Incidental Mutation 'R1147:Oog3'
ID |
102479 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Oog3
|
Ensembl Gene |
ENSMUSG00000050810 |
Gene Name |
oogenesin 3 |
Synonyms |
|
MMRRC Submission |
039220-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.071)
|
Stock # |
R1147 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
143884126-143889221 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 143884982 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Serine
at position 318
(F318S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000059834
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000050933]
|
AlphaFold |
Q3UWY1 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000050933
AA Change: F318S
PolyPhen 2
Score 0.807 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000059834 Gene: ENSMUSG00000050810 AA Change: F318S
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
26 |
N/A |
INTRINSIC |
low complexity region
|
31 |
42 |
N/A |
INTRINSIC |
SCOP:d1a4ya_
|
226 |
428 |
7e-5 |
SMART |
|
Meta Mutation Damage Score |
0.5008 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 97.7%
- 10x: 89.5%
- 20x: 66.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam20 |
T |
C |
8: 41,248,655 (GRCm39) |
I255T |
possibly damaging |
Het |
Aknad1 |
T |
A |
3: 108,659,857 (GRCm39) |
N290K |
possibly damaging |
Het |
Ano8 |
C |
A |
8: 71,934,661 (GRCm39) |
V447F |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Ash1l |
A |
T |
3: 88,892,194 (GRCm39) |
M1358L |
possibly damaging |
Het |
Ccdc110 |
A |
G |
8: 46,397,121 (GRCm39) |
K837E |
possibly damaging |
Het |
Cd19 |
T |
A |
7: 126,010,217 (GRCm39) |
D384V |
possibly damaging |
Het |
Ces1f |
C |
T |
8: 93,984,909 (GRCm39) |
V473I |
possibly damaging |
Het |
Chd6 |
C |
T |
2: 160,832,191 (GRCm39) |
E994K |
probably damaging |
Het |
Col5a2 |
G |
T |
1: 45,415,931 (GRCm39) |
N1405K |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,379,426 (GRCm39) |
D3720G |
probably damaging |
Het |
Dsel |
T |
C |
1: 111,789,939 (GRCm39) |
T199A |
possibly damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Flacc1 |
A |
T |
1: 58,708,622 (GRCm39) |
Y215N |
probably damaging |
Het |
Hrg |
G |
T |
16: 22,779,754 (GRCm39) |
C344F |
probably damaging |
Het |
Htt |
T |
C |
5: 35,008,596 (GRCm39) |
Y1462H |
probably damaging |
Het |
Kcnh2 |
T |
A |
5: 24,529,385 (GRCm39) |
I784F |
probably damaging |
Het |
Kifc3 |
T |
C |
8: 95,864,546 (GRCm39) |
T55A |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Or2a20 |
A |
T |
6: 43,194,146 (GRCm39) |
T100S |
probably damaging |
Het |
Or52w1 |
G |
A |
7: 105,018,484 (GRCm39) |
R308Q |
probably benign |
Het |
Pde5a |
C |
T |
3: 122,587,962 (GRCm39) |
T376M |
probably damaging |
Het |
Pkhd1l1 |
A |
G |
15: 44,400,837 (GRCm39) |
I2204V |
probably null |
Het |
Ppp1r13l |
A |
G |
7: 19,109,772 (GRCm39) |
D731G |
probably damaging |
Het |
Ptk6 |
C |
T |
2: 180,837,590 (GRCm39) |
G443D |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Ptprs |
T |
C |
17: 56,730,504 (GRCm39) |
D749G |
probably damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,749,265 (GRCm39) |
D1212E |
probably damaging |
Het |
Rsad1 |
T |
C |
11: 94,434,966 (GRCm39) |
Y290C |
probably damaging |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Slc6a11 |
T |
A |
6: 114,221,831 (GRCm39) |
I507N |
possibly damaging |
Het |
Sp140l1 |
C |
G |
1: 85,077,226 (GRCm39) |
K113N |
probably benign |
Het |
Sybu |
A |
T |
15: 44,609,651 (GRCm39) |
F78I |
