Mutagenetix > Incidental Mutation

Incidental Mutation 'R1946:Olfr1469'

216724

Institutional Source

Beutler Lab

Gene Symbol

Olfr1469

Ensembl Gene

ENSMUSG00000063777

Gene Name

olfactory receptor 1469

Synonyms

GA_x6K02T2RE5P-3743369-3744289, MOR202-11

MMRRC Submission

039964-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.101) question?

Stock #

R1946 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

13407849-13414540 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 13410779 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 70 (V70A)

Ref Sequence

ENSEMBL: ENSMUSP00000150006 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077538] [ENSMUST00000216910]

AlphaFold

Q8VFW5

Predicted Effect

possibly damaging
Transcript: ENSMUST00000077538
AA Change: V70A

PolyPhen 2 Score 0.640 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000076741
Gene: ENSMUSG00000063777
AA Change: V70A

Domain	Start	End	E-Value	Type
Pfam:7tm_4	32	308	2e-47	PFAM
Pfam:7tm_1	42	290	2.3e-19	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000216910
AA Change: V70A

PolyPhen 2 Score 0.640 (Sensitivity: 0.87; Specificity: 0.91)

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.7%
20x: 93.8%

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: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdh	A	G	5: 76,891,704 (GRCm38)	S253P	probably damaging	Het
Adamts5	C	A	16: 85,899,243 (GRCm38)	C342F	probably damaging	Het
Adgrv1	C	T	13: 81,374,249 (GRCm38)	C5923Y	probably damaging	Het
Aen	G	C	7: 78,902,672 (GRCm38)	E32Q	probably damaging	Het
Apba2	T	C	7: 64,744,630 (GRCm38)		probably null	Het
Arhgap44	A	G	11: 65,012,096 (GRCm38)	M509T	probably damaging	Het
Arpc1b	A	G	5: 145,122,633 (GRCm38)	T56A	probably null	Het
Atoh1	T	C	6: 64,729,459 (GRCm38)	V46A	probably benign	Het
Bmpr2	T	C	1: 59,868,397 (GRCm38)	V883A	possibly damaging	Het
Bpifa1	A	T	2: 154,145,634 (GRCm38)	I135F	probably damaging	Het
Bsn	A	G	9: 108,114,651 (GRCm38)	F1301L	probably damaging	Het
Capn13	T	C	17: 73,350,525 (GRCm38)	E240G	possibly damaging	Het
Ccdc18	A	G	5: 108,228,995 (GRCm38)	E1434G	probably damaging	Het
Coq8b	G	A	7: 27,239,874 (GRCm38)	V150I	possibly damaging	Het
Cpn1	G	A	19: 43,956,518 (GRCm38)	T450M	probably benign	Het
Dlg4	A	G	11: 70,039,575 (GRCm38)	Y432C	probably damaging	Het
Dnah8	C	A	17: 30,712,385 (GRCm38)	T1458K	probably benign	Het
Dock5	A	T	14: 67,786,316 (GRCm38)	M1132K	probably damaging	Het
Dsg2	A	G	18: 20,580,548 (GRCm38)	D192G	probably damaging	Het
F930017D23Rik	G	A	10: 43,593,444 (GRCm38)		noncoding transcript	Het
Fndc11	A	T	2: 181,221,834 (GRCm38)	D144V	probably benign	Het
Fut2	A	G	7: 45,651,324 (GRCm38)	F8S	probably damaging	Het
Gad2	A	T	2: 22,685,428 (GRCm38)	T515S	probably benign	Het
Ganab	T	A	19: 8,910,808 (GRCm38)	D439E	probably damaging	Het
Gm10228	C	A	16: 89,041,353 (GRCm38)	G21V	unknown	Het
Gm13119	T	A	4: 144,361,865 (GRCm38)	V77E	probably benign	Het
Gm9573	A	T	17: 35,622,524 (GRCm38)		probably benign	Het
