ID MIXL1_HUMAN Reviewed; 232 AA. AC Q9H2W2; B7ZLF9; DT 13-NOV-2007, integrated into UniProtKB/Swiss-Prot. DT 01-MAR-2001, sequence version 1. DT 24-JAN-2024, entry version 186. DE RecName: Full=Homeobox protein MIXL1; DE AltName: Full=Homeodomain protein MIX; DE Short=hMix; DE AltName: Full=MIX1 homeobox-like protein 1; DE AltName: Full=Mix.1 homeobox-like protein; GN Name=MIXL1; Synonyms=MIXL; 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] (ISOFORM 1), SUBCELLULAR LOCATION, AND TISSUE RP SPECIFICITY. RX PubMed=12070013; DOI=10.1182/blood.v100.1.89; RA Guo W., Chan A.P., Liang H., Wieder E.D., Molldrem J.J., Etkin L.D., RA Nagarajan L.; RT "A human Mix-like homeobox gene MIXL shows functional similarity to Xenopus RT Mix.1."; RL Blood 100:89-95(2002). RN [2] RP NUCLEOTIDE SEQUENCE [GENOMIC DNA]. RX PubMed=11084649; RX DOI=10.1002/1097-0177(2000)9999:9999<::aid-dvdy1070>3.0.co;2-o; RA Robb L., Hartley L., Begley C.G., Brodnicki T.C., Copeland N.G., RA Gilbert D.J., Jenkins N.A., Elefanty A.G.; RT "Cloning, expression analysis, and chromosomal localization of murine and RT human homologues of a Xenopus mix gene."; RL Dev. Dyn. 219:497-504(2000). RN [3] 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 [4] 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 (JUL-2005) to the EMBL/GenBank/DDBJ databases. RN [5] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2). RC TISSUE=Brain; 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 [6] RP TISSUE SPECIFICITY. RX PubMed=16433620; DOI=10.1089/scd.2005.14.656; RA Mossman A.K., Sourris K., Ng E., Stanley E.G., Elefanty A.G.; RT "Mixl1 and oct4 proteins are transiently co-expressed in differentiating RT mouse and human embryonic stem cells."; RL Stem Cells Dev. 14:656-663(2005). RN [7] RP PHOSPHORYLATION AT TYR-20. RX PubMed=17224082; DOI=10.1186/1750-2187-1-6; RA Guo W., Nagarajan L.; RT "Amino terminal tyrosine phosphorylation of human MIXL1."; RL J. Mol. Signal. 1:6-6(2006). RN [8] RP SUBCELLULAR LOCATION, AND TISSUE SPECIFICITY. RX PubMed=17303500; DOI=10.1016/j.humpath.2006.09.020; RA Drakos E., Rassidakis G.Z., Leventaki V., Guo W., Medeiros L.J., RA Nagarajan L.; RT "Differential expression of the human MIXL1 gene product in non-Hodgkin and RT Hodgkin lymphomas."; RL Hum. Pathol. 38:500-507(2007). CC -!- FUNCTION: Transcription factor that play a central role in proper axial CC mesendoderm morphogenesis and endoderm formation. Required for CC efficient differentiation of cells from the primitive streak stage to CC blood, by acting early in the recruitment and/or expansion of CC mesodermal progenitors to the hemangioblastic and hematopoietic CC lineages. Also involved in the morphogenesis of the heart and the gut CC during embryogenesis. Acts as a negative regulator of brachyury CC expression (By similarity). {ECO:0000250}. CC -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000255|PROSITE-ProRule:PRU00108, CC ECO:0000269|PubMed:12070013, ECO:0000269|PubMed:17303500}. CC -!- ALTERNATIVE PRODUCTS: CC Event=Alternative splicing; Named isoforms=2; CC Name=1; CC IsoId=Q9H2W2-1; Sequence=Displayed; CC Name=2; CC IsoId=Q9H2W2-2; Sequence=VSP_054305; CC -!