ADNP
Sign in to saveAlso known as ADNP1, MRD28, HVDAS, activity-dependent neuroprotector homeobox, activity dependent neuroprotector homeobox
protein-coding gene in the species Homo sapiens
In the Vinony graph
Vinony's link graph records 8 inbound references to ADNP, and connects out to PubMed, human chromosome 20 and Ensembl genome database project.
It is catalogued under the topic Genes on human chromosome 20.
Vinony links it to 4 Wikipedia language editions.
Gene data
ADNP- Name
- activity dependent neuroprotector homeobox
- Type
- protein-coding
- Position
- 50,854,048–50,931,437 (−)
- Aliases
- ADNP1, HVDAS, MRD28
- Ensembl
- ENSG00000101126
- RefSeq RNA
- NM_001282531.3, NM_001282532.2, NM_001347511.2, NM_001439000.1, NM_001439001.1
- RefSeq protein
- NP_001269460.1, NP_001269461.1, NP_001334440.1, NP_001425929.1, NP_001425930.1
Vasoactive intestinal peptide is a neuroprotective factor that has a stimulatory effect on the growth of some tumor cells and an inhibitory effect on others. This gene encodes a protein that is upregulated by vasoactive intestinal peptide and may be involved in its stimulatory effect on certain tumor cells. The encoded protein contains one homeobox and nine zinc finger domains, suggesting that it functions as a transcription factor. This gene is also upregulated in normal proliferative tissues. Finally, the encoded protein may increase the viability of certain cell types through modulation of p53 activity. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
activity dependent neuroprotector homeobox
- Symbol
- ADNP
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 20:50,854,048-50,931,437
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
Show 8 more facts
- HomoloGene ID
- 7617
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/23394
- genomic end
- 50931437
- genomic start
- 50888916
- chromosome
- human chromosome 20
- cytogenetic location
- 20q13.13
- genetic association
- Helsmoortel-Van Der Aa syndrome
Sources (9)
via Wikidata · CC0