Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
25789
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 59 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM59L
Synonyms (NCBI Gene) Gene synonyms aliases
BSMAP, C19orf4
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.11
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a predicted type-I membrane glycoprotein. The encoded protein may play a role in functioning of the central nervous system. [provided by RefSeq, Jul 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1438220 hsa-miR-10a CLIP-seq
MIRT1438221 hsa-miR-10b CLIP-seq
MIRT1438222 hsa-miR-320e CLIP-seq
MIRT1438223 hsa-miR-339-5p CLIP-seq
MIRT1438224 hsa-miR-3620 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0001658 Process Branching involved in ureteric bud morphogenesis IEA
GO:0005515 Function Protein binding IPI 28514442, 33961781
GO:0005794 Component Golgi apparatus IEA
GO:0016020 Component Membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617096 13237 ENSG00000105696
Protein
UniProt ID Q9UK28
Protein name Transmembrane protein 59-like (Brain-specific membrane-anchored protein)
Protein function Modulates the O-glycosylation and complex N-glycosylation steps occurring during the Golgi maturation of APP. Inhibits APP transport to the cell surface and further shedding.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12280 BSMAP 79 284 Brain specific membrane anchored protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed preferentially at high level in the brain.
Sequence
MAAVALMPPPLLLLLLLASPPAASAPSARDPFAPQLGDTQNCQLRCRDRDLGPQPSQAGL
EGASESPYDRAVLISACERGCRLFSICRFVARSSKPNATQTECEAACVEAYVKEAEQQAC
SHGCWSQPAEPEPEQKRKVLEAPSGALSLLDLFSTLCNDLVNSAQGFVSSTWTYYLQTDN
GKVVVFQTQPIVESLGFQGGRLQRVEVTWRGSHPEALEVHVDPVGPLDKVRKAKIRVKTS
SKAKVESEEPQDNDFLSCMSRRSGLPRWILACCLFLSVLVMLWL
SCSTLVTAPGQHLKFQ
PLTLEQHKGFMMEPDWPLYPPPSHACEDSLPPYKLKLDLTKL
Sequence length 342
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
Dental caries Dental caries N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Renal Cell Associate 36618425
Colonic Neoplasms Stimulate 36618425
Colorectal Neoplasms Associate 38466182
Glioblastoma Stimulate 37439405
Glioma Associate 37439405
Neoplasms Associate 35361846, 36618425
Recombinant chromosome 8 syndrome Inhibit 36618425
Urinary Bladder Neoplasms Stimulate 36618425