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Record Information
Record ID 61
Pubmed ID 30088198
SNP DQB104
Gene ID 3119
Protein ID P01920
Vaccine Adverse Events chronic hepatitis B
Vaccine Hepatitis B recombinant vaccine
Gene Name HLA-DQB1
Official Symbol major histocompatibility complex, class II, DQ beta 1 [Homo sapiens (human)]
Aliases CELIAC1, HLA-DQB, IDDM1
Other Designations HLA class II histocompatibility antigen, DQ beta 1 chain; MHC class II DQ beta chain; MHC class II HLA-DQ beta glycoprotein; MHC class II antigen DQB1; MHC class II antigen HLA-DQ-beta-1
Chromosome 6
Location 6p21.32
Annotation Chromosome 6 NC_000006.12 (32659467..32666657, complement)
MIM 604305
DNA Sequence >NC_000006.12:32659467-32666657 Homo sapiens chromosome 6, GRCh38.p14 Primary Assembly TTTAGACTCAAAAATAGTATTTTTATTGCTGGTTATGCTTTCTTAAAAATAAAAAATATTCTTGATCGAT GTGACTTTCCAGAATGTTTGAAACACCAGTGACCAAGGATCACTATATATGTCTCCAAACAATTCTACCA TGCTTATTTACACAGCACTCACCAAACCAGAAGAGAGGCTGGGATATTCTAAGGCCAATGCACTGAGCAT CAGTATTAAAGAACCATGAATGATGCGACAATTGAATTATTTTCTACCTCCTCTGCCCACCCTTACTTCA CACCCCAAAATGCTTTCAGTGTCTTTTCAAGGTACAATCCTCCTTCTGGCCACAGGTTTGCTGGGTCACC TCAAGGGATGTTCCTTCATTCTGCAGTGATTTCCTGCCTCTTCTCAATTAAGAAAGTTCAGAATACAGAT AACTCAGGATCATGTTTAATTATGTAAAAAAGCTCTAAAGTCAGGTAATGTTTTTCATGTGCTTCTCTTG AGCAGTCTGAGGAAAGAATAGAAACAGAAACCCCTTGGGACCTGAGTAGACGCAGCTGGCCATGCACAGG CAGAGGCTCTGGGTCAGTGCAGGAAGCAGAGTCACAGCCAGCGCCTTGGGGTGGGGATGAAAGGAGATGA CCTGGTGGCTGCGTGACAGCCACTGTAGGACTTTGATCTCAGGGGGACAAGCTGACACAGGCAGCTGGGA ATTCTGGGCAGGCATAAGCAGGCATCACAGAAGAGTGATAACCAATCCTAGTTAAAATAGTCTCAGGAGT CAGTGCAGAAGCCCTGGAGAAGAGAGAAGAGCATTGATCAGCACAGGGTATCCTGGTGGGCCTGCCATCT CCCCCACCCTTCAGGGGCCCCCTGCAGCTTCAGACAGAGAAAGTTGAGGTCCAGGGTGTATTGTCATCAC CTCCCCCAAGATCTGTGCAAAGGTGAAATCAGCTCATGAGGACACAGAACTTCAGCTTGATGCAGATGTG TGGGAGGTGGGGAACAGCTGTTATTCTTCTGGGGAATATGAAGGGTTCAGTCTTTTTAGGAAATTGGATG ATATCTCTTCCCGACCACTAGCAGCCTCTTTCAGTCACTGGAAAATGCTTACAGGCAGTAGCCACCATCA TGTGGCACAAAGTGGGCATCATCCTAGTGTCTAACATTTAAGCTGTGGTTCTGGCTCCACATTTCACAAG AAGATGCCACCAAAGTTAAGGCTTGGTTCTGGGGAACAATGTCTGGAGATTCCTAGAAACTGGCAAACTT CTCCCCTAAGTCTTGATCCTCATAGCAGCAAATAGGCCATGAACATGGACCACTGTGGTCAGGTACACTC AGCTCATGCTCTTCCCTCTTATACCTGTGCCTCCCCACACTGGATCATGGCTGAAATATTACCTGCTGGT GGAGGCCCTTGAGGTCTTACAAAAGGAAGTTATGCAGAGAAAGGTCTCATTACACAAACAGCCACTCTCT CACCCCAAAGGAAAATGACACACATGACTTAGAGTTACATTCTCTTCCCACCCATGTTCTTCCAGGCCTT CAGCACCCTAATTTAAAATCCCCTAAAACAAAGGAAATTGTCACTAGAAAGAAAGGAAGCTGAGGCTCTG