Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
65998
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger translocation associated
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZFTA
Synonyms (NCBI Gene) Gene synonyms aliases
C11orf95
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q13.1
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
GO:0045892 Process Negative regulation of DNA-templated transcription IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
615699 28449 ENSG00000188070
Protein
UniProt ID C9JLR9
Protein name Zinc finger translocation-associated protein (ZFTA)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF18658 zf-C2H2_12 106 169 Spin-doc zinc-finger Domain
PF18658 zf-C2H2_12 265 328 Spin-doc zinc-finger Domain
PF18658 zf-C2H2_12 419 482 Spin-doc zinc-finger Domain
PF18658 zf-C2H2_12 582 645 Spin-doc zinc-finger Domain
Sequence
MEPGGDHRSRSSGGRGGPGPAVASARGRRLPPAGSSGSAEPEEDEGGQDLQLEGGALGSW
GSAPLPSSRARGPASSGRKYSDHCEARASRPGKSRIPGRDHRRYYHDHWRLEYLMDFNPA
RHGMVCMVCGSSLATLKLSTIKRHIRQKHPYSLHWSPREKEVISNSWDA
HLGLGACGEAE
GLGVQGAEEEEEEEEEEEEEGAGVPACPPKGPGKAPAGGGCRRQRRGGPVAPRARRLRLS
ASRRAGGSRGLGARRLERRLKESLQNWFRAECLMDYDPRGNRLVCMACGRALPSLHLDDI
RAHVLEVHPGSLGLSGPQRSALLQAWGG
QPEALSELTQSPPGDDLAPQDLTGKSRDSASA
AGAPSSQDLSPPDVKEEAGWVPERPGPAEEEEELEEGEGERAGVPGRSPRGRAHRRHPQE
RWRLEYLMELDGGRRGLVCGVCGGALASLKMSTIERHIRRRHPGSTRLGGPVQALIAREW
SE
KAAHLLALGPPRPESPQGPIPPGTAAASDEGGGDEEEEPEEEEEEWGDVPLSPGAPLE
RPAEEEEDEEDGQEPGGLALPPPPPPPPPPPPRSREQRRNYQPRWRGEYLMDYDGSRRGL
VCMVCGGALATLKVSTIKRHILQVHPFSMDFTPEERQTILEAYEE
AALRCYGHEGFGPPA
PAPRDGGADLKSGAVCRA
Sequence length 678
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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS