Description: | growth factor independent 1 transcriptional repressor [Source:HGNC Symbol;Acc:HGNC:4237] |
Synonyms: | ZNF163, GFI-1, SCN2, GFI1A |
Other ID(s): | HGNC:4237, ENSG00000162676 |
Protein Accession Numbers: | ENST00000294702, NP_001120687, ENST00000370332, NP_005254, ENST00000427103, ENST00000294702.5, NP_001120688, ENST00000370332.1 |
Statistics: | ClinVar(261) gnomAD(1143) COSMIC(418) PTM(17) |
∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000294702 You are here now!
ENST00000370332 You are here now!
ENST00000427103 You are here now!
NP_001120687 You are here now!
NP_001120688 You are here now!
NP_005254 You are here now!
Pfam Domain filter_list | Domain Name filter_list | Description filter_list | Positions filter_list | Clan filter_list | Clan Name filter_list | Organism filter_list |
---|---|---|---|---|---|---|
NO RESULT FOUND | ||||||
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 312-334 | CL0361 | C2H2-zf | Homo sapiens |
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 368-390 | CL0361 | C2H2-zf | Homo sapiens |
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 255-278 | CL0361 | C2H2-zf | Homo sapiens |
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 340-362 | CL0361 | C2H2-zf | Homo sapiens |
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 396-419 | CL0361 | C2H2-zf | Homo sapiens |
PF00096 | zf-C2H2 | Zinc finger, C2H2 type | 284-306 | CL0361 | C2H2-zf | Homo sapiens |
Disease Name filter_list | Disease Category filter_list | DSI* filter_list | DPI** filter_list | ||
---|---|---|---|---|---|
Cytopenia | N/A | 0.604 | 0.345 | ||
Leukemia, Myelocytic, Acute | Neoplasms ; | 0.604 | 0.345 | ||
Acute Myeloid Leukemia, M1 | Neoplasms ; | 0.604 | 0.345 | ||
Ataxia, Spinocerebellar | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Congenital anemia | N/A | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 1 | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 2 | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 4 | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 5 | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 6 (disorder) | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Spinocerebellar Ataxia Type 7 | Nervous System Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Neutropenia, Nonimmune Chronic Idiopathic, Adult | Hemic and Lymphatic Diseases ; Congenital, Hereditary, and Neonatal Diseases and Abnormalities ; | 0.604 | 0.345 | ||
Neutropenia, Severe Congenital, Autosomal Dominant 1 | Hemic and Lymphatic Diseases ; | 0.604 | 0.345 | ||
Acute Myeloid Leukemia (AML-M2) | Neoplasms ; | 0.604 | 0.345 | ||
Neutropenia, Severe Congenital, Autosomal Dominant 2 | Hemic and Lymphatic Diseases ; | 0.604 | 0.345 | ||
NO RESULT FOUND |