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LOC100420320 kinesin family member 2A pseudogene [ Homo sapiens (human) ]

Gene ID: 100420320, updated on 10-Dec-2024

Summary

Gene symbol
LOC100420320
Gene description
kinesin family member 2A pseudogene
See related
Ensembl:ENSG00000235274
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 LOC100420320 in Genome Data Viewer
Location:
Xq25
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (127728732..127730932, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (126042259..126044459, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (126862713..126864913, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene patatin like phospholipase domain containing 10 pseudogene Neighboring gene Sharpr-MPRA regulatory region 1703 Neighboring gene uncharacterized LOC105373332 Neighboring gene NANOG hESC enhancer GRCh37_chrX:126884520-126885021 Neighboring gene uncharacterized LOC105373333 Neighboring gene actin related protein T1

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_026760.2 

    Range
    101..2301
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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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    127728732..127730932 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    126042259..126044459 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)