Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
140767
Gene name Gene Name - the full gene name approved by the HGNC.
Neurensin 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NRSN1
Synonyms (NCBI Gene) Gene synonyms aliases
VMP, p24
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1194439 hsa-miR-1207-5p CLIP-seq
MIRT1194440 hsa-miR-1225-3p CLIP-seq
MIRT1194441 hsa-miR-1233 CLIP-seq
MIRT1194442 hsa-miR-1252 CLIP-seq
MIRT1194443 hsa-miR-196a CLIP-seq
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 25416956, 32296183
GO:0007399 Process Nervous system development IBA 21873635
GO:0007399 Process Nervous system development ISS
GO:0016021 Component Integral component of membrane IEA
GO:0030133 Component Transport vesicle IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616630 17881 ENSG00000152954
Protein
UniProt ID Q8IZ57
Protein name Neurensin-1 (Neuro-p24) (Vesicular membrane protein of 24 kDa) (Vesicular membrane protein p24)
Protein function May play an important role in neural organelle transport, and in transduction of nerve signals or in nerve growth. May play a role in neurite extension. May play a role in memory consolidation (By similarity). {ECO:0000250|UniProtKB:P97799, ECO:
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14927 Neurensin 23 153 Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain. Not detectable in other tissues tested. {ECO:0000269|PubMed:12463420}.
Sequence
Sequence length 195
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hirschsprung disease Hirschsprung Disease rs76262710, rs75996173, rs77316810, rs75076352, rs76534745, rs76764689, rs76449634, rs377767412, rs193922699, rs75030001, rs606231342, rs1553540620, rs759944122, rs1057519322, rs1057519323
View all (4 more)
22325380
Unknown
Disease term Disease name Evidence References Source
Huntington disease Huntington Disease 22325380 ClinVar
Breast Cancer Breast Cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Insomnia Insomnia GWAS
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Acquired Immunodeficiency Syndrome Associate 1696859
Attention Deficit Disorder with Hyperactivity Associate 19362708
Auditory Perceptual Disorders Associate 19362708
Disruptive Impulse Control and Conduct Disorders Associate 19362708
Dyslexia Associate 15717286, 16385449
Hirschsprung Disease Associate 29654647
HIV Infections Stimulate 25998390
Infections Associate 25341640
Leukoencephalitis Acute Hemorrhagic Associate 23347174
Psychotic Disorders Associate 29064472