KEGG   Homo sapiens (human): 84138
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
Motif
Pfam: Iwr1 Synaphin
Other DBs
NCBI-GeneID: 84138
NCBI-ProteinID: NP_115554
OMIM: 619192
HGNC: 25807
Ensembl: ENSG00000103061
UniProt: Q96CW6
Position
16:complement(68298034..68310946)
AA seq 309 aa
MEAARTAVLRVKRKRSAEPAEALVLACKRLRSDAVESAAQKTSEGLERAAENNVFHLVAT
VCSQEEPVQPLLREVLRPSRDSQQRVRRNLRASAREVRQEGRYRVLSSRRSLGTTSSGQE
SEYTPGNPEAAGNSGFQLLDLVHEEGEPEAASAGSCKTSDPDVILCNSVELIRERLTVSE
DGPGVRRQEEQKHDDYVYDIYYLETATPGWIENILSVQPYSQEWELVNDDQEPEDIYDDE
DDENSENNWRNEYPEEESSDGDEDSRGSADYNSLSEEERGSSRQRMWSKYPLDVQKEFGY
DSPHDLDSD
NT seq 930 nt   +upstreamnt  +downstreamnt
atggaggccgccaggaccgctgtactccgggtgaagcggaagcgcagtgcggagccggcg
gaggctcttgtgctcgcttgtaaacgcctccggagcgacgcggtcgagtcagcggcacag
aagacgtcggagggtttggagagagcggcggagaataatgtcttccacttggtggccact
gtgtgctcccaggaggaaccagtccagcctctcctgcgggaagttctgcgcccgtcacgg
gacagccagcagcgtgtccgccgtaatctccgcgcctcggctcgggaggtccggcaggag
ggccgctaccgggtgctttccagccgccgatccttggggaccacctcgagcggccaggag
tccgagtacacgccggggaacccagaagccgccgggaactcgggctttcagttgttagac
cttgtccacgaggagggagaacctgaagccgcctctgcaggctcctgcaaaacatctgac
ccagatgtgatcctctgcaattctgtagagttgatccgtgagcgattgactgtgtctgag
gatggaccaggagtcaggcgccaggaagaacaaaaacacgatgactatgtgtatgacatt
tactacttggagacggccactccaggctggattgagaacatcctctccgtgcagccctac
agccaagaatgggagctggtgaatgatgatcaagaaccagaggacatttacgacgatgaa
gatgacgagaacagtgagaataactggcgcaatgagtacccagaggaggagagcagtgat
ggagatgaggattccagaggctctgctgactacaacagcctgagtgaggaggaaagaggc
agcagcagacagcggatgtggagcaagtaccctctggatgtgcagaaggagttcggctat
gacagcccccacgacctggattcagactga

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