GO:0008150 | biological_process |
Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human) |
詳細情報を見る |
同義遺伝子名
AMME syndrome candidate gene 1 protein homolog, Ammecr1, 6230420G18Rik
Refseq ID | NM_019496 |
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Gene ID | 56068 |
Unigene ID | Mm.143724 |
Probe set ID | 1450546_at [Mouse430_2] |
Ensembl ID | ENSMUSG00000042225 |
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