Mutagenetix > Incidental Mutation

Incidental Mutation 'R7329:Or8c11'

569124

Institutional Source

Beutler Lab

Gene Symbol

Or8c11

Ensembl Gene

ENSMUSG00000096757

Gene Name

olfactory receptor family 8 subfamily C member 11

Synonyms

GA_x6K02T2PVTD-32071567-32072508, Olfr900, GA_x6K02T2MYUG-9124-8183, MOR170-2, MOR170-13, MOR170-15, Olfr251

MMRRC Submission

045422-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.075) question?

Stock #

R7329 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

38289179-38290129 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 38289456 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Lysine at position 87 (T87K)

Ref Sequence

ENSEMBL: ENSMUSP00000149583 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072731] [ENSMUST00000214865]

AlphaFold

E9Q891

Predicted Effect

probably benign
Transcript: ENSMUST00000072731
AA Change: T93K

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000072514
Gene: ENSMUSG00000096757
AA Change: T93K

Domain	Start	End	E-Value	Type
Pfam:7tm_4	37	313	9.8e-50	PFAM
Pfam:7tm_1	47	296	4.2e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000214865
AA Change: T87K

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

100% (78/78)

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: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actb	T	C	5: 142,890,146 (GRCm39)	N252S	probably benign	Het
Adgrb1	C	A	15: 74,411,094 (GRCm39)	T330K	probably damaging	Het
Ahnak	A	G	19: 8,979,156 (GRCm39)	T147A	probably damaging	Het
Ankfy1	T	C	11: 72,603,034 (GRCm39)	V21A	probably damaging	Het
Arrdc4	T	A	7: 68,390,775 (GRCm39)	N322Y	probably damaging	Het
Bfsp2	C	A	9: 103,327,121 (GRCm39)	E205D	probably benign	Het
C2cd4b	T	A	9: 67,667,419 (GRCm39)	S138R	possibly damaging	Het
Camkk1	C	G	11: 72,917,873 (GRCm39)	N147K	probably damaging	Het
Ckap2l	T	A	2: 129,127,284 (GRCm39)	Q298L	possibly damaging	Het
Clstn2	G	T	9: 97,343,422 (GRCm39)	A675D	probably benign	Het
Cntnap2	G	A	6: 47,248,205 (GRCm39)	V1204M	possibly damaging	Het
Col4a1	C	T	8: 11,276,494 (GRCm39)		probably null	Het
Ctrc	T	C	4: 141,571,022 (GRCm39)	T73A	probably benign	Het
Cubn	A	G	2: 13,473,582 (GRCm39)	F454L	probably damaging	Het
Cuedc1	A	T	11: 88,060,692 (GRCm39)	S12C	unknown	Het
Cyb561a3	G	T	19: 10,565,268 (GRCm39)	G211C	probably damaging	Het
D5Ertd579e	A	T	5: 36,773,739 (GRCm39)	S219T	probably benign	Het
Dennd4c	T	A	4: 86,759,318 (GRCm39)	Y1783N	probably damaging	Het
Dennd4c	C	T	4: 86,698,111 (GRCm39)	P200S	possibly damaging	Het
Dnah6	G	A	6: 73,121,705 (GRCm39)	Q1426*	probably null	Het
Dync2h1	T	G	9: 7,011,247 (GRCm39)	T3649P	probably benign	Het
E2f8	T	C	7: 48,521,858 (GRCm39)	S415G	probably damaging	Het
Fbxo22	A	G	9: 55,122,261 (GRCm39)	I147V	probably benign	Het
Gclc	A	G	9: 77,683,473 (GRCm39)	Y110C	probably damaging	Het
Gstm5	A	G	3: 107,803,647 (GRCm39)	T27A	possibly damaging	Het
Heatr4	A	G	12: 84,024,856 (GRCm39)	S322P	probably benign	Het
Htt	T	A	5: 34,987,099 (GRCm39)	I1106N	probably benign	Het
Hunk	T	C	16: 90,183,570 (GRCm39)	V76A	probably benign	Het
