Incidental Mutation 'IGL01446:Usp17lc'
| ID |
84406 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Usp17lc
|
| Ensembl Gene |
ENSMUSG00000058976 |
| Gene Name |
ubiquitin specific peptidase 17-like C |
| Synonyms |
Dub-2, Dub2b, Dub2, Usp17l5 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01446
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
103065903-103068381 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 103067651 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Serine
at position 315
(R315S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000102505
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000079348]
[ENSMUST00000106892]
|
| AlphaFold |
G5E8I7 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000079348
AA Change: R315S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000078323
Gene: ENSMUSG00000058976
AA Change: R315S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:UCH
|
50 |
345 |
3.8e-54 |
PFAM |
|
Pfam:UCH_1
|
51 |
327 |
3.5e-25 |
PFAM |
|
low complexity region
|
374 |
385 |
N/A |
INTRINSIC |
|
low complexity region
|
529 |
539 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000106892
AA Change: R315S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000102505
Gene: ENSMUSG00000058976
AA Change: R315S
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:UCH
|
50 |
345 |
1.3e-60 |
PFAM |
|
Pfam:UCH_1
|
51 |
327 |
5.5e-30 |
PFAM |
|
low complexity region
|
374 |
385 |
N/A |
INTRINSIC |
|
low complexity region
|
529 |
539 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000116717
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic elthality before implantation, failure to hatch from the zona pellucida, decreased cell proliferation and increased apoptosis. Mice heterozygous for this allele exhibit abnormal body, testis and thymus weight and reduced sperm motility. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 41 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
A |
G |
11: 9,353,834 (GRCm39) |
T3719A |
probably damaging |
Het |
| Acaca |
A |
G |
11: 84,151,457 (GRCm39) |
K785R |
probably damaging |
Het |
| Acsm3 |
G |
A |
7: 119,377,677 (GRCm39) |
V401M |
probably damaging |
Het |
| Aff4 |
G |
T |
11: 53,306,296 (GRCm39) |
R1146L |
probably damaging |
Het |
| Alms1 |
C |
A |
6: 85,673,683 (GRCm39) |
P3562T |
probably damaging |
Het |
| Arsj |
A |
G |
3: 126,232,463 (GRCm39) |
E403G |
probably benign |
Het |
| Baiap2l1 |
C |
T |
5: 144,212,723 (GRCm39) |
V431I |
probably benign |
Het |
| Cecr2 |
T |
A |
6: 120,735,560 (GRCm39) |
M904K |
probably benign |
Het |
| Cenpe |
A |
T |
3: 134,943,300 (GRCm39) |
T775S |
probably benign |
Het |
| Dennd1b |
G |
A |
1: 138,950,848 (GRCm39) |
E30K |
possibly damaging |
Het |
| Dnah5 |
A |
G |
15: 28,326,815 (GRCm39) |
D2008G |
probably damaging |
Het |
| Dnm2 |
T |
C |
9: 21,392,672 (GRCm39) |
V460A |
probably damaging |
Het |
| Ell2 |
G |
T |
13: 75,910,110 (GRCm39) |
L285F |
probably benign |
Het |
| Erg |
A |
G |
16: 95,162,141 (GRCm39) |
S322P |
probably damaging |
Het |
| Extl3 |
A |
G |
14: 65,314,529 (GRCm39) |
F218L |
probably benign |
Het |
| Fzd9 |
T |
C |
5: 135,279,420 (GRCm39) |
E155G |
probably damaging |
Het |
| Ghr |
A |
G |
15: 3,362,837 (GRCm39) |
W212R |
probably damaging |
Het |
| Gulp1 |
A |
G |
1: 44,783,708 (GRCm39) |
|
probably benign |
Het |
| Hdgfl2 |
C |
T |
17: 56,404,281 (GRCm39) |
R332C |
possibly damaging |
Het |
| Lratd1 |
A |
T |
12: 14,199,929 (GRCm39) |
I266N |
probably damaging |
Het |
| Nsd2 |
T |
C |
5: 34,018,530 (GRCm39) |
|
probably benign |
Het |
| Or4c12 |
A |
G |
2: 89,774,282 (GRCm39) |
F59S |
probably damaging |
Het |
