Warning: The NCBI web site requires JavaScript to function. more...
An official website of the United States government
The .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Download features.
Download gene features.
NCBI Reference Sequence: XM_017025114.2
FASTA Graphics
LOCUS XM_017025114 3018 bp mRNA linear PRI 25-AUG-2024 DEFINITION PREDICTED: Homo sapiens pleckstrin homology, MyTH4 and FERM domain containing H3 (PLEKHH3), transcript variant X2, mRNA. ACCESSION XM_017025114 VERSION XM_017025114.2 DBLINK BioProject: PRJNA168 KEYWORDS RefSeq. SOURCE Homo sapiens (human) ORGANISM Homo sapiens Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo. COMMENT MODEL REFSEQ: This record is predicted by automated computational analysis. This record is derived from a genomic sequence (NC_000017.11) annotated using gene prediction method: Gnomon, supported by mRNA and EST evidence. Also see: Documentation of NCBI's Annotation Process On Apr 5, 2022 this sequence version replaced XM_017025114.1. ##Genome-Annotation-Data-START## Annotation Provider :: NCBI RefSeq Annotation Status :: Updated annotation Annotation Name :: GCF_000001405.40-RS_2024_08 Annotation Pipeline :: NCBI eukaryotic genome annotation pipeline Annotation Software Version :: 10.3 Annotation Method :: Best-placed RefSeq; Gnomon; RefSeqFE; cmsearch; tRNAscan-SE Features Annotated :: Gene; mRNA; CDS; ncRNA Annotation Date :: 08/23/2024 ##Genome-Annotation-Data-END## FEATURES Location/Qualifiers source 1..3018 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="17" gene 1..3018 /gene="PLEKHH3" /note="pleckstrin homology, MyTH4 and FERM domain containing H3; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 ESTs, 53 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns" /db_xref="GeneID:79990" /db_xref="HGNC:HGNC:26105" CDS 166..2805 /gene="PLEKHH3" /codon_start=1 /product="pleckstrin homology domain-containing family H member 3 isoform X2" /protein_id="XP_016880603.1" /db_xref="GeneID:79990" /db_xref="HGNC:HGNC:26105" /translation="MCLWASRCRLGAIHLLGALRQGRRHAWPDLALPLPSPLGPRPIP SPSASASAEECGEAGWAARTPGSPSAPSSQVRRPDARAPAAETWTRGRSHPRIGGGSV EEGKMRRRGCLGAWQNELTSPVSKMGKLRPGDGKRLAQGSTGPLEVTLTQPVRSGPVS NRLQSWEETWSLIPEKGLPEDDPDIVVKGWLYREPRGGGARPWLPPRRAWFVLTRDSL DQFSSSGKGARRLGSLVLTSLCSVTGPERRRKETGLWSVTVSGRKHSVRLCSPRQAEA ERWGVALREVIASKAPLETPTQLLLRDIQESCGDPEAVALIYLRNPILRHTSGALYAP LLPLPYGVSAPGPGYAPLREEAVRLFLALQALEGARRPGPLMQGVLQTCRDLPALRDE LFLQLAKQTSGPAGPPGLPATQDPAALRYWQLLTCMSCTFRPGGAVRGHLLGHLERTE QALPDSELAEYARFIRKALGRTRGRELVPSLAEISALSQRQELLCTVHCPGAGACAVA IDSHTTAGEVARELVGRLGLARSRNAFALYEQRGAQERALAGGTLVADVLTSLAAEEA GLEDSPDSGWRLCLRLHGPLHPEGLSPDGHELPFLFEQAHALLLRGRPPPPDDTLRAL AALRLQSLQRDFSPRVPLPRLDRLLPPPAPPREDPPRPTPRPPPSAALLAGALWSPGL AKRRAERARRGGAGRTAGSIAREGGGGAGTAAAVLGGWKRLRGMGRAEAMAAYLALAA QCPGFGAARYDVLELSTEPGRGAPQKLCLGLGAKAMSLSRPGETEPIHSVSYGHVAAC QLMGPHTLALRVGESQLLLQSPQVEEIMQLVNAYLANPSPERPCSSSSPPCQDLPDTS PPSQRPGLDEPQGQSGCLGQLQD" ORIGIN 1 ggttcggagc ctcgtctcaa tcactctcgc tgtaaccggc cgtcacgctg atccgctcca 61 gcctccagcc acacgctgcg cgcttggcga actagggatg agggagagtt ttttgcctgg 121 gggccaaagc ccccgggagc tctcggagca gcagccctac tcgggatgtg cctgtgggcc 181 tcccgctgca ggctgggcgc tatccacctg ctgggggccc tgaggcaggg gaggcgtcac 241 gcgtggcccg acctggccct gcctctccct tccccgctgg gcccgcgtcc catcccgtct 301 ccttccgcct ccgccagcgc cgaggaatgt ggcgaggccg gctgggcggc tcgaacgcct 