Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01996:Or10j7'

182897

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Or10j7

Ensembl Gene

ENSMUSG00000058981

Gene Name

olfactory receptor family 10 subfamily J member 7

Synonyms

GA_x6K02T2R7CC-664297-665229, MOR267-5, Olfr1406

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

IGL01996

Quality Score

Status

Chromosome

Chromosomal Location

173011009-173012071 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 173011294 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 236 (T236A)

Ref Sequence

ENSEMBL: ENSMUSP00000151023 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000072395] [ENSMUST00000201132] [ENSMUST00000215878]

AlphaFold

E9Q8X1

Predicted Effect

probably benign
Transcript: ENSMUST00000072395
AA Change: T236A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000072231
Gene: ENSMUSG00000058981
AA Change: T236A

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	307	3.9e-55	PFAM
Pfam:7tm_1	41	289	2.7e-17	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000201132
AA Change: T236A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000144530
Gene: ENSMUSG00000058981
AA Change: T236A

Domain	Start	End	E-Value	Type
Pfam:7tm_4	31	88	5.4e-11	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000215878
AA Change: T236A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

Coding Region Coverage

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: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3110009E18Rik	T	C	1: 120,078,430 (GRCm39)	V29A	possibly damaging	Het
Adarb1	A	G	10: 77,158,051 (GRCm39)	L132P	probably damaging	Het
Afg3l1	T	G	8: 124,228,633 (GRCm39)	M733R	probably damaging	Het
Aox1	C	T	1: 58,121,225 (GRCm39)	R899C	probably benign	Het
Arhgap44	T	A	11: 64,896,322 (GRCm39)		probably benign	Het
Asns	T	C	6: 7,682,378 (GRCm39)	D189G	possibly damaging	Het
Brap	A	G	5: 121,816,910 (GRCm39)		probably benign	Het
Ccdc138	T	A	10: 58,397,852 (GRCm39)	L564H	probably damaging	Het
Ccdc167	A	G	17: 29,924,461 (GRCm39)		probably null	Het
Ccdc178	A	G	18: 22,230,813 (GRCm39)	Y353H	probably damaging	Het
Clca3b	A	T	3: 144,554,924 (GRCm39)	S41R	probably benign	Het
Dpep3	T	C	8: 106,701,358 (GRCm39)	N397S	probably damaging	Het
Eif1	T	C	11: 100,211,826 (GRCm39)	I83T	probably benign	Het
Enah	A	T	1: 181,784,070 (GRCm39)	W80R	unknown	Het
F2rl1	C	T	13: 95,650,432 (GRCm39)	C150Y	probably damaging	Het
Fbxw24	T	C	9: 109,434,440 (GRCm39)	R387G	possibly damaging	Het
Fsd1l	A	G	4: 53,647,760 (GRCm39)	T68A	probably benign	Het
Greb1	T	C	12: 16,740,846 (GRCm39)	K1412R	possibly damaging	Het
Grin2b	T	C	6: 135,709,584 (GRCm39)	S1321G	probably damaging	Het
H4c11	G	A	13: 21,919,308 (GRCm39)	G15S	unknown	Het
Itgb7	C	T	15: 102,126,412 (GRCm39)	G508D	probably damaging	Het
Kcnq3	A	G	15: 65,895,545 (GRCm39)	I333T	probably damaging	Het
Knl1	A	G	2: 118,934,542 (GRCm39)	D2115G	probably damaging	Het
Lmtk3	G	A	7: 45,442,871 (GRCm39)		probably null	Het
Lrpprc	A	G	17: 85,080,698 (GRCm39)	Y176H	probably benign	Het
Mier1	T	C	4: 102,984,473 (GRCm39)	S22P	possibly damaging	Het
Mme	A	T	3: 63,250,970 (GRCm39)	N337I	probably benign	Het
Mthfd1	A	G	12: 76,350,679 (GRCm39)	Y687C	probably damaging	Het
Nrp2	T	C	1: 62,788,419 (GRCm39)	M373T	probably damaging	Het
Nudcd1	A	T	15: 44,269,357 (GRCm39)	F101Y	probably benign	Het
Nup133	T	A	8: 124,673,334 (GRCm39)	I66L	probably benign	Het
Or11j4	T	G	14: 50,631,116 (GRCm39)	M301R	probably damaging	Het
Or1e19	T	A	11: 73,316,794 (GRCm39)	N5I	probably damaging	Het
Osbpl5	A	G	7: 143,261,081 (GRCm39)		probably null	Het
Paqr8	T	C	1: 21,005,628 (GRCm39)	F261L	probably damaging	Het
Plxna2	A	G	1: 194,482,084 (GRCm39)	E1452G	probably damaging	Het
Polh	T	C	17: 46,483,927 (GRCm39)	D446G	probably benign	Het
Psg19	A	T	7: 18,523,986 (GRCm39)	M353K	possibly damaging	Het
Sap25	T	C	5: 137,640,080 (GRCm39)		probably null	Het
Sap30l	C	T	11: 57,700,777 (GRCm39)	R144*	probably null	Het
Sema6b	C	T	17: 56,438,157 (GRCm39)	V144M	probably damaging	Het
Sfmbt2	T	C	2: 10,444,837 (GRCm39)	Y228H	probably benign	Het
Shank2	A	G	7: 143,965,230 (GRCm39)	D946G	probably damaging	Het
Slc11a1	T	A	1: 74,415,965 (GRCm39)	L52Q	possibly damaging	Het
Sptlc3	T	C	2: 139,423,424 (GRCm39)		probably benign	Het
Tgfb1i1	T	C	7: 127,848,464 (GRCm39)		probably benign	Het
Tifa	T	C	3: 127,590,229 (GRCm39)		probably benign	Het
Tomm40l	C	T	1: 171,047,224 (GRCm39)	V265M	possibly damaging	Het
Trim45	C	A	3: 100,835,425 (GRCm39)	Y469*	probably null	Het
Ttc21a	G	T	9: 119,787,182 (GRCm39)	A730S	probably damaging	Het
Vmn1r18	A	T	6: 57,367,001 (GRCm39)	D184E	possibly damaging	Het
Vmn2r120	A	T	17: 57,832,222 (GRCm39)	I189N	possibly damaging	Het