| Or5a3 |
T |
C |
19: 12,400,165 (GRCm39) |
I164T |
possibly damaging |
Het |
| Or5b121 |
C |
T |
19: 13,507,616 (GRCm39) |
T237I |
probably benign |
Het |
| Phf11b |
A |
C |
14: 59,578,740 (GRCm39) |
S9A |
probably benign |
Het |
| Psd4 |
T |
C |
2: 24,295,407 (GRCm39) |
S854P |
probably damaging |
Het |
| Reln |
C |
T |
5: 22,174,315 (GRCm39) |
D1963N |
probably damaging |
Het |
| Rpe65 |
T |
A |
3: 159,306,042 (GRCm39) |
|
probably benign |
Het |
| Sdccag8 |
T |
C |
1: 176,672,811 (GRCm39) |
S235P |
probably damaging |
Het |
| Sgip1 |
G |
T |
4: 102,786,110 (GRCm39) |
|
probably null |
Het |
| Skint5 |
G |
A |
4: 113,800,019 (GRCm39) |
P36L |
probably damaging |
Het |
| Slc26a3 |
G |
T |
12: 31,502,490 (GRCm39) |
|
probably benign |
Het |
| Snx13 |
T |
A |
12: 35,174,479 (GRCm39) |
C669* |
probably null |
Het |
| Svil |
A |
T |
18: 5,062,385 (GRCm39) |
T902S |
probably damaging |
Het |
| Syne2 |
T |
C |
12: 76,088,149 (GRCm39) |
S4989P |
probably damaging |
Het |
| Ttn |
G |
A |
2: 76,640,283 (GRCm39) |
T13775M |
probably damaging |
Het |
| Ubr4 |
T |
C |
4: 139,165,351 (GRCm39) |
|
probably benign |
Het |
| Ush1c |
C |
T |
7: 45,858,380 (GRCm39) |
R636H |
possibly damaging |
Het |
| Vmn1r236 |
T |
A |
17: 21,506,918 (GRCm39) |
V12D |
probably benign |
Het |
| Wsb2 |
T |
G |
5: 117,509,229 (GRCm39) |
I170S |
probably damaging |
Het |
| Zfp800 |
G |
A |
6: 28,242,983 (GRCm39) |
L661F |
possibly damaging |
Het |
|
| Other mutations in Usp17lc |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00338:Usp17lc
|
APN |
7 |
103,068,148 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
IGL00499:Usp17lc
|
APN |
7 |
103,067,672 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00499:Usp17lc
|
APN |
7 |
103,067,673 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1466:Usp17lc
|
UTSW |
7 |
103,068,148 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1466:Usp17lc
|
UTSW |
7 |
103,068,148 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1584:Usp17lc
|
UTSW |
7 |
103,068,148 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1754:Usp17lc
|
UTSW |
7 |
103,068,055 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2987:Usp17lc
|
UTSW |
7 |
103,067,509 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3969:Usp17lc
|
UTSW |
7 |
103,067,626 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4661:Usp17lc
|
UTSW |
7 |
103,067,797 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5118:Usp17lc
|
UTSW |
7 |
103,067,868 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5413:Usp17lc
|
UTSW |
7 |
103,067,763 (GRCm39) |
missense |
probably benign |
|
|
R6962:Usp17lc
|
UTSW |
7 |
103,068,118 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7412:Usp17lc
|
UTSW |
7 |
103,067,575 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7638:Usp17lc
|
UTSW |
7 |
103,067,706 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7748:Usp17lc
|
UTSW |
7 |
103,067,688 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8194:Usp17lc
|
UTSW |
7 |
103,067,407 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8303:Usp17lc
|
UTSW |
7 |
103,067,389 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8815:Usp17lc
|
UTSW |
7 |
103,067,524 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8859:Usp17lc
|
UTSW |
7 |
103,064,316 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9023:Usp17lc
|
UTSW |
7 |
103,067,539 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9200:Usp17lc
|
UTSW |
7 |
103,068,105 (GRCm39) |
missense |
probably benign |
0.14 |
|
R9658:Usp17lc
|
UTSW |
7 |
103,067,389 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
| Posted On |
2013-11-11 |
Incidental Mutation