Mutagenetix > Incidental Mutation

Incidental Mutation 'R4698:Or5m10b'

355811

Institutional Source

Beutler Lab

Gene Symbol

Or5m10b

Ensembl Gene

ENSMUSG00000057761

Gene Name

olfactory receptor family 5 subfamily M member 10B

Synonyms

GA_x6K02T2Q125-47347069-47348016, Olfr1022, MOR196-1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R4698 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

85698938-85699885 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 85699596 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 220 (Y220C)

Ref Sequence

ENSEMBL: ENSMUSP00000059312 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054736] [ENSMUST00000121914]

AlphaFold

L7MTT3

Predicted Effect

possibly damaging
Transcript: ENSMUST00000054736
AA Change: Y220C

PolyPhen 2 Score 0.905 (Sensitivity: 0.82; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000059312
Gene: ENSMUSG00000057761
AA Change: Y220C

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	312	4.8e-51	PFAM
Pfam:7TM_GPCR_Srsx	35	304	8e-6	PFAM
Pfam:7tm_1	41	290	9.8e-22	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000121914

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.3%

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: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700122O11Rik	A	G	17: 48,349,049 (GRCm39)	V11A	possibly damaging	Het
6030452D12Rik	T	C	8: 107,230,979 (GRCm39)	I55T	unknown	Het
Aadacl2	A	G	3: 59,932,460 (GRCm39)	D325G	probably benign	Het
Adh1	A	G	3: 137,988,274 (GRCm39)	S113G	probably benign	Het
Agxt2	T	C	15: 10,392,130 (GRCm39)		probably null	Het
Aicda	C	T	6: 122,530,847 (GRCm39)		probably benign	Het
Aifm2	T	C	10: 61,563,535 (GRCm39)	M135T	probably benign	Het
Asah2	T	C	19: 32,031,871 (GRCm39)		probably null	Het
Btbd17	T	C	11: 114,682,543 (GRCm39)	R390G	probably damaging	Het
Cadps	T	C	14: 12,705,654 (GRCm38)	E247G	possibly damaging	Het
Cds2	T	C	2: 132,146,873 (GRCm39)	I383T	probably damaging	Het
Celf3	T	A	3: 94,392,174 (GRCm39)		probably null	Het
Crhr2	T	C	6: 55,079,852 (GRCm39)	S162G	possibly damaging	Het
Dapl1	A	T	2: 59,335,118 (GRCm39)	K91*	probably null	Het
Ddx60	A	C	8: 62,465,458 (GRCm39)	M1372L	probably benign	Het
Dnah2	A	T	11: 69,389,358 (GRCm39)	F845I	probably damaging	Het
Dscam	T	C	16: 96,411,524 (GRCm39)	D1784G	probably damaging	Het
Ech1	T	C	7: 28,531,478 (GRCm39)	V310A	probably benign	Het
Eef1g	A	G	19: 8,955,330 (GRCm39)	D393G	possibly damaging	Het
Eif3k	T	C	7: 28,671,969 (GRCm39)	I172V	possibly damaging	Het
Foxd4	A	G	19: 24,877,625 (GRCm39)	F192L	probably damaging	Het
Gpr153	T	A	4: 152,366,240 (GRCm39)	S268R	probably damaging	Het
H3c13	C	A	3: 96,176,394 (GRCm39)	R129S	probably damaging	Het
Ivl	T	C	3: 92,478,698 (GRCm39)	K456E	unknown	Het
Kif20b	A	T	19: 34,928,944 (GRCm39)	D1190V	probably damaging	Het
Kif21a	T	A	15: 90,840,508 (GRCm39)	I1223L	possibly damaging	Het
Lmf1	T	C	17: 25,798,324 (GRCm39)	V55A	probably damaging	Het
Loxhd1	A	G	18: 77,459,987 (GRCm39)	E659G	possibly damaging	Het
Lrrc37a	T	C	11: 103,394,930 (GRCm39)	E165G	possibly damaging	Het
Mios	T	C	6: 8,228,113 (GRCm39)	Y677H	possibly damaging	Het
Mnx1	T	A	5: 29,679,057 (GRCm39)	K342M	unknown	Het
Mtpap	A	T	18: 4,375,724 (GRCm39)	T35S	possibly damaging	Het
Ndc1	C	G	4: 107,268,334 (GRCm39)	D623E	probably benign	Het
Nedd4l	A	G	18: 65,336,951 (GRCm39)	Y666C	probably damaging	Het
Or52s6	T	A	7: 103,091,842 (GRCm39)	I163F	possibly damaging	Het
Or5ac22	T	C	16: 59,135,720 (GRCm39)	T17A	probably damaging	Het
Or5b12b	T	G	19: 12,861,985 (GRCm39)	F247V	probably benign	Het
Papss1	G	T	3: 131,313,092 (GRCm39)	V369F	probably damaging	Het
Pcdhac2	T	A	18: 37,278,822 (GRCm39)	Y601N	probably damaging	Het
Pde7a	C	T	3: 19,365,095 (GRCm39)	R24Q	probably damaging	Het
Phf21a	A	G	2: 92,187,297 (GRCm39)	D445G	probably damaging	Het
Plekho1	T	A	3: 95,902,964 (GRCm39)	N15I	possibly damaging	Het
Pprc1	T	C	19: 46,057,634 (GRCm39)		probably benign	Het
Ralgapa1	A	T	12: 55,724,061 (GRCm39)		probably null	Het
Rrp12	T	C	19: 41,861,481 (GRCm39)	E942G	probably benign	Het
Skor1	T	C	9: 63,051,830 (GRCm39)	D685G	probably benign	Het
Smim23	A	T	11: 32,774,510 (GRCm39)	I3N	possibly damaging	Het
Spata7	A	T	12: 98,630,536 (GRCm39)	I333F	probably damaging	Het
Sppl2c	T	C	11: 104,079,141 (GRCm39)	I647T	probably benign	Het
Srgap1	C	A	10: 121,628,392 (GRCm39)	R837L	probably benign	Het
Stpg2	C	A	3: 139,014,990 (GRCm39)	P385H	probably damaging	Het
Tmem238	C	A	7: 4,792,016 (GRCm39)	E19*	probably null	Het
Top2b	A	T	14: 16,387,331 (GRCm38)	K140*	probably null	Het
Trp53	T	A	11: 69,479,248 (GRCm39)	L142*	probably null	Het
Tyro3	A	T	2: 119,633,751 (GRCm39)	D133V	probably damaging	Het
Virma	T	A	4: 11,528,636 (GRCm39)	I1291N	probably damaging	Het
Vmn1r213	A	G	13: 23,195,507 (GRCm39)		probably benign	Het
Zbtb10	T	C	3: 9,329,610 (GRCm39)	S323P	possibly damaging	Het
Zfp521	A	T	18: 13,978,660 (GRCm39)	N584K	probably damaging	Het
Zfp944	A	G	17: 22,558,180 (GRCm39)	C356R	probably damaging	Het

