Mutagenetix > Incidental Mutations

Incidental Mutation 'R5503:Olfr912'

430740

Institutional Source

Beutler Lab

Gene Symbol

Olfr912

Ensembl Gene

ENSMUSG00000111448

Gene Name

olfactory receptor 912

Synonyms

MOR165-4, GA_x6K02T2PVTD-32283590-32284522

MMRRC Submission

043064-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.314) question?

Stock #

R5503 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

38580178-38586876 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 38582072 bp

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 265 (V265A)

Ref Sequence

ENSEMBL: ENSMUSP00000150014 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071681] [ENSMUST00000217160]

Predicted Effect

probably benign
Transcript: ENSMUST00000071681
AA Change: V265A

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

SMART Domains

Protein: ENSMUSP00000071604
Gene: ENSMUSG00000049926
AA Change: V265A

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	9.8e-51	PFAM
Pfam:7tm_1	41	290	1.3e-21	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000217160
AA Change: V265A

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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 98.3%
3x: 97.4%
10x: 95.4%
20x: 91.5%

Validation Efficiency

96% (103/107)

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: 88 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700049A03Rik	G	T	12: 71,164,546	E685*	probably null	Het
2700049A03Rik	A	T	12: 71,164,547	E685V	possibly damaging	Het
Abca6	A	G	11: 110,218,257	S696P	probably damaging	Het
Abca9	G	A	11: 110,141,610	T727M	probably damaging	Het
Alpk2	T	C	18: 65,306,241	R1161G	probably benign	Het
Amy1	T	C	3: 113,556,060	D487G	probably benign	Het
Arap2	G	A	5: 62,630,186	A1409V	probably damaging	Het
B020004J07Rik	A	T	4: 101,835,802	Y334N	probably benign	Het
B4galt6	C	A	18: 20,745,352		probably null	Het
Cacna1s	G	A	1: 136,086,742	G382D	probably damaging	Het
Camk2a	A	G	18: 60,978,000	D87G	probably damaging	Het
Cdh18	A	G	15: 23,436,534	Y492C	probably damaging	Het
Col18a1	C	T	10: 77,071,620	G861D	probably damaging	Het
Col4a3bp	C	T	13: 96,543,239	R26C	possibly damaging	Het
Crybg1	C	A	10: 43,998,766	S782I	probably benign	Het
Csgalnact1	G	A	8: 68,461,473	L27F	probably damaging	Het
Dab1	T	A	4: 104,512,264	C3S	probably benign	Het
Dapk1	T	C	13: 60,725,312	F343L	probably benign	Het
Dgat1	A	T	15: 76,502,194		probably benign	Het
Dnah11	C	A	12: 117,880,451		probably null	Het
Dsg2	T	A	18: 20,580,651	Y226*	probably null	Het
Epg5	T	A	18: 77,951,207	M351K	possibly damaging	Het
F13b	A	G	1: 139,522,543	T648A	probably benign	Het
Fgf17	T	C	14: 70,636,968	Y127C	probably damaging	Het
Fkbp15	G	A	4: 62,327,887	P435S	probably benign	Het
Gfm1	G	A	3: 67,453,727		probably null	Het
Gigyf1	T	C	5: 137,523,467		probably benign	Het
Gm12830	A	T	4: 114,821,739	T6S	unknown	Het
Gm6465	A	T	5: 11,848,183	N88I	probably damaging	Het
Gpr18	C	T	14: 121,911,747	V289I	probably damaging	Het
Ipp	G	T	4: 116,537,938	E557*	probably null	Het
Klhl12	T	A	1: 134,485,915		probably null	Het
Klhl38	A	G	15: 58,322,349	V328A	possibly damaging	Het
Kndc1	A	G	7: 139,931,889	T1470A	probably damaging	Het
Kntc1	T	A	5: 123,819,876	D2173E	possibly damaging	Het
Lipi	T	C	16: 75,573,976	K118E	probably benign	Het
Marf1	A	C	16: 14,152,231	L208R	probably damaging	Het
Misp	G	A	10: 79,826,718	R323K	probably damaging	Het
Mlxip	T	A	5: 123,395,327	M133K	probably damaging	Het
Mon2	A	T	10: 123,032,645	M501K	possibly damaging	Het
Myh2	A	G	11: 67,173,449	I77V	probably benign	Het
Napa	C	A	7: 16,115,624	Q254K	probably benign	Het
Nckap5l	C	A	15: 99,425,622	G1000V	probably damaging	Het
Neo1	A	T	9: 58,985,650	S236R	possibly damaging	Het
Neurl4	T	A	11: 69,906,368	Y594N	probably damaging	Het
Nmral1	G	A	16: 4,715,629	P94L	probably benign	Het
Notch3	A	T	17: 32,147,055	I1024N	probably benign	Het
Nsd1	T	A	13: 55,245,939	I451K	probably damaging	Het
Nt5c3b	T	C	11: 100,433,057	D143G	probably benign	Het
Olfr1415	C	A	1: 92,491,196	K186N	probably benign	Het
Olfr27	A	G	9: 39,144,484	N128S	probably benign	Het
Olfr316	T	A	11: 58,758,328	V221E	probably damaging	Het
Olfr45	A	C	7: 140,691,396	M164L	probably benign	Het
Olfr77	A	G	9: 19,920,379	T57A	probably benign	Het
Oplah	A	G	15: 76,305,446		probably null	Het
Phb2	T	A	6: 124,713,022		probably benign	Het
Plcl2	A	G	17: 50,509,929	I108V	probably benign	Het
Plpp6	T	A	19: 28,964,746	M249K	probably damaging	Het
Pnpt1	G	A	11: 29,138,156	G189E	probably damaging	Het
Ptprn	C	T	1: 75,251,875	V853M	probably damaging	Het
Ptprq	T	C	10: 107,688,328		probably null	Het
Rai1	G	A	11: 60,186,453	V448I	probably benign	Het
Rbm20	T	A	19: 53,851,354	C925S	possibly damaging	Het
Rin3	C	A	12: 102,313,055	P41Q	probably benign	Het
Rpl31-ps21	T	C	5: 21,119,507		noncoding transcript	Het
Rpl39-ps	A	T	15: 102,635,126		noncoding transcript	Het
Rtn4ip1	T	A	10: 43,907,883	D133E	probably benign	Het
Ryr1	T	C	7: 29,069,028	K2839E	possibly damaging	Het
Sept5	T	C	16: 18,623,368	K268R	probably benign	Het
Serpinb6b	T	A	13: 32,977,659	D238E	possibly damaging	Het
Slc15a2	C	T	16: 36,762,385	V214M	probably damaging	Het
Smarca2	T	C	19: 26,623,936	M18T	probably damaging	Het
Smarca2	C	A	19: 26,682,046	T912K	possibly damaging	Het
Smdt1	A	T	15: 82,347,900	R46S	possibly damaging	Het
Spa17	A	C	9: 37,611,977	F5V	probably damaging	Het
Spag17	A	G	3: 100,027,244	E614G	possibly damaging	Het
Sstr4	CGAGGAGGAGGAGGA	CGAGGAGGAGGAGGAGGA	2: 148,395,551		probably benign	Het
Tlr1	A	T	5: 64,926,292	V314D	probably damaging	Het
Trappc8	A	T	18: 20,836,900	L1011Q	probably benign	Het
Tsga10	A	G	1: 37,760,947	*691Q	probably null	Het
Vav1	A	T	17: 57,303,079	K420*	probably null	Het
Vmn1r174	C	G	7: 23,754,137	T76R	probably benign	Het
Vmn2r116	A	G	17: 23,386,804	E230G	probably benign	Het
Vps13b	A	G	15: 35,452,166	T637A	probably damaging	Het
Zbtb7a	A	G	10: 81,144,797	E275G	probably damaging	Het
Zfp280b	A	G	10: 76,039,462		probably null	Het
Zfp763	A	G	17: 33,019,533	Y213H	possibly damaging	Het
Zfp78	T	A	7: 6,378,529	W161R	probably benign	Het

