Gene Gene information from NCBI Gene database.
Entrez ID 58513
Gene name Epidermal growth factor receptor pathway substrate 15 like 1
Gene symbol EPS15L1
Synonyms (NCBI Gene)
EPS15R
Chromosome 19
Chromosome location 19p13.11
miRNA miRNA information provided by mirtarbase database.
222
miRTarBase ID miRNA Experiments Reference
MIRT514105 hsa-miR-3609 PAR-CLIP 20371350
MIRT514106 hsa-miR-548ah-5p PAR-CLIP 20371350
MIRT514104 hsa-miR-106a-5p PAR-CLIP 20371350
MIRT514103 hsa-miR-106b-5p PAR-CLIP 20371350
MIRT514102 hsa-miR-17-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 16159959, 18200045, 19262564, 25416956, 32203420, 32296183, 33961781, 35271311, 35914814
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616826 24634 ENSG00000127527
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UBC2
Protein name Epidermal growth factor receptor substrate 15-like 1 (Eps15-related protein) (Eps15R)
Protein function Seems to be a constitutive component of clathrin-coated pits that is required for receptor-mediated endocytosis. Involved in endocytosis of integrin beta-1 (ITGB1) and transferrin receptor (TFR); internalization of ITGB1 as DAB2-dependent cargo
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12763 EF-hand_4 17 93 Cytoskeletal-regulatory complex EF hand Family
PF12763 EF-hand_4 122 218 Cytoskeletal-regulatory complex EF hand Family
PF12763 EF-hand_4 273 365 Cytoskeletal-regulatory complex EF hand Family
Sequence
MAAPLIPLSQQIPTGNSLYESYYKQVDPAYTGRVGASEAALFLKKSGLSDIILGKIWDLA
DPEGKGFLDKQGFYVALRLVACAQSGHEVTLSN
LNLSMPPPKFHDTSSPLMVTPPSAEAH
WAVRVEEKAKFDGIFESLLPINGLLSGDKVKPVLMNSKLPLDVLGRVWDLSDIDKDGHLD
RDEFAVAMHLVYRALEKEPVPSALPPSLIPPSKRKKTV
FPGAVPVLPASPPPKDSLRSTP
SHGSVSSLNSTGSLSPKHSLKQTQPTVNWVVPVADKMRFDEIFLKTDLDLDGYVSGQEVK
EIFMHSGLTQNLLAHIWALADTRQTGKLSKDQFALAMYFIQQKVSKGIDPPQVLSPDMVP
PSERG
TPGPDSSGSLGSGEFTGVKELDDISQEIAQLQREKYSLEQDIREKEEAIRQKTSE
VQELQNDLDRETSSLQELEAQKQDAQDRLDEMDQQKAKLRDMLSDVRQKCQDETQMISSL
KTQIQSQESDLKSQEDDLNRAKSELNRLQQEETQLEQSIQAGRVQLETIIKSLKSTQDEI
NQARSKLSQLHESRQEAHRSLEQYDQVLDGAHGASLTDLANLSEGVSLAERGSFGAMDDP
FKNKALLFSNNTQELHPDPFQTEDPFKSDPFKGADPFKGDPFQNDPFAEQQTTSTDPFGG
DPFKESDPFRGSATDDFFKKQTKNDPFTSDPFTKNPSLPSKLDPFESSDPFSSSSVSSKG
SDPFGTLDPFGSGSFNSAEGFADFSQMSKPPPSGPFTSSLGGAGFSDDPFKSKQDTPALP
PKKPAPPRPKPPSGKSTPVSQLGSADFPEAPDPFQPLGADSGDPFQSKKGFGDPFSGKDP
FVPSSAAKPSKASASGFADFTSVS
Sequence length 864
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Endocytosis   EGFR downregulation
Cargo recognition for clathrin-mediated endocytosis
Clathrin-mediated endocytosis
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ECTRODACTYLY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MULTIPLE SCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SPLIT HAND-FOOT MALFORMATION CTD
★★☆☆☆
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
Aniridia Aniridia HPO_DG
★☆☆☆☆
Found in Text Mining only
Congenital Foot Deformity Congenital deformity of foot BEFREE 21700002
★☆☆☆☆
Found in Text Mining only
Cornelia De Lange Syndrome Cornelia De Lange Syndrome BEFREE 30302754
★☆☆☆☆
Found in Text Mining only
Ectrodactyly Ectrodactyly ORPHANET_DG 29023680
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Isolated split hand-split foot malformation Isolated Split Hand-Split Foot Malformation Orphanet
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 18395097, 31355249
★☆☆☆☆
Found in Text Mining only
Multiple Sclerosis Multiple Sclerosis GWASDB_DG 22190364
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Multiple Sclerosis Multiple Sclerosis GWASCAT_DG 22190364, 24076602
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Oligodactyly Oligodactyly HPO_DG
★☆☆☆☆
Found in Text Mining only
Sensorineural Hearing Loss (disorder) Hearing Loss HPO_DG
★☆☆☆☆
Found in Text Mining only