ACCCTCTTAATGGAGGAAGCTTTTGGAAAGGAGCCAGTGAGACAATGATGAATGGTAAGGATGCCCTGGA ATAAGCTCTATCAGTCAGCTCTGTGACAGCGCTACCTTTCAACCAGTAAAATCAGATTCCAATGCCTCCT CCCATCTTGTCCTGTCTCCTCGCACTTCTTCTCAGGGTCAGGAGGAAAGAGCTAATCTACAGACAGGACC ACTCTGAACAGAGGGTCTGGGTCACAGCCCATCTTCCCCTTTTCCCCTGGGGTTCCTCACCTTTCTGACT CCTTTGACGGATGATAAGGCCCAGCCCAAGGAAGATCAGCCCCAGCACGAAGCCTCCAACGCCACTCAGC ATCTTGCTCTGGGCAGATTCAGACTGAGCCCCTAAAGAGCAGAACTGAGTGTCTGTGTTTGTCCCCACAC CCCATAGCATCCCTGCTGAGGAGTTGAAGTCCAGTCTGAGGTGCAGAAGGTGAAGGCATCAAAGGAACCT AGTTCTCCATTCAGACCACCCCTAAGGAGGGGAAAGACCAGCCAATAGGTCCTTGGATACAGTGAATAGG TGAGAGAGTGGGGAAGCAAATCTCTGCTCTTCAAGAACTCATCCATAACCTTAGACCCTAAGATCCCAGT CACCAGCCCTAAGAATCAGTCCCTCAGAGCTATCAGGACTGGGATTCAGAGCAACAGTATGTAGAGTAAT TTCCCTAGCATCTGGAAAGGTGATGAGACCAGGATTCTTCTGATGCACTTGCCATGGAGCAAGAGGTGCT CTAGTCTCCTGTGATTCCCAGCTCAGTAGTGACATCAGGGATAAGAGATGGGAAGGAATGGGTCAGAAGG AGCTCTTTGTCTTGTGGGCCCATAGTAACAGAAACTCAATATCCCCTTACGCCACTCCACGGTGATGGGG CTCTGGAGGCTGGGGTGCTCCACGTGGCAGGTGTAGACATCTCCACGCTGGGGAGTCATTTCCAGCATCA CCAGGATCTGGAAAGTCCAGTCACCATTCCTAATAAGGGGGGTGGACACAACGCCGGCTGTCTCCTCCTG ATCATTCCGAAACCACCGGACTTTGATCTGGCCTGGATAGAAATCTGTCACCGAGCAGACCAGCAGGTTG TGGTGGTTGAGGGCCTCTGTCCTGGATGGGGAGATGGTCACTGTGGGCTCCACTGAGGGCAGTAACAGAC AGGAAAAGACATAGGAGTGAGATGTGAGAACACACACCACGTCTACCATGAGGAAGGATCCCTCCTTGGA CCAGAGTGGAAAGATACCTGGAGTCGAAGTCTTGGATTAAGGTTCATTCAACAAATATAAATTTGACAAT CACTGAGAATTCAAAGATAAATAACATACTATGGTCCCTGCATTTATAGAATGTGCAATCTAGTAACAGA CAGCAAAAAACAAAAAGAATGTTATTTCAAAAGTTTGTAATATTTGAAAAAAAAGTAGAATGTTATTTCA AAAGTTTGTAATATTTGAAAAAAAAGTAGGCAGGCCTTCAAAACAAATAACCCTTGATCAAACATCATGT TTGTCCACAACTCAATTCCTTTATCTTCTCAGATTGCTGCTCATAGTAAAAAAAATGACACATCTTTCCC CGCCTCTTTTACACATCTCATCCTTTCCTTTTAGGCCACTTTATCACATTTCCTTTATTCTCTTAGTGTG AAACTATAGCAAATATTTAATGTGTGCTTTCTTTATTTAGTAATATGTTCTCTCATTTTCTTTTTTTCCT TAATTTCTTTTTAACGCACAAGTGAGTTTAATTACTAGCTGTCTACCCTACTCCATTTCCTTGCTATTGA CAATTACTTTCTTGTTCTGAAATCAGACATTATCGTGTATGTTCTCCACAGAAAATATTCTGAGATCCGT GCAGAGGTCGGCCTGGGCTAATGAGCCTGTAATGTGAACATATACATATAACTGGGATTTGCTGAGGTCA GCAGGTGGCACCCCAATTAAATGGCACTCTTGAGCCATCATCCGGAAGGAATCATGGTTTCTGCTTGGAC TTGAACTTTTCTTTAGGTTCTCCTTCCTGGAGGCCAACTGAAATCAGAGTCAGCTATGTGGCCTTATAAG ATTTGTTCATCTTCAACAGACTGGGAGTAAAAATAGAGGGCACAAATTTATGAGAAAAGATGATAAAATA AATTTTATGGAAATAAAACTGAAATAGCAAAAATATAAGTACTTGCTGGCATTAGGATGTGAGTCAAAAG AAGGCAAGGGAGTGTAAAGCAAACTAAAAGTTTTGTGAACCTGCATAGATAACACCGGGGTCAGACTAGG GATTGATTAATCATGAATTTTCAATGCCGCATTAACACACAGAACAAACAGGAATAGACTCATTGCTGCT TCTGGTCAAAACTGGCTTTAACAAGGCCTTACATCCCTTAGACTCTACATATGTGTAGTGAGGAACATAA