Mutagenetix > Incidental Mutation

Incidental Mutation 'R1847:Or5d16'

265979

Institutional Source

Beutler Lab

Gene Symbol

Or5d16

Ensembl Gene

ENSMUSG00000075145

Gene Name

olfactory receptor family 5 subfamily D member 16

Synonyms

Olfr1155, GA_x6K02T2Q125-49426894-49425950, MOR174-10

MMRRC Submission

039872-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.100) question?

Stock #

R1847 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

87773026-87773970 bp(-) (GRCm39)

Type of Mutation

splice site (4332 bp from exon)

DNA Base Change (assembly)

T to C at 87773065 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000149665 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099843] [ENSMUST00000214641] [ENSMUST00000215903] [ENSMUST00000216191] [ENSMUST00000216726]

AlphaFold

Q8VFR3

Predicted Effect

probably null
Transcript: ENSMUST00000099843

SMART Domains

Protein: ENSMUSP00000097431
Gene: ENSMUSG00000075145

Domain	Start	End	E-Value	Type
Pfam:7tm_4	33	310	2.7e-44	PFAM
Pfam:7tm_1	43	292	5.3e-16	PFAM

Predicted Effect

silent
Transcript: ENSMUST00000214641

Predicted Effect

silent
Transcript: ENSMUST00000215903

Predicted Effect

probably null
Transcript: ENSMUST00000216191

Predicted Effect

probably null
Transcript: ENSMUST00000216726

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 94.9%
20x: 91.2%

Validation Efficiency

97% (68/70)

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: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc1	C	A	16: 14,263,313 (GRCm39)	R758S	probably benign	Het
Acnat1	A	T	4: 49,447,716 (GRCm39)	H288Q	possibly damaging	Het
Adamts1	T	C	16: 85,599,114 (GRCm39)	E162G	possibly damaging	Het
Akap11	A	G	14: 78,751,101 (GRCm39)	S429P	probably benign	Het
Alg14	T	C	3: 121,155,415 (GRCm39)	Y212H	probably damaging	Het
Cacna1g	T	C	11: 94,357,007 (GRCm39)	T97A	probably damaging	Het
Ccdc112	T	A	18: 46,420,821 (GRCm39)	N310Y	possibly damaging	Het
Cenpl	A	T	1: 160,913,574 (GRCm39)	Y328F	probably damaging	Het
Cep162	G	A	9: 87,086,133 (GRCm39)	H1064Y	probably benign	Het
Cnksr3	T	A	10: 7,104,324 (GRCm39)	E126D	probably benign	Het
Ctsh	T	A	9: 89,943,618 (GRCm39)	M81K	probably benign	Het
D6Wsu163e	A	G	6: 126,932,112 (GRCm39)	T284A	probably damaging	Het
Dab1	C	T	4: 104,588,948 (GRCm39)	A524V	probably benign	Het
Dnaaf1	T	A	8: 120,309,616 (GRCm39)	M196K	probably benign	Het
Dnah9	C	A	11: 65,725,212 (GRCm39)	G4314C	probably damaging	Het
Dph1	A	G	11: 75,070,557 (GRCm39)	Y361H	probably damaging	Het
Ect2	C	T	3: 27,204,221 (GRCm39)	M29I	probably benign	Het
Eif3h	T	C	15: 51,661,066 (GRCm39)	Y167C	probably damaging	Het
Epc2	C	T	2: 49,422,101 (GRCm39)	R332C	probably damaging	Het
Fras1	C	A	5: 96,897,282 (GRCm39)		probably null	Het
Gfm2	A	G	13: 97,299,442 (GRCm39)	I386V	probably benign	Het
Gpd1l	G	A	9: 114,743,399 (GRCm39)	T167I	probably damaging	Het
Hsph1	T	A	5: 149,546,950 (GRCm39)	K567*	probably null	Het
Igfn1	T	G	1: 135,897,126 (GRCm39)	S1147R	probably benign	Het
Itgb4	T	C	11: 115,874,590 (GRCm39)	V406A	probably benign	Het
Kcna2	A	G	3: 107,012,429 (GRCm39)	I337V	possibly damaging	Het
Kcnab1	T	C	3: 65,209,615 (GRCm39)		probably null	Het
Kri1	G	T	9: 21,191,788 (GRCm39)		probably benign	Het
Lrguk	T	A	6: 34,110,322 (GRCm39)	I801K	possibly damaging	Het
Magi2	A	T	5: 20,807,458 (GRCm39)	N871Y	probably damaging	Het
Map3k10	G	T	7: 27,360,981 (GRCm39)		probably null	Het
Mrps25	T	C	6: 92,155,721 (GRCm39)	T71A	probably damaging	Het
Myo15a	G	A	11: 60,390,321 (GRCm39)	W945*	probably null	Het
Ncan	A	T	8: 70,555,104 (GRCm39)	I1021N	probably damaging	Het
Ncf4	C	A	15: 78,134,582 (GRCm39)	S11R	probably benign	Het
Neb	A	C	2: 52,086,307 (GRCm39)	S5255R	possibly damaging	Het
Nop2	TGATGAAGATGAAGATGA	TGATGAAGATGA	6: 125,114,042 (GRCm39)		probably benign	Het
Or4c102	G	A	2: 88,422,516 (GRCm39)	A123T	probably damaging	Het
Or5ak22	A	T	2: 85,230,785 (GRCm39)	F31I	probably damaging	Het
Pacs1	T	C	19: 5,203,742 (GRCm39)	I328V	probably damaging	Het
Pafah2	GCCCC	GCCCCC	4: 134,152,852 (GRCm39)		probably null	Het
Pan2	A	G	10: 128,140,247 (GRCm39)	H56R	possibly damaging	Het
Pigo	G	A	4: 43,024,710 (GRCm39)	R124*	probably null	Het
Ppfia2	A	G	10: 106,763,571 (GRCm39)	D1188G	probably benign	Het
Ppp1r16b	A	G	2: 158,603,355 (GRCm39)	N327D	probably damaging	Het
Psd3	A	G	8: 68,172,656 (GRCm39)	C223R	possibly damaging	Het
Rad50	A	G	11: 53,592,934 (GRCm39)	V72A	possibly damaging	Het
Rcor3	T	A	1: 191,785,133 (GRCm39)	D445V	possibly damaging	Het
Rundc1	T	A	11: 101,324,507 (GRCm39)	H404Q	probably benign	Het
Ryr1	T	C	7: 28,779,236 (GRCm39)	K2083E	probably benign	Het
Scd3	C	A	19: 44,224,281 (GRCm39)	H171Q	probably damaging	Het
Scrn2	T	C	11: 96,923,021 (GRCm39)	F155L	probably benign	Het
Serpina12	A	T	12: 103,998,769 (GRCm39)	L323Q	probably damaging	Het
Sptlc3	T	A	2: 139,467,843 (GRCm39)	M467K	probably benign	Het
Stard9	G	T	2: 120,528,970 (GRCm39)	R1742S	possibly damaging	Het
Thbd	A	T	2: 148,249,604 (GRCm39)	L88*	probably null	Het
Tln2	G	A	9: 67,269,969 (GRCm39)	Q477*	probably null	Het
Tnn	T	A	1: 159,943,752 (GRCm39)	E1020D	possibly damaging	Het
Trip12	A	T	1: 84,726,990 (GRCm39)	H3Q	probably damaging	Het
Vmn2r115	ATCTTCT	ATCT	17: 23,578,962 (GRCm39)		probably benign	Het
Vmp1	G	A	11: 86,534,413 (GRCm39)	Q165*	probably null	Het
Zfp758	T	A	17: 22,594,204 (GRCm39)	M230K	probably benign	Het

