Gene

ncaph

ID
ZDB-GENE-070112-652
Name
non-SMC condensin I complex, subunit H
Symbol
ncaph Nomenclature History
Previous Names
  • si:dkeyp-86b9.4
  • zgc:158618
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Is predicted to enable chromatin binding activity. Involved in mitotic chromosome condensation. Acts upstream of or within mitotic sister chromatid segregation. Predicted to be located in chromosome and cytoplasm. Predicted to be part of condensin complex. Is expressed in brain; ciliary marginal zone; optic cup; and spinal cord. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly. Orthologous to human NCAPH (non-SMC condensin I complex subunit H).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Seipold et al., 2009
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
2 figures from Seipold et al., 2009
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With ncaph Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
?Microcephaly 23, primary, autosomal recessive 617985
Associated With ncaph Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR022816 Condensin complex subunit 2/barren
Domain Details Per Protein
Protein Length Condensin complex subunit 2/barren
UniProtKB:A2BG39 690
UniProtKB:A1L231 690
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations