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)
|
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
Domain | Start | End | E-Value | Type |
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
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
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 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH 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 |