Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
2036
Gene name Gene Name - the full gene name approved by the HGNC.
Erythrocyte membrane protein band 4.1 like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EPB41L1
Synonyms (NCBI Gene) Gene synonyms aliases
4.1N, MRD11
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MRD11
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q11.23
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 information of associated ontologies with gene provided by GO database.
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:0005829 Component Cytosol TAS
GO:0005856 Component Cytoskeleton IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602879 3378 ENSG00000088367
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Mental retardation Severe intellectual disability, MENTAL RETARDATION, AUTOSOMAL DOMINANT 11, Intellectual Disability rs5742905, rs267607136, rs267607137, rs2131714307, rs267607038, rs267607042, rs80338685, rs137853127, rs80338815, rs28940893, rs387906309, rs121908096, rs121908099, rs587784365, rs121918315
View all (1024 more)
25572454, 21376300
Non-syndromic intellectual disability Autosomal dominant non-syndromic intellectual disability rs121918049, rs1135401819, rs1553638614, rs1561846159, rs1564493599, rs1563978827
Unknown
Disease term Disease name Evidence References Source
Non-Syndromic Intellectual Disability autosomal dominant non-syndromic intellectual disability GenCC
Neurodevelopmental Disorders complex neurodevelopmental disorder GenCC
Melanoma Melanoma SMAD3 and SLC9A5 gain?of?function increases invasion capability of melanoma cells. GWAS, CBGDA
Carcinoma Carcinoma GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 27448302
Glioblastoma Associate 38167429
Neoplasms Inhibit 20860828, 27448302
Prostatic Neoplasms Associate 20860828