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GRAMD4P2 GRAM domain containing 4 pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100873881, updated on 10-Oct-2023

Summary

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Official Symbol
GRAMD4P2provided by HGNC
Official Full Name
GRAM domain containing 4 pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:39654
See related
AllianceGenome:HGNC:39654
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:
22q11.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (15750362..15750824, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (16324248..16324710, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (16227139..16227601)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene neurofibromin 1 pseudogene 6 Neighboring gene mediator complex subunit 15 pseudogene 7 Neighboring gene POTEH antisense RNA 1 Neighboring gene RNA, U6 small nuclear 816, pseudogene Neighboring gene POTE ankyrin domain family member H Neighboring gene OCT4 hESC enhancer GRCh37_chr22:16212624-16213125 Neighboring gene prostate enriched lncRNA Neighboring gene double homeobox A pseudogene 8 Neighboring gene BMS1 pseudogene 22 Neighboring gene TOMM40 pseudogene 2 Neighboring gene neurobeachin pseudogene 3

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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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_032336.1 

    Range
    101..563
    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_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    15750362..15750824 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    16324248..16324710 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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