Incidental Mutation 'IGL03241:Cdc25a'
| ID |
414296 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cdc25a
|
| Ensembl Gene |
ENSMUSG00000032477 |
| Gene Name |
cell division cycle 25A |
| Synonyms |
D9Ertd393e |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL03241
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
9 |
| Chromosomal Location |
109704647-109722963 bp(+) (GRCm39) |
| Type of Mutation |
splice site (6 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 109713267 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094324]
[ENSMUST00000198308]
[ENSMUST00000198848]
|
| AlphaFold |
P48964 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000094324
|
| SMART Domains |
Protein: ENSMUSP00000091882
Gene: ENSMUSG00000032477
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:M-inducer_phosp
|
85 |
318 |
3.6e-69 |
PFAM |
|
RHOD
|
356 |
469 |
2.6e-25 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000197945
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000198219
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000198308
|
| SMART Domains |
Protein: ENSMUSP00000142958
Gene: ENSMUSG00000032477
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:M-inducer_phosp
|
24 |
258 |
1.2e-88 |
PFAM |
|
RHOD
|
295 |
408 |
5.97e-25 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000198848
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199353
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000199787
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] CDC25A is a member of the CDC25 family of phosphatases. CDC25A is required for progression from G1 to the S phase of the cell cycle. It activates the cyclin-dependent kinase CDC2 by removing two phosphate groups. CDC25A is specifically degraded in response to DNA damage, which prevents cells with chromosomal abnormalities from progressing through cell division. CDC25A is an oncogene, although its exact role in oncogenesis has not been demonstrated. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a spontaneous mutation exhibit elevated levels of early erythroid progenitor cell cycling but erythropoiesis is normally unaffected. Homozygous deletion of this gene is lethal and male heterozygotes display decreased vertebral trabecular bone. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 27 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc12 |
T |
A |
8: 87,236,436 (GRCm39) |
E1126V |
possibly damaging |
Het |
| Acnat1 |
A |
G |
4: 49,447,702 (GRCm39) |
V275A |
probably benign |
Het |
| Adamts15 |
G |
A |
9: 30,815,781 (GRCm39) |
P692S |
probably damaging |
Het |
| Aqp7 |
A |
T |
4: 41,045,270 (GRCm39) |
|
probably benign |
Het |
| Arhgap26 |
A |
T |
18: 39,362,970 (GRCm39) |
I413F |
probably damaging |
Het |
| Cdh18 |
C |
T |
15: 23,227,019 (GRCm39) |
T160I |
probably benign |
Het |
| Cfap206 |
T |
C |
4: 34,711,553 (GRCm39) |
Y448C |
probably damaging |
Het |
| Clec4a4 |
T |
C |
6: 122,967,332 (GRCm39) |
S3P |
probably damaging |
Het |
| Dhx38 |
A |
T |
8: 110,289,288 (GRCm39) |
H37Q |
possibly damaging |
Het |
| F7 |
A |
T |
8: 13,078,779 (GRCm39) |
E70V |
probably damaging |
Het |
| Nbeal1 |
A |
T |
1: 60,274,027 (GRCm39) |
Q418H |
possibly damaging |
Het |
| Nbeal1 |
G |
A |
1: 60,274,028 (GRCm39) |
E419K |
probably benign |
Het |
| Nebl |
A |
G |
2: 17,397,975 (GRCm39) |
|
probably null |
Het |
| Or4k15b |
T |
A |
14: 50,272,525 (GRCm39) |
M112L |
possibly damaging |
Het |
| Pfkm |
T |
C |
15: 98,021,061 (GRCm39) |
V293A |
probably benign |
Het |
| Slc36a3 |
A |
G |
11: 55,015,934 (GRCm39) |
S407P |
possibly damaging |
Het |
| Slc5a1 |
T |
C |
5: 33,290,749 (GRCm39) |
V111A |
probably benign |
Het |
| St6galnac5 |
G |
T |
3: 152,552,223 (GRCm39) |
Q115K |
probably benign |
Het |
| Tex56 |
G |
T |
13: 35,128,313 (GRCm39) |
A177S |
probably damaging |
Het |
| Timmdc1 |
G |
A |
16: 38,331,071 (GRCm39) |
|
probably benign |
Het |
| Trim34b |
T |
C |
7: 103,983,820 (GRCm39) |
|
probably benign |
Het |
| Trim75 |
A |
T |
8: 65,435,358 (GRCm39) |
I364N |
probably damaging |
Het |
| Vmn1r27 |
T |
A |
6: 58,192,126 (GRCm39) |
N293Y |
probably benign |
Het |
| Vmn2r88 |
A |
G |
14: 51,655,830 (GRCm39) |
T689A |
probably benign |
Het |
| Vmn2r97 |
T |
C |
17: 19,148,438 (GRCm39) |
V111A |
probably benign |
Het |
| Zfp114 |
C |
T |
7: 23,880,437 (GRCm39) |
T261I |
probably benign |
Het |
| Zfp516 |
A |
G |
18: 83,005,645 (GRCm39) |
T850A |
probably benign |
Het |
|
| Other mutations in Cdc25a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01658:Cdc25a
|
APN |
9 |
109,705,194 (GRCm39) |
splice site |
probably null |
|
|
IGL01761:Cdc25a
|
APN |
9 |
109,720,933 (GRCm39) |
intron |
probably benign |
|
|
IGL02808:Cdc25a
|
APN |
9 |
109,712,667 (GRCm39) |
splice site |
probably null |
|
|
P4748:Cdc25a
|
UTSW |
9 |
109,713,176 (GRCm39) |
splice site |
probably benign |
|
|
R1472:Cdc25a
|
UTSW |
9 |
109,705,157 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1571:Cdc25a
|
UTSW |
9 |
109,710,614 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R1598:Cdc25a
|
UTSW |
9 |
109,708,961 (GRCm39) |
frame shift |
probably null |
|
|
R4135:Cdc25a
|
UTSW |
9 |
109,710,585 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R4301:Cdc25a
|
UTSW |
9 |
109,718,810 (GRCm39) |
missense |
probably benign |
0.23 |
|
R4386:Cdc25a
|
UTSW |
9 |
109,718,801 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5074:Cdc25a
|
UTSW |
9 |
109,713,208 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R5171:Cdc25a
|
UTSW |
9 |
109,706,229 (GRCm39) |
missense |
probably benign |
0.25 |
|
R5896:Cdc25a
|
UTSW |
9 |
109,713,433 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5928:Cdc25a
|
UTSW |
9 |
109,718,861 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6223:Cdc25a
|
UTSW |
9 |
109,718,842 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6240:Cdc25a
|
UTSW |
9 |
109,713,226 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6440:Cdc25a
|
UTSW |
9 |
109,710,566 (GRCm39) |
missense |
probably benign |
|
|
R6854:Cdc25a
|
UTSW |
9 |
109,708,995 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7219:Cdc25a
|
UTSW |
9 |
109,718,154 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7980:Cdc25a
|
UTSW |
9 |
109,708,949 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8506:Cdc25a
|
UTSW |
9 |
109,720,820 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8790:Cdc25a
|
UTSW |
9 |
109,716,416 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8807:Cdc25a
|
UTSW |
9 |
109,708,303 (GRCm39) |
missense |
probably benign |
0.01 |
|
| Posted On |
2016-08-02 |
Incidental Mutation