Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
202865
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 7 open reading frame 33
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C7orf33
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q36.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017497 hsa-miR-335-5p Microarray 18185580
MIRT530607 hsa-miR-5000-5p PAR-CLIP 20371350
MIRT530606 hsa-miR-3973 PAR-CLIP 20371350
MIRT530605 hsa-miR-520g-3p PAR-CLIP 20371350
MIRT530604 hsa-miR-520h PAR-CLIP 20371350
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q8WU49
Protein name Uncharacterized protein C7orf33
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17702 DUF5548 1 177 Family of unknown function (DUF5548) Family
Sequence
Sequence length 177
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
Glioblastoma Glioblastoma N/A N/A GWAS