Mutagenetix > Incidental Mutation

Incidental Mutation 'R8116:Or2g25'

631233

Institutional Source

Beutler Lab

Gene Symbol

Or2g25

Ensembl Gene

ENSMUSG00000095286

Gene Name

olfactory receptor family 2 subfamily G member 25

Synonyms

MOR256-33, GA_x6K02T2PSCP-2119438-2118485, Olfr117

MMRRC Submission

067545-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R8116 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

37970269-37971222 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 37970631 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Phenylalanine at position 198 (L198F)

Ref Sequence

ENSEMBL: ENSMUSP00000150204 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073636] [ENSMUST00000213638] [ENSMUST00000215414]

AlphaFold

L7N1Z1

Predicted Effect

probably damaging
Transcript: ENSMUST00000073636
AA Change: L198F

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

SMART Domains

Protein: ENSMUSP00000073320
Gene: ENSMUSG00000095286
AA Change: L198F

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	307	2.7e-44	PFAM
Pfam:7TM_GPCR_Srsx	34	222	2e-5	PFAM
Pfam:7tm_1	40	289	2.9e-23	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000213638
AA Change: L198F

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

Predicted Effect

probably damaging
Transcript: ENSMUST00000215414
AA Change: L198F

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

Coding Region Coverage

1x: 99.8%
3x: 99.6%
10x: 98.5%
20x: 93.9%

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: 69 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8a	A	T	11: 109,982,420 (GRCm39)	N7K	probably benign	Het
Akap9	T	A	5: 4,111,183 (GRCm39)	D3081E	probably benign	Het
Amer2	G	A	14: 60,616,854 (GRCm39)	A350T	probably damaging	Het
Amotl1	A	G	9: 14,466,868 (GRCm39)		probably null	Het
Ankib1	A	T	5: 3,752,995 (GRCm39)	V651E	probably damaging	Het
Aox1	T	C	1: 58,115,283 (GRCm39)	V756A	probably damaging	Het
Arap2	A	C	5: 62,887,954 (GRCm39)	I464S	probably benign	Het
Atp8a2	A	C	14: 60,263,657 (GRCm39)	M359R	probably damaging	Het
Aunip	T	C	4: 134,250,618 (GRCm39)	S188P	possibly damaging	Het
Cdt1	A	G	8: 123,298,728 (GRCm39)	E455G	probably benign	Het
Cyp2r1	G	T	7: 114,149,590 (GRCm39)	H475N	probably benign	Het
Dnah7a	G	T	1: 53,543,049 (GRCm39)	H2374N	probably benign	Het
Dsc2	C	T	18: 20,165,331 (GRCm39)	G881R	possibly damaging	Het
Dst	G	A	1: 34,313,261 (GRCm39)	A4343T	probably benign	Het
Efcab3	A	G	11: 105,002,677 (GRCm39)	D304G	possibly damaging	Het
Efcc1	T	C	6: 87,728,772 (GRCm39)	L409P	probably damaging	Het
Eno1	G	T	4: 150,325,526 (GRCm39)	S37I	probably damaging	Het
Ermp1	A	T	19: 29,601,196 (GRCm39)	L517Q	probably damaging	Het
Farp1	T	G	14: 121,471,232 (GRCm39)	I196S	probably damaging	Het
Fbxo21	A	G	5: 118,128,919 (GRCm39)	T310A	possibly damaging	Het
Fbxo31	C	T	8: 122,287,127 (GRCm39)	V149M	probably damaging	Het
Ggcx	C	A	6: 72,406,511 (GRCm39)	T658N	possibly damaging	Het
