Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01767:Or7g27'

153353

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Or7g27

Ensembl Gene

ENSMUSG00000061614

Gene Name

olfactory receptor family 7 subfamily G member 27

Synonyms

MOR150-1P, GA_x6K02T2PVTD-13076685-13077623, MOR150-2, Olfr1522-ps1, MOR150-1, Olfr845, MOR150-1P

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.118) question?

Stock #

IGL01767

Quality Score

Status

Chromosome

Chromosomal Location

19249755-19250696 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 19250598 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Isoleucine at position 281 (V281I)

Ref Sequence

ENSEMBL: ENSMUSP00000150474 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000071259] [ENSMUST00000213344] [ENSMUST00000215572]

AlphaFold

Q7TRG2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000071259
AA Change: V281I

PolyPhen 2 Score 0.541 (Sensitivity: 0.88; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000071239
Gene: ENSMUSG00000061614
AA Change: V281I

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	1.1e-56	PFAM
Pfam:7tm_1	41	290	2.1e-22	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212246
AA Change: V281I

Predicted Effect

possibly damaging
Transcript: ENSMUST00000213344
AA Change: V281I

PolyPhen 2 Score 0.541 (Sensitivity: 0.88; Specificity: 0.91)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000215572
AA Change: V281I

PolyPhen 2 Score 0.541 (Sensitivity: 0.88; Specificity: 0.91)

Coding Region Coverage

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: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadat	A	T	8: 60,960,126 (GRCm39)	D31V	probably damaging	Het
Acaca	A	T	11: 84,211,368 (GRCm39)	Y1560F	probably benign	Het
Actl7a	A	G	4: 56,743,980 (GRCm39)	E169G	probably damaging	Het
Adgrb3	A	G	1: 25,598,895 (GRCm39)	V270A	probably benign	Het
Adgre4	G	A	17: 56,104,740 (GRCm39)	V269I	probably benign	Het
Ankhd1	A	G	18: 36,781,427 (GRCm39)	T2160A	probably damaging	Het
Bltp1	T	C	3: 37,095,512 (GRCm39)	V4505A	probably benign	Het
Bnip2	T	A	9: 69,909,398 (GRCm39)		probably benign	Het
Casp16	A	G	17: 23,771,027 (GRCm39)	V126A	probably damaging	Het
Ccser1	C	A	6: 61,695,136 (GRCm39)	T157K	probably benign	Het
Cdh23	A	G	10: 60,151,503 (GRCm39)	S2459P	probably damaging	Het
Cdk5rap3	A	T	11: 96,804,291 (GRCm39)	C21S	probably damaging	Het
Chmp6	G	A	11: 119,807,812 (GRCm39)	E72K	probably benign	Het
Cldn23	T	C	8: 36,292,816 (GRCm39)	Y224C	probably damaging	Het
Cry1	C	T	10: 84,982,338 (GRCm39)	G336D	probably damaging	Het
Cyp4f17	T	A	17: 32,725,956 (GRCm39)	F30I	probably benign	Het
Dgcr8	T	A	16: 18,096,200 (GRCm39)	D496V	probably damaging	Het
Dhx9	A	G	1: 153,344,614 (GRCm39)		probably benign	Het
Dnah10	C	T	5: 124,820,801 (GRCm39)		probably benign	Het
Dock9	T	C	14: 121,860,282 (GRCm39)	E880G	possibly damaging	Het
Dscam	A	G	16: 96,456,136 (GRCm39)	V1264A	probably damaging	Het
Eno1	T	C	4: 150,331,167 (GRCm39)	Y270H	probably benign	Het
Eprs1	A	G	1: 185,117,112 (GRCm39)	D385G	probably damaging	Het
Ercc2	A	G	7: 19,124,346 (GRCm39)	Y215C	probably damaging	Het
Fscn2	A	G	11: 120,258,576 (GRCm39)	N400S	possibly damaging	Het
Fuca1	C	T	4: 135,666,512 (GRCm39)	T449I	probably benign	Het
Gm43638	T	C	5: 87,613,290 (GRCm39)	K492E	probably damaging	Het
Gm5263	T	G	1: 146,296,302 (GRCm39)		noncoding transcript	Het
Gm8122	T	C	14: 43,090,158 (GRCm39)	T111A	unknown	Het
Gtf3c2	T	A	5: 31,314,979 (GRCm39)	N923Y	probably benign	Het
Il17a	T	A	1: 20,803,864 (GRCm39)	D86E	probably benign	Het
Itgb2l	G	T	16: 96,231,775 (GRCm39)	N330K	probably benign	Het
Kcnj11	T	C	7: 45,748,489 (GRCm39)	H278R	probably benign	Het
Khdrbs2	T	A	1: 32,658,257 (GRCm39)	Y272*	probably null	Het
Kndc1	A	T	7: 139,509,959 (GRCm39)	Q1267L	probably damaging	Het
Loxhd1	T	A	18: 77,374,120 (GRCm39)	F64I	possibly damaging	Het
Lrig2	T	A	3: 104,398,861 (GRCm39)	K222N	probably benign	Het
Lrrcc1	T	A	3: 14,612,332 (GRCm39)	Y378N	probably damaging	Het
Mblac2	T	C	13: 81,898,434 (GRCm39)	L270P	probably damaging	Het
Med13	A	T	11: 86,210,609 (GRCm39)	I511N	probably benign	Het
Myo3a	A	T	2: 22,428,033 (GRCm39)	E763D	probably damaging	Het
Or1e25	T	A	11: 73,493,858 (GRCm39)	F151I	probably benign	Het
Or2n1	G	T	17: 38,486,577 (GRCm39)	V201L	probably benign	Het
Or4a68	C	T	2: 89,270,144 (GRCm39)	V160I	probably benign	Het
Or5b97	T	A	19: 12,879,112 (GRCm39)	T11S	probably benign	Het
Plxna4	T	A	6: 32,214,613 (GRCm39)	I623F	possibly damaging	Het
Ppp2ca	T	A	11: 52,008,882 (GRCm39)	Y127*	probably null	Het
Psg18	A	G	7: 18,087,322 (GRCm39)	V112A	possibly damaging	Het
Ptprj	A	T	2: 90,299,918 (GRCm39)	N108K	probably benign	Het
Rictor	A	G	15: 6,806,865 (GRCm39)	Y707C	probably damaging	Het
Rptn	T	C	3: 93,302,946 (GRCm39)	F93S	probably benign	Het
Rxrg	T	A	1: 167,454,884 (GRCm39)	C156S	probably damaging	Het
Slc24a4	T	C	12: 102,189,946 (GRCm39)		probably benign	Het
Slc25a27	C	T	17: 43,974,964 (GRCm39)		probably null	Het
Slx4	T	C	16: 3,808,112 (GRCm39)	K481E	probably benign	Het
Snx19	T	C	9: 30,374,560 (GRCm39)	W940R	possibly damaging	Het
Spopfm1	T	A	3: 94,173,791 (GRCm39)	D262E	probably benign	Het
Tasor2	G	A	13: 3,626,633 (GRCm39)	P1106S	probably benign	Het
Tcf20	G	A	15: 82,740,209 (GRCm39)	P414L	probably damaging	Het
Treml2	T	C	17: 48,609,838 (GRCm39)	V90A	probably benign	Het
Uckl1	C	T	2: 181,211,327 (GRCm39)	V501M	probably damaging	Het
Unc79	C	T	12: 103,108,256 (GRCm39)	T1937I	probably damaging	Het
Vmn2r17	A	T	5: 109,567,903 (GRCm39)	I9F	probably benign	Het
Vmn2r44	T	C	7: 8,383,237 (GRCm39)	H119R	probably benign	Het
Vmn2r78	A	G	7: 86,603,643 (GRCm39)	D607G	probably benign	Het
Vps13a	C	T	19: 16,641,258 (GRCm39)	G2288D	probably damaging	Het
Znfx1	G	T	2: 166,897,643 (GRCm39)	T427N	probably damaging	Het

