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Database: UniProt
Entry: HLX_HUMAN
LinkDB: HLX_HUMAN
Original site: HLX_HUMAN 
ID   HLX_HUMAN               Reviewed;         488 AA.
AC   Q14774; B2R8A8; Q15988; Q59HE7; Q9NZ75;
DT   01-NOV-1997, integrated into UniProtKB/Swiss-Prot.
DT   13-NOV-2007, sequence version 3.
DT   24-JAN-2024, entry version 198.
DE   RecName: Full=H2.0-like homeobox protein;
DE   AltName: Full=Homeobox protein HB24;
DE   AltName: Full=Homeobox protein HLX1;
GN   Name=HLX; Synonyms=HLX1;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA].
RC   TISSUE=B-cell;
RX   PubMed=1676597;
RA   Deguchi Y., Moroney J.F., Wilson G.L., Fox C.H., Winter H.S., Kehrl J.H.;
RT   "Cloning of a human homeobox gene that resembles a diverged Drosophila
RT   homeobox gene and is expressed in activated lymphocytes.";
RL   New Biol. 3:353-363(1991).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA].
RA   Hanrahan V., Kennedy M.A.;
RT   "Genomic sequence of human homeobox gene HLX1.";
RL   Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases.
RN   [3]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Small intestine;
RX   PubMed=14702039; DOI=10.1038/ng1285;
RA   Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R.,
RA   Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H.,
RA   Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S.,
RA   Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K.,
RA   Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H.,
RA   Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M.,
RA   Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K.,
RA   Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T.,
RA   Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M.,
RA   Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S.,
RA   Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H.,
RA   Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K.,
RA   Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N.,
RA   Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S.,
RA   Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O.,
RA   Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H.,
RA   Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B.,
RA   Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y.,
RA   Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K.,
RA   Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T.,
RA   Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T.,
RA   Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y.,
RA   Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H.,
RA   Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y.,
RA   Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H.,
RA   Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O.,
RA   Isogai T., Sugano S.;
RT   "Complete sequencing and characterization of 21,243 full-length human
RT   cDNAs.";
RL   Nat. Genet. 36:40-45(2004).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], AND VARIANT LEU-356.
RC   TISSUE=Brain;
RA   Totoki Y., Toyoda A., Takeda T., Sakaki Y., Tanaka A., Yokoyama S.,
RA   Ohara O., Nagase T., Kikuno R.F.;
RL   Submitted (MAR-2005) to the EMBL/GenBank/DDBJ databases.
RN   [5]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=16710414; DOI=10.1038/nature04727;
RA   Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A.,
RA   Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C.,
RA   Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K.,
RA   Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C.,
RA   Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W.,
RA   Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J.,
RA   Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J.,
RA   Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y.,
RA   Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J.,
RA   Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H.,
RA   Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L.,
RA   Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J.,
RA   Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S.,
RA   Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K.,
RA   Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R.,
RA   Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M.,
RA   Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S.,
RA   Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J.,
RA   Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W.,
RA   McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N.,
RA   Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V.,
RA   Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J.,
RA   Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E.,
RA   Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S.,
RA   Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M.,
RA   White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H.,
RA   Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E.,
RA   Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G.,
RA   Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.;
RT   "The DNA sequence and biological annotation of human chromosome 1.";
RL   Nature 441:315-321(2006).
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases.
RN   [7]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Retina;
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [8]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 1-326, AND VARIANT PRO-116.
RX   PubMed=7806220; DOI=10.1006/geno.1994.1394;
RA   Kennedy M.A., Rayner J.C., Morris C.M.;
RT   "Genomic structure, promoter sequence, and revised translation of human
RT   homeobox gene HLX1.";
RL   Genomics 22:348-355(1994).
RN   [9]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 350-369.
RX   PubMed=8095486; DOI=10.1006/geno.1993.1068;
RA   Nishimura D.Y., Purchio A.F., Murray J.C.;
RT   "Linkage localization of TGFB2 and the human homeobox gene HLX1 to
RT   chromosome 1q.";
RL   Genomics 15:357-364(1993).
RN   [10]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RX   PubMed=19413330; DOI=10.1021/ac9004309;
RA   Gauci S., Helbig A.O., Slijper M., Krijgsveld J., Heck A.J., Mohammed S.;
RT   "Lys-N and trypsin cover complementary parts of the phosphoproteome in a
RT   refined SCX-based approach.";
RL   Anal. Chem. 81:4493-4501(2009).
CC   -!- FUNCTION: Transcription factor required for TBX21/T-bet-dependent
CC       maturation of Th1 cells as well as maintenance of Th1-specific gene
CC       expression. Involved in embryogenesis and hematopoiesis (By
CC       similarity). {ECO:0000250}.
CC   -!- INTERACTION:
CC       Q14774; P0C7T5: ATXN1L; NbExp=3; IntAct=EBI-6678255, EBI-8624731;
CC       Q14774; Q9NWQ9: C14orf119; NbExp=3; IntAct=EBI-6678255, EBI-725606;
CC       Q14774; A8MQ03: CYSRT1; NbExp=3; IntAct=EBI-6678255, EBI-3867333;
CC       Q14774; Q86UW9: DTX2; NbExp=3; IntAct=EBI-6678255, EBI-740376;
CC       Q14774; O75593: FOXH1; NbExp=3; IntAct=EBI-6678255, EBI-1759806;
CC       Q14774; Q17RB8: LONRF1; NbExp=3; IntAct=EBI-6678255, EBI-2341787;
CC       Q14774; Q9BRT3: MIEN1; NbExp=3; IntAct=EBI-6678255, EBI-6137472;
CC       Q14774; P86480: PRR20D; NbExp=3; IntAct=EBI-6678255, EBI-12754095;
CC   -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000255|PROSITE-ProRule:PRU00108}.
CC   -!- TISSUE SPECIFICITY: Low level in normal B and T-cells, high level in
CC       activated lymphocytes and monocytes. Also found in thymus, tonsil, bone
CC       marrow, developing vessels, and fetal brain.
CC   -!- SIMILARITY: Belongs to the H2.0 homeobox family. {ECO:0000305}.
CC   -!- SEQUENCE CAUTION:
CC       Sequence=BAD92049.1; Type=Erroneous initiation; Note=Truncated N-terminus.; Evidence={ECO:0000305};
CC       Sequence=BAD92049.1; Type=Frameshift; Evidence={ECO:0000305};
CC       Sequence=M60721; Type=Frameshift; Evidence={ECO:0000305};
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DR   EMBL; M60721; -; NOT_ANNOTATED_CDS; mRNA.
DR   EMBL; AF217621; AAF65541.1; -; Genomic_DNA.
DR   EMBL; AK313298; BAG36105.1; -; mRNA.
DR   EMBL; AB208812; BAD92049.1; ALT_SEQ; mRNA.
DR   EMBL; AL445423; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471100; EAW93289.1; -; Genomic_DNA.
DR   EMBL; BC007294; AAH07294.1; -; mRNA.
DR   EMBL; BC033808; AAH33808.1; -; mRNA.
DR   EMBL; U14328; AAC51346.1; -; Genomic_DNA.
DR   EMBL; U14325; AAC51346.1; JOINED; Genomic_DNA.
DR   EMBL; U14326; AAC51346.1; JOINED; Genomic_DNA.
DR   EMBL; U14327; AAC51346.1; JOINED; Genomic_DNA.
DR   EMBL; S56767; AAD13883.1; -; Genomic_DNA.
DR   CCDS; CCDS1527.1; -.
DR   PIR; A55180; A55180.
DR   RefSeq; NP_068777.1; NM_021958.3.
DR   AlphaFoldDB; Q14774; -.
DR   SMR; Q14774; -.
DR   BioGRID; 109387; 37.
DR   IntAct; Q14774; 25.
DR   MINT; Q14774; -.
DR   STRING; 9606.ENSP00000355870; -.
DR   iPTMnet; Q14774; -.
