Mutagenetix > Incidental Mutation

Incidental Mutation 'R3847:Or8u10'

277410

Institutional Source

Beutler Lab

Gene Symbol

Or8u10

Ensembl Gene

ENSMUSG00000075205

Gene Name

olfactory receptor family 8 subfamily U member 10

Synonyms

MOR171-52, GA_x6K02T2Q125-47560740-47559775, Olfr1037, MOR256-34P

MMRRC Submission

040895-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.068) question?

Stock #

R3847 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

85915074-85916198 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 85915751 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 123 (Y123*)

Ref Sequence

ENSEMBL: ENSMUSP00000150319 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099911] [ENSMUST00000213333] [ENSMUST00000216020] [ENSMUST00000216886]

AlphaFold

Q7TR84

Predicted Effect

probably null
Transcript: ENSMUST00000099911
AA Change: Y123*

SMART Domains

Protein: ENSMUSP00000097495
Gene: ENSMUSG00000075205
AA Change: Y123*

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	1.8e-54	PFAM
Pfam:7tm_1	41	290	1.2e-19	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000117964

Predicted Effect

probably null
Transcript: ENSMUST00000213333
AA Change: Y123*

Predicted Effect

probably null
Transcript: ENSMUST00000216020
AA Change: Y123*

Predicted Effect

probably null
Transcript: ENSMUST00000216886
AA Change: Y123*

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.7%
20x: 96.1%

Validation Efficiency

100% (66/66)

