Mutagenetix > Incidental Mutation

Incidental Mutation 'R4603:Or6c207'

345800

Institutional Source

Beutler Lab

Gene Symbol

Or6c207

Ensembl Gene

ENSMUSG00000062914

Gene Name

olfactory receptor family 6 subfamily C member 207

Synonyms

Olfr777, MOR114-9, GA_x6K02T2PULF-10955551-10954616

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.079) question?

Stock #

R4603 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

129104255-129105190 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 129104274 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Alanine to Valine at position 306 (A306V)

Ref Sequence

ENSEMBL: ENSMUSP00000145475 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080313] [ENSMUST00000204573] [ENSMUST00000213512]

AlphaFold

Q8VFH3

Predicted Effect

probably benign
Transcript: ENSMUST00000080313
AA Change: A306V

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000079191
Gene: ENSMUSG00000062914
AA Change: A306V

Domain	Start	End	E-Value	Type
Pfam:7tm_4	28	307	1.4e-42	PFAM
Pfam:7tm_1	38	287	1.5e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204573
AA Change: A306V

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000145475
Gene: ENSMUSG00000062914
AA Change: A306V

Domain	Start	End	E-Value	Type
Pfam:7tm_4	28	307	1.4e-42	PFAM
Pfam:7tm_1	38	287	1.5e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000213512

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 94.9%

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: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810024B03Rik	A	G	2: 127,029,019 (GRCm39)	V60A	probably damaging	Het
AAdacl4fm3	A	G	4: 144,429,798 (GRCm39)	V397A	probably benign	Het
Afg3l1	A	G	8: 124,228,674 (GRCm39)	T747A	probably benign	Het
Aldh4a1	T	C	4: 139,370,740 (GRCm39)	S408P	probably damaging	Het
Ank2	T	C	3: 126,825,665 (GRCm39)	T445A	probably benign	Het
Antxrl	A	G	14: 33,797,792 (GRCm39)	E589G	possibly damaging	Het
Arhgef12	C	T	9: 42,921,489 (GRCm39)	G329R	probably benign	Het
Arsi	G	A	18: 61,049,723 (GRCm39)	G202E	probably benign	Het
AY358078	T	A	14: 52,063,532 (GRCm39)	C393S	possibly damaging	Het
Bpnt2	T	C	4: 4,767,878 (GRCm39)	I299M	probably damaging	Het
Brca2	T	A	5: 150,459,630 (GRCm39)	C302S	possibly damaging	Het
Ccdc169	T	A	3: 55,058,226 (GRCm39)	M4K	probably benign	Het
Ccdc66	T	C	14: 27,222,377 (GRCm39)	N122S	probably damaging	Het
Cd226	T	C	18: 89,225,343 (GRCm39)	V80A	probably damaging	Het
Cdc73	T	C	1: 143,553,595 (GRCm39)		probably null	Het
Cfap96	A	T	8: 46,423,505 (GRCm39)	I69N	probably damaging	Het
Cse1l	T	C	2: 166,786,452 (GRCm39)	V604A	probably benign	Het
Cxcr1	G	C	1: 74,231,896 (GRCm39)	T42S	probably benign	Het
Dhx9	TCC	TC	1: 153,342,797 (GRCm39)		probably null	Het
Ercc3	G	A	18: 32,378,624 (GRCm39)	A202T	probably benign	Het
Erp27	A	G	6: 136,896,947 (GRCm39)	V85A	probably damaging	Het
Fam3d	T	A	14: 8,358,429 (GRCm38)	S57C	probably damaging	Het
Fgf8	T	G	19: 45,726,592 (GRCm39)	I137L	probably benign	Het
Fgfrl1	T	A	5: 108,851,401 (GRCm39)	V106D	probably damaging	Het
Gaa	T	C	11: 119,169,784 (GRCm39)	W613R	probably damaging	Het
Gabarap	A	G	11: 69,885,287 (GRCm39)	N66S	probably benign	Het
Gp1bb	A	T	16: 18,439,893 (GRCm39)	L67Q	probably damaging	Het
Gpn1	T	C	5: 31,654,696 (GRCm39)		probably null	Het
Gstt1	T	C	10: 75,629,969 (GRCm39)	Y48C	probably damaging	Het
Iqcg	C	T	16: 32,861,134 (GRCm39)	R194K	probably null	Het
Iqcg	C	G	16: 32,861,133 (GRCm39)		probably null	Het
Kcnj3	C	T	2: 55,336,991 (GRCm39)	R286*	probably null	Het
Klhl38	T	A	15: 58,186,616 (GRCm39)	I38F	possibly damaging	Het
Kmo	C	A	1: 175,479,208 (GRCm39)	P248Q	probably benign	Het
Mbtps1	A	T	8: 120,262,086 (GRCm39)	D354E	probably damaging	Het
Mcpt9	C	T	14: 56,266,049 (GRCm39)	V60M	probably damaging	Het
Mical3	C	A	6: 120,911,799 (GRCm39)	E1083*	probably null	Het
Mprip	T	C	11: 59,622,399 (GRCm39)	V162A	probably damaging	Het
Mrc2	G	A	11: 105,239,257 (GRCm39)		probably null	Het
Myocd	T	C	11: 65,078,571 (GRCm39)	D408G	possibly damaging	Het
Myt1l	A	G	12: 29,892,539 (GRCm39)	T59A	probably benign	Het
Ndufb7	A	G	8: 84,293,494 (GRCm39)	E16G	probably damaging	Het
Ndufs7	T	A	10: 80,092,501 (GRCm39)	Y203*	probably null	Het
Nploc4	C	T	11: 120,276,613 (GRCm39)	V478I	probably benign	Het
Nrap	A	G	19: 56,323,456 (GRCm39)		probably null	Het
Or5e1	A	T	7: 108,354,834 (GRCm39)	Y257F	probably damaging	Het
Pald1	T	C	10: 61,184,395 (GRCm39)	T241A	probably benign	Het
Pdss2	T	C	10: 43,248,197 (GRCm39)	S234P	probably damaging	Het
Pias2	T	A	18: 77,217,803 (GRCm39)	V335E	probably damaging	Het
Ppip5k2	C	A	1: 97,682,861 (GRCm39)	K187N	probably damaging	Het
Ppp3cb	T	C	14: 20,570,714 (GRCm39)	N339S	possibly damaging	Het
Ppp4r1	T	G	17: 66,120,459 (GRCm39)	C181G	probably damaging	Het
Pramel27	T	A	4: 143,579,451 (GRCm39)	H345Q	probably benign	Het
Prkdc	G	A	16: 15,628,688 (GRCm39)	E3478K	probably damaging	Het
Prpf4b	T	C	13: 35,072,147 (GRCm39)		probably benign	Het
Psme3	T	A	11: 101,208,435 (GRCm39)		probably null	Het
Ptpre	C	A	7: 135,269,372 (GRCm39)	Y284*	probably null	Het
Scnn1a	A	G	6: 125,299,123 (GRCm39)	I94V	probably damaging	Het
Secisbp2l	C	T	2: 125,582,657 (GRCm39)	G933D	possibly damaging	Het
Shc2	T	C	10: 79,459,690 (GRCm39)	D418G	probably benign	Het
Sidt1	A	T	16: 44,075,389 (GRCm39)	D661E	probably damaging	Het
Slc35e2	T	C	4: 155,702,106 (GRCm39)	F290S	probably benign	Het
Sorcs1	A	G	19: 50,301,402 (GRCm39)		probably null	Het
Stox2	A	G	8: 47,645,970 (GRCm39)	S497P	probably damaging	Het
Tmem270	C	A	5: 134,930,482 (GRCm39)	E260*	probably null	Het
Tmtc2	T	C	10: 105,249,391 (GRCm39)	Y114C	probably benign	Het
Trim46	A	G	3: 89,150,958 (GRCm39)	F188S	probably benign	Het
Trim7	T	A	11: 48,728,355 (GRCm39)	M1K	probably null	Het
Txnip	A	G	3: 96,465,604 (GRCm39)	E18G	probably benign	Het
Usp34	A	G	11: 23,414,633 (GRCm39)	N2859D	probably damaging	Het
Vmn2r94	T	A	17: 18,477,647 (GRCm39)	I255F	probably benign	Het
Xkr5	T	A	8: 18,983,733 (GRCm39)	N603I	possibly damaging	Het
Zfp512	C	T	5: 31,637,570 (GRCm39)	A497V	probably benign	Het
Zfp518b	T	C	5: 38,830,970 (GRCm39)	N345S	probably damaging	Het

