Incidental Mutation 'R6081:Mcm8'
| ID |
482911 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Mcm8
|
| Ensembl Gene |
ENSMUSG00000027353 |
| Gene Name |
minichromosome maintenance 8 homologous recombination repair factor |
| Synonyms |
5730432L01Rik |
| MMRRC Submission |
044240-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.731)
|
| Stock # |
R6081 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
132658061-132686117 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 132670003 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Leucine
at position 359
(R359L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000066842
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028831]
[ENSMUST00000066559]
|
| AlphaFold |
Q9CWV1 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000028831
AA Change: R387L
PolyPhen 2
Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
|
| SMART Domains |
Protein: ENSMUSP00000028831
Gene: ENSMUSG00000027353
AA Change: R387L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
15 |
N/A |
INTRINSIC |
|
low complexity region
|
48 |
62 |
N/A |
INTRINSIC |
|
Blast:MCM
|
79 |
155 |
2e-28 |
BLAST |
|
MCM
|
198 |
742 |
2.42e-136 |
SMART |
|
AAA
|
439 |
590 |
5.99e-6 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000066559
AA Change: R359L
PolyPhen 2
Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
|
| SMART Domains |
Protein: ENSMUSP00000066842
Gene: ENSMUSG00000027353
AA Change: R359L
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
6 |
15 |
N/A |
INTRINSIC |
|
Blast:MCM
|
51 |
127 |
2e-28 |
BLAST |
|
MCM
|
170 |
714 |
2.42e-136 |
SMART |
|
AAA
|
411 |
562 |
5.99e-6 |
SMART |
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.6%
- 10x: 97.9%
- 20x: 93.8%
|
| 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 mini-chromosome maintenance proteins is a key component of the pre-replication complex and may be involved in the formation of replication forks and in the recruitment of other DNA replication related proteins. This protein contains the central domain that is conserved among the mini-chromosome maintenance proteins. The encoded protein may interact with other mini-chromosome maintenance proteins and play a role in DNA replication. This gene may be associated with length of reproductive lifespan and menopause. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2013]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit female and male infertility associated with impaired ovarian development and arrested male meiosis, and impaired sensitivity to homologous recombination double-strand break repair. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 29 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930522L14Rik |
A |
T |
5: 109,887,097 (GRCm39) |
M33K |
probably damaging |
Het |
| 4930556J24Rik |
T |
C |
11: 3,888,140 (GRCm39) |
Q82R |
unknown |
Het |
| Adcy9 |
T |
C |
16: 4,112,545 (GRCm39) |
D714G |
probably benign |
Het |
| Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
| Ahctf1 |
G |
T |
1: 179,609,237 (GRCm39) |
A639E |
probably benign |
Het |
| Ank3 |
G |
A |
10: 69,838,395 (GRCm39) |
R1566K |
possibly damaging |
Het |
| Anxa5 |
C |
T |
3: 36,519,436 (GRCm39) |
D18N |
probably damaging |
Het |
| Apc |
C |
T |
18: 34,423,164 (GRCm39) |
P299L |
possibly damaging |
Het |
| Btnl4 |
C |
A |
17: 34,693,210 (GRCm39) |
W68C |
probably damaging |
Het |
| Cmya5 |
T |
A |
13: 93,281,021 (GRCm39) |
|
probably benign |
Het |
| Cstf2t |
G |
T |
19: 31,060,523 (GRCm39) |
V20L |
probably benign |
Het |
| D630045J12Rik |
A |
T |
6: 38,119,633 (GRCm39) |
V1703E |
probably damaging |
Het |
| Dhx32 |
A |
G |
7: 133,323,941 (GRCm39) |
F535S |
probably damaging |
Het |
| Diras2 |
T |
C |
13: 52,662,181 (GRCm39) |
D42G |
probably damaging |
Het |
| Dppa3 |
T |
A |
6: 122,606,931 (GRCm39) |
D140E |
probably damaging |
Het |
| Gpr180 |
C |
T |
14: 118,391,086 (GRCm39) |
T205I |
probably benign |
Het |
| Gzme |
T |
G |
14: 56,355,764 (GRCm39) |
T183P |
possibly damaging |
Het |
| H2-T23 |
T |
A |
17: 36,342,707 (GRCm39) |
I144F |
possibly damaging |
Het |
| Hlx |
T |
C |
1: 184,459,894 (GRCm39) |
S415G |
probably benign |
Het |
| Krtap5-3 |
G |
A |
7: 141,755,223 (GRCm39) |
C20Y |
unknown |
Het |
| Mroh2b |
G |
C |
15: 4,973,859 (GRCm39) |
