Homo sapiens (human): 81693
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Entry
81693 CDS
T01001
Symbol
AMN, IGS2, PRO1028, amnionless
Name
(RefSeq) amnion associated transmembrane protein
KO
K18259
protein amnionless
Organism
hsa
Homo sapiens (human)
Pathway
hsa04977
Vitamin digestion and absorption
Network
nt06538
Cobalamin transport and metabolism
Element
N01806
Cobalamin (Vitamin B12) absorption
Disease
H01277
Vitamin B12 deficiency anaemia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09154 Digestive system
04977 Vitamin digestion and absorption
81693 (AMN)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
81693 (AMN)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of other body fluids (saliva and urine)
81693 (AMN)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Amnionless
Motif
Other DBs
NCBI-GeneID:
81693
NCBI-ProteinID:
NP_112205
OMIM:
605799
HGNC:
14604
Ensembl:
ENSG00000166126
UniProt:
Q9BXJ7
Structure
PDB
PDBj
LinkDB
All DBs
Position
14:102922663..102930842
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AA seq
453 aa
AA seq
DB search
MGVLGRVLLWLQLCALTQAVSKLWVPNTDFDVAANWSQNRTPCAGGAVEFPADKMVSVLV
QEGHAVSDMLLPLDGELVLASGAGFGVSDVGSHLDCGAGEPAVFRDSDRFSWHDPHLWRS
GDEAPGLFFVDAERVPCRHDDVFFPPSASFRVGLGPGASPVRVRSISALGRTFTRDEDLA
VFLASRAGRLRFHGPGALSVGPEDCADPSGCVCGNAEAQPWICAALLQPLGGRCPQAACH
SALRPQGQCCDLCGAVVLLTHGPAFDLERYRARILDTFLGLPQYHGLQVAVSKVPRSSRL
READTEIQVVLVENGPETGGAGRLARALLADVAENGEALGVLEATMRESGAHVWGSSAAG
LAGGVAAAVLLALLVLLVAPPLLRRAGRLRWRRHEAAAPAGAPLGFRNPVFDVTASEELP
LPRRLSLVPKAAADSTSHSYFVNPLFAGAEAEA
NT seq
1362 nt
NT seq
+upstream
nt +downstream
nt
atgggcgtcctgggccgggtcctgctgtggctgcagctctgcgcactgacccaggcggtc
tccaaactctgggtccccaacacggacttcgacgtcgcagccaactggagccagaaccgg
accccgtgcgccggcggcgccgttgagttcccggcggacaagatggtgtcagtcctggtg
caagaaggtcacgccgtctcagacatgctcctgccgctggatggggaactcgtcctggct
tcaggagccggattcggcgtctcagacgtgggctcgcacctggactgtggcgcgggcgaa
cctgccgtcttccgcgactctgaccgcttctcctggcatgacccgcacctgtggcgctct
ggggacgaggcacctggcctcttcttcgtggacgccgagcgcgtgccctgccgccacgac
gacgtcttctttccgcctagtgcctccttccgcgtggggctcggccctggcgctagcccc
gtgcgtgtccgcagcatctcggctctgggccggacgttcacgcgcgacgaggacctggct
gttttcctggcgtcccgcgcgggccgcctacgcttccacgggccgggcgcgctgagcgtg
ggccccgaggactgcgcggacccgtcgggctgcgtctgcggcaacgcggaggcgcagccg
tggatctgcgcggccctgctccagcccctgggcggccgctgcccccaggccgcctgccac
agcgccctccggccccaggggcagtgctgtgacctctgtggagccgttgtgttgctgacc
cacggccccgcatttgacctggagcggtaccgggcgcggatactggacaccttcctgggt
ctgcctcagtaccacgggctgcaggtggccgtgtccaaggtgccacgctcgtcccggctc
cgtgaggccgatacggagatccaggtggtgctggtggagaatgggcccgagacaggcgga
gcggggcggctggcccgggccctcctggcggacgtcgccgagaacggcgaggccctcggc
gtcctggaggcgaccatgcgggagtcgggcgcacacgtctggggcagctccgcggctggg
ctggcgggcggcgtggcggctgccgtgctgctggcgctgctggtcctgctggtggcgccg
ccgctgctgcgccgcgcggggaggctcaggtggaggaggcacgaggcggcggccccggct
ggagcgcccctcggcttccgcaacccggtgttcgacgtgacggcctccgaggagctgccc
ctgccgcggcggctcagcctggttccgaaggcggccgcagacagcaccagccacagttac
ttcgtcaaccctctgttcgccggggccgaggccgaggcctga
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