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CHTF8P1 chromosome transmission fidelity factor 8 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 677883, updated on 10-Oct-2023

Summary

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Official Symbol
CHTF8P1provided by HGNC
Official Full Name
chromosome transmission fidelity factor 8 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:35443
See related
AllianceGenome:HGNC:35443
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
CTF8P; CHTF8P
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Genomic context

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Location:
Xp11.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (44633330..44636065)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (44040119..44042854)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (44492576..44495311)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene farnesyl diphosphate synthase pseudogene 5 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29565 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29566 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29567 Neighboring gene FUN14 domain containing 1 Neighboring gene ribosomal protein L19 pseudogene 20 Neighboring gene ReSE screen-validated silencer GRCh37_chrX:44551446-44551623 Neighboring gene ribosomal protein SA pseudogene 61

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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Markers

Other Names

  • CHTF8 pseudogene 1
  • CTF8, chromosome transmission fidelity factor 8 homolog pseudogene 1

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_005539.5 

    Range
    101..2836
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    44633330..44636065
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    44040119..44042854
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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