Homo sapiens (human): 9056
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Entry
9056 CDS
T01001
Symbol
SLC7A7, LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1
Name
(RefSeq) solute carrier family 7 member 7
KO
K13867
solute carrier family 7 (L-type amino acid transporter), member 7
Organism
hsa
Homo sapiens (human)
Pathway
hsa04974
Protein digestion and absorption
Disease
H00899
Lysinuric protein intolerance
H01400
Secondary hyperammonemia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09154 Digestive system
04974 Protein digestion and absorption
9056 (SLC7A7)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
9056 (SLC7A7)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC7: Cationic amino acid transporter/glycoprotein-associated
9056 (SLC7A7)
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GFIT
Motif
Pfam:
AA_permease_2
AA_permease
Motif
Other DBs
NCBI-GeneID:
9056
NCBI-ProteinID:
NP_001119577
OMIM:
603593
HGNC:
11065
Ensembl:
ENSG00000155465
UniProt:
Q9UM01
A0A0S2Z502
Structure
PDB
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Position
14:complement(22773222..22819791)
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AA seq
511 aa
AA seq
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MVDSTEYEVASQPEVETSPLGDGASPGPEQVKLKKEISLLNGVCLIVGNMIGSGIFVSPK
GVLIYSASFGLSLVIWAVGGLFSVFGALCYAELGTTIKKSGASYAYILEAFGGFLAFIRL
WTSLLIIEPTSQAIIAITFANYMVQPLFPSCFAPYAASRLLAAACICLLTFINCAYVKWG
TLVQDIFTYAKVLALIAVIVAGIVRLGQGASTHFENSFEGSSFAVGDIALALYSALFSYS
GWDTLNYVTEEIKNPERNLPLSIGISMPIVTIIYILTNVAYYTVLDMRDILASDAVAVTF
ADQIFGIFNWIIPLSVALSCFGGLNASIVAASRLFFVGSREGHLPDAICMIHVERFTPVP
SLLFNGIMALIYLCVEDIFQLINYYSFSYWFFVGLSIVGQLYLRWKEPDRPRPLKLSVFF
PIVFCLCTIFLVAVPLYSDTINSLIGIAIALSGLPFYFLIIRVPEHKRPLYLRRIVGSAT
RYLQVLCMSVAAEMDLEDGGEMPKQRDPKSN
NT seq
1536 nt
NT seq
+upstream
nt +downstream
nt
atggttgacagcactgagtatgaagtggcctcccagcctgaggtggaaacctcccctttg
ggtgatggggccagcccagggccggagcaggtgaagctgaagaaggagatctcactgctt
aacggcgtgtgcctgattgtggggaacatgatcggctcgggcatctttgtttcccccaag
ggtgtgctcatatacagtgcctcctttggtctctctctggtcatctgggctgtcgggggc
ctcttctccgtctttggggccctttgttatgcggaactgggcaccaccattaagaaatct
ggggccagctatgcctatatcctggaggcctttggaggattccttgctttcatcagactc
tggacctccctgctcatcattgagcccaccagccaggccatcattgccatcacctttgcc
aactacatggtacagcctctcttcccgagctgcttcgccccttatgctgccagccgcctg
ctggctgctgcctgcatttgtctcttaaccttcattaactgtgcctatgtcaaatgggga
accctggtacaagatattttcacctatgctaaagtattggcactgatcgcggtcatcgtt
gcaggcattgttagacttggccagggagcctctactcattttgagaattcctttgagggt
tcatcatttgcagtgggtgacattgccctggcactgtactcagctctgttctcctactca
ggctgggacaccctcaactatgtcactgaagagatcaagaatcctgagaggaacctgccc
ctctccattggcatctccatgcccattgtcaccatcatctatatcttgaccaatgtggcc
tattatactgtgctagacatgagagacatcttggccagtgatgctgttgctgtgactttt
gcagatcagatatttggaatatttaactggataattccactgtcagttgcattatcctgt
tttggtggcctcaatgcctccattgtggctgcttctaggcttttctttgtgggctcaaga
gaaggccatctccctgatgccatctgcatgatccatgttgagcggttcacaccagtgcct
tctctgctcttcaatggtatcatggcattgatctacttgtgcgtggaagacatcttccag
ctcattaactactacagcttcagctactggttctttgtggggctttctattgtgggtcag
ctttatctgcgctggaaggagcctgatcgacctcgtcccctcaagctcagcgttttcttc
ccgattgtcttctgcctctgcaccatcttcctggtggctgttccactttacagtgatact
atcaactccctcatcggcattgccattgccctctcaggcctgcccttttacttcctcatc
atcagagtgccagaacataagcgaccgctttacctccgaaggatcgtggggtctgccaca
aggtacctccaggtcctgtgtatgtcagttgctgcagaaatggatttggaagatggagga
gagatgcccaagcaacgggatcccaaatctaactaa
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