Mutagenetix > Incidental Mutation

Incidental Mutation 'R5120:Or1e30'

392948

Institutional Source

Beutler Lab

Gene Symbol

Or1e30

Ensembl Gene

ENSMUSG00000069818

Gene Name

olfactory receptor family 1 subfamily E member 30

Synonyms

Olfr390, MOR135-26, GA_x6K02T2P1NL-3938806-3939741

MMRRC Submission

042708-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.144) question?

Stock #

R5120 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

73677766-73678701 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 73677790 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 9 (I9L)

Ref Sequence

ENSEMBL: ENSMUSP00000148992 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092919] [ENSMUST00000120081] [ENSMUST00000206815] [ENSMUST00000215161]

AlphaFold

Q8VEZ7

Predicted Effect

probably benign
Transcript: ENSMUST00000092919
AA Change: I9L

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000090598
Gene: ENSMUSG00000069818
AA Change: I9L

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	2.1e-61	PFAM
Pfam:7TM_GPCR_Srsx	35	305	7.2e-9	PFAM
Pfam:7tm_1	41	290	6.8e-28	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000120081
AA Change: I9L

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000113472
Gene: ENSMUSG00000069818
AA Change: I9L

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srsx	35	305	7.2e-9	PFAM
Pfam:7tm_1	41	290	1.4e-36	PFAM
Pfam:7tm_4	139	283	5.6e-45	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000206815
AA Change: I9L

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

Predicted Effect

probably benign
Transcript: ENSMUST00000215161
AA Change: I9L

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)

Meta Mutation Damage Score

0.1085

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.8%
20x: 90.6%

Validation Efficiency

100% (97/97)

