Mutagenetix > Incidental Mutation

Incidental Mutation 'R0863:Or7e173'

82200

Institutional Source

Beutler Lab

Gene Symbol

Or7e173

Ensembl Gene

ENSMUSG00000050803

Gene Name

olfactory receptor family 7 subfamily E member 173

Synonyms

Olfr866, MOR145-5, GA_x6K02T2PVTD-13768406-13767468

MMRRC Submission

039037-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.093) question?

Stock #

R0863 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

19938255-19939331 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 19938509 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 242 (S242T)

Ref Sequence

ENSEMBL: ENSMUSP00000054864 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000062248]

AlphaFold

Q8VFI7

Predicted Effect

probably damaging
Transcript: ENSMUST00000062248
AA Change: S242T

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

SMART Domains

Protein: ENSMUSP00000054864
Gene: ENSMUSG00000050803
AA Change: S242T

Domain	Start	End	E-Value	Type
Pfam:7tm_4	34	310	2e-47	PFAM
Pfam:7TM_GPCR_Srsx	38	282	8.7e-7	PFAM
Pfam:7tm_1	44	293	5.1e-21	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197056

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000212071

Meta Mutation Damage Score

0.3349

Coding Region Coverage

1x: 99.5%
3x: 98.9%
10x: 97.4%
20x: 94.8%

Validation Efficiency

94% (59/63)

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
2310016G11Rik	A	G	7: 44,327,232 (GRCm39)		noncoding transcript	Het
4930433I11Rik	A	T	7: 40,642,480 (GRCm39)	T141S	probably benign	Het
Abca14	A	T	7: 119,815,453 (GRCm39)	T234S	probably benign	Het
Acap1	C	A	11: 69,777,882 (GRCm39)	V119L	probably damaging	Het
Actr2	C	T	11: 20,030,760 (GRCm39)	V163I	probably benign	Het
Adcy4	T	C	14: 56,021,056 (GRCm39)	Y27C	probably damaging	Het
Arnt2	T	A	7: 83,914,792 (GRCm39)	K524M	probably damaging	Het
Brca1	T	C	11: 101,415,596 (GRCm39)	Y846C	probably benign	Het
Capn7	T	A	14: 31,091,714 (GRCm39)	C704S	possibly damaging	Het
Cep350	T	A	1: 155,737,981 (GRCm39)	I2621L	probably benign	Het
Col11a1	G	A	3: 113,932,414 (GRCm39)	R113H	unknown	Het
Ctnnbl1	C	T	2: 157,641,337 (GRCm39)		probably benign	Het
Cul9	T	C	17: 46,848,748 (GRCm39)		probably null	Het
Erc2	A	C	14: 27,747,105 (GRCm39)	N345T	probably benign	Het
Fank1	A	G	7: 133,482,352 (GRCm39)	R73G	possibly damaging	Het
Fes	A	T	7: 80,030,634 (GRCm39)	W552R	probably damaging	Het
Fsd2	A	G	7: 81,191,913 (GRCm39)	V488A	possibly damaging	Het
Gfm1	T	C	3: 67,381,928 (GRCm39)	S705P	probably damaging	Het
Gm9493	A	T	19: 23,597,173 (GRCm39)	Q23L	probably benign	Het
Gucy1b2	T	C	14: 62,656,511 (GRCm39)	D282G	probably benign	Het
H2-Ab1	T	C	17: 34,486,328 (GRCm39)	I129T	probably damaging	Het
H2-M10.3	T	A	17: 36,677,582 (GRCm39)	Y232F	probably damaging	Het
Iqca1	C	A	1: 90,070,453 (GRCm39)	G133V	probably null	Het
Lonp1	T	C	17: 56,925,331 (GRCm39)	K487R	probably damaging	Het
Ltbp1	A	G	17: 75,559,381 (GRCm39)	Y290C	probably damaging	Het
Ms4a10	C	T	19: 10,945,957 (GRCm39)	G58D	probably damaging	Het
Muc5b	A	G	7: 141,421,454 (GRCm39)	S4315G	probably benign	Het
Nlrp1b	T	A	11: 71,072,173 (GRCm39)	T557S	probably benign	Het
Nlrp3	A	G	11: 59,456,676 (GRCm39)	D946G	probably benign	Het
Obscn	T	C	11: 58,886,241 (GRCm39)		probably benign	Het
Oga	C	T	19: 45,771,425 (GRCm39)	A49T	probably benign	Het
Or10ab5	A	G	7: 108,244,865 (GRCm39)	I306T	probably benign	Het
Or5p50	T	C	7: 107,422,581 (GRCm39)	S32G	probably benign	Het
Pask	A	T	1: 93,242,061 (GRCm39)	F1219I	probably damaging	Het
Pcdhb2	G	A	18: 37,428,710 (GRCm39)	V228I	possibly damaging	Het
Phf1	T	C	17: 27,156,114 (GRCm39)		probably benign	Het
Plec	G	A	15: 76,058,280 (GRCm39)	Q3751*	probably null	Het
Plscr1l1	A	T	9: 92,233,140 (GRCm39)	I88L	possibly damaging	Het
Ppp1r12c	G	T	7: 4,489,365 (GRCm39)	Q240K	probably damaging	Het
Ralgapa1	A	T	12: 55,809,466 (GRCm39)	Y436*	probably null	Het
Ralgapa1	C	A	12: 55,829,562 (GRCm39)		probably benign	Het
Scel	T	A	14: 103,823,916 (GRCm39)	S381R	possibly damaging	Het
Sema4a	C	T	3: 88,355,456 (GRCm39)		probably benign	Het
Sltm	A	G	9: 70,469,190 (GRCm39)	T150A	probably benign	Het
Spag1	G	T	15: 36,192,193 (GRCm39)	K217N	probably damaging	Het
Ssh1	C	T	5: 114,104,792 (GRCm39)	R9H	probably damaging	Het
St3gal4	C	A	9: 34,964,744 (GRCm39)	V155F	probably damaging	Het
Stxbp5	C	T	10: 9,684,784 (GRCm39)	E539K	possibly damaging	Het
Tbc1d7	G	T	13: 43,308,161 (GRCm39)		probably benign	Het
Thnsl2	A	T	6: 71,111,208 (GRCm39)	L220*	probably null	Het
Tinf2	G	A	14: 55,917,566 (GRCm39)	P308S	probably benign	Het
Tnf	T	C	17: 35,420,120 (GRCm39)		probably benign	Het
Ttc21b	T	C	2: 66,073,117 (GRCm39)	I190V	probably benign	Het
Ttn	T	C	2: 76,537,391 (GRCm39)	T34846A	probably benign	Het
Ube4a	A	G	9: 44,861,114 (GRCm39)	V232A	possibly damaging	Het
Uri1	A	T	7: 37,669,100 (GRCm39)	D122E	probably damaging	Het
Vmn2r94	T	G	17: 18,477,973 (GRCm39)	Q146P	probably damaging	Het
Zan	T	A	5: 137,456,901 (GRCm39)	E1278D	unknown	Het
Zfhx4	T	A	3: 5,310,375 (GRCm39)	S919R	possibly damaging	Het

