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SAP18P3 SAP18 pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 106660616, updated on 13-May-2022

Summary

Official Symbol
SAP18P3provided by HGNC
Official Full Name
SAP18 pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:51569
See related
Ensembl:ENSG00000230697 AllianceGenome:HGNC:51569
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 SAP18P3 in Genome Data Viewer
Location:
3p24.3
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (20007813..20008267, complement)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (20011881..20012335, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (20049305..20049759, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene RAB5A, member RAS oncogene family Neighboring gene protein phosphatase 2C like domain containing 1 Neighboring gene RNA, U4 small nuclear 85, pseudogene Neighboring gene uncharacterized LOC124909352 Neighboring gene ribosomal protein L39 pseudogene 18 Neighboring gene CRISPRi-validated cis-regulatory element chr3.1018

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_044939.1 

    Range
    101..555
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    20007813..20008267 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    20011881..20012335 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)