Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria Kits ELISA
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Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) Kit ELISA Kit ELISA
Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) Kit ELISA Kit ELISA
Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) Kit ELISA Kit ELISA
Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) Kit ELISA Kit ELISA
Methylmalonic Aciduria (Cobalamin Deficiency) CblD Type, with Homocystinuria (MMADHC) profil antigène
Profil protéine
This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.
Gene names and symbols associated with MMADHC
- methylmalonic aciduria and homocystinuria, cblD type (MMADHC) anticorps
- methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria (Mmadhc) anticorps
- methylmalonic aciduria and homocystinuria, cblD type (Mmadhc) anticorps
- 2010311D03Rik anticorps
- AI314967 anticorps
- C2orf25 anticorps
- cblD anticorps
- CL25022 anticorps
- RGD1303272 anticorps
Protein level used designations for MMADHC
methylmalonic aciduria and homocystinuria type D homolog, mitochondrial , methylmalonic aciduria and homocystinuria type D protein, mitochondrial , protein C2orf25, mitochondrial , likely ortholog of H. sapiens chromosome 2 open reading frame 25 (C2orf25)
| GENE ID | SPECIES |
|---|---|
| 424311 | Gallus gallus |
| 27249 | Homo sapiens |
| 109129 | Mus musculus |
| 362134 | Rattus norvegicus |
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