Igkv12-98	C	T	6: 68,548,087 (GRCm39)	T72I	possibly damaging	Het
Igkv9-123	A	T	6: 67,931,629 (GRCm39)	W16R	possibly damaging	Het
Ipo7	T	C	7: 109,648,224 (GRCm39)	L674S	possibly damaging	Het
Kcnh6	T	C	11: 105,908,203 (GRCm39)	F273S	probably benign	Het
Lamb3	C	A	1: 193,002,848 (GRCm39)	Q98K	possibly damaging	Het
Lingo4	A	T	3: 94,310,162 (GRCm39)	T367S	probably benign	Het
Lypd6b	A	T	2: 49,832,512 (GRCm39)	I26F	probably benign	Het
Maneal	T	C	4: 124,750,512 (GRCm39)	T415A	probably benign	Het
Mapk1ip1l	A	G	14: 47,547,920 (GRCm39)	T23A	unknown	Het
Mrps17	T	A	5: 129,793,705 (GRCm39)		probably benign	Het
Mup13	T	G	4: 61,183,688 (GRCm39)	D45A	probably damaging	Het
Mycbpap	T	A	11: 94,400,073 (GRCm39)	D408V	probably damaging	Het
Myh10	A	G	11: 68,701,017 (GRCm39)	H1742R	probably benign	Het
Mylk4	A	G	13: 32,900,766 (GRCm39)	Y255H	probably damaging	Het
Nbeal1	A	G	1: 60,256,355 (GRCm39)	Q200R	probably benign	Het
Nkain2	TTTACTCGTT	TTT	10: 32,765,892 (GRCm39)		probably null	Het
Olfm4	T	C	14: 80,249,369 (GRCm39)	V162A	possibly damaging	Het
Or1j15	A	G	2: 36,458,708 (GRCm39)	T33A	probably benign	Het
Or51a8	T	C	7: 102,550,039 (GRCm39)	L155P	probably damaging	Het
Or5w8	T	C	2: 87,687,585 (GRCm39)	V22A	probably benign	Het
Ovol3	T	A	7: 29,934,677 (GRCm39)	R43S	probably benign	Het
Pcbp1	A	G	6: 86,502,098 (GRCm39)	V267A	probably benign	Het
Phf20	T	A	2: 156,146,552 (GRCm39)	V903E	probably damaging	Het
Pi4k2b	T	G	5: 52,914,211 (GRCm39)	S316A	probably benign	Het
Pira1	G	A	7: 3,742,875 (GRCm39)		probably benign	Het
Pkhd1	A	T	1: 20,617,743 (GRCm39)	H947Q	probably damaging	Het
Ppip5k2	A	C	1: 97,678,478 (GRCm39)		probably null	Het
Prkca	T	A	11: 107,905,103 (GRCm39)	T212S	possibly damaging	Het
Psg16	A	T	7: 16,824,611 (GRCm39)	I41F	possibly damaging	Het
Rae1	T	A	2: 172,851,238 (GRCm39)	F204I	probably benign	Het
Rasef	T	A	4: 73,662,374 (GRCm39)	N192I	probably damaging	Het
Rfc1	T	A	5: 65,420,478 (GRCm39)	R1122S	unknown	Het
Rfx2	A	T	17: 57,110,681 (GRCm39)	S102T	probably benign	Het
Sez6l	A	G	5: 112,588,773 (GRCm39)	Y647H	probably damaging	Het
Siglecf	A	G	7: 43,001,395 (GRCm39)	Y121C	probably damaging	Het
Slc27a5	T	C	7: 12,725,089 (GRCm39)	T453A	possibly damaging	Het
Slc44a2	G	A	9: 21,254,048 (GRCm39)	R171Q	probably damaging	Het
Slc4a9	A	C	18: 36,673,874 (GRCm39)	E889A	possibly damaging	Het
Snx31	C	A	15: 36,555,621 (GRCm39)	R13L	probably benign	Het
Spag6l	A	T	16: 16,584,883 (GRCm39)	Y422N	probably benign	Het
Spmip5	T	C	19: 58,777,654 (GRCm39)	E52G	probably damaging	Het
Sulf2	T	C	2: 165,959,008 (GRCm39)	T67A	probably damaging	Het
Syne2	G	A	12: 76,013,758 (GRCm39)	R2983Q	probably benign	Het
Tmtc3	A	G	10: 100,283,281 (GRCm39)	I758T	probably benign	Het
Top2a	T	A	11: 98,895,072 (GRCm39)	I843L	possibly damaging	Het
Tph1	T	C	7: 46,306,285 (GRCm39)		probably null	Het
Trdmt1	A	G	2: 13,520,933 (GRCm39)	L323P	probably damaging	Het
Ush2a	A	T	1: 188,285,395 (GRCm39)	E1977V	probably damaging	Het
Utp4	A	G	8: 107,640,095 (GRCm39)	E468G	probably benign	Het
Uts2r	A	G	11: 121,051,558 (GRCm39)	T141A	possibly damaging	Het
Vmn1r230	A	G	17: 21,066,952 (GRCm39)	Y47C	probably damaging	Het

