Homo sapiens (human): 402
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Entry
402 CDS
T01001
Symbol
ARL2, ARFL2, MRCS1
Name
(RefSeq) ARF like GTPase 2
KO
K07943
ADP-ribosylation factor-like protein 2
Organism
hsa
Homo sapiens (human)
Disease
H02794
Microcornea, rod-cone dystrophy, cataract, and posterior staphyloma
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
402 (ARL2)
09183 Protein families: signaling and cellular processes
04031 GTP-binding proteins [BR:
hsa04031
]
402 (ARL2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Other centrosome associated proteins
402 (ARL2)
GTP-binding proteins [BR:
hsa04031
]
Small (monomeric) G-proteins
Arf/Sar Family
Arl2/Arl3
402 (ARL2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Arf
Roc
G-alpha
SRPRB
Ras
Gtr1_RagA
MMR_HSR1
GTP_EFTU
TniB
Motif
Other DBs
NCBI-GeneID:
402
NCBI-ProteinID:
NP_001658
OMIM:
601175
HGNC:
693
Ensembl:
ENSG00000213465
UniProt:
P36404
Q53YD8
Structure
PDB
PDBj
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All DBs
Position
11:65014160..65022184
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AA seq
184 aa
AA seq
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MGLLTILKKMKQKERELRLLMLGLDNAGKTTILKKFNGEDIDTISPTLGFNIKTLEHRGF
KLNIWDVGGQKSLRSYWRNYFESTDGLIWVVDSADRQRMQDCQRELQSLLVEERLAGATL
LIFANKQDLPGALSSNAIREVLELDSIRSHHWCIQGCSAVTGENLLPGIDWLLDDISSRI
FTAD
NT seq
555 nt
NT seq
+upstream
nt +downstream
nt
atggggctcctgaccattctgaagaagatgaagcagaaagagcgggagctgcgactgctc
atgcttggcctggacaatgctggaaagacaaccatcctgaagaagttcaatggggaggac
atcgacaccatctccccaacgctgggcttcaacatcaagaccctggagcaccgaggattc
aagctgaacatctgggatgtgggtggccagaagtccctgcggtcctactggcggaactac
tttgagagcaccgatggcctcatctgggtagtggacagcgcagaccgccagcgcatgcag
gactgccagcgggagctccagagcctgctggtggaggagcgcctggccggagcaaccctc
ctcatctttgctaataagcaggacctgcctggagcactgtcctctaacgccatccgcgag
gtcctggagctggactccatccgcagccaccactggtgcatccagggctgcagcgccgtc
accggggagaacctgctgccgggcatcgactggctcctggatgacatttccagccgcatt
ttcacagctgactga
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integrated database retrieval system