Incidental Mutation 'IGL02036:Dpep3'
ID 184526
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dpep3
Ensembl Gene ENSMUSG00000031898
Gene Name dipeptidase 3
Synonyms MBD-3, 1700018F16Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.082) question?
Stock # IGL02036
Quality Score
Status
Chromosome 8
Chromosomal Location 106700152-106706051 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 106700417 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Proline at position 430 (T430P)
Ref Sequence ENSEMBL: ENSMUSP00000034371 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034371]
AlphaFold Q9DA79
Predicted Effect probably benign
Transcript: ENSMUST00000034371
AA Change: T430P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000034371
Gene: ENSMUSG00000031898
AA Change: T430P

DomainStartEndE-ValueType
signal peptide 1 40 N/A INTRINSIC
Pfam:Peptidase_M19 83 404 1.2e-110 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212917
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a membrane-bound glycoprotein from the family of dipeptidases involved in hydrolytic metabolism of various dipeptides, including penem and carbapenem beta-lactam antibiotics. This gene is located on chromosome 16 in a cluster with another member of this family. Alternatively spliced transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cep290 T A 10: 100,393,962 (GRCm39) C2056* probably null Het
Cyp2c38 T A 19: 39,448,760 (GRCm39) D143V probably null Het
Ddx10 T C 9: 53,115,483 (GRCm39) K617R probably benign Het
Dgat2l6 T A X: 99,589,199 (GRCm39) I336N probably damaging Het
Dop1a A G 9: 86,413,818 (GRCm39) I1906M probably benign Het
Dph1 T C 11: 75,074,991 (GRCm39) probably null Het
Epha7 T C 4: 28,950,509 (GRCm39) S775P probably damaging Het
F5 A G 1: 164,010,571 (GRCm39) probably benign Het
Fcgbpl1 G A 7: 27,836,950 (GRCm39) V290M possibly damaging Het
Hdx T A X: 110,569,564 (GRCm39) T342S probably benign Het
Inpp4a T C 1: 37,416,650 (GRCm39) probably benign Het
Itgad A G 7: 127,788,993 (GRCm39) T515A possibly damaging Het
Kcnc2 T A 10: 112,291,831 (GRCm39) S340T possibly damaging Het
Krba1 C T 6: 48,392,576 (GRCm39) T830I possibly damaging Het
Lrch1 G A 14: 75,032,733 (GRCm39) probably benign Het
Mag C T 7: 30,607,877 (GRCm39) V295M probably damaging Het
Mmp16 T A 4: 18,093,371 (GRCm39) D375E probably benign Het
Or2h2 A G 17: 37,396,559 (GRCm39) F166S probably damaging Het
Or2t44 T C 11: 58,677,923 (GRCm39) Y288H probably damaging Het
Or4c111 A G 2: 88,843,823 (GRCm39) V195A probably benign Het
Pcyox1l T C 18: 61,840,607 (GRCm39) probably benign Het
Secisbp2l A G 2: 125,600,127 (GRCm39) S403P probably benign Het
Sh3tc2 T A 18: 62,147,978 (GRCm39) H1229Q probably benign Het
Svep1 A C 4: 58,088,245 (GRCm39) W1735G possibly damaging Het
Tbxas1 T A 6: 38,998,091 (GRCm39) C220S probably benign Het
Vmn1r173 G T 7: 23,402,321 (GRCm39) M185I probably benign Het
Ywhag A G 5: 135,940,348 (GRCm39) V82A probably benign Het
Other mutations in Dpep3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00158:Dpep3 APN 8 106,705,779 (GRCm39) missense probably benign 0.22
IGL01078:Dpep3 APN 8 106,704,860 (GRCm39) missense probably damaging 1.00
IGL01543:Dpep3 APN 8 106,702,814 (GRCm39) missense probably damaging 1.00
IGL01996:Dpep3 APN 8 106,701,358 (GRCm39) missense probably damaging 1.00
R0422:Dpep3 UTSW 8 106,702,750 (GRCm39) critical splice donor site probably null
R0627:Dpep3 UTSW 8 106,705,363 (GRCm39) missense possibly damaging 0.56
R0747:Dpep3 UTSW 8 106,704,018 (GRCm39) missense probably benign 0.12
R1116:Dpep3 UTSW 8 106,705,461 (GRCm39) missense probably damaging 0.98
R1711:Dpep3 UTSW 8 106,700,325 (GRCm39) missense probably benign 0.01
R2085:Dpep3 UTSW 8 106,701,346 (GRCm39) missense probably damaging 1.00
R4385:Dpep3 UTSW 8 106,704,818 (GRCm39) missense probably damaging 1.00
R4860:Dpep3 UTSW 8 106,702,821 (GRCm39) missense probably benign 0.34
R4860:Dpep3 UTSW 8 106,702,821 (GRCm39) missense probably benign 0.34
R5784:Dpep3 UTSW 8 106,705,375 (GRCm39) missense probably benign 0.03
R6658:Dpep3 UTSW 8 106,705,728 (GRCm39) missense probably benign
R6893:Dpep3 UTSW 8 106,700,474 (GRCm39) missense probably benign
R7536:Dpep3 UTSW 8 106,704,032 (GRCm39) missense probably damaging 1.00
R9213:Dpep3 UTSW 8 106,700,245 (GRCm39) missense probably benign 0.15
R9528:Dpep3 UTSW 8 106,704,251 (GRCm39) missense probably benign 0.01
R9766:Dpep3 UTSW 8 106,705,369 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07