
AMBN ameloblastin [Homo sapiens (human)] - Gene - NCBI
2024年12月10日 · This gene encodes the nonamelogenin enamel matrix protein ameloblastin. The encoded protein may be important in enamel matrix formation and mineralization. This …
AMTN Gene - GeneCards | AMTN Protein | AMTN Antibody
2024年12月24日 · AMTN (Amelotin) is a Protein Coding gene. Diseases associated with AMTN include Amelogenesis Imperfecta, Type Iiib and Amelogenesis Imperfecta, Type Iiia. Among …
Ameloblastin - Wikipedia
Ameloblastin (abbreviated AMBN and also known as sheathlin or amelin) is an enamel matrix protein that in humans is encoded by the AMBN gene. [5] Ameloblastin is a specific protein …
Ameloblastin and its multifunctionality in amelogenesis: A review
2024年8月1日 · Ameloblastin (Ambn) is multifunctional in its facilitation of enamel formation. Human amelogenesis imperfecta cases and animal models emphasize importance of Ambn. …
AMBN protein expression summary - The Human Protein Atlas
This gene encodes the nonamelogenin enamel matrix protein ameloblastin. The encoded protein may be important in enamel m atrix formation and mineralization. This gene is located in the …
258 - Gene ResultAMBN ameloblastin [ (human)] - National …
2025年2月8日 · Ameloblastin is critical for the initiation of enamel ribbon formation, and its absence results in pathological mineralization within the enamel organ epithelia. Single …
成釉细胞(AMBN)基因 | MCE
This gene encodes the nonamelogenin enamel matrix protein ameloblastin. The encoded protein may be important in enamel matrix formation and mineralization. This gene is located in the …
Cloning and characterization of the human ameloblastin gene
2000年10月3日 · The human AMBN gene consists of 13 exons and contains a novel 78 bp (26 amino acid) insert representing two short exons produced by internal sequence duplication. …
Gene: AMBN (ENSG00000178522) - Summary - Homo_sapiens
Chromosome 4: 71,457,973-71,473,005 forward strand. This gene has 2 transcripts (splice variants) and is associated with 1 phenotype. A single transcript chosen for a gene which is …
Whole exome sequencing identifies an AMBN missense mutation …
2018年9月3日 · Whole exome sequencing of the proband identified a novel heterozygous C-T point mutation at nucleotide position 1069 of the AMBN gene, causing a Pro to Ser mutation at …