Mutagenetix > Incidental Mutation

Incidental Mutation 'R6988:Olfr791'

543092

Institutional Source

Beutler Lab

Gene Symbol

Olfr791

Ensembl Gene

ENSMUSG00000047626

Gene Name

olfactory receptor 791

Synonyms

GA_x6K02T2PULF-11205096-11206034, MOR114-1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.141) question?

Stock #

R6988 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

129521792-129528353 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 129526673 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 149 (S149T)

Ref Sequence

ENSEMBL: ENSMUSP00000150497 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057477] [ENSMUST00000217228]

AlphaFold

Q8VGJ0

Predicted Effect

probably benign
Transcript: ENSMUST00000057477
AA Change: S149T

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000052722
Gene: ENSMUSG00000047626
AA Change: S149T

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	307	7.6e-45	PFAM
Pfam:7TM_GPCR_Srsx	33	303	4.3e-6	PFAM
Pfam:7tm_1	39	288	4.7e-24	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000217228
AA Change: S149T

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.2%
20x: 97.2%

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: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013G24Rik	T	G	4: 137,454,579 (GRCm38)	L15W	probably damaging	Het
4930550C14Rik	G	A	9: 53,411,756 (GRCm38)	V31I	possibly damaging	Het
4932415D10Rik	T	C	10: 82,291,899 (GRCm38)	D1759G	possibly damaging	Het
Adgre1	C	T	17: 57,408,445 (GRCm38)	S255F	probably benign	Het
Aff4	T	G	11: 53,398,237 (GRCm38)	S404R	probably damaging	Het
Akr1c19	A	T	13: 4,233,758 (GRCm38)		probably benign	Het
Ankrd31	T	A	13: 96,878,249 (GRCm38)	I1342K	probably damaging	Het
Arhgap5	T	A	12: 52,518,125 (GRCm38)	D626E	possibly damaging	Het
Arhgef1	G	A	7: 24,916,923 (GRCm38)	V332I	probably benign	Het
AY358078	A	G	14: 51,826,187 (GRCm38)	E430G	probably damaging	Het
B4gat1	T	A	19: 5,040,434 (GRCm38)	I395N	probably benign	Het
Bub1b	T	A	2: 118,636,830 (GRCm38)	I878N	probably damaging	Het
Ccdc150	C	T	1: 54,355,709 (GRCm38)	Q745*	probably null	Het
Ccl19	A	T	4: 42,754,885 (GRCm38)	I87N	probably damaging	Het
Ces2g	G	C	8: 104,963,908 (GRCm38)	G107A	probably benign	Het
Chpt1	A	G	10: 88,488,406 (GRCm38)	V180A	probably damaging	Het
Col2a1	T	C	15: 98,004,454 (GRCm38)	T14A	unknown	Het
Dnah7a	T	C	1: 53,582,625 (GRCm38)	I1114V	possibly damaging	Het
Dnah7c	T	C	1: 46,666,213 (GRCm38)	I2462T	possibly damaging	Het
Dnah8	T	C	17: 30,643,275 (GRCm38)	F208S	probably damaging	Het
Dnhd1	A	G	7: 105,714,210 (GRCm38)	E3993G	probably damaging	Het
Erv3	C	T	2: 131,855,966 (GRCm38)	D158N	possibly damaging	Het
Exoc6	T	A	19: 37,609,091 (GRCm38)	F647I	probably damaging	Het
Fbrs	G	A	7: 127,479,508 (GRCm38)		probably benign	Het
Fgfr1op2	T	C	6: 146,589,965 (GRCm38)	F109L	probably damaging	Het
Fv1	T	C	4: 147,869,271 (GRCm38)	F98S	possibly damaging	Het
Gm436	A	G	4: 144,686,325 (GRCm38)	F15S	probably benign	Het
H2-M10.1	T	C	17: 36,325,592 (GRCm38)	K107E	probably benign	Het
Hspg2	A	T	4: 137,528,890 (GRCm38)	Q1436L	probably damaging	Het
Ighv1-74	T	C	12: 115,802,763 (GRCm38)	Y79C	probably damaging	Het
Kcnj1	G	A	9: 32,396,585 (GRCm38)	V102I	probably benign	Het
Mnt	C	A	11: 74,842,809 (GRCm38)		probably benign	Het
Mrpl15	T	C	1: 4,782,660 (GRCm38)	T112A	probably benign	Het
Ncdn	T	C	4: 126,747,189 (GRCm38)	D506G	probably benign	Het
Ogdh	C	T	11: 6,313,806 (GRCm38)	R81*	probably null	Het
Olfr815	G	C	10: 129,902,409 (GRCm38)	F100L	probably damaging	Het
Pole	G	T	5: 110,329,583 (GRCm38)	V1863F	probably damaging	Het
Pramel5	T	C	4: 144,274,007 (GRCm38)		probably benign	Het
Rabep1	A	G	11: 70,934,537 (GRCm38)	K636E	probably damaging	Het
Rasgrf2	T	A	13: 91,885,635 (GRCm38)	Y1151F	probably benign	Het
Rrad	A	G	8: 104,630,636 (GRCm38)	V93A	probably damaging	Het
Sesn3	A	T	9: 14,310,257 (GRCm38)	R118*	probably null	Het
Slc27a3	T	C	3: 90,386,290 (GRCm38)	N596S	probably benign	Het
Snx19	C	A	9: 30,428,935 (GRCm38)	D456E	probably damaging	Het
Supt20	T	C	3: 54,698,597 (GRCm38)	S35P	probably damaging	Het
Syde2	G	T	3: 146,019,809 (GRCm38)	R885L	probably benign	Het
Synm	G	A	7: 67,733,658 (GRCm38)	L1419F	probably damaging	Het
Tcrg-V6	G	T	13: 19,190,644 (GRCm38)	G40W	possibly damaging	Het
Tekt2	A	G	4: 126,323,443 (GRCm38)	F221L	probably benign	Het
Ticam1	C	T	17: 56,269,900 (GRCm38)	E732K	probably benign	Het
Tmem39b	A	G	4: 129,693,148 (GRCm38)	I90T	possibly damaging	Het
Trib2	A	G	12: 15,815,338 (GRCm38)	S79P	probably damaging	Het
Usp32	T	C	11: 85,010,143 (GRCm38)	M1084V	probably benign	Het
Vmn1r181	T	C	7: 23,984,847 (GRCm38)	F246L	probably damaging	Het
Wnt16	A	G	6: 22,288,511 (GRCm38)	D2G	probably damaging	Het
Zfp462	A	G	4: 55,080,716 (GRCm38)	E1357G	probably benign	Het
Zhx3	A	G	2: 160,779,868 (GRCm38)	M793T	probably benign	Het

