AVP V67A [extracellular region]

Stable Identifier
R-HSA-5621446
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
AVP, Arg vasopressin, RecName: Full=Vasopressin-neurophysin 2-copeptin; AltName: Full=AVP-NPII; Contains: RecName: Full=Arg-vasopressin; Contains: RecName: Full=Neurophysin 2; AltName: Full=Neurophysin-II; Contains: RecName: Full=Copeptin; Flags: Precursor;
GN Name=AVP; Synonyms=ARVP, VP;
OS Homo sapiens, NEU2_HUMAN
AVP V67A [extracellular region] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
AVP, ARVP, VP
Chain
signal peptide:1-19, peptide:20-28, chain:32-124, peptide:126-164
Other Identifiers
11732028_at
16916638
207848_at
25318
34020_at
3895225
3895226
3895227
3895228
551
71892
8064575
A_23_P109133
AAA61291
AAA98772
AAB86629
AAI26197
AAI26225
AF031476
AL160414
AVP
AVP-201
BC126196
BC126224
CAA26935
CAA44681
CAA44682
CAB025318
CCDS13045
ENSG00000101200
ENSP00000369647
ENST00000380293
EntrezGene:551
g13259532_3p_at
GE57806
GO:0000003
GO:0002125
GO:0003013
GO:0003084
GO:0003091
GO:0003674
GO:0004672
GO:0005102
GO:0005179
GO:0005184
GO:0005185
GO:0005575
GO:0005576
GO:0005615
GO:0005622
GO:0005623
GO:0005737
GO:0005829
GO:0006091
GO:0006464
GO:0006629
GO:0006810
GO:0006833
GO:0006915
GO:0006950
GO:0007005
GO:0007165
GO:0007186
GO:0007204
GO:0007267
GO:0007621
GO:0007625
GO:0007626
GO:0008150
GO:0008219
GO:0008283
GO:0008284
GO:0009058
GO:0010469
GO:0010628
GO:0014049
GO:0014070
GO:0016301
GO:0030141
GO:0030234
GO:0030307
GO:0030425
GO:0030665
GO:0031394
GO:0031410
GO:0031894
GO:0031895
GO:0032849
GO:0033138
GO:0033574
GO:0035094
GO:0035176
GO:0035813
GO:0040007
GO:0042310
GO:0042538
GO:0042592
GO:0042711
GO:0043027
GO:0043066
GO:0043084
GO:0043154
GO:0043226
GO:0044281
GO:0045471
GO:0045907
GO:0050877
GO:0050880
GO:0050891
GO:0051970
GO:0061024
GO:0070371
GO:0070528
GO:0090201
HGNC:894
HPA071892
ILMN_1811443
IPR000981
IPR022423
IPR036387
LRG_715
M11166
M25647
MIM:125700
MIM:192340
NM_000490
NP_000481
PF00184
PF00220
PR00831
SM00003
TC20000567.hg
TC20001386.hg
uc002whu.3
UPI000012FF67
X03172
X62890
X62891
X62891_s_at
XM_011529267
XP_011527569
Participant Of
Other forms of this molecule
Modified Residues
Name
L-valine 67 replaced with L-alanine
Coordinate
67
PsiMod
A protein modification that effectively removes or replaces an L-valine.
A protein modification that effectively converts a source amino acid residue to an L-alanine.
Disease
Name Identifier Synonyms
neurohypophyseal diabetes insipidus 12388 central diabetes insipidus, Vasopressin deficiency, vasopressin defective diabetes insipidus, Pituitary diabetes insipidus
Cross References
OpenTargets
GeneCards
PRO
Orphanet
Interactors (1)