Incidental Mutation 'IGL00778:Clpb'
| ID |
277931 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Clpb
|
| Ensembl Gene |
ENSMUSG00000001829 |
| Gene Name |
ClpB caseinolytic peptidase B |
| Synonyms |
Skd3 |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.912)
|
| Stock # |
IGL00778
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
101312958-101444667 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
C to T
at 101427815 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 387
(R387*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000148062
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000001884]
[ENSMUST00000106998]
[ENSMUST00000209579]
|
| AlphaFold |
Q60649 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000001884
AA Change: R387*
|
| SMART Domains |
Protein: ENSMUSP00000001884
Gene: ENSMUSG00000001829
AA Change: R387*
| Domain | Start | End | E-Value | Type |
|---|
|
ANK
|
133 |
162 |
2.03e-1 |
SMART |
|
ANK
|
166 |
195 |
1.96e-3 |
SMART |
|
ANK
|
235 |
264 |
6.65e-6 |
SMART |
|
low complexity region
|
294 |
306 |
N/A |
INTRINSIC |
|
AAA
|
343 |
497 |
6.36e-10 |
SMART |
|
ClpB_D2-small
|
541 |
630 |
6.83e-4 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000106998
AA Change: R417*
|
| SMART Domains |
Protein: ENSMUSP00000102611
Gene: ENSMUSG00000001829
AA Change: R417*
| Domain | Start | End | E-Value | Type |
|---|
|
ANK
|
133 |
162 |
2.03e-1 |
SMART |
|
ANK
|
166 |
195 |
1.96e-3 |
SMART |
|
ANK
|
265 |
294 |
6.65e-6 |
SMART |
|
low complexity region
|
324 |
336 |
N/A |
INTRINSIC |
|
AAA
|
373 |
527 |
6.36e-10 |
SMART |
|
ClpB_D2-small
|
571 |
660 |
6.83e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150355
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000150832
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000209579
AA Change: R387*
|
| 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 belongs to the ATP-ases associated with diverse cellular activities (AAA+) superfamily. Members of this superfamily form ring-shaped homo-hexamers and have highly conserved ATPase domains that are involved in various processes including DNA replication, protein degradation and reactivation of misfolded proteins. All members of this family hydrolyze ATP through their AAA+ domains and use the energy generated through ATP hydrolysis to exert mechanical force on their substrates. In addition to an AAA+ domain, the protein encoded by this gene contains a C-terminal D2 domain, which is characteristic of the AAA+ subfamily of Caseinolytic peptidases to which this protein belongs. It cooperates with Hsp70 in the disaggregation of protein aggregates. Allelic variants of this gene are associated with 3-methylglutaconic aciduria, which causes cataracts and neutropenia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 26 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930503E14Rik |
G |
A |
14: 44,401,391 (GRCm39) |
H152Y |
probably benign |
Het |
| Abca1 |
T |
C |
4: 53,086,132 (GRCm39) |
D457G |
probably benign |
Het |
| Atp8a1 |
T |
G |
5: 67,817,246 (GRCm39) |
K913N |
possibly damaging |
Het |
| Cd180 |
G |
A |
13: 102,841,917 (GRCm39) |
S321N |
probably benign |
Het |
| Cdc14b |
T |
C |
13: 64,363,470 (GRCm39) |
N264D |
probably damaging |
Het |
| Cenpf |
A |
T |
1: 189,387,109 (GRCm39) |
C1724S |
probably benign |
Het |
| Chil4 |
A |
G |
3: 106,109,113 (GRCm39) |
S397P |
probably benign |
Het |
| Csgalnact2 |
A |
T |
6: 118,103,233 (GRCm39) |
M1K |
probably null |
Het |
| Enpp3 |
C |
A |
10: 24,674,160 (GRCm39) |
C380F |
probably damaging |
Het |
| Gtf3c1 |
G |
A |
7: 125,266,546 (GRCm39) |
R967W |
probably damaging |
Het |
| Hnrnpr |
T |
A |
4: 136,066,856 (GRCm39) |
D472E |
unknown |
Het |
| Klhl28 |
A |
T |
12: 64,996,840 (GRCm39) |
D500E |
probably damaging |
Het |
| Lmo7 |
C |
T |
14: 102,148,321 (GRCm39) |
|
probably benign |
Het |
| Mphosph8 |
A |
G |
14: 56,911,900 (GRCm39) |
I308V |
probably benign |
Het |
| Myo6 |
T |
A |
9: 80,190,868 (GRCm39) |
|
probably null |
Het |
| Nsmaf |
C |
T |
4: 6,435,056 (GRCm39) |
