Human Gene VIP (ENST00000367244.8_5) from GENCODE V47lift37
Description: vasoactive intestinal peptide, transcript variant 1 (from RefSeq NM_003381.4)
Gencode Transcript: ENST00000367244.8_5
Gencode Gene: ENSG00000146469.13_7
Transcript (Including UTRs)
Position: hg19 chr6:153,071,932-153,080,895 Size: 8,964 Total Exon Count: 7 Strand: +
Coding Region
Position: hg19 chr6:153,073,313-153,078,276 Size: 4,964 Coding Exon Count: 5
Data last updated at UCSC: 2024-08-22 23:36:26
Sequence and Links to Tools and Databases
Comments and Description Text from UniProtKB
ID: VIP_HUMAN
DESCRIPTION: RecName: Full=VIP peptides; Contains: RecName: Full=Intestinal peptide PHV-42; AltName: Full=Peptide histidine valine 42; Contains: RecName: Full=Intestinal peptide PHM-27; AltName: Full=Peptide histidine methioninamide 27; Contains: RecName: Full=Vasoactive intestinal peptide; Short=VIP; AltName: Full=Vasoactive intestinal polypeptide; Flags: Precursor;
FUNCTION: VIP causes vasodilation, lowers arterial blood pressure, stimulates myocardial contractility, increases glycogenolysis and relaxes the smooth muscle of trachea, stomach and gall bladder.FUNCTION: PHM and PHV also cause vasodilation.SUBCELLULAR LOCATION: Secreted.SIMILARITY: Belongs to the glucagon family.WEB RESOURCE: Name=Wikipedia; Note=Vasoactive intestinal peptide entry; URL="http://en.wikipedia.org/wiki/Vasoactive_intestinal_peptide";
Primer design for this transcript
MalaCards Disease Associations
MalaCards Gene Search: VIP
Diseases sorted by gene-association score: vipoma (36), wdha syndrome (28), vasomotor rhinitis (27), ganglioneuroma (22), chemical colitis (21), pancreatic cholera (18), somatostatinoma (17), cholera (17), fetal alcohol syndrome (16), islet cell tumor (14), impotence (13), subcortical arteriosclerotic encephalopathy (13), glucagonoma (12), ganglioneuroblastoma (12), cluster headache (12), achalasia (12), gastrinoma (11), megaesophagus (10), amyloid neuropathy (10), holoprosencephaly 3 (10), persian gulf syndrome (9), cryptosporidiosis (9), constipation (9), megacolon (9), bronchitis (9), cervical neuroblastoma (9), extracranial neuroblastoma (9), hyperprolactinemia (8), eisenmenger syndrome (8), normal pressure hydrocephalus (7), adie pupil (7), urticaria pigmentosa (7), endocrine gland cancer (7), anismus (6), diffuse pulmonary fibrosis (6), postgastrectomy syndrome (6), secretory diarrhea (5), space motion sickness (5), hirschsprung disease 1 (5), allergic rhinitis (5), pulmonary hypertension (4), pertussis (4), autonomic nervous system neoplasm (4), acromegaly (4), binswanger's disease (3), rhinitis (3), asthma (3), pheochromocytoma (3), small cell cancer of the lung, somatic (2), cystic fibrosis (2), pancreatic cancer (2), peripheral nervous system neoplasm (1), neuroblastoma (1)
Comparative Toxicogenomics Database (CTD)
Common Gene Haplotype Alleles
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RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
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mRNA Secondary Structure of 3' and 5' UTRs
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Protein Domain and Structure Information
InterPro Domains: Graphical view of domain structure IPR000532 - Glucagon_GIP_secretin_VIP
IPR015523 - VIP
Pfam Domains: PF00123 - Peptide hormone
Protein Data Bank (PDB) 3-D Structure
ModBase Predicted Comparative 3D Structure on P01282
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Gene Ontology (GO) Annotations with Structured Vocabulary
Descriptions from all associated GenBank mRNAs
AK313950 - Homo sapiens cDNA, FLJ94595.BC009794 - Homo sapiens vasoactive intestinal peptide, mRNA (cDNA clone MGC:13587 IMAGE:4294373), complete cds.AK291959 - Homo sapiens cDNA FLJ77165 complete cds, highly similar to Homo sapiens vasoactive intestinal peptide (VIP), transcript variant 2, mRNA.M36634 - Human vasoactive intestinal peptide (VIP) mRNA, complete cds.CU679495 - Synthetic construct Homo sapiens gateway clone IMAGE:100018534 5' read VIP mRNA.HQ447888 - Synthetic construct Homo sapiens clone IMAGE:100071241; CCSB006418_02 vasoactive intestinal peptide (VIP) gene, encodes complete protein.KJ892378 - Synthetic construct Homo sapiens clone ccsbBroadEn_01772 VIP gene, encodes complete protein.M54930 - Human vasoactive intestinal peptide and peptide histidine isoleucine mRNA, 3' end.JD302050 - Sequence 283074 from Patent EP1572962.JD490725 - Sequence 471749 from Patent EP1572962.JD354538 - Sequence 335562 from Patent EP1572962.JD465294 - Sequence 446318 from Patent EP1572962.JD303042 - Sequence 284066 from Patent EP1572962.JD171402 - Sequence 152426 from Patent EP1572962.
Biochemical and Signaling Pathways
Other Names for This Gene
Alternate Gene Symbols: ENST00000367244.1, ENST00000367244.2, ENST00000367244.3, ENST00000367244.4, ENST00000367244.5, ENST00000367244.6, ENST00000367244.7, NM_003381, P01282, Q5TCY8, Q5TCY9, Q96QK3, uc318ftk.1, uc318ftk.2, VIP_HUMANUCSC ID: ENST00000367244.8_5RefSeq Accession: NM_003381.4
Protein: P01282
(aka VIP_HUMAN)
Gene Model Information
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Methods, Credits, and Use Restrictions
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for details on how this gene model was made and data restrictions if any.