Mutagenetix > Incidental Mutation

Incidental Mutation 'R7624:Or14a256'

589322

Institutional Source

Beutler Lab

Gene Symbol

Or14a256

Ensembl Gene

ENSMUSG00000062042

Gene Name

olfactory receptor family 14 subfamily A member 256

Synonyms

Olfr294, MOR219-5, GA_x6K02T2NHDJ-9504525-9505532

MMRRC Submission

045689-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.127) question?

Stock #

R7624 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

86264844-86265851 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 86265769 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Serine at position 28 (F28S)

Ref Sequence

ENSEMBL: ENSMUSP00000077662 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000078588]

AlphaFold

F7CWV4

Predicted Effect

possibly damaging
Transcript: ENSMUST00000078588
AA Change: F28S

PolyPhen 2 Score 0.468 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000077662
Gene: ENSMUSG00000062042
AA Change: F28S

Domain	Start	End	E-Value	Type
Pfam:7tm_4	29	309	1.2e-38	PFAM
Pfam:7tm_1	39	288	1.8e-22	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

99% (69/70)

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
Atm	C	A	9: 53,366,068 (GRCm39)	R2533L	probably damaging	Het
Caprin1	T	A	2: 103,603,022 (GRCm39)	M514L	possibly damaging	Het
Ccdc78	A	G	17: 26,006,126 (GRCm39)	E98G	probably damaging	Het
Cmya5	A	T	13: 93,226,865 (GRCm39)	M2741K	possibly damaging	Het
Cnot1	T	G	8: 96,478,447 (GRCm39)	R959S	probably damaging	Het
Col12a1	G	T	9: 79,553,076 (GRCm39)		probably null	Het
Col4a3	A	G	1: 82,696,605 (GRCm39)	T177A	probably benign	Het
Cpa3	T	C	3: 20,279,307 (GRCm39)	N211D	possibly damaging	Het
Cripto	C	T	9: 110,775,017 (GRCm39)		probably benign	Het
Cryba1	T	C	11: 77,613,543 (GRCm39)	Y36C	probably damaging	Het
Ctnna1	T	A	18: 35,377,897 (GRCm39)	I632N	probably benign	Het
D630045J12Rik	T	C	6: 38,126,498 (GRCm39)	N1504S	probably damaging	Het
Dgkz	C	A	2: 91,773,019 (GRCm39)	R346L	probably damaging	Het
Dnajc21	G	A	15: 10,461,318 (GRCm39)	R211C	probably benign	Het
Dnajc21	A	T	15: 10,461,320 (GRCm39)	I210N	probably damaging	Het
Dscam	T	C	16: 96,411,524 (GRCm39)	D1784G	probably damaging	Het
Eya3	A	G	4: 132,400,262 (GRCm39)	T94A	probably benign	Het
Fan1	T	A	7: 64,022,234 (GRCm39)	N340Y	probably damaging	Het
Fat3	T	C	9: 15,871,165 (GRCm39)	D3742G	possibly damaging	Het
Ficd	T	C	5: 113,876,751 (GRCm39)	F309L	probably benign	Het
Gfra1	A	T	19: 58,226,878 (GRCm39)	M451K	probably benign	Het
Gm43517	T	A	12: 49,437,961 (GRCm39)	L318Q		Het
Gsc	A	T	12: 104,439,310 (GRCm39)	V22E	possibly damaging	Het
Il4ra	T	C	7: 125,168,280 (GRCm39)	Y100H	probably damaging	Het
Ilf3	T	C	9: 21,309,340 (GRCm39)	S486P	probably benign	Het
Itga10	T	A	3: 96,560,269 (GRCm39)	H594Q	probably benign	Het
Kcnf1	T	C	12: 17,226,137 (GRCm39)	D28G	probably benign	Het
Kiss1	A	G	1: 133,257,160 (GRCm39)	K53R	possibly damaging	Het
Lcn5	A	G	2: 25,551,426 (GRCm39)	I182V	probably benign	Het
Lcorl	T	C	5: 45,859,307 (GRCm39)	D269G	probably benign	Het
Letm2	A	T	8: 26,082,553 (GRCm39)	C174*	probably null	Het
Met	T	G	6: 17,558,834 (GRCm39)	V1154G	probably damaging	Het
Mindy3	A	G	2: 12,424,000 (GRCm39)	S22P	probably benign	Het
Mroh2b	G	A	15: 4,946,613 (GRCm39)	R471Q	probably damaging	Het
Nfe2l3	T	C	6: 51,435,252 (GRCm39)	L604P	probably damaging	Het
Or12e10	A	G	2: 87,640,683 (GRCm39)	Q173R	probably damaging	Het
Or5h18	T	A	16: 58,847,382 (GRCm39)	Q296L	possibly damaging	Het
Or8b3b	C	T	9: 38,583,919 (GRCm39)	V274I	probably benign	Het
Or8u9	A	T	2: 86,001,564 (GRCm39)	I199N	possibly damaging	Het
Or9r7	A	C	10: 129,962,455 (GRCm39)	I157S	probably damaging	Het
Pcdha9	T	A	18: 37,132,849 (GRCm39)	Y639*	probably null	Het
Pom121l2	A	T	13: 22,167,699 (GRCm39)	I657L	probably damaging	Het
Prr14l	T	A	5: 32,986,967 (GRCm39)	T843S	possibly damaging	Het
Rln1	A	T	19: 29,309,499 (GRCm39)	N93K	probably damaging	Het
Rpl3l	A	T	17: 24,951,401 (GRCm39)	M101L	probably benign	Het
Rtkn	A	G	6: 83,129,158 (GRCm39)	Y551C	probably benign	Het
Rundc1	G	C	11: 101,324,305 (GRCm39)	R337P	possibly damaging	Het
Scarf1	T	A	11: 75,405,242 (GRCm39)		probably null	Het
Serpinb1b	T	A	13: 33,275,622 (GRCm39)		probably null	Het
Sgsm1	A	T	5: 113,422,201 (GRCm39)	C484*	probably null	Het
Slc22a19	T	A	19: 7,650,668 (GRCm39)	K547*	probably null	Het
Slc22a19	T	C	19: 7,671,183 (GRCm39)	T177A	probably benign	Het
Slc6a5	A	C	7: 49,591,614 (GRCm39)	K526N	probably benign	Het
Sqle	G	A	15: 59,202,603 (GRCm39)	R519Q	probably benign	Het
Stard9	T	C	2: 120,518,627 (GRCm39)	I517T	probably benign	Het
Taf15	A	T	11: 83,395,849 (GRCm39)	D518V	unknown	Het
Tenm4	A	G	7: 96,545,192 (GRCm39)	M2440V	possibly damaging	Het
Tm6sf1	A	G	7: 81,518,458 (GRCm39)	M122V	possibly damaging	Het
Tmprss9	T	A	10: 80,728,053 (GRCm39)	S548T	possibly damaging	Het
Trim62	A	T	4: 128,777,471 (GRCm39)		probably benign	Het
Ugt2b34	C	T	5: 87,039,141 (GRCm39)	V507M	possibly damaging	Het
Usp16	T	A	16: 87,273,693 (GRCm39)	M423K	probably benign	Het
Vmn1r199	T	A	13: 22,566,906 (GRCm39)	S67T	probably benign	Het
Vmn1r62	A	T	7: 5,678,600 (GRCm39)	M94L	probably benign	Het
Wnk4	G	T	11: 101,155,180 (GRCm39)	E364*	probably null	Het
Xpo1	T	A	11: 23,232,584 (GRCm39)	I368N	probably damaging	Het
Zfp366	A	G	13: 99,382,804 (GRCm39)	T656A	probably benign	Het
Zfp934	T	C	13: 62,666,338 (GRCm39)	M113V	probably benign	Het
Zkscan2	A	G	7: 123,097,994 (GRCm39)	V134A	probably damaging	Het

