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Cancer Genome Characterization Initiative

Visit the database of genomic characterization data for multiple tumor types.


Gene Info

Gene Information For:Hs. ZNF469, Zinc finger protein 469
Sequence ID:NM_001127464
RefSeqGene ID:NG_012236
Entrez Gene ID:84627
Ensembl ID:ENSG00000225614

Database Links

UniGeneEntrez GeneOMIMEnsembl GeneSNPSNP: GeneViewSNP: VarViewAssembliesCancer AberrationsRNAi

Gene Expression Data


Associated Diseases (from OMIM)

DiseaseOther Genes
BRITTLE CORNEA SYNDROME 

Cytogenetic Location (from UniGene)

Cytogenetic Location:16q24Mitelman Breakpoint Data

Chromosomal Position (from UCSC)

Chromosomal Position:16: 88498328 - 88507157

NM_001127464 exon info from UCSC:

Transcript StartTranscript EndChromosomal Start Chromosomal End
131798849387888497056
3180132038849714188507164

Protein Infomation

RefSeq
mRNAProteinSwissProtPfam
NM_001127464 NP_001120936 Q96JG9  

Related Sequences

 
mRNAGenPeptSwissProt
AB058761 BAB47487 Q96JG9

Homologs (from HomoloGene)
Note: Both orthologs and paralogs are included.
Organism Symbol Protein Homolog Similarity
(% aa unchanged)
Organism Symbol Entrez
Gene
Gene Info Protein
H.sapiens ZNF469 NP_001120936 M.musculus Gm22 195209 Gene Info XP_111398 52

Gene Ontology
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)