Mutagenetix > Incidental Mutation

Incidental Mutation 'R8942:Or4k15b'

681068

Institutional Source

Beutler Lab

Gene Symbol

Or4k15b

Ensembl Gene

ENSMUSG00000068437

Gene Name

olfactory receptor family 4 subfamily K member 15B

Synonyms

GA_x6K02T2PMLR-5725741-5724776, MOR246-7_p, Olfr725, MOR246-3

Accession Numbers

Essential gene?

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

Stock #

R8942 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

50271771-50277832 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 50272602 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Arginine at position 86 (L86R)

Ref Sequence

ENSEMBL: ENSMUSP00000145828 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089844] [ENSMUST00000206920]

AlphaFold

Q05A45

Predicted Effect

SMART Domains

Protein: ENSMUSP00000087282
Gene: ENSMUSG00000068437
AA Change: L86R

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	304	4.7e-46	PFAM
Pfam:7TM_GPCR_Srsx	36	282	1.8e-7	PFAM
Pfam:7tm_1	41	287	5.8e-21	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000206920
AA Change: L86R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

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: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc4	A	T	14: 118,790,732 (GRCm39)	D833E	probably damaging	Het
Adgrl3	A	T	5: 81,796,568 (GRCm39)	I626L	probably benign	Het
AI182371	A	C	2: 34,990,622 (GRCm39)	L25R	probably damaging	Het
Atp2b2	G	T	6: 113,790,991 (GRCm39)	Q138K	probably benign	Het
Atp8b5	T	C	4: 43,353,658 (GRCm39)	F491L	probably damaging	Het
Bcap29	T	A	12: 31,684,353 (GRCm39)	M1L	probably damaging	Het
C1qtnf7	A	G	5: 43,773,583 (GRCm39)	D294G	probably benign	Het
Ccdc170	C	T	10: 4,484,044 (GRCm39)	A290V	probably benign	Het
Cfhr2	A	T	1: 139,741,292 (GRCm39)	L228I	probably benign	Het
Clip4	T	A	17: 72,170,768 (GRCm39)	V645D	probably benign	Het
Cyp4a31	C	T	4: 115,426,918 (GRCm39)	R173W	possibly damaging	Het
Dis3l	T	C	9: 64,214,875 (GRCm39)	K898R	probably benign	Het
Efr3b	G	T	12: 4,032,091 (GRCm39)	H172Q	possibly damaging	Het
Eipr1	A	T	12: 28,917,053 (GRCm39)	N374Y	probably damaging	Het
Exoc3l4	A	T	12: 111,392,002 (GRCm39)	E414D	possibly damaging	Het
Exoc3l4	G	T	12: 111,392,003 (GRCm39)	V415L	probably benign	Het
Faap100	G	T	11: 120,267,856 (GRCm39)	H306N	possibly damaging	Het
Gapvd1	T	C	2: 34,619,134 (GRCm39)	T80A	probably benign	Het
Gen1	A	G	12: 11,292,287 (GRCm39)	S501P	probably benign	Het
Gm10643	A	G	8: 84,790,799 (GRCm39)		probably benign	Het
Hecw1	A	T	13: 14,481,395 (GRCm39)	V445D	probably benign	Het
Hells	CT	C	19: 38,942,045 (GRCm39)		probably null	Het
Hnrnpr	T	G	4: 136,059,791 (GRCm39)	D197E	possibly damaging	Het
Hspb1	G	A	5: 135,916,928 (GRCm39)	V6M	probably damaging	Het
Iglon5	A	G	7: 43,126,315 (GRCm39)	V196A	probably benign	Het
Ints2	T	C	11: 86,103,720 (GRCm39)	T1142A	probably benign	Het
Katnip	T	G	7: 125,449,975 (GRCm39)	L1013R	probably damaging	Het
Kcnq2	T	A	2: 180,724,244 (GRCm39)	D587V	probably damaging	Het
Lmln	C	T	16: 32,901,330 (GRCm39)	P242L	probably damaging	Het
Mapt	G	A	11: 104,173,307 (GRCm39)		probably null	Het
Mrgpre	T	C	7: 143,335,002 (GRCm39)	Y167C		Het
Mtx2	A	T	2: 74,699,696 (GRCm39)	I156F	probably benign	Het
Nipbl	A	T	15: 8,381,104 (GRCm39)	S563T	probably benign	Het
Nmbr	C	T	10: 14,646,197 (GRCm39)	S357L	probably benign	Het
Or10ak14	A	T	4: 118,611,594 (GRCm39)	I49N	possibly damaging	Het
Or4e1	A	C	14: 52,700,692 (GRCm39)	I258S	probably damaging	Het
Or4f14	T	A	2: 111,743,207 (GRCm39)	I23F	probably benign	Het
Or4f60	T	C	2: 111,902,802 (GRCm39)	N42S	probably damaging	Het
Or4p4	C	T	2: 88,483,308 (GRCm39)	L271F	possibly damaging	Het
Pctp	A	G	11: 89,875,554 (GRCm39)	M203T	possibly damaging	Het
Pip4k2c	A	G	10: 127,036,084 (GRCm39)	V261A	probably benign	Het
Pm20d1	G	T	1: 131,739,785 (GRCm39)	V378F	possibly damaging	Het
Ppcdc	C	T	9: 57,342,265 (GRCm39)	R19H	probably benign	Het
Pramel26	T	C	4: 143,536,861 (GRCm39)	N490S	probably benign	Het
Sdk1	A	G	5: 142,082,598 (GRCm39)	E1332G	probably damaging	Het
Sgce	G	T	6: 4,730,027 (GRCm39)	L66M	probably benign	Het
Sycp2l	G	T	13: 41,277,522 (GRCm39)		probably null	Het
Tars1	G	T	15: 11,384,183 (GRCm39)	H695N	probably benign	Het
Tdo2	A	G	3: 81,876,851 (GRCm39)	V107A	probably benign	Het
Tmem131l	A	T	3: 83,805,793 (GRCm39)	M1550K	possibly damaging	Het
Ttf2	A	C	3: 100,869,042 (GRCm39)	S431R	probably benign	Het
Unc80	A	G	1: 66,512,468 (GRCm39)	D126G	possibly damaging	Het
Usp17lb	C	T	7: 104,490,583 (GRCm39)	V115I	possibly damaging	Het
Vezf1	A	G	11: 87,972,553 (GRCm39)	T305A	probably benign	Het
Vmn1r45	A	T	6: 89,910,876 (GRCm39)	N31K	probably benign	Het
Wdr59	T	C	8: 112,211,808 (GRCm39)	K380E	probably benign	Het
Xylt1	T	A	7: 117,233,971 (GRCm39)	Y499*	probably null	Het
Zfp777	T	C	6: 48,006,125 (GRCm39)	E467G	probably benign	Het
Zkscan4	C	A	13: 21,668,680 (GRCm39)	P406Q	probably benign	Het

