Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
55871
Gene name Gene Name - the full gene name approved by the HGNC.
Zn regulated GTPase metalloprotein activator 1A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNG1A
Synonyms (NCBI Gene) Gene synonyms aliases
CBWD1, COBP
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9p24.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT048672 hsa-miR-99a-5p CLASH 23622248
MIRT047172 hsa-miR-182-3p CLASH 23622248
MIRT043329 hsa-miR-331-3p CLASH 23622248
MIRT499082 hsa-miR-7-1-3p PAR-CLIP 21572407
MIRT499081 hsa-miR-7-2-3p PAR-CLIP 21572407
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, 32814053
GO:0005524 Function ATP binding IEA
GO:0005737 Component Cytoplasm IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611078 17134 ENSG00000172785
Protein
UniProt ID Q9BRT8
Protein name Zinc-regulated GTPase metalloprotein activator 1A (EC 3.6.5.-) (Cobalamin synthase W domain-containing protein 1) (COBW domain-containing protein 1) (NPC-A-6 COBW domain-containing protein 1) (NPC-A-6)
Protein function Zinc chaperone that directly transfers zinc cofactor to target metalloproteins, thereby activating them. Catalyzes zinc insertion into the active site of methionine aminopeptidase METAP1, which function to cleave the initiator methionine from po
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02492 cobW 43 231 CobW/HypB/UreG, nucleotide-binding domain Domain
PF07683 CobW_C 274 377 Cobalamin synthesis protein cobW C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitously expressed. Up-regulated in cultured astrocytes treated with dopamine. {ECO:0000269|PubMed:15233989}.
Sequence
Sequence length 395
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Congenital anomalies of kidney and urinary tract Cakut rs267606865, rs121908436, rs281875326, rs879255515, rs75462234, rs869320679, rs760905589, rs797045022, rs869320624, rs745597204, rs1114167358, rs1555879360, rs1577330805, rs1008555507 31862704
Unknown
Disease term Disease name Evidence References Source
Carpal Tunnel Syndrome Carpal Tunnel Syndrome GWAS