Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9399
Gene name Gene Name - the full gene name approved by the HGNC.
Stomatin like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STOML1
Synonyms (NCBI Gene) Gene synonyms aliases
SLP-1, STORP, hUNC-24
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q24.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT669823 hsa-miR-125a-3p HITS-CLIP 23824327
MIRT669822 hsa-miR-764 HITS-CLIP 23824327
MIRT669821 hsa-miR-3934-5p HITS-CLIP 23824327
MIRT669820 hsa-miR-6747-3p HITS-CLIP 23824327
MIRT669819 hsa-miR-1234-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 19696025, 23082202
GO:0005575 Component Cellular_component ND
GO:0005886 Component Plasma membrane IBA 21873635
GO:0006869 Process Lipid transport IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608326 14560 ENSG00000067221
Protein
UniProt ID Q9UBI4
Protein name Stomatin-like protein 1 (SLP-1) (EPB72-like protein 1) (Protein unc-24 homolog) (Stomatin-related protein) (STORP)
Protein function May play a role in cholesterol transfer to late endosomes (PubMed:19696025). May play a role in modulating membrane acid-sensing ion channels. Can specifically inhibit proton-gated current of ASIC1 isoform 1. Can increase inactivation speed of A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01145 Band_7 80 228 SPFH domain / Band 7 family Family
PF02036 SCP2 291 395 SCP-2 sterol transfer family Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed at low levels. Expression is highest in brain. {ECO:0000269|PubMed:10997330, ECO:0000269|PubMed:9931417}.
Sequence
Sequence length 398
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Coronary artery disease Coronary Artery Disease rs137852988, rs121918313, rs121918529, rs121918531, rs137852340, rs1555800701, rs1215189537 29212778
Unknown
Disease term Disease name Evidence References Source
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Autistic Disorder Associate 11121177
Carcinogenesis Associate 19034969
Neoplasms Associate 19034969, 24007313
Squamous Cell Carcinoma of Head and Neck Associate 24007313