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GTF2IP14 general transcription factor IIi pseudogene 14 [ Homo sapiens (human) ]

Gene ID: 106481735, updated on 10-Oct-2023

Summary

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Official Symbol
GTF2IP14provided by HGNC
Official Full Name
general transcription factor IIi pseudogene 14provided by HGNC
Primary source
HGNC:HGNC:51726
See related
Ensembl:ENSG00000226002 AllianceGenome:HGNC:51726
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:
7q11.21
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (65084103..65100232)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (66290273..66306356)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 7 NC_000007.13 (64544481..64560610)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene chaperonin containing TCP1 subunit 6 pseudogene 3 Neighboring gene small nucleolar RNA, H/ACA box 15B-1 Neighboring gene small nucleolar RNA, H/ACA box 22C Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:64540973-64541867 Neighboring gene uncharacterized LOC124901662 Neighboring gene integrator complex subunit 4 pseudogene 1 Neighboring gene uncharacterized LOC124901661 Neighboring gene NANOG hESC enhancer GRCh37_chr7:64691122-64691685

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)

General gene information

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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_043494.1 

    Range
    101..16230
    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_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    65084103..65100232
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    66290273..66306356
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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