Mutagenetix > Incidental Mutation

Incidental Mutation 'R5772:Or4k35'

445426

Institutional Source

Beutler Lab

Gene Symbol

Or4k35

Ensembl Gene

ENSMUSG00000074965

Gene Name

olfactory receptor family 4 subfamily K member 35

Synonyms

MOR248-11, Olfr1277, GA_x6K02T2Q125-72321818-72320907

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.075) question?

Stock #

R5772 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

111099799-111100710 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 111100057 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 218 (Y218*)

Ref Sequence

ENSEMBL: ENSMUSP00000150703 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099619] [ENSMUST00000214760]

AlphaFold

Q8VF41

Predicted Effect

probably null
Transcript: ENSMUST00000099619
AA Change: Y218*

SMART Domains

Protein: ENSMUSP00000097214
Gene: ENSMUSG00000074965
AA Change: Y218*

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	303	5.5e-50	PFAM
Pfam:7tm_1	41	287	7.2e-20	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000214760
AA Change: Y218*

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.9%

Validation Efficiency

98% (64/65)

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: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932416K20Rik	G	A	8: 105,524,271 (GRCm39)		noncoding transcript	Het
Abcg8	A	T	17: 84,994,127 (GRCm39)	E48V	probably damaging	Het
Afap1l2	T	C	19: 56,911,406 (GRCm39)	T289A	probably benign	Het
Atf6	T	A	1: 170,574,758 (GRCm39)	D560V	probably damaging	Het
Bcl2l14	A	T	6: 134,404,362 (GRCm39)	K183N	probably damaging	Het
Carmil3	T	C	14: 55,730,696 (GRCm39)	L52P	probably damaging	Het
Cct3	T	A	3: 88,208,274 (GRCm39)	N61K	probably damaging	Het
Col18a1	A	G	10: 77,002,177 (GRCm39)	V10A	unknown	Het
Col26a1	G	A	5: 136,876,420 (GRCm39)	Q67*	probably null	Het
Cyp2d34	T	C	15: 82,501,341 (GRCm39)	D329G	probably null	Het
Dchs1	T	A	7: 105,422,247 (GRCm39)	I58F	probably damaging	Het
Ddx60	T	C	8: 62,401,931 (GRCm39)	L269P	probably damaging	Het
Dis3l2	G	A	1: 86,806,154 (GRCm39)	G325D	probably damaging	Het
Dync1h1	A	T	12: 110,612,707 (GRCm39)	K2861*	probably null	Het
Ednra	A	G	8: 78,401,696 (GRCm39)	I198T	possibly damaging	Het
Ep300	T	C	15: 81,524,115 (GRCm39)		probably benign	Het
Fam120a	G	A	13: 49,034,409 (GRCm39)	P1068S	probably benign	Het
Fsip2	A	T	2: 82,815,084 (GRCm39)	M3606L	probably benign	Het
Garre1	A	T	7: 33,953,413 (GRCm39)	W238R	probably damaging	Het
Gm7713	T	C	15: 59,866,492 (GRCm39)		noncoding transcript	Het
Gprin3	A	T	6: 59,331,398 (GRCm39)	V303D	possibly damaging	Het
Hmcn1	A	T	1: 150,570,629 (GRCm39)	V2178D	possibly damaging	Het
Hoxa11	A	G	6: 52,222,380 (GRCm39)	V107A	possibly damaging	Het
Iqub	C	A	6: 24,454,250 (GRCm39)	M544I	possibly damaging	Het
Itgb4	A	T	11: 115,879,258 (GRCm39)		probably benign	Het
Itpkb	A	G	1: 180,161,818 (GRCm39)		probably benign	Het
Kalrn	A	T	16: 33,796,190 (GRCm39)	V1195E	probably damaging	Het
Kif12	C	A	4: 63,084,178 (GRCm39)	R608M	probably damaging	Het
Lcorl	A	T	5: 45,952,709 (GRCm39)		probably null	Het
Lrrc24	T	C	15: 76,606,910 (GRCm39)	E162G	probably damaging	Het
Med6	A	G	12: 81,626,418 (GRCm39)	S119P	probably damaging	Het
Mmab	A	C	5: 114,574,775 (GRCm39)	L166R	probably damaging	Het
Myef2l	A	G	3: 10,153,566 (GRCm39)	R112G	probably damaging	Het
Nom1	A	G	5: 29,651,873 (GRCm39)	K737R	possibly damaging	Het
Obscn	T	C	11: 58,946,970 (GRCm39)	S4352G	probably damaging	Het
Or10ag60	A	T	2: 87,438,517 (GRCm39)	T262S	probably benign	Het
Or2w25	T	A	11: 59,504,712 (GRCm39)	D307E	probably benign	Het
Or6d12	A	C	6: 116,492,912 (GRCm39)	D58A	possibly damaging	Het
Pdzrn3	G	A	6: 101,149,275 (GRCm39)	S351L	probably benign	Het
Pdzrn4	A	T	15: 92,655,562 (GRCm39)	E485V	probably damaging	Het
Prkdc	T	A	16: 15,597,252 (GRCm39)	I2804K	possibly damaging	Het
Psg28	A	G	7: 18,164,640 (GRCm39)	L24P	probably damaging	Het
Resp18	A	G	1: 75,250,644 (GRCm39)	V145A	possibly damaging	Het
Rgl3	T	C	9: 21,892,908 (GRCm39)	M259V	probably benign	Het
Rhot2	A	T	17: 26,058,781 (GRCm39)	S540T	probably benign	Het
Ring1	T	C	17: 34,241,282 (GRCm39)	Y278C	possibly damaging	Het
Rpn2	A	G	2: 157,137,265 (GRCm39)	Y216C	probably damaging	Het
Scgb2b18	G	A	7: 32,873,255 (GRCm39)	L5F	unknown	Het
Slamf7	T	C	1: 171,466,838 (GRCm39)		probably null	Het
Slc22a12	T	C	19: 6,590,479 (GRCm39)	N237S	possibly damaging	Het
Spen	A	T	4: 141,205,495 (GRCm39)	V1044D	unknown	Het
Sqor	A	T	2: 122,651,261 (GRCm39)	M175L	probably benign	Het
Stx16	G	A	2: 173,935,292 (GRCm39)	G156R	probably damaging	Het
Tars3	T	G	7: 65,333,873 (GRCm39)	F632V	probably damaging	Het
Tln1	A	G	4: 43,545,191 (GRCm39)	V1008A	probably benign	Het
Tmem145	A	G	7: 25,015,039 (GRCm39)	H554R	probably benign	Het
Trank1	A	T	9: 111,195,744 (GRCm39)	D1256V	possibly damaging	Het
Trbv19	A	G	6: 41,155,794 (GRCm39)	Y55C	possibly damaging	Het
Ttc23l	C	T	15: 10,551,555 (GRCm39)	C57Y	probably benign	Het
Uap1	A	T	1: 169,988,949 (GRCm39)	C158S	probably benign	Het
Zfp353-ps	T	A	8: 42,535,647 (GRCm39)		noncoding transcript	Het
Zfp629	T	A	7: 127,210,307 (GRCm39)	I501F	probably damaging	Het
Zfp820	T	C	17: 22,037,702 (GRCm39)	Y542C	probably damaging	Het

