Mutagenetix > Incidental Mutation

Incidental Mutation 'R4366:Or8b12c'

325755

Institutional Source

Beutler Lab

Gene Symbol

Or8b12c

Ensembl Gene

ENSMUSG00000066750

Gene Name

olfactory receptor family 8 subfamily B member 12C

Synonyms

Olfr876, MOR161-1, GA_x6K02T2PVTD-31489645-31490577

MMRRC Submission

041114-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

R4366 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

37715185-37716232 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 37715486 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 93 (H93L)

Ref Sequence

ENSEMBL: ENSMUSP00000149930 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000086064] [ENSMUST00000213368] [ENSMUST00000215287]

AlphaFold

Q7TRE4

Predicted Effect

probably benign
Transcript: ENSMUST00000086064
AA Change: H93L

PolyPhen 2 Score 0.192 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000083231
Gene: ENSMUSG00000066750
AA Change: H93L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	30	307	1.6e-47	PFAM
Pfam:7tm_1	40	289	3.2e-23	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000213368
AA Change: H93L

PolyPhen 2 Score 0.192 (Sensitivity: 0.92; Specificity: 0.87)

Predicted Effect

probably benign
Transcript: ENSMUST00000215287
AA Change: H93L

PolyPhen 2 Score 0.192 (Sensitivity: 0.92; Specificity: 0.87)

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.5%
10x: 96.8%
20x: 93.7%

Validation Efficiency

95% (57/60)

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: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrf5	A	C	17: 43,752,860 (GRCm39)	T396P	probably damaging	Het
Apob	A	T	12: 8,066,083 (GRCm39)	I4318F	possibly damaging	Het
Apol7c	T	G	15: 77,410,589 (GRCm39)	D119A	probably benign	Het
App	G	T	16: 84,853,321 (GRCm39)	D252E	unknown	Het
C4a	T	A	17: 35,033,885 (GRCm39)		noncoding transcript	Het
Cacna1b	T	C	2: 24,592,632 (GRCm39)	Y515C	probably damaging	Het
Cacna1f	G	T	X: 7,476,213 (GRCm39)	A123S	probably damaging	Het
Cldn6	G	C	17: 23,900,494 (GRCm39)	A153P	probably benign	Het
Cmya5	T	C	13: 93,228,464 (GRCm39)	N2208S	probably benign	Het
Csnk1g1	A	G	9: 65,927,135 (GRCm39)	T101A	probably benign	Het
Ddx46	T	A	13: 55,811,049 (GRCm39)	D544E	probably benign	Het
Dmxl1	T	A	18: 50,011,084 (GRCm39)	C1080*	probably null	Het
Dst	T	C	1: 34,290,959 (GRCm39)	S3335P	probably damaging	Het
Efnb3	T	C	11: 69,446,771 (GRCm39)	K313R	probably damaging	Het
Elf2	G	A	3: 51,215,570 (GRCm39)	Q47*	probably null	Het
Epc2	A	G	2: 49,437,566 (GRCm39)	K657E	possibly damaging	Het
Ephx4	A	G	5: 107,551,679 (GRCm39)		probably benign	Het
Ereg	T	C	5: 91,234,659 (GRCm39)	I24T	probably benign	Het
Evc2	C	A	5: 37,496,013 (GRCm39)	A41D	possibly damaging	Het
Fkbp15	A	G	4: 62,254,651 (GRCm39)	V283A	probably benign	Het
Flrt3	T	C	2: 140,502,327 (GRCm39)	T434A	probably damaging	Het
Gm572	A	G	4: 148,739,322 (GRCm39)	D50G	possibly damaging	Het
Hecw1	C	T	13: 14,490,749 (GRCm39)	D748N	probably damaging	Het
Hivep3	A	C	4: 119,953,286 (GRCm39)	H534P	possibly damaging	Het
Hspa4l	C	A	3: 40,721,241 (GRCm39)		probably null	Het
Ipo7	T	C	7: 109,628,919 (GRCm39)	M63T	possibly damaging	Het
Ipo7	A	T	7: 109,647,423 (GRCm39)	T614S	possibly damaging	Het
Krt87	T	G	15: 101,385,395 (GRCm39)	M326L	probably benign	Het
Mbd5	T	A	2: 49,162,978 (GRCm39)	N261K	probably damaging	Het
Mcam	T	A	9: 44,045,994 (GRCm39)	L3Q	probably damaging	Het
Mcoln3	C	A	3: 145,846,247 (GRCm39)	T519K	possibly damaging	Het
Mideas	C	T	12: 84,203,245 (GRCm39)	G886S	probably benign	Het
Mrgprx1	C	A	7: 47,670,941 (GRCm39)	A269S	probably damaging	Het
Mypn	T	C	10: 63,028,487 (GRCm39)	E192G	probably benign	Het
Nup205	C	A	6: 35,168,962 (GRCm39)	P397Q	probably benign	Het
Obsl1	A	C	1: 75,464,693 (GRCm39)	L1576R	possibly damaging	Het
Ofcc1	A	G	13: 40,168,937 (GRCm39)	S817P	probably benign	Het
Or6c210	A	T	10: 129,496,400 (GRCm39)	M242L	probably benign	Het
Pcdhgb7	A	G	18: 37,887,125 (GRCm39)	Y765C	possibly damaging	Het
Pde7a	A	G	3: 19,365,026 (GRCm39)		probably null	Het
Phip	C	T	9: 82,782,922 (GRCm39)		probably benign	Het
Rhbdl2	T	A	4: 123,703,728 (GRCm39)	M1K	probably null	Het
Ripor2	C	T	13: 24,905,694 (GRCm39)	P947S	probably benign	Het
Sf3a3	A	G	4: 124,618,932 (GRCm39)	T298A	probably benign	Het
Slc25a29	C	T	12: 108,797,097 (GRCm39)		probably benign	Het
Spinkl	T	G	18: 44,307,650 (GRCm39)	T4P	possibly damaging	Het
Stk33	G	A	7: 108,879,002 (GRCm39)	S449L	probably benign	Het
Suz12	T	A	11: 79,892,988 (GRCm39)		probably benign	Het
Timp2	T	A	11: 118,201,497 (GRCm39)	I124F	probably damaging	Het
Tlr1	C	T	5: 65,083,180 (GRCm39)	D466N	probably benign	Het
Tmem200b	A	G	4: 131,649,781 (GRCm39)	I234V	possibly damaging	Het
Ubr1	C	A	2: 120,801,084 (GRCm39)		probably benign	Het
Usp33	C	A	3: 152,074,149 (GRCm39)	Q332K	probably benign	Het
Zfr	A	G	15: 12,156,416 (GRCm39)	E634G	probably damaging	Het

