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Go!
Schema
>
ReferenceIsoform
>
Entries
UniProt:P49023-2 PXN
Show undefined attributes
created
[InstanceEdit:11155652] Interactions Importer, 2026-03-20 05:00:18
crossReference
[DatabaseIdentifier:12156778] PDB:6U4M
[DatabaseIdentifier:12445156] RefSeq:NP_001074324.1
[DatabaseIdentifier:12445155] RefSeq:NP_079433.3
[DatabaseIdentifier:12445157] RefSeq:NP_001230685.1
[DatabaseIdentifier:12445154] RefSeq:NP_002850.2
[DatabaseIdentifier:12282265] Pharos - Targets:P49023
[DatabaseIdentifier:12260219] PRO:P49023
[DatabaseIdentifier:12153650] PDB:4EDN
[DatabaseIdentifier:12156772] PDB:9QWO
[DatabaseIdentifier:11507802] ENSEMBL:ENSG00000089159
[DatabaseIdentifier:11621790] ENSEMBL:ENSP00000395536
[DatabaseIdentifier:11621789] ENSEMBL:ENSP00000391283
[DatabaseIdentifier:11621791] ENSEMBL:ENSP00000228307
[DatabaseIdentifier:11621788] ENSEMBL:ENSP00000267257
[DatabaseIdentifier:11744489] ENSEMBL:ENST00000424649
[DatabaseIdentifier:11744488] ENSEMBL:ENST00000267257
[DatabaseIdentifier:11744490] ENSEMBL:ENST00000458477
[DatabaseIdentifier:11744487] ENSEMBL:ENST00000228307
[DatabaseIdentifier:11784349] GeneCards:PXN
[DatabaseIdentifier:11799821] GlyGen:P49023
[DatabaseIdentifier:11837446] HPA:ENSG00000089159-PXN
[DatabaseIdentifier:12121941] OpenTargets:ENSG00000089159
[DatabaseIdentifier:12140394] PDB:5UWH
[DatabaseIdentifier:12141050] PDB:3RQG
[DatabaseIdentifier:12152173] PDB:2VZD
[DatabaseIdentifier:12156771] PDB:6PW8
[DatabaseIdentifier:12152179] PDB:2K2R
[DatabaseIdentifier:12156779] PDB:3PY7
[DatabaseIdentifier:12156781] PDB:1OW7
[DatabaseIdentifier:12156773] PDB:2O9V
[DatabaseIdentifier:12141047] PDB:3RQE
[DatabaseIdentifier:12156783] PDB:3U3F
[DatabaseIdentifier:12141048] PDB:3RQF
[DatabaseIdentifier:12156782] PDB:1OW6
[DatabaseIdentifier:12156775] PDB:4XH2
[DatabaseIdentifier:12156774] PDB:4XGZ
[DatabaseIdentifier:12156767] PDB:4R32
[DatabaseIdentifier:12156785] PDB:6IUI
[DatabaseIdentifier:12156777] PDB:6U4N
[DatabaseIdentifier:12152175] PDB:2VZG
[DatabaseIdentifier:12156780] PDB:1OW8
[DatabaseIdentifier:12156776] PDB:3GM1
[DatabaseIdentifier:12156784] PDB:7QB0
[DatabaseIdentifier:12152178] PDB:2VZI
databaseName
UniProt
dbId
11155651
displayName
UniProt:P49023-2 PXN
geneName
PXN
identifier
P49023
moleculeType
Protein
otherIdentifier
11717617_a_at
11717618_s_at
11736017_s_at
11736018_x_at
11748796_a_at
11749054_x_at
11752827_a_at
11752828_x_at
16771242
201087_PM_at
201087_at
211823_PM_s_at
211823_s_at
3474373
3474374
3474375
3474376
3474377
3474378
3474379
3474380
3474384
3474385
3474386
3474387
3474388
3474390
3474393
3474394
3474395
3474396
3474397
3474398
3474399
3474400
3474402
3474403
3474404
3474405
3474406
3474407
3474408
3474410
3474411
3474416
3474417
3474423
3474424
3474425
3474426
38644_at
5829
7967002
7967021
A_24_P184555
A_33_P3380086
A_33_P3380098
GE58953
GO:0001725
GO:0005515
GO:0005737
GO:0005829
GO:0005856
GO:0005875
GO:0005886
GO:0005911
GO:0005925
GO:0005938
GO:0007155
GO:0007165
GO:0007172
GO:0007179
GO:0008013
GO:0016477
GO:0017166
GO:0019903
GO:0030027
GO:0034446
GO:0034614
GO:0038191
GO:0043542
GO:0046872
GO:0048870
GO:0051496
GO:0060396
GO:0065003
GO:0070161
HMNXSV003021472
HMNXSV003050104
HMNXSV003050935
TC12002037.hg
U14588_at
g1912054_3p_a_at
g4506344_3p_at
referenceDatabase
[ReferenceDatabase:2] UniProt
referenceGene
[ReferenceDNASequence:11372897] BioGPS Gene:5829 PXN
[ReferenceDNASequence:12760976] UCSC:P49023 PXN
[ReferenceDNASequence:11402828] COSMIC - genes:PXN PXN
[ReferenceDNASequence:11408250] CTD Gene:5829 PXN
[ReferenceDNASequence:11440364] dbSNP Gene:5829 PXN
[ReferenceDNASequence:11815974] HGNC:9718 PXN
[ReferenceDNASequence:11910809] KEGG:hsa:5829 PXN
[ReferenceDNASequence:12002686] Monarch:5829 PXN
[ReferenceDNASequence:12086779] NCBI Gene:5829 PXN
[ReferenceDNASequence:12107594] OMIM:602505 PXN
referenceTranscript
[ReferenceRNASequence:12626693] RefSeq:NM_001080855.3 PXN
[ReferenceRNASequence:12626694] RefSeq:NM_001243756.2 PXN
[ReferenceRNASequence:12626695] RefSeq:NM_002859.4 PXN
[ReferenceRNASequence:12626692] RefSeq:NM_025157.4 PXN
schemaClass
ReferenceIsoform
secondaryIdentifier
ENSP00000391283.2
species
[Species:48887] Homo sapiens
stId
uniprot:P49023-2
url
https://www.uniprot.org/uniprotkb/P49023-2/entry
variantIdentifier
P49023-2
Referrals
(interactor)
[UndirectedInteraction:11155653] UniProt:P51451 <-> UniProt:P49023-2 (IntAct)
[UndirectedInteraction:11186143] UniProt:Q9C005 <-> UniProt:P49023-2 (IntAct)
[UndirectedInteraction:11233061] UniProt:P07947 <-> UniProt:P49023-2 (IntAct)
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