Gpc5	A	C	14: 115,636,637 (GRCm39)	H440P	probably damaging	Het
H13	C	T	2: 152,537,446 (GRCm39)	A297V	probably damaging	Het
H2-DMb1	T	A	17: 34,374,443 (GRCm39)	L31Q	probably damaging	Het
Ifi207	G	A	1: 173,557,746 (GRCm39)	P331S	unknown	Het
Il11ra1	G	T	4: 41,766,251 (GRCm39)	A263S	probably benign	Het
Il1a	C	A	2: 129,144,864 (GRCm39)	V185F	probably damaging	Het
Ippk	C	T	13: 49,599,818 (GRCm39)	P226S		Het
Kdm4d	T	A	9: 14,375,237 (GRCm39)	K207M	probably damaging	Het
Lrrc37	A	T	11: 103,434,115 (GRCm39)	M3018K	unknown	Het
Lrrc4b	T	C	7: 44,110,533 (GRCm39)	L135P	probably damaging	Het
Lrrk1	A	G	7: 65,912,371 (GRCm39)	Y1730H	possibly damaging	Het
Mcpt2	C	A	14: 56,279,663 (GRCm39)	A18D	probably damaging	Het
Mtmr4	C	T	11: 87,502,756 (GRCm39)	R937*	probably null	Het
Muc16	T	A	9: 18,570,033 (GRCm39)	T829S	unknown	Het
Myof	A	C	19: 37,921,167 (GRCm39)	I1365S	probably damaging	Het
Npc2	C	T	12: 84,807,612 (GRCm39)	R82Q	probably benign	Het
Or10ag2	T	A	2: 87,249,081 (GRCm39)	S228T	probably damaging	Het
Or10d1c	A	T	9: 38,894,169 (GRCm39)	M57K	probably damaging	Het
Or10j2	T	A	1: 173,098,047 (GRCm39)	F102I	possibly damaging	Het
Or4k45	T	C	2: 111,395,783 (GRCm39)	D2G	probably benign	Het
Or8b3b	A	T	9: 38,584,464 (GRCm39)	I92N	possibly damaging	Het
Or8d2b	T	A	9: 38,789,026 (GRCm39)	S185T	probably damaging	Het
Pdzph1	T	C	17: 59,282,138 (GRCm39)	N48S	probably benign	Het
Plce1	A	T	19: 38,513,262 (GRCm39)	H187L	probably benign	Het
Pramel6	G	T	2: 87,338,808 (GRCm39)	V3F	probably benign	Het
Prr5l	CCTCGCTCGCTCGCTCGC	CCTCGCTCGCTCGC	2: 101,627,919 (GRCm39)		probably null	Het
Pwwp3a	G	A	10: 80,076,231 (GRCm39)	G474S	probably damaging	Het
Rabgap1l	A	G	1: 160,530,012 (GRCm39)	Y358H	probably benign	Het
Rbbp8	T	C	18: 11,855,727 (GRCm39)	S625P	probably damaging	Het
Rhot1	A	T	11: 80,141,879 (GRCm39)	K461I	probably benign	Het
Rpa1	G	A	11: 75,193,501 (GRCm39)	T610I	possibly damaging	Het
Ryr1	G	T	7: 28,810,308 (GRCm39)	H316N	probably benign	Het
Shprh	T	C	10: 11,089,205 (GRCm39)	S1648P	probably damaging	Het
Sipa1	A	T	19: 5,702,140 (GRCm39)	D923E	possibly damaging	Het
Spata6	A	G	4: 111,685,517 (GRCm39)	Y474C	possibly damaging	Het
Sptbn1	A	T	11: 30,089,117 (GRCm39)	I715N	probably damaging	Het
Stab1	A	T	14: 30,880,910 (GRCm39)	D627E	possibly damaging	Het
Stard9	T	A	2: 120,495,420 (GRCm39)	C98*	probably null	Het
Tfpi2	T	C	6: 3,963,872 (GRCm39)	T187A	probably damaging	Het
Tmem63a	G	T	1: 180,788,048 (GRCm39)	K267N	probably benign	Het
Topaz1	C	T	9: 122,604,708 (GRCm39)	A1104V	probably benign	Het
Trmt11	A	G	10: 30,442,490 (GRCm39)	I231T	possibly damaging	Het
Utp15	G	A	13: 98,387,371 (GRCm39)	T401I	probably benign	Het
Vmn2r13	T	C	5: 109,322,926 (GRCm39)	K121R	probably benign	Het
Xab2	C	T	8: 3,663,830 (GRCm39)	R363H	probably damaging	Het
Zfand2b	T	A	1: 75,145,504 (GRCm39)	F3L	possibly damaging	Het
Zfyve28	A	T	5: 34,374,944 (GRCm39)	S357T	probably damaging	Het

Other mutations in Or2g25

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01862:Or2g25	APN	17	37,970,368 (GRCm39)	missense	probably damaging	1.00
IGL01949:Or2g25	APN	17	37,970,357 (GRCm39)	missense	probably damaging	1.00
IGL02085:Or2g25	APN	17	37,970,579 (GRCm39)	missense	probably benign	0.11
IGL02481:Or2g25	APN	17	37,970,363 (GRCm39)	missense	probably damaging	1.00
IGL02483:Or2g25	APN	17	37,970,363 (GRCm39)	missense	probably damaging	1.00
IGL03274:Or2g25	APN	17	37,970,646 (GRCm39)	missense	probably benign	0.35
R0234:Or2g25	UTSW	17	37,970,997 (GRCm39)	missense	probably damaging	0.99
R0234:Or2g25	UTSW	17	37,970,997 (GRCm39)	missense	probably damaging	0.99
R1522:Or2g25	UTSW	17	37,970,661 (GRCm39)	missense	probably damaging	1.00
R1712:Or2g25	UTSW	17	37,970,799 (GRCm39)	missense	probably benign	0.42
R1750:Or2g25	UTSW	17	37,970,564 (GRCm39)	missense	probably damaging	1.00
R1865:Or2g25	UTSW	17	37,970,754 (GRCm39)	missense	possibly damaging	0.78
R2371:Or2g25	UTSW	17	37,971,044 (GRCm39)	missense	probably damaging	1.00
R2382:Or2g25	UTSW	17	37,970,822 (GRCm39)	missense	probably benign	0.00
R3798:Or2g25	UTSW	17	37,970,997 (GRCm39)	missense	probably damaging	0.99
R4831:Or2g25	UTSW	17	37,970,969 (GRCm39)	missense	probably benign	0.03
R5087:Or2g25	UTSW	17	37,970,612 (GRCm39)	missense	probably damaging	0.97
R5365:Or2g25	UTSW	17	37,970,586 (GRCm39)	missense	probably damaging	1.00
R5812:Or2g25	UTSW	17	37,970,630 (GRCm39)	missense	probably damaging	1.00
R5822:Or2g25	UTSW	17	37,971,122 (GRCm39)	missense	probably damaging	1.00
R6405:Or2g25	UTSW	17	37,971,014 (GRCm39)	missense	possibly damaging	0.58
R6945:Or2g25	UTSW	17	37,970,405 (GRCm39)	missense	possibly damaging	0.95
R7121:Or2g25	UTSW	17	37,970,699 (GRCm39)	missense	probably damaging	0.98
R7312:Or2g25	UTSW	17	37,970,403 (GRCm39)	missense	possibly damaging	0.78
R7502:Or2g25	UTSW	17	37,971,122 (GRCm39)	missense	probably damaging	1.00
R8425:Or2g25	UTSW	17	37,970,975 (GRCm39)	missense	probably damaging	1.00
R8960:Or2g25	UTSW	17	37,970,760 (GRCm39)	missense	probably benign	0.02
R9168:Or2g25	UTSW	17	37,971,047 (GRCm39)	missense	probably damaging	1.00
RF017:Or2g25	UTSW	17	37,970,672 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AACTTTCCCTGACTCTGTGCATAG -3'
(R):5'- TCTGCCAATCTCTTGCAGGAG -3'

Sequencing Primer
(F):5'- ATATAGACAGCAGTGCTTGTGCC -3'
(R):5'- CAATCTCTTGCAGGAGTGGCG -3'

Posted On

2020-06-30