Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100533467
Gene name Gene Name - the full gene name approved by the HGNC.
BIVM-ERCC5 readthrough
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
BIVM-ERCC5
Synonyms (NCBI Gene) Gene synonyms aliases
ERCC5-202
Chromosome Chromosome number
13
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
13q33.1
Summary Summary of gene provided in NCBI Entrez Gene.
This locus represents naturally occurring read-through transcription between the neighboring BIVM (basic, immunoglobulin-like variable motif containing) and ERCC5 (excision repair cross-complementing rodent repair deficiency, complementation group 5) gene
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT821725 hsa-miR-1185 CLIP-seq
MIRT821726 hsa-miR-1273c CLIP-seq
MIRT821727 hsa-miR-3125 CLIP-seq
MIRT821728 hsa-miR-3129-3p CLIP-seq
MIRT821729 hsa-miR-3679-5p 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
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Nucleotide excision repair  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cerebrooculofacioskeletal syndrome Cerebrooculofacioskeletal Syndrome 3 rs121917901, rs758341467, rs121917904, rs1590413260, rs2140538834, rs121913027, rs121913028, rs121913018, rs121913020, rs121913021, rs121913024, rs121913026, rs41556519, rs185142838, rs587778271
View all (20 more)
Polyneuropathy Polyneuropathy rs1597597437
Spastic paraplegia Spastic Paraplegia rs118204049, rs121918262, rs104894490, rs119476046, rs281865117, rs281865118, rs137853017, rs72554620, rs121908610, rs121908611, rs121908613, rs116171274, rs121434442, rs121434443, rs137852520
View all (368 more)
Xeroderma pigmentosum Xeroderma Pigmentosum, Xeroderma pigmentosum, group G, Xeroderma Pigmentosum, Type G-Cockayne Syndrome rs794729654, rs794729655, rs752088918, rs121965088, rs794729656, rs794729657, rs754532049, rs1200172747, rs104894132, rs104894133, rs104894134, rs1587755557, rs2127773185, rs2127773120, rs121908562
View all (169 more)
7951246, 15082767