GAATGTTGTGTACTTTGGGAGGCTTAAGATCTTGGTGAGTAATTGTGGGCTGATTACTTAAAGTGTTTAT CATGTACCAATATTAGGATATATAAAGTGGTGATGCTAATCTCTAATGCACAGGTAGCTGTGAGATTAAA TGACATAACATAGATGGTATTTGATAAGGCAACTGTCTAGAAATAAGTGCTTCCTGAATGGGTAAAATTG ACTTTCAGAATGTTTATTCCTGAAGTGGATAGTGATGGGGGGGAGGGGATAACCTAGGCCAAAAGCAACC TGAAACTATTTTTATCCAATAATTTAATAGCTTCAACCTATTTATTCCCAAACTTCTGATCTTTGCATAG TGCTATTTGTTCAGCTTTTCTAAGAAATTAAAACTCTGCCTTACAACATCATTCAAGCATTGTTTTTATT TTTAGCAAACACATTTTCCTCAGACTTTGTATTCACAAATTCTATTAAGATCCAAGTCAGTAAGAGTTTA CTTGAAAGCATTAAGCAAAATGTTAGAAAATAATTGATAAAGTTCATTTGTAAGCCTCTGTTTTTTTCTT GAACCTAACTGGATTGGCAGCTGAGTACATTTATTCATGAATTTAACAGAAGATCATTGAGCTCACACCA CATACCAGTCAATGTGTCAGGTACCAGGCATGCAATAATTAAACAGTCTCTCGCCTCAAAGATCTCCGCC ATTAGTGGTAGCCATTTAAGAAAACAGAATTACGATGAATAATGATTTGAAGCCAAAAAGTCAAAATATC TTATTTCGCAACTGTAATTGCTGGATGCCCTGCGCGCAGCTGTGGGGCAGCCCTAACTCCACCAGGCCAA GCCTGAAGCTTCCTGCGGCGCAAGCTGCGCACGTGGGCCTTGCTGGGTGGGGCAGTGCTAGCGAGGCCGG CGGGCAGGGGAAGAGGGTGGGCACTGGGGGCAGAGAGAACTGCTTAGCGAAGGTAAGGTACGAGGAGGCA AACACATAAGGCACGAGGCGAGAAACGTGCAGAGCGGAGGACGAGGCCGACGGACGGGGAGGCTGGGGGG GACACTAGGCAGCCTGGCCAACTCTGCTTGTCCCCCTGCTCTGCCCTAGGTCCCCGCCCCTCCGATGCAC CTGCCCCCACCACCCCGCCGCCGCCTCCTTTCCCCTGGGGTGGAATGAACTGGGCTCAGATTTCAGAGAC CTCGCCCCCATCGCCCCTCCCGGCACAGAAACTCGGGGTCTCGGCCAAGGGTGGGCCTCACGGAGGGGCG ACGACGCTCACCTCTCCTCTGCAAGATCCCGCGGAACGCCACCTCGTAGTTGTGTCTGCACACCGTGTCC AACTCCGCCCGGGTCCCCTCCAGGACTTCCTTCTGGCTGTTCCAGTACTCGGCATCAGGCCGCCCCTGCG GCGTCACCGCGCGGTACACCCCCACGTCGCTGTCGAAGCGCGCGTACTCCTCTCGGTTATAGATGTATCT GGTCACAAGACGCACGCGCTCCGTCCCGTTGGTGAAGTAGCACATGCCCTTAAACTGGAACACGAAATCC TCTGCGGGGAATCACCGGCCGGTCAGTCAGGCCCCAGCCCGGCCGCCCCCGCAGCCGCCGCCCTGACCCG GCCTGGAGCTGTGGAACCGCCCGCGCGACCTCCAGTTCCCGCCCGCCCGTGCCTGGCGCTCCAGACCTGG GATCCTCCCGGCGGCTCTGCCCAGCTCTGCCCGCCTTCTTTGCGGGCTTCTGGAATCTGCCTTCCTACAT CCAGGAAAGGGAGGAAAGCCCTGTCCCTGCCTGAGCCTGTGAACCCAGCGAAGAGGCAGTCGGGCTGATT TTACATGCACCTCTGCACTTAGAGGGATCAGGGCGTTCTCGCATGAAATCCCATTTTTCATGAAGCTCCT GGATACCTCAGAGATAAAGTTATCCACATAAATCTGAGAGTTCAACGGAATGACGAGATAGGTCCAGGAA TTAAGCCTGGCCTCGTTCTGACACGCGTATTCTCTTGGTCCCTGGGTAAAATACCTTCCTTCCCATGCCT AGATTTACCCTCCCAAGTCCCGTTGAGGTTCACTCCCTTCTATGTTGGAAAGGACCTACACCTCTGAGTC CTAGATAGAGACATTTATTCATGGAAAGAGCACAAGCTTTTGAATTTGATAAACTAGATTCCAATTAAAC TGTGGCAGTCACCAGTTTGGGCAGGTTATGTAACAGAATATCCATATCACAAGTATAATTGTGTAAAAGA AAATCATGATATCTACACACAGGATGTTAGAAGGAGTGAGAGAGAAGTTATATAAAGTATTGTTCTGTCT GAAGTGAGTGGTTTCACAATATGTGTTATTTCCCTTCTTTACATCCTCCTTCCTACTAAATTCAGTCCAC CATTAACTCGGGTCTCTGAATCCCACTCAAGTCACCATTTGCCCATAAATCAGTGAAACCCGAAGACTCC