Other mutations in Or7g27

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01546:Or7g27	APN	9	19,250,068 (GRCm39)	missense	possibly damaging	0.56
IGL01637:Or7g27	APN	9	19,250,260 (GRCm39)	missense	probably damaging	1.00
IGL01945:Or7g27	APN	9	19,250,628 (GRCm39)	missense	probably damaging	0.98
IGL02202:Or7g27	APN	9	19,250,545 (GRCm39)	missense	probably benign	0.06
IGL02877:Or7g27	APN	9	19,250,497 (GRCm39)	missense	possibly damaging	0.86
R0466:Or7g27	UTSW	9	19,250,475 (GRCm39)	missense	probably damaging	1.00
R1521:Or7g27	UTSW	9	19,249,948 (GRCm39)	missense	probably benign	0.35
R1650:Or7g27	UTSW	9	19,249,943 (GRCm39)	missense	possibly damaging	0.49
R1766:Or7g27	UTSW	9	19,250,154 (GRCm39)	missense	probably benign	0.06
R2060:Or7g27	UTSW	9	19,250,352 (GRCm39)	missense	probably benign	0.01
R2082:Or7g27	UTSW	9	19,250,574 (GRCm39)	missense	probably benign	0.36
R2257:Or7g27	UTSW	9	19,249,789 (GRCm39)	missense	probably benign	0.01
R2892:Or7g27	UTSW	9	19,250,034 (GRCm39)	missense	probably benign	0.04
R3156:Or7g27	UTSW	9	19,250,720 (GRCm39)	splice site	probably null
R3943:Or7g27	UTSW	9	19,250,371 (GRCm39)	missense	probably benign	0.05
R4116:Or7g27	UTSW	9	19,249,940 (GRCm39)	missense	probably benign	0.39
R4518:Or7g27	UTSW	9	19,250,556 (GRCm39)	missense	possibly damaging	0.86
R4814:Or7g27	UTSW	9	19,250,476 (GRCm39)	missense	probably damaging	1.00
R5339:Or7g27	UTSW	9	19,250,455 (GRCm39)	missense	possibly damaging	0.78
R6647:Or7g27	UTSW	9	19,249,925 (GRCm39)	missense	possibly damaging	0.50
R7493:Or7g27	UTSW	9	19,250,109 (GRCm39)	missense	probably damaging	0.98
R7522:Or7g27	UTSW	9	19,250,294 (GRCm39)	nonsense	probably null
R7584:Or7g27	UTSW	9	19,250,569 (GRCm39)	missense	possibly damaging	0.94
R9127:Or7g27	UTSW	9	19,250,026 (GRCm39)	missense	probably benign
R9463:Or7g27	UTSW	9	19,250,320 (GRCm39)	missense	possibly damaging	0.94

Posted On

2014-02-04