Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5064
Gene name Gene Name - the full gene name approved by the HGNC.
Paralemmin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PALM
Synonyms (NCBI Gene) Gene synonyms aliases
PALM1
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19p13.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the paralemmin protein family. The product of this gene is a prenylated and palmitoylated phosphoprotein that associates with the cytoplasmic face of plasma membranes and is implicated in plasma membrane dynamics in neurons a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT043056 hsa-miR-324-5p CLASH 23622248
MIRT718145 hsa-miR-1911-3p HITS-CLIP 19536157
MIRT718144 hsa-miR-6753-5p HITS-CLIP 19536157
MIRT718143 hsa-miR-6748-3p HITS-CLIP 19536157
MIRT718142 hsa-miR-4421 HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16386234, 32814053
GO:0005654 Component Nucleoplasm IDA
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane IDA 16386234
GO:0007010 Process Cytoskeleton organization IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608134 8594 ENSG00000099864
Protein
UniProt ID O75781
Protein name Paralemmin-1 (Paralemmin)
Protein function Involved in plasma membrane dynamics and cell process formation. Isoform 1 and isoform 2 are necessary for axonal and dendritic filopodia induction, for dendritic spine maturation and synapse formation in a palmitoylation-dependent manner. {ECO:
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03285 Paralemmin 71 387 Paralemmin Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with highest expression in brain and testis and intermediate expression in heart and adrenal gland.
Sequence
Sequence length 387
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Lung adenocarcinoma Lung adenocarcinoma Validation that loss of Tgfbr2 results in more aggressive and T cell-excluded KP lung tumors GWAS, CBGDA