Incidental Mutation 'R0687:Usp24'
ID |
61192 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Usp24
|
Ensembl Gene |
ENSMUSG00000028514 |
Gene Name |
ubiquitin specific peptidase 24 |
Synonyms |
2810030C21Rik, 2700066K03Rik |
MMRRC Submission |
038872-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0687 (G1)
|
Quality Score |
109 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
106316213-106441322 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 106420504 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Isoleucine
at position 2277
(K2277I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000133095
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094933]
[ENSMUST00000165709]
|
AlphaFold |
B1AY13 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000094933
AA Change: K2276I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000092538 Gene: ENSMUSG00000028514 AA Change: K2276I
Domain | Start | End | E-Value | Type |
Blast:UBA
|
5 |
43 |
2e-16 |
BLAST |
low complexity region
|
57 |
96 |
N/A |
INTRINSIC |
SCOP:d1gw5a_
|
348 |
882 |
6e-7 |
SMART |
low complexity region
|
1031 |
1059 |
N/A |
INTRINSIC |
low complexity region
|
1124 |
1150 |
N/A |
INTRINSIC |
low complexity region
|
1365 |
1378 |
N/A |
INTRINSIC |
Pfam:UCH
|
1685 |
2036 |
3.7e-54 |
PFAM |
Pfam:UCH_1
|
1686 |
1993 |
1.8e-27 |
PFAM |
low complexity region
|
2066 |
2081 |
N/A |
INTRINSIC |
low complexity region
|
2256 |
2267 |
N/A |
INTRINSIC |
low complexity region
|
2576 |
2592 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000165709
AA Change: K2277I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000133095 Gene: ENSMUSG00000028514 AA Change: K2277I
Domain | Start | End | E-Value | Type |
Blast:UBA
|
5 |
43 |
2e-16 |
BLAST |
low complexity region
|
57 |
96 |
N/A |
INTRINSIC |
SCOP:d1gw5a_
|
348 |
883 |
8e-7 |
SMART |
low complexity region
|
1032 |
1060 |
N/A |
INTRINSIC |
low complexity region
|
1125 |
1151 |
N/A |
INTRINSIC |
low complexity region
|
1366 |
1379 |
N/A |
INTRINSIC |
Pfam:UCH
|
1686 |
2037 |
2e-49 |
PFAM |
Pfam:UCH_1
|
1687 |
1994 |
4e-24 |
PFAM |
low complexity region
|
2067 |
2082 |
N/A |
INTRINSIC |
low complexity region
|
2257 |
2268 |
N/A |
INTRINSIC |
low complexity region
|
2577 |
2593 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.7%
- 20x: 95.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Modification of cellular proteins by ubiquitin is an essential regulatory mechanism controlled by the coordinated action of multiple ubiquitin-conjugating and deubiquitinating enzymes. USP24 belongs to a large family of cysteine proteases that function as deubiquitinating enzymes (Quesada et al., 2004 [PubMed 14715245]).[supplied by OMIM, Mar 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 16 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406P16Rik |
T |
G |
7: 34,245,418 |
Q679P |
possibly damaging |
Het |
Anxa10 |
T |
A |
8: 62,092,572 |
D42V |
possibly damaging |
Het |
B3gnt9 |
T |
A |
8: 105,254,783 |
|
probably benign |
Het |
Ccdc150 |
A |
T |
1: 54,285,631 |
|
probably null |
Het |
Fstl5 |
A |
G |
3: 76,707,812 |
I727V |
possibly damaging |
Het |
Nae1 |
C |
A |
8: 104,513,244 |
R484L |
probably damaging |
Het |
Nudt19 |
T |
A |
7: 35,551,472 |
T281S |
probably benign |
Het |
Osgin1 |
T |
A |
8: 119,445,832 |
V455E |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,684,333 |
D655E |
probably damaging |
Het |
Plch1 |
C |
T |
3: 63,716,029 |
V617M |
probably damaging |
Het |
Polk |
