Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
120400
Gene name Gene Name - the full gene name approved by the HGNC.
Neurexophilin and PC-esterase domain family member 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NXPE1
Synonyms (NCBI Gene) Gene synonyms aliases
FAM55A
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q23.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT661424 hsa-miR-3606-3p HITS-CLIP 23824327
MIRT661423 hsa-miR-513a-3p HITS-CLIP 23824327
MIRT661422 hsa-miR-513c-3p HITS-CLIP 23824327
MIRT661421 hsa-miR-296-3p HITS-CLIP 23824327
MIRT629266 hsa-miR-3653-5p HITS-CLIP 23824327
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 32814053
GO:0005576 Component Extracellular region IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q8N323
Protein name NXPE family member 1 (Protein FAM55A)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06312 Neurexophilin 80 279 Neurexophilin Family
Sequence
MSSNTMLQKTLLILISFSVVTWMIFIISQNFTKLWSALNLSISVHYWNNSAKSLFPKTSL
IPLKPLTETELRIKEIIEKLDQQIPPRPFTHVNTTTSATHSTATILNPRDTYCRGDQLDI
LLEVRDHLGQRKQYGGDFLRARMSSPALTAGASGKVMDFNNGTYLVSFTLFWEGQVSLSL
LLIHPSEGASALWRARNQGYDKIIFKGKFVNGTSHVFTECGLTLNSNAELCEYLDDRDQE
AFYCMKPQHMPCEALTYMTTRNREVSYLTDKENSLFHRS
KVGVEMMKDRKHIDVTNCNKR
EKIEETCQVGMKPPVPGGYTLQGKWITTFCNQVQLDTIKINGCLKGKLIYLLGDSTLRQW
IYYFPKVVKTLKFFDLHETGIFKKHLLLDAERHTQIQWKKHSYPFVTFQLYSLIDHDYIP
REIDRLSGDKNTAIVITFGQHFRPFPIDIFIRRAIGVQKAIERLFLRSPATKVIIKTENI
REMHIETERFGDFHGYIHYLIMKDIFKDLNVGIIDAWDMTIAYGTDTIHPPDHVIGNQIN
MFLNYIC
Sequence length 547
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Inflammatory Bowel Disease Inflammatory bowel disease N/A N/A GWAS
Ulcerative colitis Ulcerative colitis N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Colorectal Neoplasms Associate 29659199
Inflammatory Bowel Diseases Associate 25766683
Neoplasms Associate 29659199