Mutagenetix > Incidental Mutation

Incidental Mutation 'R8485:Or10ag60'

657664

Institutional Source

Beutler Lab

Gene Symbol

Or10ag60

Ensembl Gene

ENSMUSG00000059205

Gene Name

olfactory receptor family 10 subfamily AG member 60

Synonyms

GA_x6K02T2Q125-49112575-49113519, Olfr1130, MOR264-4

MMRRC Submission

067928-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.176) question?

Stock #

R8485 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

87436556-87438678 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 87438601 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 290 (M290L)

Ref Sequence

ENSEMBL: ENSMUSP00000150905 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000213103] [ENSMUST00000216580]

AlphaFold

A0A1L1SQT2

Predicted Effect

probably benign
Transcript: ENSMUST00000213103
AA Change: M290L

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

Predicted Effect

probably benign
Transcript: ENSMUST00000216580
AA Change: M290L

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (59/59)

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: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp6	A	G	3: 97,066,302 (GRCm39)		probably benign	Het
Adamts16	T	C	13: 70,886,794 (GRCm39)	T999A	possibly damaging	Het
Adgrb1	A	C	15: 74,420,153 (GRCm39)	T829P	probably damaging	Het
Ankrd12	C	T	17: 66,290,711 (GRCm39)	S1574N	probably benign	Het
Ankrd2	G	A	19: 42,030,384 (GRCm39)		probably null	Het
Ano3	T	A	2: 110,498,200 (GRCm39)		probably null	Het
Arhgap18	T	C	10: 26,722,104 (GRCm39)	I25T	probably benign	Het
Armc3	T	C	2: 19,297,945 (GRCm39)	F572S	probably damaging	Het
Aspdh	G	T	7: 44,117,093 (GRCm39)	G165W	probably damaging	Het
Btnl10	G	T	11: 58,811,142 (GRCm39)	R155L	possibly damaging	Het
Cacng7	A	G	7: 3,414,541 (GRCm39)	E168G	probably benign	Het
Cadps	G	A	14: 12,439,872 (GRCm38)	T1215M	probably damaging	Het
Cbfa2t3	C	A	8: 123,357,517 (GRCm39)	G598C	probably damaging	Het
Cdh15	T	C	8: 123,584,105 (GRCm39)	S69P	probably damaging	Het
Cwc27	G	T	13: 104,940,772 (GRCm39)	P196T	probably benign	Het
Cwc27	C	A	13: 104,940,776 (GRCm39)	L194F	possibly damaging	Het
Dlec1	T	G	9: 118,957,659 (GRCm39)	V881G	probably benign	Het
Dnah7c	A	C	1: 46,719,952 (GRCm39)	D2801A	probably benign	Het
Efhc1	T	C	1: 21,030,460 (GRCm39)	M131T	possibly damaging	Het
Ercc2	G	A	7: 19,122,165 (GRCm39)	V386I	possibly damaging	Het
Exoc4	T	A	6: 33,898,436 (GRCm39)	I885N	probably damaging	Het
Fbxl22	C	T	9: 66,421,849 (GRCm39)		probably null	Het
Flii	G	T	11: 60,607,063 (GRCm39)	A971E	probably benign	Het
Fnip2	T	A	3: 79,388,844 (GRCm39)	E599V	probably benign	Het
Glb1l2	G	A	9: 26,679,036 (GRCm39)	L453F	probably benign	Het
Gm49368	C	T	7: 127,711,611 (GRCm39)	P624L	probably damaging	Het
Gpa33	T	A	1: 165,992,261 (GRCm39)	D268E	probably benign	Het
Gpi1	A	T	7: 33,918,677 (GRCm39)		probably null	Het
Iqgap2	T	C	13: 95,796,659 (GRCm39)	N1165S	probably damaging	Het
Irag2	A	T	6: 145,117,400 (GRCm39)	N379I	probably damaging	Het
Kctd2	G	T	11: 115,320,434 (GRCm39)		probably benign	Het
L1td1	C	T	4: 98,625,911 (GRCm39)	A702V	probably damaging	Het
Lrp1	G	A	10: 127,394,519 (GRCm39)	R2565C	probably damaging	Het
Mycbpap	A	G	11: 94,402,534 (GRCm39)	L267P	probably damaging	Het
Mycbpap	T	C	11: 94,405,359 (GRCm39)	R57G	probably benign	Het
Myo1b	A	C	1: 51,818,760 (GRCm39)	L505R	probably damaging	Het
Nfatc2	A	C	2: 168,432,012 (GRCm39)	F34V	probably damaging	Het
Nphs1	A	G	7: 30,165,598 (GRCm39)	N655S	probably damaging	Het
Nsd2	A	T	5: 34,040,189 (GRCm39)	I909F	probably damaging	Het
Or8b37	T	A	9: 37,959,253 (GRCm39)	M245K	probably benign	Het
Pak2	G	A	16: 31,871,083 (GRCm39)	A33V	probably benign	Het
Phb1	A	G	11: 95,566,055 (GRCm39)	D113G	probably benign	Het
Pkhd1	T	A	1: 20,593,257 (GRCm39)	I1619F	probably damaging	Het
Pkhd1l1	A	G	15: 44,423,796 (GRCm39)	I3113V	probably damaging	Het
Plat	G	T	8: 23,262,248 (GRCm39)	G91W	probably damaging	Het
Prrc2b	T	A	2: 32,102,105 (GRCm39)	M726K	possibly damaging	Het
Rai14	A	G	15: 10,575,122 (GRCm39)	L612P	probably damaging	Het
Rapgef1	T	C	2: 29,600,186 (GRCm39)	S598P	probably damaging	Het
Rdm1	G	A	11: 101,518,816 (GRCm39)	V8I	probably benign	Het
Rrbp1	A	G	2: 143,796,933 (GRCm39)	F1148L	probably benign	Het
Slc12a2	T	C	18: 58,074,218 (GRCm39)		probably null	Het
Slc7a8	T	A	14: 54,962,264 (GRCm39)	T457S	probably benign	Het
Stk32a	T	A	18: 43,376,075 (GRCm39)	M48K	possibly damaging	Het
Svil	T	C	18: 5,064,566 (GRCm39)	S642P	probably benign	Het
Taok3	G	A	5: 117,389,142 (GRCm39)	V516M	possibly damaging	Het
Ugdh	T	C	5: 65,584,902 (GRCm39)	I7V	possibly damaging	Het
Zc3h11a	T	A	1: 133,553,633 (GRCm39)	S504C	possibly damaging	Het
Zfp512	C	T	5: 31,637,401 (GRCm39)	R497W	probably damaging	Het

