Mutagenetix > Incidental Mutation

Incidental Mutation 'R5403:Or8g22'

430113

Institutional Source

Beutler Lab

Gene Symbol

Or8g22

Ensembl Gene

ENSMUSG00000095194

Gene Name

olfactory receptor family 8 subfamily G member 22, pseudogene 1

Synonyms

Olfr936, MOR171-37, EG628171, GA_x6K02T2PVTD-32743332-32742397

MMRRC Submission

042974-MU

Accession Numbers

Essential gene?

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

Stock #

R5403 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

38957910-38958845 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 38957999 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Threonine at position 239 (P239T)

Ref Sequence

ENSEMBL: ENSMUSP00000137209 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000178303] [ENSMUST00000216912]

AlphaFold

J3KMV2

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000104850

Predicted Effect

probably damaging
Transcript: ENSMUST00000178303
AA Change: P239T

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000137209
Gene: ENSMUSG00000095194
AA Change: P239T

Domain	Start	End	E-Value	Type
Pfam:7tm_1	1	246	6e-21	PFAM
Pfam:7tm_4	1	264	6.9e-49	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000216912
AA Change: A283D

Coding Region Coverage

1x: 99.4%
3x: 98.7%
10x: 97.4%
20x: 95.7%

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, Feb 2010]

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsbg3	G	T	17: 57,183,221 (GRCm39)		probably benign	Het
Adamts6	A	G	13: 104,489,323 (GRCm39)	D392G	possibly damaging	Het
Adcy8	C	T	15: 64,588,001 (GRCm39)	V929I	probably benign	Het
Alkbh8	A	G	9: 3,385,318 (GRCm39)	K537E	probably benign	Het
Anp32a	A	T	9: 62,249,275 (GRCm39)	I16F	possibly damaging	Het
Asb18	T	C	1: 89,942,110 (GRCm39)	T64A	probably benign	Het
Bpifb4	A	T	2: 153,785,912 (GRCm39)	I17F	probably damaging	Het
Brd7	G	T	8: 89,084,169 (GRCm39)	Q148K	probably damaging	Het
Brinp1	A	G	4: 68,711,201 (GRCm39)	W336R	probably benign	Het
Ccdc88b	T	A	19: 6,835,108 (GRCm39)	T38S	unknown	Het
Cd46	C	T	1: 194,744,719 (GRCm39)	V340I	possibly damaging	Het
Cdr2	G	A	7: 120,557,968 (GRCm39)	Q186*	probably null	Het
Ces1e	T	G	8: 93,935,240 (GRCm39)	D404A	probably benign	Het
Chd3	A	T	11: 69,239,895 (GRCm39)		probably null	Het
Cmtm1	CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT	CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT	8: 105,036,102 (GRCm39)		probably benign	Het
Cntnap3	G	A	13: 64,909,792 (GRCm39)	T771I	possibly damaging	Het
Cops8	C	T	1: 90,534,342 (GRCm39)		probably benign	Het
Csmd2	C	T	4: 128,380,677 (GRCm39)	R2078C	probably benign	Het
Ddx50	A	G	10: 62,482,809 (GRCm39)	S87P	probably benign	Het
Dennd2b	A	G	7: 109,156,112 (GRCm39)	S213P	probably damaging	Het
Dlg2	A	G	7: 92,080,210 (GRCm39)	T598A	probably damaging	Het
Dnah8	G	A	17: 30,967,542 (GRCm39)	D2585N	probably benign	Het
Epha6	A	T	16: 59,595,933 (GRCm39)	D919E	probably damaging	Het
Fndc9	C	T	11: 46,128,541 (GRCm39)	S20L	probably benign	Het
Gpx6	A	G	13: 21,501,813 (GRCm39)	E145G	probably damaging	Het
Hc	A	G	2: 34,947,446 (GRCm39)	Y23H	probably damaging	Het
Insyn2b	A	T	11: 34,353,058 (GRCm39)	T367S	probably benign	Het
Jmy	G	T	13: 93,577,904 (GRCm39)	Q755K	probably benign	Het
Krtap4-7	A	T	11: 99,534,540 (GRCm39)	S108T	unknown	Het
Mgat5b	T	G	11: 116,839,483 (GRCm39)	I333S	probably benign	Het
Mrtfb	A	G	16: 13,218,877 (GRCm39)	T519A	probably damaging	Het
Naip6	G	A	13: 100,436,585 (GRCm39)	A646V	probably benign	Het
Opn4	T	C	14: 34,314,894 (GRCm39)	T460A	probably benign	Het
Or6b2	A	T	1: 92,408,019 (GRCm39)	V108E	possibly damaging	Het
Otogl	T	A	10: 107,644,617 (GRCm39)	M1210L	probably benign	Het
Pheta1	A	G	5: 121,990,794 (GRCm39)	E52G	possibly damaging	Het
Phf24	A	T	4: 42,933,831 (GRCm39)		probably null	Het
Ppargc1a	G	A	5: 51,620,167 (GRCm39)		probably benign	Het
Ptprd	G	A	4: 75,872,405 (GRCm39)	R1355*	probably null	Het
Rad50	A	G	11: 53,586,108 (GRCm39)		probably null	Het
Robo4	CGG	CG	9: 37,322,786 (GRCm39)		probably null	Het
Rsf1	GCG	GCGACGGCGACG	7: 97,229,114 (GRCm39)		probably benign	Het
Tbcd	C	A	11: 121,451,569 (GRCm39)	N546K	probably damaging	Het
Tenm4	A	G	7: 96,538,034 (GRCm39)	D1832G	probably damaging	Het
Tfap2e	T	C	4: 126,628,439 (GRCm39)	I172M	probably benign	Het
Tnip2	A	G	5: 34,671,108 (GRCm39)	L45P	probably damaging	Het
Ttc3	T	C	16: 94,260,703 (GRCm39)	V1396A	probably benign	Het
Ube2o	A	T	11: 116,439,633 (GRCm39)	I179N	possibly damaging	Het
Usp17le	T	C	7: 104,418,441 (GRCm39)	I234V	probably damaging	Het
Zfp106	T	C	2: 120,365,262 (GRCm39)	T382A	probably benign	Het
Zfp607a	A	G	7: 27,578,744 (GRCm39)	K605E	possibly damaging	Het
Zmynd10	T	A	9: 107,427,785 (GRCm39)	L363H	possibly damaging	Het

