Mutagenetix > Incidental Mutation

Incidental Mutation 'R1681:Olfr914'

188517

Institutional Source

Beutler Lab

Gene Symbol

Olfr914

Ensembl Gene

ENSMUSG00000047050

Gene Name

olfactory receptor 914

Synonyms

MOR165-7, GA_x6K02T2PVTD-32308823-32309773

MMRRC Submission

039717-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

R1681 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

38605102-38610978 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 38606948 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Glycine to Aspartic acid at position 161 (G161D)

Ref Sequence

ENSEMBL: ENSMUSP00000150241 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057755] [ENSMUST00000217057]

AlphaFold

E9PW59

Predicted Effect

probably damaging
Transcript: ENSMUST00000057755
AA Change: G161D

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000053405
Gene: ENSMUSG00000047050
AA Change: G161D

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	310	1.1e-48	PFAM
Pfam:7tm_1	41	290	5.2e-23	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000217057
AA Change: G161D

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.6%
20x: 93.6%

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: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	T	A	11: 84,226,185 (GRCm38)	I247N	probably damaging	Het
Ankle1	G	T	8: 71,407,618 (GRCm38)	S260I	probably benign	Het
Aoc2	T	C	11: 101,325,192 (GRCm38)	S34P	probably benign	Het
Ap1m1	A	C	8: 72,256,122 (GRCm38)	I397L	possibly damaging	Het
Apba1	C	A	19: 23,936,561 (GRCm38)	D649E	probably damaging	Het
Aptx	C	T	4: 40,697,274 (GRCm38)	V25M	probably benign	Het
Arhgef18	G	A	8: 3,439,645 (GRCm38)	G326R	probably damaging	Het
Atm	A	C	9: 53,522,155 (GRCm38)	I265S	possibly damaging	Het
B3galt4	A	T	17: 33,951,213 (GRCm38)	V17E	probably benign	Het
Bcl7a	T	A	5: 123,356,023 (GRCm38)	M86K	possibly damaging	Het
Cela3a	T	A	4: 137,402,684 (GRCm38)		probably null	Het
Cep85	T	A	4: 134,148,728 (GRCm38)	K456*	probably null	Het
Ces1f	C	A	8: 93,275,414 (GRCm38)	A29S	probably benign	Het
Chd9	A	T	8: 90,973,135 (GRCm38)	I598F	probably damaging	Het
Cntln	T	C	4: 84,947,635 (GRCm38)	L176S	probably damaging	Het
Cntn3	A	T	6: 102,170,668 (GRCm38)	N909K	probably damaging	Het
Cntnap5b	T	C	1: 100,076,107 (GRCm38)	S271P	probably damaging	Het
Col6a3	T	A	1: 90,773,502 (GRCm38)	H2564L	unknown	Het
Cyp2b19	C	A	7: 26,763,340 (GRCm38)		probably null	Het
Dapk1	G	T	13: 60,718,464 (GRCm38)		probably null	Het
Dnah7b	T	A	1: 46,324,712 (GRCm38)	Y3497*	probably null	Het
Duoxa2	T	C	2: 122,299,162 (GRCm38)		probably null	Het
Eny2	T	C	15: 44,432,478 (GRCm38)	W42R	probably damaging	Het
Epha3	A	G	16: 63,595,728 (GRCm38)	V635A	probably damaging	Het
Fam167b	G	C	4: 129,578,276 (GRCm38)	Q34E	probably benign	Het
Fam26f	A	G	10: 34,127,900 (GRCm38)	F4L	probably benign	Het
Fancm	T	C	12: 65,105,656 (GRCm38)	M962T	probably benign	Het
Gimap8	T	A	6: 48,656,411 (GRCm38)	I388N	probably benign	Het
Gpaa1	A	G	15: 76,331,453 (GRCm38)	T22A	probably benign	Het
Hoxc11	T	C	15: 102,955,156 (GRCm38)	S211P	possibly damaging	Het
Hsd17b12	T	C	2: 94,033,561 (GRCm38)	N312S	unknown	Het
Idh2	T	G	7: 80,099,158 (GRCm38)	E125A	probably damaging	Het
Igdcc4	A	G	9: 65,128,795 (GRCm38)	Y712C	probably damaging	Het
