USC-OGP 2-DE database Two-dimensional polyacrylamide gel electrophoresis database

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Searching in 'USC-OGP 2-DE database' for entry matching: Q13642 USC-OGP 2-DE database:  Q13642 Q13642 General information about the entry View entry in simple text format Entry name FHL1_HUMAN Primary accession number Q13642 integrated into USC-OGP 2-DE database on  January 17, 2017 (release 1) 2D Annotations were last modified on January 17, 2017 (version 1) General Annotations were last modified on  April 5, 2017 (version 2) Name and origin of the protein Description RecName: Full=Four and a half LIM domains protein 1; Short=FHL-1; AltName: Full=Skeletal muscle LIM-protein 1; Short=SLIM; Short=SLIM-1;. Gene name Name=FHL1 Synonyms=SLIM1 Annotated species Homo sapiens (Human) [TaxID: 9606] Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. References [1]   2D GEL CHARACTERIZATION Author 1., Author 2. Submitted (Mar-2011) to Current 2D PAGE maps for identified proteins How to interpret a protein UVEAL_MELANOMA_3-10 {UVEAL MELANOMA 3-10} Homo sapiens (Human)   map experimental info   UVEAL_MELANOMA_3-10 MAP LOCATIONS: SPOT OGP-1256: pI=5.39; Mw=30456 Cross-references UniProtKB/Swiss-Prot Q13642; FHL1_HUMAN. 2D PAGE maps for identified proteins How to interpret a protein map You may obtain an estimated location of the protein on various 2D PAGE maps, provided the whole amino acid sequence is known. The estimation is obtained according to the computed protein's pI and Mw. Warning 1: the displayed region reflects an area around the theoretical pI and molecular weight of the protein and is only provided for the user's information. It should be used with caution, as the experimental and theoretical positions of a protein may differ significantly. Warning 2: the 2D PAGE map is built on demand. This may take some few seconds to be computed. External data extracted from UniProtKB/Swiss-Prot Extracted from UniProtKB/Swiss-Prot, release: 0.0 Entry name FHL1_HUMAN Primary accession number Q13642 Secondary accession number(s) B7Z5T4 B7Z793 O95212 Q13230 Q13645 Q5JXI7 Q5M7Y6 Q6IB30 Q9NZ40 Q9UKZ8 Q9Y630 Sequence was last modified on  January 23, 2007 (version 4) Annotations were last modified on  March 15, 2017 (version 172) Name and origin of the protein Description RecName: Full=Four and a half LIM domains protein 1; Short=FHL-1; AltName: Full=Skeletal muscle LIM-protein 1; Short=SLIM; Short=SLIM-1; Gene name Name=FHL1 Synonyms=SLIM1 Encoded on Name=FHL1; Synonyms=SLIM1 Keywords 3D-structure; Acetylation; Alternative splicing; Complete proteome; Cytoplasm; Developmental protein; Differentiation; Direct protein sequencing; Disease mutation; Emery-Dreifuss muscular dystrophy; Isopeptide bond; LIM domain; Metal-binding; Nucleus; Polymorphism; Reference proteome; Repeat; Ubl conjugation; Zinc; Zinc-finger. Copyright Copyrighted by the UniProt Consortium, see http://www.uniprot.org/help/license. Distributed under the Creative Commons Attribution-NoDerivs License Cross-references EMBL U60115; AAC52021.1; -; mRNA EMBL U29538; AAC35421.1; -; mRNA EMBL AF110763; AAD21579.1; -; Genomic_DNA EMBL AF098518; AAC72390.1; -; mRNA EMBL AF063002; AAC72886.1; -; mRNA EMBL AF220153; AAF32351.1; -; mRNA EMBL AK122708; BAG53680.1; -; mRNA EMBL AK289411; BAF82100.1; -; mRNA EMBL AK299381; BAH13020.1; -; mRNA EMBL AK301642; BAH13529.1; -; mRNA EMBL CR456974; CAG33255.1; -; mRNA EMBL AL078638; CAC18881.1; -; Genomic_DNA EMBL AL078638; CAI41062.1; -; Genomic_DNA EMBL AL078638; CAI41055.1; ALT_INIT; Genomic_DNA EMBL CH471150; EAW88476.1; -; Genomic_DNA EMBL CH471150; EAW88478.1; -; Genomic_DNA EMBL CH471150; EAW88479.1; -; Genomic_DNA EMBL BC010998; AAH10998.1; -; mRNA EMBL BC088369; AAH88369.1; ALT_INIT; mRNA EMBL U60118; AAC50795.1; -; mRNA CCDS CCDS14655.1; -. [Q13642-1]; . CCDS CCDS55505.1; -. [Q13642-4]; . CCDS CCDS55506.1; -. [Q13642-5]; . CCDS CCDS55507.1; -. [Q13642-2]; . CCDS CCDS76036.1; -. [Q13642-3]; . PIR G01884; G01884; . PIR JC4893; G02741; . RefSeq NP_001153171.1; NM_001159699.1. [Q13642-5]; . RefSeq NP_001153172.1; NM_001159700.1. [Q13642-1]; . RefSeq NP_001153173.1; NM_001159701.1. [Q13642-4]; . RefSeq NP_001153174.1; NM_001159702.2. [Q13642-2]; . RefSeq NP_001153175.1; NM_001159703.1. [Q13642-3]; . RefSeq NP_001153176.1; NM_001159704.1. [Q13642-1]; . RefSeq