Homo sapiens (human): 84138
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Entry
84138 CDS
T01001
Symbol
SLC7A6OS, EPM12, Iwr1
Name
(RefSeq) solute carrier family 7 member 6 opposite strand
Organism
hsa
Homo sapiens (human)
Disease
H00810
Progressive myoclonic epilepsy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Iwr1
Synaphin
Motif
Other DBs
NCBI-GeneID:
84138
NCBI-ProteinID:
NP_115554
OMIM:
619192
HGNC:
25807
Ensembl:
ENSG00000103061
UniProt:
Q96CW6
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Position
16:complement(68298034..68310946)
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AA seq
309 aa
AA seq
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MEAARTAVLRVKRKRSAEPAEALVLACKRLRSDAVESAAQKTSEGLERAAENNVFHLVAT
VCSQEEPVQPLLREVLRPSRDSQQRVRRNLRASAREVRQEGRYRVLSSRRSLGTTSSGQE
SEYTPGNPEAAGNSGFQLLDLVHEEGEPEAASAGSCKTSDPDVILCNSVELIRERLTVSE
DGPGVRRQEEQKHDDYVYDIYYLETATPGWIENILSVQPYSQEWELVNDDQEPEDIYDDE
DDENSENNWRNEYPEEESSDGDEDSRGSADYNSLSEEERGSSRQRMWSKYPLDVQKEFGY
DSPHDLDSD
NT seq
930 nt
NT seq
+upstream
nt +downstream
nt
atggaggccgccaggaccgctgtactccgggtgaagcggaagcgcagtgcggagccggcg
gaggctcttgtgctcgcttgtaaacgcctccggagcgacgcggtcgagtcagcggcacag
aagacgtcggagggtttggagagagcggcggagaataatgtcttccacttggtggccact
gtgtgctcccaggaggaaccagtccagcctctcctgcgggaagttctgcgcccgtcacgg
gacagccagcagcgtgtccgccgtaatctccgcgcctcggctcgggaggtccggcaggag
ggccgctaccgggtgctttccagccgccgatccttggggaccacctcgagcggccaggag
tccgagtacacgccggggaacccagaagccgccgggaactcgggctttcagttgttagac
cttgtccacgaggagggagaacctgaagccgcctctgcaggctcctgcaaaacatctgac
ccagatgtgatcctctgcaattctgtagagttgatccgtgagcgattgactgtgtctgag
gatggaccaggagtcaggcgccaggaagaacaaaaacacgatgactatgtgtatgacatt
tactacttggagacggccactccaggctggattgagaacatcctctccgtgcagccctac
agccaagaatgggagctggtgaatgatgatcaagaaccagaggacatttacgacgatgaa
gatgacgagaacagtgagaataactggcgcaatgagtacccagaggaggagagcagtgat
ggagatgaggattccagaggctctgctgactacaacagcctgagtgaggaggaaagaggc
agcagcagacagcggatgtggagcaagtaccctctggatgtgcagaaggagttcggctat
gacagcccccacgacctggattcagactga
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