Incidental Mutation 'IGL01544:Mmp24'
| ID |
90260 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mmp24
|
| Ensembl Gene |
ENSMUSG00000027612 |
| Gene Name |
matrix metallopeptidase 24 |
| Synonyms |
Membrane type 5-MMP, MT5-MMP |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.147)
|
| Stock # |
IGL01544
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
155617262-155660286 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 155641807 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Arginine
at position 212
(G212R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000029141
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029141]
|
| AlphaFold |
Q9R0S2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000029141
AA Change: G212R
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000029141
Gene: ENSMUSG00000027612
AA Change: G212R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
42 |
N/A |
INTRINSIC |
|
Pfam:PG_binding_1
|
52 |
107 |
6.9e-14 |
PFAM |
|
ZnMc
|
132 |
301 |
1.78e-60 |
SMART |
|
low complexity region
|
323 |
346 |
N/A |
INTRINSIC |
|
HX
|
357 |
400 |
7.4e-9 |
SMART |
|
HX
|
402 |
446 |
7.01e-10 |
SMART |
|
HX
|
449 |
495 |
6.49e-14 |
SMART |
|
HX
|
497 |
542 |
6.64e-11 |
SMART |
|
Pfam:DUF3377
|
548 |
618 |
1.9e-30 |
PFAM |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the matrix metalloproteinase family of extracellular matrix-degrading enzymes that are involved in tissue remodeling, wound repair, progression of atherosclerosis and tumor invasion. The encoded preproprotein undergoes proteolytic processing to generate a mature, zinc-dependent endopeptidase enzyme. Mice lacking the encoded protein do not develop neuropathic pain with mechanical allodynia after sciatic nerve injury, display enhanced sensitivity to noxious thermal stimuli under basal conditions, and develop hyperalgesia during inflammation. [provided by RefSeq, Feb 2016]
PHENOTYPE: Mice homozygous for disruptions in this gene fail to develop neuropathic pain after peripheral nerve injury. They also experience reduced stress and enhanced mechanical coordination. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Arap3 |
G |
A |
18: 38,123,889 (GRCm39) |
R377C |
probably damaging |
Het |
| Bbx |
C |
A |
16: 50,095,140 (GRCm39) |
E59* |
probably null |
Het |
| Cep120 |
C |
T |
18: 53,819,033 (GRCm39) |
R886H |
probably benign |
Het |
| Cep350 |
C |
A |
1: 155,828,933 (GRCm39) |
V324L |
probably damaging |
Het |
| Cry1 |
T |
A |
10: 84,982,360 (GRCm39) |
K329* |
probably null |
Het |
| Dhtkd1 |
T |
C |
2: 5,918,342 (GRCm39) |
N627S |
probably benign |
Het |
| Dpp8 |
A |
T |
9: 64,962,270 (GRCm39) |
T437S |
probably benign |
Het |
| Elovl1 |
G |
A |
4: 118,288,107 (GRCm39) |
|
probably null |
Het |
| Heca |
A |
G |
10: 17,791,715 (GRCm39) |
Y114H |
probably damaging |
Het |
| Hrh4 |
A |
G |
18: 13,148,950 (GRCm39) |
N104S |
probably benign |
Het |
| Ift80 |
T |
A |
3: 68,898,115 (GRCm39) |
K73N |
probably benign |
Het |
| Ina |
T |
C |
19: 47,003,948 (GRCm39) |
V252A |
possibly damaging |
Het |
| Klhl36 |
A |
G |
8: 120,596,755 (GRCm39) |
E152G |
possibly damaging |
Het |
| Lamp5 |
T |
A |
2: 135,910,990 (GRCm39) |
L241Q |
probably damaging |
Het |
| Lrp4 |
G |
A |
2: 91,307,896 (GRCm39) |
R447H |
probably damaging |
Het |
| Mpp3 |
A |
G |
11: 101,909,485 (GRCm39) |
V191A |
possibly damaging |
Het |
| Mtmr4 |
A |
G |
11: 87,488,437 (GRCm39) |
|
probably benign |
Het |
| Mynn |
C |
A |
3: 30,661,854 (GRCm39) |
S312* |
probably null |
Het |
| Neb |
T |
A |
2: 52,182,917 (GRCm39) |
I1010F |
