Description

methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria [Source:MGI Symbol;Acc:MGI:1923786]

Location

Chromosome 2: 50,279,881-50,296,801 reverse strand.

GRCm38:CM000995.2

About this gene

This gene has 8 transcripts (splice variants), 79 orthologues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Mmadhc-001ENSMUST000001027691342296aaENSMUSP00000099830
 
Protein coding
CCDS16027Q99LS1 NM_133839
NP_598600
TSL:1GENCODE basicAPPRIS P1
Mmadhc-007ENSMUST000001441431079219aaENSMUSP00000122804
 
Protein coding
-A2AQT7 -CDS 3' incompleteTSL:3
Mmadhc-002ENSMUST00000133768711179aaENSMUSP00000115961
 
Protein coding
-A2AQT8 -CDS 3' incompleteTSL:3
Mmadhc-003ENSMUST000001473451351No protein-
 
Processed transcript
---TSL:3
Mmadhc-005ENSMUST00000140563927No protein-
 
Processed transcript
---TSL:5
Mmadhc-004ENSMUST00000134480803No protein-
 
Processed transcript
---TSL:5
Mmadhc-006ENSMUST00000154254753No protein-
 
Processed transcript
---TSL:5
Mmadhc-008ENSMUST00000152948428No protein-
 
Processed transcript
---TSL:3

Gene-based displays