Incidental Mutation 'R7541:Ooep'
ID583897
Institutional Source Beutler Lab
Gene Symbol Ooep
Ensembl Gene ENSMUSG00000032346
Gene Nameoocyte expressed protein
SynonymsMoep19, Floped, 2410146L05Rik
MMRRC Submission
Accession Numbers
Is this an essential gene? Not available question?
Stock #R7541 (G1)
Quality Score225.009
Status Validated
Chromosome9
Chromosomal Location78376109-78378725 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 78378065 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Serine at position 90 (T90S)
Ref Sequence ENSEMBL: ENSMUSP00000034900 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034900]
Predicted Effect possibly damaging
Transcript: ENSMUST00000034900
AA Change: T90S

PolyPhen 2 Score 0.931 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000034900
Gene: ENSMUSG00000032346
AA Change: T90S

DomainStartEndE-ValueType
PDB:3V69|B 33 111 8e-6 PDB
low complexity region 130 150 N/A INTRINSIC
Meta Mutation Damage Score 0.1246 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency 96% (51/53)
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele exhibit female infertility associated with a failure of embryos to progress beyond the 2 cell stage. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020D05Rik G A 19: 5,503,411 P114L probably benign Het
4930539E08Rik G A 17: 28,905,324 R335W probably damaging Het
9530053A07Rik T A 7: 28,144,256 C856* probably null Het
Acss2 G A 2: 155,574,690 probably null Het
Adamts10 G A 17: 33,531,616 R210H probably benign Het
Als2 T C 1: 59,167,616 probably null Het
Aplp2 A T 9: 31,152,356 M652K possibly damaging Het
Atrn A G 2: 130,961,571 I560M possibly damaging Het
Bicc1 T C 10: 70,946,604 D602G possibly damaging Het
Cdh4 A G 2: 179,444,810 probably null Het
Clasp1 T A 1: 118,542,997 probably null Het
Col6a6 A G 9: 105,767,324 I1255T probably damaging Het
Comp G T 8: 70,381,350 V672L probably damaging Het
Dbnl T G 11: 5,795,486 D122E probably damaging Het
Dgkz G A 2: 91,942,675 R346C probably damaging Het
Dnhd1 C T 7: 105,678,309 R54C probably damaging Het
Elmo3 T C 8: 105,306,714 I121T probably damaging Het
Fam184b A G 5: 45,542,232 L614P probably damaging Het
Fbxo18 T C 2: 11,749,537 R797G probably benign Het
Gata6 A G 18: 11,059,108 T392A probably damaging Het
Gm17783 T A 16: 45,528,492 T106S possibly damaging Het
Gm21731 A T 13: 120,240,979 M104L probably benign Het
Gm29609 A G 5: 31,154,232 F855S probably benign Het
Gm3424 T C 14: 5,829,330 N88D possibly damaging Het
Gnas T A 2: 174,298,099 S80T unknown Het
Hsd17b14 C A 7: 45,566,146 P190Q probably damaging Het
Iqch C T 9: 63,445,521 V955I possibly damaging Het
Kcnt2 T C 1: 140,376,384 V164A probably benign Het
Krt87 A G 15: 101,438,634 L46P probably damaging Het
Lef1 A G 3: 131,191,099 M237V probably benign Het
Lmbr1l A T 15: 98,909,386 probably null Het
Lrrc49 T C 9: 60,610,403 I408V probably damaging Het
Luc7l3 T C 11: 94,295,965 S365G unknown Het
March2 A T 17: 33,703,058 C109* probably null Het
Metrnl T A 11: 121,715,970 C284S probably damaging Het
Mmachc G A 4: 116,705,885 T91I probably benign Het
Mrps7 T G 11: 115,606,870 M187R probably damaging Het
Ncapd3 A G 9: 27,067,040 E845G probably damaging Het
Olfr1393 T A 11: 49,280,333 F62I probably damaging Het
Olfr272 A T 4: 52,911,376 D139E probably benign Het
Pcdhb18 A T 18: 37,491,609 D664V probably damaging Het
Pigz T C 16: 31,945,131 S336P probably benign Het
Pou2f2 A T 7: 25,116,128 D71E probably benign Het
Reep6 G T 10: 80,335,199 R303L possibly damaging Het
Rmdn2 A T 17: 79,627,868 S137C Het
Rnf220 A T 4: 117,489,930 L95H probably damaging Het
Rsf1 CGGCGGCGG CGGCGGCGGGGGCGGCGG 7: 97,579,911 probably benign Het
Stxbp1 A T 2: 32,818,505 S83T probably damaging Het
Trappc11 T C 8: 47,505,582 probably null Het
Ttn G T 2: 76,791,301 D15598E probably damaging Het
Vav2 T A 2: 27,275,002 R645W probably damaging Het
Vmn1r169 T A 7: 23,577,987 V268D probably benign Het
Zp2 A T 7: 120,136,056 C365S probably damaging Het
Other mutations in Ooep
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03144:Ooep APN 9 78378007 missense possibly damaging 0.87
R7040:Ooep UTSW 9 78378401 missense possibly damaging 0.92
R7313:Ooep UTSW 9 78378151 missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- CAGGGACAATGTAGTTTCCTGG -3'
(R):5'- AGCTCTCTGTACTCTGCTAGGG -3'

Sequencing Primer
(F):5'- CCTGGTGTTTGGAAACTGAAAG -3'
(R):5'- CTAGGGGCAGCAAGTCCATG -3'
Posted On2019-10-17