Mutagenetix > Incidental Mutation

Incidental Mutation 'R0924:Or6b2b'

83056

Institutional Source

Beutler Lab

Gene Symbol

Or6b2b

Ensembl Gene

ENSMUSG00000057464

Gene Name

olfactory receptor family 6 subfamily B member 2B

Synonyms

MOR103-12, GA_x6K02T2R7CC-81266841-81267776, Olfr1415

MMRRC Submission

039071-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.101) question?

Stock #

R0924 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

92418540-92419475 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 92419127 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 117 (S117P)

Ref Sequence

ENSEMBL: ENSMUSP00000145446 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071521] [ENSMUST00000204009] [ENSMUST00000204766]

AlphaFold

Q7TQS4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000071521
AA Change: S117P

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000084047
Gene: ENSMUSG00000057464
AA Change: S117P

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	1.3e-53	PFAM
Pfam:7tm_1	41	290	1.2e-16	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000204009
AA Change: S117P

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000145446
Gene: ENSMUSG00000057464
AA Change: S117P

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	1.3e-53	PFAM
Pfam:7tm_1	41	290	1.2e-16	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204766

SMART Domains

Protein: ENSMUSP00000144986
Gene: ENSMUSG00000057464

Domain	Start	End	E-Value	Type
Blast:CLECT	1	65	1e-7	BLAST

Meta Mutation Damage Score

0.2126

Coding Region Coverage

1x: 99.5%
3x: 98.9%
10x: 97.7%
20x: 96.2%

Validation Efficiency

97% (69/71)

