Incidental Mutation 'IGL00329:Pate12'
ID 6181
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Pate12
Ensembl Gene ENSMUSG00000023093
Gene Name prostate and testis expressed 12
Synonyms Gm7257
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # IGL00329
Quality Score
Status
Chromosome 9
Chromosomal Location 36343180-36346234 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) G to A at 36344198 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000048154 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041537]
AlphaFold D3YX25
Predicted Effect probably benign
Transcript: ENSMUST00000041537
SMART Domains Protein: ENSMUSP00000048154
Gene: ENSMUSG00000023093

DomainStartEndE-ValueType
signal peptide 1 21 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad9 A G 3: 36,123,911 (GRCm39) N72S probably benign Het
Aopep T A 13: 63,338,977 (GRCm39) I623N probably damaging Het
Apba3 C T 10: 81,108,901 (GRCm39) P555S probably damaging Het
Arcn1 C A 9: 44,670,333 (GRCm39) E98* probably null Het
Cimip2b G A 4: 43,428,158 (GRCm39) R100W possibly damaging Het
Col28a1 G T 6: 8,175,425 (GRCm39) T141K probably damaging Het
Dna2 T C 10: 62,802,222 (GRCm39) F811S probably damaging Het
Dusp19 T A 2: 80,461,269 (GRCm39) I186K probably damaging Het
Dync2li1 A G 17: 84,952,154 (GRCm39) D195G possibly damaging Het
Epm2aip1 T C 9: 111,101,855 (GRCm39) V276A possibly damaging Het
Extl3 T C 14: 65,313,070 (GRCm39) E704G probably benign Het
Gle1 T C 2: 29,829,301 (GRCm39) probably benign Het
Gm2178 C A 14: 26,235,767 (GRCm39) probably benign Het
Gm4553 T C 7: 141,718,964 (GRCm39) S155G unknown Het
Herc2 T A 7: 55,774,047 (GRCm39) L1166Q probably damaging Het
Hsd11b2 A G 8: 106,249,759 (GRCm39) E290G probably benign Het
Inpp5d T C 1: 87,595,725 (GRCm39) V157A probably benign Het
Krt72 T A 15: 101,693,434 (GRCm39) Q160L probably damaging Het
Lrrd1 A G 5: 3,900,081 (GRCm39) K129E possibly damaging Het
Mapk13 A G 17: 28,995,379 (GRCm39) Y200C probably damaging Het
Mme G A 3: 63,287,749 (GRCm39) W750* probably null Het
Nat8l C T 5: 34,155,761 (GRCm39) P139L probably damaging Het
Nrtn C A 17: 57,058,569 (GRCm39) R144L probably benign Het
Or52h9 C A 7: 104,202,299 (GRCm39) P58T probably benign Het
Pdgfa T A 5: 138,974,216 (GRCm39) probably benign Het
Rtp3 A G 9: 110,815,666 (GRCm39) V233A probably benign Het
Syne2 A G 12: 76,078,474 (GRCm39) probably benign Het
Trappc10 A T 10: 78,039,711 (GRCm39) probably benign Het
Usp24 A G 4: 106,216,288 (GRCm39) T380A probably benign Het
Vmn1r21 A T 6: 57,821,049 (GRCm39) S132T probably benign Het
Other mutations in Pate12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01799:Pate12 APN 9 36,344,179 (GRCm39) missense possibly damaging 0.59
IGL03018:Pate12 APN 9 36,344,723 (GRCm39) missense possibly damaging 0.89
IGL03178:Pate12 APN 9 36,344,132 (GRCm39) missense probably benign
IGL03284:Pate12 APN 9 36,344,759 (GRCm39) missense probably damaging 1.00
R1157:Pate12 UTSW 9 36,344,143 (GRCm39) missense probably benign 0.01
R2032:Pate12 UTSW 9 36,344,195 (GRCm39) critical splice donor site probably null
R4879:Pate12 UTSW 9 36,344,089 (GRCm39) missense probably damaging 1.00
R4954:Pate12 UTSW 9 36,344,156 (GRCm39) missense probably benign 0.28
R5019:Pate12 UTSW 9 36,343,198 (GRCm39) missense probably benign 0.05
Posted On 2012-04-20