Mutagenetix > Incidental Mutation

Incidental Mutation 'R7706:Or52k2'

594281

Institutional Source

Beutler Lab

Gene Symbol

Or52k2

Ensembl Gene

ENSMUSG00000073973

Gene Name

olfactory receptor family 52 subfamily K member 2

Synonyms

GA_x6K02T2PBJ9-5323062-5324015, Olfr552, MOR28-1

MMRRC Submission

045767-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.150) question?

Stock #

R7706 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

102253563-102254516 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 102253853 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 97 (H97Q)

Ref Sequence

ENSEMBL: ENSMUSP00000150317 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098223] [ENSMUST00000215712]

AlphaFold

E9Q545

Predicted Effect

probably benign
Transcript: ENSMUST00000098223
AA Change: H97Q

PolyPhen 2 Score 0.124 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000095826
Gene: ENSMUSG00000073973
AA Change: H97Q

Domain	Start	End	E-Value	Type
Pfam:7tm_4	33	312	6e-118	PFAM
Pfam:7TM_GPCR_Srsx	37	270	4.4e-8	PFAM
Pfam:7tm_1	43	294	9.6e-20	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000215712
AA Change: H97Q

PolyPhen 2 Score 0.124 (Sensitivity: 0.93; Specificity: 0.86)

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

98% (52/53)

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: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1600014C23Rik	G	A	17: 46,044,583 (GRCm39)	T46I	unknown	Het
Arhgef1	G	A	7: 24,616,306 (GRCm39)	D317N	probably damaging	Het
Atxn7l2	T	C	3: 108,114,719 (GRCm39)	D109G	probably damaging	Het
B4galnt3	C	A	6: 120,195,913 (GRCm39)	V305L	probably benign	Het
C9	T	A	15: 6,488,402 (GRCm39)	N85K	probably benign	Het
Cacna1g	T	C	11: 94,305,867 (GRCm39)	I1941V	probably benign	Het
Capn15	A	G	17: 26,183,125 (GRCm39)	V518A	probably benign	Het
Chst10	A	T	1: 38,905,106 (GRCm39)	Y200N	probably damaging	Het
Ciao3	T	C	17: 26,001,226 (GRCm39)	*493Q	probably null	Het
Cir1	A	G	2: 73,142,823 (GRCm39)	S4P	probably damaging	Het
Cish	G	A	9: 107,177,840 (GRCm39)	R172Q	probably benign	Het
Cnot10	A	T	9: 114,422,506 (GRCm39)	N693K	probably damaging	Het
Ddx6	A	G	9: 44,538,939 (GRCm39)	D249G	probably damaging	Het
Dennd6b	T	C	15: 89,069,447 (GRCm39)	D528G	probably benign	Het
Dmtf1	T	A	5: 9,174,489 (GRCm39)	T484S	possibly damaging	Het
Dnaaf5	T	C	5: 139,138,596 (GRCm39)	V259A	probably damaging	Het
Dzip1l	A	T	9: 99,519,589 (GRCm39)	S39C	probably damaging	Het
Efcab8	T	A	2: 153,623,695 (GRCm39)	M60K		Het
Eml2	T	A	7: 18,920,035 (GRCm39)	V113D	possibly damaging	Het
Fnip1	A	T	11: 54,406,325 (GRCm39)	I1141F	probably benign	Het
Gm7298	T	A	6: 121,712,570 (GRCm39)	S127R	probably damaging	Het
Hcn2	G	A	10: 79,570,017 (GRCm39)	R622Q	possibly damaging	Het
Ift172	C	T	5: 31,423,723 (GRCm39)	W746*	probably null	Het
Irs1	A	G	1: 82,265,412 (GRCm39)	Y935H	probably damaging	Het
Kctd17	CAGCTGGAGGAGC	CAGC	15: 78,321,113 (GRCm39)		probably benign	Het
Klhl20	T	C	1: 160,936,827 (GRCm39)	I183V	probably benign	Het
Krt1	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	15: 101,758,813 (GRCm39)		probably benign	Het
Lalba	T	C	15: 98,379,474 (GRCm39)	D103G	probably damaging	Het
Lpin3	T	C	2: 160,747,210 (GRCm39)	L822P	probably damaging	Het
Lrrc38	G	A	4: 143,076,845 (GRCm39)	C36Y	probably damaging	Het
Ly6e	T	C	15: 74,830,183 (GRCm39)	S46P	possibly damaging	Het
Nav2	T	C	7: 49,244,067 (GRCm39)	I2098T	probably benign	Het
Nipbl	T	C	15: 8,381,010 (GRCm39)	E594G	probably benign	Het
Parn	T	C	16: 13,425,117 (GRCm39)	D432G	probably damaging	Het
Pcdh20	A	G	14: 88,704,793 (GRCm39)	S836P	probably damaging	Het
Pcmtd2	C	T	2: 181,496,868 (GRCm39)	R282C	probably damaging	Het
Ppp2r3c	A	G	12: 55,328,490 (GRCm39)	I425T	probably benign	Het
Samm50	T	A	15: 84,085,081 (GRCm39)		probably null	Het
Sars1	C	T	3: 108,338,780 (GRCm39)		probably null	Het
Senp8	A	G	9: 59,645,121 (GRCm39)	Y12H	possibly damaging	Het
Slc13a4	T	C	6: 35,247,290 (GRCm39)	I577V	possibly damaging	Het
Srr	T	G	11: 74,803,961 (GRCm39)		probably null	Het
Steap2	T	A	5: 5,732,967 (GRCm39)	N19I	possibly damaging	Het
Sucla2	A	G	14: 73,806,433 (GRCm39)	Y168C	probably damaging	Het
Tha1	T	C	11: 117,760,281 (GRCm39)	Q275R	probably damaging	Het
Trim56	T	C	5: 137,143,510 (GRCm39)	N2S	probably benign	Het
Tubgcp6	T	A	15: 88,988,426 (GRCm39)	H849L	probably benign	Het
Uevld	A	G	7: 46,597,775 (GRCm39)	I72T	possibly damaging	Het
Ybx1	A	G	4: 119,136,164 (GRCm39)	*323Q	probably null	Het
Zfp354b	C	T	11: 50,819,390 (GRCm39)		probably null	Het
Zfp36l2	A	T	17: 84,494,346 (GRCm39)	L97Q	probably benign	Het
Zfp729a	T	A	13: 67,771,612 (GRCm39)	R78S	possibly damaging	Het

