Incidental Mutation 'IGL01107:Dusp11'
| ID |
51325 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Dusp11
|
| Ensembl Gene |
ENSMUSG00000030002 |
| Gene Name |
dual specificity phosphatase 11 (RNA/RNP complex 1-interacting) |
| Synonyms |
2010300F21Rik |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01107
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
6 |
| Chromosomal Location |
85919250-85938649 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to G
at 85929352 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000032071]
|
| AlphaFold |
Q6NXK5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000032071
|
| SMART Domains |
Protein: ENSMUSP00000032071
Gene: ENSMUSG00000030002
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
14 |
N/A |
INTRINSIC |
|
Pfam:DSPc
|
74 |
203 |
2.5e-18 |
PFAM |
|
low complexity region
|
230 |
243 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134793
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137527
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139164
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151394
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156821
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000201530
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the dual specificity protein phosphatase subfamily. These phosphatases inactivate their target kinases by dephosphorylating both the phosphoserine/threonine and phosphotyrosine residues. They negatively regulate members of the mitogen-activated protein (MAP) kinase superfamily (MAPK/ERK, SAPK/JNK, p38), which is associated with cellular proliferation and differentiation. Different members of the family of dual specificity phosphatases show distinct substrate specificities for various MAP kinases, different tissue distribution and subcellular localization, and different modes of inducibility of their expression by extracellular stimuli. This gene product is localized to the nucleus and binds directly to RNA and splicing factors, and thus it is suggested to participate in nuclear mRNA metabolism. [provided by RefSeq, Sep 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 32 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700001O22Rik |
A |
T |
2: 30,687,948 (GRCm39) |
F215Y |
probably damaging |
Het |
| 2700049A03Rik |
T |
C |
12: 71,241,242 (GRCm39) |
|
probably null |
Het |
| Akip1 |
C |
T |
7: 109,311,045 (GRCm39) |
T195M |
probably damaging |
Het |
| Arhgef16 |
T |
C |
4: 154,364,701 (GRCm39) |
N631S |
probably benign |
Het |
| Brat1 |
C |
T |
5: 140,702,932 (GRCm39) |
S544L |
probably damaging |
Het |
| Cfap65 |
C |
T |
1: 74,958,342 (GRCm39) |
|
probably null |
Het |
| Defa22 |
T |
A |
8: 21,653,053 (GRCm39) |
|
probably null |
Het |
| Dnajc4 |
C |
T |
19: 6,966,869 (GRCm39) |
R153H |
probably benign |
Het |
| E2f4 |
T |
A |
8: 106,030,809 (GRCm39) |
|
probably benign |
Het |
| Ece1 |
T |
A |
4: 137,665,969 (GRCm39) |
L271Q |
probably damaging |
Het |
| Fcgrt |
T |
C |
7: 44,742,752 (GRCm39) |
D343G |
probably damaging |
Het |
| Igsf10 |
T |
C |
3: 59,238,945 (GRCm39) |
E412G |
probably damaging |
Het |
| Il4ra |
G |
T |
7: 125,175,086 (GRCm39) |
L431F |
possibly damaging |
Het |
| Ilrun |
A |
T |
17: 28,005,043 (GRCm39) |
|
probably null |
Het |
| Krt86 |
T |
A |
15: 101,373,306 (GRCm39) |
L200Q |
probably damaging |
Het |
| Lpcat1 |
T |
A |
13: 73,642,947 (GRCm39) |
F126I |
probably damaging |
Het |
| Prag1 |
A |
G |
8: 36,567,085 (GRCm39) |
T79A |
probably benign |
Het |
| Pramel13 |
A |
T |
4: 144,119,664 (GRCm39) |
I301N |
probably benign |
Het |
| Psg29 |
G |
T |
7: 16,938,850 (GRCm39) |
L41F |
probably benign |
Het |
| Rai14 |
C |
T |
15: 10,599,797 (GRCm39) |
|
probably benign |
Het |
| Reg3a |
A |
G |
6: 78,360,228 (GRCm39) |
D136G |
probably benign |
Het |
| Rif1 |
A |
G |
2: 52,001,315 (GRCm39) |
T1590A |
probably benign |
Het |
| Rorb |
A |
T |
19: 18,934,692 (GRCm39) |
L300* |
probably null |
Het |
| Sin3b |
T |
C |
8: 73,457,733 (GRCm39) |
C150R |
possibly damaging |
Het |
| Smarcc1 |
C |
A |
9: 110,051,005 (GRCm39) |
H942N |
probably damaging |
Het |
| Tas2r105 |
A |
G |
6: 131,664,074 (GRCm39) |
V118A |
probably benign |
Het |
| Tmem131 |
T |
C |
1: 36,868,662 (GRCm39) |
S388G |
probably damaging |
Het |
| Ttll9 |
C |
A |
2: 152,844,809 (GRCm39) |
|
probably benign |
Het |
| Ush1c |
A |
G |
7: 45,859,325 (GRCm39) |
L498P |
probably damaging |
Het |
| Vmn2r100 |
A |
G |
17: 19,741,618 (GRCm39) |
Y110C |
probably damaging |
Het |
| Zbtb11 |
T |
C |
16: 55,826,370 (GRCm39) |
Y800H |
probably damaging |
Het |
| Zdhhc20 |
T |
A |
14: 58,103,046 (GRCm39) |
E101V |
probably damaging |
Het |
|
| Other mutations in Dusp11 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01584:Dusp11
|
APN |
6 |
85,930,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02276:Dusp11
|
APN |
6 |
85,935,599 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02727:Dusp11
|
APN |
6 |
85,938,474 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0372:Dusp11
|
UTSW |
6 |
85,935,712 (GRCm39) |
splice site |
probably benign |
|
|
R0413:Dusp11
|
UTSW |
6 |
85,929,352 (GRCm39) |
splice site |
probably benign |
|
|
R1669:Dusp11
|
UTSW |
6 |
85,927,008 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2115:Dusp11
|
UTSW |
6 |
85,935,651 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4610:Dusp11
|
UTSW |
6 |
85,927,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4678:Dusp11
|
UTSW |
6 |
85,930,363 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5288:Dusp11
|
UTSW |
6 |
85,924,587 (GRCm39) |
makesense |
probably null |
|
|
R5386:Dusp11
|
UTSW |
6 |
85,924,587 (GRCm39) |
makesense |
probably null |
|
|
R5756:Dusp11
|
UTSW |
6 |
85,929,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5987:Dusp11
|
UTSW |
6 |
85,936,215 (GRCm39) |
nonsense |
probably null |
|
|
R6591:Dusp11
|
UTSW |
6 |
85,938,507 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6691:Dusp11
|
UTSW |
6 |
85,938,507 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7684:Dusp11
|
UTSW |
6 |
85,927,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-06-21 |
Incidental Mutation