Incidental Mutation 'IGL00709:Orc1'
ID 12869
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Orc1
Ensembl Gene ENSMUSG00000028587
Gene Name origin recognition complex, subunit 1
Synonyms MmORC1, Orc1l
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL00709
Quality Score
Status
Chromosome 4
Chromosomal Location 108436651-108472030 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to T at 108447975 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000099805 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102744] [ENSMUST00000102744]
AlphaFold Q9Z1N2
PDB Structure Structure of free mouse ORC1 BAH domain [X-RAY DIFFRACTION]
Structure of mouse ORC1 BAH domain bound to H4K20me2 [X-RAY DIFFRACTION]
Predicted Effect probably null
Transcript: ENSMUST00000102744
SMART Domains Protein: ENSMUSP00000099805
Gene: ENSMUSG00000028587

DomainStartEndE-ValueType
BAH 44 170 1.88e-31 SMART
low complexity region 394 417 N/A INTRINSIC
AAA 505 656 1e-7 SMART
Cdc6_C 757 837 5.45e-12 SMART
Predicted Effect probably null
Transcript: ENSMUST00000102744
SMART Domains Protein: ENSMUSP00000099805
Gene: ENSMUSG00000028587

DomainStartEndE-ValueType
BAH 44 170 1.88e-31 SMART
low complexity region 394 417 N/A INTRINSIC
AAA 505 656 1e-7 SMART
Cdc6_C 757 837 5.45e-12 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000126668
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130162
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139772
Predicted Effect noncoding transcript
Transcript: ENSMUST00000143497
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The origin recognition complex (ORC) is a highly conserved six subunits protein complex essential for the initiation of the DNA replication in eukaryotic cells. Studies in yeast demonstrated that ORC binds specifically to origins of replication and serves as a platform for the assembly of additional initiation factors such as Cdc6 and Mcm proteins. The protein encoded by this gene is the largest subunit of the ORC complex. While other ORC subunits are stable throughout the cell cycle, the levels of this protein vary during the cell cycle, which has been shown to be controlled by ubiquitin-mediated proteolysis after initiation of DNA replication. This protein is found to be selectively phosphorylated during mitosis. It is also reported to interact with MYST histone acetyltransferase 2 (MyST2/HBO1), a protein involved in control of transcription silencing. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
Allele List at MGI
Other mutations in this stock
Total: 11 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atp6v1d T C 12: 78,896,528 (GRCm39) H113R probably benign Het
Cd59a A G 2: 103,944,425 (GRCm39) N91S probably benign Het
Ddx21 C A 10: 62,434,181 (GRCm39) E193* probably null Het
Mink1 T A 11: 70,503,845 (GRCm39) I1255N probably damaging Het
Prelid2 T A 18: 42,045,488 (GRCm39) N141Y probably damaging Het
Rad50 A G 11: 53,560,469 (GRCm39) L1051S possibly damaging Het
Sidt1 C T 16: 44,082,374 (GRCm39) probably benign Het
Slc25a24 A G 3: 109,066,670 (GRCm39) K275E probably damaging Het
Stx19 A G 16: 62,642,943 (GRCm39) N253S probably benign Het
Tanc2 A G 11: 105,689,621 (GRCm39) Y261C probably damaging Het
Wdr62 A G 7: 29,941,486 (GRCm39) L706P probably benign Het
Other mutations in Orc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00333:Orc1 APN 4 108,452,522 (GRCm39) splice site probably benign
IGL01124:Orc1 APN 4 108,445,984 (GRCm39) splice site probably benign
IGL01514:Orc1 APN 4 108,459,249 (GRCm39) missense probably damaging 0.97
