Mutagenetix > Incidental Mutations

Incidental Mutation 'R5208:Olfr668'

402154

Institutional Source

Beutler Lab

Gene Symbol

Olfr668

Ensembl Gene

ENSMUSG00000057770

Gene Name

olfactory receptor 668

Synonyms

GA_x6K02T2PBJ9-7554614-7553658, MOR34-3

MMRRC Submission

042783-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.317) question?

Stock #

R5208 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

104922291-104928057 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 104925726 bp

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 13 (F13L)

Ref Sequence

ENSEMBL: ENSMUSP00000150824 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000164391] [ENSMUST00000215359] [ENSMUST00000217177]

Predicted Effect

probably benign
Transcript: ENSMUST00000164391
AA Change: F13L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000130975
Gene: ENSMUSG00000057770
AA Change: F13L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	33	313	7.2e-103	PFAM
Pfam:7TM_GPCR_Srsx	37	210	4.7e-10	PFAM
Pfam:7tm_1	43	295	4.6e-18	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000215359
AA Change: F13L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Predicted Effect

probably benign
Transcript: ENSMUST00000217177

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.3%
20x: 95.3%

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: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5830411N06Rik	C	A	7: 140,298,036	A977D	probably benign	Het
Aadacl4	A	T	4: 144,617,828	N58I	probably benign	Het
Adgra3	T	C	5: 50,011,515	D163G	probably damaging	Het
Alcam	C	A	16: 52,295,048	E236*	probably null	Het
Ank3	G	A	10: 70,002,565	R1566K	possibly damaging	Het
Aplf	G	T	6: 87,642,026		probably null	Het
Arl4a	A	T	12: 40,036,745	M1K	probably null	Het
Asic4	A	G	1: 75,451,226	D132G	probably damaging	Het
Bbs12	T	C	3: 37,320,273	I290T	probably benign	Het
BC024139	A	G	15: 76,124,665	S290P	probably benign	Het
Bmp6	G	A	13: 38,469,697	A247T	probably benign	Het
Cadps	A	G	14: 12,457,711	S1057P	possibly damaging	Het
Caprin1	A	C	2: 103,769,433		probably null	Het
Cdc42bpg	G	A	19: 6,321,720	R1343K	probably benign	Het
Cdk18	A	T	1: 132,117,480		probably null	Het
Cenpf	A	T	1: 189,671,046		probably null	Het
Cfhr1	A	T	1: 139,556,330		probably null	Het
Chn2	A	T	6: 54,295,801	I201F	probably damaging	Het
Chrdl2	A	G	7: 100,023,922	D175G	probably damaging	Het
Disp2	G	T	2: 118,791,805	R1006L	probably damaging	Het
Dnah2	C	T	11: 69,458,920	R2399Q	probably benign	Het
Dnah3	C	G	7: 120,032,638	D1365H	probably damaging	Het
Efcab8	T	A	2: 153,802,423	Y372*	probably null	Het
Eftud2	G	A	11: 102,841,185	P768S	probably damaging	Het
Ehmt1	A	C	2: 24,801,533	S1170A	probably benign	Het
Gdpd4	A	C	7: 98,014,911	K572Q	probably benign	Het
Gm7356	T	C	17: 14,001,194	E191G	probably damaging	Het
Gm8674	A	T	13: 49,901,921		noncoding transcript	Het
Gulp1	T	G	1: 44,781,039	H235Q	probably benign	Het
Hormad1	T	C	3: 95,578,107	V202A	possibly damaging	Het
Inpp5b	G	A	4: 124,751,317	D179N	possibly damaging	Het
Kcnk4	T	A	19: 6,927,701	Y194F	possibly damaging	Het
Lars	A	C	18: 42,217,557	S896A	probably benign	Het
Lonp1	A	G	17: 56,617,793	V538A	probably damaging	Het
Map3k14	A	T	11: 103,239,146	L315Q	probably damaging	Het
Met	T	A	6: 17,526,423	Y500*	probably null	Het
Mga	T	G	2: 119,947,981	I2093M	possibly damaging	Het
Mpl	T	G	4: 118,455,881	I152L	probably benign	Het
Mthfsd	G	A	8: 121,108,319		probably benign	Het
Mup4	A	G	4: 59,958,119	F150L	probably damaging	Het
Mybph	T	A	1: 134,193,535	V11D	probably benign	Het
Olfr1278	A	T	2: 111,292,601	E111V	probably damaging	Het
Olfr988	T	A	2: 85,353,798	I43F	probably benign	Het
Pde4a	T	C	9: 21,203,558		probably null	Het
Pex2	C	T	3: 5,561,368	R127H	probably benign	Het
Pgap3	A	G	11: 98,398,048	W94R	probably damaging	Het
Prl4a1	T	C	13: 28,018,484	V14A	probably benign	Het
Psg25	A	T	7: 18,526,535	I146N	probably benign	Het
Ptprn2	A	G	12: 116,858,928	Y209C	probably damaging	Het
Sema4c	T	A	1: 36,550,326	D573V	probably damaging	Het
Setx	A	T	2: 29,166,367	I2192F	possibly damaging	Het
Sp4	A	G	12: 118,299,546	L255P	probably damaging	Het
Spaca7	A	G	8: 12,586,456	Y94C	probably damaging	Het
Stt3a	T	G	9: 36,746,595	I390L	possibly damaging	Het
Tars2	A	G	3: 95,747,593	W128R	probably damaging	Het
Tll1	G	A	8: 64,051,493	T623M	probably damaging	Het
Tmem129	A	T	5: 33,655,506	V166E	probably damaging	Het
Tmem200a	T	A	10: 25,994,153	I73F	probably benign	Het
Tnks1bp1	T	C	2: 85,070,632	M1561T	probably damaging	Het
Ttc37	G	A	13: 76,147,767	E1050K	possibly damaging	Het
Zfat	A	T	15: 68,180,721	I401N	probably damaging	Het
Zfp142	A	T	1: 74,570,868	V1153E	probably benign	Het
Zwilch	T	C	9: 64,152,923	I354V	probably benign	Het