|
probably null |
Het |
| Padi6 |
T |
A |
4: 140,454,934 (GRCm39) |
I668L |
possibly damaging |
Het |
| Pigw |
A |
G |
11: 84,768,150 (GRCm39) |
I393T |
possibly damaging |
Het |
| Prg3 |
G |
A |
2: 84,824,076 (GRCm39) |
C212Y |
probably damaging |
Het |
| Pwp1 |
T |
C |
10: 85,715,752 (GRCm39) |
V267A |
probably benign |
Het |
| Raver2 |
C |
A |
4: 100,953,468 (GRCm39) |
Q79K |
probably benign |
Het |
| Sdr9c7 |
T |
C |
10: 127,745,697 (GRCm39) |
S270P |
probably damaging |
Het |
| Sfmbt2 |
A |
G |
2: 10,406,818 (GRCm39) |
E39G |
probably damaging |
Het |
| Strada |
A |
G |
11: 106,061,976 (GRCm39) |
|
probably benign |
Het |
| Xrn1 |
T |
C |
9: 95,855,500 (GRCm39) |
|
probably benign |
Het |
| Zic3 |
A |
G |
X: 57,079,779 (GRCm39) |
Y424C |
probably damaging |
Het |
|
| Other mutations in Clpb |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00418:Clpb
|
APN |
7 |
101,436,952 (GRCm39) |
missense |
probably benign |
|
|
IGL00780:Clpb
|
APN |
7 |
101,427,815 (GRCm39) |
nonsense |
probably null |
|
|
IGL00951:Clpb
|
APN |
7 |
101,400,467 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01374:Clpb
|
APN |
7 |
101,422,335 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01542:Clpb
|
APN |
7 |
101,436,712 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02203:Clpb
|
APN |
7 |
101,428,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02989:Clpb
|
APN |
7 |
101,428,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03088:Clpb
|
APN |
7 |
101,434,656 (GRCm39) |
nonsense |
probably null |
|
|
Surfeit
|
UTSW |
7 |
101,360,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT1430001:Clpb
|
UTSW |
7 |
101,435,926 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
PIT4486001:Clpb
|
UTSW |
7 |
101,313,139 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0611:Clpb
|
UTSW |
7 |
101,436,956 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R1565:Clpb
|
UTSW |
7 |
101,434,668 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1760:Clpb
|
UTSW |
7 |
101,435,905 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1879:Clpb
|
UTSW |
7 |
101,355,690 (GRCm39) |
missense |
probably benign |
0.23 |
|
R1933:Clpb
|
UTSW |
7 |
101,428,418 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1938:Clpb
|
UTSW |
7 |
101,412,863 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2922:Clpb
|
UTSW |
7 |
101,372,035 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2923:Clpb
|
UTSW |
7 |
101,372,035 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2995:Clpb
|
UTSW |
7 |
101,428,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4492:Clpb
|
UTSW |
7 |
101,436,929 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5384:Clpb
|
UTSW |
7 |
101,428,548 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5973:Clpb
|
UTSW |
7 |
101,313,204 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6787:Clpb
|
UTSW |
7 |
101,312,866 (GRCm39) |
unclassified |
probably benign |
|
|
R7158:Clpb
|
UTSW |
7 |
101,313,039 (GRCm39) |
missense |
probably benign |
0.45 |
|
R7225:Clpb
|
UTSW |
7 |
101,360,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7239:Clpb
|
UTSW |
7 |
101,360,662 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7482:Clpb
|
UTSW |
7 |
101,435,926 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7499:Clpb
|
UTSW |
7 |
101,371,935 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R7547:Clpb
|
UTSW |
7 |
101,313,503 (GRCm39) |
splice site |
probably null |
|
|
R7769:Clpb
|
UTSW |
7 |
101,371,924 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8279:Clpb
|
UTSW |
7 |
101,355,695 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R9376:Clpb
|
UTSW |
7 |
101,360,625 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9501:Clpb
|
UTSW |
7 |
101,427,780 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9623:Clpb
|
UTSW |
7 |
101,313,399 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R9631:Clpb
|
UTSW |
7 |
101,434,605 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
| Posted On |
2015-04-16 |
Incidental Mutation