Other mutations in Or4k15b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01116:Or4k15b	APN	14	50,272,507 (GRCm39)	missense	probably benign	0.29
IGL01412:Or4k15b	APN	14	50,272,770 (GRCm39)	missense	probably benign
IGL03241:Or4k15b	APN	14	50,272,525 (GRCm39)	missense	possibly damaging	0.70
IGL03268:Or4k15b	APN	14	50,272,024 (GRCm39)	missense	probably damaging	0.98
IGL03348:Or4k15b	APN	14	50,272,212 (GRCm39)	missense	probably benign	0.00
R0358:Or4k15b	UTSW	14	50,272,743 (GRCm39)	missense	probably damaging	0.97
R0577:Or4k15b	UTSW	14	50,272,249 (GRCm39)	missense	probably damaging	1.00
R2094:Or4k15b	UTSW	14	50,272,171 (GRCm39)	missense	probably damaging	1.00
R2424:Or4k15b	UTSW	14	50,272,281 (GRCm39)	missense	probably damaging	1.00
R3421:Or4k15b	UTSW	14	50,271,997 (GRCm39)	missense	possibly damaging	0.66
R3422:Or4k15b	UTSW	14	50,271,997 (GRCm39)	missense	possibly damaging	0.66
R4436:Or4k15b	UTSW	14	50,272,287 (GRCm39)	missense	probably damaging	1.00
R4437:Or4k15b	UTSW	14	50,272,287 (GRCm39)	missense	probably damaging	1.00
R4438:Or4k15b	UTSW	14	50,272,287 (GRCm39)	missense	probably damaging	1.00
R4684:Or4k15b	UTSW	14	50,272,287 (GRCm39)	missense	probably damaging	1.00
R4717:Or4k15b	UTSW	14	50,272,821 (GRCm39)	missense	probably damaging	0.98
R5253:Or4k15b	UTSW	14	50,272,745 (GRCm39)	missense	possibly damaging	0.91
R5254:Or4k15b	UTSW	14	50,272,135 (GRCm39)	missense	possibly damaging	0.60
R5641:Or4k15b	UTSW	14	50,272,746 (GRCm39)	missense	probably benign	0.04
R5881:Or4k15b	UTSW	14	50,272,444 (GRCm39)	missense	probably benign	0.00
R5906:Or4k15b	UTSW	14	50,272,306 (GRCm39)	missense	probably benign	0.05
R6511:Or4k15b	UTSW	14	50,272,266 (GRCm39)	missense	probably damaging	1.00
R7837:Or4k15b	UTSW	14	50,272,033 (GRCm39)	missense	probably damaging	1.00
R7980:Or4k15b	UTSW	14	50,272,252 (GRCm39)	missense	probably damaging	1.00
R8118:Or4k15b	UTSW	14	50,272,608 (GRCm39)	missense	probably benign	0.13
R9084:Or4k15b	UTSW	14	50,271,916 (GRCm39)	missense	probably benign
R9797:Or4k15b	UTSW	14	50,272,224 (GRCm39)	missense	probably benign	0.19
X0062:Or4k15b	UTSW	14	50,272,317 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CCACAAACCAGGGGATGATG -3'
(R):5'- AGTTCAAAGGAGCTCCAGCC -3'

Sequencing Primer
(F):5'- GGATGATGACCAGAGTGATACAC -3'
(R):5'- AAAGGAGCTCCAGCCTTTCCTG -3'

Posted On

2021-08-31