Mutagenetix > Incidental Mutation

Incidental Mutation 'R9211:Or8k38'

698834

Institutional Source

Beutler Lab

Gene Symbol

Or8k38

Ensembl Gene

ENSMUSG00000075176

Gene Name

olfactory receptor family 8 subfamily K member 38

Synonyms

Olfr1085, MOR191-1, GA_x6K02T2Q125-48147264-48146323

MMRRC Submission

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R9211 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

86487859-86488800 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 86488024 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 259 (Y259*)

Ref Sequence

ENSEMBL: ENSMUSP00000150258 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099879] [ENSMUST00000213279] [ENSMUST00000214566]

AlphaFold

Q7TR64

Predicted Effect

probably null
Transcript: ENSMUST00000099879
AA Change: Y259*

SMART Domains

Protein: ENSMUSP00000097464
Gene: ENSMUSG00000075176
AA Change: Y259*

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	4.6e-49	PFAM
Pfam:7tm_1	41	290	1.1e-18	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000213279
AA Change: Y259*

Predicted Effect

probably null
Transcript: ENSMUST00000214566
AA Change: Y259*

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

99% (86/87)

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: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110009E18Rik	G	T	1: 120,099,161 (GRCm39)	D85Y	possibly damaging	Het
Accs	T	C	2: 93,668,614 (GRCm39)	R315G	probably damaging	Het
Adam3	A	C	8: 25,177,910 (GRCm39)	W668G	probably benign	Het
Adgrb2	T	A	4: 129,886,199 (GRCm39)	V113E	probably benign	Het
Anapc4	C	T	5: 53,007,994 (GRCm39)	T391I	possibly damaging	Het
Angpt2	C	T	8: 18,748,078 (GRCm39)	G394D	probably benign	Het
Ankrd31	C	G	13: 97,029,551 (GRCm39)	L1662V	possibly damaging	Het
Ankrd36	A	G	11: 5,612,370 (GRCm39)	D1234G	possibly damaging	Het
Ankrd6	C	T	4: 32,806,580 (GRCm39)	V558M	probably damaging	Het
Ankrd61	T	A	5: 143,828,358 (GRCm39)	M206L	probably benign	Het
Arhgap33	C	T	7: 30,223,023 (GRCm39)	G970R	possibly damaging	Het
Atf7	A	G	15: 102,437,117 (GRCm39)	V115A	unknown	Het
Atp2c2	A	T	8: 120,446,032 (GRCm39)	R65S	probably benign	Het
Atp8b5	T	A	4: 43,367,960 (GRCm39)	M861K	probably damaging	Het
Bmi1	T	C	2: 18,689,152 (GRCm39)	S279P	probably benign	Het
Bptf	T	G	11: 106,946,124 (GRCm39)	S2372R	probably damaging	Het
Cacnb2	A	T	2: 14,879,308 (GRCm39)	I15L	unknown	Het
Card11	A	G	5: 140,869,375 (GRCm39)	M807T	probably benign	Het
Ccdc175	A	T	12: 72,153,458 (GRCm39)	D704E	probably damaging	Het
Cd300ld	T	A	11: 114,878,386 (GRCm39)	Y42F	probably damaging	Het
Cdh1	A	T	8: 107,390,962 (GRCm39)	T693S	probably benign	Het
Clca4b	T	C	3: 144,638,214 (GRCm39)	Y16C	possibly damaging	Het
Col4a4	A	G	1: 82,506,501 (GRCm39)	I273T	unknown	Het
Coro2b	C	A	9: 62,427,662 (GRCm39)	V9L	probably benign	Het
Crnkl1	T	C	2: 145,774,773 (GRCm39)	D55G	probably damaging	Het
Dcps	T	A	9: 35,035,872 (GRCm39)	N338I	probably damaging	Het
Dusp2	A	T	2: 127,179,311 (GRCm39)	H222L	probably benign	Het
Dync1li1	C	A	9: 114,518,012 (GRCm39)	Y21*	probably null	Het
Efhb	T	G	17: 53,756,507 (GRCm39)	Q381H	probably damaging	Het
Elac2	A	T	11: 64,869,864 (GRCm39)		probably benign	Het
Etaa1	A	G	11: 17,896,053 (GRCm39)	V688A	possibly damaging	Het
Fam120c	C	T	X: 150,127,495 (GRCm39)	H84Y	probably benign	Het
