Incidental Mutation 'R6453:Mcm4'
ID 520130
Institutional Source Beutler Lab
Gene Symbol Mcm4
Ensembl Gene ENSMUSG00000022673
Gene Name minichromosome maintenance complex component 4
Synonyms mCdc21, Mcmd4, 19G, Cdc21
MMRRC Submission 044589-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R6453 (G1)
Quality Score 225.009
Status Not validated
Chromosome 16
Chromosomal Location 15441761-15455264 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 15448273 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Glutamine at position 428 (L428Q)
Ref Sequence ENSEMBL: ENSMUSP00000023353 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023353]
AlphaFold P49717
Predicted Effect probably damaging
Transcript: ENSMUST00000023353
AA Change: L428Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000023353
Gene: ENSMUSG00000022673
AA Change: L428Q

DomainStartEndE-ValueType
low complexity region 2 21 N/A INTRINSIC
low complexity region 23 40 N/A INTRINSIC
MCM 266 769 N/A SMART
AAA 501 653 7.04e-3 SMART
Blast:MCM 781 849 3e-11 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000229606
Predicted Effect probably benign
Transcript: ENSMUST00000230437
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.6%
  • 20x: 92.2%
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 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, 6 and 7 proteins possesses DNA helicase activity, and may act as a DNA unwinding enzyme. The phosphorylation of this protein by CDC2 kinase reduces the DNA helicase activity and chromatin binding of the MCM complex. This gene is mapped to a region on the chromosome 8 head-to-head next to the PRKDC/DNA-PK, a DNA-activated protein kinase involved in the repair of DNA double-strand breaks. Alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]
PHENOTYPE: Disruption of this allele cause chromosomal instability as assessed by micronucleus levels in erythrocytes. Mice homozygous for a spontaneous allele exhibit early onset T cell acute lymphoblastic leukemia. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik C T 17: 35,879,109 (GRCm39) S149L possibly damaging Het
A830018L16Rik A T 1: 11,868,782 (GRCm39) D354V possibly damaging Het
Acta2 G A 19: 34,224,057 (GRCm39) T150I probably damaging Het
Adgra1 T A 7: 139,455,343 (GRCm39) S324T probably benign Het
Ankrd44 A T 1: 54,696,863 (GRCm39) probably null Het
B430306N03Rik T A 17: 48,623,764 (GRCm39) W22R probably damaging Het
Ccdc162 A T 10: 41,426,821 (GRCm39) V2024E probably damaging Het
Cers6 C T 2: 68,877,513 (GRCm39) H164Y probably benign Het
Chd3 T A 11: 69,240,938 (GRCm39) K1458* probably null Het
Cimip1 A G 2: 173,370,052 (GRCm39) Y109C probably benign Het
Col3a1 G A 1: 45,378,538 (GRCm39) probably benign Het
Cyb5d2 T G 11: 72,673,586 (GRCm39) T3P probably benign Het
Dennd1b A G 1: 139,071,686 (GRCm39) Y468C probably benign Het
Dnajc14 A G 10: 128,643,359 (GRCm39) E427G probably damaging Het
Exoc7 T C 11: 116,184,795 (GRCm39) probably null Het
Fat2 A G 11: 55,173,042 (GRCm39) I2557T probably benign Het
Flt1 T C 5: 147,620,751 (GRCm39) D131G possibly damaging Het
Frem1 G T 4: 82,833,062 (GRCm39) S1858* probably null Het
Garem1 T A 18: 21,281,796 (GRCm39) I187F probably damaging Het
Gldc A T 19: 30,093,917 (GRCm39) I700N probably damaging Het
Gpatch4 A G 3: 87,962,312 (GRCm39) E175G probably damaging Het
Gria2 A G 3: 80,648,281 (GRCm39) Y152H possibly damaging Het
H2-Q2 C T 17: 35,563,871 (GRCm39) L251F probably benign Het
Hectd4 G A 5: 121,488,655 (GRCm39) G3649R probably damaging Het
Hormad1 A G 3: 95,485,568 (GRCm39) E252G probably benign Het
Kif14 A G 1: 136,410,042 (GRCm39) probably null Het
Lmcd1 A G 6: 112,292,789 (GRCm39) T214A probably benign Het
Macrod2 A G 2: 142,018,545 (GRCm39) E226G probably damaging Het
Msh6 T A 17: 88,293,167 (GRCm39) Y641N probably damaging Het
Myo7a C T 7: 97,722,374 (GRCm39) V1184M probably benign Het
Nipa2 A T 7: 55,585,569 (GRCm39) M142K probably damaging Het
Or8b1c T C 9: 38,384,871 (GRCm39) I276T probably benign Het