Other mutations in Or10ag60

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01151:Or10ag60	APN	2	87,438,323 (GRCm39)	missense	probably damaging	1.00
IGL01310:Or10ag60	APN	2	87,437,852 (GRCm39)	missense	possibly damaging	0.68
IGL02558:Or10ag60	APN	2	87,437,903 (GRCm39)	missense	probably benign	0.00
R0323:Or10ag60	UTSW	2	87,437,841 (GRCm39)	missense	probably benign
R0590:Or10ag60	UTSW	2	87,438,338 (GRCm39)	missense	probably damaging	0.98
R0718:Or10ag60	UTSW	2	87,438,271 (GRCm39)	missense	probably benign	0.08
R2445:Or10ag60	UTSW	2	87,438,302 (GRCm39)	missense	probably damaging	0.99
R3408:Or10ag60	UTSW	2	87,438,220 (GRCm39)	missense	probably benign	0.03
R4280:Or10ag60	UTSW	2	87,438,595 (GRCm39)	missense	possibly damaging	0.90
R4491:Or10ag60	UTSW	2	87,437,736 (GRCm39)	start codon destroyed	probably null	0.84
R4928:Or10ag60	UTSW	2	87,438,487 (GRCm39)	missense	probably benign	0.06
R5033:Or10ag60	UTSW	2	87,438,055 (GRCm39)	missense	probably damaging	1.00
R5061:Or10ag60	UTSW	2	87,438,176 (GRCm39)	missense	probably benign	0.00
R5109:Or10ag60	UTSW	2	87,438,319 (GRCm39)	missense	possibly damaging	0.78
R5109:Or10ag60	UTSW	2	87,437,755 (GRCm39)	missense	possibly damaging	0.64
R5772:Or10ag60	UTSW	2	87,438,517 (GRCm39)	missense	probably benign	0.12
R6004:Or10ag60	UTSW	2	87,438,253 (GRCm39)	missense	probably damaging	1.00
R6005:Or10ag60	UTSW	2	87,438,424 (GRCm39)	missense	probably damaging	0.97
R6411:Or10ag60	UTSW	2	87,438,317 (GRCm39)	missense	probably damaging	1.00
R6964:Or10ag60	UTSW	2	87,437,957 (GRCm39)	missense	probably damaging	1.00
R7085:Or10ag60	UTSW	2	87,437,750 (GRCm39)	missense	probably benign	0.00
R7484:Or10ag60	UTSW	2	87,438,281 (GRCm39)	missense	probably damaging	1.00
R8429:Or10ag60	UTSW	2	87,437,868 (GRCm39)	missense	probably benign	0.06
R8471:Or10ag60	UTSW	2	87,437,989 (GRCm39)	missense	probably damaging	0.99
R8890:Or10ag60	UTSW	2	87,438,412 (GRCm39)	missense	probably damaging	1.00
R8935:Or10ag60	UTSW	2	87,438,421 (GRCm39)	missense	possibly damaging	0.72
X0060:Or10ag60	UTSW	2	87,438,386 (GRCm39)	missense	probably benign	0.11
Z1176:Or10ag60	UTSW	2	87,438,098 (GRCm39)	missense	probably benign	0.34

Predicted Primers

PCR Primer
(F):5'- CATTGCCACCATTCTGAAGTTGC -3'
(R):5'- GGCTATTACTCAAAGCAGCACAG -3'

Sequencing Primer
(F):5'- TTCTGAAGTTGCCAACAGCC -3'
(R):5'- TCAAAGCAGCACAGGCATTATAG -3'

Posted On

2021-01-18