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MMADHCP2 MMADHC pseudogene 2 [ Homo sapiens (human) ]

Gene ID: 100216355, updated on 23-Nov-2021

Summary

Official Symbol
MMADHCP2provided by HGNC
Official Full Name
MMADHC pseudogene 2provided by HGNC
Primary source
HGNC:HGNC:54997
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

See MMADHCP2 in Genome Data Viewer
Location:
11p13
Annotation release Status Assembly Chr Location
109.20211119 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (34334784..34336108, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (34356331..34357655, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene N-acetyltransferase 10 Neighboring gene uncharacterized LOC102723539 Neighboring gene ankyrin repeat and BTB domain containing 2 Neighboring gene CRISPRi-validated cis-regulatory element chr11.1764 Neighboring gene CIR1 pseudogene 3

Genomic regions, transcripts, and products

General gene information

Other Names

  • metabolism of cobalamin associated D pseudogene
  • methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria pseudogene
  • methylmalonic aciduria and homocystinuria, cblD type pseudogene

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_009050.4 

    Range
    101..1425
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20211119

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    34334784..34336108 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
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