Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03046:Or7g25'

391865

Institutional Source

Beutler Lab

Gene Symbol

Or7g25

Ensembl Gene

ENSMUSG00000048391

Gene Name

olfactory receptor family 7 subfamily G member 25

Synonyms

GA_x6K02T2PVTD-12986331-12985390, Olfr843, MOR155-2

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.130) question?

Stock #

IGL03046 (G1)

Quality Score

116

Status

Validated

Chromosome

Chromosomal Location

19159653-19160759 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 19160441 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 85 (I85F)

Ref Sequence

ENSEMBL: ENSMUSP00000151203 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000061365] [ENSMUST00000214019] [ENSMUST00000214267]

AlphaFold

Q7TRG4

Predicted Effect

probably damaging
Transcript: ENSMUST00000061365
AA Change: I85F

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000051027
Gene: ENSMUSG00000048391
AA Change: I85F

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	2.4e-51	PFAM
Pfam:7tm_1	41	290	3.3e-24	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000214019
AA Change: I85F

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Predicted Effect

probably damaging
Transcript: ENSMUST00000214267
AA Change: I85F

PolyPhen 2 Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)

Meta Mutation Damage Score

0.3136

Coding Region Coverage

1x: 0.0%
3x: 0.0%
10x: 0.0%
20x: 0.0%

Validation Efficiency

98% (54/55)

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: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	T	A	6: 121,636,282 (GRCm39)	M717K	probably benign	Het
Acad12	C	A	5: 121,748,029 (GRCm39)	V130L	probably benign	Het
Cdca2	T	C	14: 67,937,471 (GRCm39)		probably benign	Het
Cfap100	T	A	6: 90,389,332 (GRCm39)		probably null	Het
Cfap43	T	A	19: 47,804,302 (GRCm39)	E298V	probably damaging	Het
Cic	C	T	7: 24,990,500 (GRCm39)	P1971S	probably damaging	Het
Cnga1	T	C	5: 72,761,681 (GRCm39)	D611G	probably benign	Het
Daglb	C	T	5: 143,486,948 (GRCm39)	P522L	probably damaging	Het
Dclre1b	A	T	3: 103,710,597 (GRCm39)	I438K	probably benign	Het
Ddx5	C	A	11: 106,675,871 (GRCm39)	R273M	probably damaging	Het
Eepd1	C	T	9: 25,393,981 (GRCm39)	L82F	probably damaging	Het
Emilin3	G	A	2: 160,750,649 (GRCm39)	Q320*	probably null	Het
Exoc6	T	C	19: 37,582,217 (GRCm39)		probably null	Het
Fcna	G	C	2: 25,520,693 (GRCm39)		probably benign	Het
Foxs1	T	C	2: 152,774,484 (GRCm39)	T190A	probably benign	Het
Gje1	A	G	10: 14,592,374 (GRCm39)	L136P	probably damaging	Het
Hdac11	A	G	6: 91,145,827 (GRCm39)	T176A	probably benign	Het
Hhip	C	A	8: 80,698,967 (GRCm39)	V700L	probably damaging	Het
Hps5	T	C	7: 46,426,463 (GRCm39)		probably benign	Het
Itgb1bp1	T	C	12: 21,329,436 (GRCm39)	S13G	unknown	Het
Kcna1	A	T	6: 126,619,148 (GRCm39)	L391M	possibly damaging	Het
Kif1a	C	T	1: 93,010,128 (GRCm39)	V6M	probably damaging	Het
Klhl6	T	C	16: 19,801,639 (GRCm39)	I39V	probably benign	Het
Lpcat4	C	A	2: 112,072,334 (GRCm39)		silent	Het
Ltn1	A	T	16: 87,202,509 (GRCm39)	S1047R	probably benign	Het
Mdn1	A	G	4: 32,694,495 (GRCm39)	T1073A	possibly damaging	Het
Megf10	G	T	18: 57,421,055 (GRCm39)	A898S	possibly damaging	Het
Mtmr6	T	C	14: 60,529,577 (GRCm39)		probably null	Het
Mtnr1b	T	C	9: 15,774,059 (GRCm39)	I333M	probably benign	Het
Muc5ac	G	T	7: 141,348,950 (GRCm39)	C463F	probably benign	Het
Mycbpap	G	T	11: 94,396,543 (GRCm39)	T99N	possibly damaging	Het
Myo7a	C	T	7: 97,728,534 (GRCm39)	C824Y	probably damaging	Het
N4bp2	A	G	5: 65,948,303 (GRCm39)	H311R	probably damaging	Het
Nepro	T	A	16: 44,552,509 (GRCm39)		probably benign	Het
Nop56	A	T	2: 130,117,489 (GRCm39)		probably benign	Het
Nup210	A	G	6: 90,995,978 (GRCm39)		probably benign	Het
Or4d10c	A	G	19: 12,065,391 (GRCm39)	V255A	probably damaging	Het
Pcna	C	T	2: 132,093,673 (GRCm39)	E109K	probably benign	Het
Pgap6	A	T	17: 26,338,414 (GRCm39)		probably null	Het
Pkhd1	T	G	1: 20,607,589 (GRCm39)	D1089A	possibly damaging	Het
Plb1	A	G	5: 32,485,756 (GRCm39)	R847G	probably damaging	Het
Pou6f2	A	G	13: 18,303,612 (GRCm39)		probably benign	Het
Prss43	C	G	9: 110,660,049 (GRCm39)	S371C	probably benign	Het
Ralgapa1	A	T	12: 55,741,942 (GRCm39)	V1322D	probably damaging	Het
Rrp8	A	G	7: 105,384,109 (GRCm39)	V131A	probably benign	Het
Rtp1	A	T	16: 23,248,044 (GRCm39)	K39M	probably benign	Het
Sanbr	A	T	11: 23,565,150 (GRCm39)	L279Q	possibly damaging	Het
Slc1a6	A	G	10: 78,636,008 (GRCm39)	I358V	probably benign	Het
Slc25a15	T	C	8: 22,885,726 (GRCm39)		probably benign	Het
Slc43a1	G	A	2: 84,684,897 (GRCm39)		probably benign	Het
Speer4c1	A	C	5: 15,919,214 (GRCm39)		probably benign	Het
Spock3	T	G	8: 63,802,018 (GRCm39)		probably null	Het
Tbc1d7	T	C	13: 43,308,162 (GRCm39)		probably null	Het
Tmem184c	C	T	8: 78,326,286 (GRCm39)	W260*	probably null	Het
Trnau1ap	A	G	4: 132,039,252 (GRCm39)	Y265H	probably damaging	Het
Usp25	T	C	16: 76,871,754 (GRCm39)	F363S	probably damaging	Het
Vcl	T	C	14: 21,072,085 (GRCm39)	F817L	possibly damaging	Het
Vmn1r13	T	A	6: 57,187,717 (GRCm39)	M292K	probably benign	Het
Xpc	G	T	6: 91,487,463 (GRCm39)	A89E	probably damaging	Het

