Mutagenetix > Incidental Mutation

Incidental Mutation 'R9758:Or10z1'

732829

Institutional Source

Beutler Lab

Gene Symbol

Or10z1

Ensembl Gene

ENSMUSG00000050788

Gene Name

olfactory receptor family 10 subfamily Z member 1

Synonyms

MOR267-6, Olfr419, GA_x6K02T2P20D-20891507-20892448

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

R9758 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

174077455-174078542 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 174077902 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 197 (L197P)

Ref Sequence

ENSEMBL: ENSMUSP00000149512 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027817] [ENSMUST00000061990] [ENSMUST00000214725]

AlphaFold

E9Q0Y7

Predicted Effect

probably benign
Transcript: ENSMUST00000027817

SMART Domains

Protein: ENSMUSP00000027817
Gene: ENSMUSG00000026532

Domain	Start	End	E-Value	Type
SPEC	55	153	3.62e-11	SMART
SPEC	159	259	1.84e-26	SMART
SPEC	265	365	1.56e-24	SMART
SPEC	371	471	8.35e-25	SMART
SPEC	477	577	1.19e-29	SMART
SPEC	583	682	2.43e-26	SMART
SPEC	688	788	1.3e-26	SMART
SPEC	794	894	1.66e-28	SMART
SPEC	900	1077	5.03e-19	SMART
SH3	978	1033	2.98e-15	SMART
SPEC	1083	1178	2.57e-16	SMART
SPEC	1184	1284	1.15e-27	SMART
SPEC	1290	1390	7.05e-23	SMART
SPEC	1396	1495	6.04e-22	SMART
SPEC	1501	1602	1.15e-27	SMART
SPEC	1608	1708	5.46e-29	SMART
SPEC	1714	1814	1.08e-32	SMART
SPEC	1820	1921	2.17e-23	SMART
SPEC	1927	2028	2.19e-19	SMART
SPEC	2042	2142	3.87e-11	SMART
SPEC	2156	2253	9.77e-8	SMART
low complexity region	2307	2318	N/A	INTRINSIC
efhand_Ca_insen	2346	2414	2.37e-27	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000061990
AA Change: L197P

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

SMART Domains

Protein: ENSMUSP00000050893
Gene: ENSMUSG00000050788
AA Change: L197P

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	1.4e-53	PFAM
Pfam:7tm_1	41	290	3.2e-18	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000214725
AA Change: L197P

