Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
64224
Gene name Gene Name - the full gene name approved by the HGNC.
HERPUD family member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HERPUD2
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p14.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT030766 hsa-miR-21-5p Microarray 18591254
MIRT708110 hsa-miR-1277-5p HITS-CLIP 21572407
MIRT702998 hsa-miR-3163 HITS-CLIP 21572407
MIRT708108 hsa-miR-656-3p HITS-CLIP 21572407
MIRT703006 hsa-miR-340-5p HITS-CLIP 23313552
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 32296183
GO:0007283 Process Spermatogenesis IEA
GO:0016021 Component Integral component of membrane IEA
GO:0030968 Process Endoplasmic reticulum unfolded protein response IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620829 21915 ENSG00000122557
Protein
UniProt ID Q9BSE4
Protein name Homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 2 protein
Protein function Could be involved in the unfolded protein response (UPR) pathway.
PDB 2KDB
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00240 ubiquitin 12 89 Ubiquitin family Domain
Sequence
MDQSGMEIPVTLIIKAPNQKYSDQTISCFLNWTVGKLKTHLSNVYPSKPLTKDQRLVYSG
RLLPDHLQLKDILRKQDEYHMVHLVCTSR
TPPSSPKSSTNRESHEALASSSNSSSDHSGS
TTPSSGQETLSLAVGSSSEGLRQRTLPQAQTDQAQSHQFPYVMQGNVDNQFPGQAAPPGF
PVYPAFSPLQMLWWQQMYAHQYYMQYQAAVSAQATSNVNPTQPTTSQPLNLAHVPGEEPP
PAPNLVAQENRPMNENVQMNAQGGPVLNEEDFNRDWLDWMYTFSRAAILLSIVYFYSSFS
RFIMVMGAMLLVYLHQAGWFPFRQEGGHQQAPNNNAEVNNDGQNANNLELEEMERLMDDG
LEDESGEDGGEDASAIQRPGLMASAWSFITTFFTSLIPEGPPQVAN
Sequence length 406
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Unknown
Disease term Disease name Evidence References Source
Hypertension Hypertension GWAS
Dementia Dementia GWAS
Myocardial Infarction Myocardial Infarction GWAS
Brugada Syndrome Brugada Syndrome GWAS