Incidental Mutation 'IGL02698:Pate10'
ID 304045
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Pate10
Ensembl Gene ENSMUSG00000091174
Gene Name prostate and testis expressed 10
Synonyms Gm17677
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # IGL02698
Quality Score
Status
Chromosome 9
Chromosomal Location 35652345-35653548 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 35652416 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132657 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166746]
AlphaFold B3GLJ5
Predicted Effect probably benign
Transcript: ENSMUST00000166746
SMART Domains Protein: ENSMUSP00000132657
Gene: ENSMUSG00000091174

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arpp21 T A 9: 112,014,812 (GRCm39) probably benign Het
Car8 A T 4: 8,185,598 (GRCm39) I186N probably benign Het
Ccdc174 G A 6: 91,867,834 (GRCm39) S183N probably benign Het
Ccdc66 T A 14: 27,212,749 (GRCm39) K525* probably null Het
Cebpz A G 17: 79,243,003 (GRCm39) V217A probably benign Het
Cfap36 C A 11: 29,197,014 (GRCm39) probably null Het
Cpne4 T C 9: 104,909,984 (GRCm39) V527A probably damaging Het
Crh T G 3: 19,748,354 (GRCm39) D96A possibly damaging Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Dcp1a A T 14: 30,227,499 (GRCm39) probably benign Het
Ddhd1 A T 14: 45,842,663 (GRCm39) probably benign Het
Dis3l2 C T 1: 86,976,551 (GRCm39) probably benign Het
Dop1a T C 9: 86,406,412 (GRCm39) probably benign Het
Etv3 A G 3: 87,443,885 (GRCm39) T490A possibly damaging Het
Fastkd2 A G 1: 63,787,158 (GRCm39) T531A probably benign Het
Fat1 C T 8: 45,476,201 (GRCm39) A1749V probably benign Het
Fgfr1 T A 8: 26,063,624 (GRCm39) L761* probably null Het
Gcc2 A G 10: 58,107,112 (GRCm39) K683E possibly damaging Het
Gm5117 C T 8: 32,229,767 (GRCm39) noncoding transcript Het
Hif1a T C 12: 73,977,545 (GRCm39) probably null Het
Inha A G 1: 75,486,527 (GRCm39) E274G probably damaging Het
Itih2 G T 2: 10,135,312 (GRCm39) P26H probably damaging Het
Kif23 G A 9: 61,832,283 (GRCm39) T620I possibly damaging Het
Klhl30 T C 1: 91,281,429 (GRCm39) F10S probably damaging Het
Kmt2b T C 7: 30,278,118 (GRCm39) probably benign Het
Lmf2 A C 15: 89,238,357 (GRCm39) L174R probably damaging Het
Med13l T C 5: 118,900,894 (GRCm39) L2216P probably damaging Het
Mmp1b T A 9: 7,384,877 (GRCm39) L257F probably damaging Het
Net1 A G 13: 3,937,569 (GRCm39) probably null Het
Nfasc A G 1: 132,562,475 (GRCm39) V100A probably benign Het
Nr4a2 A G 2: 56,998,172 (GRCm39) F535S probably damaging Het
Ntn4 G T 10: 93,480,521 (GRCm39) A45S probably benign Het
Or2y1c T A 11: 49,361,690 (GRCm39) F237L probably benign Het
Or4a27 T A 2: 88,559,815 (GRCm39) I43F probably damaging Het
Or52a20 T C 7: 103,366,485 (GRCm39) V228A probably damaging Het
Or5w17 T A 2: 87,584,188 (GRCm39) K50* probably null Het
Or8c9 A G 9: 38,241,506 (GRCm39) T208A probably benign Het
Pappa A T 4: 65,099,257 (GRCm39) E592V probably damaging Het
Pi4ka A T 16: 17,109,032 (GRCm39) I1630N probably damaging Het
Ptprb A G 10: 116,199,185 (GRCm39) D1997G probably benign Het
Rc3h2 A T 2: 37,295,312 (GRCm39) S235T probably damaging Het
S1pr1 T A 3: 115,505,746 (GRCm39) K283* probably null Het
Scn5a T A 9: 119,350,163 (GRCm39) T904S probably damaging Het
Sema6d T C 2: 124,495,643 (GRCm39) L30P possibly damaging Het
Slc26a7 A C 4: 14,593,867 (GRCm39) S83A possibly damaging Het
Slco1a6 C A 6: 142,048,737 (GRCm39) G348* probably null Het
Srgap3 C T 6: 112,723,889 (GRCm39) V524I probably damaging Het
Stxbp3-ps A T 19: 9,535,688 (GRCm39) noncoding transcript Het
Sv2b C T 7: 74,790,726 (GRCm39) probably null Het
Sympk T C 7: 18,779,559 (GRCm39) I663T probably benign Het
Ttn C A 2: 76,775,115 (GRCm39) V1976L probably damaging Het
Uqcrc1 T C 9: 108,777,011 (GRCm39) probably null Het
Vmn2r111 T C 17: 22,790,226 (GRCm39) Y260C probably damaging Het
Other mutations in Pate10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02593:Pate10 APN 9 35,653,438 (GRCm39) missense possibly damaging 0.92
IGL02612:Pate10 APN 9 35,653,460 (GRCm39) missense possibly damaging 0.92
IGL02648:Pate10 APN 9 35,652,405 (GRCm39) missense probably benign 0.14
R4240:Pate10 UTSW 9 35,653,449 (GRCm39) nonsense probably null
R4983:Pate10 UTSW 9 35,653,465 (GRCm39) missense probably benign 0.12
R5161:Pate10 UTSW 9 35,652,884 (GRCm39) nonsense probably null
R5545:Pate10 UTSW 9 35,652,940 (GRCm39) missense probably benign 0.10
R5980:Pate10 UTSW 9 35,652,911 (GRCm39) missense probably damaging 0.99
R6131:Pate10 UTSW 9 35,652,840 (GRCm39) nonsense probably null
R6147:Pate10 UTSW 9 35,653,528 (GRCm39) missense possibly damaging 0.66
R6147:Pate10 UTSW 9 35,653,406 (GRCm39) missense possibly damaging 0.94
R8850:Pate10 UTSW 9 35,652,391 (GRCm39) missense probably damaging 1.00
X0066:Pate10 UTSW 9 35,653,466 (GRCm39) missense possibly damaging 0.90
Posted On 2015-04-16