Mutagenetix > Incidental Mutation

Incidental Mutation 'R0441:Or8k37'

39138

Institutional Source

Beutler Lab

Gene Symbol

Or8k37

Ensembl Gene

ENSMUSG00000110804

Gene Name

olfactory receptor family 8 subfamily K member 37

Synonyms

MOR192-3, MOR192-2, GA_x6K02T2Q125-48121788-48120847, Olfr1084

MMRRC Submission

038642-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.244) question?

Stock #

R0441 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

86469109-86470062 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 86469674 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Lysine at position 126 (I126K)

Ref Sequence

ENSEMBL: ENSMUSP00000150546 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000216851]

AlphaFold

A0A1L1STZ9

Predicted Effect

probably damaging
Transcript: ENSMUST00000099880
AA Change: I126K

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

SMART Domains

Protein: ENSMUSP00000097465
Gene: ENSMUSG00000075177
AA Change: I126K

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	5.9e-48	PFAM
Pfam:7tm_1	41	290	7.6e-19	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000216851
AA Change: I126K

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

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 96.9%
20x: 94.6%

Validation Efficiency

100% (71/71)

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: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921539E11Rik	T	C	4: 103,092,689 (GRCm39)		probably benign	Het
Adgrv1	G	A	13: 81,545,345 (GRCm39)	R5647*	probably null	Het
Agbl2	C	T	2: 90,627,827 (GRCm39)	R211*	probably null	Het
Akap9	A	G	5: 4,011,714 (GRCm39)	K806E	probably benign	Het
Ampd1	C	G	3: 102,995,794 (GRCm39)	L235V	probably benign	Het
Atcay	T	C	10: 81,060,294 (GRCm39)	D14G	possibly damaging	Het
Atp8b4	C	T	2: 126,220,626 (GRCm39)		probably benign	Het
Bmp8b	T	C	4: 123,018,308 (GRCm39)	V393A	probably damaging	Het
Brca2	T	A	5: 150,465,322 (GRCm39)	D1695E	probably damaging	Het
Cdh15	A	G	8: 123,587,705 (GRCm39)	I210V	probably damaging	Het
Cep250	T	C	2: 155,813,924 (GRCm39)	L564P	possibly damaging	Het
Cmpk1	T	C	4: 114,822,220 (GRCm39)	T110A	probably benign	Het
Cpsf3	T	G	12: 21,350,085 (GRCm39)	I268S	probably damaging	Het
Csmd2	C	T	4: 128,414,023 (GRCm39)	A2621V	probably benign	Het
Cyp2c40	T	C	19: 39,795,607 (GRCm39)		probably benign	Het
D430041D05Rik	T	A	2: 103,998,292 (GRCm39)	Y1837F	probably damaging	Het
Degs2	A	G	12: 108,668,469 (GRCm39)	F10S	probably damaging	Het
Dytn	T	A	1: 63,717,933 (GRCm39)		probably benign	Het
Elfn2	G	C	15: 78,557,795 (GRCm39)	P251A	probably benign	Het
Epg5	T	C	18: 78,066,486 (GRCm39)		probably benign	Het
Evc2	A	G	5: 37,574,811 (GRCm39)	D1022G	probably damaging	Het
Fat3	A	G	9: 15,856,304 (GRCm39)		probably benign	Het
Fbn1	A	T	2: 125,151,675 (GRCm39)		probably null	Het
Gm15217	T	C	14: 46,620,676 (GRCm39)		probably null	Het
Gm17611	A	T	13: 50,130,435 (GRCm39)		noncoding transcript	Het
Gpld1	G	A	13: 25,146,303 (GRCm39)	W182*	probably null	Het
Gsc	T	C	12: 104,439,353 (GRCm39)	I8V	probably damaging	Het
Hck	A	G	2: 152,976,052 (GRCm39)	K197R	probably benign	Het
Kat6b	T	C	14: 21,720,301 (GRCm39)	L1551P	probably damaging	Het
Lrch1	C	T	14: 75,184,985 (GRCm39)	G39D	possibly damaging	Het
Macf1	T	C	4: 123,259,148 (GRCm39)		probably null	Het
Mroh9	A	T	1: 162,888,331 (GRCm39)	V248E	probably damaging	Het
Mrps15	C	A	4: 125,945,210 (GRCm39)		probably benign	Het
Naip2	A	C	13: 100,298,290 (GRCm39)	I582S	probably benign	Het
Ndufa5	T	C	6: 24,522,750 (GRCm39)	T31A	probably benign	Het
Nfyb	A	G	10: 82,586,594 (GRCm39)	V190A	possibly damaging	Het
Nos2	A	G	11: 78,819,409 (GRCm39)	I40M	probably benign	Het
Or2f2	T	C	6: 42,767,108 (GRCm39)	I45T	probably damaging	Het
Or5ar1	A	T	2: 85,671,859 (GRCm39)	I92N	probably damaging	Het
Otog	T	C	7: 45,955,301 (GRCm39)	S564P	probably damaging	Het
Pak5	C	T	2: 135,958,549 (GRCm39)	A180T	probably benign	Het
Pappa2	T	C	1: 158,590,628 (GRCm39)		probably benign	Het
Pkd1l3	C	G	8: 110,350,281 (GRCm39)	D375E	possibly damaging	Het
Plxnc1	T	A	10: 94,632,344 (GRCm39)	N1431I	probably damaging	Het
Prph	A	T	15: 98,955,319 (GRCm39)	I429L	probably damaging	Het
Prrc2a	A	G	17: 35,368,664 (GRCm39)		probably benign	Het
Pwwp3a	A	T	10: 80,064,859 (GRCm39)	N30Y	probably damaging	Het
Rad54b	A	T	4: 11,563,394 (GRCm39)	T18S	probably benign	Het
Ranbp2	A	G	10: 58,321,590 (GRCm39)	E2629G	probably benign	Het
Rec114	G	A	9: 58,565,053 (GRCm39)	T201I	probably benign	Het
Rspo1	G	A	4: 124,885,190 (GRCm39)	R22Q	probably benign	Het
Sec23b	A	G	2: 144,423,917 (GRCm39)	E522G	probably damaging	Het
Sgsm3	G	A	15: 80,893,971 (GRCm39)	R502H	possibly damaging	Het
Sh3pxd2b	C	A	11: 32,373,023 (GRCm39)	A730D	possibly damaging	Het
Spag4	A	G	2: 155,909,899 (GRCm39)	D187G	probably damaging	Het
Srgap2	G	A	1: 131,264,175 (GRCm39)	T465I	probably damaging	Het
St3gal6	G	T	16: 58,293,818 (GRCm39)	A237E	probably damaging	Het
St3gal6	C	A	16: 58,293,816 (GRCm39)	A238S	probably damaging	Het
Tecpr1	C	A	5: 144,132,759 (GRCm39)	R1159L	probably benign	Het
Tmem63b	A	T	17: 45,977,241 (GRCm39)		probably null	Het
Tmtc1	T	A	6: 148,317,256 (GRCm39)	D78V	probably damaging	Het
Tpp2	A	G	1: 44,029,722 (GRCm39)	N68D	possibly damaging	Het
Ttn	C	A	2: 76,770,269 (GRCm39)	A2641S	probably benign	Het
Uimc1	T	C	13: 55,241,032 (GRCm39)	K19E	probably damaging	Het
Utrn	T	A	10: 12,564,038 (GRCm39)	E1274V	probably null	Het
Vmn2r102	A	T	17: 19,914,630 (GRCm39)	I732F	probably damaging	Het
Wrn	A	T	8: 33,758,778 (GRCm39)	M792K	probably benign	Het
Zfp451	A	G	1: 33,816,126 (GRCm39)	I608T	probably damaging	Het