Fbxl7	T	A	15: 26,789,616 (GRCm39)	N37I	probably damaging	Het
Fndc3b	A	T	3: 27,523,086 (GRCm39)	W498R	probably damaging	Het
Galc	G	A	12: 98,173,699 (GRCm39)	A621V	probably benign	Het
Gch1	A	T	14: 47,426,519 (GRCm39)	I69N	probably damaging	Het
Gdpd4	T	C	7: 97,615,466 (GRCm39)	V97A	possibly damaging	Het
Hirip3	C	T	7: 126,463,567 (GRCm39)	R485*	probably null	Het
Hmgcs2	C	T	3: 98,204,748 (GRCm39)	T302I	possibly damaging	Het
Ing5	A	T	1: 93,740,409 (GRCm39)	K137I	possibly damaging	Het
Kcnh8	T	A	17: 53,146,236 (GRCm39)	Y375N	probably damaging	Het
Kdm3a	C	A	6: 71,573,674 (GRCm39)	W963L	probably benign	Het
Klra17	T	G	6: 129,842,651 (GRCm39)	I216L	possibly damaging	Het
Kmt2e	A	G	5: 23,669,770 (GRCm39)	K86E	possibly damaging	Het
Krt42	T	C	11: 100,155,867 (GRCm39)	N293S	possibly damaging	Het
Lrrc8d	T	A	5: 105,960,216 (GRCm39)	W209R	probably damaging	Het
Mettl23	C	T	11: 116,734,469 (GRCm39)	P13S	unknown	Het
Ncln	T	C	10: 81,323,527 (GRCm39)	Y540C	probably damaging	Het
Neb	C	G	2: 52,135,360 (GRCm39)	G3250A	probably damaging	Het
Nebl	A	G	2: 17,393,501 (GRCm39)		probably null	Het
Nqo2	A	T	13: 34,156,399 (GRCm39)	T38S	probably benign	Het
Obscn	A	T	11: 59,026,693 (GRCm39)	I170N	probably benign	Het
Or2bd2	G	T	7: 6,443,417 (GRCm39)	G173W	probably damaging	Het
Or4c100	A	G	2: 88,356,170 (GRCm39)	D81G	probably benign	Het
Or5af2	A	T	11: 58,708,709 (GRCm39)	N292Y	probably damaging	Het
Or5p6	C	T	7: 107,630,798 (GRCm39)	V251I	probably damaging	Het
Or7g28	T	A	9: 19,271,824 (GRCm39)	I276F	possibly damaging	Het
Pacs1	A	T	19: 5,189,057 (GRCm39)	V775E	probably damaging	Het
Pheta2	A	T	15: 82,225,227 (GRCm39)		probably benign	Het
Pmfbp1	T	C	8: 110,262,445 (GRCm39)	I713T	probably benign	Het
Pnma8b	A	G	7: 16,679,589 (GRCm39)	D191G	unknown	Het
Polr1a	T	C	6: 71,943,521 (GRCm39)	I1252T	probably damaging	Het
Prss16	A	T	13: 22,192,754 (GRCm39)	M110K	probably benign	Het
Pygo2	T	C	3: 89,338,038 (GRCm39)		probably null	Het
Rab5b	C	A	10: 128,519,063 (GRCm39)		probably null	Het
Reln	G	T	5: 22,549,200 (GRCm39)	Y69*	probably null	Het
Rgs12	T	A	5: 35,123,165 (GRCm39)	M316K	probably damaging	Het
Rmi2	T	C	16: 10,657,743 (GRCm39)	C118R	possibly damaging	Het
Rnf223	T	A	4: 156,216,834 (GRCm39)	C70S	probably damaging	Het
Rxrb	T	A	17: 34,255,626 (GRCm39)	F371Y	probably damaging	Het
Smurf2	T	A	11: 106,759,463 (GRCm39)	S78C	probably damaging	Het
Sorbs1	A	T	19: 40,332,798 (GRCm39)		probably null	Het
Spag17	C	T	3: 100,032,614 (GRCm39)		probably benign	Het
Spidr	T	C	16: 15,871,319 (GRCm39)	H217R	probably benign	Het
Tiam2	T	G	17: 3,498,729 (GRCm39)	V835G	possibly damaging	Het
Tm2d2	C	T	8: 25,510,548 (GRCm39)	R136*	probably null	Het
Tnks	C	T	8: 35,316,489 (GRCm39)	D877N	probably damaging	Het
Tns1	A	G	1: 73,956,948 (GRCm39)	L491P	possibly damaging	Het
Trps1	A	G	15: 50,694,840 (GRCm39)	I485T	probably damaging	Het
Tubgcp5	A	G	7: 55,456,331 (GRCm39)	S308G	probably benign	Het
Ugt8a	T	C	3: 125,661,130 (GRCm39)	H454R	probably damaging	Het
Usp32	G	T	11: 84,913,559 (GRCm39)	T924K	probably damaging	Het
Vmn2r91	A	T	17: 18,356,819 (GRCm39)	K829*	probably null	Het
Zfc3h1	T	C	10: 115,248,328 (GRCm39)	F1146L	possibly damaging	Het
Zfp729a	G	T	13: 67,767,820 (GRCm39)	A803E	probably benign	Het
Zfp990	A	G	4: 145,264,171 (GRCm39)	T390A	probably damaging	Het

