Homo sapiens (human): 6948
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Entry
6948 CDS
T01001
Symbol
TCN2, D22S676, D22S750, II, TC, TC_II, TC-2, TC2, TCII
Name
(RefSeq) transcobalamin 2
KO
K14619
transcobalamin-2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04977
Vitamin digestion and absorption
hsa04980
Cobalamin transport and metabolism
Network
nt06538
Cobalamin transport and metabolism
Element
N01807
Transfer of cobalamin to the portal blood
Disease
H01190
Transcobalamin II deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09154 Digestive system
04977 Vitamin digestion and absorption
6948 (TCN2)
04980 Cobalamin transport and metabolism
6948 (TCN2)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cobalamin_bind
DUF4430
Motif
Other DBs
NCBI-GeneID:
6948
NCBI-ProteinID:
NP_000346
OMIM:
613441
HGNC:
11653
Ensembl:
ENSG00000185339
UniProt:
P20062
Structure
PDB
PDBj
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All DBs
Position
22:30607174..30627271
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AA seq
427 aa
AA seq
DB search
MRHLGAFLFLLGVLGALTEMCEIPEMDSHLVEKLGQHLLPWMDRLSLEHLNPSIYVGLRL
SSLQAGTKEDLYLHSLKLGYQQCLLGSAFSEDDGDCQGKPSMGQLALYLLALRANCEFVR
GHKGDRLVSQLKWFLEDEKRAIGHDHKGHPHTSYYQYGLGILALCLHQKRVHDSVVDKLL
YAVEPFHQGHHSVDTAAMAGLAFTCLKRSNFNPGRRQRITMAIRTVREEILKAQTPEGHF
GNVYSTPLALQFLMTSPMRGAELGTACLKARVALLASLQDGAFQNALMISQLLPVLNHKT
YIDLIFPDCLAPRVMLEPAAETIPQTQEIISVTLQVLSLLPPYRQSISVLAGSTVEDVLK
KAHELGGFTYETQASLSGPYLTSVMGKAAGEREFWQLLRDPNTPLLQGIADYRPKDGETI
ELRLVSW
NT seq
1284 nt
NT seq
+upstream
nt +downstream
nt
atgaggcaccttggggccttcctcttccttctgggggtcctgggggccctcactgagatg
tgtgaaataccagagatggacagccatctggtagagaagttgggccagcacctcttacct
tggatggaccggctttccctggagcacttgaaccccagcatctatgtgggcctacgcctc
tccagtctgcaggctgggaccaaggaagacctctacctgcacagcctcaagcttggttac
cagcagtgcctcctagggtctgccttcagcgaggatgacggtgactgccagggcaagcct
tccatgggccagctggccctctacctgctcgctctcagagccaactgtgagtttgtcagg
ggccacaagggggacaggctggtctcacagctcaaatggttcctggaggatgagaagaga
gccattgggcatgatcacaagggccacccccacactagctactaccagtatggcctgggc
attctggccctgtgtctccaccagaagcgggtccatgacagcgtggtggacaaacttctg
tatgctgtggaacctttccaccagggccaccattctgtggacacagcagccatggcaggc
ttggcattcacctgtctgaagcgctcaaacttcaaccctggtcggagacaacggatcacc
atggccatcagaacagtgcgagaggagatcttgaaggcccagacccccgagggccacttt
gggaatgtctacagcaccccattggcattacagttcctcatgacttcccccatgcgtggg
gcagaactgggaacagcatgtctcaaggcgagggttgctttgctggccagtctgcaggat
ggagccttccagaatgctctcatgatttcccagctgctgcccgttctgaaccacaagacc
tacattgatctgatcttcccagactgtctggcaccacgagtcatgttggaaccagctgct
gagaccattcctcagacccaagagatcatcagtgtcacgctgcaggtgcttagtctcttg
ccgccgtacagacagtccatctctgttctggccgggtccaccgtggaagatgtcctgaag
aaggcccatgagttaggaggattcacatatgaaacacaggcctccttgtcaggcccctac
ttaacctccgtgatggggaaagcggccggagaaagggagttctggcagcttctccgagac
cccaacaccccactgttgcaaggtattgctgactacagacccaaggatggagaaaccatt
gagctgaggctggttagctggtag
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