Mutagenetix > Incidental Mutations

Incidental Mutation 'R7784:Olfr434'

599432

Institutional Source

Beutler Lab

Gene Symbol

Olfr434

Ensembl Gene

ENSMUSG00000059411

Gene Name

olfactory receptor 434

Synonyms

GA_x6K02T2P3E9-4341246-4340281, MOR261-10

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.067) question?

Stock #

R7784 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

43213021-43218113 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 43217388 bp

Zygosity

Heterozygous

Amino Acid Change

Histidine to Glutamine at position 158 (H158Q)

Ref Sequence

ENSEMBL: ENSMUSP00000149678 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076752] [ENSMUST00000216562]

Predicted Effect

possibly damaging
Transcript: ENSMUST00000076752
AA Change: H158Q

PolyPhen 2 Score 0.817 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000076039
Gene: ENSMUSG00000059411
AA Change: H158Q

Domain	Start	End	E-Value	Type
Pfam:7tm_4	30	307	7.7e-62	PFAM
Pfam:7tm_1	40	289	2.1e-29	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000216562
AA Change: H158Q

PolyPhen 2 Score 0.817 (Sensitivity: 0.84; Specificity: 0.93)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

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: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	A	T	14: 32,659,840	S1389R	probably benign	Het
Abca9	A	T	11: 110,154,417	C363*	probably null	Het
Actbl2	T	A	13: 111,255,411	N93K	probably damaging	Het
Adamtsl3	T	C	7: 82,573,989	Y993H	probably damaging	Het
Adgrg1	G	A	8: 95,012,882	W653*	probably null	Het
Akap13	T	A	7: 75,610,328	V97D	probably benign	Het
Cacna1d	T	A	14: 30,123,439	D613V	probably damaging	Het
Col10a1	C	A	10: 34,394,218	P62H	unknown	Het
Cpb2	A	T	14: 75,275,040	N298Y	probably damaging	Het
Ddc	A	G	11: 11,839,396		probably null	Het
Ddx6	T	C	9: 44,630,142		probably null	Het
Epb42	T	G	2: 121,034,435	K58N	probably benign	Het
Eps8	T	A	6: 137,499,587	I605L	probably benign	Het
Eps8l1	T	C	7: 4,472,122	L304P	probably damaging	Het
Erbb4	T	A	1: 68,075,499	I929F	probably damaging	Het
Erc2	A	T	14: 27,898,594	N393I	probably damaging	Het
Fbxw25	C	T	9: 109,650,119	D355N		Het
Ffar2	T	C	7: 30,819,258	K286E	probably benign	Het
Gabrd	A	G	4: 155,388,932		probably null	Het
Ganc	G	A	2: 120,436,668	W488*	probably null	Het
Gm5724	C	T	6: 141,713,193		probably null	Het
Ifi207	T	A	1: 173,730,132	M347L	unknown	Het
Kat6b	A	T	14: 21,660,841	I619F	probably damaging	Het
Kif26a	A	G	12: 112,178,147	R1612G	possibly damaging	Het
Kifc3	A	G	8: 95,110,692		probably null	Het
Krt39	A	T	11: 99,521,031	C76*	probably null	Het
Lcmt1	G	T	7: 123,401,495	R84L	probably benign	Het
Lrit1	A	G	14: 37,061,780	Y355C	probably benign	Het
Med23	C	T	10: 24,902,448	T870M	probably damaging	Het
Mtmr6	A	G	14: 60,300,445	D593G	probably benign	Het
Myo15b	G	A	11: 115,861,340	V683M		Het
Neb	T	A	2: 52,235,488	M506L		Het
Olfr103	T	C	17: 37,336,578	Y218C	probably benign	Het
Olfr103	A	G	17: 37,337,055	F59S	probably damaging	Het
Olfr1154	G	A	2: 87,903,193	T161I	probably benign	Het
Pdzd8	A	G	19: 59,327,863	F294L	probably damaging	Het
Rabgap1	G	A	2: 37,487,532	S347N	possibly damaging	Het
Rasgrf2	T	C	13: 91,896,082	T350A		Het
Rbp3	A	T	14: 33,954,158	H21L	probably benign	Het
Rp1	C	A	1: 4,142,658	V1069F	unknown	Het
Rtn4	T	A	11: 29,741,048	L1113*	probably null	Het
Ryr3	A	G	2: 112,775,695	F2407L	probably damaging	Het
Sept2	T	A	1: 93,497,444	D107E	probably damaging	Het
Sept4	A	G	11: 87,579,008	T7A	probably benign	Het
Slc34a3	T	A	2: 25,232,225	I123F	probably damaging	Het
Slc9a4	T	C	1: 40,600,776	Y243H	probably damaging	Het
Slco1a1	T	A	6: 141,943,388	E66V	probably damaging	Het
Spata33	A	G	8: 123,213,252	R68G	unknown	Het
Spta1	G	A	1: 174,202,451	D928N	probably damaging	Het
St8sia5	A	G	18: 77,254,550	S319G	probably benign	Het
Tmem208	A	G	8: 105,328,833	D149G	possibly damaging	Het
Trank1	A	T	9: 111,364,103	I583F	probably damaging	Het
Trio	C	T	15: 27,763,994	V2015M	probably damaging	Het
Tsc22d1	C	T	14: 76,416,701	Q207*	probably null	Het
Tshr	A	G	12: 91,505,305	D143G	probably benign	Het
Txlna	C	T	4: 129,632,157	R299H	probably damaging	Het
Ush2a	A	T	1: 188,444,592	T1318S	possibly damaging	Het
Utp14b	A	G	1: 78,664,943	K186R	probably damaging	Het
Vars2	C	T	17: 35,658,158	A884T	possibly damaging	Het
Zfp354c	TCACACTCGGCACA	TCACA	11: 50,815,240		probably benign	Het
Zfp775	A	G	6: 48,619,249	Q19R	possibly damaging	Het

Other mutations in Olfr434

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00339:Olfr434	APN	6	43217848	missense	probably benign	0.00
R0347:Olfr434	UTSW	6	43217362	missense	probably benign
R1099:Olfr434	UTSW	6	43217624	missense	probably damaging	1.00
R1147:Olfr434	UTSW	6	43217212	missense	probably damaging	0.99
R1147:Olfr434	UTSW	6	43217212	missense	probably damaging	0.99
R1353:Olfr434	UTSW	6	43217690	missense	probably benign	0.41
R1570:Olfr434	UTSW	6	43217351	missense	probably benign
R1720:Olfr434	UTSW	6	43217560	missense	probably damaging	1.00
R2098:Olfr434	UTSW	6	43217503	missense	probably benign	0.02
R4707:Olfr434	UTSW	6	43216949	missense	probably benign	0.27
R4942:Olfr434	UTSW	6	43216994	missense	probably damaging	1.00
R5008:Olfr434	UTSW	6	43217057	missense	probably damaging	0.98
R5084:Olfr434	UTSW	6	43217660	missense	probably damaging	1.00
R6472:Olfr434	UTSW	6	43217359	missense	probably benign
R7592:Olfr434	UTSW	6	43217245	missense	probably damaging	1.00
R7756:Olfr434	UTSW	6	43217016	nonsense	probably null
R8056:Olfr434	UTSW	6	43217044	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GATGCATGACACAGACCTTTC -3'
(R):5'- TGACTGGATCCTCAGGATGG -3'

Sequencing Primer
(F):5'- GATGCATGACACAGACCTTTCTCTTC -3'
(R):5'- CACCAGGATGCGTGTGTAG -3'

Posted On

2019-11-26