CTCTCTGTGGTCAGCCAGTCAGCTTCCCTCAGCACCAAGATTTTGCCTCCACAAATGCTCCACTCGGTCA GGAATAGAGACAAATTTTCCTCAAATACAGAGACTACAGACACCATTGCTGCCTCACATTTTCCAATGCA GGATCTCATAATCCTAAGTCCAGGCAGTCTTGGGGCACGCCTAAATGACAAATCCTGCTGTGTCTTTGGA GAAATTCATATCTTCAAAAATAACCCCATGCTCACTTTGTCCTATCGCTGGTAGTAAATGTACACTTTAT CTCCTCTTTCTCTCCTCTCTCCTCCTCTTCCAGGCTTAAGCCTGTAGGATGGGGATTGGATTGTCCTCAT CTCATCACTAAAAGATAAATGGGAATGCAACATAGCTTTCTTTCCCAAGAGAGAGGAAATGTTGATGAAA GATTGTGTCCAAGATCATAGAGATCACCATCCCCCATACCCCAGCCCAAGGAGAGCCTGTTCCCAGAGTG GCGGCTCTGGAGAGCAGCTGCCCTGCACTTACCGGGAGAGTCTCTGCCCTCAGCCAGTAGGGAGCTCAGC ATCGCCAGCATCAAGGTGACAGTTGCTACCCGAAGGTCTCCGGGGATCCGCAAAGCCTTCTTCCAAGACA TAACTGAGACGAAGGGAAAAGCAGTGGTAGTCAACACAGCTCGGACCTGAT
Protein Name DQB1_HUMAN
Length 261
Moltype AA
Topology linear
Division PRI
Update Date 03-AUG-2022
Create Date 21-JUL-1986
Definition RecName: Full=HLA class II histocompatibility antigen, DQ beta 1 chain; AltName: Full=MHC class II antigen DQB1; Flags: Precursor
Primary Accession P01920
Accession Version P01920.2
Other SeqIDs sp|P01920.2|DQB1_HUMAN,gi|290457643
Organism Homo sapiens
Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Comment On or before Mar 2, 2010 this sequence version replaced gi:74739599, gi:74739651, gi:74739714, gi:74739717, P01918.1, P01919.2, P03992.2, P05537.1, gi:74739741, gi:74739742, gi:74739748, gi:121940129, gi:74739765, gi:121940216, gi:121940764, gi:74739933, gi:74739988, gi:74754534, gi:74740007, gi:121941628, gi:121941702, gi:74754550, gi:74740085, gi:74740086, gi:74740090, gi:74740091, gi:74740092, gi:74740093, gi:74754569, gi:121942322, gi:121943209, gi:82066185, gi:74740626, gi:74741001, gi:74741479, gi:74755527, gi:74755528, gi:74748054, gi:74757241, gi:74748151, gi:74748395, gi:74749748, gi:74749993, gi:74750604, gi:74750862, gi:74751330, gi:74751338, gi:74751343, gi:74751492, gi:74752211, gi:74752871, gi:74753162, gi:74753459, gi:74753460, gi:74753461, P01920.1.; [FUNCTION] Binds peptides derived from antigens that access the endocytic route of antigen presenting cells (APC) and presents them on the cell surface for recognition by the CD4 T-cells. The peptide binding cleft accommodates peptides of 10-30 residues. The peptides presented by MHC class II molecules are generated mostly by degradation of proteins that access the endocytic route, where they are processed by lysosomal proteases and other hydrolases. Exogenous antigens that have been endocytosed by the APC are thus