Incidental Mutation 'R9290:Oog2'
ID 704203
Institutional Source Beutler Lab
Gene Symbol Oog2
Ensembl Gene ENSMUSG00000066030
Gene Name oogenesin 2
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9290 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 143917289-143923504 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 143923015 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 427 (F427L)
Ref Sequence ENSEMBL: ENSMUSP00000079267 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080405] [ENSMUST00000143978]
AlphaFold Q7TPX8
Predicted Effect probably benign
Transcript: ENSMUST00000080405
AA Change: F427L

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000079267
Gene: ENSMUSG00000066030
AA Change: F427L

DomainStartEndE-ValueType
SCOP:d1a4ya_ 204 391 2e-7 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000143978
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 99% (67/68)
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abl2 A G 1: 156,457,538 (GRCm39) K268R probably damaging Het
Acvr1 T C 2: 58,338,330 (GRCm39) D464G probably damaging Het
Adra1d G T 2: 131,403,898 (GRCm39) T64K probably benign Het
Cct3 T C 3: 88,216,536 (GRCm39) V164A probably benign Het
Cdhr2 T C 13: 54,882,009 (GRCm39) V1153A possibly damaging Het
Cdkn2c A C 4: 109,518,512 (GRCm39) Y147* probably null Het
Ces1g A T 8: 94,029,545 (GRCm39) H562Q probably benign Het
Cfap221 A G 1: 119,853,381 (GRCm39) L771P probably benign Het
Chsy3 A G 18: 59,542,928 (GRCm39) M689V probably benign Het
Ciita T A 16: 10,326,513 (GRCm39) S235T probably damaging Het
Cracdl T A 1: 37,663,634 (GRCm39) R755W probably damaging Het
Dcdc2a A G 13: 25,386,313 (GRCm39) K396E probably benign Het
Dgki C T 6: 37,276,780 (GRCm39) C35Y unknown Het
Dnah11 C T 12: 117,991,251 (GRCm39) E2372K probably damaging Het
Dnai7 T C 6: 145,148,688 (GRCm39) E57G unknown Het
Eif3a A G 19: 60,765,221 (GRCm39) V322A probably damaging Het
Foxp2 A T 6: 15,197,120 (GRCm39) Q54L possibly damaging Het
Garin2 T A 12: 78,759,028 (GRCm39) V116E possibly damaging Het
Gm19410 T A 8: 36,269,386 (GRCm39) C1074S probably damaging Het
Gtf3c3 T G 1: 54,477,997 (GRCm39) E26A possibly damaging Het
Hps5 T C 7: 46,424,331 (GRCm39) E514G probably damaging Het
Ide A T 19: 37,302,647 (GRCm39) D154E Het
Insm1 T C 2: 146,065,273 (GRCm39) V363A probably benign Het
Iqgap2 A T 13: 95,886,523 (GRCm39) M120K probably damaging Het
Kcnh5 T A 12: 75,023,488 (GRCm39) I527F probably benign Het
Lrtm2 A G 6: 119,297,792 (GRCm39) L83P probably damaging Het
Map1a A G 2: 121,131,014 (GRCm39) E372G probably damaging Het
Mycbp2 A T 14: 103,425,960 (GRCm39) H2421Q probably damaging Het
Myh15 A G 16: 48,997,375 (GRCm39) E1731G probably damaging Het
Myt1 A T 2: 181,437,667 (GRCm39) H168L probably benign Het
Nxph4 A T 10: 127,362,546 (GRCm39) V115E probably damaging Het
Ofcc1 A T 13: 40,433,802 (GRCm39) I101N possibly damaging Het
Or4c115 A G 2: 88,928,076 (GRCm39) L65P probably damaging Het
Or4f14b A T 2: 111,774,967 (GRCm39) I278N possibly damaging Het
Or5w11 A G 2: 87,459,209 (GRCm39) N18S probably benign Het
Or8b48 T C 9: 38,493,334 (GRCm39) S254P probably damaging Het
Or8g27 A G 9: 39,129,531 (GRCm39) R293G probably damaging Het
Otop1 T G 5: 38,455,302 (GRCm39) I232S probably benign Het
Pak6 G A 2: 118,523,883 (GRCm39) R346Q probably damaging Het
Pbk A T 14: 66,054,713 (GRCm39) M282L probably benign Het
Pmpcb T C 5: 21,944,009 (GRCm39) probably null Het
Pou5f2 T A 13: 78,173,585 (GRCm39) W176R probably damaging Het
Prkra G T 2: 76,478,147 (GRCm39) S18R probably benign Het
Prune2 G T 19: 17,145,691 (GRCm39) A2764S probably benign Het
Ptpdc1 A T 13: 48,740,221 (GRCm39) D403E probably benign Het
Pxylp1 T C 9: 96,722,089 (GRCm39) E54G probably damaging Het
Rap1gap G A 4: 137,446,222 (GRCm39) A325T probably damaging Het
Raver2 G A 4: 100,977,387 (GRCm39) probably benign Het
Rbpj T C 5: 53,810,745 (GRCm39) V455A probably damaging Het
Rptor A T 11: 119,702,823 (GRCm39) I397F probably benign Het
Sacs G A 14: 61,421,499 (GRCm39) M148I probably benign Het
Sec16b A G 1: 157,373,816 (GRCm39) Q496R probably damaging Het
Sned1 C A 1: 93,199,385 (GRCm39) C488* probably null Het
Snupn G T 9: 56,882,547 (GRCm39) V187F possibly damaging Het
Sorcs2 T C 5: 36,183,225 (GRCm39) D1016G probably damaging Het
Spta1 T C 1: 174,045,204 (GRCm39) M1517T possibly damaging Het
Them4 G T 3: 94,231,630 (GRCm39) G156C probably damaging Het
Tnik T C 3: 28,675,124 (GRCm39) S721P probably benign Het
Trpm8 T C 1: 88,246,767 (GRCm39) S26P probably damaging Het
Ube2e3 A G 2: 78,750,324 (GRCm39) I183M probably damaging Het
Uhrf2 A G 19: 30,055,416 (GRCm39) Y389C probably damaging Het
Utp4 T A 8: 107,642,828 (GRCm39) D495E possibly damaging Het
Vill C A 9: 118,890,562 (GRCm39) N158K probably benign Het
Vmn1r219 G A 13: 23,347,399 (GRCm39) G196E probably damaging Het
Vmn2r101 C T 17: 19,811,395 (GRCm39) S493L probably benign Het
Vmn2r61 A G 7: 41,915,385 (GRCm39) T111A probably benign Het
Zbtb40 G T 4: 136,745,529 (GRCm39) A168E probably benign Het
Zscan18 A T 7: 12,508,054 (GRCm39) I482N probably damaging Het
Other mutations in Oog2
AlleleSourceChrCoordTypePredicted EffectPPH 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
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
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
Predicted Primers PCR Primer
(F):5'- GGAAACTCACTTCAATGCCCTG -3'
(R):5'- ATTCCCAATAGTACGCTACCATTTC -3'

Sequencing Primer
(F):5'- TGCCCTAAGTCAATGTTACCAG -3'
(R):5'- TTCTCTCTTCCAAAATCAAGCCCAG -3'
Posted On 2022-03-25