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TMLHEP1 TMLHE pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 553939, updated on 13-May-2022

Summary

Official Symbol
TMLHEP1provided by HGNC
Official Full Name
TMLHE pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:55622
See related
AllianceGenome:HGNC:55622
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 TMLHEP1 in Genome Data Viewer
Location:
Xq28
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (155349581..155352238)
110 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (153586917..153589577)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (154578893..154581552)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene chloride intracellular channel 2 Neighboring gene twinfilin 1 pseudogene 2 Neighboring gene PHD finger protein 10 pseudogene 1 Neighboring gene uncharacterized LOC101927830 Neighboring gene int22h-2 recombination region Neighboring gene microRNA 1184-2 Neighboring gene H2A.B variant histone 2 Neighboring gene coagulation factor VIII associated 2

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_029356.2 

    Range
    101..2758
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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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    155349581..155352238
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    153586917..153589577
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)