Homo sapiens (human): 55889
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Entry
55889 CDS
T01001
Symbol
GOLGA6B, GOLGA, GOLGA6D
Name
(RefSeq) golgin A6 family member B
Organism
hsa
Homo sapiens (human)
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
GOLGA2L5
GM130_C
Motif
Other DBs
NCBI-GeneID:
55889
NCBI-ProteinID:
NP_061122
HGNC:
32205
Ensembl:
ENSG00000215186
UniProt:
A6NDN3
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All DBs
Position
15:72654697..72669599
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AA seq
693 aa
AA seq
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MWPQPYLPPHPMMLEESRQNKLAAAKKKLKEYQQRKSPGIPAGAKTKKKKTDSSPETTTS
GGGHSPGDSQYQELAVALESSSVTISQLNENIESLKQQKKQVEHQLEEAKKTNNEIHKAQ
MERLETINILTLEKADLKTTLYHTKRAARHFEEESKDLAGRLQYSLQRIQELERALCAVS
TQQQEEDRSSSCREAVLHRRLQQTIKERALLNAHVTQVTESLKQVQLERDEYAKHIKGER
ARWQERMWKMSVEARTLKEEKKRDIHRIQELERSLSELKNQMAKPPSLAPPAVTSVVEQL
QDEAKHLRQEVEGLEGKLQSQVENNQALSLLSKEQKQRLQEQEEMLREQEVQRVREQERL
CEQNERLREQQKTLQEQGERLRKQEQRLRKQEERLRKEEERLQKQEKRLWDQEERLWKKE
ERLQKQEERLALSQNHKLDKQLAEPQCSFEDLNNEKKSALQLEQQVKELQEKLDEEHLEA
ASQQNQQLETQLSLVALPGEGDGGQHLDSEEEEAPRPTPNIPEDLESREATSSFMDLPKE
KADGTEQVERRELGFVQPSGVTDGMRESFTVYESQGAVPNTRHQEMEDVIRLAQKEEEMK
VKLLELQELVLPLVGNHEGHGKFLIAAQNPADEPTPGAPAPQELGAAGEQDDFYEVSLDN
NVEPAPGAAREGSPHDNPTVQQIVQLSPVMQDT
NT seq
2082 nt
NT seq
+upstream
nt +downstream
nt
atgtggccccaaccctacctccctccccaccccatgatgttagaagaatctcgacagaat
aaattggcagcagccaagaaaaagctaaaagaatatcagcaaaggaagagccctggtatt
ccagcaggagcaaagacaaaaaagaaaaaaactgacagtagccctgagacaaccacttcc
ggtggtggccactcacctggggatagccagtaccaagaactagcagtagccctggagtca
agctcagtgacaatcagtcaactcaatgaaaacatagaatcattgaaacagcagaagaaa
caagtggaacatcagctggaagaagcaaagaaaacaaacaatgaaatacacaaagcacaa
atggagcggttagagacaatcaacatcctcacattggaaaaggcagacttgaagaccacc
ctttaccatactaaacgtgctgcccgacacttcgaagaagagtccaaggatctggctggc
cgcctgcaatactccttacagcgtattcaagaattggagcgggctctctgtgctgtgtct
acacagcagcaggaagaggacaggtcctcgagctgcagagaagcggtcctccaccggcgg
ttacagcagaccataaaggagcgggcgctgctgaacgcacacgtgacacaggtgacagag
tcactaaaacaagtccagctagagcgagacgaatatgctaaacacataaaaggagagagg
gcccggtggcaggagaggatgtggaaaatgtcggtggaggctcgaacattgaaggaagag
aagaagcgtgacatacatcggatacaggagctggagaggagcttgtccgaactcaaaaac
cagatggctaagcccccatccctggcgcccccagcagtgacctctgtggtggaacagcta
caagatgaggccaaacacctgaggcaggaggtggaaggtctggagggaaagctccaatcc
caggtggaaaacaatcaggccttgagtctccttagcaaggaacaaaagcagagactccag
gagcaggaggagatgctccgagagcaggaggtgcagagagtgcgggagcaggagagactg
tgtgaacaaaacgagaggcttcgggagcagcagaagacgctacaggagcagggtgagagg
ctgcgaaagcaggagcagaggctacgcaaacaggaggagaggctgcgaaaggaggaggag
aggctgcaaaagcaggaaaagaggctgtgggaccaggaggagaggctgtggaagaaggag
gagaggctacaaaagcaggaggagaggctcgcgctctcccagaaccacaagctcgacaag
cagctggccgagccacagtgcagcttcgaggatctgaacaacgagaaaaagagcgcactg
cagttggagcagcaagtaaaggagctgcaggagaagctagacgaggagcacctagaagct
gccagccagcagaaccaacagctagagacccagctaagcctcgtggctctcccgggagaa
ggagatggaggacaacatctggacagtgaggaggaggaggcgcctcggcccacgccaaac
atcccagaggacctggagagccgggaggccacgagcagctttatggacctcccgaaggag
aaggcggacgggacggagcaggtggagagacgagagcttggattcgtccagccttctgga
gtgacagacggcatgagagagtccttcaccgtatatgaaagccagggggcagtgccaaac
acgcggcaccaggagatggaggatgtcatcaggctggcccagaaggaggaggagatgaag
gtgaagctgctggagctgcaagagttggtgttgccccttgtgggcaaccatgaggggcat
ggcaaattcctcatcgctgcccagaaccctgctgatgagcccactccaggggccccagcc
ccccaggaacttggggctgccggtgagcaggatgatttttatgaagtgagcctggacaac
aacgtggagcctgcaccaggagcggccagggagggttctccccatgacaaccccactgta
cagcagatcgtgcagctgtctcctgtcatgcaggacacctag
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