IGL01677:Orc1 APN 4 108,461,782 (GRCm39) missense probably damaging 1.00
IGL01782:Orc1 APN 4 108,463,465 (GRCm39) missense possibly damaging 0.78
IGL01886:Orc1 APN 4 108,461,154 (GRCm39) splice site probably null
IGL01912:Orc1 APN 4 108,447,941 (GRCm39) missense probably damaging 1.00
IGL02057:Orc1 APN 4 108,445,926 (GRCm39) missense possibly damaging 0.53
IGL02155:Orc1 APN 4 108,447,874 (GRCm39) missense probably benign 0.00
IGL02311:Orc1 APN 4 108,457,171 (GRCm39) missense probably benign
IGL02616:Orc1 APN 4 108,452,676 (GRCm39) missense probably benign 0.00
R0012:Orc1 UTSW 4 108,452,843 (GRCm39) critical splice donor site probably null
R0195:Orc1 UTSW 4 108,471,505 (GRCm39) nonsense probably null
R0239:Orc1 UTSW 4 108,452,843 (GRCm39) critical splice donor site probably null
R0239:Orc1 UTSW 4 108,452,843 (GRCm39) critical splice donor site probably null
R0611:Orc1 UTSW 4 108,459,229 (GRCm39) missense probably benign
R1351:Orc1 UTSW 4 108,452,564 (GRCm39) missense probably benign 0.01
R1966:Orc1 UTSW 4 108,469,414 (GRCm39) missense probably damaging 1.00
R2018:Orc1 UTSW 4 108,447,897 (GRCm39) missense possibly damaging 0.95
R2398:Orc1 UTSW 4 108,459,166 (GRCm39) missense possibly damaging 0.68
R3110:Orc1 UTSW 4 108,461,757 (GRCm39) missense probably benign 0.01
R3112:Orc1 UTSW 4 108,461,757 (GRCm39) missense probably benign 0.01
R3712:Orc1 UTSW 4 108,461,218 (GRCm39) missense probably damaging 1.00
R3716:Orc1 UTSW 4 108,471,656 (GRCm39) missense probably damaging 1.00
R3829:Orc1 UTSW 4 108,462,828 (GRCm39) missense probably damaging 1.00
R4282:Orc1 UTSW 4 108,463,471 (GRCm39) missense probably benign 0.18
R4320:Orc1 UTSW 4 108,445,973 (GRCm39) missense probably benign
R4321:Orc1 UTSW 4 108,445,973 (GRCm39) missense probably benign
R4322:Orc1 UTSW 4 108,445,973 (GRCm39) missense probably benign
R4348:Orc1 UTSW 4 108,450,649 (GRCm39) missense probably damaging 0.98
R4562:Orc1 UTSW 4 108,459,252 (GRCm39) critical splice donor site probably null
R4772:Orc1 UTSW 4 108,436,765 (GRCm39) utr 5 prime probably benign
R4914:Orc1 UTSW 4 108,461,755 (GRCm39) missense probably damaging 1.00
R4964:Orc1 UTSW 4 108,471,670 (GRCm39) makesense probably null
R5219:Orc1 UTSW 4 108,447,966 (GRCm39) missense probably damaging 1.00
R5428:Orc1 UTSW 4 108,457,137 (GRCm39) missense probably benign 0.00
R5655:Orc1 UTSW 4 108,450,636 (GRCm39) missense probably benign 0.09
R5693:Orc1 UTSW 4 108,470,276 (GRCm39) missense probably benign 0.01
R5936:Orc1 UTSW 4 108,459,180 (GRCm39) missense probably benign 0.10
R5960:Orc1 UTSW 4 108,463,495 (GRCm39) missense possibly damaging 0.67
R6294:Orc1 UTSW 4 108,447,867 (GRCm39) missense probably benign 0.01
R6504:Orc1 UTSW 4 108,447,914 (GRCm39) missense probably benign 0.15
R6533:Orc1 UTSW 4 108,454,644 (GRCm39) missense probably benign 0.05
R6775:Orc1 UTSW 4 108,460,652 (GRCm39) missense probably damaging 1.00
R7123:Orc1 UTSW 4 108,445,884 (GRCm39) start codon destroyed probably damaging 0.99
R7156:Orc1 UTSW 4 108,452,656 (GRCm39) missense probably benign 0.00
R7327:Orc1 UTSW 4 108,445,911 (GRCm39) missense probably benign 0.01
R7552:Orc1 UTSW 4 108,445,951 (GRCm39) missense probably benign 0.41
R7842:Orc1 UTSW 4 108,462,744 (GRCm39) missense probably benign 0.00
R7899:Orc1 UTSW 4 108,460,568 (GRCm39) splice site probably null
R8033:Orc1 UTSW 4 108,462,761 (GRCm39) missense probably damaging 1.00
R9442:Orc1 UTSW 4 108,469,357 (GRCm39) missense probably benign 0.06
R9762:Orc1 UTSW 4 108,447,874 (GRCm39) missense probably benign 0.00
Posted On 2012-12-06