Incidental Mutation 'R6174:Cdc45'
| ID |
501846 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cdc45
|
| Ensembl Gene |
ENSMUSG00000000028 |
| Gene Name |
cell division cycle 45 |
| Synonyms |
Cdc45l |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R6174 (G1)
|
| Quality Score |
148.008 |
|
Status
|
Not validated
|
| Chromosome |
16 |
| Chromosomal Location |
18780447-18811987 bp(-) (GRCm38) |
| Type of Mutation |
splice site (58 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 18794704 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000094753
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000000028]
[ENSMUST00000096990]
|
| AlphaFold |
Q9Z1X9 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000000028
|
| SMART Domains |
Protein: ENSMUSP00000000028
Gene: ENSMUSG00000000028
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CDC45
|
19 |
564 |
1.6e-152 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000096990
|
| SMART Domains |
Protein: ENSMUSP00000094753
Gene: ENSMUSG00000000028
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CDC45
|
18 |
74 |
7.9e-24 |
PFAM |
|
Pfam:CDC45
|
73 |
520 |
4.5e-138 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 98.1%
- 20x: 94.7%
|
| 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 was identified by its strong similarity with Saccharomyces cerevisiae Cdc45, an essential protein required to the initiation of DNA replication. Cdc45 is a member of the highly conserved multiprotein complex including Cdc6/Cdc18, the minichromosome maintenance proteins (MCMs) and DNA polymerase, which is important for early steps of DNA replication in eukaryotes. This protein has been shown to interact with MCM7 and DNA polymerase alpha. Studies of the similar gene in Xenopus suggested that this protein play a pivotal role in the loading of DNA polymerase alpha onto chromatin. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
PHENOTYPE: Homozygous mutant embryos do not develop after implantation, resulting in embryonic lethality between E4.5-E5.5. Heterozygous animals appear normal and fertile. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 59 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930590J08Rik |
T |
A |
6: 91,942,536 (GRCm38) |
D725E |
probably damaging |
Het |
| 9530053A07Rik |
A |
G |
7: 28,139,959 (GRCm38) |
Y399C |
probably damaging |
Het |
| Bco1 |
T |
A |
8: 117,113,534 (GRCm38) |
Y264N |
probably damaging |
Het |
| Cd109 |
G |
A |
9: 78,665,546 (GRCm38) |
|
probably null |
Het |
| Ckap5 |
A |
G |
2: 91,568,219 (GRCm38) |
E578G |
probably benign |
Het |
| Cracr2b |
T |
A |
7: 141,464,836 (GRCm38) |
L193Q |
probably damaging |
Het |
| D11Wsu47e |
C |
A |
11: 113,688,975 (GRCm38) |
H399N |
possibly damaging |
Het |
| Dmxl2 |
G |
A |
9: 54,393,727 (GRCm38) |
L2367F |
probably damaging |
Het |
| Dopey2 |
T |
G |
16: 93,766,222 (GRCm38) |
D871E |
probably damaging |
Het |
| Emc1 |
T |
C |
4: 139,366,531 (GRCm38) |
Y651H |
probably benign |
Het |
| Enox1 |
T |
C |
14: 77,508,187 (GRCm38) |
S41P |
possibly damaging |
Het |
| Foxa1 |
A |
G |
12: 57,542,900 (GRCm38) |
L178P |
probably damaging |
Het |
| Gm10639 |
T |
A |
9: 78,304,455 (GRCm38) |
Y166* |
probably null |
Het |
| Grm7 |
T |
A |
6: 111,246,297 (GRCm38) |
Y433N |
probably benign |
Het |
| Gtf3c2 |
G |
A |
5: 31,158,211 (GRCm38) |
R813C |
probably damaging |
Het |
| Hacd3 |
T |
C |
9: 65,005,627 (GRCm38) |
E117G |
probably damaging |
Het |
| Hist1h4i |
T |
A |
13: 22,041,077 (GRCm38) |
T83S |
probably benign |
Het |
| Hmcn1 |
G |
A |
1: 150,646,784 (GRCm38) |
T3455M |
probably benign |
Het |
| Itga6 |
A |
G |
2: 71,833,709 (GRCm38) |
I61V |
possibly damaging |
Het |
| Jaml |
T |
C |
9: 45,088,773 (GRCm38) |
L81P |
probably damaging |
Het |
| Loxhd1 |
T |
C |
18: 77,412,178 (GRCm38) |
F782S |
probably damaging |
Het |
| Lrp1b |
T |
C |
2: 41,449,263 (GRCm38) |
H742R |
probably benign |
Het |
| Macrod2 |
G |
T |
2: 140,400,975 (GRCm38) |
M1I |
probably null |
Het |
| Mcf2l |
G |
A |
8: 13,013,849 (GRCm38) |
W1020* |
probably null |
