TMEM238L (transmembrane protein 238 like)

Gene
Gene Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100289255
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 238 like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM238L
Synonyms (NCBI Gene) Gene synonyms aliases
FORCP, LINC00675
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1-p12
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide all(6)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 33112233
GO:0005783 Component Endoplasmic reticulum IEA
GO:0005789 Component Endoplasmic reticulum membrane IDA 33112233
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0016020 Component Membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
Gene Gene ontology Other IDs Protein Associated diseases
UniProt ID A6NJY4
Protein name Transmembrane protein 238-like (FOXA1-regulated conserved small protein) (FORCP)
Protein function May play a role in inducing apoptosis during endoplasmic reticulum (ER) stress and in the inhibition of proliferation and tumorigenicity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15125 TMEM238 13 → 76 TMEM238 protein family Family
Sequence
Sequence length 79
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)
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
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
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Show/Hide Text Mining Associations (15)
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Inhibit 34738869
Carcinogenesis Inhibit 30556869
Carcinoma Pancreatic Ductal Associate 26309360
Carcinoma Renal Cell Inhibit 32196582
Colorectal Neoplasms Associate 30061182, 31442207
Esophageal Squamous Cell Carcinoma Inhibit 30556869
Glioma Associate 30061182
Lymphatic Metastasis Stimulate 26309360
Lymphatic Metastasis Inhibit 30556869
Neoplasm Invasiveness Inhibit 34738869