Other mutations in Olfr791

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01153:Olfr791	APN	10	129,526,995 (GRCm38)	missense	probably damaging	0.97
IGL03034:Olfr791	APN	10	129,526,658 (GRCm38)	missense	probably benign
IGL03281:Olfr791	APN	10	129,526,403 (GRCm38)	missense	probably benign	0.31
R0555:Olfr791	UTSW	10	129,526,896 (GRCm38)	missense	possibly damaging	0.90
R1474:Olfr791	UTSW	10	129,526,955 (GRCm38)	missense	probably benign	0.03
R1638:Olfr791	UTSW	10	129,526,619 (GRCm38)	missense	probably benign	0.00
R1917:Olfr791	UTSW	10	129,527,049 (GRCm38)	missense	probably damaging	0.99
R1918:Olfr791	UTSW	10	129,527,049 (GRCm38)	missense	probably damaging	0.99
R1919:Olfr791	UTSW	10	129,527,049 (GRCm38)	missense	probably damaging	0.99
R2303:Olfr791	UTSW	10	129,527,049 (GRCm38)	missense	probably benign	0.10
R3113:Olfr791	UTSW	10	129,527,143 (GRCm38)	missense	probably benign	0.08
R3929:Olfr791	UTSW	10	129,526,231 (GRCm38)	start codon destroyed	probably null	1.00
R4704:Olfr791	UTSW	10	129,526,302 (GRCm38)	missense	possibly damaging	0.90
R4831:Olfr791	UTSW	10	129,526,580 (GRCm38)	missense	probably damaging	1.00
R5207:Olfr791	UTSW	10	129,526,904 (GRCm38)	missense	probably benign	0.08
R5313:Olfr791	UTSW	10	129,527,081 (GRCm38)	missense	probably damaging	1.00
R5644:Olfr791	UTSW	10	129,527,103 (GRCm38)	missense	probably damaging	1.00
R5661:Olfr791	UTSW	10	129,526,749 (GRCm38)	missense	probably benign	0.45
R5894:Olfr791	UTSW	10	129,526,488 (GRCm38)	missense	probably damaging	0.98
R6996:Olfr791	UTSW	10	129,526,863 (GRCm38)	missense	probably damaging	1.00
R7380:Olfr791	UTSW	10	129,526,661 (GRCm38)	missense	probably benign
R7539:Olfr791	UTSW	10	129,527,105 (GRCm38)	nonsense	probably null
R7552:Olfr791	UTSW	10	129,526,560 (GRCm38)	missense	possibly damaging	0.95
R7635:Olfr791	UTSW	10	129,526,682 (GRCm38)	missense	probably benign	0.00
R8084:Olfr791	UTSW	10	129,526,940 (GRCm38)	missense	probably damaging	1.00
R8260:Olfr791	UTSW	10	129,527,088 (GRCm38)	missense	possibly damaging	0.55
R8755:Olfr791	UTSW	10	129,526,463 (GRCm38)	missense	possibly damaging	0.60
X0066:Olfr791	UTSW	10	129,526,745 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AGAAGTTTCCTTTACCACTGTCTG -3'
(R):5'- ATGAGTGCAAAGACAGCCAC -3'

Sequencing Primer
(F):5'- ATACCATCACCTATAATGCTTGTGC -3'
(R):5'- GCCACAAGTATAACCATCTGTTC -3'

Posted On

2018-11-28