Mutagenetix > Incidental Mutation

Incidental Mutation 'R6943:Or5m9b'

540637

Institutional Source

Beutler Lab

Gene Symbol

Or5m9b

Ensembl Gene

ENSMUSG00000099820

Gene Name

olfactory receptor family 5 subfamily M member 9B

Synonyms

Olfr1036, GA_x6K02T2Q125-47549689-47550621, MOR262-13, MOR245-25

MMRRC Submission

045057-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.284) question?

Stock #

R6943 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

85905048-85906062 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 85905264 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 60 (F60S)

Ref Sequence

ENSEMBL: ENSMUSP00000130843 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164985]

AlphaFold

Q7TR85

Predicted Effect

probably damaging
Transcript: ENSMUST00000164985
AA Change: F60S

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

SMART Domains

Protein: ENSMUSP00000130843
Gene: ENSMUSG00000099820
AA Change: F60S

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	306	2.2e-51	PFAM
Pfam:7tm_1	39	288	1.1e-21	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.8%
10x: 98.9%
20x: 96.2%

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: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aacs	T	A	5: 125,583,362 (GRCm39)		probably null	Het
Arhgef1	A	G	7: 24,623,156 (GRCm39)	I423V	probably benign	Het
Aspm	T	C	1: 139,408,280 (GRCm39)	L2389P	probably damaging	Het
B4galt1	T	C	4: 40,812,860 (GRCm39)	M222V	probably benign	Het
Bsn	C	A	9: 107,985,016 (GRCm39)	G3013C	unknown	Het
Camsap2	T	C	1: 136,232,187 (GRCm39)	H136R	probably damaging	Het
Ccar1	A	G	10: 62,582,715 (GRCm39)	V1047A	unknown	Het
Ccdc80	A	G	16: 44,915,445 (GRCm39)	E67G	probably benign	Het
Ces3b	G	T	8: 105,819,710 (GRCm39)	G511V	probably damaging	Het
Cops6	T	A	5: 138,161,790 (GRCm39)	H224Q	probably benign	Het
Dnah5	A	T	15: 28,235,866 (GRCm39)	D331V	probably damaging	Het
Dusp29	T	C	14: 21,727,135 (GRCm39)	D171G	probably damaging	Het
Echs1	G	A	7: 139,688,007 (GRCm39)	T266I	probably damaging	Het
Ehmt2	G	A	17: 35,130,406 (GRCm39)	C1017Y	probably damaging	Het
Epb41l5	C	T	1: 119,536,859 (GRCm39)	R344Q	probably damaging	Het
Fcgbp	G	A	7: 27,791,477 (GRCm39)	V913I	probably benign	Het
Foxd4	A	G	19: 24,877,240 (GRCm39)	F320S	probably damaging	Het
Frmpd4	C	T	X: 166,387,579 (GRCm39)	R133K	probably damaging	Het
Glmp	A	G	3: 88,233,917 (GRCm39)	Y258C	probably damaging	Het
Gphn	C	G	12: 78,538,955 (GRCm39)	S200R	possibly damaging	Het
Gvin2	G	A	7: 105,551,187 (GRCm39)	Q622*	probably null	Het
H2-Q7	T	G	17: 35,658,560 (GRCm39)	M66R	probably benign	Het
Hivep2	T	A	10: 14,004,058 (GRCm39)	C219S	probably damaging	Het
Hlcs	A	T	16: 93,942,261 (GRCm39)	M90K	possibly damaging	Het
Itga8	C	A	2: 12,160,182 (GRCm39)		probably null	Het
Klrk1	T	A	6: 129,598,203 (GRCm39)	M1L	possibly damaging	Het
Kmo	T	A	1: 175,485,941 (GRCm39)	F385I	probably benign	Het
Lrit1	G	C	14: 36,782,052 (GRCm39)	V242L	probably damaging	Het
Lrrc3c	A	G	11: 98,490,075 (GRCm39)	D144G	probably damaging	Het
Lyzl4	C	T	9: 121,412,047 (GRCm39)	W123*	probably null	Het
Map3k1	A	G	13: 111,909,246 (GRCm39)	S77P	probably benign	Het
Mark1	T	C	1: 184,630,984 (GRCm39)	T709A	probably damaging	Het
Nbr1	A	T	11: 101,468,777 (GRCm39)	I878F	probably damaging	Het
Nedd1	A	T	10: 92,547,168 (GRCm39)	H118Q	probably damaging	Het
Nfatc1	C	T	18: 80,678,770 (GRCm39)	G873S	probably damaging	Het
Ngly1	T	G	14: 16,283,467 (GRCm38)	N415K	probably damaging	Het
Nol6	C	A	4: 41,118,962 (GRCm39)	R677L	probably damaging	Het
Nop9	T	C	14: 55,990,270 (GRCm39)	V471A	probably benign	Het
Notch4	A	G	17: 34,802,577 (GRCm39)	N1333D	probably benign	Het
Nsun2	G	A	13: 69,778,152 (GRCm39)	G478R	probably damaging	Het
Or10x4	T	A	1: 174,219,407 (GRCm39)	Y257*	probably null	Het
Or1ad8	T	A	11: 50,898,153 (GRCm39)	M118K	probably damaging	Het
Or8g34	A	T	9: 39,373,159 (GRCm39)	Y144F	probably benign	Het
Pcp4l1	T	C	1: 171,002,022 (GRCm39)	E46G	possibly damaging	Het
Plek2	T	C	12: 78,936,083 (GRCm39)		probably null	Het
Rbl1	T	G	2: 157,030,206 (GRCm39)	I434L	probably benign	Het
Ryr2	A	G	13: 11,581,834 (GRCm39)	V4777A	possibly damaging	Het
Sgk1	T	C	10: 21,758,593 (GRCm39)	F19S	probably damaging	Het
Stard9	C	T	2: 120,532,677 (GRCm39)	A2978V	probably benign	Het
Syne1	T	C	10: 5,033,940 (GRCm39)	T7711A	probably benign	Het
Taf10	G	A	7: 105,393,383 (GRCm39)	T48I	probably benign	Het
Tgfbi	T	G	13: 56,784,989 (GRCm39)	S649A	possibly damaging	Het
Thbs3	T	C	3: 89,132,171 (GRCm39)	V749A	probably benign	Het
Tmem241	G	T	18: 12,180,641 (GRCm39)	H218N	possibly damaging	Het
Tmem266	C	T	9: 55,284,851 (GRCm39)		probably benign	Het
Tnc	T	C	4: 63,900,982 (GRCm39)	I1586M	probably damaging	Het
Ubr4	T	A	4: 139,164,442 (GRCm39)	C2676*	probably null	Het
Unc13a	A	T	8: 72,105,021 (GRCm39)	I747N	probably damaging	Het
Vangl1	A	T	3: 102,073,097 (GRCm39)		probably benign	Het
Vmn1r184	C	T	7: 25,966,563 (GRCm39)	T103I	possibly damaging	Het
Vmn1r204	T	C	13: 22,740,474 (GRCm39)	V35A	probably benign	Het
Vps13b	A	G	15: 35,448,835 (GRCm39)	H603R	possibly damaging	Het
Zfp105	A	G	9: 122,754,303 (GRCm39)	D44G	probably benign	Het
Zfp11	T	C	5: 129,735,152 (GRCm39)	H103R	probably damaging	Het
Zfp335	A	G	2: 164,736,795 (GRCm39)	F947L	possibly damaging	Het

