Mutagenetix > Incidental Mutation

Incidental Mutation 'R5240:Or1e1f'

400750

Institutional Source

Beutler Lab

Gene Symbol

Or1e1f

Ensembl Gene

ENSMUSG00000057050

Gene Name

olfactory receptor family 1 subfamily E member 1F

Synonyms

Olfr397, GA_x6K02T2P1NL-4121434-4122381, MOR135-28

MMRRC Submission

042811-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.092) question?

Stock #

R5240 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

73855436-73856383 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 73855632 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 66 (L66P)

Ref Sequence

ENSEMBL: ENSMUSP00000150172 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000108465] [ENSMUST00000121280] [ENSMUST00000213134] [ENSMUST00000216291]

AlphaFold

Q8VEZ6

Predicted Effect

probably damaging
Transcript: ENSMUST00000108465
AA Change: L66P

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

SMART Domains

Protein: ENSMUSP00000104105
Gene: ENSMUSG00000062128
AA Change: L66P

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	7.9e-60	PFAM
Pfam:7TM_GPCR_Srsx	35	305	7.8e-8	PFAM
Pfam:7tm_1	41	290	1e-23	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000121280
AA Change: L66P

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

SMART Domains

Protein: ENSMUSP00000113870
Gene: ENSMUSG00000057050
AA Change: L66P

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	35	305	1.3e-6	PFAM
Pfam:7tm_1	41	290	4.3e-35	PFAM
Pfam:7tm_4	139	283	1.2e-44	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000213134
AA Change: L66P

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000215020

Predicted Effect

probably damaging
Transcript: ENSMUST00000216291
AA Change: L66P

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

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 95.1%

Validation Efficiency

100% (69/69)

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
Aadacl2fm2	A	C	3: 59,659,449 (GRCm39)	T301P	probably damaging	Het
Cdc42bpg	T	G	19: 6,365,929 (GRCm39)	L786R	probably damaging	Het
Cfap73	C	T	5: 120,767,772 (GRCm39)	V260I	probably damaging	Het
Chchd10	A	T	10: 75,773,283 (GRCm39)	N131I	probably damaging	Het
Chn2	T	C	6: 54,197,680 (GRCm39)	V190A	probably benign	Het
Clec2l	C	T	6: 38,650,387 (GRCm39)	T64I	probably damaging	Het
Cpeb3	T	A	19: 37,151,915 (GRCm39)	T154S	probably damaging	Het
D130043K22Rik	A	G	13: 25,061,960 (GRCm39)	E643G	probably damaging	Het
Ddx31	A	G	2: 28,736,042 (GRCm39)	M127V	probably benign	Het
Dennd1b	A	G	1: 138,990,615 (GRCm39)	Y193C	probably damaging	Het
Dgke	T	A	11: 88,941,511 (GRCm39)	D288V	probably damaging	Het
Dst	T	A	1: 34,247,639 (GRCm39)	L1683*	probably null	Het
Dusp29	G	A	14: 21,727,091 (GRCm39)	R186W	probably benign	Het
E130116L18Rik	G	T	5: 25,428,018 (GRCm39)		probably benign	Het
Eif2b5	G	A	16: 20,320,148 (GRCm39)	V115I	possibly damaging	Het
Fchsd1	C	T	18: 38,092,926 (GRCm39)		probably benign	Het
Fgfr3	A	T	5: 33,887,382 (GRCm39)	T234S	probably damaging	Het
Gipc2	A	T	3: 151,808,299 (GRCm39)	D251E	possibly damaging	Het
Gm11787	A	C	4: 3,511,810 (GRCm39)		noncoding transcript	Het
Haus6	A	G	4: 86,501,415 (GRCm39)	Y819H	possibly damaging	Het
Homez	G	A	14: 55,095,531 (GRCm39)	A59V	probably damaging	Het
Iffo1	T	C	6: 125,129,423 (GRCm39)	V363A	probably benign	Het
Ifit2	T	A	19: 34,551,796 (GRCm39)	D445E	probably benign	Het
Ipo9	A	C	1: 135,317,344 (GRCm39)		probably benign	Het
Kcnv1	C	T	15: 44,976,640 (GRCm39)	G216R	probably damaging	Het
Kdm6b	A	C	11: 69,292,730 (GRCm39)		probably benign	Het
Mplkip	T	C	13: 17,870,304 (GRCm39)	S79P	probably damaging	Het
Nae1	T	C	8: 105,249,776 (GRCm39)		probably benign	Het
Nfe2l2	A	T	2: 75,506,353 (GRCm39)	N582K	possibly damaging	Het
Nsmce4a	G	A	7: 130,138,754 (GRCm39)	R297C	probably damaging	Het
Or3a1d	T	A	11: 74,238,068 (GRCm39)	D114V	probably damaging	Het
Or5p70	A	T	7: 107,994,909 (GRCm39)	D194V	probably damaging	Het
Osbp	T	A	19: 11,955,654 (GRCm39)	F357I	probably damaging	Het
Pcdhb4	A	G	18: 37,442,979 (GRCm39)	D763G	possibly damaging	Het
Pcdhgb2	A	C	18: 37,824,103 (GRCm39)	I365L	possibly damaging	Het
Pde6g	A	G	11: 120,338,912 (GRCm39)		probably benign	Het
Pigo	C	A	4: 43,020,675 (GRCm39)	V756L	possibly damaging	Het
Pkhd1	G	T	1: 20,345,865 (GRCm39)	T2721K	probably benign	Het
Pls1	A	T	9: 95,658,675 (GRCm39)		probably null	Het
Prim2	A	G	1: 33,519,397 (GRCm39)		probably benign	Het
Prkd2	T	A	7: 16,589,711 (GRCm39)	I471N	probably benign	Het
Prrc2b	C	T	2: 32,096,408 (GRCm39)	T593I	probably benign	Het
Ptch2	C	A	4: 116,963,335 (GRCm39)		probably benign	Het
Pth	A	T	7: 112,985,051 (GRCm39)	D107E	probably damaging	Het
Pycr2	A	C	1: 180,735,188 (GRCm39)	Q315P	probably benign	Het
Rbpj	A	T	5: 53,806,782 (GRCm39)	Y209F	probably damaging	Het
Ripk4	C	A	16: 97,544,967 (GRCm39)	R560L	probably damaging	Het
Sdr42e1	T	C	8: 118,390,021 (GRCm39)	R207G	probably benign	Het
Sipa1l1	A	G	12: 82,388,362 (GRCm39)	Y196C	possibly damaging	Het
Smarcc2	T	C	10: 128,316,875 (GRCm39)		probably null	Het
Stom	T	A	2: 35,226,889 (GRCm39)	I15F	probably benign	Het
Sugp2	G	T	8: 70,695,925 (GRCm39)	L299F	probably benign	Het
Tbrg4	A	T	11: 6,567,516 (GRCm39)		probably null	Het
Tkt	G	T	14: 30,287,635 (GRCm39)	G210C	probably damaging	Het
Tmem163	G	A	1: 127,419,289 (GRCm39)		probably benign	Het
Trip12	A	G	1: 84,771,854 (GRCm39)	I98T	probably benign	Het
Unc5b	A	G	10: 60,610,419 (GRCm39)	I466T	probably damaging	Het
Unc79	T	A	12: 103,037,010 (GRCm39)	F599L	probably damaging	Het
Vav1	G	A	17: 57,604,122 (GRCm39)	E151K	probably damaging	Het
Vcan	T	G	13: 89,840,651 (GRCm39)	D1631A	probably benign	Het
Vmn2r4	A	C	3: 64,314,358 (GRCm39)	S208A	possibly damaging	Het
Zfp619	A	G	7: 39,186,642 (GRCm39)	T891A	possibly damaging	Het
Zfp672	A	G	11: 58,220,527 (GRCm39)		probably benign	Het
Znhit1	T	A	5: 137,011,235 (GRCm39)		probably null	Het

