Mutagenetix > Incidental Mutation

Incidental Mutation 'R8708:Or1af1'

669326

Institutional Source

Beutler Lab

Gene Symbol

Or1af1

Ensembl Gene

ENSMUSG00000068947

Gene Name

olfactory receptor family 1 subfamily AF member 1

Synonyms

Olfr366, MOR138-5P, MOR138-6, GA_x6K02T2NLDC-33902472-33903401

MMRRC Submission

068562-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R8708 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

37109503-37110432 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 37109956 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 152 (S152T)

Ref Sequence

ENSEMBL: ENSMUSP00000150608 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000091001] [ENSMUST00000214897]

AlphaFold

Q7TRY4

Predicted Effect

probably damaging
Transcript: ENSMUST00000091001
AA Change: S152T

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000088524
Gene: ENSMUSG00000068947
AA Change: S152T

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	5e-62	PFAM
Pfam:7tm_1	41	290	3.7e-25	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000214897
AA Change: S152T

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

Meta Mutation Damage Score

0.4367

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

98% (99/101)

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: 103 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adra1d	T	C	2: 131,403,400 (GRCm39)	K230R	probably damaging	Het
Ajm1	C	A	2: 25,467,814 (GRCm39)	R699L	possibly damaging	Het
Akp3	T	A	1: 87,054,091 (GRCm39)	Y236*	probably null	Het
Alg11	T	C	8: 22,555,129 (GRCm39)	F130S	probably damaging	Het
Ankfn1	A	T	11: 89,394,756 (GRCm39)	S276R	possibly damaging	Het
Ankhd1	T	A	18: 36,727,344 (GRCm39)	H486Q	probably damaging	Het
Ankrd23	T	C	1: 36,573,169 (GRCm39)	T68A	probably benign	Het
Arhgap23	A	G	11: 97,343,238 (GRCm39)	T507A	probably benign	Het
Arid1a	A	T	4: 133,409,145 (GRCm39)	D1787E	unknown	Het
Atad2b	T	A	12: 5,011,253 (GRCm39)	D504E	probably damaging	Het
Atg2b	T	A	12: 105,635,687 (GRCm39)		probably benign	Het
Bptf	C	A	11: 106,964,139 (GRCm39)	S1685I	probably damaging	Het
Bptf	T	A	11: 106,964,140 (GRCm39)	S1685C	probably damaging	Het
Cacna1c	A	T	6: 118,604,416 (GRCm39)	I1437N		Het
Capn1	T	C	19: 6,061,328 (GRCm39)	K197E	probably damaging	Het
Ccdc177	T	C	12: 80,805,891 (GRCm39)	T128A	probably benign	Het
Ccdc7b	G	T	8: 129,863,095 (GRCm39)	M9I	probably benign	Het
Celf1	T	A	2: 90,840,925 (GRCm39)		probably null	Het
Ckap5	T	A	2: 91,425,823 (GRCm39)	N1285K	probably benign	Het