Grm3	A	G	5: 9,512,123 (GRCm38)	W576R	probably damaging	Het
Gsdmc4	C	A	15: 63,902,780 (GRCm38)	D51Y	probably benign	Het
Hmcn2	T	C	2: 31,405,635 (GRCm38)	S2619P	probably damaging	Het
Kcnq2	T	A	2: 181,088,451 (GRCm38)	D446V	probably benign	Het
Kera	A	G	10: 97,609,147 (GRCm38)	K123E	probably benign	Het
Kmt2c	A	T	5: 25,315,154 (GRCm38)	V1986E	probably benign	Het
Lrp11	T	C	10: 7,623,776 (GRCm38)	Y244H	probably damaging	Het
Lrp1b	T	A	2: 40,665,147 (GRCm38)	D320V	unknown	Het
Lrrcc1	A	G	3: 14,550,393 (GRCm38)	R394G	probably benign	Het
Lrrk2	G	A	15: 91,736,661 (GRCm38)		probably null	Het
Map4k5	A	T	12: 69,845,755 (GRCm38)	D133E	probably damaging	Het
Megf11	A	T	9: 64,679,276 (GRCm38)	D461V	probably damaging	Het
Msrb3	A	G	10: 120,852,008 (GRCm38)	V54A	probably damaging	Het
Ncoa3	T	A	2: 166,059,177 (GRCm38)	N896K	possibly damaging	Het
Ncor2	G	A	5: 125,034,412 (GRCm38)	T1314I	probably damaging	Het
Nes	A	G	3: 87,978,514 (GRCm38)	Q1316R	possibly damaging	Het
Nfe2l3	A	C	6: 51,457,315 (GRCm38)	Q285P	probably damaging	Het
Nkd1	C	T	8: 88,592,117 (GRCm38)	H357Y	probably damaging	Het
Nmt2	T	A	2: 3,322,635 (GRCm38)	I355N	probably benign	Het
Olfr1333	T	C	4: 118,830,026 (GRCm38)	N139S	probably benign	Het
Olfr1354	T	A	10: 78,916,924 (GRCm38)	I28N	probably damaging	Het
Olfr147	T	A	9: 38,402,886 (GRCm38)	M1K	probably null	Het
Olfr290	T	C	7: 84,916,279 (GRCm38)	S167P	probably benign	Het
Olfr353	A	T	2: 36,890,446 (GRCm38)	M134K	possibly damaging	Het
Otx1	G	T	11: 21,998,482 (GRCm38)	T46K	probably damaging	Het
Panx1	A	G	9: 15,007,526 (GRCm38)	C346R	probably benign	Het
Pcdhb16	T	A	18: 37,478,899 (GRCm38)	L304*	probably null	Het
Plet1	A	G	9: 50,504,352 (GRCm38)		probably null	Het
Plod2	A	G	9: 92,607,135 (GRCm38)	S707G	probably damaging	Het
Plscr4	G	A	9: 92,483,836 (GRCm38)	V120I	probably damaging	Het
Ppp1r12b	A	G	1: 134,892,270 (GRCm38)	V245A	probably damaging	Het
Ppp2r2d	A	G	7: 138,868,467 (GRCm38)	D19G	probably damaging	Het
Rimbp3	G	A	16: 17,210,427 (GRCm38)	V572I	probably benign	Het
Ror2	T	C	13: 53,131,849 (GRCm38)	I110V	probably damaging	Het
Sec24d	A	T	3: 123,353,394 (GRCm38)	H667L	probably benign	Het
Sema3d	A	G	5: 12,573,843 (GRCm38)	Q573R	probably damaging	Het
Snx19	T	A	9: 30,432,324 (GRCm38)	N593K	probably damaging	Het
Sulf1	T	C	1: 12,796,907 (GRCm38)	V105A	probably benign	Het
Syngr3	T	C	17: 24,687,706 (GRCm38)	N45S	probably benign	Het
Tenm4	A	T	7: 96,735,808 (GRCm38)	H524L	probably damaging	Het
Tex30	C	T	1: 44,091,404 (GRCm38)	G68D	probably damaging	Het
Tmem43	A	T	6: 91,486,909 (GRCm38)	I389F	probably benign	Het
Trpm1	A	T	7: 64,223,808 (GRCm38)	N488Y	probably damaging	Het
Usf2	T	C	7: 30,956,238 (GRCm38)	T1A	probably null	Het
Vill	A	T	9: 119,058,492 (GRCm38)	H108L	probably benign	Het
Vmn1r16	T	C	6: 57,322,900 (GRCm38)	I246V	probably benign	Het
Vmn1r188	T	G	13: 22,088,645 (GRCm38)	S256R	possibly damaging	Het
Zfp12	G	A	5: 143,245,378 (GRCm38)	E487K	probably damaging	Het
Zfp24	AC	A	18: 24,014,419 (GRCm38)		probably null	Het

