Homo sapiens (human): 81031
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Entry
81031 CDS
T01001
Symbol
SLC2A10, ATORS, ATS, GLUT10
Name
(RefSeq) solute carrier family 2 member 10
KO
K08147
MFS transporter, SP family, solute carrier family 2 (facilitated glucose transporter), member 10
Organism
hsa
Homo sapiens (human)
Disease
H00919
Arterial tortuosity syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
81031 (SLC2A10)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC2: Facilitative GLUT transporter
81031 (SLC2A10)
Major facilitator superfamily (MFS)
Sugar transporters
Sugar porter (SP) family [TC:
2.A.1.1
]
81031 (SLC2A10)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Sugar_tr
MFS_1
Motif
Other DBs
NCBI-GeneID:
81031
NCBI-ProteinID:
NP_110404
OMIM:
606145
HGNC:
13444
Ensembl:
ENSG00000197496
UniProt:
O95528
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All DBs
Position
20:46708320..46736347
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AA seq
541 aa
AA seq
DB search
MGHSPPVLPLCASVSLLGGLTFGYELAVISGALLPLQLDFGLSCLEQEFLVGSLLLGALL
ASLVGGFLIDCYGRKQAILGSNLVLLAGSLTLGLAGSLAWLVLGRAVVGFAISLSSMACC
IYVSELVGPRQRGVLVSLYEAGITVGILLSYALNYALAGTPWGWRHMFGWATAPAVLQSL
SLLFLPAGTDETATHKDLIPLQGGEAPKLGPGRPRYSFLDLFRARDNMRGRTTVGLGLVL
FQQLTGQPNVLCYASTIFSSVGFHGGSSAVLASVGLGAVKVAATLTAMGLVDRAGRRALL
LAGCALMALSVSGIGLVSFAVPMDSGPSCLAVPNATGQTGLPGDSGLLQDSSLPPIPRTN
EDQREPILSTAKKTKPHPRSGDPSAPPRLALSSALPGPPLPARGHALLRWTALLCLMVFV
SAFSFGFGPVTWLVLSEIYPVEIRGRAFAFCNSFNWAANLFISLSFLDLIGTIGLSWTFL
LYGLTAVLGLGFIYLFVPETKGQSLAEIDQQFQKRRFTLSFGHRQNSTGIPYSRIEISAA
S
NT seq
1626 nt
NT seq
+upstream
nt +downstream
nt
atgggccactccccacctgtcctgcctttgtgtgcctctgtgtctttgctgggtggcctg
acctttggttatgaactggcagtcatatcaggtgccctgctgccactgcagcttgacttt
gggctaagctgcttggagcaggagttcctggtgggcagcctgctcctgggggctctcctc
gcctccctggttggtggcttcctcattgactgctatggcaggaagcaagccatcctcggg
agcaacttggtgctgctggcaggcagcctgaccctgggcctggctggttccctggcctgg
ctggtcctgggccgcgctgtggttggcttcgccatttccctctcctccatggcttgctgt
atctacgtgtcagagctggtggggccacggcagcggggagtgctggtgtccctctatgag
gcaggcatcaccgtgggcatcctgctctcctatgccctcaactatgcactggctggtacc
ccctggggatggaggcacatgttcggctgggccactgcacctgctgtcctgcaatccctc
agcctcctcttcctccctgctggtacagatgagactgcaacacacaaggacctcatccca
ctccagggaggtgaggcccccaagctgggcccggggaggccacggtactcctttctggac
ctcttcagggcacgcgataacatgcgaggccggaccacagtgggcctggggctggtgctc
ttccagcaactaacagggcagcccaacgtgctgtgctatgcctccaccatcttcagctcc
gttggtttccatgggggatcctcagccgtgctggcctctgtggggcttggcgcagtgaag
gtggcagctaccctgaccgccatggggctggtggaccgtgcaggccgcagggctctgttg
ctagctggctgtgccctcatggccctgtccgtcagtggcataggcctcgtcagctttgcc
gtgcccatggactcaggcccaagctgtctggctgtgcccaatgccaccgggcagacaggc
ctccctggagactctggcctgctgcaggactcctctctacctcccattccaaggaccaat
gaggaccaaagggagccaatcttgtccactgctaagaaaaccaagccccatcccagatct
ggagacccctcagcccctcctcggctggccctgagctctgccctccctgggccccctctg
cccgctcgggggcatgcactgctgcgctggaccgcactgctgtgcctgatggtctttgtc
agtgccttctcctttgggtttgggccagtgacctggcttgtcctcagcgagatctaccct
gtggagatacgaggaagagccttcgccttctgcaacagcttcaactgggcggccaacctc
ttcatcagcctctccttcctcgatctcattggcaccatcggcttgtcctggaccttcctg
ctctacggactgaccgctgtcctcggcctgggcttcatctatttatttgttcctgaaaca
aaaggccagtcgttggcagagatagaccagcagttccagaagagacggttcaccctgagc
tttggccacaggcagaactccactggcatcccgtacagccgcatcgagatctctgcggcc
tcctga
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