Mutagenetix > Incidental Mutation

Incidental Mutation 'R1184:Or4c111'

101865

Institutional Source

Beutler Lab

Gene Symbol

Or4c111

Ensembl Gene

ENSMUSG00000075107

Gene Name

olfactory receptor family 4 subfamily C member 111

Synonyms

Olfr1216, MOR233-9, GA_x6K02T2Q125-50494588-50493653

MMRRC Submission

039256-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.053) question?

Stock #

R1184 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

88843471-88844406 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 88844057 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Threonine at position 117 (M117T)

Ref Sequence

ENSEMBL: ENSMUSP00000149441 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099800] [ENSMUST00000216000] [ENSMUST00000217000]

AlphaFold

Q7TR05

Predicted Effect

probably damaging
Transcript: ENSMUST00000099800
AA Change: M117T

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000097388
Gene: ENSMUSG00000075107
AA Change: M117T

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	303	1.8e-46	PFAM
Pfam:7tm_1	39	286	4.2e-17	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000216000
AA Change: M117T

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

probably damaging
Transcript: ENSMUST00000217000
AA Change: M117T

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218738

Meta Mutation Damage Score

0.3475

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.5%

Validation Efficiency

100% (83/83)

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: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700003E16Rik	A	G	6: 83,137,894 (GRCm39)	R7G	probably damaging	Het
Ahdc1	T	A	4: 132,792,707 (GRCm39)	M1316K	probably benign	Het
Alkal1	A	G	1: 6,459,712 (GRCm39)	Y96C	probably damaging	Het
Anxa2r1	A	T	13: 120,496,667 (GRCm39)	N67K	probably benign	Het
Arhgap17	T	C	7: 122,913,913 (GRCm39)	Y199C	probably damaging	Het
Bmp2	T	C	2: 133,403,388 (GRCm39)	V313A	probably damaging	Het
Cacna1b	C	T	2: 24,577,757 (GRCm39)		probably null	Het
Cars1	T	C	7: 143,140,876 (GRCm39)	T141A	probably damaging	Het
Ccdc57	A	G	11: 120,764,637 (GRCm39)		probably benign	Het
Cenpe	T	C	3: 134,970,183 (GRCm39)		probably null	Het
Chadl	T	C	15: 81,577,258 (GRCm39)	S198G	probably benign	Het
Chd6	G	C	2: 160,872,722 (GRCm39)	P286R	probably damaging	Het
Clec4a4	G	T	6: 122,989,671 (GRCm39)	W104L	probably benign	Het
Coq4	G	A	2: 29,678,346 (GRCm39)		probably benign	Het
Cplane1	G	T	15: 8,245,971 (GRCm39)	V1448L	probably benign	Het
Crtc2	T	A	3: 90,169,940 (GRCm39)	Y445*	probably null	Het
Dapk1	A	T	13: 60,844,112 (GRCm39)	I44F	probably damaging	Het
Dcbld2	T	A	16: 58,270,204 (GRCm39)		probably null	Het
Dcun1d4	T	C	5: 73,668,455 (GRCm39)		probably benign	Het
Depdc7	A	T	2: 104,560,523 (GRCm39)		probably benign	Het
Dna2	A	G	10: 62,794,977 (GRCm39)	D416G	probably benign	Het
Dnah2	A	T	11: 69,390,016 (GRCm39)	I743N	probably damaging	Het
Dnah9	A	G	11: 65,975,438 (GRCm39)		probably null	Het
Dock3	A	G	9: 106,846,999 (GRCm39)	S877P	probably damaging	Het
Eif3l	T	A	15: 78,959,966 (GRCm39)		probably null	Het
Epha5	A	T	5: 84,219,134 (GRCm39)		probably null	Het
Ffar3	T	A	7: 30,554,529 (GRCm39)	N264Y	probably damaging	Het
Fyb1	A	T	15: 6,668,381 (GRCm39)	I525F	probably damaging	Het