Other mutations in Or4k35

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01552:Or4k35	APN	2	111,100,257 (GRCm39)	missense	probably damaging	1.00
IGL02550:Or4k35	APN	2	111,100,349 (GRCm39)	missense	probably damaging	0.99
IGL02661:Or4k35	APN	2	111,099,811 (GRCm39)	missense	possibly damaging	0.56
IGL02940:Or4k35	APN	2	111,100,073 (GRCm39)	missense	probably damaging	0.99
R0121:Or4k35	UTSW	2	111,100,659 (GRCm39)	missense	probably benign	0.01
R0402:Or4k35	UTSW	2	111,100,208 (GRCm39)	missense	probably damaging	1.00
R0903:Or4k35	UTSW	2	111,100,701 (GRCm39)	missense	probably benign
R1804:Or4k35	UTSW	2	111,100,275 (GRCm39)	missense	probably benign
R1806:Or4k35	UTSW	2	111,100,622 (GRCm39)	missense	possibly damaging	0.65
R1965:Or4k35	UTSW	2	111,099,938 (GRCm39)	missense	probably damaging	1.00
R3718:Or4k35	UTSW	2	111,100,571 (GRCm39)	missense	probably benign
R4044:Or4k35	UTSW	2	111,099,927 (GRCm39)	missense	probably benign	0.01
R4401:Or4k35	UTSW	2	111,100,178 (GRCm39)	missense	probably damaging	1.00
R4518:Or4k35	UTSW	2	111,100,263 (GRCm39)	missense	probably benign
R5309:Or4k35	UTSW	2	111,100,655 (GRCm39)	missense	probably benign	0.00
R5312:Or4k35	UTSW	2	111,100,655 (GRCm39)	missense	probably benign	0.00
R5367:Or4k35	UTSW	2	111,100,235 (GRCm39)	missense	possibly damaging	0.81
R5727:Or4k35	UTSW	2	111,100,197 (GRCm39)	nonsense	probably null
R5827:Or4k35	UTSW	2	111,100,266 (GRCm39)	missense	probably damaging	1.00
R5882:Or4k35	UTSW	2	111,100,484 (GRCm39)	missense	probably damaging	0.99
R6036:Or4k35	UTSW	2	111,099,957 (GRCm39)	missense	probably damaging	1.00
R6036:Or4k35	UTSW	2	111,099,957 (GRCm39)	missense	probably damaging	1.00
R6728:Or4k35	UTSW	2	111,100,018 (GRCm39)	missense	probably benign	0.00
R7629:Or4k35	UTSW	2	111,100,221 (GRCm39)	missense	probably benign	0.00
R8377:Or4k35	UTSW	2	111,099,983 (GRCm39)	missense	probably damaging	1.00
R8870:Or4k35	UTSW	2	111,100,464 (GRCm39)	missense	possibly damaging	0.61
R9100:Or4k35	UTSW	2	111,100,094 (GRCm39)	missense	probably benign	0.35
R9668:Or4k35	UTSW	2	111,100,287 (GRCm39)	missense	probably benign	0.03
R9690:Or4k35	UTSW	2	111,099,822 (GRCm39)	missense	probably damaging	0.98
R9715:Or4k35	UTSW	2	111,100,623 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CTGGATTCAGAAGAGGTGTGATAAC -3'
(R):5'- TGGCTTTGTGCATTCAATAAGC -3'

Sequencing Primer
(F):5'- GTGTGATAACTGCATAAAACACAGC -3'
(R):5'- GTGCATTCAATAAGCCAACTGG -3'

Posted On

2016-11-21