Mutagenetix > Incidental Mutation

Incidental Mutation 'R8692:Or2w3b'

668453

Institutional Source

Beutler Lab

Gene Symbol

Or2w3b

Ensembl Gene

ENSMUSG00000060030

Gene Name

olfactory receptor family 2 subfamily W member 3B

Synonyms

Olfr317, GA_x6K02T2NKPP-680866-681849, MOR256-47

MMRRC Submission

068546-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

R8692 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

58622922-58624049 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 58623595 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 132 (Y132C)

Ref Sequence

ENSEMBL: ENSMUSP00000150575 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000075607] [ENSMUST00000215513] [ENSMUST00000216196]

AlphaFold

Q5NCD6

Predicted Effect

probably damaging
Transcript: ENSMUST00000075607
AA Change: Y132C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000075034
Gene: ENSMUSG00000060030
AA Change: Y132C

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	1.4e-50	PFAM
Pfam:7tm_1	41	290	5.8e-24	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000215513
AA Change: Y132C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Predicted Effect

probably damaging
Transcript: ENSMUST00000216196
AA Change: Y132C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.1%

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: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca12	A	C	1: 71,327,874 (GRCm39)	I1402S	probably damaging	Het
Abca9	T	C	11: 110,032,409 (GRCm39)	D736G	probably benign	Het
Acy1	T	C	9: 106,310,377 (GRCm39)	E377G	probably damaging	Het
Apob	G	A	12: 8,058,270 (GRCm39)	V2251M	probably damaging	Het
Arhgap23	C	A	11: 97,345,322 (GRCm39)	T657K	probably damaging	Het
Cabin1	T	C	10: 75,587,410 (GRCm39)	K129R	probably benign	Het
Cdh24	A	T	14: 54,875,793 (GRCm39)	F259I	probably benign	Het
Cops6	A	G	5: 138,162,083 (GRCm39)	N307S	probably benign	Het
Cyp4a31	G	A	4: 115,423,769 (GRCm39)	V143M	probably damaging	Het
Deaf1	A	T	7: 140,877,444 (GRCm39)	I561K	probably benign	Het
Dnah7a	A	C	1: 53,472,175 (GRCm39)	S3531A	probably benign	Het
Dnajc14	T	A	10: 128,642,900 (GRCm39)	I274N	probably damaging	Het
Dnmt1	A	G	9: 20,853,077 (GRCm39)	L48S	probably damaging	Het
Efna4	A	T	3: 89,242,549 (GRCm39)	I115N	probably damaging	Het
Ermp1	T	A	19: 29,594,093 (GRCm39)	L692F	probably benign	Het
Fcho2	GT	G	13: 98,882,382 (GRCm39)		probably null	Het
Fcsk	A	T	8: 111,615,722 (GRCm39)	C536S	probably benign	Het
Fermt2	A	T	14: 45,742,099 (GRCm39)	C82*	probably null	Het
Gabra6	G	T	11: 42,210,537 (GRCm39)	D61E	probably damaging	Het
Gdpd4	T	A	7: 97,690,140 (GRCm39)	S611T	probably benign	Het
Gm10800	AAGAAAACTGAAAATCAT	A	2: 98,497,379 (GRCm39)		probably benign	Het
Gm17430	G	A	18: 9,726,336 (GRCm39)	A112V	probably benign	Het
Gm2381	A	T	7: 42,472,071 (GRCm39)	L2Q	probably damaging	Het
Hif3a	A	T	7: 16,788,701 (GRCm39)	L90Q	probably benign	Het
Irf3	C	T	7: 44,649,889 (GRCm39)	Q168*	probably null	Het
Krt82	T	G	15: 101,456,828 (GRCm39)	D184A	possibly damaging	Het
Lgals4	C	T	7: 28,540,921 (GRCm39)	R282C	probably damaging	Het
Lrrc49	A	G	9: 60,594,445 (GRCm39)	S28P	probably damaging	Het
Mfsd11	T	A	11: 116,752,443 (GRCm39)	N197K	probably benign	Het
Mindy1	A	G	3: 95,199,587 (GRCm39)	D243G	probably damaging	Het
Mphosph9	A	T	5: 124,450,875 (GRCm39)	W299R	probably damaging	Het
Mst1r	G	T	9: 107,792,050 (GRCm39)	R862L	possibly damaging	Het
Nasp	T	A	4: 116,469,280 (GRCm39)		probably null	Het
Ncapg2	T	C	12: 116,414,049 (GRCm39)	I1073T	probably damaging	Het
Nek2	A	T	1: 191,554,745 (GRCm39)	K152N	probably benign	Het
Neurod2	T	C	11: 98,218,960 (GRCm39)	E68G	probably benign	Het
Or1j4	A	T	2: 36,740,096 (GRCm39)	I13F	probably benign	Het
P4ha3	T	A	7: 99,955,228 (GRCm39)	I361N	probably damaging	Het
Pcdh15	T	A	10: 74,289,805 (GRCm39)	S875T	possibly damaging	Het
Pde7b	G	T	10: 20,423,639 (GRCm39)	P79Q	probably benign	Het
Phb2	G	A	6: 124,692,097 (GRCm39)	A228T	probably damaging	Het
Piezo2	A	T	18: 63,225,971 (GRCm39)	C888*	probably null	Het
Pkhd1	A	T	1: 20,462,374 (GRCm39)	L2060Q	probably damaging	Het
Pms1	T	C	1: 53,246,052 (GRCm39)	M496V	probably benign	Het
Ppfibp1	C	T	6: 146,892,013 (GRCm39)	T91I	probably benign	Het
Ppp1r9b	T	C	11: 94,891,077 (GRCm39)	L557P	probably damaging	Het
Ppp2r5c	G	T	12: 110,489,032 (GRCm39)	V68L	probably benign	Het
Qrfp	T	A	2: 31,698,797 (GRCm39)	H45L	probably benign	Het
Rasgrp1	G	A	2: 117,115,353 (GRCm39)	T745I	probably damaging	Het
Rnf144a	G	A	12: 26,370,972 (GRCm39)	T163I	probably benign	Het
Sbsn	A	T	7: 30,451,522 (GRCm39)	H179L	unknown	Het
Simc1	G	A	13: 54,673,193 (GRCm39)	V514I	probably benign	Het
Slc35d1	A	G	4: 103,047,051 (GRCm39)	M249T		Het
Slfn4	T	A	11: 83,079,709 (GRCm39)	H466Q	possibly damaging	Het
Stab2	A	T	10: 86,808,794 (GRCm39)	C172S	probably damaging	Het
Tanc1	T	C	2: 59,673,989 (GRCm39)	I1698T	probably benign	Het
Tenm4	C	T	7: 96,555,148 (GRCm39)	P2618S	probably benign	Het
Tiam2	A	C	17: 3,479,082 (GRCm39)	D605A	probably damaging	Het
Tmed4	A	T	11: 6,223,822 (GRCm39)	D151E	probably benign	Het
Trim62	A	T	4: 128,794,465 (GRCm39)	I211F	possibly damaging	Het
Ttpa	A	G	4: 20,008,585 (GRCm39)	D49G	probably benign	Het
Usf3	T	C	16: 44,040,103 (GRCm39)	S1528P	probably benign	Het
Usp34	C	T	11: 23,379,325 (GRCm39)	T1991I		Het
Vash1	G	A	12: 86,735,863 (GRCm39)	V250M	possibly damaging	Het
Vmn1r199	T	C	13: 22,567,809 (GRCm39)	*368Q	probably null	Het
Vmn1r74	A	G	7: 11,580,972 (GRCm39)	T91A	probably benign	Het
Vmn1r8	T	C	6: 57,013,557 (GRCm39)	F203L	probably benign	Het
Vmn2r13	G	T	5: 109,319,514 (GRCm39)	Q489K	probably benign	Het
Vmn2r-ps158	G	T	7: 42,697,108 (GRCm39)	A722S	probably benign	Het
Zfp385b	A	T	2: 77,549,971 (GRCm39)	V38E	probably damaging	Het
Zfp820	A	G	17: 22,037,876 (GRCm39)	I484T	probably benign	Het

