Homo sapiens (human): 342979
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Entry
342979 CDS
T01001
Symbol
PALM3
Name
(RefSeq) paralemmin 3
KO
K27974
paralemmin-3
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
342979 (PALM3)
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Gene cluster
GFIT
Motif
Pfam:
Paralemmin
Motif
Other DBs
NCBI-GeneID:
342979
NCBI-ProteinID:
NP_001138500
OMIM:
621051
HGNC:
33274
Ensembl:
ENSG00000187867
UniProt:
A6NDB9
A0A590UJ36
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Position
19:complement(14053367..14062076)
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AA seq
688 aa
AA seq
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MALQSQVWSLATPMPMAESSLYRQRLEVIAEKRRLQEEIRAARREVEEEKLRVERLKRKS
LRERWLMDGAAAVPEPSEDPTSKDPQSPEGQAQARIRNLEDSLFTLQSQLQLLQSASTGA
QHKPSGRPSWRRQGHRPLSQSIVEAGSVGQTDLNKRASLPAGLVGTPPESPSEPREDVLG
FLPGPRQVPGAAGDSSEANGPCPSPIPTPEQGLSQRAVPSEGRVGEAKGGGVVSVVWEGL
RATEDCATGATGPELEAKVEEVVLEAIGDRKGAGSLELPAWVKEDRGIVEVVWEGVGGSD
AEAMGEIGRVPEVVQTSSPRLQERLEAAASIEGEDVPQGSPEGDGQGGSGGEEGSFIWVE
RVTLSEEWEELLVEGLEGPEVAGRERGDESPLGAEGAKTGGGEETWEAEKRKAEESMGIG
SEEKPGTGRDEAEMSPVVERKGGEKKLELESRGSAEKLGTEREGGEEPLGIERKVEGHLR
AEKEGDEEKRGAEEEEVEEPLGVEKKGGEEEPEATKEPLEAERKGGEETLEAEKRGGEES
LETEKTQGTEGDLNLEQGSREGSESQAEEMNEAGPPLEANTETRPEKEGPQPQEKPVGAL
EEEGVKPQTAAEGQGPLGDATPLLAETPAPEQPAECQPLLQGEGPSANPSAHPVPTYAPA
RQPEPSAPTEGEEASGPKQKTCQCCAVM
NT seq
2067 nt
NT seq
+upstream
nt +downstream
nt
atggccctgcagagccaggtgtggtctctggccacacccatgcccatggcggagagctcc
ctctaccggcagcggctagaagtcatcgctgagaagcggcggctgcaggaggagatccgc
gccgcgcgccgggaggtggaggaggagaaactccgcgtggagcgtctcaagaggaagtct
ctccgggaacgttggctaatggatggggcagctgcagtgccagagccatccgaagacccc
acctcgaaggacccccagtcacccgagggccaggctcaggcccgaatccggaacctggaa
gacagtttgttcacactccagtcccagctgcaactgttgcaaagtgcttccacaggtgcc
cagcacaagccctcaggcaggcccagctggcgcagacagggtcaccgtcctctctcccag
tccattgtcgaggcaggttctgtaggccagactgatctgaacaagagagcctccctgccg
gctggactagtgggcacgcctccagagtccccctctgagcccagggaggatgtcttgggg
tttctgccaggcccgaggcaggtccccggggcagcaggagactcctcagaagccaatggc
ccatgccccagccccatccccactccagagcaggggctaagtcagagggcagtgccatcc
gaagggcgggtgggtgaggccaaaggagggggcgtggtgagtgtggtgtgggaagggctg
agggccacagaggactgtgccacaggggccacgggccccgagctggaggctaaggtggag
gaagtggtgctggaagccatcggagacaggaagggagctggtagcctggagctcccggcc
tgggtgaaggaggacaggggcatcgtggaggtggtctgggagggggtgggtggcagtgat
gcagaggccatgggggagataggcagggtccctgaggtcgtgcagactagctcgcctagg
ctccaggagagattagaggcagcagcttccatagaaggggaagatgtgccccagggcagc
cctgagggtgatgggcagggaggctctggaggagaggagggatccttcatttgggtggag
agagtgaccctcagtgaagagtgggaggagctgctggtggaggggttggaagggcccgag
gtggcagggagggagagaggagatgaaagcccgctgggggccgagggggccaagacggga
ggaggcgaggagacctgggaggcagagaagagaaaagcggaagaatccatgggaatagga
agtgaggaaaagccagggacagggagggatgaagcggagatgtcaccagtggtagagagg
aaaggaggagagaagaagttggagctggagagcagaggaagtgcagaaaagctgggaaca
gagagggaaggaggtgaggaaccactgggcatagagagaaaagttgagggacatttgagg
gcagagaaggaaggagatgaggaaaagcgaggggcagaggaggaggaggtagaagaacca
ttgggagtagagaagaaaggaggtgaggaagagccagaggcaaccaaagaaccactggag
gcagagagaaagggaggggaggagacactggaggcagagaaaaggggaggtgaggaatca
ttggagacagagaagacccaagggacggagggagatctgaatctagaacaagggtctagg
gaaggaagtgaatcccaggcagaggagatgaatgaggcagggcctccccttgaggctaac
acggagacaaggccagagaaggaaggaccccagccccaggagaagccagtaggagccctg
gaggaggaaggagtgaagccccaaaccgctgctgagggccaaggccccttgggggatgcc
acacctcttctggcagagaccccagccccagagcagcccgccgaatgccagccactgctt
cagggggaggggcccagcgccaaccccagtgcccaccctgtgcccacctacgcgcctgcc
cggcagcctgagccatctgcccccaccgagggtgaagaggcaagtggccctaagcaaaag
acgtgccagtgttgtgcggtcatgtga
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