Other mutations in Or7g25

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02104:Or7g25	APN	9	19,160,166 (GRCm39)	missense	probably benign	0.21
IGL02338:Or7g25	APN	9	19,159,960 (GRCm39)	missense	probably damaging	0.98
IGL03197:Or7g25	APN	9	19,160,098 (GRCm39)	missense	probably benign	0.37
IGL03227:Or7g25	APN	9	19,160,518 (GRCm39)	missense	probably damaging	1.00
IGL03052:Or7g25	UTSW	9	19,159,938 (GRCm39)	nonsense	probably null
R0423:Or7g25	UTSW	9	19,160,248 (GRCm39)	nonsense	probably null
R1316:Or7g25	UTSW	9	19,160,035 (GRCm39)	missense	probably benign	0.06
R1759:Or7g25	UTSW	9	19,160,384 (GRCm39)	missense	probably benign	0.36
R1782:Or7g25	UTSW	9	19,159,877 (GRCm39)	missense	probably benign	0.04
R2517:Or7g25	UTSW	9	19,160,357 (GRCm39)	missense	probably benign	0.21
R3196:Or7g25	UTSW	9	19,160,495 (GRCm39)	missense	probably damaging	1.00
R3742:Or7g25	UTSW	9	19,159,979 (GRCm39)	missense	possibly damaging	0.91
R4191:Or7g25	UTSW	9	19,160,383 (GRCm39)	missense	probably benign	0.05
R4320:Or7g25	UTSW	9	19,160,052 (GRCm39)	missense	probably damaging	1.00
R4523:Or7g25	UTSW	9	19,160,525 (GRCm39)	missense	probably damaging	0.98
R4756:Or7g25	UTSW	9	19,160,153 (GRCm39)	missense	possibly damaging	0.56
R4908:Or7g25	UTSW	9	19,160,149 (GRCm39)	missense	probably benign	0.00
R5319:Or7g25	UTSW	9	19,160,329 (GRCm39)	missense	possibly damaging	0.60
R5554:Or7g25	UTSW	9	19,160,039 (GRCm39)	missense	probably benign	0.02
R6011:Or7g25	UTSW	9	19,159,807 (GRCm39)	missense	probably damaging	0.98
R7330:Or7g25	UTSW	9	19,160,567 (GRCm39)	missense	probably benign	0.01
R7862:Or7g25	UTSW	9	19,160,736 (GRCm39)	start gained	probably benign
R9544:Or7g25	UTSW	9	19,160,561 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AACAACATCAGACTATGCAGTAGTG -3'
(R):5'- GACTGACATATTCTCCAGCCATTG -3'

Sequencing Primer
(F):5'- CAATGAAAGTAAAACGAGCAGTACAC -3'
(R):5'- CAGCCATTGAATCATTTATCTTCAGC -3'

Posted On

2016-06-07