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
4930522L14Rik	T	C	5: 109,884,190 (GRCm39)		probably null	Het
Abcc12	C	T	8: 87,280,020 (GRCm39)	E338K	probably benign	Het
Abcc5	A	T	16: 20,190,906 (GRCm39)	S815T	probably benign	Het
Ankrd16	G	A	2: 11,794,619 (GRCm39)	E335K	probably benign	Het
Atm	A	G	9: 53,414,375 (GRCm39)	F905S	possibly damaging	Het
Bckdha	C	T	7: 25,331,077 (GRCm39)	R281H	probably damaging	Het
Blvra	C	T	2: 126,937,111 (GRCm39)	T188I	probably damaging	Het
Bmp8b	C	A	4: 123,009,961 (GRCm39)		probably benign	Het
Cacna2d3	A	G	14: 29,069,077 (GRCm39)		probably null	Het
Cacng8	T	C	7: 3,442,990 (GRCm39)	S84P	probably damaging	Het
Cad	T	A	5: 31,218,994 (GRCm39)	V605E	probably damaging	Het
Ccny	A	G	18: 9,449,641 (GRCm39)	S11P	probably benign	Het
Col3a1	C	A	1: 45,361,150 (GRCm39)	P112T	unknown	Het
Corin	T	C	5: 72,579,508 (GRCm39)	E155G	probably benign	Het
Cul9	T	C	17: 46,836,061 (GRCm39)	Y1195C	probably damaging	Het
Cyp27a1	A	G	1: 74,776,718 (GRCm39)	E501G	probably damaging	Het
Dennd3	T	A	15: 73,414,581 (GRCm39)	N457K	possibly damaging	Het
Dnah7a	T	G	1: 53,540,815 (GRCm39)	I2520L	probably benign	Het
Dst	C	T	1: 34,251,400 (GRCm39)	S4165F	probably damaging	Het
Fgf14	A	C	14: 124,217,801 (GRCm39)	I234R	probably benign	Het
Foxp4	A	G	17: 48,186,453 (GRCm39)	I442T	unknown	Het
Gad2	T	G	2: 22,575,000 (GRCm39)	D472E	probably benign	Het
Garnl3	G	T	2: 32,882,240 (GRCm39)	H832N	probably benign	Het
Gm13941	T	C	2: 110,935,198 (GRCm39)	M11V	unknown	Het
Gnptab	T	A	10: 88,269,439 (GRCm39)	L714*	probably null	Het
Golgb1	C	A	16: 36,719,095 (GRCm39)	Q334K	probably benign	Het
Gp9	A	G	6: 87,756,133 (GRCm39)	I49M	probably benign	Het
Guf1	A	G	5: 69,718,500 (GRCm39)	N213S	probably damaging	Het
H2-K2	T	G	17: 34,216,303 (GRCm39)	H281P	probably damaging	Het
Hhip	T	A	8: 80,724,124 (GRCm39)	M373L	probably benign	Het
Ifi203	C	T	1: 173,761,362 (GRCm39)	C229Y	possibly damaging	Het
Ighv13-2	A	G	12: 114,321,418 (GRCm39)	L88S	probably damaging	Het
Kcna3	T	C	3: 106,944,012 (GRCm39)	Y92H	possibly damaging	Het
Lmo7	A	G	14: 102,159,531 (GRCm39)		probably null	Het
Lrguk	A	G	6: 34,050,703 (GRCm39)	D387G	probably damaging	Het
Mki67	A	C	7: 135,297,859 (GRCm39)	S2392A	probably benign	Het
Mknk2	C	T	10: 80,503,809 (GRCm39)	W367*	probably null	Het
Mocos	A	G	18: 24,809,719 (GRCm39)	K441E	probably damaging	Het
Mpnd	T	C	17: 56,318,692 (GRCm39)	S150P	probably damaging	Het
Naip2	G	C	13: 100,315,941 (GRCm39)	L280V	probably damaging	Het
Naip2	A	T	13: 100,315,940 (GRCm39)	L280Q	probably damaging	Het
Neurod4	C	T	10: 130,106,351 (GRCm39)	V308I	probably benign	Het
Nxf3	C	T	X: 134,974,732 (GRCm39)	V474I	probably benign	Het
Or10d5j	A	T	9: 39,867,877 (GRCm39)	M118K	probably damaging	Het
Pam	T	A	1: 97,782,481 (GRCm39)		probably benign	Het
Pde5a	T	C	3: 122,596,809 (GRCm39)	Y467H	probably damaging	Het
Pibf1	T	A	14: 99,374,557 (GRCm39)	V332E	possibly damaging	Het
Plxna1	C	A	6: 89,333,501 (GRCm39)	R376L	probably damaging	Het
Proz	A	G	8: 13,123,533 (GRCm39)	E268G	probably benign	Het
Rimbp3	A	T	16: 17,028,163 (GRCm39)	H529L	probably benign	Het
Rnf103	C	G	6: 71,485,859 (GRCm39)	C163W	probably damaging	Het
Rnf17	T	C	14: 56,749,753 (GRCm39)	V1433A	probably damaging	Het
Septin11	G	T	5: 93,310,026 (GRCm39)	M276I	probably damaging	Het
Slc30a4	A	G	2: 122,544,192 (GRCm39)	V50A	probably damaging	Het
Sorbs1	A	G	19: 40,302,887 (GRCm39)	V570A	probably damaging	Het
Spout1	T	C	2: 30,067,419 (GRCm39)		probably null	Het
Syne2	T	C	12: 76,095,396 (GRCm39)	L5241P	probably damaging	Het
Tas2r110	T	A	6: 132,845,638 (GRCm39)	I223N	probably damaging	Het
Tead2	T	A	7: 44,881,752 (GRCm39)		probably null	Het
Thsd1	A	G	8: 22,749,427 (GRCm39)	H713R	probably damaging	Het
Ttc21b	A	G	2: 66,073,023 (GRCm39)	L221S	probably damaging	Het
Ugcg	C	T	4: 59,207,798 (GRCm39)	P46S	probably benign	Het
Vmn2r105	A	G	17: 20,428,952 (GRCm39)	I708T	possibly damaging	Het
Vmn2r117	G	T	17: 23,679,389 (GRCm39)	H612N	probably damaging	Het
Wnk1	C	T	6: 119,946,315 (GRCm39)	G613S	possibly damaging	Het
Zbtb41	T	A	1: 139,351,734 (GRCm39)	H282Q	probably benign	Het
Zfp335	C	A	2: 164,742,026 (GRCm39)		probably null	Het
Zmym2	T	A	14: 57,158,956 (GRCm39)		probably benign	Het

