Incidental Mutation 'IGL03002:Cdc123'
ID 407408
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cdc123
Ensembl Gene ENSMUSG00000039128
Gene Name cell division cycle 123
Synonyms G431001I09Rik
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL03002
Quality Score
Status
Chromosome 2
Chromosomal Location 5799105-5849975 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 5803166 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000043033 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043864]
AlphaFold Q8CII2
Predicted Effect probably benign
Transcript: ENSMUST00000043864
SMART Domains Protein: ENSMUSP00000043033
Gene: ENSMUSG00000039128

DomainStartEndE-ValueType
Pfam:D123 14 314 3e-107 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124662
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130142
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acadl T C 1: 66,876,128 (GRCm39) I398V probably benign Het
Adcy4 A T 14: 56,011,013 (GRCm39) C635S probably benign Het
Aoc1l3 A G 6: 48,964,052 (GRCm39) H20R probably benign Het
Asic4 C A 1: 75,427,967 (GRCm39) D164E possibly damaging Het
C8g T A 2: 25,388,823 (GRCm39) *203L probably null Het
Cad T C 5: 31,212,330 (GRCm39) V11A probably benign Het
Cckar T C 5: 53,860,247 (GRCm39) N194S probably damaging Het
Chrm5 T C 2: 112,310,706 (GRCm39) T137A probably damaging Het
Cyp1a1 A G 9: 57,609,724 (GRCm39) probably benign Het
Dapk3 G T 10: 81,026,437 (GRCm39) E187* probably null Het
Dmtf1 T C 5: 9,190,474 (GRCm39) E80G probably damaging Het
Dusp19 T A 2: 80,461,279 (GRCm39) N189K probably damaging Het
Gfral A G 9: 76,104,520 (GRCm39) V164A possibly damaging Het
Hk1 A T 10: 62,107,578 (GRCm39) V799E probably damaging Het
Iars2 C T 1: 185,055,013 (GRCm39) probably null Het
Jcad T A 18: 4,675,153 (GRCm39) Y972N probably benign Het
Lrp1 A T 10: 127,425,505 (GRCm39) D708E probably damaging Het
Mbtd1 T A 11: 93,815,316 (GRCm39) H301Q probably benign Het
Med12 A G X: 100,339,461 (GRCm39) T2004A probably benign Het
Mib1 T C 18: 10,798,356 (GRCm39) I739T possibly damaging Het
Mthfsd C T 8: 121,835,018 (GRCm39) probably benign Het
Mybpc3 T G 2: 90,954,234 (GRCm39) F369C probably damaging Het
Nfatc2 C T 2: 168,376,904 (GRCm39) V329M probably damaging Het
Ngef A T 1: 87,437,114 (GRCm39) probably null Het
Nlrp1b T C 11: 71,059,685 (GRCm39) E759G probably benign Het
Or10aa3 C A 1: 173,878,191 (GRCm39) T84N probably benign Het
Prdm4 T C 10: 85,729,016 (GRCm39) E790G probably benign Het
Psmd12 A G 11: 107,376,607 (GRCm39) D81G probably benign Het
Rnf144b A G 13: 47,396,359 (GRCm39) H232R probably damaging Het
Sec63 C T 10: 42,686,905 (GRCm39) T475M possibly damaging Het
Slc16a4 A T 3: 107,208,102 (GRCm39) N204I probably benign Het
Socs1 T C 16: 10,602,404 (GRCm39) N111S probably damaging Het
Srpra A G 9: 35,126,017 (GRCm39) N432D probably damaging Het
Srrm2 A G 17: 24,034,708 (GRCm39) probably benign Het
Tgoln1 A G 6: 72,593,055 (GRCm39) S142P possibly damaging Het
Trbv13-1 A G 6: 41,093,169 (GRCm39) N34S probably benign Het
Vmn2r26 T C 6: 124,016,754 (GRCm39) V406A possibly damaging Het
Vsig1 G T X: 139,827,088 (GRCm39) G79V probably damaging Het
Other mutations in Cdc123
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Cdc123 APN 2 5,809,746 (GRCm39) missense probably benign 0.01
IGL00422:Cdc123 APN 2 5,803,260 (GRCm39) missense probably benign 0.07
IGL01860:Cdc123 APN 2 5,808,752 (GRCm39) splice site probably benign
Sinking UTSW 2 5,803,174 (GRCm39) missense possibly damaging 0.82
R0563:Cdc123 UTSW 2 5,803,212 (GRCm39) missense probably benign
R1412:Cdc123 UTSW 2 5,808,776 (GRCm39) missense possibly damaging 0.80
R1584:Cdc123 UTSW 2 5,808,788 (GRCm39) critical splice acceptor site probably null
R1838:Cdc123 UTSW 2 5,799,702 (GRCm39) splice site probably null
R2064:Cdc123 UTSW 2 5,800,354 (GRCm39) splice site probably benign
R2144:Cdc123 UTSW 2 5,815,617 (GRCm39) missense probably benign 0.19
R4082:Cdc123 UTSW 2 5,815,566 (GRCm39) intron probably benign
R4679:Cdc123 UTSW 2 5,849,703 (GRCm39) missense probably damaging 1.00
R4970:Cdc123 UTSW 2 5,809,748 (GRCm39) missense possibly damaging 0.59
R5089:Cdc123 UTSW 2 5,809,811 (GRCm39) missense probably benign 0.00
R5112:Cdc123 UTSW 2 5,809,748 (GRCm39) missense possibly damaging 0.59
R5691:Cdc123 UTSW 2 5,827,986 (GRCm39) missense probably benign 0.00
R5914:Cdc123 UTSW 2 5,803,174 (GRCm39) missense possibly damaging 0.82
R7860:Cdc123 UTSW 2 5,808,775 (GRCm39) missense probably benign 0.00
R8695:Cdc123 UTSW 2 5,826,174 (GRCm39) missense possibly damaging 0.69
R8865:Cdc123 UTSW 2 5,800,235 (GRCm39) intron probably benign
R9018:Cdc123 UTSW 2 5,849,683 (GRCm39) missense probably benign 0.00
R9265:Cdc123 UTSW 2 5,808,765 (GRCm39) missense possibly damaging 0.50
Z1176:Cdc123 UTSW 2 5,809,796 (GRCm39) missense probably damaging 0.97
Posted On 2016-08-02