Incidental Mutation 'IGL01475:Cdc16'
| ID |
88423 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Cdc16
|
| Ensembl Gene |
ENSMUSG00000038416 |
| Gene Name |
CDC16 cell division cycle 16 |
| Synonyms |
2700071J12Rik, 2810431D22Rik |
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.972)
|
| Stock # |
IGL01475
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
13807676-13831938 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 13831542 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 592
(S592P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000047950
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043767]
[ENSMUST00000043962]
|
| AlphaFold |
Q8R349 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043767
|
| SMART Domains |
Protein: ENSMUSP00000037354
Gene: ENSMUSG00000038398
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
18 |
N/A |
INTRINSIC |
|
Pfam:Smg4_UPF3
|
63 |
224 |
1.4e-54 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000043962
AA Change: S592P
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000047950
Gene: ENSMUSG00000038416
AA Change: S592P
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:TPR_9
|
11 |
63 |
1.8e-3 |
PFAM |
|
Pfam:ANAPC3
|
15 |
95 |
3.5e-23 |
PFAM |
|
TPR
|
130 |
163 |
1.17e1 |
SMART |
|
Blast:TPR
|
299 |
333 |
2e-8 |
BLAST |
|
Blast:TPR
|
334 |
367 |
1e-14 |
BLAST |
|
TPR
|
368 |
401 |
1.48e1 |
SMART |
|
Blast:TPR
|
402 |
435 |
7e-15 |
BLAST |
|
TPR
|
445 |
478 |
6.68e-6 |
SMART |
|
TPR
|
479 |
512 |
1.74e-4 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137360
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211643
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000211724
|
| 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 functions as a protein ubiquitin ligase and is a component of the multiprotein APC complex. The APC complex is a cyclin degradation system that governs exit from mitosis by targeting cell cycle proteins for degredation by the 26S proteasome. Each component protein of the APC complex is highly conserved among eukaryotic organisms. This protein, and other APC complex proteins, contain a tetratricopeptide repeat (TPR) domain; a protein domain that is often involved in protein-protein interactions and the assembly of multiprotein complexes. Multiple alternatively spliced transcript variants, encoding distinct proteins, have been identified. [provided by RefSeq, Jan 2016]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 45 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700129C05Rik |
A |
T |
14: 59,380,252 (GRCm39) |
N15K |
possibly damaging |
Het |
| Adam32 |
A |
T |
8: 25,362,664 (GRCm39) |
I587K |
probably damaging |
Het |
| Adamtsl4 |
T |
C |
3: 95,584,843 (GRCm39) |
S942G |
probably benign |
Het |
| Adamtsl5 |
A |
G |
10: 80,180,750 (GRCm39) |
F104S |
probably damaging |
Het |
| Adgrf5 |
A |
G |
17: 43,761,245 (GRCm39) |
D980G |
probably benign |
Het |
| Apba1 |
A |
T |
19: 23,894,950 (GRCm39) |
D462V |
possibly damaging |
Het |
| Arhgef11 |
T |
C |
3: 87,634,433 (GRCm39) |
|
probably benign |
Het |
| Cd74 |
T |
C |
18: 60,943,393 (GRCm39) |
|
probably benign |
Het |
| Cenpj |
A |
G |
14: 56,802,502 (GRCm39) |
M21T |
possibly damaging |
Het |
| Col28a1 |
A |
G |
6: 8,103,521 (GRCm39) |
L425S |
probably damaging |
Het |
| Dbt |
C |
T |
3: 116,313,908 (GRCm39) |
T25I |
possibly damaging |
Het |
| Dguok |
C |
A |
6: 83,467,552 (GRCm39) |
M98I |
possibly damaging |
Het |
| Dmxl1 |
T |
C |
18: 50,004,781 (GRCm39) |
L943P |
probably damaging |
Het |
| Eloa |
G |
A |
4: 135,738,231 (GRCm39) |
S243L |
probably benign |
Het |
| Enkur |
C |
A |
2: 21,201,530 (GRCm39) |
A52S |
probably damaging |
Het |
| Ezh1 |
T |
C |
11: 101,083,787 (GRCm39) |
E744G |
probably damaging |
Het |
| Fbxw11 |
T |
C |
11: 32,672,101 (GRCm39) |
S190P |
possibly damaging |
Het |
| Foxb1 |
G |
A |
9: 69,666,550 (GRCm39) |
|
probably benign |
Het |
| Gabra5 |
C |
T |
7: 57,058,432 (GRCm39) |
G439S |
probably damaging |
Het |
| Gtf2h2 |
A |
T |
13: 100,617,541 (GRCm39) |
V207D |
probably damaging |
Het |
| Hoatz |
A |
G |
9: 51,011,358 (GRCm39) |
I93T |
probably benign |
Het |
| Krt76 |
A |
G |
15: 101,796,948 (GRCm39) |
V317A |
probably benign |
Het |
| Lair1 |
C |
A |
7: 4,012,683 (GRCm39) |
|
probably benign |
Het |
| Lrit2 |
T |
A |
14: 36,791,051 (GRCm39) |
H243Q |
probably damaging |
Het |
| Mast3 |
C |
T |
8: 71,232,174 (GRCm39) |