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: 84 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310033P09Rik	A	G	11: 59,101,061 (GRCm39)	H225R	probably benign	Het
Abcc9	T	A	6: 142,602,344 (GRCm39)	I690F	probably benign	Het
Acp4	A	T	7: 43,906,395 (GRCm39)	D52E	probably damaging	Het
Adam17	T	C	12: 21,393,020 (GRCm39)		probably benign	Het
Adamts15	T	C	9: 30,832,872 (GRCm39)	E221G	probably damaging	Het
Aoc2	A	G	11: 101,216,540 (GRCm39)	T208A	probably benign	Het
Apoa4	T	G	9: 46,154,035 (GRCm39)	I212S	probably damaging	Het
Bptf	A	T	11: 106,964,211 (GRCm39)	M1598K	probably damaging	Het
Camsap3	G	A	8: 3,650,680 (GRCm39)	R209Q	probably damaging	Het
Ccdc171	C	A	4: 83,476,763 (GRCm39)		probably benign	Het
Celsr2	G	C	3: 108,300,436 (GRCm39)	P2875A	probably benign	Het
Cenpb	A	G	2: 131,021,738 (GRCm39)	V20A	probably benign	Het
Cfap61	A	T	2: 145,985,080 (GRCm39)	K975*	probably null	Het
Cfhr4	T	C	1: 139,680,841 (GRCm39)	S226G	probably benign	Het
Col9a2	G	T	4: 120,896,969 (GRCm39)	A20S	unknown	Het
Crnn	A	T	3: 93,056,203 (GRCm39)	I330F	probably benign	Het
Csf3r	C	A	4: 125,929,620 (GRCm39)	P381Q	probably benign	Het
Csmd3	G	A	15: 48,536,891 (GRCm39)	Q104*	probably null	Het
Ctnna1	G	A	18: 35,315,607 (GRCm39)		probably null	Het
Cwf19l2	C	T	9: 3,418,761 (GRCm39)	Q183*	probably null	Het
Ddx60	T	C	8: 62,398,940 (GRCm39)	Y220H	probably benign	Het
Dhh	T	C	15: 98,796,038 (GRCm39)	Q39R	probably benign	Het
Dynlrb2	T	A	8: 117,242,437 (GRCm39)	I89N	possibly damaging	Het
Dytn	T	C	1: 63,662,202 (GRCm39)	E645G	probably benign	Het
Efcab7	A	G	4: 99,754,688 (GRCm39)	T287A	probably damaging	Het
Eogt	A	G	6: 97,111,276 (GRCm39)	V195A	probably benign	Het
Ep400	G	T	5: 110,904,224 (GRCm39)	P125Q	probably damaging	Het
Fasn	A	G	11: 120,702,217 (GRCm39)	V1815A	probably benign	Het
Gm5866	T	C	5: 52,740,224 (GRCm39)		noncoding transcript	Het
Gm8674	C	A	13: 50,055,984 (GRCm39)		noncoding transcript	Het
Gpat4	G	T	8: 23,670,218 (GRCm39)	H270Q	possibly damaging	Het
Grik5	A	G	7: 24,710,065 (GRCm39)	L890P	probably damaging	Het
Gsap	A	G	5: 21,474,934 (GRCm39)	N500S	probably damaging	Het
H2-M10.1	T	C	17: 36,636,048 (GRCm39)	D173G	probably benign	Het
Igfn1	T	A	1: 135,901,240 (GRCm39)	I413F	possibly damaging	Het
Ighv1-52	G	T	12: 115,109,406 (GRCm39)	H17N	probably benign	Het
Kcnu1	T	A	8: 26,424,516 (GRCm39)	D270E	possibly damaging	Het
Kif16b	A	C	2: 142,690,259 (GRCm39)	N274K	probably damaging	Het
Klk1b11	C	T	7: 43,648,446 (GRCm39)	T151I	probably benign	Het
Krtap13	A	G	16: 88,548,458 (GRCm39)	F10S	probably damaging	Het
Large1	A	T	8: 73,585,969 (GRCm39)	I379N	probably damaging	Het
Lhx8	T	C	3: 154,017,332 (GRCm39)	H301R	probably damaging	Het
Lrriq3	T	C	3: 154,835,021 (GRCm39)	V252A	probably benign	Het
Lysmd3	T	A	13: 81,817,311 (GRCm39)	I96N	probably damaging	Het
Mpeg1	C	T	19: 12,438,793 (GRCm39)	Q84*	probably null	Het
Myoz1	C	T	14: 20,700,722 (GRCm39)	G165D	probably benign	Het
Myt1	G	A	2: 181,439,413 (GRCm39)	V312I	probably benign	Het
Ndufb7	T	C	8: 84,293,606 (GRCm39)		probably benign	Het
Numa1	C	T	7: 101,626,644 (GRCm39)	T10M	probably damaging	Het
Or10d1b	T	A	9: 39,613,366 (GRCm39)	H233L	probably benign	Het
Or2g7	A	T	17: 38,378,157 (GRCm39)	I32F	probably damaging	Het
Or4f14d	A	T	2: 111,960,903 (GRCm39)	D84E	probably damaging	Het
Or4k39	T	C	2: 111,239,585 (GRCm39)		noncoding transcript	Het
Osmr	A	T	15: 6,856,756 (GRCm39)	S464T	probably benign	Het
Pak5	G	A	2: 135,925,149 (GRCm39)	H718Y	probably damaging	Het
Pan2	T	A	10: 128,150,864 (GRCm39)		probably null	Het
Pik3r4	T	C	9: 105,546,208 (GRCm39)	S853P	probably benign	Het
Pnkp	C	T	7: 44,511,827 (GRCm39)	S113L	probably damaging	Het
Polr3gl	T	A	3: 96,485,795 (GRCm39)		probably benign	Het
Psd2	G	A	18: 36,112,863 (GRCm39)	R186Q	possibly damaging	Het
Psd4	T	C	2: 24,295,450 (GRCm39)	V868A	probably benign	Het
Ralgapa2	G	T	2: 146,254,004 (GRCm39)	T852K	probably benign	Het
Rbm43	T	C	2: 51,822,435 (GRCm39)		probably benign	Het
Rps6kl1	C	A	12: 85,186,122 (GRCm39)	G329C	probably damaging	Het
Scaf11	T	C	15: 96,317,423 (GRCm39)	T714A	probably benign	Het
Selenoo	C	A	15: 88,978,508 (GRCm39)	N310K	possibly damaging	Het
Sepsecs	T	C	5: 52,818,003 (GRCm39)	Q258R	probably damaging	Het
Sgcz	T	C	8: 37,993,420 (GRCm39)	S226G	probably benign	Het
Slfn5	A	G	11: 82,851,754 (GRCm39)	K627E	probably damaging	Het
Sos1	A	T	17: 80,715,677 (GRCm39)	F1027I	probably damaging	Het
Ssh1	C	G	5: 114,095,459 (GRCm39)	V228L	possibly damaging	Het
Sugp1	C	A	8: 70,501,317 (GRCm39)	P65T	probably benign	Het
Tas2r106	T	A	6: 131,655,779 (GRCm39)	N24I	probably damaging	Het
Tex10	T	C	4: 48,459,272 (GRCm39)	E534G	possibly damaging	Het
Tmem182	C	T	1: 40,894,061 (GRCm39)	T192I	possibly damaging	Het
Traf7	T	A	17: 24,737,718 (GRCm39)	K51*	probably null	Het
Trap1	C	A	16: 3,861,952 (GRCm39)	R604L	probably damaging	Het
Trim6	T	A	7: 103,877,447 (GRCm39)	L179Q	probably damaging	Het
Ubfd1	T	C	7: 121,670,973 (GRCm39)	S264P	probably damaging	Het
Upk3bl	T	C	5: 136,093,045 (GRCm39)		probably benign	Het
Wdfy3	T	A	5: 102,015,972 (GRCm39)	Q2601L	possibly damaging	Het
Wdr89	A	G	12: 75,679,412 (GRCm39)	Y281H	probably damaging	Het
Zfp286	A	T	11: 62,671,551 (GRCm39)	M174K	probably benign	Het
Zmym1	T	C	4: 126,945,230 (GRCm39)		probably null	Het