Col24a1	C	T	3: 145,251,020 (GRCm39)	T1673I	probably damaging	Het
Dbp	A	G	7: 45,359,225 (GRCm39)	E300G	probably damaging	Het
Dchs2	C	A	3: 83,036,049 (GRCm39)	H265Q	probably benign	Het
Dicer1	A	T	12: 104,694,704 (GRCm39)	S198T	possibly damaging	Het
Dnase1l2	A	T	17: 24,661,266 (GRCm39)	F86L	probably benign	Het
Dnhd1	T	G	7: 105,343,487 (GRCm39)	Y1610*	probably null	Het
Dock5	A	G	14: 68,004,820 (GRCm39)	V1529A	probably benign	Het
Egfr	G	T	11: 16,817,300 (GRCm39)		probably benign	Het
Exph5	T	A	9: 53,287,096 (GRCm39)	H1392Q	probably benign	Het
Fam78b	A	G	1: 166,906,332 (GRCm39)	K164E	possibly damaging	Het
Fignl2	C	A	15: 100,950,734 (GRCm39)	R516L	unknown	Het
Fndc7	C	T	3: 108,774,528 (GRCm39)	E577K	probably benign	Het
Fryl	T	C	5: 73,289,905 (GRCm39)	E107G	probably benign	Het
Gbp10	A	T	5: 105,368,831 (GRCm39)	M336K	probably damaging	Het
Gm11444	A	T	11: 85,737,723 (GRCm39)	C156S		Het
Golga3	C	A	5: 110,350,721 (GRCm39)	A752E	probably benign	Het
Gper1	G	T	5: 139,411,690 (GRCm39)	V12L	probably benign	Het
Hmbox1	G	T	14: 65,061,089 (GRCm39)	A394E	probably damaging	Het
Ighv1-71	T	A	12: 115,705,955 (GRCm39)	I77L	probably benign	Het
Ing4	A	T	6: 125,024,895 (GRCm39)	N214Y	probably damaging	Het
Ints8	A	G	4: 11,208,824 (GRCm39)		probably null	Het
Itpa	T	A	2: 130,517,639 (GRCm39)	V129E	probably damaging	Het
Itpripl1	T	A	2: 126,983,262 (GRCm39)	M287L	probably benign	Het
Klc3	T	C	7: 19,129,784 (GRCm39)	I362V	probably damaging	Het
Ky	T	A	9: 102,402,590 (GRCm39)		probably benign	Het
Lasp1	A	G	11: 97,697,709 (GRCm39)	N43S	possibly damaging	Het
Limk2	A	G	11: 3,300,763 (GRCm39)	M380T	probably benign	Het
Lrp2	T	A	2: 69,289,957 (GRCm39)	E3627D	probably damaging	Het
Lrrc25	T	C	8: 71,070,459 (GRCm39)	L80P	probably damaging	Het
Mcoln3	A	T	3: 145,846,276 (GRCm39)	K529*	probably null	Het
Mdn1	A	C	4: 32,725,854 (GRCm39)	D2591A	probably damaging	Het
Med12l	A	G	3: 59,159,751 (GRCm39)	I1267V	probably benign	Het
Mei4	C	A	9: 81,809,595 (GRCm39)	S226*	probably null	Het
Mios	G	A	6: 8,234,255 (GRCm39)	V809M	probably benign	Het
Mmp17	G	A	5: 129,672,486 (GRCm39)	R146Q	possibly damaging	Het
Mob3a	G	A	10: 80,527,218 (GRCm39)	Q36*	probably null	Het
Myo3a	T	A	2: 22,296,607 (GRCm39)		probably benign	Het
Naca	A	T	10: 127,883,943 (GRCm39)	I2125F	probably damaging	Het
Ndst3	A	C	3: 123,322,564 (GRCm39)	S840A	probably benign	Het
Nlrp4c	T	C	7: 6,068,603 (GRCm39)	M168T	probably damaging	Het
Nt5c3	A	G	6: 56,874,758 (GRCm39)		probably null	Het
Or4a72	C	A	2: 89,405,623 (GRCm39)	G149V	probably damaging	Het
