Incidental Mutation 'IGL03191:Pate8'
ID 412650
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Pate8
Ensembl Gene ENSMUSG00000091248
Gene Name prostate and testis expressed 8
Synonyms Gm17689
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL03191
Quality Score
Status
Chromosome 9
Chromosomal Location 36492574-36493931 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 36492698 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 69 (D69G)
Ref Sequence ENSEMBL: ENSMUSP00000126891 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000170030]
AlphaFold B3GLJ4
Predicted Effect probably benign
Transcript: ENSMUST00000170030
AA Change: D69G

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 A G 1: 58,398,228 (GRCm39) D1323G probably null Het
Asxl2 A G 12: 3,550,094 (GRCm39) D612G probably damaging Het
Cacna1c A T 6: 118,718,864 (GRCm39) F395L probably damaging Het
Cct8 A G 16: 87,283,198 (GRCm39) S380P probably damaging Het
Cltb T C 13: 54,746,883 (GRCm39) E31G probably damaging Het
Cobl T C 11: 12,203,364 (GRCm39) M1031V probably benign Het
Colgalt1 C A 8: 72,075,731 (GRCm39) probably null Het
Dcstamp A G 15: 39,617,620 (GRCm39) I10V probably benign Het
Diaph3 T C 14: 87,310,738 (GRCm39) I138V possibly damaging Het
Dnah8 T C 17: 30,945,804 (GRCm39) V1827A probably damaging Het
Dpf1 T A 7: 29,015,986 (GRCm39) probably benign Het
Dscam A T 16: 96,621,969 (GRCm39) L494Q probably benign Het
Eif2ak4 C T 2: 118,252,693 (GRCm39) H422Y probably damaging Het
Galnt10 T C 11: 57,662,326 (GRCm39) V324A probably damaging Het
Hcfc1 T C X: 72,999,220 (GRCm39) I309V probably benign Het
Il24 T C 1: 130,812,584 (GRCm39) T96A probably benign Het
Itga2 T C 13: 114,973,020 (GRCm39) probably benign Het
Lrrc32 A G 7: 98,147,454 (GRCm39) H78R possibly damaging Het
Lrrk1 T C 7: 65,909,707 (GRCm39) E2001G probably damaging Het
Lztr1 T A 16: 17,336,392 (GRCm39) M199K probably damaging Het
Mcm8 A G 2: 132,663,362 (GRCm39) Y160C possibly damaging Het
Msh4 G A 3: 153,575,245 (GRCm39) T710M probably damaging Het
Pilrb1 A T 5: 137,853,227 (GRCm39) L192Q probably damaging Het
Pim1 T A 17: 29,712,693 (GRCm39) probably benign Het
Slc12a1 A T 2: 125,048,009 (GRCm39) Q817L possibly damaging Het
Trip11 T C 12: 101,865,184 (GRCm39) D163G probably damaging Het
Tsc2 A T 17: 24,847,028 (GRCm39) V179E probably damaging Het
Zfp641 C T 15: 98,186,568 (GRCm39) V352M probably damaging Het
Other mutations in Pate8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01455:Pate8 APN 9 36,492,659 (GRCm39) missense probably benign 0.00
IGL01693:Pate8 APN 9 36,492,662 (GRCm39) missense probably benign 0.31
IGL02268:Pate8 APN 9 36,493,166 (GRCm39) missense possibly damaging 0.71
PIT4354001:Pate8 UTSW 9 36,492,597 (GRCm39) missense possibly damaging 0.71
R0401:Pate8 UTSW 9 36,493,924 (GRCm39) missense unknown
R0743:Pate8 UTSW 9 36,492,597 (GRCm39) missense probably benign 0.03
R1483:Pate8 UTSW 9 36,492,620 (GRCm39) missense probably benign 0.00
R1701:Pate8 UTSW 9 36,493,114 (GRCm39) critical splice donor site probably benign
R2258:Pate8 UTSW 9 36,493,161 (GRCm39) missense probably benign 0.03
R3764:Pate8 UTSW 9 36,493,114 (GRCm39) critical splice donor site probably null
R5143:Pate8 UTSW 9 36,493,200 (GRCm39) missense probably benign 0.31
R6783:Pate8 UTSW 9 36,492,631 (GRCm39) splice site probably null
R7013:Pate8 UTSW 9 36,493,854 (GRCm39) missense unknown
R7014:Pate8 UTSW 9 36,493,854 (GRCm39) missense unknown
Posted On 2016-08-02