Other mutations in Or1e30

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00402:Or1e30	APN	11	73,678,406 (GRCm39)	missense	probably damaging	1.00
IGL01621:Or1e30	APN	11	73,678,103 (GRCm39)	missense	probably damaging	0.99
IGL01630:Or1e30	APN	11	73,678,687 (GRCm39)	missense	probably benign	0.14
IGL01866:Or1e30	APN	11	73,678,654 (GRCm39)	missense	probably benign	0.28
IGL02577:Or1e30	APN	11	73,677,872 (GRCm39)	missense	probably damaging	1.00
IGL02617:Or1e30	APN	11	73,678,560 (GRCm39)	missense	probably benign	0.01
IGL03017:Or1e30	APN	11	73,678,344 (GRCm39)	missense	probably benign	0.01
IGL03215:Or1e30	APN	11	73,678,211 (GRCm39)	missense	probably damaging	1.00
IGL03342:Or1e30	APN	11	73,678,309 (GRCm39)	missense	probably benign	0.03
IGL03098:Or1e30	UTSW	11	73,678,529 (GRCm39)	missense	probably benign	0.29
R0115:Or1e30	UTSW	11	73,678,141 (GRCm39)	missense	possibly damaging	0.45
R0217:Or1e30	UTSW	11	73,678,214 (GRCm39)	missense	possibly damaging	0.90
R1971:Or1e30	UTSW	11	73,678,616 (GRCm39)	missense	probably damaging	1.00
R2033:Or1e30	UTSW	11	73,678,264 (GRCm39)	missense	probably benign	0.15
R2058:Or1e30	UTSW	11	73,678,100 (GRCm39)	missense	probably benign	0.00
R3051:Or1e30	UTSW	11	73,678,060 (GRCm39)	missense	probably benign	0.01
R3622:Or1e30	UTSW	11	73,678,567 (GRCm39)	missense	probably benign	0.00
R3913:Or1e30	UTSW	11	73,678,522 (GRCm39)	missense	probably damaging	1.00
R4545:Or1e30	UTSW	11	73,677,992 (GRCm39)	missense	probably damaging	1.00
R4656:Or1e30	UTSW	11	73,678,337 (GRCm39)	missense	probably damaging	1.00
R5635:Or1e30	UTSW	11	73,678,460 (GRCm39)	missense	probably benign	0.26
R6020:Or1e30	UTSW	11	73,678,378 (GRCm39)	missense	probably benign	0.03
R6151:Or1e30	UTSW	11	73,678,521 (GRCm39)	nonsense	probably null
R6885:Or1e30	UTSW	11	73,677,926 (GRCm39)	missense	possibly damaging	0.94
R6984:Or1e30	UTSW	11	73,678,603 (GRCm39)	missense	possibly damaging	0.91
R7057:Or1e30	UTSW	11	73,677,974 (GRCm39)	missense	possibly damaging	0.88
R7120:Or1e30	UTSW	11	73,677,940 (GRCm39)	missense	probably damaging	0.98
R7704:Or1e30	UTSW	11	73,678,616 (GRCm39)	missense	probably damaging	1.00
R8323:Or1e30	UTSW	11	73,677,766 (GRCm39)	start codon destroyed	probably damaging	1.00
R9100:Or1e30	UTSW	11	73,678,687 (GRCm39)	missense	probably benign	0.14
R9258:Or1e30	UTSW	11	73,678,281 (GRCm39)	missense	probably benign	0.28
R9384:Or1e30	UTSW	11	73,677,796 (GRCm39)	missense	probably benign
R9421:Or1e30	UTSW	11	73,677,927 (GRCm39)	missense	probably benign	0.23
R9450:Or1e30	UTSW	11	73,678,101 (GRCm39)	missense	possibly damaging	0.56
R9698:Or1e30	UTSW	11	73,678,442 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCAAAGCATTAAGTTACTTATCACT -3'
(R):5'- GCAACTTGGGCATAGTGACA -3'

Sequencing Primer
(F):5'- TGTAAAGCACTTGTCTT -3'
(R):5'- TCAGAGAAGGACAAGTTGCTG -3'

Posted On

2016-06-15