	missense	probably benign	0.00
R6690:Olfr951	UTSW	9	39394549	missense	probably benign	0.00
R6925:Olfr951	UTSW	9	39393860	missense	probably benign	0.32
R6982:Olfr951	UTSW	9	39394322	missense	probably damaging	1.00
R7662:Olfr951	UTSW	9	39394093	missense	probably benign	0.01
R8074:Olfr951	UTSW	9	39393946	missense	probably damaging	1.00
R8389:Olfr951	UTSW	9	39394616	missense	probably damaging	1.00
R9444:Olfr951	UTSW	9	39394069	missense	probably benign	0.19
R9642:Olfr951	UTSW	9	39394561	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCTCAACACAGGCACTTTC -3'
(R):5'- GGTAACAACTGTGGACTGACC -3'

Sequencing Primer
(F):5'- GGCACTTTCACTCACTAATACAG -3'
(R):5'- CAAAGTCAATGAAGGACAAACTGCTG -3'

Posted On

2018-11-28