Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
66000
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 108
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM108
Synonyms (NCBI Gene) Gene synonyms aliases
CT124, RTLN
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT047062 hsa-miR-183-5p CLASH 23622248
MIRT734803 hsa-miR-3148 RNA-seq 31540331
MIRT1429816 hsa-miR-1287 CLIP-seq
MIRT1429817 hsa-miR-150 CLIP-seq
MIRT1429818 hsa-miR-2964a-5p CLIP-seq
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:0005768 Component Endosome IEA
GO:0005769 Component Early endosome IBA
GO:0005769 Component Early endosome IEA
GO:0005769 Component Early endosome ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617361 28451 ENSG00000144868
Protein
UniProt ID Q6UXF1
Protein name Transmembrane protein 108 (Retrolinkin)
Protein function Transmembrane protein required for proper cognitive functions. Involved in the development of dentate gyrus (DG) neuron circuitry, is necessary for AMPA receptors surface expression and proper excitatory postsynaptic currents of DG granule neuro
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15759 TMEM108 61 575 TMEM108 family Family
Sequence
Sequence length 575
Interactions View interactions
<
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
Dementia Dementia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Cognition Disorders Associate 33958783
Colorectal Neoplasms Associate 36932973
Dementia Associate 33958783
Parkinson Disease Associate 33958783