2024-11-01 10:23:38, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS XM_054319735 1439 bp mRNA linear PRI 26-AUG-2024 DEFINITION PREDICTED: Homo sapiens claudin domain containing 2 (CLDND2), transcript variant X7, mRNA. ACCESSION XM_054319735 VERSION XM_054319735.1 DBLINK BioProject: PRJNA807723 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_060943) annotated using gene prediction method: Gnomon, supported by EST evidence. Also see: Documentation of NCBI's Annotation Process ##Genome-Annotation-Data-START## Annotation Provider :: NCBI RefSeq Annotation Status :: Updated annotation Annotation Name :: GCF_009914755.1-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..1439 /organism="Homo sapiens" /mol_type="mRNA" /isolate="CHM13" /db_xref="taxon:9606" /chromosome="19" /sex="female" /cell_line="CHM13htert" /tissue_type="hydatidiform mole" /note="haploid cell line" gene 1..1439 /gene="CLDND2" /note="claudin domain containing 2; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 54 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:125875" /db_xref="HGNC:HGNC:28511" CDS 292..1173 /gene="CLDND2" /codon_start=1 /product="claudin domain-containing protein 2 isoform X1" /protein_id="XP_054175710.1" /db_xref="GeneID:125875" /db_xref="HGNC:HGNC:28511" /translation="
MGVKRSLQSGGILLSLVANVLMVLSTATNYWTRQQEGHSGLWQECNHGICSSIPCQTTLAVTVACMVLAVGVGVVGMVMGLRIRCDEGESLRGQTTSAFLFLGGLLLLTALIGYTVKNAWKNNVFFSWSYFSGWLALPFSILAGKLDSGKRVEETAQKTLTPEAPQLPSQETPGTSRGLPNTLTTPADPAETPLEPQTPVPGALPAIRPRAHLPLPAPHPRPPRLLLSAGRHDHAEHRRHQWIPRVSVTAACLGQNKGTAFFSAAAPRAFLRVVGTQARGCIEAQGRHKDMNS"
misc_feature 319..729 /gene="CLDND2" /note="PMP-22/EMP/MP20/Claudin family; Region: PMP22_Claudin; cl21598" /db_xref="CDD:473919" ORIGIN
tgggcgacagagcaagactccatctcaaaaaataataatgataataatgataaaagaaggactcggcctatcatgtaacggcccccaaagctgagatctgaatctaagcagtcactcagttgagagctgcgggggtgtatgcgatggtggtggggggagtgattatccctttaaacagccactgggggagggggttctggaacccctggcctcacagagacccagcctccctccccccgtctctctgggctctgtgtctaaggagccctagggcactgggtcctcagtggcatgggggtgaagcggagcctccagagtgggggcattctgctcagcctcgtggccaacgtcctcatggtgctctccacggccaccaactactggacccgccaacaagagggccacagtggcctgtggcaggaatgcaaccacggcatctgctccagcatcccctgccagaccacgctggcggtgactgtggcgtgcatggtgctggcggtgggtgtcggcgtggtgggcatggtgatgggactgcggattcggtgcgacgagggcgagtcgctgcggggccagaccacgagcgccttcctcttcctcggcggactgctgctgctgaccgccttgataggctacaccgtgaagaatgcgtggaagaacaacgtcttcttctcttggtcctatttttctgggtggctggccttacccttctcaattctcgcgggtaaactggacagcgggaagagggtggaggagactgcccagaagaccctcaccccagaggctccccagctgccctcccaggaaaccccggggacctctcggggactccccaacacactaacgactcccgcagacccggcagagacccccttggagccccaaaccccagtccccggggccctcccggccatccgccccagggcccaccttcctctccctgctccgcacccccgtccccccaggcttctgctttctgctggcagacatgatcatgcagagcaccgacgccatcagtggattccccgtgtgtctgtgactgcagcctgcctggggcagaataaaggaacggctttttttagcgctgcggctccgcgtgcttttctgcgggtcgtggggacgcaggcacggggttgcatagaggctcagggaagacataaggacatgaactcatagggaacgtggagacagggagacacagacatggagacacaagtctccatggattgggatgggaacagggacatgtgggaggggcggggccaggaggggacgtgggcctttggagagggtgtggagaggctgtggggacgacatggaggtgaagtagagacacggacaggggaggatacggatatggaagggacagggaacacggggatggagagagtggagagaccgacgcgcgaggattcagaggcgtgggaatacgagtaccgcga
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Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
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