- TISSUE SPECIFICITY: Restricted to progenitors and secondary lymph CC tissues. In normal hematopoiesis, it is restricted to immature B- and CC T-lymphoid cells. Present in differentiating embryonic stem cells (at CC protein level). {ECO:0000269|PubMed:12070013, CC ECO:0000269|PubMed:16433620, ECO:0000269|PubMed:17303500}. CC -!- PTM: Phosphorylated at multiple sites. {ECO:0000269|PubMed:17224082}. CC -!- SIMILARITY: Belongs to the paired homeobox family. {ECO:0000305}. CC -!- WEB RESOURCE: Name=Atlas of Genetics and Cytogenetics in Oncology and CC Haematology; CC URL="https://atlasgeneticsoncology.org/gene/47624/MIXL1"; CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AF211891; AAG35776.1; -; mRNA. DR EMBL; AF218357; AAK01479.1; -; Genomic_DNA. DR EMBL; AL592045; -; NOT_ANNOTATED_CDS; Genomic_DNA. DR EMBL; CH471098; EAW69778.1; -; Genomic_DNA. DR EMBL; BC111974; AAI11975.1; -; mRNA. DR EMBL; BC113441; AAI13442.1; -; mRNA. DR EMBL; BC143784; AAI43785.1; -; mRNA. DR CCDS; CCDS1552.1; -. [Q9H2W2-1] DR CCDS; CCDS60432.1; -. [Q9H2W2-2] DR RefSeq; NP_001269331.1; NM_001282402.1. [Q9H2W2-2] DR RefSeq; NP_114150.1; NM_031944.2. [Q9H2W2-1] DR AlphaFoldDB; Q9H2W2; -. DR SMR; Q9H2W2; -. DR IntAct; Q9H2W2; 1. DR STRING; 9606.ENSP00000442439; -. DR GlyGen; Q9H2W2; 1 site, 1 O-linked glycan (1 site). DR iPTMnet; Q9H2W2; -. DR PhosphoSitePlus; Q9H2W2; -. DR BioMuta; MIXL1; -. DR DMDM; 74762734; -. DR MassIVE; Q9H2W2; -. DR PaxDb; 9606-ENSP00000442439; -. DR PeptideAtlas; Q9H2W2; -. DR ProteomicsDB; 7224; -. DR ProteomicsDB; 80609; -. [Q9H2W2-1] DR Antibodypedia; 20764; 168 antibodies from 31 providers. DR DNASU; 83881; -. DR Ensembl; ENST00000366810.6; ENSP00000355775.4; ENSG00000185155.12. [Q9H2W2-1] DR Ensembl; ENST00000542034.5; ENSP00000442439.1; ENSG00000185155.12. [Q9H2W2-2] DR GeneID; 83881; -. DR KEGG; hsa:83881; -. DR MANE-Select; ENST00000366810.6; ENSP00000355775.4; NM_031944.3; NP_114150.1. DR UCSC; uc010pvm.4; human. [Q9H2W2-1] DR AGR; HGNC:13363; -. DR CTD; 83881; -. DR DisGeNET; 83881; -. DR GeneCards; MIXL1; -. DR HGNC; HGNC:13363; MIXL1. DR HPA; ENSG00000185155; Tissue enhanced (lymphoid). DR MIM; 609852; gene. DR neXtProt; NX_Q9H2W2; -. DR OpenTargets; ENSG00000185155; -. DR PharmGKB; PA134976348; -. DR VEuPathDB; HostDB:ENSG00000185155; -. DR eggNOG; KOG0849; Eukaryota. DR GeneTree; ENSGT00940000162190; -. DR HOGENOM; CLU_104890_0_0_1; -. DR InParanoid; Q9H2W2; -. DR OMA; HHSACET; -. DR OrthoDB; 4202152at2759; -. DR PhylomeDB; Q9H2W2; -. DR TreeFam; TF334098; -. DR PathwayCommons; Q9H2W2; -. DR Reactome; R-HSA-9754189; Germ layer formation at gastrulation. DR Reactome; R-HSA-9823730; Formation of definitive endoderm. DR SignaLink; Q9H2W2; -. DR BioGRID-ORCS; 83881; 38 hits in 1176 CRISPR screens. DR GenomeRNAi; 83881; -. DR Pharos; Q9H2W2; Tbio. DR PRO; PR:Q9H2W2; -. DR Proteomes; UP000005640; Chromosome 1. DR RNAct; Q9H2W2; Protein. DR Bgee; ENSG00000185155; Expressed in oocyte and 85 other cell types or tissues. DR ExpressionAtlas; Q9H2W2; baseline and differential. DR