Kank1	T	C	19: 25,410,304 (GRCm38)	V447A	possibly damaging	Het
Kif1b	T	A	4: 149,195,501 (GRCm38)		probably null	Het
Klc4	A	T	17: 46,636,770 (GRCm38)	D335E	probably damaging	Het
Klhl33	T	A	14: 50,893,077 (GRCm38)	D320V	probably benign	Het
Krt73	A	T	15: 101,802,047 (GRCm38)	M84K	possibly damaging	Het
Kti12	T	A	4: 108,848,858 (GRCm38)	I323N	probably damaging	Het
Kynu	T	C	2: 43,679,825 (GRCm38)	L373P	probably damaging	Het
Lats1	T	C	10: 7,705,914 (GRCm38)	M821T	probably damaging	Het
Lnx1	A	T	5: 74,685,410 (GRCm38)	H126Q	probably benign	Het
Lonrf2	G	A	1: 38,813,276 (GRCm38)	P165S	probably benign	Het
Lrrc4b	T	A	7: 44,461,177 (GRCm38)	Y158N	probably damaging	Het
Lrrc74b	C	A	16: 17,559,753 (GRCm38)	R87L	probably damaging	Het
Meig1	T	C	2: 3,409,274 (GRCm38)	D63G	probably damaging	Het
Mrpl38	G	A	11: 116,138,429 (GRCm38)		probably benign	Het
Naip2	C	T	13: 100,161,860 (GRCm38)	G556D	probably benign	Het
Naip2	T	C	13: 100,161,854 (GRCm38)	E558G	probably benign	Het
Nlrp1a	T	A	11: 71,142,358 (GRCm38)	E3D	unknown	Het
Nphs2	T	A	1: 156,320,898 (GRCm38)	D110E	probably damaging	Het
Nxn	T	A	11: 76,272,464 (GRCm38)	K244N	probably benign	Het
Oas3	A	T	5: 120,769,908 (GRCm38)	F322L	probably benign	Het
Obscn	T	A	11: 59,103,325 (GRCm38)	Y1577F	probably damaging	Het
Olfr1122	G	A	2: 87,388,620 (GRCm38)	R305K	possibly damaging	Het
Olfr911-ps1	T	A	9: 38,524,117 (GRCm38)	N128K	probably benign	Het
Olfr917	A	G	9: 38,665,320 (GRCm38)	Y175H	probably benign	Het
Olfr924	T	C	9: 38,848,513 (GRCm38)	M133T	probably damaging	Het
Panx1	T	C	9: 15,007,783 (GRCm38)	D260G	probably benign	Het
Pcdhb15	T	C	18: 37,473,813 (GRCm38)	Y33H	probably damaging	Het
Pik3ap1	C	A	19: 41,308,529 (GRCm38)	V461F	probably damaging	Het
Plpp3	G	A	4: 105,208,805 (GRCm38)		probably null	Het
Prtn3	A	T	10: 79,880,541 (GRCm38)	T61S	probably benign	Het
Psen1	T	A	12: 83,724,620 (GRCm38)	Y225N	probably damaging	Het
Rab44	T	A	17: 29,140,124 (GRCm38)	S429T	possibly damaging	Het
Ralgapa1	T	C	12: 55,762,603 (GRCm38)	I462M	probably benign	Het
Rbfox3	T	C	11: 118,505,669 (GRCm38)	N105S	probably damaging	Het
Rbm7	A	C	9: 48,489,721 (GRCm38)	Y236D	possibly damaging	Het
Samhd1	T	C	2: 157,101,732 (GRCm38)	T621A	probably benign	Het
Samt3	C	A	X: 86,046,650 (GRCm38)	D49E	probably benign	Het
Sass6	T	C	3: 116,603,473 (GRCm38)	V26A	possibly damaging	Het
Scn11a	C	T	9: 119,804,412 (GRCm38)	M418I	possibly damaging	Het
Scrib	T	C	15: 76,064,567 (GRCm38)	E480G	probably damaging	Het
Sec24a	T	G	11: 51,695,189 (GRCm38)	T1071P	probably damaging	Het
Siglecg	A	C	7: 43,408,941 (GRCm38)	E84A	probably benign	Het
Slc6a17	C	T	3: 107,474,386 (GRCm38)	V419I	probably damaging	Het
Soga1	T	C	2: 157,030,530 (GRCm38)	T966A	possibly damaging	Het
Ssr2	T	C	3: 88,581,042 (GRCm38)	M75T	possibly damaging	Het
Tbc1d22b	A	G	17: 29,575,177 (GRCm38)	T275A	possibly damaging	Het
Tbx15	T	A	3: 99,351,824 (GRCm38)		probably null	Het
Tll1	A	C	8: 64,085,551 (GRCm38)	L353R	possibly damaging	Het
Tlr4	C	T	4: 66,841,105 (GRCm38)	P712S	probably damaging	Het
Tmem145	T	A	7: 25,314,734 (GRCm38)	F424L	possibly damaging	Het
Tnrc18	T	C	5: 142,773,817 (GRCm38)	K755E	unknown	Het
Trmt44	A	G	5: 35,569,977 (GRCm38)	I298T	probably benign	Het
Vmn1r69	A	G	7: 10,580,252 (GRCm38)	V184A	probably benign	Het
Zfp84	T	C	7: 29,777,400 (GRCm38)	C506R	probably damaging	Het