A |
T |
13: 96,484,017 |
N579K |
probably damaging |
Het |
Scube2 |
C |
A |
7: 109,829,128 |
V513F |
possibly damaging |
Het |
Skiv2l2 |
T |
C |
13: 112,914,361 |
T227A |
probably damaging |
Het |
Spen |
T |
C |
4: 141,488,028 |
M498V |
unknown |
Het |
Tm7sf3 |
T |
A |
6: 146,621,890 |
N163I |
possibly damaging |
Het |
Tmem144 |
G |
A |
3: 79,839,273 |
|
probably benign |
Het |
|
Other mutations in Usp24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00329:Usp24
|
APN |
4 |
106359091 |
missense |
probably benign |
|
IGL00340:Usp24
|
APN |
4 |
106401139 |
missense |
probably damaging |
0.99 |
IGL00480:Usp24
|
APN |
4 |
106368106 |
missense |
probably damaging |
0.99 |
IGL00548:Usp24
|
APN |
4 |
106341298 |
missense |
probably damaging |
0.96 |
IGL00655:Usp24
|
APN |
4 |
106390318 |
missense |
probably damaging |
0.99 |
IGL00674:Usp24
|
APN |
4 |
106372679 |
splice site |
probably benign |
|
IGL00718:Usp24
|
APN |
4 |
106409704 |
missense |
probably benign |
0.10 |
IGL00803:Usp24
|
APN |
4 |
106385526 |
splice site |
probably benign |
|
IGL01161:Usp24
|
APN |
4 |
106436844 |
missense |
probably benign |
0.02 |
IGL01344:Usp24
|
APN |
4 |
106379385 |
missense |
possibly damaging |
0.73 |
IGL01374:Usp24
|
APN |
4 |
106380099 |
missense |
possibly damaging |
0.86 |
IGL01485:Usp24
|
APN |
4 |
106362232 |
missense |
probably benign |
0.01 |
IGL01736:Usp24
|
APN |
4 |
106423461 |
missense |
probably benign |
0.00 |
IGL01737:Usp24
|
APN |
4 |
106387734 |
missense |
probably benign |
0.03 |
IGL01862:Usp24
|
APN |
4 |
106408898 |
splice site |
probably benign |
|
IGL01981:Usp24
|
APN |
4 |
106375768 |
splice site |
probably benign |
|
IGL02090:Usp24
|
APN |
4 |
106411426 |
missense |
possibly damaging |
0.55 |
IGL02275:Usp24
|
APN |
4 |
106387493 |
missense |
probably damaging |
1.00 |
IGL02352:Usp24
|
APN |
4 |
106403925 |
missense |
probably damaging |
1.00 |
IGL02359:Usp24
|
APN |
4 |
106403925 |
missense |
probably damaging |
1.00 |
IGL02391:Usp24
|
APN |
4 |
106407129 |
missense |
possibly damaging |
0.60 |
IGL02418:Usp24
|
APN |
4 |
106436360 |
missense |
probably benign |
0.07 |
IGL02537:Usp24
|
APN |
4 |
106392367 |
missense |
probably damaging |
1.00 |
IGL02638:Usp24
|
APN |
4 |
106438770 |
splice site |
probably benign |
|
IGL02638:Usp24
|
APN |
4 |
106438772 |
splice site |
probably benign |
|
IGL02830:Usp24
|
APN |
4 |
106347387 |
missense |
possibly damaging |
0.79 |
IGL03125:Usp24
|
APN |
4 |
106392402 |
missense |
probably benign |
0.09 |
IGL03280:Usp24
|
APN |
4 |
106380430 |
missense |
probably damaging |
1.00 |
IGL03350:Usp24
|
APN |
4 |
106371079 |
nonsense |
probably null |
|
BB010:Usp24
|
UTSW |
4 |
106428489 |
missense |
probably benign |
|
BB020:Usp24
|
UTSW |
4 |
106428489 |
missense |
probably benign |
|
IGL03098:Usp24
|
UTSW |
4 |
106371033 |
missense |
probably benign |
0.11 |
R0035:Usp24
|
UTSW |
4 |
106368027 |
missense |
probably benign |
0.18 |
R0044:Usp24
|
UTSW |
4 |
106412084 |
splice site |
probably benign |
|
R0086:Usp24
|
UTSW |
4 |
106392360 |
missense |
probably damaging |
0.98 |
R0125:Usp24
|
UTSW |
4 |
106397299 |
missense |
possibly damaging |
0.76 |
R0197:Usp24
|
UTSW |
4 |
106407133 |
missense |
probably damaging |
1.00 |
R0240:Usp24
|
UTSW |
4 |
106414404 |
nonsense |
probably null |
|
R0240:Usp24
|
UTSW |
4 |
106414404 |
nonsense |
probably null |
|
R0491:Usp24
|
UTSW |
4 |
106402105 |
missense |
probably benign |
0.41 |
R0973:Usp24
|
UTSW |
4 |
106371079 |
