MSeqDR-LSDB Mitochondrial Disease Locus Specific Database
MMAA (methylmalonic aciduria (cobalamin deficiency)...)
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MMAA gene homepage
MSeqDR-LSDB: Mitochondrial Disease LSDB
General information
Gene symbol
MMAA
Gene name
methylmalonic aciduria (cobalamin deficiency) cblA type
Chromosome
4
Chromosomal band
q31.1
Imprinted
Unknown
Genomic reference
NC_000004.11
Transcript reference
NM_172250.2
Associated with diseases
-
Citation reference(s)
-
Curators (0)
-
Total number of public variants reported
0
Unique public DNA variants reported
0
Individuals with public variants
0
Hidden variants
0
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Notes
MSeqDR-LSDB
Date created
November 12, 2013
Links to other resources
HGNC
18871
Entrez Gene
166785
PubMed articles
MMAA
OMIM - Gene
607481
HGMD
MMAA
GeneCards
MMAA
GeneTests
MMAA
Active transcripts
Legend
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ID
Chr
Name
NCBI ID
NCBI Protein ID
Variants
00000895
4
methylmalonic aciduria (cobalamin deficiency) cblA type
NM_172250.2
NP_758454.1
0
Copyright & disclaimer
; NuclearMitome http://www.transgenomic.com ; MitoPhenome http://mitophenome.org
Mitochondrial Disease Sequence Data Resource (MSeqDR) Consortium
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