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SMU1P1 SMU1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 246784, updated on 17-Sep-2024

Summary

Official Symbol
SMU1P1provided by HGNC
Official Full Name
SMU1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:54527
See related
AllianceGenome:HGNC:54527
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 SMU1P1 in Genome Data Viewer
Location:
1q23.1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (157058710..157060804, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (156195525..156197618, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (157028502..157030596, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene Rho guanine nucleotide exchange factor 11 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:156961673-156962173 Neighboring gene RNA, 7SL, cytoplasmic 612, pseudogene Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1443 Neighboring gene uncharacterized LOC102724222 Neighboring gene MPRA-validated peak427 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:157044311-157044941 Neighboring gene keratin 8 pseudogene 45 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:157059291-157059812 Neighboring gene ETS variant transcription factor 3 like

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • SMU1, DNA replication regulator and spliceosomal factor pseudogene
  • smu-1 suppressor of mec-8 and unc-52 homolog 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_001588.5 

    Range
    101..2195
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    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    157058710..157060804 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    156195525..156197618 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)