Other mutations in Or8b12c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00973:Or8b12c	APN	9	37,716,078 (GRCm39)	missense	probably damaging	1.00
IGL01330:Or8b12c	APN	9	37,715,516 (GRCm39)	missense	probably damaging	1.00
IGL02105:Or8b12c	APN	9	37,715,891 (GRCm39)	missense	possibly damaging	0.53
IGL02505:Or8b12c	APN	9	37,715,627 (GRCm39)	missense	probably benign	0.08
R1543:Or8b12c	UTSW	9	37,715,243 (GRCm39)	missense	possibly damaging	0.94
R1768:Or8b12c	UTSW	9	37,715,599 (GRCm39)	missense	probably damaging	1.00
R1960:Or8b12c	UTSW	9	37,715,242 (GRCm39)	missense	probably benign	0.01
R2567:Or8b12c	UTSW	9	37,715,509 (GRCm39)	missense	probably damaging	1.00
R3815:Or8b12c	UTSW	9	37,715,465 (GRCm39)	missense	probably benign	0.05
R3816:Or8b12c	UTSW	9	37,715,465 (GRCm39)	missense	probably benign	0.05
R3817:Or8b12c	UTSW	9	37,715,465 (GRCm39)	missense	probably benign	0.05
R3819:Or8b12c	UTSW	9	37,715,465 (GRCm39)	missense	probably benign	0.05
R4364:Or8b12c	UTSW	9	37,715,486 (GRCm39)	missense	probably benign	0.19
R4620:Or8b12c	UTSW	9	37,716,115 (GRCm39)	missense	probably benign	0.02
R5530:Or8b12c	UTSW	9	37,716,103 (GRCm39)	missense	probably benign	0.00
R6199:Or8b12c	UTSW	9	37,716,177 (GRCm39)	splice site	probably null
R6238:Or8b12c	UTSW	9	37,715,317 (GRCm39)	missense	probably benign	0.26
R6893:Or8b12c	UTSW	9	37,716,141 (GRCm39)	makesense	probably null
R7404:Or8b12c	UTSW	9	37,715,257 (GRCm39)	missense	possibly damaging	0.80
R7806:Or8b12c	UTSW	9	37,715,872 (GRCm39)	missense	probably damaging	0.99
R8855:Or8b12c	UTSW	9	37,715,709 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTCATCCTTGCAGGCCTGAC -3'
(R):5'- GTCAGCCTTGCCATGGATATG -3'

Sequencing Primer
(F):5'- TTGCAGGCCTGACAGACCAG -3'
(R):5'- GGGCCATGGCTCCAACAAAAC -3'

Posted On

2015-07-06