Mutagenetix > Incidental Mutation

Incidental Mutation 'R5604:Or1e35'

439201

Institutional Source

Beutler Lab

Gene Symbol

Or1e35

Ensembl Gene

ENSMUSG00000062186

Gene Name

olfactory receptor family 1 subfamily E member 35

Synonyms

MOR135-10, GA_x6K02T2P1NL-4062605-4061667, Olfr395

MMRRC Submission

043156-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R5604 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

73797378-73798316 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 73797853 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 155 (H155L)

Ref Sequence

ENSEMBL: ENSMUSP00000149064 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072991] [ENSMUST00000215690]

AlphaFold

Q8VGR3

Predicted Effect

probably benign
Transcript: ENSMUST00000072991
AA Change: H155L

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

SMART Domains

Protein: ENSMUSP00000072756
Gene: ENSMUSG00000062186
AA Change: H155L

Domain	Start	End	E-Value	Type
low complexity region	8	17	N/A	INTRINSIC
Pfam:7tm_4	31	309	6.2e-56	PFAM
Pfam:7TM_GPCR_Srsx	35	305	2.8e-8	PFAM
Pfam:7tm_1	41	290	3.7e-24	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000215690
AA Change: H155L

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.6%
20x: 96.3%

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: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310034C09Rik	A	T	16: 88,556,278 (GRCm39)	N164I	possibly damaging	Het
4933402J07Rik	C	A	8: 88,295,125 (GRCm39)	R88S	possibly damaging	Het
Abca1	A	T	4: 53,067,168 (GRCm39)		probably null	Het
Abca13	T	A	11: 9,516,279 (GRCm39)	I4406K	probably damaging	Het
Adam6b	T	A	12: 113,454,420 (GRCm39)	Y412*	probably null	Het
Ahcyl2	C	T	6: 29,908,366 (GRCm39)	H370Y	probably damaging	Het
Ahi1	A	G	10: 20,862,904 (GRCm39)	Y693C	probably damaging	Het
Anapc4	T	A	5: 52,999,076 (GRCm39)	Y129*	probably null	Het
Ankrd35	A	G	3: 96,592,215 (GRCm39)	T834A	probably benign	Het
Antxr2	T	C	5: 98,096,169 (GRCm39)	K372E	probably damaging	Het
Arhgef1	C	T	7: 24,612,210 (GRCm39)	H198Y	probably benign	Het
Barhl2	T	C	5: 106,603,412 (GRCm39)	E249G	probably benign	Het
C2cd5	T	C	6: 142,957,747 (GRCm39)	E987G	probably benign	Het
C87436	T	C	6: 86,424,337 (GRCm39)	S290P	probably benign	Het
Ccser1	C	T	6: 61,290,788 (GRCm39)	T490M	probably damaging	Het
Cd8b1	T	C	6: 71,303,159 (GRCm39)	V78A	probably benign	Het
Cdc25c	A	G	18: 34,866,701 (GRCm39)	Y374H	probably damaging	Het
Cmya5	C	T	13: 93,229,271 (GRCm39)	R1939H	probably benign	Het
Cyp2d40	A	G	15: 82,648,256 (GRCm39)	F19S	probably damaging	Het
Dll3	A	G	7: 27,994,057 (GRCm39)	V460A	probably benign	Het
Dnajb12	GC	G	10: 59,728,574 (GRCm39)		probably null	Het
E4f1	A	G	17: 24,663,118 (GRCm39)	I729T	probably damaging	Het
Endou	A	C	15: 97,618,800 (GRCm39)	S75A	probably benign	Het
Epas1	C	T	17: 87,113,200 (GRCm39)	H129Y	probably damaging	Het
Grm1	T	A	10: 10,622,479 (GRCm39)	N415Y	probably damaging	Het
Hdc	A	T	2: 126,436,583 (GRCm39)	S429R	probably benign	Het
Hnf4g	C	T	3: 3,722,186 (GRCm39)	Q447*	probably null	Het
Htr6	C	T	4: 138,788,814 (GRCm39)	A414T	probably benign	Het
Insig1	T	C	5: 28,280,080 (GRCm39)	L224P	probably damaging	Het
Ipo9	G	A	1: 135,329,983 (GRCm39)	L486F	probably damaging	Het
Irak2	T	A	6: 113,667,792 (GRCm39)	S458T	possibly damaging	Het
Irs2	A	G	8: 11,055,007 (GRCm39)	S1142P	possibly damaging	Het
Kirrel1	T	A	3: 86,996,462 (GRCm39)	N379I	possibly damaging	Het
L3mbtl4	T	A	17: 69,084,917 (GRCm39)	D609E	probably benign	Het
Lama3	A	G	18: 12,572,405 (GRCm39)	T537A	probably benign	Het
Lce1i	A	T	3: 92,685,056 (GRCm39)	V40E	unknown	Het
Mprip	T	A	11: 59,649,293 (GRCm39)	V999D	probably benign	Het
Myd88	G	T	9: 119,168,829 (GRCm39)	T85K	possibly damaging	Het
Padi6	A	T	4: 140,458,473 (GRCm39)	M473K	probably damaging	Het
Pcdh12	T	A	18: 38,401,935 (GRCm39)	S97C	probably damaging	Het
Pkd1l1	T	A	11: 8,783,877 (GRCm39)	D2026V	probably damaging	Het
Plcxd1	T	C	5: 110,250,451 (GRCm39)	V264A	probably benign	Het
Plekha4	T	C	7: 45,198,580 (GRCm39)	S558P	probably damaging	Het
Ppm1a	T	A	12: 72,837,455 (GRCm39)	M334K	probably benign	Het
Ppp1r13l	T	C	7: 19,109,524 (GRCm39)	S684P	possibly damaging	Het
Prdm4	TCTCCTCCT	TCTCCT	10: 85,728,987 (GRCm39)		probably null	Het
Prl2a1	T	C	13: 27,990,369 (GRCm39)		probably benign	Het
Ptch1	T	C	13: 63,672,936 (GRCm39)	K753E	probably benign	Het
Qrich1	A	G	9: 108,436,502 (GRCm39)		probably benign	Het
Ror2	G	A	13: 53,271,201 (GRCm39)	R373C	probably benign	Het
Rtn4	C	A	11: 29,658,140 (GRCm39)	L765I	probably damaging	Het
Sema3a	T	C	5: 13,523,487 (GRCm39)		probably null	Het
Setd2	T	A	9: 110,433,284 (GRCm39)	D62E	probably damaging	Het
Ss18	A	T	18: 14,769,577 (GRCm39)	Y327N	unknown	Het
Ticam1	G	A	17: 56,578,756 (GRCm39)	T113I	probably benign	Het
Tnrc6a	A	G	7: 122,773,459 (GRCm39)	I1134V	probably damaging	Het
Top3b	T	G	16: 16,707,399 (GRCm39)	Y526*	probably null	Het
Tph2	T	C	10: 114,926,614 (GRCm39)	E384G	probably damaging	Het
Ttll11	A	T	2: 35,707,798 (GRCm39)	I503N	probably benign	Het
Zfp87	T	G	13: 67,665,945 (GRCm39)	K172N	probably damaging	Het

