Mutagenetix > Incidental Mutation

Incidental Mutation 'R0318:Or2z8'

65262

Institutional Source

Beutler Lab

Gene Symbol

Or2z8

Ensembl Gene

ENSMUSG00000069998

Gene Name

olfactory receptor family 2 subfamily Z member 8

Synonyms

MOR282-1, GA_x6K02T2NUPS-191522-192466, Olfr372

MMRRC Submission

038528-MU

Accession Numbers

Essential gene?

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

Stock #

R0318 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

72811504-72812519 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 72812244 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Methionine at position 240 (T240M)

Ref Sequence

ENSEMBL: ENSMUSP00000149288 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000093434] [ENSMUST00000215324]

AlphaFold

Q7TRY2

Predicted Effect

probably damaging
Transcript: ENSMUST00000093434
AA Change: T240M

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

SMART Domains

Protein: ENSMUSP00000132724
Gene: ENSMUSG00000069998
AA Change: T240M

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	2e-57	PFAM
Pfam:7TM_GPCR_Srsx	35	221	1.1e-7	PFAM
Pfam:7tm_1	41	290	6.4e-26	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000215324
AA Change: T240M

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

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 98.8%
3x: 97.7%
10x: 94.4%
20x: 86.5%

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: 54 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9130401M01Rik	A	T	15: 57,892,370 (GRCm39)	L79Q	probably damaging	Het
Add1	T	C	5: 34,782,684 (GRCm39)	V130A	probably damaging	Het
Ankrd23	G	T	1: 36,573,153 (GRCm39)	T73K	probably benign	Het
Blk	A	G	14: 63,611,646 (GRCm39)	Y430H	probably damaging	Het
C3	C	T	17: 57,531,709 (GRCm39)	V272M	probably damaging	Het
Cerk	C	T	15: 86,035,766 (GRCm39)	A254T	possibly damaging	Het
Ces2a	G	A	8: 105,467,456 (GRCm39)	A494T	probably damaging	Het
Cfap46	T	C	7: 139,234,482 (GRCm39)	Y258C	probably damaging	Het
Chaf1a	C	T	17: 56,369,227 (GRCm39)	T486I	possibly damaging	Het
Colec12	A	G	18: 9,848,446 (GRCm39)	N208S	possibly damaging	Het
Coro7	T	A	16: 4,493,671 (GRCm39)	H63L	probably benign	Het
Cps1	T	A	1: 67,216,173 (GRCm39)	W833R	probably damaging	Het
Csmd3	A	T	15: 47,522,549 (GRCm39)	W2707R	probably damaging	Het
Dbn1	C	T	13: 55,622,729 (GRCm39)	E585K	probably damaging	Het
Ddx50	A	T	10: 62,478,616 (GRCm39)	I190K	probably damaging	Het
Dnmt3l	G	A	10: 77,890,889 (GRCm39)	V264M	probably damaging	Het
Dnpep	A	G	1: 75,293,270 (GRCm39)	V33A	probably damaging	Het
Fam163a	A	G	1: 155,955,715 (GRCm39)	C26R	probably damaging	Het
Fam83h	A	G	15: 75,875,478 (GRCm39)	S620P	probably benign	Het
Fcna	A	G	2: 25,515,071 (GRCm39)	S263P	probably benign	Het
Fnip2	A	T	3: 79,419,685 (GRCm39)	S165R	probably damaging	Het
Fpr-rs3	T	C	17: 20,844,410 (GRCm39)	T244A	probably benign	Het
Gpr152	T	C	19: 4,193,541 (GRCm39)	S361P	possibly damaging	Het
Grm5	A	T	7: 87,252,175 (GRCm39)	I142L	probably damaging	Het
Gucy2g	A	G	19: 55,226,230 (GRCm39)	S229P	probably benign	Het
Htr7	C	T	19: 35,946,886 (GRCm39)	G376D	probably damaging	Het
Irgc	T	C	7: 24,131,896 (GRCm39)	D307G	probably benign	Het
Irs1	A	T	1: 82,266,381 (GRCm39)	S612T	probably benign	Het
Maml2	C	T	9: 13,531,890 (GRCm39)	T368I	probably damaging	Het
Mapkapk2	A	G	1: 131,025,072 (GRCm39)	V64A	probably damaging	Het
Marf1	C	T	16: 13,960,398 (GRCm39)	A549T	probably damaging	Het
Nptx1	C	T	11: 119,433,367 (GRCm39)	E411K	probably damaging	Het
Or5ak25	C	A	2: 85,268,581 (GRCm39)	R307M	possibly damaging	Het
Pcgf5	A	T	19: 36,389,590 (GRCm39)	K22N	possibly damaging	Het
Psmd9	C	A	5: 123,372,712 (GRCm39)	A65E	possibly damaging	Het
Sh3bp1	A	G	15: 78,795,907 (GRCm39)	T679A	probably damaging	Het
Sipa1l2	G	A	8: 126,174,436 (GRCm39)	P1281S	possibly damaging	Het
Slc17a3	C	T	13: 24,039,841 (GRCm39)	S293F	probably damaging	Het
Slc25a24	A	G	3: 109,064,316 (GRCm39)	M222V	probably benign	Het
Smg9	T	C	7: 24,120,313 (GRCm39)	F429S	possibly damaging	Het
Snapc1	C	T	12: 74,021,806 (GRCm39)	R81C	probably damaging	Het
Sorl1	T	A	9: 41,993,250 (GRCm39)	Y258F	probably damaging	Het
Srp72	C	T	5: 77,132,047 (GRCm39)	T242I	probably benign	Het
Stc1	A	T	14: 69,275,867 (GRCm39)	Q220L	probably damaging	Het
Tas2r122	T	C	6: 132,688,795 (GRCm39)	T33A	possibly damaging	Het
Tbc1d10b	A	G	7: 126,798,206 (GRCm39)	L645P	probably damaging	Het
Thoc2l	T	C	5: 104,665,619 (GRCm39)	F47S	probably benign	Het
Timd4	T	A	11: 46,727,898 (GRCm39)	H272Q	probably benign	Het
Ttll5	T	G	12: 85,923,368 (GRCm39)		probably null	Het
Veph1	G	T	3: 65,964,680 (GRCm39)	S783Y	probably damaging	Het
Vmn1r230	T	C	17: 21,067,078 (GRCm39)	L89S	possibly damaging	Het
Xcr1	A	G	9: 123,685,219 (GRCm39)	V165A	possibly damaging	Het
Zfp286	T	C	11: 62,675,788 (GRCm39)	D58G	probably damaging	Het
Zfyve26	C	T	12: 79,323,055 (GRCm39)	R897H	probably damaging	Het

