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CDRT15P7 CDRT15 pseudogene 7 [ Homo sapiens (human) ]

Gene ID: 100420788, updated on 17-Sep-2024

Summary

Official Symbol
CDRT15P7provided by HGNC
Official Full Name
CDRT15 pseudogene 7provided by HGNC
Primary source
HGNC:HGNC:54915
See related
AllianceGenome:HGNC:54915
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
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Genomic context

See CDRT15P7 in Genome Data Viewer
Location:
9q13
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (63719860..63720642)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (47839263..47840045, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (68315594..68316376)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124902167 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:68298872-68299728 Neighboring gene uncharacterized LOC100419925 Neighboring gene myosin VB pseudogene 3 Neighboring gene cyclin dependent kinase 2 associated protein 2 pseudogene 3

Genomic regions, transcripts, and products

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_023922.2 

    Range
    192..974
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    63719860..63720642
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    47839263..47840045 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)