Incidental Mutation 'IGL02940:Stk39'
| ID |
364482 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Stk39
|
| Ensembl Gene |
ENSMUSG00000027030 |
| Gene Name |
serine/threonine kinase 39 |
| Synonyms |
SPAK, DCHT, Rnl5, RF005 |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.506)
|
| Stock # |
IGL02940
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
2 |
| Chromosomal Location |
68040789-68302381 bp(-) (GRCm39) |
| Type of Mutation |
splice site (5 bp from exon) |
| DNA Base Change (assembly) |
C to T
at 68051243 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000099776
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102715]
[ENSMUST00000102715]
|
| AlphaFold |
Q9Z1W9 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000102715
|
| SMART Domains |
Protein: ENSMUSP00000099776
Gene: ENSMUSG00000027030
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
65 |
N/A |
INTRINSIC |
|
S_TKc
|
75 |
349 |
4.44e-80 |
SMART |
|
Pfam:OSR1_C
|
463 |
494 |
1.3e-15 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000102715
|
| SMART Domains |
Protein: ENSMUSP00000099776
Gene: ENSMUSG00000027030
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
14 |
65 |
N/A |
INTRINSIC |
|
S_TKc
|
75 |
349 |
4.44e-80 |
SMART |
|
Pfam:OSR1_C
|
463 |
494 |
1.3e-15 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126663
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000130380
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134442
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139407
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144457
|
| 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 encodes a serine/threonine kinase that is thought to function in the cellular stress response pathway. The kinase is activated in response to hypotonic stress, leading to phosphorylation of several cation-chloride-coupled cotransporters. The catalytically active kinase specifically activates the p38 MAP kinase pathway, and its interaction with p38 decreases upon cellular stress, suggesting that this kinase may serve as an intermediate in the response to cellular stress. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a null allele exhibit reduced bumetanide-sensitive thallium, a potassium tracer, uptake in dorsal root ganglion neurons and reduced fertility. Mice with an ENU mutation in intron 8 exhibit elevated albumin-creatinine (ACR) ratios. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 33 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrg3 |
T |
A |
8: 95,760,084 (GRCm39) |
V101D |
possibly damaging |
Het |
| Brca1 |
T |
C |
11: 101,380,738 (GRCm39) |
D1765G |
probably benign |
Het |
| Cadps2 |
T |
C |
6: 23,496,808 (GRCm39) |
K450R |
probably benign |
Het |
| Cc2d2a |
A |
T |
5: 43,885,636 (GRCm39) |
|
probably null |
Het |
| Dbh |
A |
G |
2: 27,058,321 (GRCm39) |
Y163C |
probably damaging |
Het |
| Drc7 |
T |
A |
8: 95,800,925 (GRCm39) |
I649N |
probably damaging |
Het |
| Dst |
G |
A |
1: 34,328,668 (GRCm39) |
A7097T |
probably benign |
Het |
| Fbxo46 |
A |
G |
7: 18,869,537 (GRCm39) |
H52R |
probably benign |
Het |
| Gm9944 |
T |
C |
4: 144,179,709 (GRCm39) |
|
probably benign |
Het |
| Lsm14a |
G |
T |
7: 34,070,596 (GRCm39) |
S100* |
probably null |
Het |
| Mrc2 |
C |
T |
11: 105,231,997 (GRCm39) |
R850C |
probably damaging |
Het |
| Musk |
A |
G |
4: 58,373,364 (GRCm39) |
D763G |
probably damaging |
Het |
| Ncan |
C |
T |
8: 70,562,735 (GRCm39) |
V508I |
probably benign |
Het |
| Or4k35 |
A |
T |
2: 111,100,073 (GRCm39) |
L213Q |
probably damaging |
Het |
| Pgls |
C |
T |
8: 72,046,741 (GRCm39) |
S18L |
probably damaging |
Het |
| Phf20l1 |
A |
G |
15: 66,467,000 (GRCm39) |
T98A |
probably damaging |
Het |
| Ppp1r36dn |
A |
C |
12: 76,497,944 (GRCm39) |
|
noncoding transcript |
Het |
| Prdm13 |
T |
A |
4: 21,683,421 (GRCm39) |
K180* |
probably null |
Het |
| Rai1 |
T |
C |
11: 60,077,844 (GRCm39) |
V636A |
probably benign |
Het |
| Setd5 |
T |
C |
6: 113,091,899 (GRCm39) |
F240S |
possibly damaging |
Het |
| Slco1a5 |
A |
G |
6: 142,187,731 (GRCm39) |
L536P |
probably damaging |
Het |
| Tenm2 |
T |
C |
11: 35,932,471 (GRCm39) |
T1707A |
probably damaging |
Het |
| Tlr2 |
A |
T |