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

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 99.3%
20x: 98.5%

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: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actc1	T	C	2: 113,879,799 (GRCm39)	Y220C	probably damaging	Het
Actmap	T	C	7: 26,896,655 (GRCm39)	S73P	possibly damaging	Het
Bmper	G	A	9: 23,286,902 (GRCm39)	G276D	possibly damaging	Het
C2cd5	A	T	6: 142,984,613 (GRCm39)	M549K	probably benign	Het
Caprin1	A	G	2: 103,606,283 (GRCm39)	V319A	possibly damaging	Het
Cchcr1	G	A	17: 35,839,285 (GRCm39)		probably null	Het
Cdc42bpb	A	T	12: 111,265,783 (GRCm39)	V1383E	possibly damaging	Het
Cep350	T	C	1: 155,770,433 (GRCm39)	E1819G	probably damaging	Het
Ces4a	A	G	8: 105,869,054 (GRCm39)	E163G	possibly damaging	Het
Chrnd	C	T	1: 87,118,792 (GRCm39)	R50*	probably null	Het
Cntn3	A	G	6: 102,183,511 (GRCm39)	S715P	probably damaging	Het
Creb1	A	T	1: 64,598,909 (GRCm39)	R95S	probably benign	Het
Ctdp1	T	C	18: 80,492,710 (GRCm39)	Y595C	probably damaging	Het
Cts7	C	T	13: 61,504,223 (GRCm39)	E86K	probably damaging	Het
Dazap1	A	G	10: 80,113,440 (GRCm39)	N113S	unknown	Het
Dhdds	T	C	4: 133,727,706 (GRCm39)		probably null	Het
Dnaaf9	A	G	2: 130,554,938 (GRCm39)	S998P	probably damaging	Het
Dnah1	T	C	14: 30,985,395 (GRCm39)	D3832G	probably damaging	Het
Drd1	A	G	13: 54,207,182 (GRCm39)	L344P	probably damaging	Het
Fam135b	G	A	15: 71,324,199 (GRCm39)	T1256I	probably benign	Het
Fam234a	A	T	17: 26,432,627 (GRCm39)	D507E	probably benign	Het
Fbxw16	A	T	9: 109,278,169 (GRCm39)	I3N	probably benign	Het
Foxd4	A	T	19: 24,877,670 (GRCm39)	W177R	probably damaging	Het
Fyb2	A	G	4: 104,802,961 (GRCm39)	S288G	probably benign	Het
Gadl1	A	G	9: 115,789,519 (GRCm39)	H275R	probably benign	Het
Gbp5	A	G	3: 142,206,366 (GRCm39)	T17A	probably benign	Het
Gm1110	A	T	9: 26,800,894 (GRCm39)	Y433*	probably null	Het
Gm6408	C	A	5: 146,420,628 (GRCm39)	D169E	probably benign	Het
Gramd2b	T	A	18: 56,611,972 (GRCm39)	V145E	probably damaging	Het
Grip1	G	A	10: 119,874,569 (GRCm39)	E778K	possibly damaging	Het
Hcn1	GCA	GCAACA	13: 118,112,305 (GRCm39)		probably benign	Het
Hif1an	G	A	19: 44,558,378 (GRCm39)	V293M	probably damaging	Het
Hyal3	A	G	9: 107,462,347 (GRCm39)	D127G	probably damaging	Het
Ighg1	T	A	12: 113,293,252 (GRCm39)	D146V	possibly damaging	Het
Iws1	T	A	18: 32,216,347 (GRCm39)	D362E	probably damaging	Het
Kif21b	G	A	1: 136,080,961 (GRCm39)	E601K	probably damaging	Het
Kndc1	C	A	7: 139,500,620 (GRCm39)	P662T	possibly damaging	Het
Krtap13-1	C	T	16: 88,526,229 (GRCm39)	T151I	probably benign	Het
Ndufa10	A	T	1: 92,379,752 (GRCm39)	I327N	probably benign	Het
Or10ag53	A	G	2: 87,082,439 (GRCm39)	I53V	possibly damaging	Het
Pcdhb14	T	C	18: 37,582,040 (GRCm39)	V382A	probably benign	Het
Pex1	A	T	5: 3,685,876 (GRCm39)	I1206F	probably damaging	Het
Pi4k2b	T	A	5: 52,918,331 (GRCm39)	D386E	probably benign	Het
Pik3c2a	A	G	7: 115,945,427 (GRCm39)	F1460L	probably damaging	Het
Plcb2	A	C	2: 118,545,921 (GRCm39)	M588R	probably damaging	Het
Prl7d1	C	A	13: 27,893,260 (GRCm39)	R216L	possibly damaging	Het
Psg28	G	T	7: 18,156,887 (GRCm39)	Y449*	probably null	Het
Psg28	T	A	7: 18,164,602 (GRCm39)	T37S	probably benign	Het
Psmd9	G	T	5: 123,372,745 (GRCm39)	R76M	probably damaging	Het
Rfc1	T	C	5: 65,459,391 (GRCm39)	D189G	probably benign	Het
Rnf207	A	G	4: 152,397,666 (GRCm39)	S363P	probably benign	Het
Sco1	T	A	11: 66,949,250 (GRCm39)	D239E	probably damaging	Het
Sec24d	C	T	3: 123,136,803 (GRCm39)	T512M	probably damaging	Het
Shkbp1	T	C	7: 27,046,442 (GRCm39)	K441E	probably benign	Het
Slc44a5	A	T	3: 153,959,322 (GRCm39)	I338F	probably damaging	Het
Slc4a3	A	T	1: 75,534,319 (GRCm39)	I1161F	probably damaging	Het
Spmip11	T	A	15: 98,483,264 (GRCm39)	L65I	probably damaging	Het
Tnfsf9	T	A	17: 57,414,355 (GRCm39)	L261M	probably damaging	Het
Trim55	C	T	3: 19,699,498 (GRCm39)	R77C	probably damaging	Het
Vmn2r27	A	G	6: 124,168,637 (GRCm39)	I831T	possibly damaging	Het
Vwa3b	A	G	1: 37,081,438 (GRCm39)	I60V	probably benign	Het
Vwf	A	G	6: 125,603,230 (GRCm39)	N860S		Het
Zfp54	T	A	17: 21,654,149 (GRCm39)	N214K	probably benign	Het
Zfp707	T	C	15: 75,845,418 (GRCm39)	I94T		Het

