Mutagenetix > Incidental Mutation

Incidental Mutation 'R5946:Or8b12'

472182

Institutional Source

Beutler Lab

Gene Symbol

Or8b12

Ensembl Gene

ENSMUSG00000063350

Gene Name

olfactory receptor family 8 subfamily B member 12

Synonyms

GA_x6K02T2PVTD-31428850-31429782, MOR161-2, Olfr874

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.094) question?

Stock #

R5946 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

37656596-37658402 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 37658330 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Glutamine at position 300 (L300Q)

Ref Sequence

ENSEMBL: ENSMUSP00000150088 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000115004] [ENSMUST00000216982]

AlphaFold

Q7TRE6

Predicted Effect

probably damaging
Transcript: ENSMUST00000115004
AA Change: L300Q

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000110656
Gene: ENSMUSG00000063350
AA Change: L300Q

Domain	Start	End	E-Value	Type
Pfam:7tm_4	30	307	5.9e-49	PFAM
Pfam:7tm_1	40	289	6.2e-22	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000216982
AA Change: L300Q

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.4%

Validation Efficiency

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: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc9	A	G	6: 142,571,678 (GRCm39)	F1137S	probably damaging	Het
Actr6	G	T	10: 89,564,054 (GRCm39)	Q73K	probably benign	Het
Adamtsl3	G	A	7: 82,225,265 (GRCm39)	G358D	probably damaging	Het
Aggf1	A	G	13: 95,508,084 (GRCm39)	V94A	probably damaging	Het
Arpc3	A	G	5: 122,541,459 (GRCm39)	Y57C	probably damaging	Het
Asb2	A	G	12: 103,287,814 (GRCm39)	Y630H	probably benign	Het
Atp1a1	A	T	3: 101,497,090 (GRCm39)	N405K	probably benign	Het
C6	G	T	15: 4,837,996 (GRCm39)	D869Y	possibly damaging	Het
Cds2	A	G	2: 132,139,168 (GRCm39)	Y137C	probably damaging	Het
Ceacam12	A	T	7: 17,803,131 (GRCm39)	E179V	probably damaging	Het
Chgb	T	A	2: 132,634,516 (GRCm39)	Y153N	probably benign	Het
Cit	T	A	5: 116,135,593 (GRCm39)	L1831Q	probably damaging	Het
Cpne8	C	A	15: 90,373,191 (GRCm39)	*578L	probably null	Het
Cspg5	A	G	9: 110,080,151 (GRCm39)	T440A	probably damaging	Het
Dnah7a	A	C	1: 53,598,467 (GRCm39)	V1393G	probably damaging	Het
Dnajb8	A	G	6: 88,199,575 (GRCm39)	D37G	probably benign	Het
Dst	A	G	1: 34,213,273 (GRCm39)	I1063M	probably benign	Het
Efs	T	G	14: 55,156,951 (GRCm39)		probably null	Het
Gpatch1	A	G	7: 34,991,257 (GRCm39)	S596P	probably damaging	Het
Hbs1l	C	A	10: 21,217,655 (GRCm39)	H190Q	probably benign	Het
Ighm	A	G	12: 113,386,329 (GRCm39)	V7A	unknown	Het
Ivd	A	T	2: 118,707,370 (GRCm39)	I295F	possibly damaging	Het
Kcnq5	A	C	1: 21,575,931 (GRCm39)	S258A	probably damaging	Het
Mad1l1	G	T	5: 140,247,334 (GRCm39)	P331Q	probably damaging	Het
Mcf2l	G	T	8: 13,063,922 (GRCm39)	G1045C	probably damaging	Het
Mcoln1	T	A	8: 3,558,701 (GRCm39)	I233N	probably damaging	Het
Mmp13	T	C	9: 7,276,580 (GRCm39)	L225P	probably damaging	Het
Muc5ac	G	A	7: 141,371,644 (GRCm39)	C2615Y	possibly damaging	Het
Myh7b	T	C	2: 155,463,315 (GRCm39)	F516L	probably damaging	Het
Obsl1	A	T	1: 75,467,851 (GRCm39)	S1347R	probably damaging	Het
Ogn	A	G	13: 49,771,761 (GRCm39)	N207S	probably benign	Het
Or2h15	C	A	17: 38,441,598 (GRCm39)	A162S	probably benign	Het
Pcdha2	G	T	18: 37,074,159 (GRCm39)	V597L	probably damaging	Het
Pcnt	T	A	10: 76,217,897 (GRCm39)	Y2126F	possibly damaging	Het
Pgbd5	A	T	8: 125,101,056 (GRCm39)	M400K	possibly damaging	Het
Pklr	A	T	3: 89,043,503 (GRCm39)	E5V	probably benign	Het
Pkp4	T	A	2: 59,135,411 (GRCm39)	D94E	probably benign	Het
Ppan	C	T	9: 20,800,969 (GRCm39)	Q111*	probably null	Het
Prkcb	A	G	7: 122,143,926 (GRCm39)	N330S	probably benign	Het
Prl4a1	T	A	13: 28,202,499 (GRCm39)	W25R	probably damaging	Het
Rars2	T	A	4: 34,656,855 (GRCm39)	H501Q	possibly damaging	Het
Ryr2	T	C	13: 11,741,839 (GRCm39)	D2114G	probably damaging	Het
Serinc2	G	T	4: 130,149,314 (GRCm39)	T351K	possibly damaging	Het
Slc22a12	A	G	19: 6,587,881 (GRCm39)	F358L	probably damaging	Het
Sorcs2	A	C	5: 36,186,427 (GRCm39)	V905G	probably damaging	Het
Tekt3	G	C	11: 62,985,573 (GRCm39)	A460P	probably damaging	Het
Tm4sf1	T	G	3: 57,200,289 (GRCm39)	I109L	possibly damaging	Het
Tmc5	A	T	7: 118,269,948 (GRCm39)	E899D	probably damaging	Het
Tmem268	C	T	4: 63,486,746 (GRCm39)	P90S	probably damaging	Het
Trim38	A	G	13: 23,966,717 (GRCm39)	M55V	probably benign	Het
Trip10	T	G	17: 57,557,963 (GRCm39)	V50G	probably damaging	Het
Usp25	T	A	16: 76,911,942 (GRCm39)	C990*	probably null	Het
Uts2	A	G	4: 151,083,506 (GRCm39)	D39G	probably benign	Het
Vezf1	T	A	11: 87,964,560 (GRCm39)	C49*	probably null	Het
Wee2	T	A	6: 40,440,146 (GRCm39)	N431K	probably null	Het
Yeats2	C	A	16: 20,026,513 (GRCm39)	Y796*	probably null	Het
Zfp592	G	A	7: 80,687,645 (GRCm39)	G890D	possibly damaging	Het
Zfp647	G	A	15: 76,796,285 (GRCm39)	P125L	probably damaging	Het

