Description

methylmalonic aciduria (cobalamin deficiency) type B homolog (human) [Source:MGI Symbol;Acc:MGI:1924947]

INSDC coordinates

chromosome:GRCm38:CM000998.2:114431034:114444059:1

Transcripts

This gene has 4 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLengthProteinBiotypeCCDSUniProtRefSeqFlags
Mmab-001ENSMUST000000315603019 bp237 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS19565Q9D273 NM_029956
NP_084232
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Mmab-003ENSMUST00000112245644 bp180 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3Z1G7 -GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Mmab-002ENSMUST00000150519542 bp No protein product
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
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Mmab-004ENSMUST000001232561138 bp No protein product
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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Gene-based displays