Mutagenetix > Incidental Mutation

Incidental Mutation 'R8033:Or5m9b'

618069

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

067470-MU

Accession Numbers

Essential gene?

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

Stock #

R8033 (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 A at 85905219 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 45 (I45N)

Ref Sequence

ENSEMBL: ENSMUSP00000130843 (fasta)

Gene Model

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

AlphaFold

Q7TR85

Predicted Effect

possibly damaging
Transcript: ENSMUST00000164985
AA Change: I45N

PolyPhen 2 Score 0.613 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000130843
Gene: ENSMUSG00000099820
AA Change: I45N

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: 100.0%
10x: 99.7%
20x: 99.1%

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: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8a	A	T	11: 109,927,348 (GRCm39)	I1335K	probably damaging	Het
Adgrb2	A	G	4: 129,912,805 (GRCm39)	E1277G	probably benign	Het
Agbl3	A	G	6: 34,816,429 (GRCm39)	T785A	possibly damaging	Het
Ahnak	T	C	19: 8,981,074 (GRCm39)	V786A	probably benign	Het
Armc2	A	G	10: 41,884,680 (GRCm39)	I87T	possibly damaging	Het
Asap2	T	C	12: 21,274,390 (GRCm39)	S373P	probably damaging	Het
Casd1	A	T	6: 4,619,773 (GRCm39)	I173F	probably benign	Het
Chd2	A	G	7: 73,085,628 (GRCm39)	Y1669H	probably damaging	Het
Clic3	A	G	2: 25,348,617 (GRCm39)	E199G	probably benign	Het
Cpa4	G	A	6: 30,590,799 (GRCm39)	V366I	probably benign	Het
Creg2	T	C	1: 39,689,795 (GRCm39)	Y105C	probably damaging	Het
Cyp20a1	T	C	1: 60,411,750 (GRCm39)	I266T	probably benign	Het
Dido1	T	C	2: 180,316,635 (GRCm39)	D685G	probably damaging	Het
Dop1b	C	G	16: 93,566,371 (GRCm39)	R1051G	probably benign	Het
Fam114a2	A	G	11: 57,398,333 (GRCm39)	S202P	probably damaging	Het
Fance	G	T	17: 28,532,659 (GRCm39)		probably benign	Het
Farsa	T	A	8: 85,594,198 (GRCm39)	L316Q	probably benign	Het
Fcrl6	T	C	1: 172,426,748 (GRCm39)	D66G	probably benign	Het
Gatad1	T	C	5: 3,693,540 (GRCm39)	R210G	probably benign	Het
Gh	A	T	11: 106,191,381 (GRCm39)	D154E	probably benign	Het
Kmt2a	A	T	9: 44,756,767 (GRCm39)	V1160E	probably damaging	Het
Lct	T	C	1: 128,212,996 (GRCm39)	T1886A	probably benign	Het
Lrwd1	G	A	5: 136,152,079 (GRCm39)	L633F	probably damaging	Het
Mmp15	A	T	8: 96,094,590 (GRCm39)	N155Y	probably benign	Het
Msantd5f6	T	C	4: 73,321,329 (GRCm39)	N143D	probably benign	Het
Mtf2	T	G	5: 108,234,951 (GRCm39)	C125G	probably damaging	Het
Muc16	A	T	9: 18,547,902 (GRCm39)	D6130E	probably benign	Het
Orc1	T	A	4: 108,462,761 (GRCm39)	Y613N	probably damaging	Het
Pak1	A	G	7: 97,535,590 (GRCm39)	N227S	probably benign	Het
Pex3	G	A	10: 13,407,024 (GRCm39)	Q306*	probably null	Het
Pld1	A	T	3: 28,083,359 (GRCm39)	M160L	probably benign	Het
Plekhh1	G	A	12: 79,117,710 (GRCm39)	R902H	probably benign	Het
Prp2	A	G	6: 132,577,391 (GRCm39)	H226R	unknown	Het
Rad21	T	G	15: 51,827,628 (GRCm39)	T578P	probably damaging	Het
Sp140	G	A	1: 85,547,815 (GRCm39)	V181I	probably benign	Het
Spen	A	G	4: 141,199,057 (GRCm39)	V3190A	probably benign	Het
Spg11	A	C	2: 121,917,432 (GRCm39)	C1011W	probably damaging	Het
Syngr3	G	A	17: 24,905,579 (GRCm39)	R132*	probably null	Het
Tbc1d10c	A	G	19: 4,238,013 (GRCm39)	F254L	possibly damaging	Het
Tcea1	T	A	1: 4,962,141 (GRCm39)	I176K	probably damaging	Het
Timm50	G	A	7: 28,006,258 (GRCm39)	A281V	possibly damaging	Het
Tmem144	C	T	3: 79,732,624 (GRCm39)	R218K	probably benign	Het
Upp2	A	G	2: 58,670,071 (GRCm39)	Y259C	probably damaging	Het
Vcan	A	G	13: 89,852,479 (GRCm39)	V827A	probably benign	Het
Vps41	T	A	13: 18,994,635 (GRCm39)	W161R	possibly damaging	Het
Zfp994	A	T	17: 22,419,665 (GRCm39)	I428N	probably 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
R6943:Or5m9b	UTSW	2	85,905,264 (GRCm39)	missense	probably damaging	1.00
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'- GCTACCCTGTAACACATTTGAAC -3'
(R):5'- AAGTAGCACTGTACCAAGCATC -3'

Sequencing Primer
(F):5'- ACCCTGTAACACATTTGAACATTTAG -3'
(R):5'- GCACTGTACCAAGCATCCAACATAAG -3'

Posted On

2020-01-23