Other mutations in Or6c207

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01302:Or6c207	APN	10	129,104,392 (GRCm39)	missense	probably benign	0.18
IGL01782:Or6c207	APN	10	129,104,908 (GRCm39)	missense	probably benign	0.00
R0554:Or6c207	UTSW	10	129,104,368 (GRCm39)	missense	probably benign	0.00
R0594:Or6c207	UTSW	10	129,105,021 (GRCm39)	missense	possibly damaging	0.95
R1792:Or6c207	UTSW	10	129,105,112 (GRCm39)	missense	probably benign	0.20
R2357:Or6c207	UTSW	10	129,104,642 (GRCm39)	missense	probably benign	0.31
R2426:Or6c207	UTSW	10	129,105,135 (GRCm39)	missense	probably benign	0.00
R3757:Or6c207	UTSW	10	129,104,934 (GRCm39)	missense	probably damaging	0.99
R3758:Or6c207	UTSW	10	129,104,934 (GRCm39)	missense	probably damaging	0.99
R3962:Or6c207	UTSW	10	129,104,535 (GRCm39)	missense	probably damaging	1.00
R4600:Or6c207	UTSW	10	129,104,274 (GRCm39)	missense	probably benign	0.01
R4611:Or6c207	UTSW	10	129,104,274 (GRCm39)	missense	probably benign	0.01
R5113:Or6c207	UTSW	10	129,104,535 (GRCm39)	missense	probably damaging	0.98
R6415:Or6c207	UTSW	10	129,104,890 (GRCm39)	missense	probably benign	0.01
R7540:Or6c207	UTSW	10	129,105,003 (GRCm39)	missense	probably benign	0.31
R7909:Or6c207	UTSW	10	129,105,136 (GRCm39)	missense	probably benign	0.00
R8170:Or6c207	UTSW	10	129,104,917 (GRCm39)	missense	possibly damaging	0.80
R9079:Or6c207	UTSW	10	129,104,466 (GRCm39)	missense	possibly damaging	0.90

Predicted Primers

PCR Primer
(F):5'- TGGTACTGCTCCATCATTGTTG -3'
(R):5'- ACCTATGGAAGCTGCATCTTCATC -3'

Sequencing Primer
(F):5'- ACTGCTCCATCATTGTTGTTTTAAC -3'
(R):5'- ATGGAAGCTGCATCTTCATCTACATC -3'

Posted On

2015-09-25