Mutagenetix > Incidental Mutation

Incidental Mutation 'R9112:Or5b3'

692335

Institutional Source

Beutler Lab

Gene Symbol

Or5b3

Ensembl Gene

ENSMUSG00000063777

Gene Name

olfactory receptor family 5 subfamily B member 3

Synonyms

MOR202-11, Olfr1469, GA_x6K02T2RE5P-3743369-3744289

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.073) question?

Stock #

R9112 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

13387935-13388864 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 13388475 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 181 (I181F)

Ref Sequence

ENSEMBL: ENSMUSP00000150006 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000077538] [ENSMUST00000216910]

AlphaFold

Q8VFW5

Predicted Effect

probably benign
Transcript: ENSMUST00000077538
AA Change: I181F

PolyPhen 2 Score 0.049 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000076741
Gene: ENSMUSG00000063777
AA Change: I181F

Domain	Start	End	E-Value	Type
Pfam:7tm_4	32	308	2e-47	PFAM
Pfam:7tm_1	42	290	2.3e-19	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000216910
AA Change: I181F

PolyPhen 2 Score 0.049 (Sensitivity: 0.94; Specificity: 0.83)

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (56/56)

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: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310033P09Rik	A	G	11: 59,100,806 (GRCm39)	S181G	possibly damaging	Het
5730596B20Rik	A	G	6: 52,156,413 (GRCm39)	R160G	unknown	Het
Acy1	A	G	9: 106,311,952 (GRCm39)	Y262H	probably benign	Het
Adamts13	T	C	2: 26,880,379 (GRCm39)	S681P	possibly damaging	Het
Adgra3	C	A	5: 50,118,395 (GRCm39)	C1051F	probably damaging	Het
Afp	T	C	5: 90,652,289 (GRCm39)		probably null	Het
Agrn	A	T	4: 156,261,514 (GRCm39)	V568E	probably damaging	Het
Ahnak	A	G	19: 8,987,149 (GRCm39)	E2811G	probably damaging	Het
Ap1m1	C	A	8: 72,994,066 (GRCm39)	Y7*	probably null	Het
Apobec1	T	A	6: 122,555,837 (GRCm39)	T207S	probably benign	Het
Arhgap32	G	A	9: 32,157,309 (GRCm39)	R102Q	probably damaging	Het
Bcat2	T	C	7: 45,237,446 (GRCm39)		probably null	Het
Cd209f	T	A	8: 4,155,802 (GRCm39)		probably benign	Het
Cox7c	G	A	13: 86,194,837 (GRCm39)		probably benign	Het
Cyp2d11	A	G	15: 82,276,203 (GRCm39)	V156A	possibly damaging	Het
Dhrs3	A	T	4: 144,653,769 (GRCm39)	T297S	probably benign	Het
Dip2c	T	C	13: 9,660,766 (GRCm39)	C876R	probably damaging	Het
Eprs1	A	T	1: 185,129,273 (GRCm39)	I587F	probably damaging	Het
Fam13c	A	G	10: 70,286,978 (GRCm39)	T81A	probably benign	Het
Flt4	A	G	11: 49,524,064 (GRCm39)	Y548C	probably damaging	Het
Garin2	T	C	12: 78,757,202 (GRCm39)		probably null	Het
Gimap4	T	A	6: 48,667,629 (GRCm39)	V128E	probably benign	Het
Gm32742	A	G	9: 51,060,735 (GRCm39)	L856P	possibly damaging	Het
Gm5916	A	G	9: 36,032,258 (GRCm39)	Y59H	probably damaging	Het
Gnai3	A	T	3: 108,030,990 (GRCm39)	H57Q		Het
Golga3	G	T	5: 110,333,757 (GRCm39)	R131L	probably benign	Het
Gpc6	A	T	14: 117,424,088 (GRCm39)	I59F	probably benign	Het
H2bc6	T	C	13: 23,769,753 (GRCm39)	M63V	possibly damaging	Het
Herc6	T	C	6: 57,596,604 (GRCm39)	S515P	probably damaging	Het
Ift74	T	C	4: 94,575,103 (GRCm39)	I518T	probably benign	Het
Kat6b	T	C	14: 21,675,256 (GRCm39)	S474P	possibly damaging	Het
Klhl3	A	C	13: 58,248,212 (GRCm39)	I28S	unknown	Het
Klrh1	T	A	6: 129,743,697 (GRCm39)	I196F	probably benign	Het
Lipi	A	G	16: 75,359,159 (GRCm39)	F259S	probably damaging	Het
Lrrc8a	T	A	2: 30,145,782 (GRCm39)	S199T	probably damaging	Het
Map2	T	A	1: 66,472,723 (GRCm39)	C1709*	probably null	Het
Mrgprf	A	G	7: 144,861,503 (GRCm39)	S22G	probably benign	Het
Myo1e	G	T	9: 70,274,983 (GRCm39)	R712L	probably benign	Het
Nras	A	T	3: 102,967,658 (GRCm39)	N85Y	probably benign	Het
Or4a71	C	T	2: 89,358,337 (GRCm39)	C139Y	probably damaging	Het
Or6ae1	A	G	7: 139,742,660 (GRCm39)	S68P		Het
Or9q2	T	C	19: 13,772,780 (GRCm39)	H65R	probably damaging	Het
Pcp2	T	A	8: 3,674,638 (GRCm39)		probably benign	Het
Pigv	T	C	4: 133,392,079 (GRCm39)	R364G	probably benign	Het
Plekhh3	T	A	11: 101,061,625 (GRCm39)	S30C	probably damaging	Het
Poglut3	A	G	9: 53,295,530 (GRCm39)	Y44C	probably damaging	Het
Pramel11	A	C	4: 143,623,334 (GRCm39)	V280G	possibly damaging	Het
Pramel51	C	T	12: 88,144,055 (GRCm39)	A261T	possibly damaging	Het
Rhof	T	C	5: 123,258,571 (GRCm39)		probably benign	Het
Rufy3	A	T	5: 88,780,336 (GRCm39)	E361D		Het
Serpina1b	T	C	12: 103,698,699 (GRCm39)	D50G	probably benign	Het
Sgsm2	G	A	11: 74,756,222 (GRCm39)	Q376*	probably null	Het
Slc18b1	A	T	10: 23,692,262 (GRCm39)	I246F	probably damaging	Het
Slc38a9	A	T	13: 112,850,777 (GRCm39)	N387I	probably damaging	Het
Synrg	C	G	11: 83,862,409 (GRCm39)	P35A	probably damaging	Het
Tdrp	T	C	8: 14,005,796 (GRCm39)	K42E	probably damaging	Het
Trappc10	A	C	10: 78,029,201 (GRCm39)	M1112R	probably damaging	Het
Ube2e1	A	G	14: 18,285,203 (GRCm38)	V90A	probably damaging	Het
Vwde	C	A	6: 13,205,051 (GRCm39)	V277F	possibly damaging	Het
Zfyve16	A	G	13: 92,659,563 (GRCm39)	M116T	possibly damaging	Het