Other mutations in Or1e1f

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01797:Or1e1f	APN	11	73,855,644 (GRCm39)	missense	probably damaging	1.00
IGL01839:Or1e1f	APN	11	73,855,437 (GRCm39)	start codon destroyed	probably null	1.00
IGL02247:Or1e1f	APN	11	73,855,688 (GRCm39)	missense	probably benign	0.05
IGL02876:Or1e1f	APN	11	73,855,539 (GRCm39)	missense	possibly damaging	0.95
IGL03051:Or1e1f	APN	11	73,855,860 (GRCm39)	missense	probably benign	0.04
IGL03123:Or1e1f	APN	11	73,855,812 (GRCm39)	missense	probably damaging	1.00
IGL03401:Or1e1f	APN	11	73,856,388 (GRCm39)	utr 3 prime	probably benign
3-1:Or1e1f	UTSW	11	73,855,803 (GRCm39)	missense	possibly damaging	0.84
R0496:Or1e1f	UTSW	11	73,855,706 (GRCm39)	missense	probably benign	0.42
R0811:Or1e1f	UTSW	11	73,856,246 (GRCm39)	missense	probably benign	0.02
R0812:Or1e1f	UTSW	11	73,856,246 (GRCm39)	missense	probably benign	0.02
R1503:Or1e1f	UTSW	11	73,855,394 (GRCm39)	utr 5 prime	probably null
R2067:Or1e1f	UTSW	11	73,855,740 (GRCm39)	missense	probably damaging	1.00
R2111:Or1e1f	UTSW	11	73,855,740 (GRCm39)	missense	probably damaging	1.00
R4912:Or1e1f	UTSW	11	73,856,166 (GRCm39)	missense	probably damaging	1.00
R5656:Or1e1f	UTSW	11	73,855,536 (GRCm39)	missense	probably damaging	0.99
R5801:Or1e1f	UTSW	11	73,855,772 (GRCm39)	missense	probably benign	0.39
R6329:Or1e1f	UTSW	11	73,855,568 (GRCm39)	missense	possibly damaging	0.73
R6720:Or1e1f	UTSW	11	73,856,291 (GRCm39)	missense	probably damaging	1.00
R7149:Or1e1f	UTSW	11	73,856,257 (GRCm39)	missense	probably benign	0.01
R7283:Or1e1f	UTSW	11	73,855,634 (GRCm39)	missense	probably damaging	1.00
R8194:Or1e1f	UTSW	11	73,856,240 (GRCm39)	missense	probably benign	0.00
R8466:Or1e1f	UTSW	11	73,855,913 (GRCm39)	missense	probably damaging	1.00
R8472:Or1e1f	UTSW	11	73,856,223 (GRCm39)	missense	possibly damaging	0.78
R8882:Or1e1f	UTSW	11	73,855,940 (GRCm39)	missense	probably damaging	0.97
R9256:Or1e1f	UTSW	11	73,856,135 (GRCm39)	missense	probably benign	0.18
Z1176:Or1e1f	UTSW	11	73,856,123 (GRCm39)	frame shift	probably null
Z1177:Or1e1f	UTSW	11	73,855,586 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCAGAATTCCTCCTCCTGGG -3'
(R):5'- GTAGCCAAGATAGTGCCACCAG -3'

Sequencing Primer
(F):5'- GGGCTTGCCTATTGAACCACAC -3'
(R):5'- GCAGATGGCCACATAGCGATC -3'

Posted On

2016-07-06