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VNN1 (vanin 1)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8876
Gene nameGene Name - the full gene name approved by the HGNC.
Vanin 1
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
VNN1
SynonymsGene synonyms aliases
HDLCQ8, Tiff66
ChromosomeChromosome number
6
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q23.2
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the vanin family of proteins, which 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 participa
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT446019 hsa-miR-5004-5p PAR-CLIP 22100165
MIRT446018 hsa-miR-4751 PAR-CLIP 22100165
MIRT446016 hsa-miR-924 PAR-CLIP 22100165
MIRT446017 hsa-miR-1289 PAR-CLIP 22100165
MIRT446015 hsa-miR-4294 PAR-CLIP 22100165
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002526 Process Acute inflammatory response ISS 14966568
GO:0002544 Process Chronic inflammatory response ISS 14966568
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane TAS
GO:0006954 Process Inflammatory response ISS 15282320
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID O95497
Protein name Pantetheinase (EC 3.5.1.92) (Pantetheine hydrolase) (Tiff66) (Vascular non-inflammatory molecule 1) (Vanin-1)
Protein function Amidohydrolase that hydrolyzes specifically one of the carboamide linkages in D-pantetheine thus recycling pantothenic acid (vitamin B5) and releasing cysteamine. {ECO:0000269|PubMed:10567687, ECO:0000269|PubMed:11491533, ECO:0000269|PubMed:2547
PDB 4CYF , 4CYG , 4CYY , 7SLV , 7SLX , 7SLY , 9IZL
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00795 CN_hydrolase
50 299
Carbon-nitrogen hydrolase
Family
PF19018 Vanin_C
331 483
Vanin C-terminal domain
Domain
Sequence
Sequence length 513
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Pantothenate and CoA biosynthesis
Metabolic pathways
  Post-translational modification: synthesis of GPI-anchored proteins
Vitamin B5 (pantothenate) metabolism
Neutrophil degranulation
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Dermatitis Dermatitis, Atopic rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 19322213
Inflammatory bowel disease Inflammatory Bowel Diseases rs137853579, rs137853580, rs121909601, rs149491038, rs368287711, rs387907326, rs587777338, rs758439420, rs139868987, rs750447828, rs368138379, rs1329427406, rs1264862631, rs1192830343, rs1373354533, rs1419560997, rs1591263883, rs1989014468 17145956
Psoriasis Psoriasis rs281875215, rs587777763, rs281875213, rs281875212 19322213
Unknown
Disease name Disease term dbSNP ID References
Celiac disease Celiac Disease rs2305764, rs35218876 30097691
Dyslipidemias Dyslipidemias 17873875
Eczema Eczema, Infantile 19322213
Palmoplantar pustules Pustulosis of Palms and Soles 19322213

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