Other mutations in Or8u10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01390:Or8u10	APN	2	85,915,984 (GRCm39)	missense	probably benign	0.05
IGL02534:Or8u10	APN	2	85,915,713 (GRCm39)	missense	probably damaging	1.00
IGL03204:Or8u10	APN	2	85,916,015 (GRCm39)	nonsense	probably null
R0054:Or8u10	UTSW	2	85,915,705 (GRCm39)	missense	probably benign	0.38
R0054:Or8u10	UTSW	2	85,915,705 (GRCm39)	missense	probably benign	0.38
R0131:Or8u10	UTSW	2	85,915,844 (GRCm39)	missense	probably damaging	1.00
R0131:Or8u10	UTSW	2	85,915,844 (GRCm39)	missense	probably damaging	1.00
R0666:Or8u10	UTSW	2	85,915,557 (GRCm39)	missense	probably benign	0.03
R0732:Or8u10	UTSW	2	85,915,928 (GRCm39)	missense	probably benign	0.00
R1167:Or8u10	UTSW	2	85,915,635 (GRCm39)	missense	probably benign	0.16
R1899:Or8u10	UTSW	2	85,916,064 (GRCm39)	missense	probably benign
R3082:Or8u10	UTSW	2	85,916,053 (GRCm39)	missense	probably benign
R3848:Or8u10	UTSW	2	85,915,751 (GRCm39)	nonsense	probably null
R4079:Or8u10	UTSW	2	85,915,656 (GRCm39)	missense	possibly damaging	0.67
R4193:Or8u10	UTSW	2	85,916,044 (GRCm39)	missense	probably benign	0.01
R4832:Or8u10	UTSW	2	85,915,190 (GRCm39)	missense	probably benign	0.00
R5244:Or8u10	UTSW	2	85,915,300 (GRCm39)	missense	probably damaging	1.00
R5643:Or8u10	UTSW	2	85,915,503 (GRCm39)	missense	probably damaging	0.98
R5644:Or8u10	UTSW	2	85,915,503 (GRCm39)	missense	probably damaging	0.98
R5974:Or8u10	UTSW	2	85,915,225 (GRCm39)	missense	probably benign
R6136:Or8u10	UTSW	2	85,915,245 (GRCm39)	missense	probably damaging	1.00
R6189:Or8u10	UTSW	2	85,915,257 (GRCm39)	missense	possibly damaging	0.53
R6483:Or8u10	UTSW	2	85,915,784 (GRCm39)	missense	probably benign	0.00
R6569:Or8u10	UTSW	2	85,915,849 (GRCm39)	missense	possibly damaging	0.87
R6724:Or8u10	UTSW	2	85,915,701 (GRCm39)	missense	possibly damaging	0.81
R6867:Or8u10	UTSW	2	85,916,082 (GRCm39)	missense	possibly damaging	0.59
R7081:Or8u10	UTSW	2	85,915,939 (GRCm39)	missense	probably damaging	1.00
R7207:Or8u10	UTSW	2	85,915,159 (GRCm39)	missense	possibly damaging	0.93
R7436:Or8u10	UTSW	2	85,915,251 (GRCm39)	missense	probably damaging	1.00
R8699:Or8u10	UTSW	2	85,915,518 (GRCm39)	missense	probably damaging	0.98
R9347:Or8u10	UTSW	2	85,915,911 (GRCm39)	missense	possibly damaging	0.78
R9798:Or8u10	UTSW	2	85,915,606 (GRCm39)	missense	probably damaging	0.99
X0062:Or8u10	UTSW	2	85,915,458 (GRCm39)	missense	probably damaging	1.00
Z1088:Or8u10	UTSW	2	85,915,326 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- AAATCTCCTTGAGGCTGGTG -3'
(R):5'- TAATCTGGCCTTTGTAGACCTTTG -3'

Sequencing Primer
(F):5'- CTGGTGTCTGAGCAGGCAAG -3'
(R):5'- AGACCTTTGCTATTCCTCTTCGGTAG -3'

Posted On

2015-04-06