GO; GO:0000785; C:chromatin; ISS:BHF-UCL. DR GO; GO:0005654; C:nucleoplasm; IDA:HPA. DR GO; GO:0000987; F:cis-regulatory region sequence-specific DNA binding; ISS:BHF-UCL. DR GO; GO:0001228; F:DNA-binding transcription activator activity, RNA polymerase II-specific; ISS:BHF-UCL. DR GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; ISA:NTNU_SB. DR GO; GO:0042803; F:protein homodimerization activity; ISS:BHF-UCL. DR GO; GO:0000978; F:RNA polymerase II cis-regulatory region sequence-specific DNA binding; ISS:BHF-UCL. DR GO; GO:0061629; F:RNA polymerase II-specific DNA-binding transcription factor binding; IPI:BHF-UCL. DR GO; GO:1990837; F:sequence-specific double-stranded DNA binding; IDA:ARUK-UCL. DR GO; GO:0042074; P:cell migration involved in gastrulation; IEA:Ensembl. DR GO; GO:0048565; P:digestive tract development; ISS:BHF-UCL. DR GO; GO:0007492; P:endoderm development; ISS:BHF-UCL. DR GO; GO:0001706; P:endoderm formation; IBA:GO_Central. DR GO; GO:0035987; P:endodermal cell differentiation; ISS:BHF-UCL. DR GO; GO:0007369; P:gastrulation; ISS:BHF-UCL. DR GO; GO:0007507; P:heart development; ISS:BHF-UCL. DR GO; GO:0002244; P:hematopoietic progenitor cell differentiation; ISS:BHF-UCL. DR GO; GO:1901533; P:negative regulation of hematopoietic progenitor cell differentiation; ISS:BHF-UCL. DR GO; GO:2000382; P:positive regulation of mesoderm development; ISS:BHF-UCL. DR GO; GO:0045944; P:positive regulation of transcription by RNA polymerase II; ISS:BHF-UCL. DR GO; GO:0006357; P:regulation of transcription by RNA polymerase II; IBA:GO_Central. 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; IPR042917; MIXL1. DR PANTHER; PTHR47656; HOMEOBOX PROTEIN MIXL; 1. DR PANTHER; PTHR47656:SF1; HOMEOBOX PROTEIN MIXL1; 1. DR Pfam; PF00046; Homeodomain; 1. DR SMART; SM00389; HOX; 1. DR SUPFAM; SSF46689; Homeodomain-like; 1. DR PROSITE; PS00027; HOMEOBOX_1; 1. DR PROSITE; PS50071; HOMEOBOX_2; 1. DR Genevisible; Q9H2W2; HS. PE 1: Evidence at protein level; KW Alternative splicing; Developmental protein; Differentiation; DNA-binding; KW Homeobox; Nucleus; Phosphoprotein; Reference proteome; Transcription; KW Transcription regulation. FT CHAIN 1..232 FT /note="Homeobox protein MIXL1" FT /id="PRO_0000311333" FT DNA_BIND 86..145 FT /note="Homeobox" FT /evidence="ECO:0000255|PROSITE-ProRule:PRU00108" FT REGION 22..92 FT /note="Disordered" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT COMPBIAS 28..48 FT /note="Pro residues" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT COMPBIAS 59..73 FT /note="Pro residues" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT MOD_RES 20 FT /note="Phosphotyrosine" FT /evidence="ECO:0000269|PubMed:17224082" FT VAR_SEQ 130 FT /note="I -> IQLLFSPLF (in isoform 2)" FT /evidence="ECO:0000303|PubMed:15489334" FT /id="VSP_054305" SQ SEQUENCE 232 AA; 24659 MW; 2E8A6A811799A8F0 CRC64; MATAESRALQ FAEGAAFPAY RAPHAGGALL PPPSPAAALL PAPPAGPGPA TFAGFLGRDP GPAPPPPASL GSPAPPKGAA APSASQRRKR TSFSAEQLQL LELVFRRTRY PDIHLRERLA ALTLLPESRI QVWFQNRRAK SRRQSGKSFQ PLARPEIILN HCAPGTETKC LKPQLPLEVD VNCLPEPNGV GGGISDSSSQ GQNFETCSPL SEDIGSKLDS WEEHIFSAFG NF //