Mutagenetix > Incidental Mutation

Incidental Mutation 'R7611:Or5an10'

588642

Institutional Source

Beutler Lab

Gene Symbol

Or5an10

Ensembl Gene

ENSMUSG00000067513

Gene Name

olfactory receptor family 5 subfamily AN member 10

Synonyms

Olfr1436, GA_x6K02T2RE5P-2634596-2633658, MOR214-2

MMRRC Submission

045715-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.060) question?

Stock #

R7611 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

12275547-12276494 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 12276242 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Methionine to Leucine at position 85 (M85L)

Ref Sequence

ENSEMBL: ENSMUSP00000085113 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087812]

AlphaFold

A0PK57

Predicted Effect

probably damaging
Transcript: ENSMUST00000087812
AA Change: M85L

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000085113
Gene: ENSMUSG00000067513
AA Change: M85L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	35	311	2.4e-54	PFAM
Pfam:7tm_1	45	294	1.3e-19	PFAM

Coding Region Coverage

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

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: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acta2	G	A	19: 34,229,931 (GRCm39)	T8I	probably benign	Het
Adcy8	C	T	15: 64,792,882 (GRCm39)	G25S	probably benign	Het
Ahnak2	G	T	12: 112,751,749 (GRCm39)	D35E		Het
Birc6	T	C	17: 74,969,713 (GRCm39)	M4261T	probably damaging	Het
Caln1	T	G	5: 130,534,918 (GRCm39)	F45V	probably damaging	Het
Camta2	A	T	11: 70,572,372 (GRCm39)	I313N	possibly damaging	Het
Capns1	T	A	7: 29,889,539 (GRCm39)	E220V	probably damaging	Het
Carmil1	C	A	13: 24,197,315 (GRCm39)	V1374L	probably benign	Het
Casp2	T	G	6: 42,250,972 (GRCm39)	L290R	possibly damaging	Het
Cdkn2b	C	A	4: 89,228,980 (GRCm39)	V19L	probably benign	Het
Ces1c	T	C	8: 93,851,139 (GRCm39)	N162D	probably benign	Het
Cfap96	A	G	8: 46,423,488 (GRCm39)	Y75H	probably damaging	Het
Chd9	T	C	8: 91,763,017 (GRCm39)	S2281P	probably damaging	Het
Chst13	T	C	6: 90,285,999 (GRCm39)	D321G	probably damaging	Het
Ckap2l	G	T	2: 129,127,600 (GRCm39)	P193T	possibly damaging	Het
Clca4b	T	A	3: 144,627,757 (GRCm39)	T405S	probably benign	Het
Cmah	T	C	13: 24,619,630 (GRCm39)	V265A	probably benign	Het
Cyp3a11	A	T	5: 145,797,191 (GRCm39)	M396K	probably benign	Het
Ddr2	A	T	1: 169,825,727 (GRCm39)	M291K	possibly damaging	Het
Ddx43	T	A	9: 78,309,635 (GRCm39)	I145N	probably benign	Het
Ephb2	T	A	4: 136,388,212 (GRCm39)		probably null	Het
Fgfr1	A	T	8: 26,048,221 (GRCm39)	K106*	probably null	Het
Gpr6	A	G	10: 40,946,875 (GRCm39)	F236L	probably benign	Het
Grin2c	A	G	11: 115,143,511 (GRCm39)	S750P	probably damaging	Het
Hecw2	A	G	1: 53,952,459 (GRCm39)	S925P	probably damaging	Het