Other mutations in Or8g22

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01928:Or8g22	APN	9	38,958,709 (GRCm39)	missense	unknown
R0086:Or8g22	UTSW	9	38,958,191 (GRCm39)	missense	probably benign	0.00
R0561:Or8g22	UTSW	9	38,958,669 (GRCm39)	missense	probably damaging	0.99
R0650:Or8g22	UTSW	9	38,957,996 (GRCm39)	missense	probably benign	0.01
R1221:Or8g22	UTSW	9	38,958,483 (GRCm39)	missense	probably damaging	1.00
R1384:Or8g22	UTSW	9	38,958,200 (GRCm39)	missense	possibly damaging	0.70
R1680:Or8g22	UTSW	9	38,958,296 (GRCm39)	missense	probably benign	0.43
R1733:Or8g22	UTSW	9	38,958,678 (GRCm39)	missense	unknown
R3767:Or8g22	UTSW	9	38,958,707 (GRCm39)	missense	unknown
R4786:Or8g22	UTSW	9	38,958,783 (GRCm39)	nonsense	probably null
R4944:Or8g22	UTSW	9	38,958,158 (GRCm39)	missense	probably damaging	1.00
R5186:Or8g22	UTSW	9	38,958,265 (GRCm39)	nonsense	probably null
R6037:Or8g22	UTSW	9	38,958,403 (GRCm39)	missense	probably damaging	1.00
R6037:Or8g22	UTSW	9	38,958,403 (GRCm39)	missense	probably damaging	1.00
R6156:Or8g22	UTSW	9	38,958,671 (GRCm39)	missense	possibly damaging	0.90
R6217:Or8g22	UTSW	9	38,958,039 (GRCm39)	makesense	probably null
R6711:Or8g22	UTSW	9	38,958,162 (GRCm39)	makesense	probably null
R6919:Or8g22	UTSW	9	38,958,827 (GRCm39)	utr 5 prime	probably benign
R7022:Or8g22	UTSW	9	38,958,379 (GRCm39)	nonsense	probably null
R7275:Or8g22	UTSW	9	38,958,815 (GRCm39)	utr 5 prime	probably benign
R7290:Or8g22	UTSW	9	38,958,694 (GRCm39)	missense	unknown
R7644:Or8g22	UTSW	9	38,958,638 (GRCm39)	missense	probably damaging	1.00
R8906:Or8g22	UTSW	9	38,958,077 (GRCm39)	missense	possibly damaging	0.87
R9099:Or8g22	UTSW	9	38,958,026 (GRCm39)	missense	probably benign	0.00
Z1176:Or8g22	UTSW	9	38,958,215 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- TTGGCAGTGACCACCAAGAAG -3'
(R):5'- CCTGCGCATTAAATCTACTGAGGG -3'

Sequencing Primer
(F):5'- CAGTGACCACCAAGAAGAAGATATG -3'
(R):5'- CTACTGAGGGAAGATCTAAAGCCTTC -3'

Posted On

2016-09-06