Other mutations in Or8c11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02013:Or8c11	APN	9	38,289,373 (GRCm39)	missense	probably benign	0.31
IGL02131:Or8c11	APN	9	38,289,203 (GRCm39)	missense	probably benign	0.01
IGL02311:Or8c11	APN	9	38,289,194 (GRCm39)	nonsense	probably null
IGL02377:Or8c11	APN	9	38,289,542 (GRCm39)	missense	probably damaging	1.00
R0284:Or8c11	UTSW	9	38,289,880 (GRCm39)	missense	probably benign	0.00
R0412:Or8c11	UTSW	9	38,290,090 (GRCm39)	missense	probably damaging	0.98
R0903:Or8c11	UTSW	9	38,290,097 (GRCm39)	missense	probably benign	0.00
R1664:Or8c11	UTSW	9	38,289,548 (GRCm39)	missense	possibly damaging	0.93
R2902:Or8c11	UTSW	9	38,289,337 (GRCm39)	missense	possibly damaging	0.89
R3970:Or8c11	UTSW	9	38,289,222 (GRCm39)	missense	probably damaging	0.98
R4191:Or8c11	UTSW	9	38,289,648 (GRCm39)	missense	probably damaging	0.98
R4650:Or8c11	UTSW	9	38,289,699 (GRCm39)	missense	probably damaging	1.00
R4910:Or8c11	UTSW	9	38,290,038 (GRCm39)	missense	probably null	0.98
R5256:Or8c11	UTSW	9	38,289,213 (GRCm39)	missense	probably benign	0.00
R5385:Or8c11	UTSW	9	38,289,281 (GRCm39)	missense	probably benign
R5386:Or8c11	UTSW	9	38,289,281 (GRCm39)	missense	probably benign
R6005:Or8c11	UTSW	9	38,289,605 (GRCm39)	missense	probably damaging	1.00
R6268:Or8c11	UTSW	9	38,289,384 (GRCm39)	missense	probably benign	0.10
R6486:Or8c11	UTSW	9	38,289,200 (GRCm39)	missense	probably benign
R7019:Or8c11	UTSW	9	38,290,098 (GRCm39)	missense	possibly damaging	0.89
R7045:Or8c11	UTSW	9	38,289,729 (GRCm39)	missense	probably damaging	0.99
R7120:Or8c11	UTSW	9	38,289,945 (GRCm39)	missense	probably damaging	1.00
R7703:Or8c11	UTSW	9	38,289,357 (GRCm39)	missense	probably benign	0.01
R8333:Or8c11	UTSW	9	38,289,912 (GRCm39)	missense	probably damaging	0.98
R8352:Or8c11	UTSW	9	38,289,647 (GRCm39)	missense	probably benign	0.01
R8452:Or8c11	UTSW	9	38,289,647 (GRCm39)	missense	probably benign	0.01
R8461:Or8c11	UTSW	9	38,289,777 (GRCm39)	missense	probably damaging	0.96
R8870:Or8c11	UTSW	9	38,289,720 (GRCm39)	missense	probably benign	0.16

Predicted Primers

PCR Primer
(F):5'- AAGAGCTCCAGTTGCCTCTG -3'
(R):5'- AGCCTGATCATAAACCCTGTATGAG -3'

Sequencing Primer
(F):5'- AGCTCCAGTTGCCTCTGTTCATC -3'
(R):5'- CCTGTATGAGTCAGGGCAC -3'

Posted On

2019-09-13