Other mutations in Or10z1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01133:Or10z1	APN	1	174,078,092 (GRCm39)	missense	probably benign	0.41
IGL01765:Or10z1	APN	1	174,077,703 (GRCm39)	missense	probably damaging	1.00
IGL02718:Or10z1	APN	1	174,078,273 (GRCm39)	nonsense	probably null
IGL03208:Or10z1	APN	1	174,077,959 (GRCm39)	missense	probably damaging	1.00
BB009:Or10z1	UTSW	1	174,078,260 (GRCm39)	missense	probably benign	0.00
BB019:Or10z1	UTSW	1	174,078,260 (GRCm39)	missense	probably benign	0.00
R1406:Or10z1	UTSW	1	174,078,427 (GRCm39)	missense	possibly damaging	0.51
R1406:Or10z1	UTSW	1	174,078,427 (GRCm39)	missense	possibly damaging	0.51
R1760:Or10z1	UTSW	1	174,077,926 (GRCm39)	missense	probably damaging	0.99
R2138:Or10z1	UTSW	1	174,078,302 (GRCm39)	splice site	probably null
R2139:Or10z1	UTSW	1	174,078,302 (GRCm39)	splice site	probably null
R2869:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2869:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2871:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2871:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2872:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2872:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2873:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R2874:Or10z1	UTSW	1	174,078,092 (GRCm39)	missense	probably benign	0.41
R3854:Or10z1	UTSW	1	174,077,716 (GRCm39)	missense	probably damaging	1.00
R4614:Or10z1	UTSW	1	174,078,188 (GRCm39)	missense	possibly damaging	0.93
R4858:Or10z1	UTSW	1	174,078,262 (GRCm39)	missense	probably damaging	1.00
R5015:Or10z1	UTSW	1	174,078,448 (GRCm39)	missense	possibly damaging	0.91
R5138:Or10z1	UTSW	1	174,078,395 (GRCm39)	missense	probably damaging	0.97
R5296:Or10z1	UTSW	1	174,078,322 (GRCm39)	missense	possibly damaging	0.75
R5369:Or10z1	UTSW	1	174,078,007 (GRCm39)	missense	probably damaging	1.00
R6285:Or10z1	UTSW	1	174,078,395 (GRCm39)	missense	possibly damaging	0.62
R7655:Or10z1	UTSW	1	174,077,784 (GRCm39)	missense	probably damaging	1.00
R7656:Or10z1	UTSW	1	174,077,784 (GRCm39)	missense	probably damaging	1.00
R7753:Or10z1	UTSW	1	174,078,236 (GRCm39)	missense	probably benign	0.01
R7932:Or10z1	UTSW	1	174,078,260 (GRCm39)	missense	probably benign	0.00
R8179:Or10z1	UTSW	1	174,078,130 (GRCm39)	missense	possibly damaging	0.75
R9336:Or10z1	UTSW	1	174,077,679 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAAGAGAGTAGCTGGCTTTGG -3'
(R):5'- TGAATCCCACTGTCTGTGCC -3'

Sequencing Primer
(F):5'- CTTTGGGTCTCAAGTACATGAAG -3'
(R):5'- ACTGTCTGTGCCCAGCTAG -3'

Posted On

2022-11-14