Mutagenetix > Incidental Mutation

Incidental Mutation 'R6159:Or9i1b'

489784

Institutional Source

Beutler Lab

Gene Symbol

Or9i1b

Ensembl Gene

ENSMUSG00000062314

Gene Name

olfactory receptor family 9 subfamily I member 1B

Synonyms

Olfr1505, MOR211-10_i, MOR211-4P, GA_x6K02T2RE5P-4250267-4251217

MMRRC Submission

044306-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.139) question?

Stock #

R6159 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

13896386-13897336 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 13897104 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Isoleucine at position 240 (T240I)

Ref Sequence

ENSEMBL: ENSMUSP00000148945 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081520] [ENSMUST00000216623] [ENSMUST00000216835]

AlphaFold

Q7TQQ2

Predicted Effect

probably damaging
Transcript: ENSMUST00000081520
AA Change: T240I

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

SMART Domains

Protein: ENSMUSP00000080235
Gene: ENSMUSG00000062314
AA Change: T240I

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	8.2e-43	PFAM
Pfam:7tm_1	41	290	2.2e-17	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000216623
AA Change: T240I

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

Predicted Effect

probably damaging
Transcript: ENSMUST00000216835
AA Change: T240I

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

Meta Mutation Damage Score

0.5997

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 98.0%
20x: 94.2%

Validation Efficiency

96% (54/56)

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: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahcyl2	A	C	6: 29,908,457 (GRCm39)	N609T	possibly damaging	Het
Ankzf1	G	A	1: 75,170,888 (GRCm39)	C98Y	probably damaging	Het
Atg101	T	A	15: 101,188,519 (GRCm39)	M208K	possibly damaging	Het
Baiap2l2	A	G	15: 79,143,930 (GRCm39)	I388T	probably benign	Het
Cabs1	C	T	5: 88,127,613 (GRCm39)	T88I	possibly damaging	Het
Chrnd	T	A	1: 87,118,812 (GRCm39)	D56E	probably benign	Het
Col28a1	A	T	6: 8,162,247 (GRCm39)		probably null	Het
Col4a1	G	T	8: 11,270,007 (GRCm39)	P899Q	probably damaging	Het
Cts3	C	A	13: 61,714,655 (GRCm39)	A217S	probably damaging	Het
Dab2	A	G	15: 6,465,941 (GRCm39)	N495S	possibly damaging	Het
Dnah2	T	A	11: 69,349,368 (GRCm39)	I2423F	probably damaging	Het
Dnah2	C	T	11: 69,349,746 (GRCm39)	R2399Q	probably benign	Het
Dock6	T	C	9: 21,733,041 (GRCm39)	H1053R	probably benign	Het
Eif1ad14	G	A	12: 87,886,521 (GRCm39)	A36V	probably damaging	Het
Fam184a	G	A	10: 53,574,869 (GRCm39)	L191F	probably damaging	Het
Fbxl9	T	C	8: 106,049,925 (GRCm39)	Y33C	probably damaging	Het
Fip1l1	C	T	5: 74,752,608 (GRCm39)	R472W	probably damaging	Het
Gbp2	T	C	3: 142,338,018 (GRCm39)	F378S	probably damaging	Het
Ggt1	A	T	10: 75,420,799 (GRCm39)	E388V	probably damaging	Het
Gm14496	A	G	2: 181,638,050 (GRCm39)	T375A	probably benign	Het
Gm43302	A	G	5: 105,436,894 (GRCm39)	S71P	probably benign	Het
Gnrhr	G	T	5: 86,330,216 (GRCm39)	T268K	probably damaging	Het
Htt	T	C	5: 34,962,020 (GRCm39)	V335A	probably benign	Het
Klhl20	A	T	1: 160,933,037 (GRCm39)	L257H	probably damaging	Het
Med27	C	A	2: 29,414,376 (GRCm39)		probably null	Het
Muc5ac	T	A	7: 141,369,323 (GRCm39)	C2433S	possibly damaging	Het
Nasp	A	G	4: 116,461,086 (GRCm39)		probably null	Het
Nipal2	A	C	15: 34,600,172 (GRCm39)	V215G	probably damaging	Het
Or10al5	A	T	17: 38,063,038 (GRCm39)	I98F	probably damaging	Het
Oxct2b	G	A	4: 123,011,244 (GRCm39)	R388H	probably damaging	Het
Pbrm1	A	G	14: 30,774,240 (GRCm39)	I469V	possibly damaging	Het
Phyhip	A	G	14: 70,704,294 (GRCm39)	H171R	possibly damaging	Het
Pigs	C	T	11: 78,219,326 (GRCm39)	T9M	probably benign	Het
Plek	T	C	11: 16,935,539 (GRCm39)	D256G	probably damaging	Het
Prss50	T	C	9: 110,693,371 (GRCm39)	V369A	probably benign	Het
Psmc5	A	G	11: 106,152,088 (GRCm39)	K82E	possibly damaging	Het
Qrsl1	A	T	10: 43,758,189 (GRCm39)	F301L	probably benign	Het
Rasal1	T	C	5: 120,797,673 (GRCm39)	L135P	probably damaging	Het
Rbm47	A	G	5: 66,184,159 (GRCm39)	V148A	probably damaging	Het
Scyl1	T	A	19: 5,814,785 (GRCm39)	D381V	probably benign	Het
Selplg	G	T	5: 113,957,162 (GRCm39)	D381E	probably benign	Het
Sh3rf2	C	A	18: 42,289,200 (GRCm39)	Q674K	probably damaging	Het
Sned1	A	G	1: 93,210,659 (GRCm39)	T987A	probably benign	Het
Sntb1	A	G	15: 55,539,698 (GRCm39)		probably null	Het
Synj2	A	T	17: 6,036,327 (GRCm39)	I14F	probably damaging	Het
Taf2	A	T	15: 54,926,440 (GRCm39)	M170K	possibly damaging	Het
Tg	A	G	15: 66,607,096 (GRCm39)	E211G	possibly damaging	Het
Thnsl1	G	T	2: 21,217,016 (GRCm39)	E257*	probably null	Het
Tlr4	A	G	4: 66,758,070 (GRCm39)	R288G	possibly damaging	Het
Trbc1	T	C	6: 41,515,385 (GRCm39)		probably benign	Het
Trim37	G	A	11: 87,107,374 (GRCm39)		probably null	Het
Txnrd3	T	C	6: 89,640,176 (GRCm39)		probably null	Het
Tyk2	C	A	9: 21,021,800 (GRCm39)	Q875H	probably damaging	Het
Vmn2r55	A	G	7: 12,385,698 (GRCm39)	Y761H	probably damaging	Het
Zswim5	T	C	4: 116,836,876 (GRCm39)	L720P	probably damaging	Het