Other mutations in Or10j7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00946:Or10j7	APN	1	173,011,190 (GRCm39)	missense	probably benign	0.45
IGL01609:Or10j7	APN	1	173,011,843 (GRCm39)	missense	probably benign	0.00
F5770:Or10j7	UTSW	1	173,011,531 (GRCm39)	missense	probably benign	0.05
PIT4378001:Or10j7	UTSW	1	173,011,381 (GRCm39)	missense	probably benign	0.00
R0053:Or10j7	UTSW	1	173,011,845 (GRCm39)	missense	probably benign	0.35
R0800:Or10j7	UTSW	1	173,011,627 (GRCm39)	missense	probably damaging	1.00
R1793:Or10j7	UTSW	1	173,011,976 (GRCm39)	missense	probably benign
R2230:Or10j7	UTSW	1	173,011,182 (GRCm39)	missense	probably benign	0.04
R2232:Or10j7	UTSW	1	173,011,182 (GRCm39)	missense	probably benign	0.04
R5395:Or10j7	UTSW	1	173,011,247 (GRCm39)	nonsense	probably null
R5455:Or10j7	UTSW	1	173,011,818 (GRCm39)	missense	probably damaging	1.00
R5457:Or10j7	UTSW	1	173,011,180 (GRCm39)	missense	probably damaging	1.00
R5558:Or10j7	UTSW	1	173,011,585 (GRCm39)	missense	probably benign	0.01
R5760:Or10j7	UTSW	1	173,011,318 (GRCm39)	missense	probably benign	0.05
R6285:Or10j7	UTSW	1	173,011,477 (GRCm39)	missense	probably damaging	1.00
R7159:Or10j7	UTSW	1	173,011,890 (GRCm39)	missense	possibly damaging	0.95
R7676:Or10j7	UTSW	1	173,011,120 (GRCm39)	nonsense	probably null
R8700:Or10j7	UTSW	1	173,011,429 (GRCm39)	missense	probably benign
R8829:Or10j7	UTSW	1	173,011,458 (GRCm39)	missense	probably benign	0.06
R9721:Or10j7	UTSW	1	173,011,915 (GRCm39)	missense	probably benign	0.07
R9785:Or10j7	UTSW	1	173,011,458 (GRCm39)	missense	probably benign	0.06
R9788:Or10j7	UTSW	1	173,011,458 (GRCm39)	missense	probably benign	0.06
R9789:Or10j7	UTSW	1	173,011,458 (GRCm39)	missense	probably benign	0.06
V7580:Or10j7	UTSW	1	173,011,531 (GRCm39)	missense	probably benign	0.05
V7581:Or10j7	UTSW	1	173,011,531 (GRCm39)	missense	probably benign	0.05
V7582:Or10j7	UTSW	1	173,011,531 (GRCm39)	missense	probably benign	0.05

Posted On

2014-05-07