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YWHAQP3 YWHAQ pseudogene 3 [ Homo sapiens (human) ]

Gene ID: 100128944, updated on 17-Sep-2024

Summary

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Official Symbol
YWHAQP3provided by HGNC
Official Full Name
YWHAQ pseudogene 3provided by HGNC
Primary source
HGNC:HGNC:37682
See related
AllianceGenome:HGNC:37682
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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See YWHAQP3 in Genome Data Viewer
Location:
12q13.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (56871606..56872601)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (56839494..56840489)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 12 NC_000012.11 (57265390..57266385)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene hydroxysteroid 17-beta dehydrogenase 6 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr12:57198454-57199103 Neighboring gene small nucleolar RNA SNORA48 Neighboring gene Sharpr-MPRA regulatory region 4868 Neighboring gene retinol dehydrogenase 16 (all-trans) pseudogene Neighboring gene short chain dehydrogenase/reductase family 9C member 7

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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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_028176.2 

    Range
    9..1004
    Download
    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    56871606..56872601
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    56839494..56840489
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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