NP_001161291.1; NM_001167819.1. [Q13642-1]; . RefSeq NP_001440.2; NM_001449.4. [Q13642-1]; . RefSeq XP_006724807.1; XM_006724744.2. [Q13642-2]; . RefSeq XP_006724808.1; XM_006724745.3. [Q13642-2]; . RefSeq XP_006724809.1; XM_006724746.2. [Q13642-2]; . RefSeq XP_006724810.1; XM_006724747.2. [Q13642-1]; . RefSeq XP_016884846.1; XM_017029357.1. [Q13642-1]; . UniGene Hs.435369; -; . PDB 1X63; NMR; -; A=91-159 PDB 2CUP; NMR; -; A=40-127 PDB 2CUR; NMR; -; A=162-217 PDB 2EGQ; NMR; -; A=211-280 PDBsum 1X63; -; . PDBsum 2CUP; -; . PDBsum 2CUR; -; . PDBsum 2EGQ; -; . ProteinModelPortal Q13642; -; . SMR Q13642; -; . BioGrid 108564; 34; . IntAct Q13642; 29; . STRING 9606.ENSP00000071281; -; . iPTMnet Q13642; -; . PhosphoSitePlus Q13642; -; . BioMuta FHL1; -; . DMDM 59800384; -; . EPD Q13642; -; . PaxDb Q13642; -; . PeptideAtlas Q13642; -; . PRIDE Q13642; -; . TopDownProteomics Q13642-1; -. [Q13642-1]; . DNASU 2273; -; . Ensembl ENST00000345434; ENSP00000071281; ENSG00000022267. [Q13642-2]; . Ensembl ENST00000370683; ENSP00000359717; ENSG00000022267. [Q13642-5]; . Ensembl ENST00000370690; ENSP00000359724; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000394153; ENSP00000377709; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000394155; ENSP00000377710; ENSG00000022267. [Q13642-2]; . Ensembl ENST00000535737; ENSP00000444815; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000539015; ENSP00000437673; ENSG00000022267. [Q13642-4]; . Ensembl ENST00000543669; ENSP00000443333; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000618438; ENSP00000477609; ENSG00000022267. [Q13642-3]; . Ensembl ENST00000628568; ENSP00000486782; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000629039; ENSP00000486439; ENSG00000022267. [Q13642-1]; . Ensembl ENST00000630084; ENSP00000485897; ENSG00000022267. [Q13642-1]; . GeneID 2273; -; . KEGG hsa:2273; -; . UCSC uc004ezl.3; human. [Q13642-2]; . CTD 2273; -; . DisGeNET 2273; -; . GeneCards FHL1; -; . GeneReviews FHL1; -; . HGNC HGNC:3702; FHL1; . HPA CAB020817; -; . HPA HPA001040; -; . HPA HPA001391; -; . MalaCards FHL1; -; . MIM 300163; gene; . MIM 300695; phenotype; . MIM 300696; phenotype; . MIM 300717; phenotype; . MIM 300718; phenotype; . neXtProt NX_Q13642; -; . OpenTargets ENSG00000022267; -; . Orphanet 155; Familial isolated hypertrophic cardiomyopathy; . Orphanet 97239; Reducing body myopathy; . Orphanet 98863; X-linked Emery-Dreifuss muscular dystrophy; . Orphanet 178461; X-linked myopathy with postural muscle atrophy; . PharmGKB PA28141; -; . eggNOG ENOG410INGD; Eukaryota; . eggNOG ENOG410YDMU; LUCA; . GeneTree ENSGT00760000118910; -; . HOVERGEN HBG074526; -; . InParanoid Q13642; -; . KO K14365; -; . OMA EDQFYCV; -; . OrthoDB EOG091G07C5; -; . PhylomeDB Q13642; -; . TreeFam TF318571; -; . SIGNOR Q13642; -; . ChiTaRS FHL1; human; . EvolutionaryTrace Q13642; -; . GeneWiki FHL1; -; . GenomeRNAi 2273; -; . PRO PR:Q13642; -; . Proteomes UP000005640; Chromosome X; . Bgee ENSG00000022267; -; . ExpressionAtlas Q13642; baseline and differential; . Genevisible Q13642; HS; . GO GO:0005737; C:cytoplasm; IDA:UniProtKB; . GO GO:0005829; C:cytosol; IDA:HPA; . GO GO:0005925; C:focal adhesion; IDA:UniProtKB; . GO GO:0005634; C:nucleus; IDA:UniProtKB; . GO GO:0005886; C:plasma membrane; IDA:BHF-UCL; . GO GO:0044325; F:ion channel binding; IPI:BHF-UCL; . GO GO:0008270; F:zinc ion binding; IEA:InterPro; . GO GO:0009887; P:animal organ morphogenesis; NAS:UniProtKB; . GO GO:0030154; P:cell differentiation; IEA:UniProtKB-KW; . GO GO:0007517; P:muscle organ development; NAS:UniProtKB; . GO GO:0030308; P:negative regulation of cell growth; IDA:UniProtKB; . GO GO:2000134; P:negative regulation of G1/S transition of mitotic cell cycle; IDA:UniProtKB; . GO GO:0010972; P:negative regulation of G2/M transition of mitotic cell cycle; IDA:UniProtKB; . GO GO:0043268; P:positive regulation of potassium ion transport; IDA:BHF-UCL; . GO GO:0003254; P:regulation of membrane depolarization; IDA:BHF-UCL; . GO GO:1901016; P:regulation of potassium ion transmembrane transporter activity; IDA:BHF-UCL; . Gene3D 2.10.110.10; -; 4; . InterPro IPR001781; Znf_LIM; . Pfam PF00412; LIM; 3; . SMART SM00132; LIM; 3; . PROSITE PS00478; LIM_DOMAIN_1; 3; . PROSITE PS50023; LIM_DOMAIN_2; 3; .

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