Mutagenetix > Incidental Mutation

Incidental Mutation 'R6452:Or5p66'

519413

Institutional Source

Beutler Lab

Gene Symbol

Or5p66

Ensembl Gene

ENSMUSG00000109884

Gene Name

olfactory receptor family 5 subfamily P member 66

Synonyms

Olfr490, GA_x6K02T2PBJ9-10617173-10616229, MOR204-17

MMRRC Submission

044588-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.164) question?

Stock #

R6452 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

107885387-107886331 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 107886100 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 78 (S78P)

Ref Sequence

ENSEMBL: ENSMUSP00000147922 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000210114] [ENSMUST00000211345]

AlphaFold

Q8VFD2

Predicted Effect

probably damaging
Transcript: ENSMUST00000210114
AA Change: S78P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

Predicted Effect

probably damaging
Transcript: ENSMUST00000211345
AA Change: S78P

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
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: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110070M22Rik	A	G	13: 119,624,651 (GRCm39)		probably benign	Het
Alox12e	A	T	11: 70,210,831 (GRCm39)	V296E	probably damaging	Het
Bmal2	G	A	6: 146,724,705 (GRCm39)	E400K	probably benign	Het
Ccdc171	A	G	4: 83,782,527 (GRCm39)	D1273G	probably damaging	Het
Cetn3	C	T	13: 81,932,797 (GRCm39)	R19*	probably null	Het
Chd6	G	T	2: 160,807,418 (GRCm39)	P1932H	possibly damaging	Het
Cimip1	C	A	2: 173,369,700 (GRCm39)	F71L	probably benign	Het
Cyp2d34	A	T	15: 82,500,290 (GRCm39)	I483N	probably benign	Het
Dglucy	T	C	12: 100,801,468 (GRCm39)	V71A	possibly damaging	Het
Dhx35	A	G	2: 158,673,607 (GRCm39)	E346G	probably damaging	Het
Dnajc14	A	G	10: 128,643,359 (GRCm39)	E427G	probably damaging	Het
Enpp5	G	A	17: 44,396,155 (GRCm39)	G356S	probably damaging	Het
Fasn	G	T	11: 120,706,237 (GRCm39)	Q1036K	probably damaging	Het
Fermt3	A	T	19: 6,992,105 (GRCm39)	F92I	probably benign	Het
Filip1l	C	A	16: 57,327,163 (GRCm39)	D64E	possibly damaging	Het
Fnbp1l	A	G	3: 122,338,198 (GRCm39)	F491S	probably damaging	Het
Fzd2	T	G	11: 102,495,811 (GRCm39)	V85G	probably damaging	Het
Gjd4	G	A	18: 9,280,457 (GRCm39)	T207M	possibly damaging	Het
Gm32742	T	C	9: 51,057,490 (GRCm39)	E1096G	probably damaging	Het
Itgb3	T	A	11: 104,524,290 (GRCm39)	L142*	probably null	Het
Kctd21	T	A	7: 96,996,869 (GRCm39)	I114N	probably benign	Het
Klra4	G	T	6: 130,042,329 (GRCm39)		probably null	Het
Larp4b	T	C	13: 9,197,503 (GRCm39)	V240A	probably damaging	Het
Lrriq4	T	C	3: 30,709,882 (GRCm39)	S409P	probably damaging	Het
Magel2	A	G	7: 62,030,132 (GRCm39)	E1012G	unknown	Het
Mmp24	A	T	2: 155,657,673 (GRCm39)	D521V	possibly damaging	Het
Mocos	A	G	18: 24,828,998 (GRCm39)	I768V	probably benign	Het
Mprip	A	T	11: 59,643,609 (GRCm39)	E553V	probably damaging	Het
Myh8	A	T	11: 67,196,565 (GRCm39)	I1762F	possibly damaging	Het
Myh8	A	T	11: 67,183,275 (GRCm39)	Y718F	probably benign	Het
Myo7a	C	T	7: 97,722,374 (GRCm39)	V1184M	probably benign	Het
Neb	A	T	2: 52,069,495 (GRCm39)	D5775E	probably benign	Het
Or10h5	T	C	17: 33,434,919 (GRCm39)	N133S	probably benign	Het
Pramel19	T	C	4: 101,798,640 (GRCm39)	Y204H	probably benign	Het
Prl8a2	T	C	13: 27,536,780 (GRCm39)	I134T	probably benign	Het
Qrich2	G	A	11: 116,346,714 (GRCm39)	T1370I	probably benign	Het
Rabgap1l	A	G	1: 160,281,331 (GRCm39)	L630P	probably damaging	Het
Ranbp2	G	T	10: 58,313,979 (GRCm39)	L1566F	probably benign	Het
Rnf43	T	A	11: 87,623,079 (GRCm39)	W727R	probably damaging	Het
Rundc3b	A	T	5: 8,629,175 (GRCm39)		probably null	Het
Samm50	T	G	15: 84,088,298 (GRCm39)		probably benign	Het
Sema4f	G	A	6: 82,894,643 (GRCm39)	A476V	probably benign	Het
Slc4a4	A	G	5: 89,376,839 (GRCm39)	N1031S	probably benign	Het
Slc4a9	A	G	18: 36,664,512 (GRCm39)	Y390C	probably damaging	Het
Slco6d1	C	A	1: 98,348,937 (GRCm39)	Q3K	probably benign	Het
Smim1	T	C	4: 154,108,071 (GRCm39)		probably benign	Het
Spg7	A	G	8: 123,806,162 (GRCm39)	K291E	possibly damaging	Het
Sppl2c	A	T	11: 104,079,017 (GRCm39)	T606S	probably benign	Het
Tex15	A	G	8: 34,062,844 (GRCm39)	D758G	probably damaging	Het
Tigd5	A	T	15: 75,783,287 (GRCm39)	R550*	probably null	Het
Tlcd3a	G	T	11: 76,097,972 (GRCm39)	G60*	probably null	Het
Tnrc18	A	C	5: 142,712,767 (GRCm39)	L2594R	probably damaging	Het
Vezf1	A	G	11: 87,972,496 (GRCm39)	T468A	possibly damaging	Het
Vmn1r210	T	A	13: 23,011,840 (GRCm39)	I149F	probably damaging	Het
Vmn2r96	A	C	17: 18,804,117 (GRCm39)	T264P	probably benign	Het
Zfp217	C	G	2: 169,961,214 (GRCm39)	S371T	probably benign	Het
Zfp442	G	A	2: 150,250,028 (GRCm39)	H568Y	probably damaging	Het
Zfp53	A	C	17: 21,729,875 (GRCm39)	H636P	probably damaging	Het
Zscan4d	C	T	7: 10,895,999 (GRCm39)	C457Y	probably damaging	Het