Other mutations in Or1e35

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01288:Or1e35	APN	11	73,798,139 (GRCm39)	missense	probably damaging	1.00
IGL01618:Or1e35	APN	11	73,798,303 (GRCm39)	missense	probably damaging	1.00
IGL01995:Or1e35	APN	11	73,798,261 (GRCm39)	missense	possibly damaging	0.52
IGL02494:Or1e35	APN	11	73,797,550 (GRCm39)	missense	possibly damaging	0.55
IGL02995:Or1e35	APN	11	73,798,045 (GRCm39)	missense	possibly damaging	0.90
IGL03256:Or1e35	APN	11	73,797,522 (GRCm39)	missense	probably benign	0.07
R0018:Or1e35	UTSW	11	73,797,452 (GRCm39)	missense	probably damaging	1.00
R0701:Or1e35	UTSW	11	73,797,655 (GRCm39)	missense	probably damaging	1.00
R0839:Or1e35	UTSW	11	73,798,138 (GRCm39)	missense	probably damaging	0.99
R1222:Or1e35	UTSW	11	73,798,240 (GRCm39)	missense	probably damaging	1.00
R1737:Or1e35	UTSW	11	73,797,911 (GRCm39)	missense	possibly damaging	0.69
R1819:Or1e35	UTSW	11	73,797,505 (GRCm39)	missense	probably benign	0.02
R2994:Or1e35	UTSW	11	73,797,541 (GRCm39)	missense	probably damaging	1.00
R3195:Or1e35	UTSW	11	73,797,484 (GRCm39)	missense	possibly damaging	0.91
R4622:Or1e35	UTSW	11	73,797,737 (GRCm39)	missense	possibly damaging	0.55
R4753:Or1e35	UTSW	11	73,797,677 (GRCm39)	missense	probably damaging	1.00
R5137:Or1e35	UTSW	11	73,797,452 (GRCm39)	missense	probably damaging	1.00
R5448:Or1e35	UTSW	11	73,797,437 (GRCm39)	missense	probably damaging	1.00
R5748:Or1e35	UTSW	11	73,797,721 (GRCm39)	missense	probably damaging	0.98
R5899:Or1e35	UTSW	11	73,797,755 (GRCm39)	missense	probably damaging	1.00
R6156:Or1e35	UTSW	11	73,797,447 (GRCm39)	nonsense	probably null
R6388:Or1e35	UTSW	11	73,798,118 (GRCm39)	missense	probably damaging	1.00
R6572:Or1e35	UTSW	11	73,797,629 (GRCm39)	missense	possibly damaging	0.91
R7241:Or1e35	UTSW	11	73,798,058 (GRCm39)	missense	probably benign	0.05
R8870:Or1e35	UTSW	11	73,797,725 (GRCm39)	missense	probably benign	0.03
R9358:Or1e35	UTSW	11	73,797,451 (GRCm39)	missense	probably damaging	1.00
R9544:Or1e35	UTSW	11	73,797,637 (GRCm39)	missense	probably benign	0.14
R9645:Or1e35	UTSW	11	73,797,713 (GRCm39)	missense	probably benign
R9667:Or1e35	UTSW	11	73,798,097 (GRCm39)	missense	possibly damaging	0.83
R9707:Or1e35	UTSW	11	73,798,090 (GRCm39)	missense	possibly damaging	0.79
Z1177:Or1e35	UTSW	11	73,797,439 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTCCTGAGAAGATGGAACCTTG -3'
(R):5'- GCCTGACACAGCTGTACTTC -3'

Sequencing Primer
(F):5'- CCTGAGAAGATGGAACCTTGAGAATG -3'
(R):5'- GACACAGCTGTACTTCTTTATGG -3'

Posted On

2016-10-26