Other mutations in Or2w3b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02692:Or2w3b	APN	11	58,623,343 (GRCm39)	missense	probably benign	0.07
IGL03330:Or2w3b	APN	11	58,623,745 (GRCm39)	missense	probably damaging	1.00
R0554:Or2w3b	UTSW	11	58,623,865 (GRCm39)	missense	probably damaging	1.00
R1109:Or2w3b	UTSW	11	58,623,742 (GRCm39)	missense	probably benign	0.03
R2012:Or2w3b	UTSW	11	58,623,214 (GRCm39)	missense	possibly damaging	0.60
R2243:Or2w3b	UTSW	11	58,623,271 (GRCm39)	missense	probably damaging	1.00
R2253:Or2w3b	UTSW	11	58,623,821 (GRCm39)	missense	probably benign	0.23
R5400:Or2w3b	UTSW	11	58,623,146 (GRCm39)	missense	possibly damaging	0.74
R6551:Or2w3b	UTSW	11	58,623,583 (GRCm39)	missense	probably damaging	0.99
R6944:Or2w3b	UTSW	11	58,623,068 (GRCm39)	missense	possibly damaging	0.93
R7144:Or2w3b	UTSW	11	58,623,571 (GRCm39)	missense	probably damaging	1.00
R7636:Or2w3b	UTSW	11	58,623,273 (GRCm39)	missense	possibly damaging	0.83
R7985:Or2w3b	UTSW	11	58,623,532 (GRCm39)	missense	possibly damaging	0.49
R8201:Or2w3b	UTSW	11	58,623,940 (GRCm39)	missense	probably damaging	1.00
R8374:Or2w3b	UTSW	11	58,623,724 (GRCm39)	missense	probably damaging	0.97
R9006:Or2w3b	UTSW	11	58,623,188 (GRCm39)	nonsense	probably null
Z1186:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1186:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1186:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1187:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1187:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1187:Or2w3b	UTSW	11	58,623,295 (GRCm39)	missense	probably benign	0.04
Z1187:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1188:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1188:Or2w3b	UTSW	11	58,623,295 (GRCm39)	missense	probably benign	0.04
Z1188:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1188:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1189:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1189:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1190:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1190:Or2w3b	UTSW	11	58,623,295 (GRCm39)	missense	probably benign	0.04
Z1190:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1190:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1191:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1191:Or2w3b	UTSW	11	58,623,295 (GRCm39)	missense	probably benign	0.04
Z1191:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1191:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign
Z1192:Or2w3b	UTSW	11	58,623,475 (GRCm39)	missense	probably benign
Z1192:Or2w3b	UTSW	11	58,623,295 (GRCm39)	missense	probably benign	0.04
Z1192:Or2w3b	UTSW	11	58,623,200 (GRCm39)	missense	probably benign	0.02
Z1192:Or2w3b	UTSW	11	58,624,048 (GRCm39)	intron	probably benign

Predicted Primers

PCR Primer
(F):5'- TGCCTATTGCCAGGATGAAGG -3'
(R):5'- AGCTTCACCAGTAGCTCCATCC -3'

Sequencing Primer
(F):5'- TCAACGACAGCTGTGTTGAC -3'
(R):5'- GTAGCTCCATCCCACAGCTG -3'

Posted On

2021-04-30