Incidental Mutation 'IGL02648:Pate10'
ID 302012
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: 0.067) question?
Stock # IGL02648
Quality Score
Status
Chromosome 9
Chromosomal Location 35652345-35653548 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 35652405 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 21 (M21L)
Ref Sequence ENSEMBL: ENSMUSP00000132657 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166746]
AlphaFold B3GLJ5
Predicted Effect probably benign
Transcript: ENSMUST00000166746
AA Change: M21L

PolyPhen 2 Score 0.135 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000132657
Gene: ENSMUSG00000091174
AA Change: M21L

DomainStartEndE-ValueType
signal peptide 1 22 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4 A T 4: 144,344,392 (GRCm39) probably null Het
Acp4 A G 7: 43,904,414 (GRCm39) probably benign Het
Adgrv1 A T 13: 81,659,738 (GRCm39) M1997K probably benign Het
Arhgdib T C 6: 136,910,647 (GRCm39) D38G probably damaging Het
Bbox1 T G 2: 110,135,871 (GRCm39) D36A probably damaging Het
Cacna1c T C 6: 118,734,457 (GRCm39) K104R probably damaging Het
Cacna1i G A 15: 80,182,839 (GRCm39) C75Y probably damaging Het
Ccdc14 T C 16: 34,517,528 (GRCm39) L70S probably damaging Het
Ccdc88a T G 11: 29,451,051 (GRCm39) V1580G probably benign Het
Cdadc1 C A 14: 59,823,812 (GRCm39) D227Y probably damaging Het
Chd3 T C 11: 69,242,976 (GRCm39) Y1415C probably damaging Het
Cngb3 A G 4: 19,428,489 (GRCm39) N493S probably benign Het
Dock10 T A 1: 80,551,840 (GRCm39) Y665F probably damaging Het
Gm10549 C A 18: 33,597,303 (GRCm39) probably benign Het
Greb1 C T 12: 16,758,683 (GRCm39) V678M probably damaging Het
Gucy2c G A 6: 136,706,211 (GRCm39) R497* probably null Het
Itgad T C 7: 127,782,546 (GRCm39) probably benign Het
Lgr4 C A 2: 109,842,718 (GRCm39) T877K probably damaging Het
Lrig3 A G 10: 125,802,463 (GRCm39) D40G probably benign Het
Myo3b T C 2: 69,935,716 (GRCm39) probably benign Het
Neb A G 2: 52,161,093 (GRCm39) Y2193H possibly damaging Het
Or4b1 T A 2: 89,979,697 (GRCm39) I218F possibly damaging Het
Or8b3b T C 9: 38,584,312 (GRCm39) M143V probably benign Het
Pard6b A G 2: 167,940,847 (GRCm39) Q278R probably benign Het
Pkd2l1 T C 19: 44,143,975 (GRCm39) Y366C possibly damaging Het
Prl2c1 A G 13: 28,041,542 (GRCm39) D188G probably benign Het
Prl3a1 G T 13: 27,454,218 (GRCm39) M65I probably benign Het
Psg26 T A 7: 18,216,691 (GRCm39) E49D probably benign Het
Rapgef3 G A 15: 97,656,273 (GRCm39) R38W probably damaging Het
Rrn3 T C 16: 13,629,453 (GRCm39) F590L probably benign Het
Serpina12 T C 12: 104,004,267 (GRCm39) K122E probably benign Het
Slc39a6 T C 18: 24,715,424 (GRCm39) I699V probably damaging Het
Tmem259 G A 10: 79,813,651 (GRCm39) P443S probably damaging Het
Vmn1r75 T A 7: 11,615,091 (GRCm39) F274L probably benign 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
IGL02698:Pate10 APN 9 35,652,416 (GRCm39) splice site probably benign
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