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SUMO1P2 SUMO1 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 474337, updated on 13-May-2022

Summary

Official Symbol
SUMO1P2provided by HGNC
Official Full Name
SUMO1 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:33149
See related
AllianceGenome:HGNC:33149
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
bA375F2.1
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Genomic context

See SUMO1P2 in Genome Data Viewer
Location:
1q24.2
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (168898097..168899044)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (168253336..168254283)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (168867335..168868282)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 626 Neighboring gene uncharacterized LOC105371606 Neighboring gene long intergenic non-protein coding RNA 970 Neighboring gene ribosomal protein L29 pseudogene 7 Neighboring gene RNA, 5S ribosomal pseudogene 66

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_004725.4 

    Range
    101..1048
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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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    168898097..168899044
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    168253336..168254283
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)