Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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84522 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Jagunal vesicle mediated transporter 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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JAGN1 |
SynonymsGene synonyms aliases
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GL009, SCN6 |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p25.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
SNPsSNP information provided by dbSNP.
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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 |
rs777966677 |
G>A |
Pathogenic |
5 prime UTR variant, coding sequence variant, missense variant |
rs786205704 |
G>A,T |
Pathogenic |
Coding sequence variant, missense variant, 5 prime UTR variant |
rs786205705 |
C>G |
Pathogenic |
Stop gained, coding sequence variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF07086 |
Jagunal |
1 → 177 |
Jagunal, ER re-organisation during oogenesis |
Family |
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Sequence |
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Sequence length |
183 |
Interactions |
View interactions |
Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Congenital neutropenia |
Congenital neutropenia, Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency |
rs118203968, rs118203969, rs118203970, rs118203971, rs267606834, rs28936381, rs137854447, rs137854448, rs137854450, rs28931611, rs137854451, rs200478425, rs587777730, rs606231474, rs606231475, rs606231473, rs775224457, rs769441127, rs148559256, rs797044567, rs796065343, rs797045009, rs878855315, rs1555710005, rs879253750, rs879253882, rs1555354200, rs1555354198, rs1555354750, rs890101650, rs759302795, rs57246956, rs138156467, rs1194477276, rs1570588220, rs757401069, rs745582203, rs1191239079, rs1597905369, rs1599294750, rs1594996301, rs1595004126, rs1595004676, rs756667927, rs34019455 |
25129144 |
Neutropenia |
Neutropenia, NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE |
rs879253882 |
25129144, 25129145, 25129144, 11101832 |
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