Other mutations in Or8k37

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01132:Or8k37	APN	2	86,469,510 (GRCm39)	missense	probably benign	0.01
IGL01376:Or8k37	APN	2	86,469,953 (GRCm39)	missense	probably benign	0.00
IGL01387:Or8k37	APN	2	86,469,594 (GRCm39)	missense	probably benign	0.03
IGL01549:Or8k37	APN	2	86,469,876 (GRCm39)	missense	possibly damaging	0.95
IGL01549:Or8k37	APN	2	86,469,705 (GRCm39)	missense	probably benign	0.29
IGL01572:Or8k37	APN	2	86,469,283 (GRCm39)	missense	possibly damaging	0.92
IGL02084:Or8k37	APN	2	86,469,980 (GRCm39)	missense	possibly damaging	0.89
IGL02289:Or8k37	APN	2	86,469,863 (GRCm39)	missense	probably damaging	1.00
IGL02422:Or8k37	APN	2	86,469,560 (GRCm39)	missense	probably damaging	0.99
IGL02691:Or8k37	APN	2	86,469,182 (GRCm39)	missense	probably damaging	1.00
IGL02829:Or8k37	APN	2	86,469,599 (GRCm39)	missense	possibly damaging	0.60
IGL02859:Or8k37	APN	2	86,469,992 (GRCm39)	missense	probably benign	0.01
R0546:Or8k37	UTSW	2	86,469,573 (GRCm39)	missense	possibly damaging	0.86
R1186:Or8k37	UTSW	2	86,469,807 (GRCm39)	missense	probably damaging	1.00
R4465:Or8k37	UTSW	2	86,469,478 (GRCm39)	missense	probably benign	0.28
R4554:Or8k37	UTSW	2	86,469,123 (GRCm39)	missense	possibly damaging	0.74
R4670:Or8k37	UTSW	2	86,469,512 (GRCm39)	missense	possibly damaging	0.95
R4945:Or8k37	UTSW	2	86,469,833 (GRCm39)	missense	probably damaging	0.99
R5348:Or8k37	UTSW	2	86,469,150 (GRCm39)	missense	probably benign	0.39
R5888:Or8k37	UTSW	2	86,469,488 (GRCm39)	missense	probably damaging	0.98
R7001:Or8k37	UTSW	2	86,469,495 (GRCm39)	missense	probably benign	0.20
R7258:Or8k37	UTSW	2	86,469,345 (GRCm39)	nonsense	probably null
R7526:Or8k37	UTSW	2	86,470,013 (GRCm39)	missense	possibly damaging	0.93
R7646:Or8k37	UTSW	2	86,469,513 (GRCm39)	missense	probably damaging	1.00
R7915:Or8k37	UTSW	2	86,469,110 (GRCm39)	makesense	probably null

Predicted Primers

PCR Primer
(F):5'- TTGTAACCACTGTCAGGTGGGACC -3'
(R):5'- TGGGAATCACTGAGAACCCTGAGC -3'

Sequencing Primer
(F):5'- GAGTTCATCCTGAGAACAGCTATG -3'
(R):5'- GGGATAATCATCCTCACCAATGTAG -3'

Posted On

2013-05-23