Mutagenetix > Incidental Mutation

Incidental Mutation 'R6144:Or2n1'

488772

Institutional Source

Beutler Lab

Gene Symbol

Or2n1

Ensembl Gene

ENSMUSG00000096009

Gene Name

olfactory receptor family 2 subfamily N member 1

Synonyms

GA_x6K02T2PSCP-2623613-2624551, MOR256-5, Olfr134

MMRRC Submission

044291-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.084) question?

Stock #

R6144 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

38485977-38486915 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 38486116 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Histidine at position 47 (L47H)

Ref Sequence

ENSEMBL: ENSMUSP00000151069 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000074883] [ENSMUST00000215900]

AlphaFold

Q8VG95

Predicted Effect

probably damaging
Transcript: ENSMUST00000074883
AA Change: L47H

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

SMART Domains

Protein: ENSMUSP00000074423
Gene: ENSMUSG00000096009
AA Change: L47H

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	3.4e-50	PFAM
Pfam:7tm_1	41	290	2e-25	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000215900
AA Change: L47H

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

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.4%
20x: 95.6%

Validation Efficiency

96% (65/68)

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: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3300002I08Rik	A	T	2: 150,186,564 (GRCm39)	D40E	possibly damaging	Het
4921517D22Rik	C	T	13: 59,837,347 (GRCm39)	R246H	probably damaging	Het
Agbl1	A	G	7: 76,069,832 (GRCm39)	T203A	probably benign	Het
Alms1	T	A	6: 85,600,056 (GRCm39)	D2096E	probably damaging	Het
Ankrd53	T	C	6: 83,739,639 (GRCm39)		probably benign	Het
Arap3	C	A	18: 38,118,486 (GRCm39)	G814C	probably damaging	Het
Armc9	T	G	1: 86,172,301 (GRCm39)	I5S	probably benign	Het
Catsperg1	T	C	7: 28,910,120 (GRCm39)	T74A	probably damaging	Het
Cdca7l	T	A	12: 117,837,446 (GRCm39)		probably null	Het
Cfhr2	T	A	1: 139,733,153 (GRCm39)		probably benign	Het
Chpt1	A	G	10: 88,288,955 (GRCm39)		probably benign	Het
Cntrl	A	C	2: 35,055,745 (GRCm39)	D1213A	possibly damaging	Het
Col7a1	C	T	9: 108,803,148 (GRCm39)	R2149C	unknown	Het
Cpa4	T	C	6: 30,585,082 (GRCm39)	S289P	probably damaging	Het
Cpsf3	G	A	12: 21,356,887 (GRCm39)		probably null	Het
Creb3l1	T	C	2: 91,822,350 (GRCm39)	H212R	possibly damaging	Het
Cybb	C	G	X: 9,316,989 (GRCm39)	D246H	probably benign	Het
Cyp2c29	A	G	19: 39,310,053 (GRCm39)	D254G	possibly damaging	Het
Dennd1b	A	G	1: 139,008,993 (GRCm39)	H232R	probably damaging	Het
Dhx29	T	C	13: 113,101,105 (GRCm39)	L1216P	probably damaging	Het
Dsg1b	T	C	18: 20,529,476 (GRCm39)	I307T	possibly damaging	Het
Ep300	A	G	15: 81,485,435 (GRCm39)	S141G	unknown	Het
Evl	A	C	12: 108,619,290 (GRCm39)	K101T	probably damaging	Het
Exph5	G	A	9: 53,284,328 (GRCm39)	G470R	probably benign	Het
Flg	A	T	3: 93,190,515 (GRCm39)		probably benign	Het
Gm45704	T	A	8: 73,510,920 (GRCm39)			Het
Grm1	T	C	10: 10,955,640 (GRCm39)	M215V	probably benign	Het
Hadha	T	C	5: 30,345,994 (GRCm39)	D210G	probably benign	Het
Hmcn1	T	C	1: 150,598,175 (GRCm39)	Y1709C	probably damaging	Het
Hrc	A	T	7: 44,986,157 (GRCm39)	H436L	possibly damaging	Het
Hycc1	T	C	5: 24,171,367 (GRCm39)	S352G	possibly damaging	Het
Ido1	T	A	8: 25,075,306 (GRCm39)	T259S	possibly damaging	Het
Itgb7	C	A	15: 102,131,917 (GRCm39)	R222L	probably benign	Het
Khnyn	T	C	14: 56,125,296 (GRCm39)	V485A	probably damaging	Het
Kifc5b	T	C	17: 27,140,826 (GRCm39)	V100A	probably benign	Het
Lsm10	T	C	4: 125,991,794 (GRCm39)	M50T	probably damaging	Het
Map3k6	T	G	4: 132,972,986 (GRCm39)	W382G	probably damaging	Het
Mink1	T	A	11: 70,501,478 (GRCm39)	F922I	possibly damaging	Het
Mrap2	T	C	9: 87,057,871 (GRCm39)	V53A	probably damaging	Het
Mrps7	C	A	11: 115,495,000 (GRCm39)	A5E	probably benign	Het
Muc4	A	G	16: 32,587,298 (GRCm39)	N2713S	possibly damaging	Het
Nckipsd	T	C	9: 108,689,585 (GRCm39)	S249P	probably damaging	Het
Neil3	T	C	8: 54,052,447 (GRCm39)	T384A	probably benign	Het
Noc3l	A	T	19: 38,787,399 (GRCm39)	I504K	probably damaging	Het
Nudt13	A	G	14: 20,357,839 (GRCm39)	N107S	probably benign	Het
Or11h4b	C	A	14: 50,918,392 (GRCm39)	R233L	probably benign	Het
Or5c1	T	A	2: 37,222,125 (GRCm39)	M122K	probably damaging	Het
Otub1	G	T	19: 7,176,518 (GRCm39)	Y205*	probably null	Het
Pals1	T	C	12: 78,871,563 (GRCm39)	V381A	possibly damaging	Het
Pierce2	C	A	9: 72,887,270 (GRCm39)	C79F	probably damaging	Het
Plpp7	T	A	2: 31,986,100 (GRCm39)	S93T	probably damaging	Het
Pxk	T	G	14: 8,138,011 (GRCm38)	Y188D	probably damaging	Het
Rigi	T	C	4: 40,229,551 (GRCm39)	I78V	probably benign	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rpap1	A	T	2: 119,603,128 (GRCm39)	C602*	probably null	Het
Sbds	T	C	5: 130,275,185 (GRCm39)	K248E	probably benign	Het
Serpina10	A	T	12: 103,595,092 (GRCm39)	N42K	probably benign	Het
Slc7a8	A	G	14: 54,966,797 (GRCm39)	L368P	probably damaging	Het
Srrm1	T	C	4: 135,065,184 (GRCm39)		probably benign	Het
Sun2	C	T	15: 79,614,533 (GRCm39)	V288I	probably benign	Het
Tas2r107	C	A	6: 131,636,966 (GRCm39)	A28S	possibly damaging	Het
Tbc1d9b	T	C	11: 50,037,155 (GRCm39)	I268T	probably benign	Het
Tjp2	A	G	19: 24,097,437 (GRCm39)	F495L	probably damaging	Het
Top2b	T	C	14: 16,423,740 (GRCm38)	L1434P	possibly damaging	Het
Top3b	A	G	16: 16,697,005 (GRCm39)		probably null	Het
Trdv2-2	A	T	14: 54,198,761 (GRCm39)	E17V	possibly damaging	Het
Ttc6	T	A	12: 57,719,886 (GRCm39)	L819Q	possibly damaging	Het
Txlnb	A	G	10: 17,718,914 (GRCm39)	T582A	probably benign	Het
Zfp788	T	C	7: 41,299,193 (GRCm39)	S558P	probably damaging	Het