Other mutations in Or5p66

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0395:Or5p66	UTSW	7	107,885,478 (GRCm39)	missense	probably benign	0.00
R0634:Or5p66	UTSW	7	107,885,503 (GRCm39)	missense	probably benign	0.00
R0940:Or5p66	UTSW	7	107,886,264 (GRCm39)	missense	probably benign	0.01
R1990:Or5p66	UTSW	7	107,885,566 (GRCm39)	nonsense	probably null
R1991:Or5p66	UTSW	7	107,885,566 (GRCm39)	nonsense	probably null
R2860:Or5p66	UTSW	7	107,886,169 (GRCm39)	missense	probably damaging	0.98
R2861:Or5p66	UTSW	7	107,886,169 (GRCm39)	missense	probably damaging	0.98
R3712:Or5p66	UTSW	7	107,885,663 (GRCm39)	nonsense	probably null
R4735:Or5p66	UTSW	7	107,885,520 (GRCm39)	missense	probably benign
R4895:Or5p66	UTSW	7	107,885,802 (GRCm39)	missense	probably damaging	0.97
R4976:Or5p66	UTSW	7	107,885,818 (GRCm39)	missense	probably damaging	1.00
R5686:Or5p66	UTSW	7	107,885,949 (GRCm39)	missense	probably damaging	1.00
R5719:Or5p66	UTSW	7	107,885,599 (GRCm39)	missense	probably damaging	0.97
R5883:Or5p66	UTSW	7	107,885,451 (GRCm39)	missense	probably damaging	1.00
R5911:Or5p66	UTSW	7	107,885,605 (GRCm39)	missense	probably damaging	1.00
R7018:Or5p66	UTSW	7	107,885,551 (GRCm39)	missense	probably benign	0.34
R7233:Or5p66	UTSW	7	107,885,923 (GRCm39)	missense	probably benign	0.36
R8085:Or5p66	UTSW	7	107,885,620 (GRCm39)	missense	probably benign	0.01
R8166:Or5p66	UTSW	7	107,885,904 (GRCm39)	missense	probably benign	0.06
R8919:Or5p66	UTSW	7	107,886,289 (GRCm39)	missense	probably damaging	1.00
R9209:Or5p66	UTSW	7	107,885,526 (GRCm39)	missense	probably benign	0.06
R9612:Or5p66	UTSW	7	107,885,487 (GRCm39)	missense	probably benign
R9789:Or5p66	UTSW	7	107,885,898 (GRCm39)	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- AGGATCCTACAATCAACTGGAC -3'
(R):5'- GGTTTGACAGATGACCCAGTC -3'

Sequencing Primer
(F):5'- TGGACATTTTGGTGGAATAAAGC -3'
(R):5'- GTTTGACAGATGACCCAGTCCTTAG -3'

Posted On

2018-05-24