possibly damaging |
Het |
| Nes |
T |
C |
3: 87,885,271 (GRCm39) |
S1177P |
possibly damaging |
Het |
| Noct |
T |
C |
3: 51,155,469 (GRCm39) |
V79A |
probably damaging |
Het |
| Rad1 |
A |
G |
15: 10,490,465 (GRCm39) |
D114G |
probably damaging |
Het |
| Slc26a9 |
T |
C |
1: 131,687,233 (GRCm39) |
|
probably null |
Het |
| Sqor |
G |
A |
2: 122,634,266 (GRCm39) |
|
probably benign |
Het |
| Sspo |
G |
T |
6: 48,467,953 (GRCm39) |
W4309L |
probably damaging |
Het |
| Thoc7 |
A |
C |
14: 13,953,435 (GRCm38) |
Y72D |
probably damaging |
Het |
| Thra |
A |
G |
11: 98,647,754 (GRCm39) |
I43V |
possibly damaging |
Het |
| Timm44 |
G |
T |
8: 4,325,888 (GRCm39) |
|
probably benign |
Het |
| Trmo |
C |
T |
4: 46,386,169 (GRCm39) |
G119R |
probably damaging |
Het |
| Trpc4 |
T |
C |
3: 54,209,567 (GRCm39) |
M644T |
probably damaging |
Het |
| Wdr72 |
C |
T |
9: 74,056,007 (GRCm39) |
L300F |
probably damaging |
Het |
| Wrn |
T |
C |
8: 33,814,554 (GRCm39) |
T54A |
probably benign |
Het |
|
| Other mutations in Mmp24 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02089:Mmp24
|
APN |
2 |
155,654,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02452:Mmp24
|
APN |
2 |
155,657,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0600:Mmp24
|
UTSW |
2 |
155,634,517 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1381:Mmp24
|
UTSW |
2 |
155,656,047 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R4497:Mmp24
|
UTSW |
2 |
155,655,908 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R4498:Mmp24
|
UTSW |
2 |
155,655,908 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R4727:Mmp24
|
UTSW |
2 |
155,657,819 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R4985:Mmp24
|
UTSW |
2 |
155,656,016 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5020:Mmp24
|
UTSW |
2 |
155,652,204 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5501:Mmp24
|
UTSW |
2 |
155,640,056 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5686:Mmp24
|
UTSW |
2 |
155,641,697 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5709:Mmp24
|
UTSW |
2 |
155,634,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5773:Mmp24
|
UTSW |
2 |
155,641,829 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6452:Mmp24
|
UTSW |
2 |
155,657,673 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R6657:Mmp24
|
UTSW |
2 |
155,640,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7015:Mmp24
|
UTSW |
2 |
155,634,544 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7699:Mmp24
|
UTSW |
2 |
155,640,096 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8076:Mmp24
|
UTSW |
2 |
155,649,481 (GRCm39) |
nonsense |
probably null |
|
|
R8111:Mmp24
|
UTSW |
2 |
155,649,345 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R8139:Mmp24
|
UTSW |
2 |
155,655,965 (GRCm39) |
nonsense |
probably null |
|
|
R8304:Mmp24
|
UTSW |
2 |
155,641,759 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R8344:Mmp24
|
UTSW |
2 |
155,652,223 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8411:Mmp24
|
UTSW |
2 |
155,655,935 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8527:Mmp24
|
UTSW |
2 |
155,641,634 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8542:Mmp24
|
UTSW |
2 |
155,641,634 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9198:Mmp24
|
UTSW |
2 |
155,640,041 (GRCm39) |
missense |
probably benign |
0.19 |
|
R9500:Mmp24
|
UTSW |
2 |
155,654,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Mmp24
|
UTSW |
2 |
155,652,312 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Posted On |
2013-12-03 |
Incidental Mutation