Or5b124	T	C	19: 13,611,401 (GRCm39)	S309P	probably benign	Het
Or6c5	T	A	10: 129,074,678 (GRCm39)	I220N	possibly damaging	Het
Pcgf3	A	G	5: 108,634,063 (GRCm39)	D107G	probably benign	Het
Pde2a	A	G	7: 101,159,588 (GRCm39)	D816G	probably damaging	Het
Phf10	T	A	17: 15,176,261 (GRCm39)	T131S	possibly damaging	Het
Phf11	A	T	14: 59,482,262 (GRCm39)	C164S	probably damaging	Het
Phrf1	A	G	7: 140,812,446 (GRCm39)	D70G	unknown	Het
Piezo2	A	G	18: 63,226,086 (GRCm39)	L850S	probably damaging	Het
Plcg1	T	A	2: 160,596,473 (GRCm39)		probably benign	Het
Plekhh2	A	T	17: 84,882,421 (GRCm39)	I676L	probably benign	Het
Ppp1r9a	T	G	6: 5,115,196 (GRCm39)	V804G	probably damaging	Het
Ppt2	T	C	17: 34,844,613 (GRCm39)	H180R	possibly damaging	Het
Prdm15	T	C	16: 97,618,066 (GRCm39)	H398R	unknown	Het
Rab26	A	T	17: 24,748,772 (GRCm39)	M208K	probably damaging	Het
Rab31	A	C	17: 65,974,859 (GRCm39)		probably benign	Het
Radil	A	G	5: 142,471,204 (GRCm39)	V1024A	probably damaging	Het
Rorb	A	G	19: 18,960,780 (GRCm39)	I65T	probably damaging	Het
Sall1	A	T	8: 89,759,483 (GRCm39)	V207E	probably damaging	Het
Sart3	A	T	5: 113,882,728 (GRCm39)	M864K	possibly damaging	Het
Sdcbp2	T	A	2: 151,431,457 (GRCm39)	S277T	probably benign	Het
Septin5	A	G	16: 18,443,622 (GRCm39)	V100A	probably benign	Het
Sipa1	C	T	19: 5,710,980 (GRCm39)	R10Q	probably damaging	Het
Ski	A	T	4: 155,245,119 (GRCm39)	S376T	probably damaging	Het
Slc15a4	A	T	5: 127,673,715 (GRCm39)	D566E	probably benign	Het
Srgap2	G	A	1: 131,273,544 (GRCm39)	Q372*	probably null	Het
Stard9	A	G	2: 120,534,059 (GRCm39)	T3439A	probably damaging	Het
Tln1	T	C	4: 43,534,769 (GRCm39)		probably benign	Het
Tmco3	A	G	8: 13,345,998 (GRCm39)	M279V	probably benign	Het
Tmem39b	T	C	4: 129,570,191 (GRCm39)		probably benign	Het
Trio	T	A	15: 27,732,632 (GRCm39)	N3083I	probably damaging	Het
Ube3b	G	A	5: 114,531,151 (GRCm39)	R215Q	probably benign	Het
Ubr1	T	C	2: 120,696,964 (GRCm39)	N1646S	probably benign	Het
Uqcrc1	T	G	9: 108,776,108 (GRCm39)	F270C	probably damaging	Het
Vmn2r108	T	A	17: 20,682,687 (GRCm39)	N839I	probably damaging	Het
Vmn2r75	A	T	7: 85,812,476 (GRCm39)	S514R	probably damaging	Het
Wdfy4	C	G	14: 32,689,489 (GRCm39)	V3016L		Het
Wdr11	A	G	7: 129,200,780 (GRCm39)	N77S	probably benign	Het
Wdr17	C	A	8: 55,093,127 (GRCm39)		probably benign	Het
Wrn	T	A	8: 33,782,671 (GRCm39)	N753I	probably damaging	Het
Zan	A	G	5: 137,461,539 (GRCm39)		probably null	Het
Zfat	T	A	15: 67,956,278 (GRCm39)	T1203S	possibly damaging	Het
Zfhx2	A	C	14: 55,312,509 (GRCm39)	S62A	probably benign	Het

