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CTSLP4 cathepsin L pseudogene 4 [ Homo sapiens (human) ]

Gene ID: 644496, updated on 10-Oct-2023

Summary

Official Symbol
CTSLP4provided by HGNC
Official Full Name
cathepsin L pseudogene 4provided by HGNC
Primary source
HGNC:HGNC:23645
See related
AllianceGenome:HGNC:23645
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
CTSLL4; CTSL1P4; bA564C4.3
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Genomic context

Location:
10q11.23
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (50704658..50708918, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (51553251..51557509, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (52464418..52468678, complement)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene POM121 transmembrane nucleoporin pseudogene Neighboring gene nuclear pore associated protein 1 pseudogene 1 Neighboring gene protein geranylgeranyltransferase type I subunit beta pseudogene 1 Neighboring gene N-acylsphingosine amidohydrolase 2B

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_021158.3 

    Range
    101..4361
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    50704658..50708918 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    51553251..51557509 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)