Mutagenetix > Incidental Mutation

Incidental Mutation 'R3112:Or14a256'

263740

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

040585-MU

Accession Numbers

Essential gene?

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

Stock #

R3112 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

86264844-86265851 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 86264884 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 323 (Y323C)

Ref Sequence

ENSEMBL: ENSMUSP00000077662 (fasta)

Gene Model

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

AlphaFold

F7CWV4

Predicted Effect

probably benign
Transcript: ENSMUST00000078588
AA Change: Y323C

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000077662
Gene: ENSMUSG00000062042
AA Change: Y323C

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

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 97.2%
20x: 94.9%

Validation Efficiency

100% (38/38)

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: 74 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca6	T	A	11: 110,069,655 (GRCm39)	K1554*	probably null	Het
Acads	T	C	5: 115,255,757 (GRCm39)	H26R	probably benign	Het
Acer1	G	A	17: 57,265,406 (GRCm39)	T141I	probably damaging	Het
Adam15	C	G	3: 89,254,764 (GRCm39)	V99L	probably benign	Het
Ankrd13b	A	G	11: 77,368,331 (GRCm39)	V97A	possibly damaging	Het
Anpep	T	C	7: 79,491,720 (GRCm39)	T94A	probably benign	Het
Atp1a3	T	C	7: 24,694,119 (GRCm39)	N345S	probably damaging	Het
Btn1a1	T	A	13: 23,645,721 (GRCm39)	N216I	possibly damaging	Het
Cacna1s	G	A	1: 136,002,831 (GRCm39)	W62*	probably null	Het
Ccdc141	C	T	2: 76,869,830 (GRCm39)	V892I	probably benign	Het
Ccdc180	T	A	4: 45,900,470 (GRCm39)	I278K	possibly damaging	Het
Cdc7	T	G	5: 107,122,564 (GRCm39)		probably null	Het
Cpb1	C	T	3: 20,319,521 (GRCm39)	V188M	probably damaging	Het
Dock5	A	G	14: 68,095,371 (GRCm39)	I101T	possibly damaging	Het
Dqx1	T	C	6: 83,035,953 (GRCm39)	V95A	probably damaging	Het
Dvl1	T	A	4: 155,938,123 (GRCm39)	D90E	probably damaging	Het
Fam135b	T	C	15: 71,335,879 (GRCm39)	I438M	probably benign	Het
Fpr1	A	T	17: 18,096,897 (GRCm39)	M364K	probably benign	Het
Gpat4	G	A	8: 23,670,171 (GRCm39)	P286L	probably damaging	Het
Gpx7	C	A	4: 108,260,470 (GRCm39)	V109F	probably damaging	Het
Grhl2	T	C	15: 37,336,591 (GRCm39)		probably null	Het
Grn	A	G	11: 102,324,069 (GRCm39)	T53A	probably benign	Het
H1f4	T	C	13: 23,805,829 (GRCm39)		probably benign	Het
H2-T9	T	C	17: 36,440,038 (GRCm39)	Y32C	probably damaging	Het
Hmgxb3	T	C	18: 61,280,454 (GRCm39)	N683S	probably damaging	Het
Iigp1	T	C	18: 60,523,983 (GRCm39)	I367T	probably benign	Het
Itfg2	T	C	6: 128,388,632 (GRCm39)	E285G	probably damaging	Het
Itgav	T	A	2: 83,622,915 (GRCm39)	C662*	probably null	Het
Jarid2	T	A	13: 45,059,752 (GRCm39)	N661K	probably damaging	Het
Lipe	T	C	7: 25,097,848 (GRCm39)	T32A	probably benign	Het
Lrrk2	A	G	15: 91,698,898 (GRCm39)	Y2475C	probably benign	Het
Mcc	T	C	18: 44,582,330 (GRCm39)	D607G	probably damaging	Het