Other mutations in Olfr912

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00913:Olfr912	APN	9	38581376	missense	probably damaging	0.97
IGL01099:Olfr912	APN	9	38582077	missense	probably benign	0.00
IGL01749:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL01750:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL01751:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL01752:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL01753:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02262:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02264:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02298:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02305:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02309:Olfr912	APN	9	38581433	missense	probably damaging	1.00
IGL02309:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02317:Olfr912	APN	9	38581513	missense	probably damaging	1.00
IGL02401:Olfr912	APN	9	38581355	missense	probably damaging	1.00
R0311:Olfr912	UTSW	9	38539297	missense	probably benign	0.42
R0973:Olfr912	UTSW	9	38581283	missense	possibly damaging	0.74
R1552:Olfr912	UTSW	9	38581379	missense	probably benign	0.00
R1720:Olfr912	UTSW	9	38581289	missense	probably benign
R2149:Olfr912	UTSW	9	38581508	missense	probably benign	0.02
R2241:Olfr912	UTSW	9	38581805	missense	probably damaging	1.00
R3622:Olfr912	UTSW	9	38581496	missense	probably damaging	1.00
R4384:Olfr912	UTSW	9	38582053	missense	probably damaging	1.00
R4686:Olfr912	UTSW	9	38582031	missense	probably damaging	1.00
R4780:Olfr912	UTSW	9	38581969	missense	possibly damaging	0.84
R5221:Olfr912	UTSW	9	38581852	missense	probably damaging	1.00
R5887:Olfr912	UTSW	9	38581784	missense	probably damaging	1.00
R6062:Olfr912	UTSW	9	38539144	missense	probably damaging	0.97
R6516:Olfr912	UTSW	9	38581472	missense	probably damaging	1.00
R6542:Olfr912	UTSW	9	38539437	missense	probably benign	0.01
R6766:Olfr912	UTSW	9	38581773	missense	probably damaging	1.00
R7057:Olfr912	UTSW	9	38581754	missense	probably damaging	1.00
R7112:Olfr912	UTSW	9	38582034	nonsense	probably null
R7414:Olfr912	UTSW	9	38581468	missense	probably benign	0.00
R7514:Olfr912	UTSW	9	38582051	missense	probably damaging	0.96
Z1176:Olfr912	UTSW	9	38581885	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCACAAGCACCTATATAAATGAGGTAG -3'
(R):5'- TTGCATTTGACACAGCTGTC -3'

Sequencing Primer
(F):5'- TTCATTGTAGGGGGAAAAGATATCAC -3'
(R):5'- CTCAGGGCAAGTTTAACATC -3'

Posted On

2016-10-05