Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64097
Gene name Gene Name - the full gene name approved by the HGNC.
Erythrocyte membrane protein band 4.1 like 4A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
EPB41L4A
Synonyms (NCBI Gene) Gene synonyms aliases
EPB41L4, NBL4
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q22.1-q22.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the band 4.1 protein superfamily. Members of this superfamily are thought to play an important role in regulating interactions between the cytoskeleton and plasma membrane, and contain an amino terminal cons
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs730882207 G>A Likely-pathogenic Non coding transcript variant, coding sequence variant, missense variant, genic downstream transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019149 hsa-miR-335-5p Microarray 18185580
MIRT965665 hsa-miR-1193 CLIP-seq
MIRT965666 hsa-miR-1273d CLIP-seq
MIRT965667 hsa-miR-1275 CLIP-seq
MIRT965668 hsa-miR-128 CLIP-seq
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:0005575 Component Cellular_component ND
GO:0005737 Component Cytoplasm IEA
GO:0005856 Component Cytoskeleton IBA 21873635
GO:0008092 Function Cytoskeletal protein binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612141 13278 ENSG00000129595
Protein
UniProt ID Q9HCS5
Protein name Band 4.1-like protein 4A (Erythrocyte membrane protein band 4.1-like 4A) (Protein NBL4)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09379 FERM_N 15 83 FERM N-terminal domain Domain
PF00373 FERM_M 102 211 FERM central domain Domain
PF09380 FERM_C 215 303 FERM C-terminal PH-like domain Domain
PF08736 FA 311 355 FERM adjacent (FA) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in many tissues. High levels of expression in brain, liver, thymus and peripheral blood leukocytes and low levels of expression in heart, kidney, testis and colon.
Sequence
MGCFCAVPEEFYCEVLLLDESKLTLTTQQQGIKKSTKGSVVLDHVFHHVNLVEIDYFGLR
YCDRSHQTYWLDPAKTLAEHKEL
INTGPPYTLYFGIKFYAEDPCKLKEEITRYQFFLQVK
QDVLQGRLPCPVNTAAQLGAYAIQSELGDYDPYKHTAGYVSEYRFVPDQKEELEEAIERI
HKTLMGQIPSEAELNYLRTAKSLEMYGVDLH
PVYGENKSEYFLGLTPVGVVVYKNKKQVG
KYFWPRITKVHFKETQFELRVLGKDCNETSFFFEARSKTACKHLWKCSVEHHTFFRMPEN
ESN
SLSRKLSKFGSIRYKHRYSGRTALQMSRDLSIQLPRPDQNVTRSRSKTYPKRIAQTQ
PAESNSISRITANMENGENEGTIKIIAPSPVKSFKKAKNENSPDTQRSKSHAPWEENGPQ
SGLYNSPSDRTKSPKFPYTRRRNPSCGSDNDSVQPVRRRKAHNSGEDSDLKQRRRSRSRC
NTSSGSESENSNREYRKKRNRIRQENDMVDSAPQWEAVLRRQKEKNQADPNNRRSRHRSR
SRSPDIQAKEELWKHIQKELVDPSGLSEEQLKEIPYTKIETQGDPIRIRHSHSPRSYRQY
RRSQCSDGERSVLSEVNSKTDLVPPLPVTRSSDAQGSGDATVHQRRNGSKDSLMEEKPQT
STNNLAGKHTAKTIKTIQASRLKTET
Sequence length 686
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Spastic paraplegia Spastic Paraplegia rs118204049, rs121918262, rs104894490, rs119476046, rs281865117, rs281865118, rs137853017, rs72554620, rs121908610, rs121908611, rs121908613, rs116171274, rs121434442, rs121434443, rs137852520
View all (368 more)
Unknown
Disease term Disease name Evidence References Source
Coronary artery disease Coronary artery disease GWAS
Neuroblastoma Neuroblastoma Loss of SNAI2 function reduces self-renewal, 3D invasion as well as metastatic spread in vivo, while strongly sensitizing neuroblastoma cells to RA-induced growth inhibition. GWAS, CBGDA
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Dementia Dementia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Inhibit 30764831, 36274054
Carcinoma Ductal Associate 30959550
Carcinoma Renal Cell Associate 34040677, 36611858
Carotid Stenosis Associate 36187128
Colorectal Neoplasms Associate 29703930
Diabetes Mellitus Associate 36187128
Diabetes Mellitus Type 2 Stimulate 35184403
Diabetes Mellitus Type 2 Associate 36187128
Dyskeratosis Congenita Associate 29703930
Insulin Resistance Stimulate 35184403