DR   PhosphoSitePlus; Q14774; -.
DR   BioMuta; HLX; -.
DR   DMDM; 160291960; -.
DR   MassIVE; Q14774; -.
DR   MaxQB; Q14774; -.
DR   PaxDb; 9606-ENSP00000355870; -.
DR   PeptideAtlas; Q14774; -.
DR   ProteomicsDB; 60168; -.
DR   Antibodypedia; 910; 283 antibodies from 32 providers.
DR   DNASU; 3142; -.
DR   Ensembl; ENST00000366903.8; ENSP00000355870.5; ENSG00000136630.13.
DR   GeneID; 3142; -.
DR   KEGG; hsa:3142; -.
DR   MANE-Select; ENST00000366903.8; ENSP00000355870.5; NM_021958.4; NP_068777.1.
DR   UCSC; uc001hmv.5; human.
DR   AGR; HGNC:4978; -.
DR   CTD; 3142; -.
DR   DisGeNET; 3142; -.
DR   GeneCards; HLX; -.
DR   HGNC; HGNC:4978; HLX.
DR   HPA; ENSG00000136630; Tissue enhanced (bone).
DR   MalaCards; HLX; -.
DR   MIM; 142995; gene.
DR   neXtProt; NX_Q14774; -.
DR   OpenTargets; ENSG00000136630; -.
DR   Orphanet; 527468; Diaphragmatic hernia-short bowel-asplenia syndrome.
DR   PharmGKB; PA162391017; -.
DR   VEuPathDB; HostDB:ENSG00000136630; -.
DR   eggNOG; KOG0488; Eukaryota.
DR   GeneTree; ENSGT00950000183093; -.
DR   HOGENOM; CLU_043671_1_0_1; -.
DR   InParanoid; Q14774; -.
DR   OMA; EPMNEAS; -.
DR   OrthoDB; 2911948at2759; -.
DR   PhylomeDB; Q14774; -.
DR   TreeFam; TF350735; -.
DR   PathwayCommons; Q14774; -.
DR   SignaLink; Q14774; -.
DR   SIGNOR; Q14774; -.
DR   BioGRID-ORCS; 3142; 18 hits in 1175 CRISPR screens.
DR   GeneWiki; HLX_(gene); -.
DR   GenomeRNAi; 3142; -.
DR   Pharos; Q14774; Tbio.
DR   PRO; PR:Q14774; -.
DR   Proteomes; UP000005640; Chromosome 1.
DR   RNAct; Q14774; Protein.
DR   Bgee; ENSG00000136630; Expressed in stromal cell of endometrium and 100 other cell types or tissues.
DR   ExpressionAtlas; Q14774; baseline and differential.
DR   Genevisible; Q14774; HS.
DR   GO; GO:0000785; C:chromatin; ISA:NTNU_SB.
DR   GO; GO:0005634; C:nucleus; IEA:UniProtKB-SubCell.
DR   GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; ISA:NTNU_SB.
DR   GO; GO:0043565; F:sequence-specific DNA binding; IDA:MGI.
DR   GO; GO:0048557; P:embryonic digestive tract morphogenesis; IEA:Ensembl.
DR   GO; GO:0048484; P:enteric nervous system development; IEA:Ensembl.
DR   GO; GO:0050673; P:epithelial cell proliferation; IEA:Ensembl.
DR   GO; GO:0001889; P:liver development; IEA:Ensembl.
DR   GO; GO:0045629; P:negative regulation of T-helper 2 cell differentiation; IEA:Ensembl.
DR   GO; GO:0035265; P:organ growth; IEA:Ensembl.
DR   GO; GO:0050679; P:positive regulation of epithelial cell proliferation; IEA:Ensembl.
DR   GO; GO:0046622; P:positive regulation of organ growth; IEA:Ensembl.
DR   GO; GO:0045627; P:positive regulation of T-helper 1 cell differentiation; IEA:Ensembl.
DR   GO; GO:0007165; P:signal transduction; TAS:ProtInc.
