Homo sapiens (human): 265
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Entry
265 CDS
T01001
Symbol
AMELX, AI1E, AIH1, ALGN, AMG, AMGL, AMGX
Name
(RefSeq) amelogenin, X isoform isoform 1 precursor
KO
K23443
amelogenin
Organism
hsa
Homo sapiens (human)
Disease
H00615
Amelogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99992 Structural proteins
265 (AMELX)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Amelogenin
Motif
Other DBs
NCBI-GeneID:
265
NCBI-ProteinID:
NP_001133
OMIM:
300391
HGNC:
461
Ensembl:
ENSP00000370090.3
UniProt:
Q99217
LinkDB
All DBs
Position
X:11293413..11309588
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AA seq
191 aa
AA seq
DB search
MGTWILFACLLGAAFAMPLPPHPGHPGYINFSYEVLTPLKWYQSIRPPYPSYGYEPMGGW
LHHQIIPVLSQQHPPTHTLQPHHHIPVVPAQQPVIPQQPMMPVPGQHSMTPIQHHQPNLP
PPAQQPYQPQPVQPQPHQPMQPQPPVHPMQPLPPQPPLPPMFPMQPLPPMLPDLTLEAWP
STDKTKREEVD
NT seq
576 nt
NT seq
+upstream
nt +downstream
nt
atggggacctggattttatttgcctgcctcctgggagcagcttttgccatgcctctacca
cctcatcctgggcaccctggttatatcaacttcagctatgaggtgcttacccctttgaag
tggtaccagagcataaggccaccgtacccttcctatggttacgagcccatgggtggatgg
ctgcaccaccaaatcatccccgtgctgtcccaacagcaccccccgactcacaccctgcag
cctcatcaccacatcccagtggtgccagctcagcagcccgtgatcccccagcaaccaatg
atgcccgttcctggccaacactccatgactccaatccaacaccaccagccaaacctccct
ccgcccgcccagcagccctaccagccccagcctgttcagccacagcctcaccagcccatg
cagccccagccacctgtgcaccccatgcagcccctgccgccacagccacctctgcctccg
atgttccccatgcagcccctgcctcccatgcttcctgatctgactctggaagcttggcca
tcaacagacaagaccaagcgggaggaagtggattaa
DBGET
integrated database retrieval system
