Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4291
Gene name Gene Name - the full gene name approved by the HGNC.
Myeloid leukemia factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MLF1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q25.32
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes an oncoprotein which is thought to play a role in the phenotypic determination of hemopoetic cells. Translocations between this gene and nucleophosmin have been associated with myelodysplastic syndrome and acute myeloid leukemia. Multipl
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT043951 hsa-miR-378a-3p CLASH 23622248
MIRT042653 hsa-miR-422a CLASH 23622248
MIRT1150959 hsa-miR-4698 CLIP-seq
MIRT1150960 hsa-miR-802 CLIP-seq
MIRT1150961 hsa-miR-105 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002318 Process Myeloid progenitor cell differentiation ISS
GO:0003677 Function DNA binding ISS
GO:0005515 Function Protein binding IPI 12176995, 15861129, 16189514, 20374249, 22151054, 23414517, 25036637, 26871637, 28514442, 31515488
GO:0005634 Component Nucleus HDA 21630459
GO:0005634 Component Nucleus IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601402 7125 ENSG00000178053
Protein
UniProt ID P58340
Protein name Myeloid leukemia factor 1 (Myelodysplasia-myeloid leukemia factor 1)
Protein function Involved in lineage commitment of primary hemopoietic progenitors by restricting erythroid formation and enhancing myeloid formation. Interferes with erythropoietin-induced erythroid terminal differentiation by preventing cells from exiting the
PDB 3UAL , 3UBW , 6Y8E
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10248 Mlf1IP 26 202 Myelodysplasia-myeloid leukemia factor 1-interacting protein Family
Tissue specificity TISSUE SPECIFICITY: Most abundant in testis, ovary, skeletal muscle, heart, kidney and colon. Low expression in spleen, thymus and peripheral blood leukocytes.
Sequence
Sequence length 268
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Transcriptional misregulation in cancer  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Gastric cancer Hereditary Diffuse Gastric Cancer rs137854571, rs63751108, rs34612342, rs121908383, rs121909144, rs121909775, rs121909219, rs121909223, rs63750871, rs80359530, rs121964873, rs121913530, rs606231203, rs121918505, rs587776802
View all (244 more)
16367923
Leukemia Leukemia, Myelocytic, Acute, Acute Myeloid Leukemia (AML-M2) rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Neuroticism Neuroticism GWAS
Mental Depression Mental Depression GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 28358038
Cholangiocarcinoma Associate 37486965
Genetic Diseases Inborn Associate 39711284
Leukemia Associate 31675375
Leukemia Myeloid Acute Associate 25027285, 31648321, 31675375
Myelodysplastic Syndromes Associate 39711284
Neoplasms Associate 23676460, 37486965
Neuroblastoma Associate 28545128
Neuroendocrine Tumors Associate 23676460
Stomach Neoplasms Associate 16367923, 19375421