Other mutations in Or1af1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01691:Or1af1	APN	2	37,110,038 (GRCm39)	missense	probably damaging	1.00
IGL01925:Or1af1	APN	2	37,110,058 (GRCm39)	missense	probably benign	0.14
IGL02355:Or1af1	APN	2	37,109,681 (GRCm39)	missense	probably damaging	1.00
IGL02362:Or1af1	APN	2	37,109,681 (GRCm39)	missense	probably damaging	1.00
IGL02671:Or1af1	APN	2	37,110,257 (GRCm39)	missense	probably damaging	1.00
IGL02821:Or1af1	APN	2	37,110,112 (GRCm39)	missense	probably damaging	1.00
R0603:Or1af1	UTSW	2	37,110,118 (GRCm39)	missense	probably damaging	1.00
R0707:Or1af1	UTSW	2	37,110,208 (GRCm39)	nonsense	probably null
R1204:Or1af1	UTSW	2	37,109,651 (GRCm39)	missense	probably benign
R1457:Or1af1	UTSW	2	37,109,671 (GRCm39)	missense	possibly damaging	0.95
R1509:Or1af1	UTSW	2	37,109,966 (GRCm39)	missense	probably damaging	1.00
R1676:Or1af1	UTSW	2	37,109,653 (GRCm39)	nonsense	probably null
R1823:Or1af1	UTSW	2	37,110,344 (GRCm39)	missense	probably damaging	0.96
R2163:Or1af1	UTSW	2	37,110,089 (GRCm39)	missense	probably damaging	1.00
R2909:Or1af1	UTSW	2	37,110,188 (GRCm39)	missense	probably damaging	0.98
R3696:Or1af1	UTSW	2	37,110,188 (GRCm39)	missense	probably damaging	0.98
R3698:Or1af1	UTSW	2	37,110,188 (GRCm39)	missense	probably damaging	0.98
R4004:Or1af1	UTSW	2	37,109,960 (GRCm39)	missense	probably benign	0.00
R4655:Or1af1	UTSW	2	37,109,885 (GRCm39)	missense	probably benign	0.03
R5311:Or1af1	UTSW	2	37,109,633 (GRCm39)	missense	probably benign	0.00
R5385:Or1af1	UTSW	2	37,109,599 (GRCm39)	missense	possibly damaging	0.77
R5433:Or1af1	UTSW	2	37,109,684 (GRCm39)	missense	probably damaging	1.00
R5499:Or1af1	UTSW	2	37,109,777 (GRCm39)	missense	possibly damaging	0.81
R5707:Or1af1	UTSW	2	37,109,901 (GRCm39)	missense	probably benign	0.00
R6330:Or1af1	UTSW	2	37,110,136 (GRCm39)	missense	probably benign	0.00
R6338:Or1af1	UTSW	2	37,109,834 (GRCm39)	missense	probably damaging	1.00
R6666:Or1af1	UTSW	2	37,110,331 (GRCm39)	missense	probably damaging	1.00
R6872:Or1af1	UTSW	2	37,109,989 (GRCm39)	missense	possibly damaging	0.60
R7412:Or1af1	UTSW	2	37,109,774 (GRCm39)	missense	possibly damaging	0.48
R7789:Or1af1	UTSW	2	37,109,672 (GRCm39)	missense	probably benign	0.01
R7831:Or1af1	UTSW	2	37,109,723 (GRCm39)	missense	probably damaging	0.98
R8220:Or1af1	UTSW	2	37,109,791 (GRCm39)	missense	probably benign	0.06
R8391:Or1af1	UTSW	2	37,110,277 (GRCm39)	missense	probably damaging	1.00
R9049:Or1af1	UTSW	2	37,109,959 (GRCm39)	missense	probably damaging	0.98
R9231:Or1af1	UTSW	2	37,109,989 (GRCm39)	missense	possibly damaging	0.60
R9294:Or1af1	UTSW	2	37,110,122 (GRCm39)	missense	possibly damaging	0.63
R9471:Or1af1	UTSW	2	37,110,400 (GRCm39)	missense	probably damaging	1.00
R9595:Or1af1	UTSW	2	37,110,281 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CGTGCCACAGATGTTAGTGAAC -3'
(R):5'- AGGGCTCATGATTACAACAGAG -3'

Sequencing Primer
(F):5'- CCACAGATGTTAGTGAACTTGCTGAC -3'
(R):5'- AGCCCTCTGTGAAGGCCAAG -3'

Posted On

2021-04-30