Other mutations in Or5m9b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02260:Or5m9b	APN	2	85,905,816 (GRCm39)	missense	possibly damaging	0.90
IGL02370:Or5m9b	APN	2	85,905,132 (GRCm39)	missense	probably damaging	0.98
R0269:Or5m9b	UTSW	2	85,905,485 (GRCm39)	missense	probably benign	0.03
R0409:Or5m9b	UTSW	2	85,905,646 (GRCm39)	nonsense	probably null
R0412:Or5m9b	UTSW	2	85,905,435 (GRCm39)	missense	probably benign	0.16
R0617:Or5m9b	UTSW	2	85,905,485 (GRCm39)	missense	probably benign	0.03
R0846:Or5m9b	UTSW	2	85,905,510 (GRCm39)	missense	possibly damaging	0.66
R1251:Or5m9b	UTSW	2	85,905,164 (GRCm39)	missense	probably benign	0.20
R1646:Or5m9b	UTSW	2	85,905,960 (GRCm39)	missense	probably damaging	0.98
R1670:Or5m9b	UTSW	2	85,905,594 (GRCm39)	missense	probably benign
R1775:Or5m9b	UTSW	2	85,905,104 (GRCm39)	missense	possibly damaging	0.88
R1968:Or5m9b	UTSW	2	85,905,549 (GRCm39)	missense	probably damaging	1.00
R2877:Or5m9b	UTSW	2	85,905,675 (GRCm39)	missense	possibly damaging	0.82
R4639:Or5m9b	UTSW	2	85,905,923 (GRCm39)	missense	probably benign	0.24
R4957:Or5m9b	UTSW	2	85,905,854 (GRCm39)	missense	probably damaging	1.00
R5267:Or5m9b	UTSW	2	85,905,882 (GRCm39)	missense	probably benign	0.28
R5862:Or5m9b	UTSW	2	85,905,990 (GRCm39)	missense	probably benign	0.00
R6235:Or5m9b	UTSW	2	85,905,510 (GRCm39)	missense	possibly damaging	0.66
R6355:Or5m9b	UTSW	2	85,905,216 (GRCm39)	missense	probably benign	0.04
R8033:Or5m9b	UTSW	2	85,905,219 (GRCm39)	missense	possibly damaging	0.61
R8796:Or5m9b	UTSW	2	85,905,518 (GRCm39)	missense	possibly damaging	0.94
R8861:Or5m9b	UTSW	2	85,905,960 (GRCm39)	missense	probably damaging	0.98
Z1088:Or5m9b	UTSW	2	85,905,667 (GRCm39)	missense	possibly damaging	0.66
Z1177:Or5m9b	UTSW	2	85,905,768 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AGGCTACCCTGTAACACATTTG -3'
(R):5'- TAGCGATCGAAGGCCATCAC -3'

Sequencing Primer
(F):5'- ACAGACACTATATTAAGGCAATGC -3'
(R):5'- TCGAAGGCCATCACTGCCAG -3'

Posted On

2018-11-06