Other mutations in Olfr1469

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01064:Olfr1469	APN	19	13,411,226 (GRCm38)	missense	probably benign	0.01
IGL01520:Olfr1469	APN	19	13,410,750 (GRCm38)	missense	probably damaging	0.97
IGL01671:Olfr1469	APN	19	13,410,891 (GRCm38)	missense	probably benign	0.29
IGL02247:Olfr1469	APN	19	13,411,467 (GRCm38)	missense	probably benign	0.01
IGL02297:Olfr1469	APN	19	13,411,475 (GRCm38)	missense	probably benign	0.00
IGL02417:Olfr1469	APN	19	13,410,895 (GRCm38)	missense	possibly damaging	0.52
IGL02442:Olfr1469	APN	19	13,410,987 (GRCm38)	missense	probably benign	0.00
IGL02989:Olfr1469	APN	19	13,411,486 (GRCm38)	missense	probably benign
IGL03269:Olfr1469	APN	19	13,411,428 (GRCm38)	missense	probably damaging	0.99
IGL02988:Olfr1469	UTSW	19	13,411,462 (GRCm38)	missense	possibly damaging	0.75
R0707:Olfr1469	UTSW	19	13,411,420 (GRCm38)	missense	probably benign	0.22
R1055:Olfr1469	UTSW	19	13,411,390 (GRCm38)	missense	probably benign	0.10
R1102:Olfr1469	UTSW	19	13,411,090 (GRCm38)	missense	probably damaging	1.00
R2111:Olfr1469	UTSW	19	13,410,943 (GRCm38)	missense	probably damaging	0.99
R4072:Olfr1469	UTSW	19	13,410,935 (GRCm38)	missense	possibly damaging	0.49
R4073:Olfr1469	UTSW	19	13,410,935 (GRCm38)	missense	possibly damaging	0.49
R4076:Olfr1469	UTSW	19	13,410,935 (GRCm38)	missense	possibly damaging	0.49
R4726:Olfr1469	UTSW	19	13,411,105 (GRCm38)	missense	probably damaging	1.00
R4939:Olfr1469	UTSW	19	13,410,855 (GRCm38)	missense	probably benign	0.10
R5914:Olfr1469	UTSW	19	13,410,962 (GRCm38)	missense	probably benign	0.31
R6003:Olfr1469	UTSW	19	13,411,039 (GRCm38)	missense	probably benign	0.34
R6743:Olfr1469	UTSW	19	13,410,593 (GRCm38)	missense	probably damaging	1.00
R6825:Olfr1469	UTSW	19	13,411,150 (GRCm38)	missense	probably benign	0.01
R6826:Olfr1469	UTSW	19	13,411,088 (GRCm38)	missense	probably benign	0.05
R6970:Olfr1469	UTSW	19	13,411,428 (GRCm38)	missense	probably damaging	0.99
R7558:Olfr1469	UTSW	19	13,410,991 (GRCm38)	missense	probably damaging	1.00
R7596:Olfr1469	UTSW	19	13,411,147 (GRCm38)	missense	probably benign	0.01
R7923:Olfr1469	UTSW	19	13,410,818 (GRCm38)	missense	probably benign	0.17
R8014:Olfr1469	UTSW	19	13,410,811 (GRCm38)	missense	not run
R8506:Olfr1469	UTSW	19	13,411,240 (GRCm38)	missense	possibly damaging	0.49
R8746:Olfr1469	UTSW	19	13,410,728 (GRCm38)	missense	probably benign	0.44
R8803:Olfr1469	UTSW	19	13,410,673 (GRCm38)	missense	probably damaging	0.99
R9112:Olfr1469	UTSW	19	13,411,111 (GRCm38)	missense	probably benign	0.05
R9721:Olfr1469	UTSW	19	13,410,970 (GRCm38)	missense	probably benign	0.17
Z1177:Olfr1469	UTSW	19	13,410,719 (GRCm38)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- ACCGATGTTACACAGTTTCTCCTG -3'
(R):5'- CACACATTTGCAGTCATGGTG -3'

Sequencing Primer
(F):5'- TGCTGGGACTCACTGATGAC -3'
(R):5'- CAAGGGCTTGCACACTGCTG -3'

Posted On

2014-08-01