Other mutations in Or5b3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01064:Or5b3	APN	19	13,388,590 (GRCm39)	missense	probably benign	0.01
IGL01520:Or5b3	APN	19	13,388,114 (GRCm39)	missense	probably damaging	0.97
IGL01671:Or5b3	APN	19	13,388,255 (GRCm39)	missense	probably benign	0.29
IGL02247:Or5b3	APN	19	13,388,831 (GRCm39)	missense	probably benign	0.01
IGL02297:Or5b3	APN	19	13,388,839 (GRCm39)	missense	probably benign	0.00
IGL02417:Or5b3	APN	19	13,388,259 (GRCm39)	missense	possibly damaging	0.52
IGL02442:Or5b3	APN	19	13,388,351 (GRCm39)	missense	probably benign	0.00
IGL02989:Or5b3	APN	19	13,388,850 (GRCm39)	missense	probably benign
IGL03269:Or5b3	APN	19	13,388,792 (GRCm39)	missense	probably damaging	0.99
IGL02988:Or5b3	UTSW	19	13,388,826 (GRCm39)	missense	possibly damaging	0.75
R0707:Or5b3	UTSW	19	13,388,784 (GRCm39)	missense	probably benign	0.22
R1055:Or5b3	UTSW	19	13,388,754 (GRCm39)	missense	probably benign	0.10
R1102:Or5b3	UTSW	19	13,388,454 (GRCm39)	missense	probably damaging	1.00
R1946:Or5b3	UTSW	19	13,388,143 (GRCm39)	missense	possibly damaging	0.64
R2111:Or5b3	UTSW	19	13,388,307 (GRCm39)	missense	probably damaging	0.99
R4072:Or5b3	UTSW	19	13,388,299 (GRCm39)	missense	possibly damaging	0.49
R4073:Or5b3	UTSW	19	13,388,299 (GRCm39)	missense	possibly damaging	0.49
R4076:Or5b3	UTSW	19	13,388,299 (GRCm39)	missense	possibly damaging	0.49
R4726:Or5b3	UTSW	19	13,388,469 (GRCm39)	missense	probably damaging	1.00
R4939:Or5b3	UTSW	19	13,388,219 (GRCm39)	missense	probably benign	0.10
R5914:Or5b3	UTSW	19	13,388,326 (GRCm39)	missense	probably benign	0.31
R6003:Or5b3	UTSW	19	13,388,403 (GRCm39)	missense	probably benign	0.34
R6743:Or5b3	UTSW	19	13,387,957 (GRCm39)	missense	probably damaging	1.00
R6825:Or5b3	UTSW	19	13,388,514 (GRCm39)	missense	probably benign	0.01
R6826:Or5b3	UTSW	19	13,388,452 (GRCm39)	missense	probably benign	0.05
R6970:Or5b3	UTSW	19	13,388,792 (GRCm39)	missense	probably damaging	0.99
R7558:Or5b3	UTSW	19	13,388,355 (GRCm39)	missense	probably damaging	1.00
R7596:Or5b3	UTSW	19	13,388,511 (GRCm39)	missense	probably benign	0.01
R7923:Or5b3	UTSW	19	13,388,182 (GRCm39)	missense	probably benign	0.17
R8014:Or5b3	UTSW	19	13,388,175 (GRCm39)	missense	not run
R8506:Or5b3	UTSW	19	13,388,604 (GRCm39)	missense	possibly damaging	0.49
R8746:Or5b3	UTSW	19	13,388,092 (GRCm39)	missense	probably benign	0.44
R8803:Or5b3	UTSW	19	13,388,037 (GRCm39)	missense	probably damaging	0.99
R9721:Or5b3	UTSW	19	13,388,334 (GRCm39)	missense	probably benign	0.17
Z1177:Or5b3	UTSW	19	13,388,083 (GRCm39)	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- ACTGTGGAAAATTACCTGTTGGC -3'
(R):5'- GCACAAGTGGATATAGCCTTTCG -3'

Sequencing Primer
(F):5'- CAATGGCCTATGATCGTTATGCAGC -3'
(R):5'- GCCTTTCGATATCCAGAACTTGAGTG -3'

Posted On

2021-12-30