Other mutations in Or2n1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01677:Or2n1	APN	17	38,486,766 (GRCm39)	missense	probably damaging	1.00
IGL01749:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01750:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01751:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01753:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01757:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01765:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01766:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01767:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL01822:Or2n1	APN	17	38,486,339 (GRCm39)	missense	probably damaging	1.00
IGL02256:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02257:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02258:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02259:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02275:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02293:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02295:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02317:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
IGL02318:Or2n1	APN	17	38,486,577 (GRCm39)	missense	probably benign	0.04
R0230:Or2n1	UTSW	17	38,486,841 (GRCm39)	missense	probably damaging	1.00
R0363:Or2n1	UTSW	17	38,486,338 (GRCm39)	missense	probably damaging	1.00
R1074:Or2n1	UTSW	17	38,486,331 (GRCm39)	missense	probably damaging	1.00
R1506:Or2n1	UTSW	17	38,486,091 (GRCm39)	missense	probably benign
R2300:Or2n1	UTSW	17	38,486,441 (GRCm39)	nonsense	probably null
R3743:Or2n1	UTSW	17	38,486,793 (GRCm39)	missense	probably damaging	1.00
R3975:Or2n1	UTSW	17	38,486,386 (GRCm39)	missense	probably benign	0.03
R4230:Or2n1	UTSW	17	38,486,772 (GRCm39)	missense	possibly damaging	0.67
R5158:Or2n1	UTSW	17	38,486,345 (GRCm39)	nonsense	probably null
R5439:Or2n1	UTSW	17	38,486,917 (GRCm39)	splice site	probably null
R6309:Or2n1	UTSW	17	38,486,410 (GRCm39)	missense	probably benign	0.00
R6675:Or2n1	UTSW	17	38,486,905 (GRCm39)	missense	probably benign
R6800:Or2n1	UTSW	17	38,486,013 (GRCm39)	missense	probably benign	0.01
R6873:Or2n1	UTSW	17	38,486,259 (GRCm39)	missense	probably benign
R7193:Or2n1	UTSW	17	38,485,987 (GRCm39)	missense	probably benign	0.44
R7534:Or2n1	UTSW	17	38,486,188 (GRCm39)	missense	probably benign	0.22
R7869:Or2n1	UTSW	17	38,486,830 (GRCm39)	missense	possibly damaging	0.94
R7912:Or2n1	UTSW	17	38,486,158 (GRCm39)	missense	probably damaging	0.99
R8048:Or2n1	UTSW	17	38,486,419 (GRCm39)	missense	probably benign	0.11
R8305:Or2n1	UTSW	17	38,486,464 (GRCm39)	missense	probably damaging	1.00
R9396:Or2n1	UTSW	17	38,486,421 (GRCm39)	missense	probably damaging	1.00
R9445:Or2n1	UTSW	17	38,486,694 (GRCm39)	missense	probably damaging	1.00
X0011:Or2n1	UTSW	17	38,486,742 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCAATGCATCATGAGACTTTGC -3'
(R):5'- AGGAGGACACACTCTGTACC -3'

Sequencing Primer
(F):5'- TGCATCATGAGACTTTGCTATTC -3'
(R):5'- GCATCTGAGGTACAATGC -3'

Posted On

2017-10-10