Other mutations in Or5d16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02507:Or5d16	APN	2	87,773,262 (GRCm39)	nonsense	probably null
IGL03245:Or5d16	APN	2	87,773,086 (GRCm39)	missense	possibly damaging	0.75
B5639:Or5d16	UTSW	2	87,773,942 (GRCm39)	missense	probably benign	0.03
PIT4531001:Or5d16	UTSW	2	87,773,571 (GRCm39)	missense	probably damaging	1.00
R0212:Or5d16	UTSW	2	87,773,435 (GRCm39)	missense	probably damaging	1.00
R0393:Or5d16	UTSW	2	87,773,909 (GRCm39)	missense	possibly damaging	0.62
R1178:Or5d16	UTSW	2	87,773,490 (GRCm39)	missense	probably benign	0.02
R1180:Or5d16	UTSW	2	87,773,490 (GRCm39)	missense	probably benign	0.02
R1181:Or5d16	UTSW	2	87,773,490 (GRCm39)	missense	probably benign	0.02
R1266:Or5d16	UTSW	2	87,773,877 (GRCm39)	missense	probably benign	0.01
R1998:Or5d16	UTSW	2	87,773,490 (GRCm39)	missense	probably benign	0.02
R2000:Or5d16	UTSW	2	87,773,490 (GRCm39)	missense	probably benign	0.02
R4119:Or5d16	UTSW	2	87,773,787 (GRCm39)	missense	probably damaging	1.00
R4213:Or5d16	UTSW	2	87,773,465 (GRCm39)	missense	probably benign	0.00
R5157:Or5d16	UTSW	2	87,773,232 (GRCm39)	missense	probably benign
R5688:Or5d16	UTSW	2	87,773,552 (GRCm39)	missense	probably benign	0.02
R5731:Or5d16	UTSW	2	87,773,771 (GRCm39)	missense	possibly damaging	0.89
R6064:Or5d16	UTSW	2	87,773,828 (GRCm39)	missense	probably benign	0.00
R6372:Or5d16	UTSW	2	87,773,319 (GRCm39)	missense	probably benign	0.00
R6505:Or5d16	UTSW	2	87,773,518 (GRCm39)	nonsense	probably null
R6555:Or5d16	UTSW	2	87,773,632 (GRCm39)	missense	probably damaging	1.00
R6909:Or5d16	UTSW	2	87,773,034 (GRCm39)	missense	probably benign	0.27
R7257:Or5d16	UTSW	2	87,773,915 (GRCm39)	missense	probably damaging	1.00
R8037:Or5d16	UTSW	2	87,773,319 (GRCm39)	missense	probably benign	0.00
R8367:Or5d16	UTSW	2	87,773,441 (GRCm39)	missense	possibly damaging	0.75
R9301:Or5d16	UTSW	2	87,773,297 (GRCm39)	missense	probably benign	0.00
Z1088:Or5d16	UTSW	2	87,773,792 (GRCm39)	missense	probably damaging	1.00
Z1176:Or5d16	UTSW	2	87,773,811 (GRCm39)	missense	probably damaging	1.00
Z1176:Or5d16	UTSW	2	87,773,553 (GRCm39)	missense	possibly damaging	0.57

Predicted Primers

Posted On

2015-02-05