Fyco1	A	G	9: 123,648,218 (GRCm39)	F1239L	probably damaging	Het
Gcdh	T	C	8: 85,620,071 (GRCm39)		probably benign	Het
Gk5	T	C	9: 96,032,473 (GRCm39)		probably benign	Het
Grm1	A	G	10: 10,595,778 (GRCm39)	Y617H	probably benign	Het
Gvin-ps3	A	G	7: 105,683,159 (GRCm39)	V32A	probably benign	Het
Hhipl2	A	T	1: 183,206,042 (GRCm39)	I131L	probably damaging	Het
Larp4b	T	C	13: 9,216,345 (GRCm39)		probably benign	Het
Lrig2	T	A	3: 104,398,227 (GRCm39)	I301F	possibly damaging	Het
Man2a2	A	T	7: 80,012,713 (GRCm39)	I600N	possibly damaging	Het
Mylk2	G	C	2: 152,755,661 (GRCm39)		probably null	Het
Myo6	C	T	9: 80,193,664 (GRCm39)	Q870*	probably null	Het
Napg	T	G	18: 63,127,409 (GRCm39)	H204Q	probably benign	Het
Neb	G	A	2: 52,153,959 (GRCm39)	T2384M	probably damaging	Het
Nek10	A	G	14: 14,931,325 (GRCm38)		probably benign	Het
Or11h23	A	C	14: 50,948,071 (GRCm39)	T95P	probably benign	Het
Or5an6	T	C	19: 12,372,221 (GRCm39)	V198A	probably benign	Het
Or5b108	T	G	19: 13,168,739 (GRCm39)	L236R	probably damaging	Het
Pclo	A	G	5: 14,572,276 (GRCm39)	T554A	unknown	Het
Perm1	C	A	4: 156,301,771 (GRCm39)	T105K	probably damaging	Het
Pik3r1	T	C	13: 101,822,866 (GRCm39)		probably null	Het
Pld5	A	G	1: 175,872,462 (GRCm39)	I225T	probably damaging	Het
Plxnc1	T	C	10: 94,667,195 (GRCm39)		probably benign	Het
Ptpn12	A	C	5: 21,203,354 (GRCm39)	S475A	possibly damaging	Het
Ptprt	A	G	2: 161,769,692 (GRCm39)	V391A	possibly damaging	Het
Rac2	T	G	15: 78,450,145 (GRCm39)	D65A	possibly damaging	Het
Rgl3	A	G	9: 21,888,676 (GRCm39)		probably null	Het
Rif1	GCCACCA	GCCA	2: 52,000,336 (GRCm39)		probably benign	Het
Sebox	A	T	11: 78,394,675 (GRCm39)	T47S	probably damaging	Het
Sema4b	A	G	7: 79,874,388 (GRCm39)	T593A	probably benign	Het
Serpina3a	C	T	12: 104,082,787 (GRCm39)	Q187*	probably null	Het
Serpinb1a	T	C	13: 33,027,199 (GRCm39)	K248E	probably benign	Het
Serpinb9e	A	C	13: 33,443,757 (GRCm39)	E259A	probably benign	Het
Slc30a3	T	A	5: 31,247,510 (GRCm39)	H44L	probably damaging	Het
Smarca2	T	C	19: 26,748,333 (GRCm39)		probably benign	Het
Snrnp200	T	A	2: 127,078,737 (GRCm39)	C1801S	probably damaging	Het
Soat1	G	A	1: 156,269,944 (GRCm39)		probably null	Het
Spink6	T	C	18: 44,204,605 (GRCm39)		probably benign	Het
Spta1	G	A	1: 174,012,256 (GRCm39)	R354H	probably damaging	Het
Tbck	T	A	3: 132,543,733 (GRCm39)	H861Q	probably benign	Het
Tgfbrap1	G	A	1: 43,088,856 (GRCm39)	T849M	possibly damaging	Het
Tnrc6a	A	G	7: 122,769,563 (GRCm39)	N451S	possibly damaging	Het
Trim36	T	C	18: 46,329,318 (GRCm39)	T41A	probably damaging	Het
Trmt112	C	A	19: 6,887,721 (GRCm39)		probably benign	Het
Trpc4ap	A	G	2: 155,486,990 (GRCm39)		probably benign	Het
Ttll7	C	T	3: 146,645,746 (GRCm39)	P535S	probably damaging	Het
Ttn	A	T	2: 76,691,776 (GRCm39)		probably benign	Het
Txndc11	C	T	16: 10,946,364 (GRCm39)	R149Q	probably benign	Het
Ubr4	C	T	4: 139,164,509 (GRCm39)		probably benign	Het
Usp30	G	A	5: 114,241,888 (GRCm39)		probably null	Het
Vmn1r195	A	G	13: 22,463,181 (GRCm39)	Y217C	probably damaging	Het
Vps33b	T	A	7: 79,932,234 (GRCm39)	D135E	probably benign	Het
Vrk2	A	G	11: 26,433,331 (GRCm39)		probably benign	Het
Wdr81	G	T	11: 75,343,809 (GRCm39)	P486Q	probably damaging	Het
Zfp788	T	C	7: 41,297,750 (GRCm39)	Y129H	probably damaging	Het

