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TMEM97P2 transmembrane protein 97 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 724059, updated on 17-Jun-2024

Summary

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Official Symbol
TMEM97P2provided by HGNC
Official Full Name
transmembrane protein 97 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39641
See related
AllianceGenome:HGNC:39641
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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See TMEM97P2 in Genome Data Viewer
Location:
8p21.3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (20932572..20934863, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (21198930..21201221, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (20790083..20792374, complement)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105379314 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr8:20210567-20211189 Neighboring gene NANOG hESC enhancer GRCh37_chr8:20212340-20212863 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:20241249-20241750 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr8:20269567-20270766 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_102562 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:20290912-20291613 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_102576 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:20315593-20316153 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:20316154-20316713 Neighboring gene NANOG hESC enhancer GRCh37_chr8:20350867-20351405 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:20364504-20365243 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:20365983-20366722 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:20365244-20365982 Neighboring gene ReSE screen-validated silencer GRCh37_chr8:20367115-20367326 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_102632 Neighboring gene small nucleolar RNA, C/D box 3F Neighboring gene uncharacterized LOC105379315 Neighboring gene NANOG hESC enhancer GRCh37_chr8:20554878-20555391 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:20662002-20662502 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr8:20662503-20663003 Neighboring gene NANOG hESC enhancer GRCh37_chr8:20676219-20676765 Neighboring gene uncharacterized LOC105379316 Neighboring gene long intergenic non-protein coding RNA 3023 Neighboring gene long intergenic non-protein coding RNA 2153

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

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_005603.5 

    Range
    101..2392
    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_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    20932572..20934863 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    21198930..21201221 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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