Parvg A T 15: 84,213,126 (GRCm39) E122V probably null Het
Pclo T A 5: 14,726,803 (GRCm39) probably benign Het
Pik3cd A G 4: 149,736,759 (GRCm39) V933A probably damaging Het
Pira1 C G 7: 3,740,319 (GRCm39) A301P probably damaging Het
Qpctl C T 7: 18,875,222 (GRCm39) V337I probably damaging Het
Qrfprl G A 6: 65,430,014 (GRCm39) G237S possibly damaging Het
Ralgapa1 A G 12: 55,785,104 (GRCm39) W719R probably damaging Het
Rangrf A G 11: 68,864,378 (GRCm39) L28P probably damaging Het
Rbbp9 G T 2: 144,391,054 (GRCm39) Q38K probably benign Het
Rnf169 C T 7: 99,584,434 (GRCm39) M246I probably benign Het
Rsf1 CGGCGGCGG CGGCGGCGGGGGCGGCGG 7: 97,229,124 (GRCm39) probably benign Het
Sdk1 A G 5: 142,082,676 (GRCm39) D1098G probably damaging Het
Sgsm3 T A 15: 80,895,515 (GRCm39) S689T probably damaging Het
Slc13a3 C T 2: 165,253,867 (GRCm39) V429M possibly damaging Het
Slc30a5 A T 13: 100,951,197 (GRCm39) D228E probably benign Het
Slc46a3 A G 5: 147,823,200 (GRCm39) I214T possibly damaging Het
Slc7a15 T C 12: 8,584,490 (GRCm39) M347V possibly damaging Het
Slc9a2 A T 1: 40,781,781 (GRCm39) I337F possibly damaging Het
Sostdc1 C A 12: 36,364,407 (GRCm39) P39T probably benign Het
Speg A G 1: 75,394,616 (GRCm39) N1775S probably benign Het
Spg7 A G 8: 123,806,162 (GRCm39) K291E possibly damaging Het
Sptbn2 A T 19: 4,794,208 (GRCm39) R1471W possibly damaging Het
Thada T C 17: 84,723,751 (GRCm39) E1101G probably damaging Het
Trpm6 G A 19: 18,807,354 (GRCm39) A1033T probably damaging Het
Ttll6 G A 11: 96,049,553 (GRCm39) R757H probably benign Het
Other mutations in Mcm4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01823:Mcm4 APN 16 15,443,995 (GRCm39) missense probably damaging 1.00
IGL01982:Mcm4 APN 16 15,448,284 (GRCm39) missense possibly damaging 0.57
IGL02382:Mcm4 APN 16 15,442,602 (GRCm39) missense probably damaging 1.00
PIT4687001:Mcm4 UTSW 16 15,454,577 (GRCm39) missense probably benign 0.01
R0200:Mcm4 UTSW 16 15,447,503 (GRCm39) missense probably benign 0.41
R0540:Mcm4 UTSW 16 15,449,979 (GRCm39) critical splice donor site probably null
R0607:Mcm4 UTSW 16 15,449,979 (GRCm39) critical splice donor site probably null
R2064:Mcm4 UTSW 16 15,452,333 (GRCm39) missense possibly damaging 0.75
R4240:Mcm4 UTSW 16 15,445,570 (GRCm39) nonsense probably null
R4604:Mcm4 UTSW 16 15,447,527 (GRCm39) missense probably damaging 1.00
R4871:Mcm4 UTSW 16 15,452,374 (GRCm39) nonsense probably null
R5070:Mcm4 UTSW 16 15,443,434 (GRCm39) missense probably damaging 1.00
R5125:Mcm4 UTSW 16 15,453,167 (GRCm39) missense probably benign 0.21
R5178:Mcm4 UTSW 16 15,453,167 (GRCm39) missense probably benign 0.21
R5245:Mcm4 UTSW 16 15,448,289 (GRCm39) missense probably benign 0.02
R5513:Mcm4 UTSW 16 15,448,378 (GRCm39) missense probably benign 0.26
R5696:Mcm4 UTSW 16 15,443,434 (GRCm39) missense probably damaging 1.00
R6753:Mcm4 UTSW 16 15,447,226 (GRCm39) missense possibly damaging 0.91
R6909:Mcm4 UTSW 16 15,446,561 (GRCm39) missense probably damaging 1.00
R6937:Mcm4 UTSW 16 15,454,199 (GRCm39) missense probably benign
R7402:Mcm4 UTSW 16 15,455,042 (GRCm39) start codon destroyed probably null
R7483:Mcm4 UTSW 16 15,448,306 (GRCm39) missense probably benign 0.05
R8275:Mcm4 UTSW 16 15,452,435 (GRCm39) missense probably damaging 0.98
R8487:Mcm4 UTSW 16 15,450,042 (GRCm39) missense probably damaging 1.00
R8683:Mcm4 UTSW 16 15,453,138 (GRCm39) missense probably damaging 0.99
R8742:Mcm4 UTSW 16 15,443,430 (GRCm39) missense possibly damaging 0.52
R8929:Mcm4 UTSW 16 15,448,289 (GRCm39) missense probably benign 0.02
R9138:Mcm4 UTSW 16 15,447,200 (GRCm39) missense probably damaging 1.00
R9440:Mcm4 UTSW 16 15,453,175 (GRCm39) nonsense probably null
Z1177:Mcm4 UTSW 16 15,450,080 (GRCm39) missense possibly damaging 0.55
Z1177:Mcm4 UTSW 16 15,447,318 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TACCCATAGAAGACAGTAACAGTGG -3'
(R):5'- GCTGTCGACTGAGCTTACAG -3'

Sequencing Primer
(F):5'- AAGACAGTAACAGTGGCAAATATATC -3'
(R):5'- CTGTCGACTGAGCTTACAGAGAAG -3'
Posted On 2018-06-06