Comparative GO Graph (mouse, human, rat, zebrafish)

• Source: Alliance of Genome Resources

Graphs for Molecular Function, Cellular Component, Biological Process generated Fri Mar 10 16:36:22 2023.

Complete table of the annotations represented in this image is provided below.

Graphs display curated GO classifications for mouse, human, rat and zebrafish orthologs annotated from the biomedical literature.

• This class contains
  • Human genes CHD1L
  • Mouse genes Chd1l
  • Rat genes Chd1l
  • Zfish genes chd1l
• Annotations are indicated with nodes colored by organism: Human, Mouse, Rat, Zfish
• Relations between GO terms are indicated by colored edges "is_a"; "part_of"; "regulates"; "positively_regulates"; "negatively_regulates"
• GO annotations: Human from GOA; Mouse from MGI; Rat from RGD; Zebrafish from ZFIN.
• Only experimental annotations are displayed: EXP, IDA, IEP, IGI, IMP, IPI, HTP, HDA, HMP, HGI, HEP. Evidence codes are listed at the bottom of the page.

Molecular Function

Cellular Component

Biological Process

Full set of experimental annotations for Human-Rat-Zebrafish genes considered orthologs of Mouse in the Alliance stringent orthology set Chd1l

Category	ID	Classification term	Gene	Evidence	Inferred from	Organism	Reference
Molecular Function	GO:0016887	ATP hydrolysis activity	CHD1L	IMP		Human	PMID:19661379
Molecular Function	GO:0140658	ATP-dependent chromatin remodeler activity	CHD1L	IDA		Human	PMID:29220652
Molecular Function	GO:0140658	ATP-dependent chromatin remodeler activity	CHD1L	IDA		Human	PMID:29220653
Molecular Function	GO:0140658	ATP-dependent chromatin remodeler activity	CHD1L	IDA		Human	PMID:33357431
Molecular Function	GO:0140658	ATP-dependent chromatin remodeler activity	CHD1L	IDA		Human	PMID:34210977
Molecular Function	GO:0140658	ATP-dependent chromatin remodeler activity	CHD1L	IDA		Human	PMID:34486521
Molecular Function	GO:0140566	histone reader activity	CHD1L	IDA		Human	PMID:34874266
Molecular Function	GO:0031491	nucleosome binding	CHD1L	IDA		Human	PMID:33357431
Molecular Function	GO:0031491	nucleosome binding	CHD1L	IDA		Human	PMID:34210977
Molecular Function	GO:0031491	nucleosome binding	CHD1L	IDA		Human	PMID:34486521
Molecular Function	GO:0000166	nucleotide binding	CHD1L	IDA		Human	PMID:19661379
Molecular Function	GO:0160004	poly-ADP-D-ribose modification-dependent protein binding	CHD1L	IDA		Human	PMID:29220652
Molecular Function	GO:0160004	poly-ADP-D-ribose modification-dependent protein binding	CHD1L	IDA		Human	PMID:29220653
Molecular Function	GO:0160004	poly-ADP-D-ribose modification-dependent protein binding	CHD1L	IDA		Human	PMID:34486521
Molecular Function	GO:0160004	poly-ADP-D-ribose modification-dependent protein binding	CHD1L	IDA		Human	PMID:34874266
Molecular Function	GO:0005515	protein binding	CHD1L	IPI	UniProtKB:P09874	Human	PMID:19661379
Molecular Function	GO:0005515	protein binding	CHD1L	IPI	UniProtKB:O76071	Human	PMID:23891004
Cellular Component	GO:0005829	cytosol	CHD1L	IDA		Human	GO_REF:0000052
Cellular Component	GO:0005654	nucleoplasm	CHD1L	IDA		Human	GO_REF:0000052
Cellular Component	GO:0005634	nucleus	CHD1L	IDA		Human	PMID:19661379
Cellular Component	GO:0005886	plasma membrane	CHD1L	IDA		Human	GO_REF:0000052
Cellular Component	GO:0035861	site of double-strand break	CHD1L	IDA		Human	PMID:29220652
Cellular Component	GO:0035861	site of double-strand break	CHD1L	IDA		Human	PMID:29220653
Biological Process	GO:0006338	chromatin remodeling	CHD1L	IDA		Human	PMID:19661379
Biological Process	GO:0006974	DNA damage response	CHD1L	IDA		Human	PMID:19661379
Biological Process	GO:0006974	DNA damage response	CHD1L	IDA		Human	PMID:29220652
Biological Process	GO:0006974	DNA damage response	CHD1L	IDA		Human	PMID:29220653

Gene Ontology Evidence Code Abbreviations:

  EXP Inferred from experiment

  IDA Inferred from direct assay

  IEP Inferred from expression pattern

  IGI Inferred from genetic interaction

  IMP Inferred from mutant phenotype

  IPI Inferred from physical interaction

  HTP Inferred from High Throughput Experiment

  HDA Inferred from High Throughput Direct Assay

  HMP Inferred from High Throughput Mutant Phenotype

  HGI Inferred from High Throughput Genetic Interaction

  HEP Inferred from High Throughput Expression Pattern