Mutagenetix > Incidental Mutation

Incidental Mutation 'R9303:Or5h23'

705089

Institutional Source

Beutler Lab

Gene Symbol

Or5h23

Ensembl Gene

ENSMUSG00000094539

Gene Name

olfactory receptor family 5 subfamily H member 23

Synonyms

Olfr191, MOR183-5P, GA_x54KRFPKG5P-55314632-55313703

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.067) question?

Stock #

R9303 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

58905915-58906844 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 58906802 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 15 (S15P)

Ref Sequence

ENSEMBL: ENSMUSP00000150473 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078517] [ENSMUST00000215647]

AlphaFold

L7N1Z8

Predicted Effect

probably benign
Transcript: ENSMUST00000078517
AA Change: S15P

PolyPhen 2 Score 0.106 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000077604
Gene: ENSMUSG00000094539
AA Change: S15P

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	308	4e-47	PFAM
Pfam:7tm_1	41	290	6.2e-16	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000215647
AA Change: S15P

PolyPhen 2 Score 0.106 (Sensitivity: 0.93; Specificity: 0.86)

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (57/57)

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: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca16	A	G	7: 120,126,989 (GRCm39)	I1227V	probably benign	Het
Acte1	G	T	7: 143,434,902 (GRCm39)		probably null	Het
Adamts17	T	C	7: 66,489,645 (GRCm39)	L21P	probably damaging	Het
Adcy1	T	C	11: 7,094,766 (GRCm39)	V564A	probably damaging	Het
Adgre1	A	G	17: 57,748,275 (GRCm39)	N492D	probably benign	Het
Aldh1b1	G	A	4: 45,803,811 (GRCm39)	V450M	probably damaging	Het
Arv1	T	A	8: 125,457,685 (GRCm39)	H196Q	probably damaging	Het
Atp9a	A	T	2: 168,517,163 (GRCm39)	I390N	probably benign	Het
Bltp1	A	G	3: 37,098,969 (GRCm39)	I1277V		Het
Capn10	T	C	1: 92,871,665 (GRCm39)		probably null	Het
Casq2	A	G	3: 102,052,700 (GRCm39)	D404G	unknown	Het
Cenpf	T	C	1: 189,392,271 (GRCm39)		probably null	Het
Cep295nl	G	A	11: 118,224,766 (GRCm39)	P26L	possibly damaging	Het
Chmp4c	T	G	3: 10,454,974 (GRCm39)	S214A	probably benign	Het
Chrna5	T	C	9: 54,912,156 (GRCm39)	F319L	probably benign	Het
Csmd1	G	T	8: 16,011,532 (GRCm39)	T2507K	probably benign	Het
Ctnnd2	T	C	15: 30,967,037 (GRCm39)	M996T	probably damaging	Het
Dbf4	T	C	5: 8,448,102 (GRCm39)	T328A	unknown	Het
Ddc	C	T	11: 11,779,132 (GRCm39)	V331I	probably benign	Het
Fads2b	A	T	2: 85,330,649 (GRCm39)	C219*	probably null	Het
Fat1	T	A	8: 45,463,498 (GRCm39)	W1347R	probably damaging	Het
Fbxw21	A	G	9: 108,986,727 (GRCm39)	F51L	probably benign	Het
Gng2	G	T	14: 19,925,961 (GRCm39)	H44N	probably damaging	Het
Hps5	G	A	7: 46,438,619 (GRCm39)	T38I	possibly damaging	Het
Igf2	G	A	7: 142,208,153 (GRCm39)	R64C	probably damaging	Het
Inpp4b	C	T	8: 82,759,758 (GRCm39)	A601V	probably damaging	Het
Kdm2a	A	G	19: 4,395,606 (GRCm39)	Y342H	probably benign	Het
Kidins220	C	A	12: 25,107,110 (GRCm39)	T1430K	probably benign	Het
Knl1	T	C	2: 118,898,829 (GRCm39)	C177R	possibly damaging	Het
Krt32	T	C	11: 99,972,029 (GRCm39)	T440A	probably benign	Het
Kynu	T	A	2: 43,569,768 (GRCm39)	F350Y	probably damaging	Het
Lama4	T	C	10: 38,973,137 (GRCm39)	L1568P	probably damaging	Het
Lrp1b	A	T	2: 41,618,574 (GRCm39)	S281T		Het
Or2y3	A	T	17: 38,393,629 (GRCm39)	V80D	probably damaging	Het
Or8c19-ps1	C	T	9: 38,220,463 (GRCm39)	T124M	probably benign	Het
Orc3	G	A	4: 34,607,181 (GRCm39)	R50*	probably null	Het
Osbpl6	T	A	2: 76,378,716 (GRCm39)	D124E	probably damaging	Het
Parp4	TG	T	14: 56,832,790 (GRCm39)		probably null	Het
Parp4	T	C	14: 56,852,224 (GRCm39)		probably null	Het
Pcdhb18	A	C	18: 37,625,004 (GRCm39)	H778P	probably benign	Het
Polg	A	T	7: 79,105,860 (GRCm39)	Y710N	probably benign	Het
Ppp2r2b	C	A	18: 42,779,025 (GRCm39)	R370L	possibly damaging	Het
Raet1e	C	T	10: 22,057,872 (GRCm39)	T213I	possibly damaging	Het
Reln	T	A	5: 22,193,705 (GRCm39)	S1418C	possibly damaging	Het
Reln	T	C	5: 22,285,689 (GRCm39)	S427G	probably benign	Het
Rhobtb2	G	A	14: 70,025,376 (GRCm39)	H633Y	probably damaging	Het
Serpina3i	T	C	12: 104,234,881 (GRCm39)	V404A	probably damaging	Het
Serpinb8	T	C	1: 107,526,769 (GRCm39)		probably null	Het
Sorl1	G	T	9: 41,900,739 (GRCm39)	Q1658K	probably damaging	Het
Tmem26	G	A	10: 68,559,816 (GRCm39)	W29*	probably null	Het
Togaram2	A	G	17: 71,996,408 (GRCm39)	E137G	probably damaging	Het
Ttc39b	A	G	4: 83,151,023 (GRCm39)	L524S	probably damaging	Het
Usp43	T	C	11: 67,767,345 (GRCm39)	N675S	probably damaging	Het
Vmn2r104	A	G	17: 20,268,439 (GRCm39)	L10P	possibly damaging	Het
Zbtb1	G	A	12: 76,432,773 (GRCm39)	R253Q	probably damaging	Het
Zfp354b	T	A	11: 50,820,256 (GRCm39)	R36S	probably damaging	Het

Other mutations in Or5h23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00951:Or5h23	APN	16	58,906,756 (GRCm39)	missense	possibly damaging	0.86
IGL01553:Or5h23	APN	16	58,906,685 (GRCm39)	missense	probably benign	0.35
R0233:Or5h23	UTSW	16	58,906,038 (GRCm39)	missense	probably benign	0.01
R0233:Or5h23	UTSW	16	58,906,038 (GRCm39)	missense	probably benign	0.01
R1367:Or5h23	UTSW	16	58,906,706 (GRCm39)	missense	probably benign	0.00
R1631:Or5h23	UTSW	16	58,906,408 (GRCm39)	missense	probably benign
R1660:Or5h23	UTSW	16	58,906,706 (GRCm39)	missense	probably benign	0.00
R2166:Or5h23	UTSW	16	58,905,949 (GRCm39)	missense	probably benign	0.07
R2167:Or5h23	UTSW	16	58,905,949 (GRCm39)	missense	probably benign	0.07
R2168:Or5h23	UTSW	16	58,905,949 (GRCm39)	missense	probably benign	0.07
R2191:Or5h23	UTSW	16	58,906,038 (GRCm39)	missense	probably benign	0.01
R3836:Or5h23	UTSW	16	58,906,586 (GRCm39)	missense	possibly damaging	0.61
R4999:Or5h23	UTSW	16	58,906,765 (GRCm39)	missense	probably damaging	1.00
R5386:Or5h23	UTSW	16	58,906,253 (GRCm39)	missense	probably benign
R5589:Or5h23	UTSW	16	58,906,334 (GRCm39)	missense	probably benign	0.03
R5590:Or5h23	UTSW	16	58,906,360 (GRCm39)	missense	probably benign	0.06
R5609:Or5h23	UTSW	16	58,906,439 (GRCm39)	missense	possibly damaging	0.96
R5965:Or5h23	UTSW	16	58,906,666 (GRCm39)	missense	probably damaging	1.00
R5989:Or5h23	UTSW	16	58,906,697 (GRCm39)	missense	probably benign	0.00
R6049:Or5h23	UTSW	16	58,906,509 (GRCm39)	nonsense	probably null
R6058:Or5h23	UTSW	16	58,906,792 (GRCm39)	missense	probably benign
R6058:Or5h23	UTSW	16	58,906,273 (GRCm39)	missense	probably damaging	0.99
R6250:Or5h23	UTSW	16	58,906,195 (GRCm39)	missense	probably damaging	1.00
R6319:Or5h23	UTSW	16	58,906,384 (GRCm39)	missense	probably benign	0.08
R6473:Or5h23	UTSW	16	58,906,406 (GRCm39)	missense	probably benign	0.09
R6524:Or5h23	UTSW	16	58,906,640 (GRCm39)	missense	possibly damaging	0.76
R6748:Or5h23	UTSW	16	58,906,253 (GRCm39)	missense	probably benign
R6874:Or5h23	UTSW	16	58,906,312 (GRCm39)	missense	probably benign	0.02

Predicted Primers

PCR Primer
(F):5'- GAGAAAGAGATCAGTTTACTCTTGG -3'
(R):5'- TGAAATTTTGTGGCCAACCTG -3'

Sequencing Primer
(F):5'- CTGTGGATGATAACCAAGTATCCAC -3'
(R):5'- GCCAACCTGATAACTACAGAGTTGTG -3'

Posted On

2022-03-25