Other mutations in Or9i1b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01814:Or9i1b	APN	19	13,896,892 (GRCm39)	nonsense	probably null
IGL03388:Or9i1b	APN	19	13,896,984 (GRCm39)	missense	probably damaging	0.99
R0143:Or9i1b	UTSW	19	13,896,614 (GRCm39)	missense	probably damaging	1.00
R0326:Or9i1b	UTSW	19	13,896,873 (GRCm39)	missense	probably benign	0.13
R0602:Or9i1b	UTSW	19	13,897,145 (GRCm39)	missense	probably benign	0.13
R0624:Or9i1b	UTSW	19	13,896,808 (GRCm39)	missense	probably damaging	0.99
R0947:Or9i1b	UTSW	19	13,896,535 (GRCm39)	missense	probably benign	0.00
R1472:Or9i1b	UTSW	19	13,897,208 (GRCm39)	missense	probably damaging	1.00
R1691:Or9i1b	UTSW	19	13,896,783 (GRCm39)	missense	probably benign	0.00
R2991:Or9i1b	UTSW	19	13,896,675 (GRCm39)	missense	probably damaging	1.00
R4296:Or9i1b	UTSW	19	13,896,717 (GRCm39)	missense	probably damaging	1.00
R4688:Or9i1b	UTSW	19	13,896,605 (GRCm39)	missense	probably benign	0.01
R4814:Or9i1b	UTSW	19	13,896,817 (GRCm39)	missense	possibly damaging	0.50
R4823:Or9i1b	UTSW	19	13,897,022 (GRCm39)	missense	probably benign	0.02
R5038:Or9i1b	UTSW	19	13,896,822 (GRCm39)	missense	possibly damaging	0.58
R5243:Or9i1b	UTSW	19	13,897,025 (GRCm39)	missense	probably damaging	1.00
R5323:Or9i1b	UTSW	19	13,896,980 (GRCm39)	missense	possibly damaging	0.95
R5542:Or9i1b	UTSW	19	13,896,411 (GRCm39)	missense	probably benign	0.04
R5918:Or9i1b	UTSW	19	13,897,139 (GRCm39)	missense	probably damaging	1.00
R6011:Or9i1b	UTSW	19	13,896,521 (GRCm39)	missense	probably benign	0.00
R7535:Or9i1b	UTSW	19	13,896,449 (GRCm39)	missense	probably benign
R8262:Or9i1b	UTSW	19	13,897,226 (GRCm39)	missense	probably benign	0.02
R9190:Or9i1b	UTSW	19	13,896,967 (GRCm39)	missense	probably benign	0.23
R9459:Or9i1b	UTSW	19	13,896,674 (GRCm39)	missense	possibly damaging	0.76

Predicted Primers

PCR Primer
(F):5'- TTCTGCGTACCACATGCACC -3'
(R):5'- AATGCAGCCTTGACATCCTTG -3'

Sequencing Primer
(F):5'- CTCTCTCCTTCTGTGAAAATAATCAG -3'
(R):5'- CCTTGTTTCTTAGGCTGTAGACAAG -3'

Posted On

2017-10-10