Homo sapiens (human): 92344
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Entry
92344 CDS
T01001
Symbol
GORAB, GO, NTKLBP1, SCYL1BP1
Name
(RefSeq) golgin, RAB6 interacting
KO
K19748
RAB6-interacting golgin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04115
p53 signaling pathway
Disease
H00558
Geroderma osteodysplasticum
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04115 p53 signaling pathway
92344 (GORAB)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
92344 (GORAB)
Membrane trafficking [BR:
hsa04131
]
Endosome - Golgi transport
Rab GTPases and associated proteins
Rab associated proteins
92344 (GORAB)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Transcrip_act
DUF1127
MIT_C
Motif
Other DBs
NCBI-GeneID:
92344
NCBI-ProteinID:
NP_689494
OMIM:
607983
HGNC:
25676
Ensembl:
ENSG00000120370
UniProt:
Q5T7V8
B3KQ87
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Position
1:170532166..170553834
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AA seq
369 aa
AA seq
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MAQGWAGFSEEELRRLKQTKDPFEPQRRLPAKKSRQQLQREKALVEQSQKLGLQDGSTSL
LPEQLLSAPKQRVNVQKPPFSSPTLPSHFTLTSPVGDGQPQGIESQPKELGLENSHDGHN
NVEILPPKPDCKLEKKKVELQEKSRWEVLQQEQRLMEEKNKRKKALLAKAIAERSKRTQA
ETMKLKRIQKELQALDDMVSADIGILRNRIDQASLDYSYARKRFDRAEAEYIAAKLDIQR
KTEIKEQLTEHLCTIIQQNELRKAKKLEELMQQLDVEADEETLELEVEVERLLHEQEVES
RRPVVRLERPFQPAEESVTLEFAKENRKCQEQAVSPKVDDQCGNSSSIPFLSPNCPNQEG
NDISAALAT
NT seq
1110 nt
NT seq
+upstream
nt +downstream
nt
atggcgcaaggttgggcaggattctctgaggaggaactgaggagactaaagcagactaaa
gatccatttgaaccacagcgacgtctccccgcgaagaaaagtcgacaacaacttcagcga
gaaaaagcccttgtagagcaaagccaaaaacttgggcttcaagatggatcaacctcatta
cttccagagcagctgctttcagcaccaaaacagagagttaacgttcaaaaaccacctttt
tcttcccctactcttccgagtcatttcactctcacctcccccgttggtgatggacaacca
cagggcattgaaagtcagccaaaggaactgggacttgagaattcccatgatggtcacaac
aatgttgagattctacctccaaagccagattgcaaattggagaaaaagaaagtggaattg
caagaaaaatctcgttgggaagtcctccaacaagaacaacggctaatggaagagaaaaat
aaacgtaaaaaagctcttttggctaaagctattgcagaaagatccaaaagaactcaggca
gagaccatgaaactaaagcggatccagaaggagttgcaggctttagatgacatggtgtca
gctgacattggaattctcaggaaccggattgatcaggccagcttagactattcatacgct
cggaagcggtttgacagggctgaagcagagtacattgcagcaaagctagatatacagcgc
aagactgagataaaagagcaactcactgaacacctttgtacgatcatacagcaaaatgag
ctccgaaaggccaagaagttggaggagttgatgcaacaactagatgtagaagccgatgaa
gagactttggagcttgaggtggaggtcgagagattgctacacgaacaagaagtagaatca
aggagaccagtggttcgtttagagaggccatttcagcctgcggaggagagtgtgacatta
gaatttgctaaagagaacagaaagtgtcaagaacaagctgtttccccaaaggtagatgac
cagtgtggaaattccagtagcatcccctttcttagtccaaactgcccaaatcaagaaggt
aatgacatttcagctgctttggccacatga
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