Incidental Mutation 'IGL01813:Oosp2'
ID 154324
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Oosp2
Ensembl Gene ENSMUSG00000055895
Gene Name oocyte secreted protein 2
Synonyms Plac1l, Tmem122, LOC225922
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # IGL01813
Quality Score
Status
Chromosome 19
Chromosomal Location 11624648-11637923 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 11628847 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 85 (T85A)
Gene Model predicted gene model for transcript(s): [ENSMUST00000121793] [ENSMUST00000135994]
AlphaFold Q4FZG8
Predicted Effect probably benign
Transcript: ENSMUST00000069681
AA Change: T85A

PolyPhen 2 Score 0.140 (Sensitivity: 0.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000065120
Gene: ENSMUSG00000055895
AA Change: T85A

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Pfam:Zona_pellucida 30 165 7.1e-8 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121793
AA Change: T85A

PolyPhen 2 Score 0.082 (Sensitivity: 0.93; Specificity: 0.85)
SMART Domains Protein: ENSMUSP00000113931
Gene: ENSMUSG00000055895
AA Change: T85A

DomainStartEndE-ValueType
signal peptide 1 17 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000135994
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 T A 2: 69,117,936 (GRCm39) probably benign Het
Adgrb2 T C 4: 129,906,359 (GRCm39) V929A probably benign Het
Aldh2 T C 5: 121,710,136 (GRCm39) I400V probably benign Het
Atxn2l T C 7: 126,099,425 (GRCm39) D84G probably damaging Het
Avpr1a T A 10: 122,284,916 (GRCm39) N69K probably damaging Het
BC034090 G A 1: 155,102,085 (GRCm39) Q60* probably null Het
Bltp1 G A 3: 36,982,669 (GRCm39) S778N possibly damaging Het
Bub3 T C 7: 131,170,362 (GRCm39) S295P probably benign Het
Cacna1b T C 2: 24,499,902 (GRCm39) S161G probably damaging Het
Clba1 C T 12: 112,779,179 (GRCm39) T272M probably damaging Het
Col6a4 T A 9: 105,954,452 (GRCm39) S296C probably damaging Het
Cyp4f15 G A 17: 32,905,131 (GRCm39) R38H probably benign Het
Dync2h1 T C 9: 7,122,799 (GRCm39) I2052M probably damaging Het
Gm11627 T C 11: 102,469,634 (GRCm39) probably benign Het
Jmjd8 A T 17: 26,048,212 (GRCm39) probably null Het
Kmt2c A G 5: 25,495,802 (GRCm39) V629A possibly damaging Het
Kremen1 T C 11: 5,149,667 (GRCm39) T335A probably benign Het
Or12d17 A G 17: 37,777,649 (GRCm39) E184G probably damaging Het
Or8s10 A G 15: 98,335,530 (GRCm39) Y60C possibly damaging Het
Pex5l T C 3: 33,136,204 (GRCm39) E5G probably benign Het
Pigk A T 3: 152,448,156 (GRCm39) Q173L probably damaging Het
Pik3c2g T A 6: 139,599,407 (GRCm39) N174K possibly damaging Het
Plb1 C T 5: 32,486,429 (GRCm39) H893Y probably damaging Het
Pus7 T C 5: 23,965,302 (GRCm39) probably benign Het
R3hdm1 G A 1: 128,102,970 (GRCm39) probably null Het
Samd7 C T 3: 30,808,435 (GRCm39) P83S probably benign Het
Supt5 T A 7: 28,023,400 (GRCm39) Y293F probably damaging Het
Tbc1d30 T C 10: 121,102,956 (GRCm39) D692G probably benign Het
Tmpo G A 10: 90,999,104 (GRCm39) R228C probably benign Het
Tnn A T 1: 159,916,008 (GRCm39) H1236Q probably damaging Het
Ubr3 T C 2: 69,781,914 (GRCm39) I667T probably benign Het
Vmn1r183 T A 7: 23,754,985 (GRCm39) F263I probably benign Het
Other mutations in Oosp2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01323:Oosp2 APN 19 11,624,825 (GRCm39) missense probably damaging 1.00
IGL01818:Oosp2 APN 19 11,627,053 (GRCm39) missense probably benign 0.02
IGL02484:Oosp2 APN 19 11,628,847 (GRCm39) missense probably benign 0.14
IGL03358:Oosp2 APN 19 11,628,933 (GRCm39) nonsense probably null
R0938:Oosp2 UTSW 19 11,628,904 (GRCm39) nonsense probably null
R1867:Oosp2 UTSW 19 11,626,959 (GRCm39) critical splice donor site probably null
R1944:Oosp2 UTSW 19 11,626,959 (GRCm39) critical splice donor site probably null
R1945:Oosp2 UTSW 19 11,626,959 (GRCm39) critical splice donor site probably null
R2149:Oosp2 UTSW 19 11,626,978 (GRCm39) nonsense probably null
R4604:Oosp2 UTSW 19 11,627,047 (GRCm39) missense probably benign 0.01
R4684:Oosp2 UTSW 19 11,627,017 (GRCm39) missense probably damaging 0.98
R5034:Oosp2 UTSW 19 11,628,899 (GRCm39) missense probably damaging 0.99
R6034:Oosp2 UTSW 19 11,628,879 (GRCm39) missense probably damaging 1.00
R6034:Oosp2 UTSW 19 11,628,879 (GRCm39) missense probably damaging 1.00
R9695:Oosp2 UTSW 19 11,628,994 (GRCm39) missense
Posted On 2014-02-04