Incidental Mutation 'IGL01558:Stk33'
ID |
90786 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Stk33
|
Ensembl Gene |
ENSMUSG00000031027 |
Gene Name |
serine/threonine kinase 33 |
Synonyms |
4921505G21Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.068)
|
Stock # |
IGL01558
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
108878430-109038288 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
T to C
at 108940491 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000147147
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090414]
[ENSMUST00000106745]
[ENSMUST00000121378]
[ENSMUST00000121748]
[ENSMUST00000141210]
|
AlphaFold |
Q924X7 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000090414
|
SMART Domains |
Protein: ENSMUSP00000087897 Gene: ENSMUSG00000031027
Domain | Start | End | E-Value | Type |
S_TKc
|
111 |
377 |
4.7e-102 |
SMART |
low complexity region
|
399 |
414 |
N/A |
INTRINSIC |
low complexity region
|
445 |
467 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000106745
|
SMART Domains |
Protein: ENSMUSP00000102356 Gene: ENSMUSG00000031027
Domain | Start | End | E-Value | Type |
S_TKc
|
111 |
377 |
4.7e-102 |
SMART |
low complexity region
|
399 |
414 |
N/A |
INTRINSIC |
low complexity region
|
445 |
467 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000121378
|
SMART Domains |
Protein: ENSMUSP00000112560 Gene: ENSMUSG00000031027
Domain | Start | End | E-Value | Type |
S_TKc
|
2 |
254 |
1.01e-83 |
SMART |
low complexity region
|
276 |
291 |
N/A |
INTRINSIC |
low complexity region
|
322 |
344 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000121748
|
SMART Domains |
Protein: ENSMUSP00000112515 Gene: ENSMUSG00000031027
Domain | Start | End | E-Value | Type |
S_TKc
|
111 |
377 |
4.8e-102 |
SMART |
low complexity region
|
399 |
414 |
N/A |
INTRINSIC |
low complexity region
|
445 |
467 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000141210
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 21 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
C |
5: 77,036,464 (GRCm39) |
E359G |
possibly damaging |
Het |
Agtr1b |
T |
C |
3: 20,370,424 (GRCm39) |
T61A |
probably damaging |
Het |
Casd1 |
T |
A |
6: 4,624,143 (GRCm39) |
I312N |
possibly damaging |
Het |
Cebpz |
A |
T |
17: 79,242,734 (GRCm39) |
F307I |
probably damaging |
Het |
Dhx33 |
T |
C |
11: 70,890,579 (GRCm39) |
R207G |
probably benign |
Het |
G0s2 |
T |
C |
1: 192,955,003 (GRCm39) |
Y27C |
probably damaging |
Het |
Glg1 |
A |
T |
8: 111,914,362 (GRCm39) |
M474K |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,346,798 (GRCm39) |
N2490S |
probably benign |
Het |
Mpdz |
C |
A |
4: 81,213,767 (GRCm39) |
E1565* |
probably null |
Het |
Mthfsl |
A |
G |
9: 88,570,870 (GRCm39) |
I126T |
possibly damaging |
Het |
Nectin4 |
A |
G |
1: 171,212,257 (GRCm39) |
D285G |
probably benign |
Het |
Neurod1 |
T |
C |
2: 79,284,363 (GRCm39) |
H340R |
possibly damaging |
Het |
Nop53 |
G |
A |
7: 15,679,751 (GRCm39) |
|
probably benign |
Het |
Siglec1 |
A |
G |
2: 130,920,419 (GRCm39) |
L795P |
probably damaging |
Het |
Sntg1 |
A |
T |
1: 8,533,612 (GRCm39) |
|
probably benign |
Het |
Stox1 |
C |
T |
10: 62,503,651 (GRCm39) |
V135M |
probably damaging |
Het |
Sult2a8 |
C |
A |
7: 14,159,377 (GRCm39) |
E81* |
probably null |
Het |
Tdrd6 |
A |
G |
17: 43,936,659 (GRCm39) |
V1463A |
probably damaging |
Het |
Tdrd6 |
C |
T |
17: 43,935,657 (GRCm39) |
G1797D |
probably benign |
Het |
Trmt2b |
C |
A |
X: 133,139,305 (GRCm39) |
R389I |
possibly damaging |
Het |
Ttc28 |
G |
T |
5: 111,431,828 (GRCm39) |
V1903L |
probably damaging |
Het |
|
Other mutations in Stk33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01137:Stk33
|
APN |
7 |
108,928,775 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01467:Stk33
|
APN |
7 |
108,928,796 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01775:Stk33
|
APN |
7 |
108,911,574 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Stk33
|
UTSW |
7 |
108,878,876 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0336:Stk33
|
UTSW |
7 |
108,930,681 (GRCm39) |
missense |
probably benign |
0.01 |
R0394:Stk33
|
UTSW |
7 |
108,940,696 (GRCm39) |
missense |
probably benign |
|
R0579:Stk33
|
UTSW |
7 |
108,924,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Stk33
|
UTSW |
7 |
108,920,725 (GRCm39) |
missense |
probably damaging |
0.96 |
R1363:Stk33
|
UTSW |
7 |
108,879,028 (GRCm39) |
missense |
probably benign |
0.06 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R1574:Stk33
|
UTSW |
7 |
108,879,027 (GRCm39) |
missense |
probably benign |
0.01 |
R2153:Stk33
|
UTSW |
7 |
108,940,527 (GRCm39) |
missense |
probably benign |
0.01 |
R4366:Stk33
|
UTSW |
7 |
108,879,002 (GRCm39) |
missense |
probably benign |
0.06 |
R4896:Stk33
|
UTSW |
7 |
108,926,802 (GRCm39) |
missense |
probably damaging |
1.00 |
R4994:Stk33
|
UTSW |
7 |
108,939,605 (GRCm39) |
missense |
probably benign |
0.08 |
R5283:Stk33
|
UTSW |
7 |
108,935,334 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6339:Stk33
|
UTSW |
7 |
108,920,672 (GRCm39) |
missense |
probably benign |
0.03 |
R6547:Stk33
|
UTSW |
7 |
108,920,042 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6717:Stk33
|
UTSW |
7 |
108,926,823 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6894:Stk33
|
UTSW |
7 |
108,935,269 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8975:Stk33
|
UTSW |
7 |
108,935,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R9168:Stk33
|
UTSW |
7 |
108,928,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R9175:Stk33
|
UTSW |
7 |
108,920,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9204:Stk33
|
UTSW |
7 |
108,940,686 (GRCm39) |
missense |
probably benign |
0.00 |
R9416:Stk33
|
UTSW |
7 |
108,940,689 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Stk33
|
UTSW |
7 |
108,935,266 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
Posted On |
2013-12-09 |