Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
50626
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger TRAF-type containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZFTRAF1
Synonyms (NCBI Gene) Gene synonyms aliases
CHRP, CYHR1
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q24.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT920213 hsa-miR-3153 CLIP-seq
MIRT920214 hsa-miR-3665 CLIP-seq
MIRT920215 hsa-miR-3689a-3p CLIP-seq
MIRT920216 hsa-miR-3689c CLIP-seq
MIRT920217 hsa-miR-4514 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 28514442, 33961781
GO:0005634 Component Nucleus IBA
GO:0005635 Component Nuclear envelope IEA
GO:0005737 Component Cytoplasm IEA
GO:0008270 Function Zinc ion binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616635 17806 ENSG00000187954
Protein
UniProt ID P0DTL6
Protein name Zinc finger TRAF-type-containing protein 1 (Cysteine and histidine-rich protein 1)
Family and domains
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Neurodevelopmental Disorders complex neurodevelopmental disorder, neurodevelopmental disorder N/A N/A GenCC
Non-Syndromic Intellectual Disability autosomal recessive non-syndromic intellectual disability N/A N/A ClinVar