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KRTAP20-4 keratin associated protein 20-4 [ Homo sapiens (human) ]

Gene ID: 100151643, updated on 8-Mar-2024

Summary

Official Symbol
KRTAP20-4provided by HGNC
Official Full Name
keratin associated protein 20-4provided by HGNC
Primary source
HGNC:HGNC:34002
See related
Ensembl:ENSG00000206105 AllianceGenome:HGNC:34002
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
KAP20.4
Summary
Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Apr 2022]
Orthologs
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Genomic context

Location:
21q22.11
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 21 NC_000021.9 (30620627..30620850)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 21 NC_060945.1 (28987568..28987791)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (31992946..31993169)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene keratin associated protein 6-1 Neighboring gene keratin associated protein 20-1 Neighboring gene keratin associated protein 20-2 Neighboring gene keratin associated protein 20-3

Genomic regions, transcripts, and products

General protein information

Preferred Names
putative keratin-associated protein 20-4

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.

mRNA and Protein(s)

  1. NM_001350977.1NP_001337906.1  putative keratin-associated protein 20-4

    Status: VALIDATED

    Source sequence(s)
    AB096956
    Consensus CDS
    CCDS86982.1
    UniProtKB/Swiss-Prot
    Q3LI62
    Related
    ENSP00000372278.2, ENST00000382828.2

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_000021.9 Reference GRCh38.p14 Primary Assembly

    Range
    30620627..30620850
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060945.1 Alternate T2T-CHM13v2.0

    Range
    28987568..28987791
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NR_023342.1: Suppressed sequence

    Description
    NR_023342.1: This RefSeq was removed because it is now thought that this gene does encode a protein.