Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84522
Gene name Gene Name - the full gene name approved by the HGNC.
Jagunal vesicle mediated transporter 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
JAGN1
Synonyms (NCBI Gene) Gene synonyms aliases
GL009, SCN6
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p25.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a transmembrane protein. It functions in the early secretory pathway and is necessary for neutrophil differentiation and survival. Mutations in this gene result in severe congenital neutropenia. [provided by RefSeq, Oct
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs587777727 G>A Pathogenic 5 prime UTR variant, missense variant, initiator codon variant
rs587777728 C>T Pathogenic 5 prime UTR variant, coding sequence variant, missense variant
rs587777729 G>T Pathogenic 5 prime UTR variant, coding sequence variant, missense variant
rs587777730 A>G Pathogenic Missense variant, coding sequence variant
rs587777731 CCGACGGCA>- Pathogenic 5 prime UTR variant, coding sequence variant, inframe deletion
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT648137 hsa-miR-34b-3p HITS-CLIP 23824327
MIRT648136 hsa-miR-1266-3p HITS-CLIP 23824327
MIRT648135 hsa-miR-6734-3p HITS-CLIP 23824327
MIRT648134 hsa-miR-3667-3p HITS-CLIP 23824327
MIRT648133 hsa-miR-6515-3p 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:0002376 Process Immune system process IEA
GO:0002446 Process Neutrophil mediated immunity IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005783 Component Endoplasmic reticulum IDA 25129144
GO:0005783 Component Endoplasmic reticulum IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616012 26926 ENSG00000171135
Protein
UniProt ID Q8N5M9
Protein name Protein jagunal homolog 1
Protein function Endoplasmic reticulum transmembrane protein involved in vesicle-mediated transport, which is required for neutrophil function. Required for vesicle-mediated transport; it is however unclear whether it is involved in early secretory pathway or in
PDB 6WVD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07086 Jagunal 1 177 Jagunal, ER re-organisation during oogenesis Family
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed. {ECO:0000269|PubMed:25129144}.
Sequence
Sequence length 183
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)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Congenital Neutropenia autosomal recessive severe congenital neutropenia due to jagn1 deficiency rs587777730 N/A
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Bacterial Infections Associate 39286252
Daneman Davy Mancer syndrome Associate 32419428
Facial Neoplasms Associate 32419428
Genetic Diseases Inborn Associate 32419428
Infections Associate 39286252
Neutropenia Associate 39286252
Neutropenia Severe Congenital Autosomal Recessive 3 Associate 25129144, 30040071, 32419428, 33206996, 39286252