Gene Gene information from NCBI Gene database.
Entrez ID 2036
Gene name Erythrocyte membrane protein band 4.1 like 1
Gene symbol EPB41L1
Synonyms (NCBI Gene)
4.1NMRD11
Chromosome 20
Chromosome location 20q11.23
Summary Erythrocyte membrane protein band 4.1 (EPB41) is a multifunctional protein that mediates interactions between the erythrocyte cytoskeleton and the overlying plasma membrane. The encoded protein binds and stabilizes D2 and D3 dopamine receptors at the neur
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs1060499773 C>T Likely-pathogenic Intron variant, coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
347
miRTarBase ID miRNA Experiments Reference
MIRT022061 hsa-miR-128-3p Microarray 17612493
MIRT036447 hsa-miR-1226-3p CLASH 23622248
MIRT703944 hsa-miR-4740-3p HITS-CLIP 23313552
MIRT703943 hsa-miR-4258 HITS-CLIP 23313552
MIRT703942 hsa-miR-7108-3p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IEA
GO:0005198 Function Structural molecule activity IEA
GO:0005515 Function Protein binding IPI 21044950
GO:0005737 Component Cytoplasm IEA
GO:0005829 Component Cytosol TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602879 3378 ENSG00000088367
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H4G0
Protein name Band 4.1-like protein 1 (Erythrocyte membrane protein band 4.1-like 1) (Neuronal protein 4.1) (4.1N)
Protein function May function to confer stability and plasticity to neuronal membrane via multiple interactions, including the spectrin-actin-based cytoskeleton, integral membrane channels and membrane-associated guanylate kinases.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09379 FERM_N 101 164 FERM N-terminal domain Domain
PF00373 FERM_M 179 288 FERM central domain Domain
PF09380 FERM_C 292 382 FERM C-terminal PH-like domain Domain
PF08736 FA 385 428 FERM adjacent (FA) Family
PF04382 SAB 493 544 SAB domain Domain
PF05902 4_1_CTD 743 868 4.1 protein C-terminal domain (CTD) Domain
Tissue specificity TISSUE SPECIFICITY: Highest expression in brain, lower in heart, kidney, pancreas, placenta, lung and skeletal muscle.
Sequence
MTTETGPDSEVKKAQEEAPQQPEAAAAVTTPVTPAGHGHPEANSNEKHPSQQDTRPAEQS
LDMEEKDYSEADGLSERTTPSKAQKSPQKIAKKYKSAICRVTLLDASEYECEVEKHGRGQ
VLFDLVCEHLNLLEKDYFGLTFCDADSQKNWLDPSKEIKKQIRS
SPWNFAFTVKFYPPDP
AQLTEDITRYYLCLQLRADIITGRLPCSFVTHALLGSYAVQAELGDYDAEEHVGNYVSEL
RFAPNQTRELEERIMELHKTYRGMTPGEAEIHFLENAKKLSMYGVDLH
HAKDSEGIDIML
GVCANGLLIYRDRLRINRFAWPKILKISYKRSNFYIKIRPGEYEQFESTIGFKLPNHRSA
KRLWKVCIEHHTFFRLVSPEPP
PKGFLVMGSKFRYSGRTQAQTRQASALIDRPAPFFERS
SSKRYTMS
RSLDGAEFSRPASVSENHDAGPDGDKRDEDGESGGQRSEAEEGEVRTPTKIK
ELKPEQETTPRHKQEFLDKPEDVLLKHQASINELKRTLKEPNSKLIHRDRDWERERRLPS
SPAS
PSPKGTPEKANERAGLREGSEEKVKPPRPRAPESDTGDEDQDQERDTVFLKDNHLA
IERKCSSITVSSTSSLEAEVDFTVIGDYHGSAFEDFSRSLPELDRDKSDSDTEGLLFSRD
LNKGAPSQDDESGGIEDSPDRGACSTPDMPQFEPVKTETMTVSSLAIRKKIEPEAVLQTR
VSAMDNTQQVDGSASVGREFIATTPSITTETISTTMENSLKSGKGAAAMIPGPQTVATEI
RSLSPIIGKDVLTSTYGATAETLSTSTTTHVTKTVKGGFSETRIEKRIIITGDEDVDQDQ
ALALAIKEAKLQHPDMLVTKAVVYRETD
PSPEERDKKPQES
Sequence length 881
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Trafficking of AMPA receptors
Neurexins and neuroligins
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
45
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Abnormal brain morphology Likely pathogenic rs1060499773 RCV000454281
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Benign; Likely benign rs144426436 RCV005892276
Complex neurodevelopmental disorder Conflicting classifications of pathogenicity rs778642222 RCV005361108
EPB41L1-related disorder Benign; Likely benign; Uncertain significance rs2295568, rs147654123, rs144426436, rs145893462, rs1600984787, rs2063036322, rs150389879, rs756577865, rs766993119, rs201212477, rs574706898, rs78442416 RCV003975020
RCV003907683
RCV003977512
RCV003919002
RCV003894535
RCV003896361
RCV003933924
RCV003944065
RCV003934748
RCV003957253
RCV003969186
RCV003960162
Gastric cancer Benign; Likely benign rs144426436 RCV005892277
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 27448302
Glioblastoma Associate 38167429
Neoplasms Inhibit 20860828, 27448302
Prostatic Neoplasms Associate 20860828