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: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts18	A	T	8: 114,432,028 (GRCm39)		probably null	Het
Ahcyl2	A	C	6: 29,870,627 (GRCm39)		probably null	Het
Ajap1	T	A	4: 153,470,929 (GRCm39)	I293F	probably damaging	Het
Akap10	T	C	11: 61,795,689 (GRCm39)		probably benign	Het
Aldh3b2	T	C	19: 4,029,350 (GRCm39)	V241A	probably benign	Het
Anxa6	A	T	11: 54,885,214 (GRCm39)		probably null	Het
Atpaf1	T	A	4: 115,652,635 (GRCm39)	V12D	probably damaging	Het
Aurkb	C	A	11: 68,936,822 (GRCm39)	Y12*	probably null	Het
Bicdl1	A	G	5: 115,799,587 (GRCm39)		probably benign	Het
Bnc1	A	T	7: 81,628,156 (GRCm39)		probably benign	Het
Bpi	A	G	2: 158,103,346 (GRCm39)	I114V	possibly damaging	Het
Cacna1c	A	T	6: 118,652,857 (GRCm39)	I772N	probably damaging	Het
Cacna2d1	A	G	5: 16,570,860 (GRCm39)	N1045D	possibly damaging	Het
Ccrl2	A	G	9: 110,885,036 (GRCm39)	V154A	probably benign	Het
Celsr3	C	A	9: 108,723,224 (GRCm39)	Q2831K	possibly damaging	Het
Cplane1	T	C	15: 8,280,554 (GRCm39)		probably benign	Het
Cul3	A	T	1: 80,267,835 (GRCm39)	M102K	probably damaging	Het
Cwf19l2	T	C	9: 3,441,047 (GRCm39)		probably benign	Het
Dlg5	G	A	14: 24,185,645 (GRCm39)	P1920L	probably damaging	Het
Dnah2	T	C	11: 69,312,134 (GRCm39)	H4393R	probably damaging	Het
Eif2b3	T	A	4: 116,938,775 (GRCm39)	V408D	possibly damaging	Het
Eml3	T	C	19: 8,910,675 (GRCm39)		probably null	Het
Enpp2	T	C	15: 54,770,355 (GRCm39)		probably benign	Het
Fcgbpl1	A	T	7: 27,839,555 (GRCm39)	Y456F	probably damaging	Het
Gm14178	T	A	11: 99,638,326 (GRCm39)	T18S		Het
H2bc12	G	A	13: 22,220,210 (GRCm39)	D52N	probably damaging	Het
H2-M11	A	G	17: 36,860,106 (GRCm39)	M324V	probably benign	Het
H2-T13	A	T	17: 36,394,824 (GRCm39)	V33E	probably damaging	Het
Hdac10	T	C	15: 89,010,065 (GRCm39)	T298A	probably benign	Het
Hepacam	A	C	9: 37,295,224 (GRCm39)		probably benign	Het
Hmx3	A	T	7: 131,144,813 (GRCm39)	H41L	probably benign	Het
Ifi27l2a	A	G	12: 103,408,639 (GRCm39)	V68A	probably damaging	Het
Itga11	A	G	9: 62,683,956 (GRCm39)	E1079G	probably benign	Het
Krt6a	T	C	15: 101,599,235 (GRCm39)		probably benign	Het
L1td1	A	G	4: 98,625,862 (GRCm39)	N686D	probably damaging	Het
Lrrtm2	G	A	18: 35,346,808 (GRCm39)	R165C	probably damaging	Het
Macf1	G	T	4: 123,279,271 (GRCm39)	A3910E	probably damaging	Het
Muc5ac	A	T	7: 141,361,252 (GRCm39)	Y1521F	possibly damaging	Het
Myo7a	A	T	7: 97,747,463 (GRCm39)	I129N	probably damaging	Het
Ncam1	A	T	9: 49,473,476 (GRCm39)		probably benign	Het
Nckap1	A	T	2: 80,384,593 (GRCm39)	C114S	probably benign	Het
Nf1	T	G	11: 79,344,692 (GRCm39)	W1260G	probably damaging	Het
Or3a1d	T	C	11: 74,237,624 (GRCm39)	Y262C	probably damaging	Het
Or6c76b	A	T	10: 129,692,515 (GRCm39)	I43F	probably damaging	Het
Oxtr	A	T	6: 112,466,598 (GRCm39)		probably null	Het
Pabpc4	C	T	4: 123,188,458 (GRCm39)	R356C	possibly damaging	Het
Pcbp2	T	A	15: 102,398,197 (GRCm39)	D182E	probably damaging	Het
Pgm2	A	T	5: 64,269,490 (GRCm39)	I526F	possibly damaging	Het
Rab43	A	T	6: 87,769,752 (GRCm39)	Y151*	probably null	Het
Rbm19	A	G	5: 120,264,269 (GRCm39)	E343G	probably benign	Het
Rel	A	T	11: 23,692,439 (GRCm39)	D531E	probably benign	Het
Rfx4	T	A	10: 84,704,291 (GRCm39)	V262E	probably damaging	Het
Rnf31	T	C	14: 55,830,459 (GRCm39)		probably benign	Het
Robo3	T	A	9: 37,340,778 (GRCm39)		probably benign	Het
Ryr3	A	G	2: 112,672,178 (GRCm39)	L1431P	probably damaging	Het
Sema3d	A	C	5: 12,513,183 (GRCm39)	D51A	possibly damaging	Het
Sema6a	A	G	18: 47,381,559 (GRCm39)	L996P	probably damaging	Het
Sh2d4a	T	A	8: 68,787,775 (GRCm39)	F294I	probably damaging	Het
Sorl1	T	A	9: 41,919,470 (GRCm39)		probably benign	Het
Sox1ot	G	T	8: 12,480,455 (GRCm39)		noncoding transcript	Het
Spsb3	A	T	17: 25,110,358 (GRCm39)	N395I	probably damaging	Het
Sptan1	A	G	2: 29,906,040 (GRCm39)	N1662S	probably damaging	Het
Srd5a2	G	T	17: 74,331,516 (GRCm39)	N160K	probably damaging	Het
Sting1	A	G	18: 35,868,154 (GRCm39)		probably null	Het
Tmem132d	G	A	5: 128,061,503 (GRCm39)		probably benign	Het
Unc80	A	T	1: 66,549,800 (GRCm39)	Q686L	possibly damaging	Het
Vmn2r93	A	G	17: 18,524,443 (GRCm39)	T146A	probably benign	Het
Wdr19	A	G	5: 65,413,782 (GRCm39)		probably benign	Het
Zfp646	C	T	7: 127,482,982 (GRCm39)	Q1500*	probably null	Het
Zfp683	T	C	4: 133,783,138 (GRCm39)	Y201H	probably benign	Het