Het |
| Msgn1 |
A |
G |
12: 11,208,923 (GRCm38) |
L9P |
probably damaging |
Het |
| Ngdn |
C |
A |
14: 55,022,099 (GRCm38) |
S202R |
probably benign |
Het |
| Notch1 |
C |
T |
2: 26,485,442 (GRCm38) |
G50R |
possibly damaging |
Het |
| Olfr1162 |
A |
T |
2: 88,050,302 (GRCm38) |
C107* |
probably null |
Het |
| Olfr310 |
A |
T |
7: 86,268,801 (GRCm38) |
D329E |
probably benign |
Het |
| Olfr43 |
A |
T |
11: 74,206,640 (GRCm38) |
I192N |
probably damaging |
Het |
| Olfr715b |
A |
T |
7: 107,106,507 (GRCm38) |
M118K |
probably damaging |
Het |
| Osbpl10 |
A |
G |
9: 115,109,487 (GRCm38) |
S211G |
probably benign |
Het |
| Pabpc6 |
G |
A |
17: 9,668,155 (GRCm38) |
A489V |
probably benign |
Het |
| Pcdhb13 |
A |
T |
18: 37,443,421 (GRCm38) |
D284V |
possibly damaging |
Het |
| Pde6c |
T |
C |
19: 38,140,229 (GRCm38) |
S214P |
possibly damaging |
Het |
| Pofut1 |
C |
T |
2: 153,259,616 (GRCm38) |
H192Y |
probably damaging |
Het |
| Pou3f2 |
T |
C |
4: 22,486,960 (GRCm38) |
D391G |
possibly damaging |
Het |
| Prc1 |
G |
A |
7: 80,304,796 (GRCm38) |
S165N |
probably benign |
Het |
| Prex1 |
A |
G |
2: 166,572,963 (GRCm38) |
V304A |
probably benign |
Het |
| Ptpru |
T |
C |
4: 131,785,754 (GRCm38) |
I881V |
probably benign |
Het |
| Radil |
A |
G |
5: 142,487,115 (GRCm38) |
S847P |
probably benign |
Het |
| Rimklb |
A |
G |
6: 122,456,412 (GRCm38) |
S317P |
probably damaging |
Het |
| Sdhc |
A |
T |
1: 171,138,702 (GRCm38) |
L78* |
probably null |
Het |
| Skint6 |
T |
A |
4: 112,839,313 (GRCm38) |
I1042F |
possibly damaging |
Het |
| Slc1a6 |
T |
A |
10: 78,801,907 (GRCm38) |
D422E |
probably damaging |
Het |
| Slc29a1 |
A |
T |
17: 45,589,928 (GRCm38) |
H71Q |
probably damaging |
Het |
| Slfn14 |
A |
T |
11: 83,276,603 (GRCm38) |
D695E |
probably damaging |
Het |
| Spg11 |
A |
T |
2: 122,086,805 (GRCm38) |
|
probably null |
Het |
| Srgap2 |
A |
G |
1: 131,289,616 (GRCm38) |
V986A |
probably benign |
Het |
| Stab1 |
A |
T |
14: 31,162,519 (GRCm38) |
C172* |
probably null |
Het |
| Tigd4 |
A |
G |
3: 84,595,267 (GRCm38) |
H497R |
probably benign |
Het |
| Ubn2 |
G |
A |
6: 38,461,536 (GRCm38) |
G60D |
probably damaging |
Het |
| Uckl1 |
C |
T |
2: 181,573,073 (GRCm38) |
|
probably null |
Het |
| Vmn2r24 |
A |
T |
6: 123,816,277 (GRCm38) |
K854N |
probably benign |
Het |
| Vps13d |
G |
A |
4: 144,975,193 (GRCm38) |
Q3193* |
probably null |
Het |
| Wdr26 |
G |
A |
1: 181,191,868 (GRCm38) |
L315F |
probably damaging |
Het |
| Zc3h8 |
C |
A |
2: 128,943,855 (GRCm38) |
E24* |
probably null |
Het |
| Zfp39 |
A |
G |
11: 58,891,387 (GRCm38) |
V183A |
probably benign |
Het |
| Zfp608 |
C |
A |
18: 54,988,544 (GRCm38) |
|
probably benign |
Het |
|
| Other mutations in Cdc45 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01528:Cdc45
|
APN |
16 |
18,811,561 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01677:Cdc45
|
APN |
16 |
18,787,000 (GRCm38) |
missense |
probably benign |
0.02 |
|
IGL02079:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02080:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02105:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02106:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02237:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02238:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02239:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02371:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02441:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02442:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02465:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02466:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02468:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02469:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02470:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02471:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02472:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02473:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02489:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