Homo sapiens (human): 60482
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Entry
60482 CDS
T01001
Symbol
SLC5A7, CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1
Name
(RefSeq) solute carrier family 5 member 7
KO
K14387
solute carrier family 5 (high affinity choline transporter), member 7
Organism
hsa
Homo sapiens (human)
Pathway
hsa04082
Neuroactive ligand signaling
hsa04725
Cholinergic synapse
hsa05231
Choline metabolism in cancer
Network
nt06544
Neuroactive ligand signaling
Element
N01896
Acetylcholine metabolism and transport in neuron
Disease
H00770
Congenital myasthenic syndrome
H00856
Distal hereditary motor neuropathies
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04082 Neuroactive ligand signaling
60482 (SLC5A7)
09150 Organismal Systems
09156 Nervous system
04725 Cholinergic synapse
60482 (SLC5A7)
09160 Human Diseases
09161 Cancer: overview
05231 Choline metabolism in cancer
60482 (SLC5A7)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
60482 (SLC5A7)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC5: Sodium glucose cotransporter
60482 (SLC5A7)
BRITE hierarchy
SSDB
Ortholog
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Gene cluster
GFIT
Motif
Pfam:
SSF
Motif
Other DBs
NCBI-GeneID:
60482
NCBI-ProteinID:
NP_001291934
OMIM:
608761
HGNC:
14025
Ensembl:
ENSG00000115665
UniProt:
Q9GZV3
B2RCU2
Structure
PDB
PDBj
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All DBs
Position
2:107986524..108013994
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AA seq
580 aa
AA seq
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MAFHVEGLIAIIVFYLLILLVGIWAAWRTKNSGSAEERSEAIIVGGRDIGLLVGGFTMTA
TWVGGGYINGTAEAVYVPGYGLAWAQAPIGYSLSLILGGLFFAKPMRSKGYVTMLDPFQQ
IYGKRMGGLLFIPALMGEMFWAAAIFSALGATISVIIDVDMHISVIISALIATLYTLVGG
LYSVAYTDVVQLFCIFVGLWISVPFALSHPAVADIGFTAVHAKYQKPWLGTVDSSEVYSW
LDSFLLLMLGGIPWQAYFQRVLSSSSATYAQVLSFLAAFGCLVMAIPAILIGAIGASTDW
NQTAYGLPDPKTTEEADMILPIVLQYLCPVYISFFGLGAVSAAVMSSADSSILSASSMFA
RNIYQLSFRQNASDKEIVWVMRITVFVFGASATAMALLTKTVYGLWYLSSDLVYIVIFPQ
LLCVLFVKGTNTYGAVAGYVSGLFLRITGGEPYLYLQPLIFYPGYYPDDNGIYNQKFPFK
TLAMVTSFLTNICISYLAKYLFESGTLPPKLDVFDAVVARHSEENMDKTILVKNENIKLD
ELALVKPRQSMTLSSTFTNKEAFLDVDSSPEGSGTEDNLQ
NT seq
1743 nt
NT seq
+upstream
nt +downstream
nt
atggctttccatgtggaaggactgatagctatcatcgtgttctaccttctaattttgctg
gttggaatatgggctgcctggagaaccaaaaacagtggcagcgcagaagagcgcagcgaa
gccatcatagttggtggccgagatattggtttattggttggtggatttaccatgacagct
acctgggtcggaggagggtatatcaatggcacagctgaagcagtttatgtaccaggttat
ggcctagcttgggctcaggcaccaattggatattctcttagtctgattttaggtggcctg
ttctttgcaaaacctatgcgttcaaaggggtatgtgaccatgttagacccgtttcagcaa
atctatggaaaacgcatgggcggactcctgtttattcctgcactgatgggagaaatgttc
tgggctgcagcaattttctctgctttgggagccaccatcagcgtgatcatcgatgtggat
atgcacatttctgtcatcatctctgcactcattgccactctgtacacactggtgggaggg
ctctattctgtggcctacactgatgtcgttcagctcttttgcatttttgtagggctgtgg
atcagcgtcccctttgcattgtcacatcctgcagtcgcagacatcgggttcactgctgtg
catgccaaataccaaaagccgtggctgggaactgttgactcatctgaagtctactcttgg
cttgatagttttctgttgttgatgctgggtggaatcccatggcaagcatactttcagagg
gttctctcttcttcctcagccacctatgctcaagtgctgtccttcctggcagctttcggg
tgcctggtgatggccatcccagccatactcattggggccattggagcatcaacagactgg
aaccagactgcatatgggcttccagatcccaagactacagaagaggcagacatgatttta
ccaattgttctgcagtatctctgccctgtgtatatttctttctttggtcttggtgcagtt
tctgctgctgttatgtcatcagcagattcttccatcttgtcagcaagttccatgtttgca
cggaacatctaccagctttccttcagacaaaatgcttcggacaaagaaatcgtttgggtt
atgcgaatcacagtgtttgtgtttggagcatctgcaacagccatggccttgctgacgaaa
actgtgtatgggctctggtacctcagttctgaccttgtttacatcgttatcttcccccag
ctgctttgtgtactctttgttaagggaaccaacacctatggggccgtggcaggttatgtt
tctggcctcttcctgagaataactggaggggagccatatctgtatcttcagcccttgatc
ttctaccctggctattaccctgatgataatggtatatataatcagaaatttccatttaaa
acacttgccatggttacatcattcttaaccaacatttgcatctcctatctagccaagtat
ctatttgaaagtggaaccttgccacctaaattagatgtatttgatgctgttgttgcaaga
cacagtgaagaaaacatggataagacaattcttgtcaaaaatgaaaatattaaattagat
gaacttgcacttgtgaagccacgacagagcatgaccctcagctcaactttcaccaataaa
gaggccttccttgatgttgattccagtccagaagggtctgggactgaagataatttacag
tga
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