Other mutations in Or5m10b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02701:Or5m10b	APN	2	85,699,802 (GRCm39)	missense	probably benign	0.22
IGL03265:Or5m10b	APN	2	85,699,494 (GRCm39)	missense	possibly damaging	0.80
PIT4366001:Or5m10b	UTSW	2	85,699,226 (GRCm39)	missense	probably damaging	1.00
R0057:Or5m10b	UTSW	2	85,699,597 (GRCm39)	nonsense	probably null
R0057:Or5m10b	UTSW	2	85,699,597 (GRCm39)	nonsense	probably null
R0554:Or5m10b	UTSW	2	85,699,863 (GRCm39)	missense	probably benign	0.00
R3873:Or5m10b	UTSW	2	85,699,306 (GRCm39)	nonsense	probably null
R3913:Or5m10b	UTSW	2	85,699,115 (GRCm39)	missense	probably damaging	1.00
R5628:Or5m10b	UTSW	2	85,699,149 (GRCm39)	missense	probably damaging	0.99
R6467:Or5m10b	UTSW	2	85,699,714 (GRCm39)	nonsense	probably null
R6947:Or5m10b	UTSW	2	85,699,271 (GRCm39)	missense	probably benign	0.01
R7092:Or5m10b	UTSW	2	85,698,951 (GRCm39)	missense	probably damaging	1.00
R7351:Or5m10b	UTSW	2	85,694,415 (GRCm39)	unclassified	probably benign
R7574:Or5m10b	UTSW	2	85,699,350 (GRCm39)	missense	probably benign	0.03
R8430:Or5m10b	UTSW	2	85,699,526 (GRCm39)	missense	probably benign	0.00
R8771:Or5m10b	UTSW	2	85,699,712 (GRCm39)	missense	probably damaging	0.99
R8969:Or5m10b	UTSW	2	85,699,832 (GRCm39)	missense	probably benign	0.19
R9101:Or5m10b	UTSW	2	85,694,523 (GRCm39)	unclassified	probably benign
R9630:Or5m10b	UTSW	2	85,699,493 (GRCm39)	missense	probably benign	0.00
R9649:Or5m10b	UTSW	2	85,699,819 (GRCm39)	missense	probably damaging	1.00
R9649:Or5m10b	UTSW	2	85,699,278 (GRCm39)	missense	possibly damaging	0.96

Predicted Primers

PCR Primer
(F):5'- CTGAATGGGCTGTCTCAGACTC -3'
(R):5'- GGGTTCAGGAATGGACTCAG -3'

Sequencing Primer
(F):5'- GGGCTGTCTCAGACTCTGCTC -3'
(R):5'- TTCAGGAATGGACTCAGAAAAGTG -3'

Posted On

2015-10-21