3: 83,743,781 (GRCm39) |
D767E |
probably benign |
Het |
| Tlr7 |
C |
T |
X: 166,090,830 (GRCm39) |
V219I |
probably benign |
Het |
| Tmprss7 |
A |
G |
16: 45,476,818 (GRCm39) |
S815P |
probably damaging |
Het |
| Trav12-1 |
T |
A |
14: 53,776,017 (GRCm39) |
W57R |
probably damaging |
Het |
| Uxt |
T |
C |
X: 20,826,025 (GRCm39) |
E66G |
possibly damaging |
Het |
| Vmn2r45 |
A |
T |
7: 8,475,369 (GRCm39) |
M553K |
probably damaging |
Het |
| Vmn2r67 |
A |
G |
7: 84,785,951 (GRCm39) |
W685R |
probably benign |
Het |
| Vstm5 |
A |
C |
9: 15,168,962 (GRCm39) |
D144A |
probably damaging |
Het |
| Zfp592 |
A |
G |
7: 80,674,575 (GRCm39) |
H513R |
probably damaging |
Het |
| Zfp830 |
T |
A |
11: 82,656,295 (GRCm39) |
|
probably benign |
Het |
| Zfp990 |
A |
G |
4: 145,261,492 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Stk39 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00946:Stk39
|
APN |
2 |
68,144,908 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
IGL00966:Stk39
|
APN |
2 |
68,042,302 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL01936:Stk39
|
APN |
2 |
68,144,908 (GRCm39) |
missense |
probably benign |
0.21 |
|
IGL02301:Stk39
|
APN |
2 |
68,042,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
claimjumper
|
UTSW |
2 |
68,144,923 (GRCm39) |
missense |
probably damaging |
0.96 |
|
outlaw
|
UTSW |
2 |
68,137,383 (GRCm39) |
critical splice donor site |
probably null |
|
|
rustler
|
UTSW |
2 |
68,093,647 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0570:Stk39
|
UTSW |
2 |
68,240,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0609:Stk39
|
UTSW |
2 |
68,196,511 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0670:Stk39
|
UTSW |
2 |
68,196,526 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0980:Stk39
|
UTSW |
2 |
68,222,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1024:Stk39
|
UTSW |
2 |
68,240,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1573:Stk39
|
UTSW |
2 |
68,221,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1713:Stk39
|
UTSW |
2 |
68,137,460 (GRCm39) |
splice site |
probably benign |
|
|
R2223:Stk39
|
UTSW |
2 |
68,144,923 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R3700:Stk39
|
UTSW |
2 |
68,222,462 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4207:Stk39
|
UTSW |
2 |
68,051,264 (GRCm39) |
missense |
probably benign |
0.42 |
|
R4298:Stk39
|
UTSW |
2 |
68,221,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4726:Stk39
|
UTSW |
2 |
68,093,647 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4975:Stk39
|
UTSW |
2 |
68,051,336 (GRCm39) |
intron |
probably benign |
|
|
R5057:Stk39
|
UTSW |
2 |
68,051,292 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5384:Stk39
|
UTSW |
2 |
68,240,383 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5921:Stk39
|
UTSW |
2 |
68,196,449 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6125:Stk39
|
UTSW |
2 |
68,222,468 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6251:Stk39
|
UTSW |
2 |
68,137,383 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6332:Stk39
|
UTSW |
2 |
68,240,387 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6375:Stk39
|
UTSW |
2 |
68,222,582 (GRCm39) |
missense |
probably benign |
0.34 |
|
R7057:Stk39
|
UTSW |
2 |
68,240,471 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R7064:Stk39
|
UTSW |
2 |
68,189,156 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7691:Stk39
|
UTSW |
2 |
68,301,983 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7921:Stk39
|
UTSW |
2 |
68,137,383 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8155:Stk39
|
UTSW |
2 |
68,097,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8920:Stk39
|
UTSW |
2 |
68,302,191 (GRCm39) |
missense |
unknown |
|
|
R9003:Stk39
|
UTSW |
2 |
68,222,462 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9530:Stk39
|
UTSW |
2 |
68,198,755 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9682:Stk39
|
UTSW |
2 |
68,196,449 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9784:Stk39
|
UTSW |
2 |
68,198,775 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Stk39
|
UTSW |
2 |
68,222,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-12-18 |
Incidental Mutation