DR   GO; GO:0007519; P:skeletal muscle tissue development; IEA:Ensembl.
DR   GO; GO:0045063; P:T-helper 1 cell differentiation; IEA:Ensembl.
DR   GO; GO:0045064; P:T-helper 2 cell differentiation; IEA:Ensembl.
DR   CDD; cd00086; homeodomain; 1.
DR   Gene3D; 1.10.10.60; Homeodomain-like; 1.
DR   InterPro; IPR009057; Homeobox-like_sf.
DR   InterPro; IPR017970; Homeobox_CS.
DR   InterPro; IPR001356; Homeobox_dom.
DR   InterPro; IPR020479; Homeobox_metazoa.
DR   InterPro; IPR000047; HTH_motif.
DR   PANTHER; PTHR46808; H2.0-LIKE HOMEOBOX PROTEIN; 1.
DR   PANTHER; PTHR46808:SF1; H2.0-LIKE HOMEOBOX PROTEIN; 1.
DR   Pfam; PF00046; Homeodomain; 1.
DR   PRINTS; PR00024; HOMEOBOX.
DR   PRINTS; PR00031; HTHREPRESSR.
DR   SMART; SM00389; HOX; 1.
DR   SUPFAM; SSF46689; Homeodomain-like; 1.
DR   PROSITE; PS00027; HOMEOBOX_1; 1.
DR   PROSITE; PS50071; HOMEOBOX_2; 1.
PE   1: Evidence at protein level;
KW   Differentiation; DNA-binding; Homeobox; Nucleus; Reference proteome;
KW   Transcription; Transcription regulation.
FT   CHAIN           1..488
FT                   /note="H2.0-like homeobox protein"
FT                   /id="PRO_0000048978"
FT   DNA_BIND        276..335
FT                   /note="Homeobox"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00108"
FT   REGION          118..173
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   REGION          331..488
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        331..350
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        362..376
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        416..454
FT                   /note="Polar residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   VARIANT         116
FT                   /note="S -> P (in dbSNP:rs12141189)"
FT                   /evidence="ECO:0000269|PubMed:7806220"
FT                   /id="VAR_037162"
FT   VARIANT         356
FT                   /note="P -> L (in dbSNP:rs2738755)"
FT                   /evidence="ECO:0000269|Ref.4"
FT                   /id="VAR_037163"
FT   VARIANT         387
FT                   /note="A -> G (in dbSNP:rs11578466)"
FT                   /id="VAR_049582"
FT   CONFLICT        63
FT                   /note="Missing (in Ref. 1; M60721)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        134..136
FT                   /note="QQQ -> RRE (in Ref. 1; M60721)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   488 AA;  50789 MW;  FC2EA805DACAA0C1 CRC64;
     MFAAGLAPFY ASNFSLWSAA YCSSAGPGGC SFPLDPAAVK KPSFCIADIL HAGVGDLGAA
     PEGLAGASAA ALTAHLGSVH PHASFQAAAR SPLRPTPVVA PSEVPAGFPQ RLSPLSAAYH
     HHHPQQQQQQ QQPQQQQPPP PPRAGALQPP ASGTRVVPNP HHSGSAPAPS SKDLKFGIDR
     ILSAEFDPKV KEGNTLRDLT SLLTGGRPAG VHLSGLQPSA GQFFASLDPI NEASAILSPL
     NSNPRNSVQH QFQDTFPGPY AVLTKDTMPQ TYKRKRSWSR AVFSNLQRKG LEKRFEIQKY
     VTKPDRKQLA AMLGLTDAQV KVWFQNRRMK WRHSKEAQAQ KDKDKEAGEK PSGGAPAADG
     EQDERSPSRS EGEAESESSD SESLDMAPSD TERTEGSERS LHQTTVIKAP VTGALITASS
     AGSGGSSGGG GNSFSFSSAS SLSSSSTSAG CASSLGGGGA SELLPATQPT ASSAPKSPEP
     AQGALGCL
//
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