Other mutations in Or14a256

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01365:Or14a256	APN	7	86,265,205 (GRCm39)	missense	probably damaging	1.00
IGL02617:Or14a256	APN	7	86,264,872 (GRCm39)	missense	probably benign	0.14
IGL02694:Or14a256	APN	7	86,265,518 (GRCm39)	missense	probably benign	0.00
IGL02828:Or14a256	APN	7	86,265,277 (GRCm39)	missense	possibly damaging	0.67
IGL03229:Or14a256	APN	7	86,265,286 (GRCm39)	missense	probably benign	0.00
IGL03351:Or14a256	APN	7	86,264,885 (GRCm39)	missense	possibly damaging	0.68
PIT4802001:Or14a256	UTSW	7	86,265,763 (GRCm39)	missense	probably null	1.00
R0848:Or14a256	UTSW	7	86,264,848 (GRCm39)	missense	probably damaging	0.96
R1448:Or14a256	UTSW	7	86,265,569 (GRCm39)	missense	probably damaging	1.00
R1720:Or14a256	UTSW	7	86,265,664 (GRCm39)	missense	probably damaging	1.00
R1734:Or14a256	UTSW	7	86,265,425 (GRCm39)	missense	probably benign	0.07
R1959:Or14a256	UTSW	7	86,265,639 (GRCm39)	missense	probably benign	0.00
R2116:Or14a256	UTSW	7	86,265,286 (GRCm39)	missense	probably benign	0.00
R2518:Or14a256	UTSW	7	86,265,395 (GRCm39)	missense	probably benign	0.03
R3034:Or14a256	UTSW	7	86,264,970 (GRCm39)	missense	possibly damaging	0.50
R3110:Or14a256	UTSW	7	86,264,884 (GRCm39)	missense	probably benign
R3112:Or14a256	UTSW	7	86,264,884 (GRCm39)	missense	probably benign
R3690:Or14a256	UTSW	7	86,265,686 (GRCm39)	missense	probably damaging	1.00
R4612:Or14a256	UTSW	7	86,264,944 (GRCm39)	missense	probably benign	0.00
R6476:Or14a256	UTSW	7	86,265,218 (GRCm39)	missense	probably benign	0.04
R6895:Or14a256	UTSW	7	86,265,323 (GRCm39)	missense	probably damaging	1.00
R7102:Or14a256	UTSW	7	86,265,475 (GRCm39)	missense	probably benign	0.25
R7104:Or14a256	UTSW	7	86,264,900 (GRCm39)	missense	probably null	0.07
R7179:Or14a256	UTSW	7	86,265,574 (GRCm39)	missense	possibly damaging	0.76
R7256:Or14a256	UTSW	7	86,264,873 (GRCm39)	missense	probably benign	0.03
R8422:Or14a256	UTSW	7	86,265,466 (GRCm39)	missense	probably benign	0.13
R9432:Or14a256	UTSW	7	86,265,065 (GRCm39)	missense	possibly damaging	0.66
R9700:Or14a256	UTSW	7	86,265,618 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- ACAATTGGAGGGCACAACC -3'
(R):5'- GGGCAGTATCTAGGTAGTGTCC -3'

Sequencing Primer
(F):5'- GGCACAACCCAGAATAGAAATTG -3'
(R):5'- CTGGGTCCATTTCCACTGAG -3'

Posted On

2019-10-24