Other mutations in Or8b12

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00158:Or8b12	APN	9	37,657,685 (GRCm39)	missense	possibly damaging	0.89
IGL02349:Or8b12	APN	9	37,657,502 (GRCm39)	missense	probably benign	0.03
IGL02799:Or8b12	UTSW	9	37,657,805 (GRCm39)	missense	probably damaging	1.00
R0498:Or8b12	UTSW	9	37,657,550 (GRCm39)	missense	probably damaging	1.00
R0690:Or8b12	UTSW	9	37,657,513 (GRCm39)	missense	probably benign	0.01
R1053:Or8b12	UTSW	9	37,658,131 (GRCm39)	missense	probably damaging	0.99
R1777:Or8b12	UTSW	9	37,657,607 (GRCm39)	missense	possibly damaging	0.78
R1862:Or8b12	UTSW	9	37,658,264 (GRCm39)	missense	probably benign
R1907:Or8b12	UTSW	9	37,657,729 (GRCm39)	missense	probably benign	0.35
R4524:Or8b12	UTSW	9	37,658,162 (GRCm39)	missense	possibly damaging	0.50
R4731:Or8b12	UTSW	9	37,657,831 (GRCm39)	missense	probably benign	0.06
R4746:Or8b12	UTSW	9	37,657,453 (GRCm39)	missense	probably benign	0.02
R4768:Or8b12	UTSW	9	37,658,177 (GRCm39)	missense	probably damaging	1.00
R5130:Or8b12	UTSW	9	37,657,805 (GRCm39)	missense	probably damaging	1.00
R5406:Or8b12	UTSW	9	37,657,943 (GRCm39)	missense	probably benign	0.23
R5546:Or8b12	UTSW	9	37,657,820 (GRCm39)	missense	probably benign	0.05
R5882:Or8b12	UTSW	9	37,657,928 (GRCm39)	missense	probably benign	0.02
R6226:Or8b12	UTSW	9	37,657,433 (GRCm39)	start codon destroyed	probably null	1.00
R6705:Or8b12	UTSW	9	37,658,030 (GRCm39)	missense	possibly damaging	0.94
R6965:Or8b12	UTSW	9	37,657,433 (GRCm39)	start codon destroyed	probably null	1.00
R8008:Or8b12	UTSW	9	37,658,089 (GRCm39)	missense	probably damaging	0.99
R8743:Or8b12	UTSW	9	37,658,174 (GRCm39)	missense	probably benign
R9066:Or8b12	UTSW	9	37,657,871 (GRCm39)	missense	possibly damaging	0.65
R9068:Or8b12	UTSW	9	37,657,963 (GRCm39)	missense	probably damaging	1.00
R9756:Or8b12	UTSW	9	37,658,314 (GRCm39)	missense	possibly damaging	0.88

Predicted Primers

PCR Primer
(F):5'- GCAGCTCCCACTTGATTGTG -3'
(R):5'- ATCCATGAAGACCTAGTTTCTCCATAG -3'

Sequencing Primer
(F):5'- CACTTGATTGTGGTTTGTCTTTTC -3'
(R):5'- CTAGTTTCTCCATAGTGCCATAAAC -3'

Posted On

2017-03-31