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SAGE3P sarcoma antigen 3, pseudogene [ Homo sapiens (human) ]

Gene ID: 100419054, updated on 10-Oct-2023

Summary

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Official Symbol
SAGE3Pprovided by HGNC
Official Full Name
sarcoma antigen 3, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:51338
See related
AllianceGenome:HGNC:51338
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

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Location:
Xq26.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (135637624..135638932, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (133963404..133964712, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (134771549..134772857, complement)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ETS2 pseudogene 1 Neighboring gene sarcoma antigen 4, pseudogene Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chrX:134744552-134745751 Neighboring gene sarcoma antigen 2, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29985 Neighboring gene cancer/testis antigen family 45 member A1

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Other Names

  • sarcoma antigen 1 pseudogene

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_026767.1 

    Range
    101..1409
    Download
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    135637624..135638932 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    133963404..133964712 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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