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MYADML myeloid associated differentiation marker like (pseudogene) [ Homo sapiens (human) ]

Gene ID: 151325, updated on 17-Sep-2024

Summary

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Official Symbol
MYADMLprovided by HGNC
Official Full Name
myeloid associated differentiation marker like (pseudogene)provided by HGNC
Primary source
HGNC:HGNC:31019
See related
Ensembl:ENSG00000293267 AllianceGenome:HGNC:31019
Gene type
pseudo
RefSeq status
VALIDATED
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 MYADML in Genome Data Viewer
Location:
2p22.3
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (33726061..33728217, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (33774225..33776382, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (33951128..33953284, complement)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105374455 Neighboring gene heterogeneous nuclear ribonucleoprotein A1 pseudogene 61 Neighboring gene uncharacterized LOC124905986 Neighboring gene Sharpr-MPRA regulatory region 135 Neighboring gene long intergenic non-protein coding RNA 1317 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:34087984-34089183 Neighboring gene solute carrier family 25 member 5 pseudogene 2 Neighboring gene uncharacterized LOC124905987 Neighboring gene uncharacterized LOC105374456

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. Yang HC, et al. PLoS One, 2009. PMID 19421330, Free PMC Article
  2. Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women. Schuh-Huerta SM, et al. Hum Reprod, 2012 Feb. PMID 22116950, Free PMC Article
  3. Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K, et al. Genome Res, 2006 Jan. PMID 16344560, Free PMC Article
  4. Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T, et al. Nat Genet, 2004 Jan. PMID 14702039
  5. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

EBI GWAS Catalog

Description
Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women.
EBI GWAS Catalog
Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan.
EBI GWAS Catalog

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Markers

Other Names

  • myeloid-associated differentiation marker-like

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.

RNA

  1. NR_003143.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AC093393, BC031088, DB059579
    Related
    ENST00000474610.1

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    33726061..33728217 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    33774225..33776382 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_207329.1: Suppressed sequence

    Description
    NM_207329.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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