Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03284:Oog2'

415672

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Oog2

Ensembl Gene

ENSMUSG00000066030

Gene Name

oogenesin 2

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL03284

Quality Score

Status

Chromosome

Chromosomal Location

143917289-143923504 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to G at 143923177 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000115150 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080405] [ENSMUST00000143978]

AlphaFold

Q7TPX8

Predicted Effect

probably benign
Transcript: ENSMUST00000080405

SMART Domains

Protein: ENSMUSP00000079267
Gene: ENSMUSG00000066030

Domain	Start	End	E-Value	Type
SCOP:d1a4ya_	204	391	2e-7	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129781

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000141847

Predicted Effect

probably benign
Transcript: ENSMUST00000143978

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 19 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam5	A	T	8: 25,276,354 (GRCm39)		probably benign	Het
Atxn7l3b	T	C	10: 112,764,431 (GRCm39)	D66G	probably benign	Het
Dmac2	T	C	7: 25,321,851 (GRCm39)		probably null	Het
Ephb2	A	G	4: 136,388,827 (GRCm39)	M590T	probably damaging	Het
Fbxo41	C	T	6: 85,456,747 (GRCm39)	R474H	probably damaging	Het
Fcgbp	G	T	7: 27,784,857 (GRCm39)	A306S	possibly damaging	Het
Hapstr1	A	G	16: 8,673,786 (GRCm39)	I238V	possibly damaging	Het
Hmg20a	A	G	9: 56,388,901 (GRCm39)	D156G	probably benign	Het
Mast4	A	G	13: 102,887,905 (GRCm39)	V1168A	probably damaging	Het
Pate12	T	A	9: 36,344,759 (GRCm39)	C96S	probably damaging	Het
Pkhd1l1	T	A	15: 44,410,914 (GRCm39)		probably benign	Het
Psmd6	A	T	14: 14,112,546 (GRCm38)	N351K	probably benign	Het
Ralgps1	T	C	2: 33,036,577 (GRCm39)		probably benign	Het
Rbl1	C	T	2: 157,035,989 (GRCm39)		probably benign	Het
Smarcc1	G	A	9: 110,004,142 (GRCm39)	V399I	probably benign	Het
Srek1	C	A	13: 103,897,045 (GRCm39)	V99F	probably damaging	Het
Styxl1	A	G	5: 135,785,949 (GRCm39)	V32A	possibly damaging	Het
Tnn	C	T	1: 159,953,022 (GRCm39)	V673I	probably benign	Het
Vmn2r107	T	A	17: 20,577,173 (GRCm39)	D390E	probably benign	Het

Other mutations in Oog2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00843:Oog2	APN	4	143,921,742 (GRCm39)	missense	probably damaging	1.00
IGL01317:Oog2	APN	4	143,921,837 (GRCm39)	missense	probably benign	0.16
IGL01697:Oog2	APN	4	143,921,754 (GRCm39)	missense	possibly damaging	0.90
IGL02237:Oog2	APN	4	143,923,016 (GRCm39)	missense	possibly damaging	0.95
IGL02411:Oog2	APN	4	143,921,618 (GRCm39)	missense	probably damaging	0.99
IGL02476:Oog2	APN	4	143,921,799 (GRCm39)	missense	probably benign	0.02
IGL03394:Oog2	APN	4	143,920,576 (GRCm39)	missense	probably benign	0.17
R0538:Oog2	UTSW	4	143,922,654 (GRCm39)	nonsense	probably null
R0892:Oog2	UTSW	4	143,923,069 (GRCm39)	missense	probably benign	0.00
R1024:Oog2	UTSW	4	143,922,856 (GRCm39)	missense	probably damaging	1.00
R4156:Oog2	UTSW	4	143,920,523 (GRCm39)	intron	probably benign
R4157:Oog2	UTSW	4	143,920,523 (GRCm39)	intron	probably benign
R4166:Oog2	UTSW	4	143,921,411 (GRCm39)	missense	probably damaging	1.00
R4167:Oog2	UTSW	4	143,922,782 (GRCm39)	missense	probably benign	0.18
R4732:Oog2	UTSW	4	143,920,511 (GRCm39)	intron	probably benign
R4734:Oog2	UTSW	4	143,923,021 (GRCm39)	missense	probably benign	0.00
R4741:Oog2	UTSW	4	143,921,715 (GRCm39)	missense	possibly damaging	0.94
R4909:Oog2	UTSW	4	143,921,669 (GRCm39)	missense	possibly damaging	0.78
R4954:Oog2	UTSW	4	143,917,302 (GRCm39)	start gained	probably benign
R6437:Oog2	UTSW	4	143,921,678 (GRCm39)	splice site	probably null
R6487:Oog2	UTSW	4	143,923,055 (GRCm39)	missense	possibly damaging	0.48
R6946:Oog2	UTSW	4	143,923,034 (GRCm39)	missense	possibly damaging	0.95
R7000:Oog2	UTSW	4	143,921,897 (GRCm39)	missense	probably damaging	1.00
R7167:Oog2	UTSW	4	143,921,745 (GRCm39)	missense	probably benign	0.04
R7303:Oog2	UTSW	4	143,921,912 (GRCm39)	missense	probably benign	0.04
R7399:Oog2	UTSW	4	143,921,851 (GRCm39)	missense	probably benign	0.01
R8004:Oog2	UTSW	4	143,920,821 (GRCm39)	missense	probably benign	0.00
R8141:Oog2	UTSW	4	143,920,777 (GRCm39)	missense	probably damaging	0.97
R8411:Oog2	UTSW	4	143,920,743 (GRCm39)	missense	probably damaging	1.00
R8932:Oog2	UTSW	4	143,920,685 (GRCm39)	missense	probably benign	0.00
R9290:Oog2	UTSW	4	143,923,015 (GRCm39)	missense	probably benign	0.02
R9348:Oog2	UTSW	4	143,921,789 (GRCm39)	missense	probably damaging	1.00
R9614:Oog2	UTSW	4	143,922,707 (GRCm39)	missense	probably damaging	1.00
RF009:Oog2	UTSW	4	143,921,855 (GRCm39)	missense	probably benign	0.36
Z1177:Oog2	UTSW	4	143,920,585 (GRCm39)	missense	probably damaging	0.99

Posted On

2016-08-02