E1126Q |
probably damaging |
Het |
| Nav1 |
C |
T |
1: 135,398,560 (GRCm39) |
R674H |
probably damaging |
Het |
| Otx1 |
A |
T |
11: 21,949,406 (GRCm39) |
L24H |
probably damaging |
Het |
| Rnaset2b |
T |
A |
17: 7,256,193 (GRCm39) |
|
probably null |
Het |
| Samd12 |
T |
C |
15: 53,583,074 (GRCm39) |
K87E |
probably benign |
Het |
| Sec16b |
T |
C |
1: 157,388,324 (GRCm39) |
S564P |
probably benign |
Het |
| Speer4a1 |
A |
T |
5: 26,239,960 (GRCm39) |
C263* |
probably null |
Het |
| Susd1 |
C |
A |
4: 59,411,359 (GRCm39) |
C158F |
possibly damaging |
Het |
| Vmn2r6 |
C |
T |
3: 64,463,953 (GRCm39) |
V294M |
probably benign |
Het |
|
| Other mutations in Mcm8 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00470:Mcm8
|
APN |
2 |
132,669,457 (GRCm39) |
missense |
probably benign |
|
|
IGL00479:Mcm8
|
APN |
2 |
132,659,094 (GRCm39) |
missense |
probably benign |
|
|
IGL00573:Mcm8
|
APN |
2 |
132,674,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL00847:Mcm8
|
APN |
2 |
132,661,594 (GRCm39) |
missense |
probably benign |
0.29 |
|
IGL00978:Mcm8
|
APN |
2 |
132,663,326 (GRCm39) |
missense |
probably benign |
|
|
IGL01390:Mcm8
|
APN |
2 |
132,679,998 (GRCm39) |
splice site |
probably benign |
|
|
IGL01785:Mcm8
|
APN |
2 |
132,669,868 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL01786:Mcm8
|
APN |
2 |
132,669,868 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL02216:Mcm8
|
APN |
2 |
132,681,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03191:Mcm8
|
APN |
2 |
132,663,362 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
madamina
|
UTSW |
2 |
132,674,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4687001:Mcm8
|
UTSW |
2 |
132,659,097 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R0329:Mcm8
|
UTSW |
2 |
132,661,914 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R0330:Mcm8
|
UTSW |
2 |
132,661,914 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
R1520:Mcm8
|
UTSW |
2 |
132,681,375 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1771:Mcm8
|
UTSW |
2 |
132,685,476 (GRCm39) |
nonsense |
probably null |
|
|
R1967:Mcm8
|
UTSW |
2 |
132,684,662 (GRCm39) |
missense |
probably benign |
|
|
R2228:Mcm8
|
UTSW |
2 |
132,662,041 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R2418:Mcm8
|
UTSW |
2 |
132,666,658 (GRCm39) |
missense |
probably benign |
|
|
R4728:Mcm8
|
UTSW |
2 |
132,674,774 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4827:Mcm8
|
UTSW |
2 |
132,665,174 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4847:Mcm8
|
UTSW |
2 |
132,661,923 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4928:Mcm8
|
UTSW |
2 |
132,681,399 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4932:Mcm8
|
UTSW |
2 |
132,680,629 (GRCm39) |
missense |
probably benign |
0.09 |
|
R4962:Mcm8
|
UTSW |
2 |
132,680,689 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6044:Mcm8
|
UTSW |
2 |
132,673,600 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6650:Mcm8
|
UTSW |
2 |
132,663,327 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6685:Mcm8
|
UTSW |
2 |
132,684,570 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7006:Mcm8
|
UTSW |
2 |
132,665,181 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7176:Mcm8
|
UTSW |
2 |
132,661,992 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7328:Mcm8
|
UTSW |
2 |
132,674,777 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7486:Mcm8
|
UTSW |
2 |
132,681,440 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7631:Mcm8
|
UTSW |
2 |
132,669,963 (GRCm39) |
missense |
not run |
|
|
R7664:Mcm8
|
UTSW |
2 |
132,685,453 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7820:Mcm8
|
UTSW |
2 |
132,682,692 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R8090:Mcm8
|
UTSW |
2 |
132,673,569 (GRCm39) |
missense |
probably benign |
0.30 |
|
R8228:Mcm8
|
UTSW |
2 |
132,684,714 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8738:Mcm8
|
UTSW |
2 |
132,665,141 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Mcm8
|
UTSW |
2 |
132,669,487 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CAGGGAATTCCTTGTTCATTATGTG -3'
(R):5'- AAACACCCATTGCCAAGTGG -3'
Sequencing Primer
(F):5'- GCTCAGGCTTGAAATTGCAC -3'
(R):5'- AACTCCTATACGTGCCTGAAGGTG -3'
|
| Posted On |
2017-07-14 |
Incidental Mutation