Other mutations in Olfr914

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01613:Olfr914	APN	9	38,606,554 (GRCm38)	missense	probably null	0.00
IGL01758:Olfr914	APN	9	38,607,293 (GRCm38)	missense	probably damaging	0.99
IGL02003:Olfr914	APN	9	38,606,840 (GRCm38)	missense	probably damaging	1.00
IGL02203:Olfr914	APN	9	38,607,423 (GRCm38)	utr 3 prime	probably benign
IGL02233:Olfr914	APN	9	38,607,242 (GRCm38)	missense	probably damaging	1.00
IGL02408:Olfr914	APN	9	38,607,121 (GRCm38)	missense	possibly damaging	0.62
IGL02882:Olfr914	APN	9	38,606,938 (GRCm38)	missense	probably benign	0.04
IGL03081:Olfr914	APN	9	38,606,870 (GRCm38)	missense	probably benign	0.01
IGL03088:Olfr914	APN	9	38,607,301 (GRCm38)	missense	probably damaging	0.99
IGL03177:Olfr914	APN	9	38,606,571 (GRCm38)	nonsense	probably null
IGL03219:Olfr914	APN	9	38,606,951 (GRCm38)	missense	probably benign	0.28
P0023:Olfr914	UTSW	9	38,606,645 (GRCm38)	missense	probably damaging	1.00
R0630:Olfr914	UTSW	9	38,606,896 (GRCm38)	missense	probably benign	0.01
R0948:Olfr914	UTSW	9	38,606,491 (GRCm38)	missense	possibly damaging	0.65
R1451:Olfr914	UTSW	9	38,606,938 (GRCm38)	missense	probably benign	0.04
R2402:Olfr914	UTSW	9	38,607,101 (GRCm38)	missense	probably benign	0.02
R5854:Olfr914	UTSW	9	38,606,663 (GRCm38)	missense	probably damaging	1.00
R6857:Olfr914	UTSW	9	38,607,011 (GRCm38)	missense	probably benign	0.07
R7452:Olfr914	UTSW	9	38,607,088 (GRCm38)	missense	probably benign	0.34
R7838:Olfr914	UTSW	9	38,606,412 (GRCm38)	start gained	probably benign
R8039:Olfr914	UTSW	9	38,607,389 (GRCm38)	missense	probably benign
R8489:Olfr914	UTSW	9	38,606,936 (GRCm38)	missense	probably benign	0.07
R8768:Olfr914	UTSW	9	38,607,145 (GRCm38)	missense	probably benign	0.01
R9373:Olfr914	UTSW	9	38,606,846 (GRCm38)	missense	possibly damaging	0.91
R9380:Olfr914	UTSW	9	38,607,119 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GCTTAACAGACCAGCCTGACCTTC -3'
(R):5'- GCAATTATGTGGGAACTGCAAGTGC -3'

Sequencing Primer
(F):5'- TACATGGGGTGCATGACTCAG -3'
(R):5'- CTTTGGACCTGCCTGAAGTG -3'

Posted On

2014-05-09