Mutagenetix > Incidental Mutation

Incidental Mutation 'R1169:Or8k28'

101426

Institutional Source

Beutler Lab

Gene Symbol

Or8k28

Ensembl Gene

ENSMUSG00000075181

Gene Name

olfactory receptor family 8 subfamily K member 28

Synonyms

Olfr1066, MOR188-8, MOR256-52P, GA_x6K02T2Q125-47925557-47924616

MMRRC Submission

039242-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R1169 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

86285672-86286613 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 86285931 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 228 (I228T)

Ref Sequence

ENSEMBL: ENSMUSP00000097470 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099885] [ENSMUST00000213789] [ENSMUST00000216162] [ENSMUST00000217586]

AlphaFold

A2AK62

Predicted Effect

possibly damaging
Transcript: ENSMUST00000099885
AA Change: I228T

PolyPhen 2 Score 0.848 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000097470
Gene: ENSMUSG00000075181
AA Change: I228T

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	1.1e-50	PFAM
Pfam:7TM_GPCR_Srsx	35	172	1.9e-6	PFAM
Pfam:7tm_1	41	290	1.3e-15	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000213789

Predicted Effect

probably benign
Transcript: ENSMUST00000216162

Predicted Effect

probably benign
Transcript: ENSMUST00000217586

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.0%

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: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd17a	T	C	10: 80,419,781 (GRCm39)	E275G	probably damaging	Het
Adam10	T	A	9: 70,653,574 (GRCm39)	I123N	probably damaging	Het
Adam8	A	T	7: 139,563,842 (GRCm39)	L715Q	probably benign	Het
Adcyap1r1	T	A	6: 55,471,101 (GRCm39)	F418L	probably damaging	Het
Ankrd50	A	T	3: 38,508,401 (GRCm39)	I1322K	probably damaging	Het
Arid4a	G	A	12: 71,122,112 (GRCm39)	S509N	probably benign	Het
Atxn7	T	C	14: 14,095,468 (GRCm38)	S389P	possibly damaging	Het
C4b	A	T	17: 34,961,946 (GRCm39)	L100Q	probably benign	Het
Cacul1	G	A	19: 60,568,846 (GRCm39)	A104V	probably damaging	Het
Camsap3	T	C	8: 3,653,866 (GRCm39)	F512S	probably damaging	Het
Casp1	T	C	9: 5,299,454 (GRCm39)	V61A	possibly damaging	Het
Cfap251	GGGAGGAGGAGGAGGAGGAGGA	GGGAGGAGGAGGAGGAGGA	5: 123,392,673 (GRCm39)		probably benign	Het
Chd1	T	A	17: 15,955,994 (GRCm39)	F531Y	probably damaging	Het
Clec2h	C	T	6: 128,651,758 (GRCm39)	Q156*	probably null	Het
Clip2	T	A	5: 134,521,104 (GRCm39)	E978V	probably benign	Het
Cnpy2	T	G	10: 128,159,465 (GRCm39)	L34R	probably damaging	Het
Cog6	A	T	3: 52,921,265 (GRCm39)	C114S	probably benign	Het
Col6a3	A	T	1: 90,749,736 (GRCm39)	V366E	possibly damaging	Het
Col6a5	A	G	9: 105,774,173 (GRCm39)		probably null	Het
Cplx3	T	C	9: 57,517,278 (GRCm39)	T369A	probably damaging	Het
Dmbt1	G	A	7: 130,676,254 (GRCm39)		probably null	Het
Dok1	A	G	6: 83,009,029 (GRCm39)	F218L	possibly damaging	Het
Dph7	T	A	2: 24,856,583 (GRCm39)	N178K	probably benign	Het
Enam	A	T	5: 88,651,117 (GRCm39)	E800D	probably damaging	Het
Fads3	A	T	19: 10,031,463 (GRCm39)	Q205L	possibly damaging	Het
Fbxo44	T	C	4: 148,240,433 (GRCm39)	H265R	probably benign	Het
