UniProt:P13942 COL11A2

chain
  • signal peptide:1-27
  • chain:28-1736
  • propeptide:1501-1736
checksum D687B7AAD6A7774C
comment
  • FUNCTION May play an important role in fibrillogenesis by controlling lateral growth of collagen II fibrils.SUBUNIT Trimers composed of three different chains: alpha 1(XI), alpha 2(XI), and alpha 3(XI). Alpha 3(XI) is a post-translational modification of alpha 1(II). Alpha 1(V) can also be found instead of alpha 3(XI)=1(II).INTERACTION Isoforms lack exons 6, 7 or 8 or a combination of these exons. Experimental confirmation may be lacking for some isoforms.DOMAIN The C-terminal propeptide, also known as COLFI domain, have crucial roles in tissue growth and repair by controlling both the intracellular assembly of procollagen molecules and the extracellular assembly of collagen fibrils. It binds a calcium ion which is essential for its function (By similarity).PTM Prolines at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains.PTM A disulfide-bonded peptide called proline/arginine-rich protein or PARP is released from the N-terminus during extracellular processing and is subsequently retained in the cartilage matrix from which it can be isolated in significant amounts.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.DISEASE The disease is caused by variants affecting the gene represented in this entry.SIMILARITY Belongs to the fibrillar collagen family.ONLINE INFORMATION Gene page
crossReference
databaseName UniProt
dbId 51172
description
  • recommendedName: Collagen alpha-2(XI) chain
displayName UniProt:P13942 COL11A2
geneName
  • COL11A2
identifier P13942
isSequenceChanged false
keyword
  • Alternative splicing
  • Calcium
  • Collagen
  • Deafness
  • Disease variant
  • Disulfide bond
  • Dwarfism
  • Extracellular matrix
  • Glycoprotein
  • Hydroxylation
  • Metal-binding
  • Non-syndromic deafness
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
  • Stickler syndrome
modified [InstanceEdit:9926675] Weiser, Joel, 2024-11-03
moleculeType Protein
name
  • COL11A2
otherIdentifier
  • 1026_s_at
  • 1027_at
  • 11743769_a_at
  • 11744676_a_at
  • 11755914_a_at
  • 1302
  • 17018053
  • 17029860
  • 17032547
  • 17034867
  • 17037347
  • 17040053
  • 17042562
  • 213870_PM_at
  • 213870_at
  • 216993_PM_s_at
  • 216993_s_at
  • 2950368
  • 2950389
  • 2950390
  • 2950391
  • 2950392
  • 2950393
  • 2950394
  • 2950396
  • 2950397
  • 2950398
  • 2950399
  • 2950400
  • 2950401
  • 2950402
  • 2950403
  • 2950404
  • 2950405
  • 2950406
  • 2950407
  • 2950408
  • 2950409
  • 2950410
  • 2950412
  • 2950413
  • 2950414
  • 2950415
  • 2950416
  • 2950417
  • 2950418
  • 2950419
  • 2950420
  • 2950421
  • 2950422
  • 2950423
  • 2950424
  • 2950425
  • 2950426
  • 2950427
  • 2950429
  • 2950430
  • 2950431
  • 2950432
  • 2950433
  • 2950434
  • 2950435
  • 2950437
  • 2950438
  • 2950440
  • 2950441
  • 2950442
  • 2950443
  • 2950444
  • 2950445
  • 2950446
  • 2950447
  • 2950448
  • 2950449
  • 2950450
  • 2950451
  • 2950452
  • 2950453
  • 2950454
  • 2950455
  • 2950456
  • 2950458
  • 2950459
  • 2950460
  • 2950461
  • 2950462
  • 2950463
  • 2950465
  • 2950466
  • 2950467
  • 2950468
  • 2950469
  • 2950470
  • 2950471
  • 2950472
  • 2950473
  • 3002979
  • 41652_at
  • 65322_at
  • 8125568
  • 8178897
  • 8180105
  • A_33_P3216442
  • A_33_P3216448
  • GE56078
  • GO:0001501
  • GO:0001894
  • GO:0002062
  • GO:0005198
  • GO:0005201
  • GO:0005515
  • GO:0005576
  • GO:0005581
  • GO:0005585
  • GO:0005592
  • GO:0005788
  • GO:0005840
  • GO:0007605
  • GO:0030020
  • GO:0030154
  • GO:0030198
  • GO:0030199
  • GO:0030312
  • GO:0030674
  • GO:0031012
  • GO:0046872
  • GO:0048705
  • GO:0048856
  • GO:0050877
  • GO:0051216
  • GO:0060021
  • GO:0060023
  • GO:0060090
  • HMNXSV003006397
  • HMNXSV003055751
  • Hs.121509.0.S1_3p_at
  • Hs.121509.1.S1_3p_a_at
  • ILMN_1748166
  • ILMN_2311456
  • PH_hs_0024520
  • TC06001579.hg
  • TC6_cox_hap2000203.hg
  • TC6_dbb_hap3000189.hg
  • TC6_mann_hap4000171.hg
  • TC6_mcf_hap5000178.hg
  • TC6_qbl_hap6000191.hg
  • TC6_ssto_hap7000173.hg
  • U41068_cds2_s_at
physicalEntity
referenceDatabase [ReferenceDatabase:2] UniProt
referenceGene
referenceTranscript
schemaClass ReferenceGeneProduct
secondaryIdentifier
  • COBA2_HUMAN
  • A6NLX2
  • E7ER90
  • Q07751
  • Q13271
  • Q13272
  • Q13273
  • Q5JP94
  • Q5SUI8
  • Q7Z6C3
  • Q99866
  • Q9UIP9
sequenceLength 1736
species [Species:48887] Homo sapiens
stId uniprot:P13942
url http://purl.uniprot.org/uniprot/P13942

Referrals

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