Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10467
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger HIT-type containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNHIT1
Synonyms (NCBI Gene) Gene synonyms aliases
CG1I, ZNFN4A1, p18(Hamlet)
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT029663 hsa-miR-26b-5p Microarray 19088304
MIRT1542907 hsa-miR-1324 CLIP-seq
MIRT1542908 hsa-miR-1915 CLIP-seq
MIRT1542909 hsa-miR-2467-5p CLIP-seq
MIRT1542910 hsa-miR-3119 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000812 Component Swr1 complex IBA 21873635
GO:0005515 Function Protein binding IPI 15647280, 16230350, 17380123, 17577209, 17892483, 18624398, 20473270, 24463511, 25416956, 28514442, 32296183, 32814053
GO:0005634 Component Nucleus IDA 17892483
GO:0005654 Component Nucleoplasm IDA
GO:0031491 Function Nucleosome binding IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618617 21688 ENSG00000106400
Protein
UniProt ID O43257
Protein name Zinc finger HIT domain-containing protein 1 (Cyclin-G1-binding protein 1) (Zinc finger protein subfamily 4A member 1) (p18 Hamlet)
Protein function Plays a role in chromatin remodeling by promoting the incorporation of histone variant H2AZ1/H2A.Z into the genome to regulate gene expression (PubMed:20473270, PubMed:35175558). Promotes SRCAP complex-mediated deposition of histone variant H2AZ
PDB 8X15 , 8X19 , 8X1C
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF04438 zf-HIT 113 142 HIT zinc finger Domain
Tissue specificity TISSUE SPECIFICITY: Expressed abundantly in liver, but weakly in skeletal muscle, ovary and small intestine. {ECO:0000269|PubMed:17892483}.
Sequence
MVEKKTSVRSQDPGQRRVLDRAARQRRINRQLEALENDNFQDDPHAGLPQLGKRLPQFDD
DADTGKKKKKTRGDHFKLRFRKNFQALLEEQNLSVAEGPNYLTACAGPPSRPQRPFCAVC
GFPSPYTCVSCGARYCTVRCLG
THQETRCLKWTV
Sequence length 154
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  ATP-dependent chromatin remodeling  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Colorectal cancer Colorectal Carcinoma rs137854568, rs137854573, rs137854575, rs387906234, rs121908380, rs121908702, rs267606674, rs794729661, rs121909055, rs281865417, rs267606884, rs28934575, rs587776769, rs104893815, rs587776800
View all (467 more)
Associations from Text Mining
Disease Name Relationship Type References
Mitochondrial Diseases Inhibit 35175558, 37178741
Parkinson Disease Associate 35175558, 37178741