Gli1	T	A	10: 127,174,320 (GRCm39)	S24C	probably damaging	Het
Gm4894	T	A	9: 49,185,526 (GRCm39)	C43*	probably null	Het
Gpbp1l1	C	T	4: 116,431,563 (GRCm39)	H74Y	possibly damaging	Het
H2-Eb2	T	A	17: 34,552,331 (GRCm39)	F59I	possibly damaging	Het
Hspa14	T	C	2: 3,499,161 (GRCm39)	N211S	possibly damaging	Het
Ifnlr1	T	G	4: 135,432,419 (GRCm39)	F285C	probably benign	Het
Igf1r	G	T	7: 67,814,875 (GRCm39)	V259L	probably benign	Het
Igf2bp2	A	T	16: 21,897,480 (GRCm39)	Y244*	probably null	Het
Ighg2c	A	T	12: 113,249,572 (GRCm39)		probably benign	Het
Ighv8-14	A	T	12: 115,772,075 (GRCm39)		probably null	Het
Iqsec2	A	G	X: 150,927,727 (GRCm39)	S87G	probably benign	Het
Itsn2	A	G	12: 4,689,694 (GRCm39)	K589R	probably damaging	Het
Khdc1a	A	C	1: 21,420,495 (GRCm39)	E38D	possibly damaging	Het
Krt42	T	G	11: 100,154,171 (GRCm39)		probably null	Het
Lpo	T	C	11: 87,708,143 (GRCm39)	N183S	possibly damaging	Het
Lrrc3	T	A	10: 77,736,764 (GRCm39)	Y224F	probably damaging	Het
Ly6g6f	T	A	17: 35,302,240 (GRCm39)	D99V	probably damaging	Het
Lyplal1	T	C	1: 185,846,531 (GRCm39)	I42V	probably benign	Het
Mis18bp1	G	A	12: 65,190,057 (GRCm39)	Q793*	probably null	Het
Myh10	T	G	11: 68,653,667 (GRCm39)	M346R	probably damaging	Het
Nav1	G	T	1: 135,382,943 (GRCm39)	H1256Q	probably damaging	Het
Nbea	A	G	3: 55,875,744 (GRCm39)	V1642A	probably benign	Het
Or4d6	C	T	19: 12,086,853 (GRCm39)	R19H	probably benign	Het
Or8b12i	T	C	9: 20,082,354 (GRCm39)	N171S	probably benign	Het
Or8i2	A	G	2: 86,852,061 (GRCm39)	F276L	probably damaging	Het
Orm3	G	A	4: 63,276,085 (GRCm39)	V166M	probably damaging	Het
Oxct1	T	A	15: 4,120,708 (GRCm39)	I264N	probably damaging	Het
Paox	G	A	7: 139,706,244 (GRCm39)	V55I	probably benign	Het
Pde4d	C	A	13: 110,087,462 (GRCm39)		probably null	Het
Pnliprp1	A	G	19: 58,723,383 (GRCm39)	N258S	probably damaging	Het
Potegl	A	G	2: 23,146,994 (GRCm39)	K275E	possibly damaging	Het
Prl7b1	C	A	13: 27,790,887 (GRCm39)	R66L	possibly damaging	Het
Ptpre	G	T	7: 135,269,341 (GRCm39)	C261F	probably benign	Het
Rho	C	G	6: 115,909,199 (GRCm39)	N78K	probably damaging	Het
Rnf17	A	G	14: 56,751,622 (GRCm39)	N1487D	possibly damaging	Het
Ryr3	G	A	2: 112,563,359 (GRCm39)	T2922I	probably benign	Het
Saxo2	A	C	7: 82,284,379 (GRCm39)	F160V	possibly damaging	Het
Sbf2	A	T	7: 109,909,391 (GRCm39)	Y1786N	probably benign	Het
Sdad1	A	T	5: 92,446,092 (GRCm39)	V280E	probably benign	Het
Sgsm1	T	C	5: 113,427,351 (GRCm39)	D90G	probably damaging	Het
Siglec1	A	T	2: 130,916,747 (GRCm39)	D1169E	probably damaging	Het
Sim1	T	A	10: 50,857,618 (GRCm39)	V456E	probably benign	Het
Skint8	T	A	4: 111,785,710 (GRCm39)	I52N	possibly damaging	Het
Slc27a1	C	A	8: 72,033,297 (GRCm39)	R280S	probably benign	Het
Slc9a3	G	A	13: 74,298,862 (GRCm39)	V94I	probably damaging	Het
Sorcs2	C	A	5: 36,185,269 (GRCm39)	V936L	possibly damaging	Het
Syce1	A	G	7: 140,358,120 (GRCm39)	F255S	probably benign	Het
Tmc7	G	A	7: 118,150,483 (GRCm39)	S350L	probably benign	Het
Tmem200a	T	A	10: 25,870,246 (GRCm39)	I8F	probably damaging	Het
Trip6	T	C	5: 137,310,182 (GRCm39)	H322R	probably benign	Het
Vmn2r72	A	T	7: 85,400,517 (GRCm39)	N177K	probably benign	Het