readily available for presentation via MHC II molecules, and for this reason this antigen presentation pathway is usually referred to as exogenous. As membrane proteins on their way to degradation in lysosomes as part of their normal turn-over are also contained in the endosomal/lysosomal compartments, exogenous antigens must compete with those derived from endogenous components. Autophagy is also a source of endogenous peptides, autophagosomes constitutively fuse with MHC class II loading compartments. In addition to APCs, other cells of the gastrointestinal tract, such as epithelial cells, express MHC class II molecules and CD74 and act as APCs, which is an unusual trait of the GI tract. To produce a MHC class II molecule that presents an antigen, three MHC class II molecules (heterodimers of an alpha and a beta chain) associate with a CD74 trimer in the ER to form a heterononamer. Soon after the entry of this complex into the endosomal/lysosomal system where antigen processing occurs, CD74 undergoes a sequential degradation by various proteases, including CTSS and CTSL, leaving a small fragment termed CLIP (class-II-associated invariant chain peptide). The removal of CLIP is facilitated by HLA-DM via direct binding to the alpha-beta-CLIP complex so that CLIP is released. HLA-DM stabilizes MHC class II molecules until primary high affinity antigenic peptides are bound. The MHC II molecule bound to a peptide is then transported to the cell membrane surface. In B-cells, the interaction between HLA-DM and MHC class II molecules is regulated by HLA-DO. Primary dendritic cells (DCs) also to express HLA-DO. Lysosomal microenvironment has been implicated in the regulation of antigen loading into MHC II molecules, increased acidification produces increased proteolysis and efficient peptide loading.; [SUBUNIT] Heterodimer of an alpha and a beta subunit; also referred as MHC class II molecule. In the endoplasmic reticulum (ER) it forms a heterononamer; 3 MHC class II molecules bind to a CD74 homotrimer (also known as invariant chain or HLA class II histocompatibility antigen gamma chain). In the endosomal/lysosomal system; CD74 undergoes sequential degradation by various proteases; leaving a small fragment termed CLIP on each MHC class II molecule. MHC class II molecule interacts with HLA_DM, and HLA_DO in B-cells, in order to release CLIP and facilitate the binding of antigenic