Gene Gene information from NCBI Gene database.
Entrez ID 54892
Gene name Non-SMC condensin II complex subunit G2
Gene symbol NCAPG2
Synonyms (NCBI Gene)
3KSCAP-G2CAPG2LUZP5MTBhCAP-G2
Chromosome 7
Chromosome location 7q36.3
Summary This gene encodes a protein that belongs to the Condensin2nSMC family of proteins. The encoded protein is a regulatory subunit of the condensin II complex which, along with the condensin I complex, plays a role in chromosome assembly and segregation durin
SNPs SNP information provided by dbSNP.
3
SNP ID Visualize variation Clinical significance Consequence
rs772209292 G>A Pathogenic Coding sequence variant, non coding transcript variant, missense variant
rs1299537743 T>C Pathogenic Missense variant, coding sequence variant, intron variant, non coding transcript variant
rs1563515856 T>G Pathogenic Coding sequence variant, non coding transcript variant, missense variant
miRNA miRNA information provided by mirtarbase database.
214
miRTarBase ID miRNA Experiments Reference
MIRT005219 hsa-let-7b-5p pSILAC 18668040
MIRT030328 hsa-miR-26b-5p Microarray 19088304
MIRT005219 hsa-let-7b-5p Proteomics;Other 18668040
MIRT052754 hsa-miR-1260b CLASH 23622248
MIRT712733 hsa-miR-3127-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0000070 Process Mitotic sister chromatid segregation IBA
GO:0000794 Component Condensed nuclear chromosome IEA
GO:0000794 Component Condensed nuclear chromosome ISO
GO:0000796 Component Condensin complex IBA
GO:0000796 Component Condensin complex IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608532 21904 ENSG00000146918
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86XI2
Protein name Condensin-2 complex subunit G2 (Chromosome-associated protein G2) (CAP-G2) (hCAP-G2) (Leucine zipper protein 5) (Non-SMC condensin II complex subunit G2)
Protein function Regulatory subunit of the condensin-2 complex, a complex which establishes mitotic chromosome architecture and is involved in physical rigidity of the chromatid axis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12422 Condensin2nSMC 212 362 Condensin II non structural maintenance of chromosomes subunit Family
Sequence
MEKRETFVQAVSKELVGEFLQFVQLDKEASDPFSLNELLDELSRKQKEELWQRLKNLLTD
VLLESPVDGWQVVEAQGEDNMETEHGSKMRKSIEIIYAITSVILASVSVINESENYEALL
ECVIILNGILYALPESERKLQSSIQDLCVTWWEKGLPAKEDTGKTAFVMLLRRSLETKTG
ADVCRLWRIHQALYCFDYDLEESGEIKDMLLECFININYIKKEEGRRFLSCLFNWNINFI
KMIHGTIKNQLQGLQKSLMVYIAEIYFRAWKKASGKILEAIENDCIQDFMFHGIHLPRRS
PVHSKVREVLSYFHHQKKVRQGVEEMLYRLYKPILWRGLKARNSEVRSNAALLFVEAFPI
RD
PNLHAIEMDSEIQKQFEELYSLLEDPYPMVRSTGILGVCKITSKYWEMMPPTILIDLL
KKVTGELAFDTSSADVRCSVFKCLPMILDNKLSHPLLEQLLPALRYSLHDNSEKVRVAFV
DMLLKIKAVRAAKFWKICPMEHILVRLETDSRPVSRRLVSLIFNSFLPVNQPEEVWCERC
VTLVQMNHAAARRFYQYAHEHTACTNIAKLIHVIRHCLNACIQRAVREPPEDEEEEDGRE
KENVTVLDKTLSVNDVACMAGLLEIIVILWKSIDRSMENNKEAKLYTINKFASVLPEYLK
VFKDDRCKIPLFMLMSFMPASAVPPFSCGVISTLRSREEGAVDKSYCTLLDCLCSWGQVG
HILELVDNWLPTEHAQAKSNTASKGRVQIHDTRPVKPELALVYIEYLLTHPKNRECLLSA
PRKKLNHLLKALETSKADLESLLQTPGGKPRGFSEAAAPRAFGLHCRLSIHLQHKFCSEG
KVYLSMLEDTGFWLESKILSFIQDQEEDYLKLHRVIYQQIIQTYLTVCKDVVMVGLGDHQ
FQMQLLQRSLGIMQTVKGFFYVSLLLDILKEITGSSLIQKTDSDEEVAMLLDTVQKVFQK
MLECIARSFRKQPEEGLRLLYSVQRPLHEFITAVQSRHTDTPVHRGVLSTLIAGPVVEIS
HQLRKVSDVEELTPPEHLSDLPPFSRCLIGIIIKSSNVVRSFLDELKACVASNDIEGIVC
LTAAVHIILVINAGKHKSSKVREVAATVHRKLKTFMEITLEEDSIERFLYESSSRTLGEL
LNS
Sequence length 1143
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Condensation of Prophase Chromosomes
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
51
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Khan-Khan-Katsanis syndrome Likely pathogenic rs1835253194 RCV002470584
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
NCAPG2-related disorder Likely benign; Uncertain significance; Benign rs144010950, rs199564693, rs61752310, rs76593772, rs61763006, rs187542564, rs192363025, rs145268029, rs61745702, rs138977477, rs61752311, rs115631698, rs372309426, rs148607072, rs3214000
View all (15 more)
RCV003910983
RCV003917831
RCV003919037
RCV003919040
RCV003954090
RCV003919217
RCV003909214
RCV003919626
RCV003929865
RCV003902139
RCV003916902
RCV003973872
RCV003944535
RCV003944583
RCV003917232
RCV003959147
RCV003969322
RCV003917371
RCV003966844
RCV003972172
RCV003926094
RCV003925875
RCV003926095
RCV003916137
RCV003918518
RCV003910468
RCV003910621
RCV003920722
RCV003920723
RCV003920533
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 27862966
Carcinogenesis Associate 37248471
Carcinoma Non Small Cell Lung Stimulate 27862966
Carcinoma Squamous Cell Associate 36138066, 37248471
Cholesteatoma Congenital Associate 26335306
Colorectal Neoplasms Stimulate 38637125
Lymphatic Metastasis Stimulate 27862966
Melanoma Associate 17611626
Microcephaly Primary Autosomal Recessive 1 Associate 23983231
Neoplasm Metastasis Inhibit 36776838