Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79870
Gene name Gene Name - the full gene name approved by the HGNC.
BAALC binder of MAP3K1 and KLF4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BAALC
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene was identified by gene expression studies in patients with acute myeloid leukemia (AML). The gene is conserved among mammals and is not found in lower organisms. Tissues that express this gene develop from the neuroectoderm. Multiple alternative
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT814085 hsa-miR-1197 CLIP-seq
MIRT814086 hsa-miR-1252 CLIP-seq
MIRT814087 hsa-miR-1825 CLIP-seq
MIRT814088 hsa-miR-1976 CLIP-seq
MIRT814089 hsa-miR-199a-5p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
RUNX1 Activation 22493267
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 11707601
GO:0005737 Component Cytoplasm IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606602 14333 ENSG00000164929
Protein
UniProt ID Q8WXS3
Protein name Brain and acute leukemia cytoplasmic protein
Protein function May play a synaptic role at the postsynaptic lipid rafts possibly through interaction with CAMK2A.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06989 BAALC_N 1 50 BAALC N-terminus Family
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in neuroectoderm-derived tissues. Expressed in the brain and spinal cord, and at low levels, in the adrenal gland. In the bone marrow, confined to the CD34+ progenitor cells. Not found in peripheral blood mononu
Sequence
MGCGGSRADAIEPRYYESWTRETESTWLTYTDSDAPPSAAAPDSGPEAGGLHSGMLEDGL
PSNGVPRSTAPGGIPNPEKKTNCETQCPNPQSLSSGPLTQKQNGLQTTEAKRDAKRMPAK
EVTINVTDSIQQMDRSRRITKNCVN
Sequence length 145
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
Breast Cancer Breast cancer and/or colorectal cancer N/A N/A GWAS
Pelvic Organ Prolapse Pelvic organ prolapse N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Albuminuria Associate 35055008
Bjornstad syndrome Associate 18378853
Death Associate 21372155
Gastrointestinal Neoplasms Associate 22493267
Glioblastoma Stimulate 22493267
HAIR AN syndrome Associate 26430723
Leukemia Associate 12750167, 14585369, 20065290, 33453340
Leukemia Myeloid Associate 22493267
Leukemia Myeloid Acute Associate 12750167, 14585369, 18378853, 20026798, 20841507, 21596848, 21967978, 22493267, 22529287, 23760853, 23937207, 24326683, 24867525, 28830460, 32811810
View all (3 more)
Melanoma Stimulate 22493267