Mutagenetix > Incidental Mutation

Incidental Mutation 'R5176:Olfr998'

399255

Institutional Source

Beutler Lab

Gene Symbol

Olfr998

Ensembl Gene

ENSMUSG00000111454

Gene Name

olfactory receptor 998

Synonyms

GA_x6K02T2Q125-47069356-47070300, MOR175-5

MMRRC Submission

042756-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.229) question?

Stock #

R5176 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

85588948-85591893 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 85591435 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Asparagine at position 298 (K298N)

Ref Sequence

ENSEMBL: ENSMUSP00000150713 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052307] [ENSMUST00000215083]

AlphaFold

Q8VF76

Predicted Effect

possibly damaging
Transcript: ENSMUST00000052307
AA Change: K298N

PolyPhen 2 Score 0.881 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000059970
Gene: ENSMUSG00000111454
AA Change: K298N

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	2.6e-54	PFAM
Pfam:7tm_1	41	308	9.5e-18	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000215083
AA Change: K298N

PolyPhen 2 Score 0.881 (Sensitivity: 0.82; Specificity: 0.94)

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.6%

Validation Efficiency

99% (69/70)

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: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A530032D15Rik	C	T	1: 85,088,800		probably benign	Het
Abca7	C	A	10: 79,998,289	H116Q	probably benign	Het
Akap12	G	T	10: 4,353,947	E252D	probably benign	Het
Apobr	A	G	7: 126,585,016	D2G	probably damaging	Het
Arhgef12	A	T	9: 43,020,686	H168Q	probably damaging	Het
Asb3	T	A	11: 31,081,357		probably null	Het
Brip1	T	C	11: 86,077,884	Y825C	probably damaging	Het
Cacna1b	A	T	2: 24,635,131	Y1679N	probably damaging	Het
Ccdc69	C	T	11: 55,060,470	A42T	probably benign	Het
Cds1	G	T	5: 101,781,420	D55Y	possibly damaging	Het
Cep135	C	A	5: 76,637,026	D989E	probably benign	Het
Cpsf6	C	A	10: 117,361,284		probably benign	Het
Ctif	C	T	18: 75,637,219	V32M	probably damaging	Het
Cylc2	T	C	4: 51,228,587		probably benign	Het
Dao	T	C	5: 114,020,009		probably null	Het
Dopey1	T	A	9: 86,521,815	N1689K	probably damaging	Het
Dopey2	A	G	16: 93,740,043	Y14C	probably damaging	Het
E130309D02Rik	G	T	5: 143,315,075	S7*	probably null	Het
Fam160b1	A	G	19: 57,371,181	N51S	probably damaging	Het
Fam187a	C	T	11: 102,886,464	R365C	probably damaging	Het
Fastkd2	A	G	1: 63,731,439		probably benign	Het
Fkbp15	G	T	4: 62,312,323	L718I	possibly damaging	Het
Gabbr2	C	A	4: 46,681,208	V118F	probably damaging	Het
Gm11492	T	A	11: 87,567,532	M244K	probably benign	Het
Gm13991	T	A	2: 116,528,027		noncoding transcript	Het
H2-M9	T	C	17: 36,641,631	I174M	probably damaging	Het
Insr	T	A	8: 3,158,742	M1240L	probably benign	Het
Itgb4	C	T	11: 115,984,157	R447W	probably benign	Het
Mad2l1bp	T	A	17: 46,152,812	E95D	probably benign	Het
March9	T	C	10: 127,059,450	D102G	probably benign	Het
Muc19	A	G	15: 91,892,180		noncoding transcript	Het
Nr1h4	T	A	10: 89,498,255	Y91F	probably benign	Het
Nr5a2	A	T	1: 136,948,802	M1K	probably null	Het
Olfr561	T	A	7: 102,775,306	S261T	probably damaging	Het
Olfr836	A	T	9: 19,121,360	Y132F	probably damaging	Het
Oprd1	T	C	4: 132,113,793	T285A	probably benign	Het
Optc	T	C	1: 133,902,084	N196S	probably benign	Het
Panx2	G	T	15: 89,060,228	R52L	probably damaging	Het
Pdzd8	A	G	19: 59,344,957	F211L	probably damaging	Het
Pot1b	T	A	17: 55,699,995	T41S	probably benign	Het
Prss56	T	C	1: 87,184,158	L37S	probably damaging	Het
Ptk2b	T	C	14: 66,156,415	T870A	probably damaging	Het
Rabep2	C	A	7: 126,434,293		probably benign	Het
Rbm48	A	C	5: 3,595,444	V80G	probably damaging	Het
Rhou	G	T	8: 123,654,109	C55F	possibly damaging	Het
Rnaseh2c	A	G	19: 5,602,042	D45G	probably benign	Het
Rusc1	A	G	3: 89,089,082	S109P	probably damaging	Het
Ryr3	T	C	2: 112,757,667	D2643G	possibly damaging	Het
Sik2	T	C	9: 50,899,403	E471G	probably benign	Het
Sipa1	A	G	19: 5,659,378	S310P	probably damaging	Het
Spen	T	C	4: 141,476,276	E1680G	unknown	Het
Steap3	C	T	1: 120,243,767		probably null	Het
Tmeff2	T	A	1: 51,071,541	C171*	probably null	Het
Tmem138	A	T	19: 10,575,270	M33K	probably benign	Het
Trappc11	C	A	8: 47,510,963	V601L	possibly damaging	Het
Ttc30a2	T	C	2: 75,977,077	M364V	probably benign	Het
Ttll4	C	A	1: 74,679,286	H99N	probably damaging	Het
Uchl4	A	T	9: 64,235,740	K168*	probably null	Het
Wdr17	C	T	8: 54,653,878		probably null	Het
Xpo1	A	G	11: 23,295,977	D1029G	probably damaging	Het
Zfp719	G	T	7: 43,591,125	K712N	probably damaging	Het

Other mutations in Olfr998

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01763:Olfr998	APN	2	85591347	missense	probably benign	0.00
R0091:Olfr998	UTSW	2	85591352	missense	probably benign	0.38
R0241:Olfr998	UTSW	2	85590810	missense	probably benign	0.20
R0241:Olfr998	UTSW	2	85590810	missense	probably benign	0.20
R0268:Olfr998	UTSW	2	85591301	missense	possibly damaging	0.78
R0481:Olfr998	UTSW	2	85591104	missense	possibly damaging	0.94
R1816:Olfr998	UTSW	2	85590925	missense	probably benign	0.00
R1988:Olfr998	UTSW	2	85590641	missense	probably benign	0.00
R2008:Olfr998	UTSW	2	85591422	missense	probably damaging	1.00
R2060:Olfr998	UTSW	2	85591283	missense	possibly damaging	0.78
R2273:Olfr998	UTSW	2	85590588	missense	probably damaging	1.00
R4409:Olfr998	UTSW	2	85590930	missense	probably damaging	1.00
R4783:Olfr998	UTSW	2	85590938	missense	probably benign	0.03
R4785:Olfr998	UTSW	2	85590938	missense	probably benign	0.03
R5098:Olfr998	UTSW	2	85590632	missense	probably benign	0.00
R5462:Olfr998	UTSW	2	85591296	missense	probably damaging	1.00
R6092:Olfr998	UTSW	2	85590606	missense	probably benign	0.14
R6278:Olfr998	UTSW	2	85590998	missense	probably benign	0.00
R7022:Olfr998	UTSW	2	85590598	missense	probably benign	0.01
R7673:Olfr998	UTSW	2	85591062	missense	possibly damaging	0.75
R8054:Olfr998	UTSW	2	85590840	missense	probably damaging	1.00
R8118:Olfr998	UTSW	2	85590988	nonsense	probably null
R8940:Olfr998	UTSW	2	85591184	missense	probably benign
R9617:Olfr998	UTSW	2	85590935	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAAGATTCAAACTGCTGATGGG -3'
(R):5'- ACAGAGGCATTTCAGATAAACTGC -3'

Sequencing Primer
(F):5'- GGGAAACAAAAAGCCTTCTCTACTTG -3'
(R):5'- GGCATTTCAGATAAACTGCATAGAG -3'

Posted On

2016-07-06