02490:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02491:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02492:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02511:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02558:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02559:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02560:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02561:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02562:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02566:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02567:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02576:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02583:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02589:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02626:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02627:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02628:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02629:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02687:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02688:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02689:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02720:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02724:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02731:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02738:Cdc45
|
APN |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
IGL02991:Cdc45
|
UTSW |
16 |
18,798,729 (GRCm38) |
missense |
probably benign |
0.06 |
|
R0051:Cdc45
|
UTSW |
16 |
18,794,774 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0051:Cdc45
|
UTSW |
16 |
18,794,774 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0458:Cdc45
|
UTSW |
16 |
18,781,972 (GRCm38) |
splice site |
probably benign |
|
|
R1398:Cdc45
|
UTSW |
16 |
18,781,971 (GRCm38) |
splice site |
probably benign |
|
|
R1413:Cdc45
|
UTSW |
16 |
18,808,741 (GRCm38) |
missense |
possibly damaging |
0.63 |
|
R1792:Cdc45
|
UTSW |
16 |
18,807,340 (GRCm38) |
missense |
probably benign |
0.01 |
|
R2919:Cdc45
|
UTSW |
16 |
18,808,793 (GRCm38) |
missense |
probably benign |
0.00 |
|
R3956:Cdc45
|
UTSW |
16 |
18,805,430 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4079:Cdc45
|
UTSW |
16 |
18,811,360 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4825:Cdc45
|
UTSW |
16 |
18,784,863 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R5028:Cdc45
|
UTSW |
16 |
18,795,180 (GRCm38) |
missense |
probably benign |
0.43 |
|
R5214:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5215:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5309:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5311:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5312:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5352:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5353:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5354:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5355:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5356:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5424:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5426:Cdc45
|
UTSW |
16 |
18,795,897 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5655:Cdc45
|
UTSW |
16 |
18,807,279 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6796:Cdc45
|
UTSW |
16 |
18,784,857 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7910:Cdc45
|
UTSW |
16 |
18,810,453 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R8519:Cdc45
|
UTSW |
16 |
18,808,847 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8987:Cdc45
|
UTSW |
16 |
18,811,550 (GRCm38) |
missense |
probably benign |
|
|
R9221:Cdc45
|
UTSW |
16 |
18,786,771 (GRCm38) |
missense |
probably benign |
0.08 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGTTTGACTCAGTCCCAGTG -3'
(R):5'- TCAGTGTCTTGTCTCATTCATACAG -3'
Sequencing Primer
(F):5'- CCAGTGGACTGCACATCTTTGG -3'
(R):5'- ATACAGCTTGCTCCCTCCAGG -3'
|
| Posted On |
2017-12-04 |
Incidental Mutation