Other mutations in Or2z8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03251:Or2z8	APN	8	72,811,920 (GRCm39)	missense	probably damaging	1.00
R0126:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0128:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0130:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0131:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0131:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0132:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0152:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0230:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0244:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0256:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0257:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0294:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0316:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0391:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0479:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0604:Or2z8	UTSW	8	72,812,244 (GRCm39)	missense	probably damaging	1.00
R0624:Or2z8	UTSW	8	72,812,006 (GRCm39)	missense	possibly damaging	0.94
R0631:Or2z8	UTSW	8	72,812,166 (GRCm39)	missense	probably damaging	0.99
R1785:Or2z8	UTSW	8	72,812,280 (GRCm39)	missense	probably damaging	1.00
R1786:Or2z8	UTSW	8	72,812,280 (GRCm39)	missense	probably damaging	1.00
R2040:Or2z8	UTSW	8	72,811,607 (GRCm39)	missense	possibly damaging	0.77
R4176:Or2z8	UTSW	8	72,812,028 (GRCm39)	missense	probably damaging	1.00
R4782:Or2z8	UTSW	8	72,811,938 (GRCm39)	missense	probably benign	0.00
R4799:Or2z8	UTSW	8	72,811,938 (GRCm39)	missense	probably benign	0.00
R6915:Or2z8	UTSW	8	72,811,574 (GRCm39)	missense	probably benign	0.19
R7512:Or2z8	UTSW	8	72,812,367 (GRCm39)	missense	probably damaging	1.00
R8255:Or2z8	UTSW	8	72,811,607 (GRCm39)	missense	possibly damaging	0.77
R9619:Or2z8	UTSW	8	72,811,605 (GRCm39)	missense	probably damaging	1.00
RF022:Or2z8	UTSW	8	72,812,468 (GRCm39)	makesense	probably null

Predicted Primers

Posted On

2013-08-08