nonsense |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106413678 |
splice site |
probably null |
|
R0973:Usp24
|
UTSW |
4 |
106371079 |
nonsense |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106371079 |
nonsense |
probably null |
|
R0974:Usp24
|
UTSW |
4 |
106413678 |
splice site |
probably null |
|
R1163:Usp24
|
UTSW |
4 |
106420960 |
missense |
probably benign |
|
R1293:Usp24
|
UTSW |
4 |
106423553 |
missense |
probably benign |
0.19 |
R1333:Usp24
|
UTSW |
4 |
106342353 |
missense |
possibly damaging |
0.55 |
R1476:Usp24
|
UTSW |
4 |
106361933 |
missense |
probably damaging |
1.00 |
R1699:Usp24
|
UTSW |
4 |
106438827 |
missense |
probably damaging |
0.99 |
R1728:Usp24
|
UTSW |
4 |
106360421 |
missense |
possibly damaging |
0.85 |
R1729:Usp24
|
UTSW |
4 |
106360421 |
missense |
possibly damaging |
0.85 |
R1753:Usp24
|
UTSW |
4 |
106377559 |
missense |
probably benign |
0.04 |
R1917:Usp24
|
UTSW |
4 |
106410286 |
missense |
probably damaging |
1.00 |
R2045:Usp24
|
UTSW |
4 |
106400980 |
missense |
possibly damaging |
0.54 |
R2424:Usp24
|
UTSW |
4 |
106399113 |
critical splice donor site |
probably null |
|
R2436:Usp24
|
UTSW |
4 |
106409645 |
nonsense |
probably null |
|
R2513:Usp24
|
UTSW |
4 |
106379405 |
splice site |
probably null |
|
R3824:Usp24
|
UTSW |
4 |
106379066 |
missense |
probably benign |
|
R3831:Usp24
|
UTSW |
4 |
106362012 |
critical splice donor site |
probably null |
|
R3833:Usp24
|
UTSW |
4 |
106362012 |
critical splice donor site |
probably null |
|
R3982:Usp24
|
UTSW |
4 |
106387883 |
missense |
probably benign |
0.38 |
R4022:Usp24
|
UTSW |
4 |
106379224 |
splice site |
probably benign |
|
R4067:Usp24
|
UTSW |
4 |
106359089 |
missense |
possibly damaging |
0.68 |
R4175:Usp24
|
UTSW |
4 |
106316773 |
missense |
probably benign |
0.00 |
R4766:Usp24
|
UTSW |
4 |
106416048 |
missense |
probably damaging |
1.00 |
R4771:Usp24
|
UTSW |
4 |
106362180 |
splice site |
probably null |
|
R4798:Usp24
|
UTSW |
4 |
106360162 |
missense |
possibly damaging |
0.82 |
R4809:Usp24
|
UTSW |
4 |
106413676 |
critical splice donor site |
probably null |
|
R4822:Usp24
|
UTSW |
4 |
106416047 |
missense |
probably damaging |
0.98 |
R4906:Usp24
|
UTSW |
4 |
106388637 |
missense |
probably benign |
0.20 |
R4934:Usp24
|
UTSW |
4 |
106426546 |
missense |
probably benign |
0.29 |
R5074:Usp24
|
UTSW |
4 |
106420447 |
missense |
probably benign |
0.12 |
R5151:Usp24
|
UTSW |
4 |
106399112 |
critical splice donor site |
probably null |
|
R5220:Usp24
|
UTSW |
4 |
106382303 |
missense |
possibly damaging |
0.69 |
R5279:Usp24
|
UTSW |
4 |
106385424 |
missense |
possibly damaging |
0.94 |
R5280:Usp24
|
UTSW |
4 |
106341214 |
missense |
probably benign |
0.18 |
R5285:Usp24
|
UTSW |
4 |
106407033 |
missense |
probably benign |
0.00 |
R5292:Usp24
|
UTSW |
4 |
106418263 |
missense |
probably benign |
0.06 |
R5294:Usp24
|
UTSW |
4 |
106362357 |
missense |
possibly damaging |
0.53 |
R5394:Usp24
|
UTSW |
4 |
106408013 |
missense |
probably damaging |
1.00 |
R5517:Usp24
|
UTSW |
4 |
106375674 |
missense |
probably benign |
0.02 |
R5522:Usp24
|
UTSW |
4 |
106372721 |
missense |
probably damaging |
1.00 |
R5546:Usp24
|
UTSW |
4 |
106416047 |
missense |
probably damaging |
0.98 |
R5756:Usp24
|
UTSW |
4 |
106362483 |
missense |
probably damaging |
1.00 |
R5910:Usp24
|
UTSW |
4 |
106380468 |
missense |
probably damaging |
0.99 |
R5972:Usp24
|
UTSW |
4 |
106368067 |
missense |
probably damaging |
0.98 |
R6285:Usp24
|
UTSW |
4 |
106374100 |
splice site |
probably null |
