Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
388327
Gene name Gene Name - the full gene name approved by the HGNC.
Chromosome 17 open reading frame 100
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
C17orf100
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018140 hsa-miR-335-5p Microarray 18185580
MIRT047274 hsa-miR-181b-5p CLASH 23622248
MIRT835598 hsa-miR-1305 CLIP-seq
MIRT835599 hsa-miR-3671 CLIP-seq
MIRT835600 hsa-miR-4477b CLIP-seq
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 A8MU93
Protein name Uncharacterized protein C17orf100
Family and domains
Sequence
MASARGAKQSSPRVGTTRYTETSTVRVETSSHRVETSSRRVETSQRRSEGPSLSPSGKRL
PRILEASSRHVESSSQRTETTSRHVRASSLRVETSLHCAESPTPRAKPAARQNEKTAR
Sequence length 118
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Epileptic encephalopathy EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 25, WITH AMELOGENESIS IMPERFECTA rs587776508, rs121918334, rs121918317, rs121918321, rs74315390, rs28939684, rs74315391, rs74315392, rs118192244, rs121918622, rs121918623, rs121917953, rs121917955, rs121918624, rs121918625
View all (860 more)
27261973, 28673551