Other mutations in Or8k38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00940:Or8k38	APN	2	86,488,070 (GRCm39)	missense	probably damaging	0.98
IGL01137:Or8k38	APN	2	86,488,055 (GRCm39)	missense	possibly damaging	0.92
IGL01329:Or8k38	APN	2	86,488,551 (GRCm39)	missense	probably benign	0.31
IGL01398:Or8k38	APN	2	86,488,032 (GRCm39)	missense	probably damaging	1.00
IGL02248:Or8k38	APN	2	86,488,061 (GRCm39)	missense	probably damaging	1.00
IGL02699:Or8k38	APN	2	86,488,691 (GRCm39)	missense	probably benign	0.34
IGL02818:Or8k38	APN	2	86,488,128 (GRCm39)	missense	probably damaging	1.00
IGL03095:Or8k38	APN	2	86,488,775 (GRCm39)	missense	possibly damaging	0.50
IGL03218:Or8k38	APN	2	86,488,703 (GRCm39)	missense	probably benign	0.32
R0121:Or8k38	UTSW	2	86,488,163 (GRCm39)	missense	probably benign	0.42
R0546:Or8k38	UTSW	2	86,488,235 (GRCm39)	missense	possibly damaging	0.91
R0583:Or8k38	UTSW	2	86,488,704 (GRCm39)	missense	probably benign	0.20
R0980:Or8k38	UTSW	2	86,488,209 (GRCm39)	missense	probably benign	0.39
R2067:Or8k38	UTSW	2	86,488,781 (GRCm39)	missense	probably damaging	1.00
R2111:Or8k38	UTSW	2	86,488,781 (GRCm39)	missense	probably damaging	1.00
R3760:Or8k38	UTSW	2	86,488,232 (GRCm39)	missense	possibly damaging	0.91
R4530:Or8k38	UTSW	2	86,487,905 (GRCm39)	missense	probably benign	0.00
R4809:Or8k38	UTSW	2	86,488,029 (GRCm39)	missense	possibly damaging	0.95
R5940:Or8k38	UTSW	2	86,488,394 (GRCm39)	missense	probably damaging	0.98
R6027:Or8k38	UTSW	2	86,488,148 (GRCm39)	missense	probably damaging	1.00
R6417:Or8k38	UTSW	2	86,488,510 (GRCm39)	nonsense	probably null
R6420:Or8k38	UTSW	2	86,488,510 (GRCm39)	nonsense	probably null
R6619:Or8k38	UTSW	2	86,488,406 (GRCm39)	missense	probably damaging	1.00
R6762:Or8k38	UTSW	2	86,488,188 (GRCm39)	missense	probably benign	0.22
R6946:Or8k38	UTSW	2	86,487,932 (GRCm39)	missense	probably damaging	1.00
R7673:Or8k38	UTSW	2	86,488,070 (GRCm39)	missense	probably damaging	1.00
R7718:Or8k38	UTSW	2	86,488,373 (GRCm39)	missense	probably benign	0.26
R8461:Or8k38	UTSW	2	86,487,890 (GRCm39)	missense	probably benign	0.02
R8506:Or8k38	UTSW	2	86,488,745 (GRCm39)	missense	probably benign	0.05
R8977:Or8k38	UTSW	2	86,488,472 (GRCm39)	missense	probably benign	0.02
R9172:Or8k38	UTSW	2	86,487,879 (GRCm39)	missense	probably benign	0.00
R9337:Or8k38	UTSW	2	86,488,476 (GRCm39)	missense	probably benign	0.01
R9713:Or8k38	UTSW	2	86,488,041 (GRCm39)	missense	possibly damaging	0.80

Predicted Primers

PCR Primer
(F):5'- GAGCCTATTCGTCTTTTCTATGAAG -3'
(R):5'- CTCTGTTCAAATACACATGAGGTTG -3'

Sequencing Primer
(F):5'- GTCATGGCTATATTTGTATGCAACC -3'
(R):5'- GTTCAAATACACATGAGGTTGAAGTG -3'

Posted On

2022-02-07