Other mutations in Or6b2b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03066:Or6b2b	APN	1	92,419,305 (GRCm39)	missense	probably damaging	1.00
R0538:Or6b2b	UTSW	1	92,419,055 (GRCm39)	missense	possibly damaging	0.77
R0930:Or6b2b	UTSW	1	92,419,127 (GRCm39)	missense	possibly damaging	0.95
R1025:Or6b2b	UTSW	1	92,419,445 (GRCm39)	missense	probably benign	0.19
R1201:Or6b2b	UTSW	1	92,418,875 (GRCm39)	missense	probably benign	0.04
R1413:Or6b2b	UTSW	1	92,418,610 (GRCm39)	missense	probably damaging	1.00
R1510:Or6b2b	UTSW	1	92,419,339 (GRCm39)	missense	probably damaging	1.00
R1846:Or6b2b	UTSW	1	92,418,822 (GRCm39)	nonsense	probably null
R1850:Or6b2b	UTSW	1	92,419,124 (GRCm39)	missense	possibly damaging	0.89
R1940:Or6b2b	UTSW	1	92,419,457 (GRCm39)	missense	probably benign	0.14
R2760:Or6b2b	UTSW	1	92,418,802 (GRCm39)	missense	probably damaging	0.99
R4066:Or6b2b	UTSW	1	92,418,911 (GRCm39)	missense	probably damaging	1.00
R4837:Or6b2b	UTSW	1	92,418,697 (GRCm39)	missense	probably benign	0.39
R5310:Or6b2b	UTSW	1	92,418,758 (GRCm39)	missense	probably damaging	1.00
R5503:Or6b2b	UTSW	1	92,418,918 (GRCm39)	missense	probably benign	0.07
R5748:Or6b2b	UTSW	1	92,418,815 (GRCm39)	missense	probably damaging	0.99
R5760:Or6b2b	UTSW	1	92,418,922 (GRCm39)	missense	possibly damaging	0.95
R5853:Or6b2b	UTSW	1	92,419,439 (GRCm39)	missense	probably benign	0.00
R5926:Or6b2b	UTSW	1	92,419,288 (GRCm39)	missense	probably damaging	1.00
R6199:Or6b2b	UTSW	1	92,419,264 (GRCm39)	missense	possibly damaging	0.89
R7585:Or6b2b	UTSW	1	92,419,042 (GRCm39)	missense	probably benign	0.10
R7627:Or6b2b	UTSW	1	92,419,107 (GRCm39)	nonsense	probably null
R7726:Or6b2b	UTSW	1	92,419,029 (GRCm39)	missense	probably benign	0.30
R8011:Or6b2b	UTSW	1	92,418,997 (GRCm39)	missense	possibly damaging	0.60
R8306:Or6b2b	UTSW	1	92,419,247 (GRCm39)	missense	possibly damaging	0.64
R9142:Or6b2b	UTSW	1	92,419,411 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ATGAAGGCCAGGATGAAGTCCACC -3'
(R):5'- GCTACTCACAGGAACCAGGAATGC -3'

Sequencing Primer
(F):5'- GATGAAGTCCACCAGCTCTG -3'
(R):5'- AACCAGGAATGCTGTCTGTC -3'

Posted On

2013-11-08