probably damaging |
Het |
Tox |
A |
T |
4: 6,823,055 (GRCm39) |
N87K |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,741,576 (GRCm39) |
G1308R |
probably damaging |
Het |
Trub2 |
A |
G |
2: 29,677,644 (GRCm39) |
|
probably benign |
Het |
Vmn2r114 |
A |
T |
17: 23,530,037 (GRCm39) |
H123Q |
probably benign |
Het |
Vmn2r15 |
T |
A |
5: 109,441,072 (GRCm39) |
Y262F |
probably damaging |
Het |
Vmn2r33 |
C |
T |
7: 7,557,144 (GRCm39) |
E519K |
probably benign |
Het |
Zfp106 |
A |
T |
2: 120,351,017 (GRCm39) |
C1545S |
probably damaging |
Het |
|
Other mutations in Oog3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02413:Oog3
|
APN |
4 |
143,884,721 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02517:Oog3
|
APN |
4 |
143,885,920 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02635:Oog3
|
APN |
4 |
143,884,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Oog3
|
UTSW |
4 |
143,884,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Oog3
|
UTSW |
4 |
143,884,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Oog3
|
UTSW |
4 |
143,886,784 (GRCm39) |
missense |
probably benign |
0.10 |
R0617:Oog3
|
UTSW |
4 |
143,886,784 (GRCm39) |
missense |
probably benign |
0.10 |
R1147:Oog3
|
UTSW |
4 |
143,884,982 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1562:Oog3
|
UTSW |
4 |
143,889,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1669:Oog3
|
UTSW |
4 |
143,885,008 (GRCm39) |
missense |
probably benign |
0.06 |
R1766:Oog3
|
UTSW |
4 |
143,885,692 (GRCm39) |
missense |
possibly damaging |
0.49 |
R2002:Oog3
|
UTSW |
4 |
143,884,675 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2109:Oog3
|
UTSW |
4 |
143,886,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R2394:Oog3
|
UTSW |
4 |
143,885,884 (GRCm39) |
missense |
probably benign |
0.00 |
R4615:Oog3
|
UTSW |
4 |
143,884,899 (GRCm39) |
missense |
probably benign |
0.00 |
R4632:Oog3
|
UTSW |
4 |
143,884,698 (GRCm39) |
missense |
probably benign |
0.00 |
R4816:Oog3
|
UTSW |
4 |
143,885,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R5459:Oog3
|
UTSW |
4 |
143,885,815 (GRCm39) |
missense |
probably benign |
|
R5547:Oog3
|
UTSW |
4 |
143,884,598 (GRCm39) |
missense |
probably benign |
0.27 |
R6811:Oog3
|
UTSW |
4 |
143,886,152 (GRCm39) |
missense |
probably benign |
0.00 |
R6931:Oog3
|
UTSW |
4 |
143,885,923 (GRCm39) |
missense |
probably benign |
0.00 |
R7052:Oog3
|
UTSW |
4 |
143,887,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R7194:Oog3
|
UTSW |
4 |
143,889,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R7312:Oog3
|
UTSW |
4 |
143,886,801 (GRCm39) |
missense |
probably benign |
0.08 |
R7486:Oog3
|
UTSW |
4 |
143,884,742 (GRCm39) |
missense |
probably benign |
0.16 |
R7622:Oog3
|
UTSW |
4 |
143,884,889 (GRCm39) |
missense |
probably benign |
0.00 |
R8782:Oog3
|
UTSW |
4 |
143,885,962 (GRCm39) |
missense |
probably benign |
0.01 |
R8790:Oog3
|
UTSW |
4 |
143,885,710 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8794:Oog3
|
UTSW |
4 |
143,884,556 (GRCm39) |
missense |
probably benign |
0.01 |
R9586:Oog3
|
UTSW |
4 |
143,884,966 (GRCm39) |
nonsense |
probably null |
|
R9652:Oog3
|
UTSW |
4 |
143,884,489 (GRCm39) |
missense |
probably benign |
0.01 |
R9653:Oog3
|
UTSW |
4 |
143,884,489 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Oog3
|
UTSW |
4 |
143,886,206 (GRCm39) |
missense |
probably benign |
0.04 |
Z1088:Oog3
|
UTSW |
4 |
143,884,877 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
|
Posted On |
2014-01-15 |