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MPHOSPH10P9 MPHOSPH10 pseudogene 9 [ Homo sapiens (human) ]

Gene ID: 100631266, updated on 27-Aug-2024

Summary

Official Symbol
MPHOSPH10P9provided by HGNC
Official Full Name
MPHOSPH10 pseudogene 9provided by HGNC
Primary source
HGNC:HGNC:55696
See related
AllianceGenome:HGNC:55696
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

Location:
15q11.2
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (22453016..22453496)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (20125113..20125593)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (23419600..23420080, complement)

Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene SPATA31 subfamily E member 3, pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:23454295-23455138 Neighboring gene golgin A8 family member E, pseudogene Neighboring gene RNA, 7SL, cytoplasmic 545, pseudogene Neighboring gene uncharacterized LOC124900355 Neighboring gene golgin A6 family like 22 Neighboring gene pectinesterase inhibitor 10-like

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_029294.2 

    Range
    101..581
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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_000015.10 Reference GRCh38.p14 Primary Assembly

    Range
    22453016..22453496
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    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 ALT_REF_LOCI_1

Genomic

  1. NT_187604.1 Reference GRCh38.p14 ALT_REF_LOCI_1

    Range
    97169..97649
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060939.1 Alternate T2T-CHM13v2.0

    Range
    20125113..20125593
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)