Homo sapiens (human): 256472
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Entry
256472 CDS
T01001
Symbol
TMEM151A, DYT36, EKD3, TMEM151
Name
(RefSeq) transmembrane protein 151A
Organism
hsa
Homo sapiens (human)
Disease
H00831
Primary dystonia
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TMEM151
Motif
Other DBs
NCBI-GeneID:
256472
NCBI-ProteinID:
NP_694998
OMIM:
620108
HGNC:
28497
Ensembl:
ENSG00000179292
UniProt:
Q8N4L1
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All DBs
Position
11:66291894..66296664
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AA seq
468 aa
AA seq
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MPEDGAGDGGEVPALIPDGEPLREEQRPLKQSLGSSLCRESHWKCLLLTLLIHACGAVVA
WCRLATVPRLVLGPEAALARGAGGPPPTYPASPCSDGYLYIPLAFVSLLYLLYLAECWHC
HVRSCQAPRTDAHTVLALIRRLQQAPPCVWWKATSYHYVRRTRQITRYRNGDAYTTTQVY
HERADSRTARGEFDYSAHGVRDVSKELVGLAEHAATRLRFTKCFSFGSAEAEASYLTQRA
RFFSANEGLDDYLEAREGMHLKDVDFRESLMVFADPRSPPWYARAWVFWLVSAATLSWPL
RVVAAYGTAHVHYQVEKLFGASSPPPGAVPSGPPLSRVATVDFTELEWHICSNRQLVPSY
SEAVVMGAGSGAYLRGCQRCRRSVSSNSLPPARPSGPRLPFSRSRLSLGAGGRATPGVFR
SLSGGPLGRRGEDTEPLESPPCYEDALYFPVLIVHGDSGCQGDGQGAL
NT seq
1407 nt
NT seq
+upstream
nt +downstream
nt
atgcccgaggacggcgctggcgacggcggggaggtgcccgcgctcatcccggacggcgag
ccgctgcgggaagagcagcggcccctgaaacagtccctgggaagctccctgtgccgcgag
tcgcactggaagtgcctgctcctcacgctgctcatccacgcctgcggggccgtggtggcc
tggtgtcgcctggccacagtgccgcggctggtcctggggcccgaggccgccttggcccgg
ggagccgggggcccgccaccgacctacccggccagcccctgctccgatggctacctgtac
atcccgctggccttcgtctccctcctctacctcctctacctggctgagtgctggcactgt
cacgtgcggtcctgccaggcgccacgcaccgacgcccacacggtgctggcgctgatccgc
cggctgcagcaggcgccgccgtgcgtctggtggaaggccaccagctatcactacgtgcgg
cgcacacgccagatcacgcgctaccgcaacggcgacgcctacaccaccacgcaggtgtac
catgagcgcgctgacagccgcacggcccgcggcgagtttgactactcggcgcacggcgtc
cgcgacgtctccaaggagctggtggggctggcggagcacgcggccacgcggctgcgcttc
accaagtgcttcagcttcggcagcgcggaggccgaggcctcgtacctcacgcagcgggcg
cgcttcttcagcgccaacgagggcctggacgactatctggaggcgcgcgagggcatgcac
ctgaaggacgtagacttccgcgagtcgctcatggtcttcgccgacccccgcagcccgccc
tggtacgcgcgcgcctgggtcttctggctcgtgtcggcggccacgctgtcgtggcccctg
cgcgtcgtggccgcctatggcacggctcacgtgcactaccaggtggagaagctctttggc
gccagctcgcccccgccgggggccgtgcccagcgggcccccgctgtcccgcgtggccaca
gtggacttcactgagctcgagtggcacatctgctccaaccggcagctggtgcccagctac
tcggaggccgtggtcatgggcgcgggctcgggcgcctacctcagaggctgccagcgctgc
cgccgctctgtcagcagcaactcgctgccccccgcccggcccagcgggccccgcctgccc
ttcagccgcagccgcctctcgctgggcgctggcggccgggccacgccaggggtcttccgc
agcctgagcggggggccgctggggcgccgtggagaggacacggaacccctggagagcccg
ccctgctatgaggacgccctctacttcccggtgctcattgtccacggagacagcggctgc
cagggggatgggcagggtgctctctga
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