Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8875
Gene name Gene Name - the full gene name approved by the HGNC.
Vanin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
VNN2
Synonyms (NCBI Gene) Gene synonyms aliases
FOAP-4, GPI-80
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q23.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene product is a member of the Vanin family of proteins that share extensive sequence similarity with each other, and also with biotinidase. The family includes secreted and membrane-associated proteins, a few of which have been reported to particip
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016760 hsa-miR-335-5p Microarray 18185580
MIRT022124 hsa-miR-124-3p Microarray 18668037
MIRT028816 hsa-miR-26b-5p Microarray 19088304
MIRT1485707 hsa-miR-1236 CLIP-seq
MIRT1485708 hsa-miR-2467-5p CLIP-seq
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 32814053
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane TAS
GO:0015939 Process Pantothenate metabolic process IBA 21873635
GO:0015939 Process Pantothenate metabolic process IDA 11491533
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603571 12706 ENSG00000112303
Protein
UniProt ID O95498
Protein name Pantetheine hydrolase VNN2 (EC 3.5.1.92) (Glycosylphosphatidyl inositol-anchored protein GPI-80) (Protein FOAP-4) (Vascular non-inflammatory molecule 2) (Vanin-2)
Protein function Amidohydrolase that hydrolyzes specifically one of the carboamide linkages in D-pantetheine thus recycling pantothenic acid (vitamin B5) and releasing cysteamine (PubMed:11491533). Involved in the thymus homing of bone marrow cells. May regulate
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00795 CN_hydrolase 51 262 Carbon-nitrogen hydrolase Family
PF19018 Vanin_C 337 487 Vanin C-terminal domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed with higher expression in spleen and blood. {ECO:0000269|PubMed:19322213}.
Sequence
Sequence length 520
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Pantothenate and CoA biosynthesis
Metabolic pathways
  Post-translational modification: synthesis of GPI-anchored proteins
Vitamin B5 (pantothenate) metabolism
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Dermatitis Dermatitis, Atopic rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 19322213
Psoriasis Psoriasis rs281875215, rs587777763, rs281875213, rs281875212 19322213
Associations from Text Mining
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 12237255, 17453718
Brain Neoplasms Inhibit 32823285
Bronchopulmonary Dysplasia Associate 34465876
Clear cell metastatic renal cell carcinoma Associate 31776298
Diabetes Mellitus Associate 37773841
Esophageal Squamous Cell Carcinoma Associate 12901795
Glioma Associate 34953280
Inflammation Associate 30826088, 32853382
Inflammatory Bowel Diseases Stimulate 17453718
Leukemia Myeloid Associate 31776298