Incidental Mutation 'IGL00843:Oog2'
ID 12863
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 # IGL00843
Quality Score
Status
Chromosome 4
Chromosomal Location 143917289-143923504 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 143921742 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 217 (L217F)
Ref Sequence ENSEMBL: ENSMUSP00000079267 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080405] [ENSMUST00000143978]
AlphaFold Q7TPX8
Predicted Effect probably damaging
Transcript: ENSMUST00000080405
AA Change: L217F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000079267
Gene: ENSMUSG00000066030
AA Change: L217F

DomainStartEndE-ValueType
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: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Bglap A G 3: 88,291,657 (GRCm39) probably null Het
Bpnt2 T C 4: 4,776,308 (GRCm39) probably benign Het
Clcn2 T C 16: 20,522,391 (GRCm39) T772A probably benign Het
Cldn18 A T 9: 99,580,874 (GRCm39) F125I probably benign Het
Ehhadh A G 16: 21,581,379 (GRCm39) S538P possibly damaging Het
Ets2 T G 16: 95,510,837 (GRCm39) F32V probably benign Het
F5 G A 1: 164,039,360 (GRCm39) R1990Q probably benign Het
Fetub A G 16: 22,748,379 (GRCm39) probably benign Het
Hecw1 C T 13: 14,422,158 (GRCm39) E983K probably benign Het
Hemgn A G 4: 46,396,240 (GRCm39) M332T probably benign Het
Hmcn1 A G 1: 150,486,464 (GRCm39) I4314T possibly damaging Het
Lonrf2 C A 1: 38,851,616 (GRCm39) probably benign Het
Lrrc9 T C 12: 72,510,191 (GRCm39) I430T possibly damaging Het
Lrrk2 T C 15: 91,641,261 (GRCm39) V1606A possibly damaging Het
Plxnc1 T C 10: 94,683,411 (GRCm39) H791R probably benign Het
Prdm2 G A 4: 142,860,884 (GRCm39) S802L probably damaging Het
Prss32 T A 17: 24,076,336 (GRCm39) L233Q probably damaging Het
Rapgef6 T A 11: 54,582,099 (GRCm39) V1337E probably benign Het
Slc15a3 T A 19: 10,830,627 (GRCm39) M326K probably null Het
Slc25a54 A T 3: 109,020,176 (GRCm39) T397S possibly damaging Het
Slfn3 C T 11: 83,104,257 (GRCm39) T376M probably damaging Het
Stradb T A 1: 59,033,568 (GRCm39) D410E probably benign Het
Tdh T C 14: 63,733,213 (GRCm39) T178A probably damaging Het
Tspan12 T A 6: 21,851,081 (GRCm39) probably benign Het
Ube2b A T 11: 51,886,202 (GRCm39) D50E probably benign Het
Zranb1 A C 7: 132,551,622 (GRCm39) H117P probably benign Het
Other mutations in Oog2
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
IGL03284:Oog2 APN 4 143,923,177 (GRCm39) unclassified probably benign
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 2012-12-06