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CLUHP9 clustered mitochondria homolog pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 100418742, updated on 10-Oct-2023

Summary

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Official Symbol
CLUHP9provided by HGNC
Official Full Name
clustered mitochondria homolog pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:51572
See related
AllianceGenome:HGNC:51572
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:
13q12.12
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 13 NC_000013.11 (24742670..24743226)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 13 NC_060937.1 (23950520..23951076)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 13 NC_000013.10 (25316808..25317364)

Chromosome 13 - NC_000013.11Genomic Context describing neighboring genes Neighboring gene ATPase H+/K+ transporting non-gastric alpha2 subunit Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:25284257-25285456 Neighboring gene ribosomal protein L26 pseudogene 34 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr13:25290040-25290684 Neighboring gene uncharacterized LOC105370118 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr13:25315583-25316404 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 7479 Neighboring gene ankyrin repeat domain 20 family member A10, pseudogene Neighboring gene iroquois homeobox 1 pseudogene 1 Neighboring gene ring finger protein 17

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

  • clustered mitochondria (cluA/CLU1) homolog pseudogene 9

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_024901.1 

    Range
    101..657
    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_000013.11 Reference GRCh38.p14 Primary Assembly

    Range
    24742670..24743226
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060937.1 Alternate T2T-CHM13v2.0

    Range
    23950520..23951076
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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