Other mutations in Or52k2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00937:Or52k2	APN	7	102,253,564 (GRCm39)	start codon destroyed	probably null	0.99
IGL03061:Or52k2	APN	7	102,253,946 (GRCm39)	missense	probably damaging	0.99
R0989:Or52k2	UTSW	7	102,253,690 (GRCm39)	missense	probably damaging	1.00
R1513:Or52k2	UTSW	7	102,254,509 (GRCm39)	missense	probably benign	0.09
R1969:Or52k2	UTSW	7	102,253,777 (GRCm39)	missense	probably damaging	0.99
R3177:Or52k2	UTSW	7	102,253,783 (GRCm39)	missense	possibly damaging	0.94
R3277:Or52k2	UTSW	7	102,253,783 (GRCm39)	missense	possibly damaging	0.94
R4019:Or52k2	UTSW	7	102,253,849 (GRCm39)	missense	probably damaging	1.00
R4028:Or52k2	UTSW	7	102,254,500 (GRCm39)	missense	possibly damaging	0.62
R5216:Or52k2	UTSW	7	102,254,028 (GRCm39)	missense	probably benign	0.00
R5444:Or52k2	UTSW	7	102,254,076 (GRCm39)	nonsense	probably null
R5461:Or52k2	UTSW	7	102,253,615 (GRCm39)	missense	probably damaging	0.99
R8348:Or52k2	UTSW	7	102,254,207 (GRCm39)	missense	probably benign	0.01
R8448:Or52k2	UTSW	7	102,254,207 (GRCm39)	missense	probably benign	0.01
R8919:Or52k2	UTSW	7	102,253,711 (GRCm39)	missense	probably damaging	1.00
R8933:Or52k2	UTSW	7	102,253,637 (GRCm39)	missense	probably damaging	1.00
R9009:Or52k2	UTSW	7	102,253,642 (GRCm39)	missense	probably benign	0.00
R9139:Or52k2	UTSW	7	102,254,185 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATACCTTGGCTGTGCTTGGC -3'
(R):5'- CTCGACAGTAATGGAAACGTCTG -3'

Sequencing Primer
(F):5'- TGCTTGGCAACTGCACC -3'
(R):5'- TGGAGTCATTAGTGTCACAGCCC -3'

Posted On

2019-11-12