Hivep3	CGG	CG	4: 119,955,108 (GRCm39)	1141	probably null	Het
Hmg20b	T	A	10: 81,185,432 (GRCm39)		probably benign	Het
Kcnk10	T	A	12: 98,484,899 (GRCm39)	Y79F	probably damaging	Het
Lrrc30	A	T	17: 67,939,424 (GRCm39)	F52Y	probably damaging	Het
Lrriq1	T	C	10: 103,036,432 (GRCm39)	K907R	possibly damaging	Het
Mbd3	T	C	10: 80,231,352 (GRCm39)	D63G	probably damaging	Het
Mettl21a	C	T	1: 64,654,266 (GRCm39)	A84T	probably benign	Het
Mmp19	A	G	10: 128,634,857 (GRCm39)	D491G	probably benign	Het
Mug1	A	T	6: 121,852,387 (GRCm39)		probably null	Het
Myh1	A	T	11: 67,101,243 (GRCm39)	H673L	possibly damaging	Het
Nlrc5	T	C	8: 95,239,276 (GRCm39)		probably null	Het
Nme9	T	A	9: 99,352,843 (GRCm39)	S264R	probably benign	Het
Nup153	T	C	13: 46,840,798 (GRCm39)	T937A	probably benign	Het
Obsl1	T	C	1: 75,482,024 (GRCm39)	E282G	probably damaging	Het
Or1o3	A	G	17: 37,573,745 (GRCm39)	V270A	probably benign	Het
Or2w2	A	G	13: 21,758,488 (GRCm39)	V46A	probably benign	Het
Or4l15	C	A	14: 50,198,368 (GRCm39)	A54S	probably benign	Het
Or5b99	T	A	19: 12,976,431 (GRCm39)	I27N	possibly damaging	Het
Or5m5	T	A	2: 85,814,407 (GRCm39)	C74*	probably null	Het
Or8k30	T	A	2: 86,339,397 (GRCm39)	I198K	possibly damaging	Het
Pcdhga12	T	C	18: 37,901,478 (GRCm39)	F770S	possibly damaging	Het
Pfkp	T	A	13: 6,655,119 (GRCm39)		probably null	Het
Prr29	C	G	11: 106,267,158 (GRCm39)	H58D	probably damaging	Het
Ptprz1	T	A	6: 23,001,219 (GRCm39)	M1103K	probably benign	Het
Rigi	T	C	4: 40,225,651 (GRCm39)	E250G	probably damaging	Het
Rsph4a	C	T	10: 33,781,473 (GRCm39)	P108S	probably benign	Het
Setd1b	A	C	5: 123,290,657 (GRCm39)	M875L	unknown	Het
Slc15a2	A	G	16: 36,576,673 (GRCm39)	S485P	probably benign	Het
Smoc1	A	G	12: 81,226,444 (GRCm39)	D423G	probably damaging	Het
Spast	T	A	17: 74,676,198 (GRCm39)	V337D	probably damaging	Het
Spesp1	T	C	9: 62,179,987 (GRCm39)	K307R	possibly damaging	Het
Sulf1	A	G	1: 12,906,467 (GRCm39)	E503G	probably benign	Het
Susd6	T	C	12: 80,921,341 (GRCm39)	Y313H	probably damaging	Het
Them4	A	T	3: 94,238,865 (GRCm39)	D224V	possibly damaging	Het
Tpsg1	G	T	17: 25,592,184 (GRCm39)	G86V	probably damaging	Het
Tspear	A	T	10: 77,717,049 (GRCm39)	T575S	probably benign	Het
Usp21	A	T	1: 171,113,142 (GRCm39)	H211Q	probably benign	Het
Vmn1r189	T	C	13: 22,286,322 (GRCm39)	S172G	probably benign	Het
Vmn2r114	T	C	17: 23,515,944 (GRCm39)	S516G	probably damaging	Het
Vmn2r28	T	A	7: 5,484,255 (GRCm39)	R648S	probably benign	Het
Vmn2r6	C	A	3: 64,472,563 (GRCm39)	V53F	probably damaging	Het
Vmn2r76	A	G	7: 85,879,388 (GRCm39)	I304T	probably benign	Het
Vmn2r88	A	C	14: 51,651,454 (GRCm39)	Y256S		Het
Zfhx4	A	T	3: 5,468,831 (GRCm39)	K3021N	probably damaging	Het
Zfp647	T	C	15: 76,795,988 (GRCm39)	H224R	probably damaging	Het
Zfp865	A	G	7: 5,034,130 (GRCm39)	E705G	probably damaging	Het

