Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79970
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger family member 767, pseudogene
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF767P
Synonyms (NCBI Gene) Gene synonyms aliases
ZNF767
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q36.1
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 Q75MW2
Protein name Protein ZNF767 (Zinc finger protein 767 pseudogene)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12417 DUF3669 11 81 Zinc finger protein Family
Sequence
MEEAAAAPISPWTMAATIQAMERKIESQAAHLLSLEGQTGMAEKKLADCEKTAVEFGNQL
EGKWAVLGTLLQEYGLLQRRL
ENVENLLHNRNFWILRLPPGSKGESPKTTPSPSPRSSPR
LNKGRSPATGAALTPRFQMFLWTPVQMQKLRPSRD
Sequence length 155
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
Amyotrophic Lateral Sclerosis Amyotrophic lateral sclerosis N/A N/A GWAS
Cerebral Aneurysm Cerebral aneurysm N/A N/A GWAS
Diabetes Type 2 diabetes N/A N/A GWAS
Glioblastoma Glioblastoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Tertiary Lymphoid Structures Associate 32345988