Gene Gene information from NCBI Gene database.
Entrez ID 284612
Gene name Synaptophysin like 2
Gene symbol SYPL2
Synonyms (NCBI Gene)
MG29
Chromosome 1
Chromosome location 1p13.3
miRNA miRNA information provided by mirtarbase database.
110
miRTarBase ID miRNA Experiments Reference
MIRT039687 hsa-miR-615-3p CLASH 23622248
MIRT1406982 hsa-miR-1185 CLIP-seq
MIRT1406983 hsa-miR-1253 CLIP-seq
MIRT1406984 hsa-miR-1303 CLIP-seq
MIRT1406985 hsa-miR-1305 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0006874 Process Intracellular calcium ion homeostasis IEA
GO:0007507 Process Heart development IEA
GO:0008021 Component Synaptic vesicle IEA
GO:0016020 Component Membrane IEA
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.
Q5VXT5
Protein name Synaptophysin-like protein 2
Protein function Involved in communication between the T-tubular and junctional sarcoplasmic reticulum (SR) membranes.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01284 MARVEL 30 232 Membrane-associating domain Domain
Sequence
Sequence length 272
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
CHRONIC KIDNEY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Embolism Fat Associate 25406998
★☆☆☆☆
Found in Text Mining only
Obesity Associate 25406998
★☆☆☆☆
Found in Text Mining only
Obesity Morbid Associate 25406998
★☆☆☆☆
Found in Text Mining only