|
R6370:Usp24
|
UTSW |
4 |
106380521 |
missense |
probably null |
0.20 |
R6630:Usp24
|
UTSW |
4 |
106387835 |
missense |
possibly damaging |
0.69 |
R6754:Usp24
|
UTSW |
4 |
106360420 |
missense |
probably damaging |
1.00 |
R7027:Usp24
|
UTSW |
4 |
106362244 |
missense |
probably benign |
0.21 |
R7088:Usp24
|
UTSW |
4 |
106387546 |
missense |
probably damaging |
1.00 |
R7129:Usp24
|
UTSW |
4 |
106362215 |
missense |
probably damaging |
1.00 |
R7131:Usp24
|
UTSW |
4 |
106382303 |
missense |
possibly damaging |
0.69 |
R7156:Usp24
|
UTSW |
4 |
106387919 |
critical splice donor site |
probably null |
|
R7174:Usp24
|
UTSW |
4 |
106362681 |
splice site |
probably null |
|
R7236:Usp24
|
UTSW |
4 |
106406305 |
splice site |
probably null |
|
R7403:Usp24
|
UTSW |
4 |
106407035 |
missense |
possibly damaging |
0.79 |
R7424:Usp24
|
UTSW |
4 |
106379107 |
missense |
probably benign |
0.00 |
R7475:Usp24
|
UTSW |
4 |
106342353 |
missense |
possibly damaging |
0.55 |
R7505:Usp24
|
UTSW |
4 |
106379079 |
missense |
probably damaging |
1.00 |
R7782:Usp24
|
UTSW |
4 |
106316574 |
missense |
probably damaging |
1.00 |
R7900:Usp24
|
UTSW |
4 |
106409400 |
missense |
probably damaging |
1.00 |
R7933:Usp24
|
UTSW |
4 |
106428489 |
missense |
probably benign |
|
R7940:Usp24
|
UTSW |
4 |
106430544 |
missense |
probably damaging |
0.98 |
R8271:Usp24
|
UTSW |
4 |
106428514 |
missense |
probably damaging |
0.98 |
R8348:Usp24
|
UTSW |
4 |
106368736 |
missense |
possibly damaging |
0.82 |
R8448:Usp24
|
UTSW |
4 |
106368736 |
missense |
possibly damaging |
0.82 |
R8483:Usp24
|
UTSW |
4 |
106373756 |
missense |
probably damaging |
1.00 |
R8546:Usp24
|
UTSW |
4 |
106402129 |
missense |
probably benign |
0.01 |
R8798:Usp24
|
UTSW |
4 |
106379239 |
missense |
probably benign |
0.00 |
R8822:Usp24
|
UTSW |
4 |
106412213 |
missense |
probably benign |
0.17 |
R8992:Usp24
|
UTSW |
4 |
106377565 |
missense |
probably benign |
0.36 |
R9002:Usp24
|
UTSW |
4 |
106418215 |
missense |
possibly damaging |
0.72 |
R9037:Usp24
|
UTSW |
4 |
106379054 |
missense |
probably damaging |
0.99 |
R9068:Usp24
|
UTSW |
4 |
106375678 |
missense |
probably benign |
0.09 |
R9096:Usp24
|
UTSW |
4 |
106397311 |
missense |
probably benign |
0.00 |
R9180:Usp24
|
UTSW |
4 |
106359050 |
missense |
possibly damaging |
0.71 |
R9199:Usp24
|
UTSW |
4 |
106387484 |
missense |
probably damaging |
1.00 |
R9201:Usp24
|
UTSW |
4 |
106420530 |
missense |
probably benign |
0.36 |
R9251:Usp24
|
UTSW |
4 |
106360518 |
missense |
probably benign |
0.19 |
R9423:Usp24
|
UTSW |
4 |
106431670 |
missense |
probably damaging |
1.00 |
R9459:Usp24
|
UTSW |
4 |
106342358 |
missense |
probably damaging |
1.00 |
R9472:Usp24
|
UTSW |
4 |
106403931 |
missense |
probably benign |
0.00 |
R9483:Usp24
|
UTSW |
4 |
106362182 |
missense |
probably damaging |
0.99 |
R9534:Usp24
|
UTSW |
4 |
106407115 |
missense |
probably damaging |
0.97 |
R9653:Usp24
|
UTSW |
4 |
106347367 |
missense |
probably benign |
0.03 |
R9712:Usp24
|
UTSW |
4 |
106347367 |
missense |
probably benign |
0.03 |
X0024:Usp24
|
UTSW |
4 |
106360446 |
missense |
probably benign |
0.09 |
X0028:Usp24
|
UTSW |
4 |
106368055 |
missense |
probably benign |
0.01 |
X0066:Usp24
|
UTSW |
4 |
106355731 |
missense |
possibly damaging |
0.82 |
|
Predicted Primers |
PCR Primer
(F):5'- ACGCTGGTTTACTTCACATTAGCCC -3'
(R):5'- AAGACTTCTGAGCCTTCCACTGCC -3'
Sequencing Primer
(F):5'- ACATTAGCCCTGTGGCAGTG -3'
(R):5'- ACTGCTGCCACTACTTGTATCAG -3'
|
Posted On |
2013-07-30 |