Gene Gene information from NCBI Gene database.
Entrez ID 199953
Gene name Transmembrane protein 201
Gene symbol TMEM201
Synonyms (NCBI Gene)
Ima1NET5SAMP1
Chromosome 1
Chromosome location 1p36.22
miRNA miRNA information provided by mirtarbase database.
152
miRTarBase ID miRNA Experiments Reference
MIRT032231 hsa-let-7b-5p Proteomics 18668040
MIRT032231 hsa-let-7b-5p CLASH 23622248
MIRT710533 hsa-miR-1306-5p HITS-CLIP 19536157
MIRT710532 hsa-miR-660-3p HITS-CLIP 19536157
MIRT710531 hsa-miR-205-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
GO ID Ontology Definition Evidence Reference
GO:0000922 Component Spindle pole IEA
GO:0001525 Process Angiogenesis IEA
GO:0001525 Process Angiogenesis IMP 35311970
GO:0005515 Function Protein binding IPI 21610090, 32296183, 35311970
GO:0005521 Function Lamin binding IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5SNT2
Protein name Transmembrane protein 201 (Spindle-associated membrane protein 1)
Protein function Critical regulator of angiogenesis and endothelial cell (EC) migration (PubMed:35311970). Promotes the migration of endothelial cells, which is essential for angiogenesis (PubMed:35311970). Interacts with the linker of nucleoskeleton and cytoske
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09779 Ima1_N 46 171 Ima1 N-terminal domain Family
PF10476 DUF2448 191 389 Protein of unknown function C-terminus (DUF2448) Family
Sequence
MEGVSALLARCPTAGLAGGLGVTACAAAGVLLYRIARRMKPTHTMVNCWFCNQDTLVPYG
NRNCWDCPHCEQYNGFQENGDYNKPIPAQYLEHLNHVVSSAPSLRDPSQPQQWVSSQVLL
CKRCNHHQTTKIKQLAAFAPREEGRYDEEVEVYRHHLEQMYKLCRPCQAAV
EYYIKHQNR
QLRALLLSHQFKRREADQTHAQNFSSAVKSPVQVILLRALAFLACAFLLTTALYGASGHF
APGTTVPLALPPGGNGSATPDNGTTPGAEGWRQLLGLLPEHMAEKLCEAWAFGQSHQTGV
VALGLLTCLLAMLLAGRIRLRRIDAFCTCLWALLLGLHLAEQHLQAASPSWLDTLKFSTT
SLCCLVGFTAAVATRKATGPRRFRPRRFF
PGDSAGLFPTSPSLAIPHPSVGGSPASLFIP
SPPSFLPLANQQLFRSPRRTSPSSLPGRLSRALSLGTIPSLTRADSGYLFSGSRPPSQVS
RSGEFPVSDYFSLLSGSCPSSPLPSPAPSVAGSVASSSGSLRHRRPLISPARLNLKGQKL
LLFPSPPGEAPTTPSSSDEHSPHNGSLFTMEPPHVPRKPPLQDVKHALDLRSKLERGSAC
SNRSIKKEDDSSQSSTCVVDTTTRGCSEEAATWRGRFGPSLVRGLLAVSLAANALFTSVF
LYQSLR
Sequence length 666
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Uveal melanoma Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Aortic valve disorder Aortic Valve Disease BEFREE 29581213
★☆☆☆☆
Found in Text Mining only
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) Emery-Dreifuss Muscular Dystrophy BEFREE 30326651
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 37373430 Associate
★☆☆☆☆
Found in Text Mining only
Colitis Colitis BEFREE 26676714, 28301579
★☆☆☆☆
Found in Text Mining only
Crohn Disease Crohn Disease BEFREE 15685547, 28301579, 29545797, 31750921
★☆☆☆☆
Found in Text Mining only
Glucocorticoid-remediable aldosteronism Hyperaldosteronism BEFREE 30222592
★☆☆☆☆
Found in Text Mining only
Histiocytosis haematophagic Histiocytosis Haematophagic BEFREE 30819910
★☆☆☆☆
Found in Text Mining only
Ileitis Ileitis BEFREE 15685547, 28301579, 29545797, 31750921
★☆☆☆☆
Found in Text Mining only
Inflammatory Bowel Diseases Inflammatory Bowel Disease BEFREE 31750921
★☆☆☆☆
Found in Text Mining only
Lymphohistiocytosis, Hemophagocytic Lymphohistiocytosis BEFREE 30819910
★☆☆☆☆
Found in Text Mining only