Other mutations in Or8k28

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01661:Or8k28	APN	2	86,285,846 (GRCm39)	missense	possibly damaging	0.92
IGL01668:Or8k28	APN	2	86,285,746 (GRCm39)	missense	probably damaging	1.00
IGL02016:Or8k28	APN	2	86,285,841 (GRCm39)	missense	probably damaging	0.99
R0396:Or8k28	UTSW	2	86,286,363 (GRCm39)	missense	possibly damaging	0.54
R0980:Or8k28	UTSW	2	86,285,704 (GRCm39)	missense	probably benign	0.01
R0987:Or8k28	UTSW	2	86,285,891 (GRCm39)	nonsense	probably null
R2001:Or8k28	UTSW	2	86,285,817 (GRCm39)	missense	probably benign	0.45
R2002:Or8k28	UTSW	2	86,285,817 (GRCm39)	missense	probably benign	0.45
R2265:Or8k28	UTSW	2	86,286,558 (GRCm39)	missense	possibly damaging	0.77
R3811:Or8k28	UTSW	2	86,285,691 (GRCm39)	missense	probably benign	0.21
R4579:Or8k28	UTSW	2	86,285,859 (GRCm39)	missense	probably damaging	0.99
R4726:Or8k28	UTSW	2	86,286,580 (GRCm39)	missense	possibly damaging	0.90
R4768:Or8k28	UTSW	2	86,285,994 (GRCm39)	nonsense	probably null
R4871:Or8k28	UTSW	2	86,286,153 (GRCm39)	missense	possibly damaging	0.95
R5304:Or8k28	UTSW	2	86,285,779 (GRCm39)	missense	probably damaging	1.00
R6037:Or8k28	UTSW	2	86,286,133 (GRCm39)	missense	probably benign	0.14
R6037:Or8k28	UTSW	2	86,286,133 (GRCm39)	missense	probably benign	0.14
R7080:Or8k28	UTSW	2	86,285,835 (GRCm39)	nonsense	probably null
R7223:Or8k28	UTSW	2	86,286,211 (GRCm39)	missense	possibly damaging	0.78
R7378:Or8k28	UTSW	2	86,286,412 (GRCm39)	missense	probably benign	0.10
R7465:Or8k28	UTSW	2	86,286,150 (GRCm39)	missense	probably benign	0.07
R7598:Or8k28	UTSW	2	86,286,234 (GRCm39)	missense	probably damaging	0.98
R8524:Or8k28	UTSW	2	86,285,961 (GRCm39)	missense	probably damaging	1.00
R8703:Or8k28	UTSW	2	86,286,244 (GRCm39)	missense	possibly damaging	0.95
R8818:Or8k28	UTSW	2	86,286,078 (GRCm39)	missense	probably damaging	1.00
R8954:Or8k28	UTSW	2	86,285,892 (GRCm39)	missense	probably damaging	1.00
R9396:Or8k28	UTSW	2	86,285,845 (GRCm39)	missense	probably benign	0.00
X0025:Or8k28	UTSW	2	86,286,213 (GRCm39)	missense	probably benign	0.16

Predicted Primers

Posted On

2014-01-15