Other mutations in Olfr668

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01664:Olfr668	APN	7	104925104	missense	probably damaging	1.00
IGL02250:Olfr668	APN	7	104925015	missense	probably damaging	1.00
IGL02743:Olfr668	APN	7	104924868	missense	probably damaging	0.98
IGL03105:Olfr668	APN	7	104925764	unclassified	probably benign
IGL03252:Olfr668	APN	7	104925387	missense	probably benign	0.16
IGL03387:Olfr668	APN	7	104925373	missense	probably benign	0.01
R1534:Olfr668	UTSW	7	104925414	missense	possibly damaging	0.95
R2509:Olfr668	UTSW	7	104925687	missense	probably benign	0.40
R2510:Olfr668	UTSW	7	104925687	missense	probably benign	0.40
R4739:Olfr668	UTSW	7	104924810	missense	possibly damaging	0.91
R4995:Olfr668	UTSW	7	104925735	missense	probably benign	0.01
R5071:Olfr668	UTSW	7	104925493	missense	probably benign
R5074:Olfr668	UTSW	7	104925493	missense	probably benign
R5293:Olfr668	UTSW	7	104925279	missense	probably benign	0.00
R6061:Olfr668	UTSW	7	104925392	missense	probably benign	0.28
R6063:Olfr668	UTSW	7	104925392	missense	probably benign	0.28
R6064:Olfr668	UTSW	7	104925392	missense	probably benign	0.28
R6172:Olfr668	UTSW	7	104925296	missense	probably benign	0.40
R6492:Olfr668	UTSW	7	104925645	missense	possibly damaging	0.60
R6933:Olfr668	UTSW	7	104925123	missense	probably benign	0.21
R7040:Olfr668	UTSW	7	104925510	missense	probably benign	0.02
R7587:Olfr668	UTSW	7	104925056	missense	probably benign	0.28
R7841:Olfr668	UTSW	7	104924859	missense	possibly damaging	0.59
R7869:Olfr668	UTSW	7	104925104	missense	probably damaging	1.00
R7902:Olfr668	UTSW	7	104925350	missense	probably damaging	1.00
R8296:Olfr668	UTSW	7	104925621	missense	probably benign	0.00
Z1177:Olfr668	UTSW	7	104924993	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACACCAGGTAACATCAGTGAAG -3'
(R):5'- ACTGCTTAATCAACTGGTCAGC -3'

Sequencing Primer
(F):5'- TAACATCAGTGAAGGAGAGTAAGGCC -3'
(R):5'- ACTGGTCAGCTTCATATATCATGTC -3'

Posted On

2016-07-22