Other mutations in Or5an10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00975:Or5an10	APN	19	12,276,149 (GRCm39)	missense	probably damaging	0.99
IGL02129:Or5an10	APN	19	12,275,822 (GRCm39)	missense	probably damaging	1.00
PIT4378001:Or5an10	UTSW	19	12,276,076 (GRCm39)	missense	probably damaging	1.00
R0727:Or5an10	UTSW	19	12,276,458 (GRCm39)	missense	probably benign	0.03
R1244:Or5an10	UTSW	19	12,275,860 (GRCm39)	missense	probably damaging	0.98
R1647:Or5an10	UTSW	19	12,276,023 (GRCm39)	missense	probably benign
R1648:Or5an10	UTSW	19	12,276,023 (GRCm39)	missense	probably benign
R1837:Or5an10	UTSW	19	12,275,740 (GRCm39)	missense	probably damaging	1.00
R1899:Or5an10	UTSW	19	12,275,707 (GRCm39)	missense	probably damaging	1.00
R2031:Or5an10	UTSW	19	12,275,740 (GRCm39)	missense	probably damaging	1.00
R2305:Or5an10	UTSW	19	12,276,451 (GRCm39)	missense	probably benign	0.01
R4624:Or5an10	UTSW	19	12,276,347 (GRCm39)	missense	probably benign
R4681:Or5an10	UTSW	19	12,276,413 (GRCm39)	missense	probably benign	0.05
R4790:Or5an10	UTSW	19	12,276,305 (GRCm39)	missense	possibly damaging	0.60
R4865:Or5an10	UTSW	19	12,275,944 (GRCm39)	missense	probably damaging	1.00
R4941:Or5an10	UTSW	19	12,276,260 (GRCm39)	missense	possibly damaging	0.95
R5138:Or5an10	UTSW	19	12,276,140 (GRCm39)	missense	possibly damaging	0.56
R5161:Or5an10	UTSW	19	12,276,153 (GRCm39)	missense	probably damaging	0.99
R5560:Or5an10	UTSW	19	12,276,008 (GRCm39)	nonsense	probably null
R5983:Or5an10	UTSW	19	12,276,467 (GRCm39)	missense	probably benign	0.00
R6736:Or5an10	UTSW	19	12,275,936 (GRCm39)	nonsense	probably null
R6882:Or5an10	UTSW	19	12,275,934 (GRCm39)	missense	probably damaging	1.00
R6883:Or5an10	UTSW	19	12,275,934 (GRCm39)	missense	probably damaging	1.00
R7465:Or5an10	UTSW	19	12,275,801 (GRCm39)	missense	probably benign	0.04
R7500:Or5an10	UTSW	19	12,276,041 (GRCm39)	missense	probably damaging	0.98
R7529:Or5an10	UTSW	19	12,276,086 (GRCm39)	missense	probably damaging	1.00
R7565:Or5an10	UTSW	19	12,276,212 (GRCm39)	missense	probably benign	0.09
R7850:Or5an10	UTSW	19	12,275,996 (GRCm39)	missense	probably benign
R7956:Or5an10	UTSW	19	12,275,666 (GRCm39)	missense	probably damaging	1.00
R7991:Or5an10	UTSW	19	12,275,639 (GRCm39)	missense	probably damaging	1.00
R9770:Or5an10	UTSW	19	12,276,464 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACATAGTGTGGGTGACATGAC -3'
(R):5'- GATCACCGAATTCATCCTCCTAGG -3'

Sequencing Primer
(F):5'- TGGGTGACATGACTGATGAGTAC -3'
(R):5'- GATTTCCCCCAAATCACAGCACTG -3'

Posted On

2019-10-24