Mip	T	A	10: 128,061,875 (GRCm39)	L42*	probably null	Het
Mlc1	A	T	15: 88,850,199 (GRCm39)	D192E	probably benign	Het
Muc2	T	C	7: 141,299,225 (GRCm39)		probably benign	Het
Mybl1	T	C	1: 9,752,095 (GRCm39)	D260G	probably damaging	Het
Ncln	C	T	10: 81,323,519 (GRCm39)	V51I	probably benign	Het
Nlrp9a	T	C	7: 26,257,297 (GRCm39)	V305A	probably benign	Het
Nodal	G	A	10: 61,260,276 (GRCm39)	R309Q	possibly damaging	Het
Olr1	T	C	6: 129,476,881 (GRCm39)	N128S	possibly damaging	Het
Or10ak14	A	T	4: 118,611,421 (GRCm39)	F105I	probably damaging	Het
Or12j5	A	G	7: 140,083,832 (GRCm39)	I180T	probably damaging	Het
Orc1	T	A	4: 108,461,757 (GRCm39)	C585S	probably benign	Het
Pcmtd2	A	T	2: 181,496,922 (GRCm39)	I300F	probably damaging	Het
Pfkfb4	C	T	9: 108,854,110 (GRCm39)		probably benign	Het
Phactr3	T	A	2: 177,920,810 (GRCm39)	L180Q	possibly damaging	Het
Pigo	T	C	4: 43,021,083 (GRCm39)	T612A	probably benign	Het
Plch1	T	A	3: 63,616,952 (GRCm39)	D766V	probably damaging	Het
Plekhh3	T	C	11: 101,054,973 (GRCm39)		probably benign	Het
Potefam1	T	G	2: 111,058,399 (GRCm39)	L131F	probably damaging	Het
Ppp1r12b	T	A	1: 134,800,570 (GRCm39)	T547S	probably damaging	Het
Prkcb	T	A	7: 122,116,079 (GRCm39)	M186K	probably damaging	Het
Prpf3	A	T	3: 95,757,112 (GRCm39)		probably benign	Het
Psg23	T	C	7: 18,344,369 (GRCm39)	D362G	possibly damaging	Het
Reg3a	T	C	6: 78,358,114 (GRCm39)	L15P	probably damaging	Het
Scrib	A	T	15: 75,941,223 (GRCm39)	I5N	probably damaging	Het
Speg	C	T	1: 75,399,326 (GRCm39)	Q2005*	probably null	Het
Sppl3	A	T	5: 115,212,923 (GRCm39)	S51C	possibly damaging	Het
Sspo	A	G	6: 48,434,534 (GRCm39)	T1009A	probably damaging	Het
Syce1l	A	G	8: 114,381,579 (GRCm39)	Q164R	probably benign	Het
Sympk	T	C	7: 18,768,409 (GRCm39)	V126A	possibly damaging	Het
Tas2r110	T	A	6: 132,844,987 (GRCm39)	I6K	unknown	Het
Tas2r120	A	T	6: 132,634,731 (GRCm39)	H271L	probably damaging	Het
Tlcd3a	A	G	11: 76,093,057 (GRCm39)	D33G	probably benign	Het
Tnn	T	A	1: 159,943,856 (GRCm39)	T986S	possibly damaging	Het
Trim5	T	C	7: 103,928,845 (GRCm39)	H32R	probably damaging	Het
Ttc13	A	G	8: 125,410,573 (GRCm39)	I360T	possibly damaging	Het
Uaca	A	G	9: 60,778,781 (GRCm39)	E1054G	probably damaging	Het
Usp16	T	A	16: 87,268,736 (GRCm39)		probably null	Het
Wee1	T	A	7: 109,730,043 (GRCm39)	S382R	probably damaging	Het
Wnt11	T	C	7: 98,495,771 (GRCm39)	S92P	probably damaging	Het
Zfp1004	C	G	2: 150,034,141 (GRCm39)	P185R	probably damaging	Het
Zfp786	A	G	6: 47,797,160 (GRCm39)	C593R	probably damaging	Het
Zfp879	T	G	11: 50,723,989 (GRCm39)	I283L	possibly 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
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
R7624:Or14a256	UTSW	7	86,265,769 (GRCm39)	missense	possibly damaging	0.47
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'- TGAGAATGGCTTTACATACAAGAGC -3'
(R):5'- CTTGCTTTGTCAATCTGAAGCC -3'

Sequencing Primer
(F):5'- GCTTTACATACAAGAGCAGAAATTGG -3'
(R):5'- ACCCTCACGTTCAGCATCAATTG -3'

Posted On

2015-02-05