peptides. {ECO:0000269|PubMed:11376336, ECO:0000269|PubMed:14769912, ECO:0000269|PubMed:15020763, ECO:0000269|PubMed:17629515}.; [INTERACTION] P01920; P01909: HLA-DQA1; NbExp=8; IntAct=EBI-1038012, EBI-713389.; [SUBCELLULAR LOCATION] Cell membrane; Single-pass type I membrane protein. Endoplasmic reticulum membrane; Single-pass type I membrane protein. Golgi apparatus, trans-Golgi network membrane; Single-pass type I membrane protein. Endosome membrane; Single-pass type I membrane protein. Lysosome membrane; Single-pass type I membrane protein. Note=The MHC class II complex transits through a number of intracellular compartments in the endocytic pathway until it reaches the cell membrane for antigen presentation.; [POLYMORPHISM] The following alleles of HLA-DQB1 are known: DQB1*02:01, DQB1*02:02, DQB1*02:03, DQB1*02:04, DQB1*02:05, DQB1*03:01, DQB1*03:02, DQB1*03:03, DQB1*03:04, DQB1*03:05, DQB1*03:06, DQB1*03:07, DQB1*03:08, DQB1*03:09, DQB1*03:10, DQB1*03:11, DQB1*03:12, DQB1*03:13, DQB1*03:14, DQB1*03:15, DQB1*03:16, DQB1*03:17, DQB1*03:18, DQB1*03:19, DQB1*03:20, DQB1*03:21, DQB1*03:22, DQB1*03:23, DQB1*03:24, DQB1*03:25, DQB1*03:26, DQB1*04:01, DQB1*04:02, DQB1*04:03, DQB1*05:01, DQB1*05:02, DQB1*05:03, DQB1*05:04, DQB1*05:05, DQB1*06:01, DQB1*06:02, DQB1*06:03, DQB1*06:04, DQB1*06:05, DQB1*06:06, DQB1*06:07, DQB1*06:08, DQB1*06:09, DQB1*06:10, DQB1*06:11, DQB1*06:12, DQB1*06:13, DQB1*06:14, DQB1*06:15, DQB1*06:16, DQB1*06:17, DQB1*06:18, DQB1*06:19, DQB1*06:20, DQB1*06:21, DQB1*06:22, DQB1*06:23, DQB1*06:24, DQB1*06:25, DQB1*06:27, DQB1*06:28, DQB1*06:29, DQB1*06:30, DQB1*06:31, DQB1*06:32, DQB1*06:33, DQB1*06:34, DQB1*06:35, DQB1*06:36, DQB1*06:37, DQB1*06:38, and DQB1*06:39. The sequence shown is that of DQB1*03:01.; [POLYMORPHISM] DQ2 (heterodimer of DQA1*05:01/DQB1*02:01) is associated with more than 90% of celiac disease patients. A minority displays DQ8 (heterodimer of DQA1*03/DQB1*03:02).; [POLYMORPHISM] DQ0602 (heterodimer of DQA1*01:02/DQB1*06:02) confers dominant protection against type 1 diabetes (T1D) and strong susceptibility to narcolepsy. DQB1*06:02 has been found to be present in most of the narcolepsy patients. As well 98% of the patients with an HCRT deficiency are positive for DQB1*06:02.; [SIMILARITY] Belongs to the MHC class II family. {ECO:0000305}.; [SEQUENCE CAUTION] Sequence=AAC64403.2; Type=Erroneous gene model prediction; Evidence={ECO:0000305}; Sequence=CAJ57391.1; Type=Erroneous gene model prediction; Evidence={ECO:0000305}.
