Incidental Mutation 'IGL02926:Mcm6'
| ID |
363862 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Mcm6
|
| Ensembl Gene |
ENSMUSG00000026355 |
| Gene Name |
minichromosome maintenance complex component 6 |
| Synonyms |
D1Wsu22e, Mcmd6 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL02926
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
1 |
| Chromosomal Location |
128259327-128287401 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 128267119 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Histidine
at position 575
(Y575H)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140308
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027601]
[ENSMUST00000190495]
|
| AlphaFold |
P97311 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000027601
AA Change: Y575H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000027601
Gene: ENSMUSG00000026355
AA Change: Y575H
| Domain | Start | End | E-Value | Type |
|---|
|
MCM
|
119 |
657 |
1.43e-270 |
SMART |
|
PDB:2LE8|A
|
710 |
821 |
1e-47 |
PDB |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000188755
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000190495
AA Change: Y575H
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000140308
Gene: ENSMUSG00000026355
AA Change: Y575H
| Domain | Start | End | E-Value | Type |
|---|
|
MCM
|
119 |
657 |
1.43e-270 |
SMART |
|
PDB:2LE8|A
|
710 |
783 |
3e-29 |
PDB |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000191454
|
| 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 one of the highly conserved mini-chromosome maintenance proteins (MCM) that are essential for the initiation of eukaryotic genome replication. The hexameric protein complex formed by the MCM proteins is a key component of the pre-replication complex (pre_RC) and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. The MCM complex consisting of this protein and MCM2, 4 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of the complex by CDC2 kinase reduces the helicase activity, suggesting a role in the regulation of DNA replication. Single nucleotide polymorphisms in the intron regions of this gene are associated with differential transcriptional activation of the promoter of the neighboring lactase gene and, thereby, influence lactose intolerance in early adulthood. [provided by RefSeq, May 2012]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit prenatal lethality. Mice heterozygous for this allele exhibit increased micronulei-containing red blood cells. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 44 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Alms1 |
A |
T |
6: 85,618,432 (GRCm39) |
D2826V |
probably damaging |
Het |
| Alpl |
C |
T |
4: 137,469,945 (GRCm39) |
A460T |
probably damaging |
Het |
| C2cd5 |
A |
G |
6: 142,976,963 (GRCm39) |
|
probably benign |
Het |
| C4b |
C |
T |
17: 34,949,686 (GRCm39) |
R1468Q |
possibly damaging |
Het |
| Calu |
A |
G |
6: 29,366,919 (GRCm39) |
T44A |
possibly damaging |
Het |
| Cgn |
T |
C |
3: 94,685,326 (GRCm39) |
K399R |
probably benign |
Het |
| Ciao3 |
A |
G |
17: 26,001,128 (GRCm39) |
H460R |
probably benign |
Het |
| Cyp2t4 |
G |
A |
7: 26,857,228 (GRCm39) |
V356M |
probably damaging |
Het |
| D430041D05Rik |
T |
C |
2: 104,044,604 (GRCm39) |
D683G |
probably damaging |
Het |
| Dhcr24 |
T |
A |
4: 106,443,552 (GRCm39) |
I410N |
probably damaging |
Het |
| Dmap1 |
T |
A |
4: 117,539,085 (GRCm39) |
E17V |
probably benign |
Het |
| Dnaaf9 |
C |
T |
2: 130,554,286 (GRCm39) |
R921K |
probably benign |
Het |
| Dnah7a |
A |
G |
1: 53,535,109 (GRCm39) |
I2717T |
possibly damaging |
Het |
| Epb41l3 |
G |
T |
17: 69,554,741 (GRCm39) |
K280N |
probably damaging |
Het |
| Espl1 |
T |
A |
15: 102,208,290 (GRCm39) |
M432K |
probably damaging |
Het |
| Fgf5 |
C |
A |
5: 98,409,874 (GRCm39) |
A141E |
probably damaging |
Het |
| Fto |
T |
A |
8: 92,211,795 (GRCm39) |
F373L |
probably damaging |
Het |
| Gpatch1 |
T |
C |
7: 35,007,694 (GRCm39) |
D122G |
probably damaging |
Het |
| Ints11 |
T |
C |
4: 155,972,568 (GRCm39) |
|
probably null |
Het |
| Jarid2 |
A |
G |
13: 45,056,405 (GRCm39) |
Q398R |
probably benign |
Het |
| Kcnh1 |
A |
G |
1: 191,959,208 (GRCm39) |
D254G |
probably damaging |
Het |
| Lamc3 |
C |
T |
2: 31,825,738 (GRCm39) |
|
probably benign |
Het |
| Lamc3 |
C |
T |
2: 31,825,737 (GRCm39) |
|
probably benign |
Het |
| Ltbp4 |
T |
C |
7: 27,028,297 (GRCm39) |
|
probably null |
Het |
| Myh9 |
A |
C |
15: 77,671,826 (GRCm39) |
Y422D |
probably damaging |
Het |
| Or4c35 |
T |
C |
2: 89,808,506 (GRCm39) |
L128P |
probably damaging |
Het |
| Or5b105 |
A |
C |
19: 13,080,187 (GRCm39) |
N160K |
possibly damaging |
Het |
| Or8b47 |
T |
C |
9: 38,435,021 (GRCm39) |
|
probably benign |
Het |
| Plcb1 |
T |
C |
2: 135,206,682 (GRCm39) |
|
probably benign |
Het |
| Pmfbp1 |
A |
G |
8: 110,246,881 (GRCm39) |
E251G |
probably damaging |
Het |
| Psg27 |
A |
T |
7: 18,291,054 (GRCm39) |