Other mutations in Or4c111

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00341:Or4c111	APN	2	88,844,268 (GRCm39)	missense	probably benign	0.22
IGL00895:Or4c111	APN	2	88,843,953 (GRCm39)	missense	probably benign	0.13
IGL01634:Or4c111	APN	2	88,843,788 (GRCm39)	missense	probably damaging	0.99
IGL01844:Or4c111	APN	2	88,843,814 (GRCm39)	missense	possibly damaging	0.95
IGL02036:Or4c111	APN	2	88,843,823 (GRCm39)	missense	probably benign	0.00
IGL02102:Or4c111	APN	2	88,843,470 (GRCm39)	utr 3 prime	probably benign
IGL02194:Or4c111	APN	2	88,844,231 (GRCm39)	missense	probably damaging	1.00
IGL02483:Or4c111	APN	2	88,843,547 (GRCm39)	missense	probably damaging	1.00
IGL02745:Or4c111	APN	2	88,844,232 (GRCm39)	missense	probably damaging	1.00
IGL02829:Or4c111	APN	2	88,844,021 (GRCm39)	missense	probably damaging	1.00
IGL03113:Or4c111	APN	2	88,844,379 (GRCm39)	missense	probably damaging	1.00
IGL03324:Or4c111	APN	2	88,843,903 (GRCm39)	nonsense	probably null
R0102:Or4c111	UTSW	2	88,844,015 (GRCm39)	missense	probably damaging	1.00
R0304:Or4c111	UTSW	2	88,843,632 (GRCm39)	missense	probably damaging	1.00
R1484:Or4c111	UTSW	2	88,843,713 (GRCm39)	nonsense	probably null
R1560:Or4c111	UTSW	2	88,843,550 (GRCm39)	missense	probably damaging	1.00
R1823:Or4c111	UTSW	2	88,843,722 (GRCm39)	missense	probably benign	0.02
R1911:Or4c111	UTSW	2	88,843,565 (GRCm39)	missense	probably damaging	1.00
R2245:Or4c111	UTSW	2	88,843,493 (GRCm39)	missense	probably benign
R2331:Or4c111	UTSW	2	88,844,265 (GRCm39)	missense	probably benign
R3859:Or4c111	UTSW	2	88,844,405 (GRCm39)	start codon destroyed	probably null	1.00
R4579:Or4c111	UTSW	2	88,843,488 (GRCm39)	missense	probably benign
R5022:Or4c111	UTSW	2	88,844,387 (GRCm39)	missense	probably damaging	0.96
R5353:Or4c111	UTSW	2	88,844,099 (GRCm39)	missense	probably benign	0.00
R5894:Or4c111	UTSW	2	88,844,399 (GRCm39)	missense	probably damaging	1.00
R6240:Or4c111	UTSW	2	88,843,970 (GRCm39)	missense	probably benign	0.03
R7101:Or4c111	UTSW	2	88,844,324 (GRCm39)	missense	possibly damaging	0.90
R7652:Or4c111	UTSW	2	88,843,893 (GRCm39)	missense	probably benign	0.01
R8243:Or4c111	UTSW	2	88,844,051 (GRCm39)	missense	probably benign	0.39
R8752:Or4c111	UTSW	2	88,844,231 (GRCm39)	missense	probably damaging	1.00
R9062:Or4c111	UTSW	2	88,843,548 (GRCm39)	missense	probably damaging	1.00
R9472:Or4c111	UTSW	2	88,843,517 (GRCm39)	missense	possibly damaging	0.81
R9628:Or4c111	UTSW	2	88,843,670 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- GGCCAGCTTCAGCAATGGAAAC -3'
(R):5'- TGTGGTGACCATCATCTACAGCCC -3'

Sequencing Primer
(F):5'- GCTTCAGCAATGGAAACAAGTC -3'
(R):5'- ATCATCTACAGCCCTGCACTG -3'

Posted On

2014-01-15