Source Db UniProtKB: locus DQB1_HUMAN, accession P01920;; class: standard.; extra accessions:A1KR27,A2RPH3,A4Q9R4,A4USG2,A4USG5,A6N8I7,A9YQA0,B0S7Y7,B1A0K6,B1GXI3,B3VLT3,B5BLN7,B7VU69,C0MQ34,C0MQ35,C8ZL52,C8ZLJ8,C8ZLJ9,C9DRQ3,O19708,O19713,O19724,O62861,O78046,O78221,O78223,O98034,O98201,P01917,P01918,P01919,P03992,P05537,P79482,P79526,P79544,P79551,Q08GC8,Q09035,Q0E4V9,Q1M312,Q29731,Q29877,Q29884,Q29915,Q29966,Q2P9N3,Q2QK85,Q30061,Q30075,Q30076,Q30080,Q30081,Q30082,Q30083,Q30084,Q30089,Q30095,Q31633,Q38I47,Q45UE3,Q4QZB5,Q53I44,Q564J6,Q5G841,Q5ISH1,Q5ISH3,Q5W1E1,Q5Y7G8,Q643R4,Q6B9X1,Q70VH8,Q7YP69,Q8HWH0,Q8MH58,Q8SNB4,Q8SND1,Q8SP70,Q8WMA3,Q9BD17,Q9MYH2,Q9TPA9,Q9XRY6,Q9XRY7,Q9XRZ2; created: Jul 21, 1986.; sequence updated: Mar 2, 2010.; annotation updated: Aug 3, 2022.; xrefs: K01499.1, AAA98746.1, K02405.1, AAA75521.1, X03068.1, CAA26872.1, M17564.1, AAA59765.1, M29613.1, M29616.1, M16996.1, AAA59770.1, M20432.1, AAA59769.1, M60028.1, AAA59755.1, X96420.1, CAA65280.1, U92032.1, AAB91991.1, AY663393.1, AAU87973.1, AY663394.1, AAU87977.1, AY663397.1, AAU87986.1, AY663409.1, AAU88017.1, AY663404.1, AAU88002.1, AY663410.1, AAU88020.1, AY663412.1, AAU88027.1, AY656681.1, AAV71028.1, AY656682.1, AAV71029.1, AY656683.1, AAV71030.1, BX927168.11, CR753846.4, CR933859.5, BC012106.1, AAH12106.1, M25327.1, AAA59677.1, U66400.1, AAB51698.1, U83582.1, AAB41231.1, AH002887.2, AAA59762.1, M26042.1, AAA36270.1, M33907.1, AAA52672.1, L34096.1, AAC41964.1, L34098.1, AAC41966.1, L34101.1, AAC41969.1, L34103.1, AAC41971.1, L34104.1, AAC41972.1, L34105.1, AAC41973.1, L34106.1, AAC41974.1, L34107.1, AAC41975.1, AF195245.1, AAF28315.1, L42626.1, AAA85335.1, X76553.1, X76554.1, M59800.1, AAA64235.1, M14189.1, AAA36268.1, AY672649.1, AAT77952.1, M17207.1, AAA59697.1, Z49215.1, AY026349.1, AAK01944.1, AF091305.2, AAC64403.2, U77344.1, AAB19215.1, FN256435.2, CAX62164.1, CAX62165.1, AM400970.1, CAL47037.1, AM421131.1, CAM07104.1, EF484936.1, ABO87661.1, EF484939.1, ABO87664.1, EU275158.1, ABY26531.1, AM944346.1, CAQ16179.1, FM200854.1, CAR31119.1, AH013029.2, AAP93137.1, EU770203.1, ACF16333.1, FM955320.1, CAW24712.1, FN552709.1, CBF35736.1, FN552710.1, CBF35739.1, X86327.1, D78569.1, BAA11413.1, AF439338.1, AAL35222.1, AF384556.1, AAM53072.1, DQ026226.1, AAY89656.1, AY762968.1, AAV97949.1, AM181332.1, CAJ57391.1, AM691798.1, CAM88661.1, AM259942.1, CAJ90956.1, U39090.1, AAB02681.1, AJ003005.1, AJ012156.1, CAA09929.1, AJ290396.1, CAC27418.1, AF469118.1, AAL77085.1, AF479569.1, AAM09472.1, AJ535315.2, CAD59445.2, AF181983.2, AAD54423.2, AY733062.1, AAU33811.1, AJ854065.1, CAH69441.1, AJ964903.1, CAI79639.1, AB211231.1, BAD95610.1, DQ114427.1, AAZ20753.1, DQ227421.1, ABB05231.1, AM403489.1, CAL48285.1, AM490069.1, CAM32717.1, EF622510.1, ABR24117.1, EU410617.1, ABZ89500.1, GQ422610.1, ACV66342.1, FN550110.1, CBE66554.1, AF087939.1, AAD39697.1, AY094140.1, AAM14401.1, AJ001257.1, CAA04631.1, U39086.1, AAA93181.1, AJ965439.1, CAI84643.1, AF112463.1, AAD23990.1, AF112464.1, AAD23991.1, M94773.1, M65042.1, AAA36241.1, M25025.1, AAA59793.1, HLHU1C, A35055, HLHUDB, B32527, B37044, HLHU2C, F30575, I54480, I68732, I72482, S46648, NP_001230891.1, NP_002114.3, 1JK8_B, 1S9V_B, 1S9V_E, 1UVQ_B, 2NNA_B, 4GG6_B, 4GG6_D, 4OZF_B, 4OZG_B, 4OZG_D, 4OZH_B, 4OZH_D, 4OZI_B, 4OZI_D; xrefs (non-sequence databases): PDBsum:1JK8, PDBsum:1S9V, PDBsum:1UVQ, PDBsum:2NNA, PDBsum:4GG6, PDBsum:4OZF, PDBsum:4OZG, PDBsum:4OZH, PDBsum:4OZI, AlphaFoldDB:P01920, SMR:P01920, BioGRID:109364, IntAct:P01920, MINT:P01920, STRING:9606.ENSP00000364080, TCDB:9.A.75.1.1, GlyGen:P01920, iPTMnet:P01920, PhosphoSitePlus:P01920, BioMuta:HLA-DQB1, DMDM:290457643, jPOST:P01920, MassIVE:P01920, PeptideAtlas:P01920, PRIDE:P01920, ProteomicsDB:51513, ABCD:P01920, CPTC:P01920, DNASU:3119, Ensembl:ENST00000399088.8, Ensembl:ENSP00000382038.4, Ensembl:ENSG00000231286.7, Ensembl:ENST00000413089.1, Ensembl:ENSP00000396539.1, Ensembl:ENST00000416192.6, Ensembl:ENSP00000410107.2, Ensembl:ENSG00000233209.6, Ensembl:ENST00000419914.6, Ensembl:ENSP00000402865.2, Ensembl:ENSG00000225824.8, Ensembl:ENST00000422950.1, Ensembl:ENSP00000414079.1, Ensembl:ENST00000424806.1, Ensembl:ENSP00000410330.1, GeneID:3119, KEGG:hsa:3119, UCSC:uc011hep.3, CTD:3119, DisGeNET:3119, GeneCards:HLA-DQB1, GeneReviews:HLA-DQB1, HGNC:4944, MalaCards:HLA-DQB1, MIM:604305, neXtProt:NX_P01920, Orphanet:703, Orphanet:930, Orphanet:2073, Orphanet:83465, Orphanet:555, Orphanet:243377, Orphanet:802, Orphanet:477738, PharmGKB:PA35068, eggNOG:ENOG502RYBQ, InParanoid:P01920, OrthoDB:1186163at2759, PhylomeDB:P01920, PathwayCommons:P01920, Reactome:R-HSA-202424, Reactome:R-HSA-202427, Reactome:R-HSA-202430, Reactome:R-HSA-202433, Reactome:R-HSA-2132295, Reactome:R-HSA-389948, Reactome:R-HSA-877300, SignaLink:P01920, SIGNOR:P01920, BioGRID-ORCS:3119, ChiTaRS:HLA-DQB1, EvolutionaryTrace:P01920, GeneWiki:HLA-DQB1, GenomeRNAi:3119, Pharos:P01920, PRO:PR:P01920, Proteomes:UP000005640, RNAct:P01920, Bgee:ENSG00000231286, GO:0030669, GO:0030666, GO:0010008, GO:0012507, GO:0000139, GO:0071556, GO:0005765, GO:0016020, GO:0042613, GO:0005886, GO:0032588, GO:0030658, GO:0023026, GO:0032395, GO:0042605, GO:0002250, GO:0019886, GO:0006959, GO:0006955, GO:0002503, GO:0050870, GO:0050852, Gene3D:2.60.40.10, Gene3D:3.10.320.10, InterPro:IPR007110, InterPro:IPR036179, InterPro:IPR013783, InterPro:IPR003006, InterPro:IPR003597, InterPro:IPR011162, InterPro:IPR014745, InterPro:IPR000353, Pfam:PF07654, Pfam:PF00969, SMART:SM00407, SMART:SM00921, SUPFAM:SSF48726, SUPFAM:SSF54452, PROSITE:PS50835, PROSITE:PS00290
Sequence mswkkalripgglraatvtlmlamlstpvaegrdspedfvyqfkamcyftngtervryvtryiynreeyarfdsdvevyravtplgppdaeywnsqkevlertraeldtvcrhnyqlelrttlqrrveptvtispsrtealnhhnllvcsvtdfypaqikvrwfrndqeettgvvstplirngdwtfqilvmlemtpqhgdvytchvehpslqnpitvewraqsesaqskmlsgiggfvlgliflglgliihhrsqkgllh