V383E |
probably damaging |
Het |
| Ptprn |
A |
T |
1: 75,224,517 (GRCm39) |
H946Q |
possibly damaging |
Het |
| Rbl1 |
A |
G |
2: 157,009,333 (GRCm39) |
V734A |
probably benign |
Het |
| Rspry1 |
T |
A |
8: 95,376,439 (GRCm39) |
N320K |
probably damaging |
Het |
| Ryr1 |
A |
T |
7: 28,760,965 (GRCm39) |
V3219D |
probably damaging |
Het |
| Ryr2 |
C |
A |
13: 11,774,721 (GRCm39) |
W1145L |
probably damaging |
Het |
| Scel |
A |
T |
14: 103,813,683 (GRCm39) |
R319* |
probably null |
Het |
| Stxbp2 |
C |
T |
8: 3,685,629 (GRCm39) |
T226I |
probably benign |
Het |
| Tac1 |
A |
T |
6: 7,562,410 (GRCm39) |
N106I |
possibly damaging |
Het |
| Trim13 |
G |
T |
14: 61,842,693 (GRCm39) |
|
probably null |
Het |
| Tspan31 |
T |
G |
10: 126,904,778 (GRCm39) |
|
probably null |
Het |
| Usp36 |
C |
T |
11: 118,155,609 (GRCm39) |
V723M |
probably benign |
Het |
| Utrn |
A |
T |
10: 12,566,504 (GRCm39) |
N1219K |
probably damaging |
Het |
| Vcan |
G |
T |
13: 89,836,742 (GRCm39) |
T2934K |
probably damaging |
Het |
|
| Other mutations in Mcm6 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00518:Mcm6
|
APN |
1 |
128,272,120 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01420:Mcm6
|
APN |
1 |
128,273,612 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01746:Mcm6
|
APN |
1 |
128,281,261 (GRCm39) |
nonsense |
probably null |
|
|
IGL02256:Mcm6
|
APN |
1 |
128,263,465 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02624:Mcm6
|
APN |
1 |
128,277,185 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL02732:Mcm6
|
APN |
1 |
128,287,227 (GRCm39) |
missense |
probably benign |
0.16 |
|
IGL02750:Mcm6
|
APN |
1 |
128,271,209 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03189:Mcm6
|
APN |
1 |
128,272,039 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03238:Mcm6
|
APN |
1 |
128,283,257 (GRCm39) |
missense |
probably benign |
0.13 |
|
IGL03397:Mcm6
|
APN |
1 |
128,272,039 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0453:Mcm6
|
UTSW |
1 |
128,261,292 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0501:Mcm6
|
UTSW |
1 |
128,283,373 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0885:Mcm6
|
UTSW |
1 |
128,276,670 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1013:Mcm6
|
UTSW |
1 |
128,276,778 (GRCm39) |
missense |
probably benign |
|
|
R1319:Mcm6
|
UTSW |
1 |
128,276,789 (GRCm39) |
missense |
probably benign |
|
|
R1396:Mcm6
|
UTSW |
1 |
128,279,213 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1656:Mcm6
|
UTSW |
1 |
128,277,155 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1891:Mcm6
|
UTSW |
1 |
128,263,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1950:Mcm6
|
UTSW |
1 |
128,273,726 (GRCm39) |
missense |
probably benign |
0.35 |
|
R3411:Mcm6
|
UTSW |
1 |
128,279,322 (GRCm39) |
missense |
probably benign |
0.35 |
|
R4564:Mcm6
|
UTSW |
1 |
128,271,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4626:Mcm6
|
UTSW |
1 |
128,279,285 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4627:Mcm6
|
UTSW |
1 |
128,279,285 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4628:Mcm6
|
UTSW |
1 |
128,279,285 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4916:Mcm6
|
UTSW |
1 |
128,276,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4965:Mcm6
|
UTSW |
1 |
128,287,223 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4967:Mcm6
|
UTSW |
1 |
128,263,586 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5016:Mcm6
|
UTSW |
1 |
128,271,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5204:Mcm6
|
UTSW |
1 |
128,261,375 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5229:Mcm6
|
UTSW |
1 |
128,261,321 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5607:Mcm6
|
UTSW |
1 |
128,283,326 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5811:Mcm6
|
UTSW |
1 |
128,263,465 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R5816:Mcm6
|
UTSW |
1 |
128,276,192 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7204:Mcm6
|
UTSW |
1 |
128,265,864 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7316:Mcm6
|
UTSW |
1 |
128,287,245 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8081:Mcm6
|
UTSW |
1 |
128,265,905 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8546:Mcm6
|
UTSW |
1 |
128,273,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8547:Mcm6
|
UTSW |
1 |
128,273,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8549:Mcm6
|
UTSW |
1 |
128,273,685 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R8785:Mcm6
|
UTSW |
1 |
128,262,535 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8878:Mcm6
|
UTSW |
1 |
128,283,248 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9043:Mcm6
|
UTSW |
1 |
128,271,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9253:Mcm6
|
UTSW |
1 |
128,279,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Mcm6
|
UTSW |
1 |
128,272,035 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2015-12-18 |
Incidental Mutation