Other mutations in Or7e173

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01353:Or7e173	APN	9	19,938,343 (GRCm39)	missense	probably damaging	1.00
IGL01554:Or7e173	APN	9	19,938,704 (GRCm39)	missense	possibly damaging	0.55
IGL01561:Or7e173	APN	9	19,938,818 (GRCm39)	missense	probably benign	0.20
IGL01597:Or7e173	APN	9	19,938,982 (GRCm39)	missense	probably damaging	0.98
IGL02986:Or7e173	APN	9	19,939,007 (GRCm39)	missense	probably benign	0.43
IGL03101:Or7e173	APN	9	19,938,725 (GRCm39)	missense	probably benign	0.03
R1747:Or7e173	UTSW	9	19,938,613 (GRCm39)	missense	probably benign	0.01
R2121:Or7e173	UTSW	9	19,938,797 (GRCm39)	missense	probably benign
R2124:Or7e173	UTSW	9	19,938,797 (GRCm39)	missense	probably benign
R2240:Or7e173	UTSW	9	19,938,440 (GRCm39)	missense	probably damaging	1.00
R3793:Or7e173	UTSW	9	19,938,359 (GRCm39)	missense	probably damaging	1.00
R4498:Or7e173	UTSW	9	19,939,029 (GRCm39)	missense	possibly damaging	0.50
R5084:Or7e173	UTSW	9	19,938,551 (GRCm39)	missense	probably damaging	0.99
R5420:Or7e173	UTSW	9	19,938,355 (GRCm39)	missense	probably damaging	0.98
R6314:Or7e173	UTSW	9	19,938,958 (GRCm39)	missense	probably damaging	0.98
R6357:Or7e173	UTSW	9	19,938,925 (GRCm39)	missense	probably damaging	1.00
R6588:Or7e173	UTSW	9	19,939,162 (GRCm39)	missense	probably damaging	0.97
R6886:Or7e173	UTSW	9	19,938,428 (GRCm39)	missense	probably benign	0.00
R7480:Or7e173	UTSW	9	19,939,230 (GRCm39)	start codon destroyed	probably null
R9026:Or7e173	UTSW	9	19,938,344 (GRCm39)	missense
R9168:Or7e173	UTSW	9	19,938,818 (GRCm39)	missense	probably benign	0.20
R9280:Or7e173	UTSW	9	19,938,639 (GRCm39)	missense	probably benign	0.00
R9559:Or7e173	UTSW	9	19,939,216 (GRCm39)	missense	probably benign
R9562:Or7e173	UTSW	9	19,939,045 (GRCm39)	missense	probably damaging	1.00
Z1088:Or7e173	UTSW	9	19,938,575 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ACCTACTGTGGAATCTCTTCAGGGC -3'
(R):5'- TTCCTATGCAGGCTGCTTGACAC -3'

Sequencing Primer
(F):5'- TGGAATCTCTTCAGGGCATTAC -3'
(R):5'- GGCTGCTTGACACAAATGTCTC -3'

Posted On

2013-11-08