A1268T |
probably damaging |
Het |
| Matn2 |
G |
A |
15: 34,316,671 (GRCm39) |
M4I |
possibly damaging |
Het |
| Mob1b |
T |
A |
5: 88,897,502 (GRCm39) |
F137I |
probably damaging |
Het |
| Mreg |
T |
C |
1: 72,203,325 (GRCm39) |
|
probably benign |
Het |
| Nom1 |
T |
C |
5: 29,651,272 (GRCm39) |
V684A |
possibly damaging |
Het |
| Pate2 |
T |
A |
9: 35,580,998 (GRCm39) |
L1Q |
probably null |
Het |
| Pla2r1 |
T |
C |
2: 60,271,425 (GRCm39) |
|
probably benign |
Het |
| Plxna1 |
A |
G |
6: 89,331,870 (GRCm39) |
F447L |
possibly damaging |
Het |
| Pno1 |
A |
T |
11: 17,160,992 (GRCm39) |
I114N |
probably damaging |
Het |
| Ppp1r7 |
T |
G |
1: 93,288,540 (GRCm39) |
|
probably benign |
Het |
| Pprc1 |
T |
A |
19: 46,059,968 (GRCm39) |
Y1503N |
probably benign |
Het |
| Rab30 |
T |
C |
7: 92,484,930 (GRCm39) |
V132A |
probably damaging |
Het |
| Slc15a4 |
T |
C |
5: 127,679,024 (GRCm39) |
T439A |
probably benign |
Het |
| Slc29a3 |
A |
G |
10: 60,559,596 (GRCm39) |
V186A |
possibly damaging |
Het |
| Stxbp5l |
G |
A |
16: 37,165,454 (GRCm39) |
T88I |
possibly damaging |
Het |
| Tarbp1 |
A |
G |
8: 127,160,701 (GRCm39) |
V1250A |
probably benign |
Het |
| Tcte2 |
A |
T |
17: 13,937,824 (GRCm39) |
|
probably benign |
Het |
| Trp53bp1 |
A |
T |
2: 121,100,800 (GRCm39) |
|
probably null |
Het |
| Trpc4 |
A |
T |
3: 54,173,828 (GRCm39) |
L407F |
possibly damaging |
Het |
| Vmn1r6 |
T |
C |
6: 56,979,896 (GRCm39) |
F164S |
probably damaging |
Het |
| Zfp579 |
C |
A |
7: 4,997,743 (GRCm39) |
R56L |
probably benign |
Het |
|
| Other mutations in Cdc16 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00850:Cdc16
|
APN |
8 |
13,817,575 (GRCm39) |
nonsense |
probably null |
|
|
IGL01109:Cdc16
|
APN |
8 |
13,814,606 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02729:Cdc16
|
APN |
8 |
13,829,250 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL03389:Cdc16
|
APN |
8 |
13,809,179 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0026:Cdc16
|
UTSW |
8 |
13,809,130 (GRCm39) |
splice site |
probably null |
|
|
R0373:Cdc16
|
UTSW |
8 |
13,829,264 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0520:Cdc16
|
UTSW |
8 |
13,810,569 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0564:Cdc16
|
UTSW |
8 |
13,831,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1470:Cdc16
|
UTSW |
8 |
13,808,992 (GRCm39) |
splice site |
probably benign |
|
|
R1487:Cdc16
|
UTSW |
8 |
13,821,445 (GRCm39) |
missense |
probably benign |
0.17 |
|
R1753:Cdc16
|
UTSW |
8 |
13,814,688 (GRCm39) |
nonsense |
probably null |
|
|
R1883:Cdc16
|
UTSW |
8 |
13,825,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3087:Cdc16
|
UTSW |
8 |
13,809,004 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3418:Cdc16
|
UTSW |
8 |
13,819,489 (GRCm39) |
nonsense |
probably null |
|
|
R3756:Cdc16
|
UTSW |
8 |
13,827,609 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4152:Cdc16
|
UTSW |
8 |
13,812,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4842:Cdc16
|
UTSW |
8 |
13,831,644 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R5122:Cdc16
|
UTSW |
8 |
13,814,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5492:Cdc16
|
UTSW |
8 |
13,813,915 (GRCm39) |
splice site |
probably null |
|
|
R5982:Cdc16
|
UTSW |
8 |
13,831,399 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6145:Cdc16
|
UTSW |
8 |
13,817,573 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
R6154:Cdc16
|
UTSW |
8 |
13,818,609 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R6611:Cdc16
|
UTSW |
8 |
13,831,512 (GRCm39) |
missense |
probably benign |
|
|
R6992:Cdc16
|
UTSW |
8 |
13,809,188 (GRCm39) |
missense |
probably benign |
0.22 |
|
R7011:Cdc16
|
UTSW |
8 |
13,819,451 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7484:Cdc16
|
UTSW |
8 |
13,827,605 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7593:Cdc16
|
UTSW |
8 |
13,827,605 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7946:Cdc16
|
UTSW |
8 |
13,812,882 (GRCm39) |
missense |
probably benign |
0.22 |
|
R9019:Cdc16
|
UTSW |
8 |
13,831,501 (GRCm39) |
missense |
probably benign |
|
|
R9655:Cdc16
|
UTSW |
8 |
13,809,153 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R9668:Cdc16
|
UTSW |
8 |
13,817,552 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9796:Cdc16
|
UTSW |
8 |
13,807,693 (GRCm39) |
start gained |
probably benign |
|
|
| Posted On |
2013-11-18 |
Incidental Mutation