361 gggtccccct ccgctcccag ttcgcaagtg cggaggccag atgcgagagc tcccgctgcg 421 gagacctgga cgagggggag aagtcatccc aggattgggg gaggcagtgt ggaagaaggg 481 aaaatgagga ggagagggtg ccttggagcc tggcagaacg agctcacctc tcctgtttca 541 aagatgggga aactaaggcc cggagacggg aagagacttg cccaaggttc cacaggtccc 601 ctggaagtga cgctgactca gccagtgagg agcgggcctg tctccaacag gctgcagagc 661 tgggaggaga cttggagcct catcccggag aaagggctgc cggaggacga cccggacatc 721 gttgtgaaag gttggctgta ccgggagccc cgcggaggag gggcgcggcc ctggctgccc 781 ccgcgccgag cctggtttgt gctcacgcgg gactccctgg atcagttcag cagcagcggg 841 aaaggggcgc ggcgtctcgg gagcctcgtg ctcaccagcc tgtgctcggt gaccggccca 901 gagcgcaggc gtaaggagac aggtctgtgg tcagtgactg tgtctggtcg gaaacacagt 961 gtccgcctct gctccccacg ccaggcagag gctgagcgct ggggggtggc attgcgggaa 1021 gtgatcgcct ccaaggcacc cctggagacc cccacccagc tactgctcag ggacatacag 1081 gaaagttgcg gggacccaga ggccgttgcc ctcatttacc tgaggaaccc gattctgaga 1141 cacactagtg gagccttgta tgccccactc ctgcccctgc cctatggagt cagcgcccca 1201 ggtccgggct atgcacccct gcgcgaggag gcggtgcggc tgttcttggc gctgcaggcg 1261 ctggaggggg cgcggcgccc cgggcccttg atgcagggtg tgctccaaac ctgccgggac 1321 ttgcccgcgc tccgggatga actcttcctg cagctggcta agcagacctc gggccctgca 1381 ggtccccccg ggctcccggc tacccaagac cctgcggccc tgcggtactg gcaactcctc 1441 acctgcatga gctgcacctt ccgacctggg ggagctgtgc gggggcacct cctggggcac 1501 ttggagagga ccgagcaggc actcccggac tcggaactgg cggaatatgc gcgcttcatc 1561 cggaaagcgc tgggccggac gcgcggcaga gagctggtgc cctcgctggc ggagatttcc 1621 gcgttgagcc aacggcagga gctgctgtgt accgtgcact gtccgggggc tggtgcctgt 1681 gctgtggcca tcgactccca caccacggcg ggggaggtgg ctcgagagct ggtggggcgg 1741 ctgggcttgg cccggagccg caacgcattc gcgctgtacg agcagcgagg ggcccaggag 1801 cgagccctgg ctggggggac cctcgtggcc gacgtgctca ccagcttggc cgcggaggaa 1861 gctgggttgg aggactcgcc cgactccggg tggagactat gtctgcgtct tcacggacct 1921 ctgcaccctg aggggctgtc cccagacggt cacgaactgc ctttcctctt tgagcaggct 1981 cacgctctgc tgctgcgggg ccggccgccc ccacccgacg acacgctgcg cgccctggcg 2041 gcgctgcgcc tgcagagcct gcagcgggac ttctctccgc gggtgcccct gccccgcctg 2101 gaccgcctgc tcccgccccc ggccccgccg cgcgaagacc cgccccgccc gacccccagg 2161 ccgccccctt ccgctgccct gctggccggg gcgctctgga gcccgggcct ggccaagagg 2221 cgggcggagc gggcccggcg cggcggggcc ggccgcactg cgggaagcat tgcccgcgag 2281 ggaggaggcg gcgccggcac ggcagctgcc gtgctgggcg gctggaagcg gctacggggc 2341 atgggccgag ctgaggccat ggccgcctac ctggccctgg cggcgcagtg tccggggttc 2401 ggcgctgctc ggtatgacgt tctggagctg agcacggagc ctggtcgggg tgctccacag 2461 aagctgtgcc tgggcttggg agccaaggcc atgtccctct cccggccagg ggagacggag 2521 cccatccaca gtgtcagcta tggccatgtg gccgcctgcc agctaatggg cccccacacc 2581 ctggccttga gggtgggaga gagccagctc ctcctgcaga gcccccaggt ggaagagatc 2641 atgcagctgg tgaatgccta cttggccaac ccctcccccg agaggccctg cagcagctct 2701 tctcctccat gccaagacct gccagacacc tcccctccca gccagcgccc gggcctggac 2761 gagccccagg gacagtctgg ctgcttgggg cagctgcagg actgagcctg ccaagaggtc 2821 acgacttccc tcctgcctgc agcctgggcc aggactgctc tgagatttga gggaaacatg 2881 gacccttttg gccctgcagg gacagggcac atcccacacc caagggctac aatgggtgtg 2941 ggtaattttc tagtttgttt cttaatttat ttgtagaaga gaagcaaaaa aaaaaaaaaa 3001 gtttcttatt tacacaaa //
Whole sequence Selected region from: to:
All features Gene, RNA, and CDS features only
SNP
Show sequence Show reverse complement Show gap features
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on