Mutagenetix > Incidental Mutation

Incidental Mutation 'R4353:Or2h1b'

327436

Institutional Source

Beutler Lab

Gene Symbol

Or2h1b

Ensembl Gene

ENSMUSG00000091601

Gene Name

olfactory receptor family 2 subfamily H member 1B

Synonyms

MOR256-39P, GA_x6K02T2PSCP-1592036-1591098, Olfr93

MMRRC Submission

040866-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

R4353 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

37461923-37462861 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 37462228 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 58 (I58F)

Ref Sequence

ENSEMBL: ENSMUSP00000146548 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000171679] [ENSMUST00000208003] [ENSMUST00000219235]

AlphaFold

Q6UAH1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000171679
AA Change: I212F

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

SMART Domains

Protein: ENSMUSP00000125907
Gene: ENSMUSG00000091601
AA Change: I212F

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	306	5.7e-50	PFAM
Pfam:7tm_1	39	288	3.3e-28	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000208003
AA Change: I58F

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000219235
AA Change: I212F

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

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.4%
20x: 95.5%

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: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	C	T	6: 128,557,349 (GRCm39)	A115T	probably benign	Het
Alpk2	C	T	18: 65,424,523 (GRCm39)	R1888H	possibly damaging	Het
Arhgap33	C	A	7: 30,223,561 (GRCm39)	V823L	possibly damaging	Het
Atp2b2	T	C	6: 113,742,745 (GRCm39)	I736V	probably benign	Het
Atp8a1	T	C	5: 67,926,451 (GRCm39)	T260A	probably damaging	Het
B4galnt3	T	C	6: 120,192,437 (GRCm39)	E433G	possibly damaging	Het
Bzw2	A	T	12: 36,173,978 (GRCm39)	F99I	probably damaging	Het
Cdh20	A	G	1: 104,906,814 (GRCm39)	D547G	probably damaging	Het
Col27a1	G	T	4: 63,143,868 (GRCm39)	A519S	probably benign	Het
Coq6	G	A	12: 84,414,923 (GRCm39)	G110D	probably damaging	Het
Cpb1	T	C	3: 20,316,708 (GRCm39)	T281A	probably benign	Het
Cttnbp2	T	C	6: 18,514,703 (GRCm39)	D11G	probably benign	Het
Cyp2c37	A	G	19: 39,988,989 (GRCm39)	Y316C	possibly damaging	Het
Dcdc2a	T	A	13: 25,240,474 (GRCm39)	I74N	probably damaging	Het
Dhx9	A	G	1: 153,347,535 (GRCm39)	L391P	probably damaging	Het
Dsc2	G	T	18: 20,183,125 (GRCm39)	L98I	probably damaging	Het
Dthd1	T	A	5: 63,000,210 (GRCm39)	S511T	probably benign	Het
Dusp2	A	G	2: 127,179,256 (GRCm39)	T204A	probably damaging	Het
Elovl5	T	C	9: 77,868,199 (GRCm39)	V37A	probably benign	Het
Etv1	A	G	12: 38,907,105 (GRCm39)	E369G	probably damaging	Het
Gem	G	A	4: 11,705,939 (GRCm39)	R9H	probably damaging	Het
Heg1	A	G	16: 33,530,847 (GRCm39)	T108A	probably benign	Het
Inava	C	T	1: 136,153,946 (GRCm39)	V180I	probably damaging	Het
Iqgap2	C	T	13: 95,807,904 (GRCm39)	V788M	probably damaging	Het
Kyat3	T	C	3: 142,437,054 (GRCm39)		probably null	Het
Llgl1	C	T	11: 60,600,394 (GRCm39)	P581L	probably benign	Het
Mecom	C	A	3: 30,020,887 (GRCm39)	V452L	possibly damaging	Het
Meis2	A	G	2: 115,890,044 (GRCm39)	M146T	probably damaging	Het
Nrp2	A	G	1: 62,777,576 (GRCm39)	D127G	probably damaging	Het
Nt5el	T	C	13: 105,255,253 (GRCm39)	Y445H	probably benign	Het
Nup214	T	C	2: 31,867,929 (GRCm39)		probably null	Het
Pabpc4	C	T	4: 123,184,060 (GRCm39)	T191I	probably damaging	Het
Pcnx2	T	C	8: 126,489,590 (GRCm39)	H1668R	probably damaging	Het
Poln	C	T	5: 34,286,796 (GRCm39)	C124Y	probably benign	Het
Ppp2r2a	T	A	14: 67,266,386 (GRCm39)	I92L	probably damaging	Het
Prb1b	T	G	6: 132,290,624 (GRCm39)	Y25S	unknown	Het
Ptch1	C	T	13: 63,682,143 (GRCm39)	R537H	probably damaging	Het
Rnf130	T	C	11: 49,978,267 (GRCm39)	V276A	possibly damaging	Het
Rnf31	AAC	A	14: 55,838,555 (GRCm39)		probably null	Het
Rnf38	A	T	4: 44,149,100 (GRCm39)	N82K	possibly damaging	Het
Scn7a	T	A	2: 66,506,780 (GRCm39)	M1370L	probably benign	Het
Sema4b	C	A	7: 79,865,399 (GRCm39)	L125I	probably damaging	Het
Slc12a7	C	T	13: 73,938,853 (GRCm39)	T210I	possibly damaging	Het
Sox8	A	C	17: 25,786,309 (GRCm39)	*465G	probably null	Het
Spg11	G	T	2: 121,943,675 (GRCm39)	T159K	possibly damaging	Het
Stk36	A	G	1: 74,671,966 (GRCm39)	R889G	possibly damaging	Het
Tmbim7	A	G	5: 3,711,796 (GRCm39)	S14G	probably benign	Het
Usp16	A	G	16: 87,267,242 (GRCm39)	N211D	probably damaging	Het
Vmn1r6	C	T	6: 56,979,677 (GRCm39)	A113V	possibly damaging	Het
Zc3h14	A	G	12: 98,730,219 (GRCm39)	N92D	possibly damaging	Het
Zfp638	T	C	6: 83,961,041 (GRCm39)	S1206P	probably damaging	Het

