Identification |
HMDB Protein ID
| HMDBP10751 |
Secondary Accession Numbers
| |
Name
| Vasopressin-neurophysin |
Synonyms
|
Not Available
|
Gene Name
| Not Available |
Protein Type
| Unknown |
Biological Properties |
General Function
| Involved in neurohypophyseal hormone activity |
Specific Function
| Not Available |
Pathways
|
Not Available
|
Reactions
| Not Available |
GO Classification
|
Component |
extracellular region |
Function |
hormone activity |
binding |
protein binding |
receptor binding |
neuropeptide hormone activity |
neurohypophyseal hormone activity |
|
Cellular Location
|
Not Available
|
Gene Properties |
Chromosome Location
| Not Available |
Locus
| Not Available |
SNPs
| Not Available |
Gene Sequence
|
>117 bp
ATGCCTGACACCATGCTGCCCGCCTGCTTCCTCGGCCTACTGGCCTTCTCCTCCGCGTGC
TACTTCCAGAACTGCCCGAGGGGCGGCAAGAGGGCCATGTCCGACCTGGAGCTGAGA
|
Protein Properties |
Number of Residues
| 39 |
Molecular Weight
| 4312.0 |
Theoretical pI
| 8.04 |
Pfam Domain Function
|
|
Signals
|
|
Transmembrane Regions
|
|
Protein Sequence
|
>Vasopressin-neurophysin
MPDTMLPACFLGLLAFSSACYFQNCPRGGKRAMSDLELR
|
External Links |
GenBank ID Protein
| 2625108 |
UniProtKB/Swiss-Prot ID
| Q9UEW6 |
UniProtKB/Swiss-Prot Entry Name
| Q9UEW6_HUMAN |
PDB IDs
|
|
GenBank Gene ID
| AF031475 |
GeneCard ID
| Not Available |
GenAtlas ID
| Not Available |
HGNC ID
| HGNC:894 |
References |
General References
| - Bahnsen U, Oosting P, Swaab DF, Nahke P, Richter D, Schmale H: A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus. EMBO J. 1992 Jan;11(1):19-23. [PubMed:1740104 ]
|