Other mutations in Or2h1b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01087:Or2h1b	APN	17	37,462,332 (GRCm39)	missense	probably damaging	1.00
IGL02369:Or2h1b	APN	17	37,462,665 (GRCm39)	missense	probably damaging	1.00
IGL02392:Or2h1b	APN	17	37,461,979 (GRCm39)	missense	probably benign	0.03
IGL02516:Or2h1b	APN	17	37,462,163 (GRCm39)	missense	possibly damaging	0.95
IGL03089:Or2h1b	APN	17	37,462,534 (GRCm39)	missense	probably damaging	1.00
PIT4515001:Or2h1b	UTSW	17	37,462,270 (GRCm39)	missense	probably benign
R0396:Or2h1b	UTSW	17	37,462,446 (GRCm39)	missense	probably damaging	1.00
R2276:Or2h1b	UTSW	17	37,462,145 (GRCm39)	nonsense	probably null
R2278:Or2h1b	UTSW	17	37,462,145 (GRCm39)	nonsense	probably null
R3419:Or2h1b	UTSW	17	37,462,242 (GRCm39)	missense	probably damaging	0.99
R4254:Or2h1b	UTSW	17	37,462,530 (GRCm39)	missense	possibly damaging	0.90
R4530:Or2h1b	UTSW	17	37,462,498 (GRCm39)	missense	possibly damaging	0.84
R4666:Or2h1b	UTSW	17	37,462,270 (GRCm39)	missense	possibly damaging	0.61
R5583:Or2h1b	UTSW	17	37,462,485 (GRCm39)	missense	probably benign	0.00
R5834:Or2h1b	UTSW	17	37,462,690 (GRCm39)	missense	probably damaging	1.00
R6348:Or2h1b	UTSW	17	37,462,497 (GRCm39)	missense	probably damaging	0.96
R6461:Or2h1b	UTSW	17	37,462,362 (GRCm39)	missense	probably damaging	1.00
R6788:Or2h1b	UTSW	17	37,462,713 (GRCm39)	missense	probably damaging	0.98
R7969:Or2h1b	UTSW	17	37,462,077 (GRCm39)	missense	possibly damaging	0.95
R8374:Or2h1b	UTSW	17	37,462,636 (GRCm39)	missense	probably damaging	0.97
R9126:Or2h1b	UTSW	17	37,462,123 (GRCm39)	missense	possibly damaging	0.90
R9298:Or2h1b	UTSW	17	37,462,572 (GRCm39)	missense	probably damaging	1.00
Z1177:Or2h1b	UTSW	17	37,462,716 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- TGCTTCTCTCTTGGGCATAG -3'
(R):5'- CTTTGACCGCTATGTGGCTG -3'

Sequencing Primer
(F):5'- CATAGGGATTTTTGGGCTGCAGATAG -3'
(R):5'- GCTATAGGTTTGGTCCAATCCATAG -3'

Posted On

2015-07-07