Homo sapiens (human): 2189
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Entry
2189 CDS
T01001
Symbol
FANCG, FAG, XRCC9
Name
(RefSeq) FA complementation group G
KO
K10894
fanconi anemia group G protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa03460
Fanconi anemia pathway
Network
nt06508
Interstrand crosslink repair
Element
N01464
Fanconi anemia pathway
Disease
H00238
Fanconi anemia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09124 Replication and repair
03460 Fanconi anemia pathway
2189 (FANCG)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03400 DNA repair and recombination proteins [BR:
hsa03400
]
2189 (FANCG)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
DSBR (double strand breaks repair)
FA (Fanconi anemia) pathway
FA core complex
2189 (FANCG)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TPR_2
TPR_8
TPR_1
TPR_7
TPR_12
Hpt
Motif
Other DBs
NCBI-GeneID:
2189
NCBI-ProteinID:
NP_004620
OMIM:
602956
HGNC:
3588
Ensembl:
ENSG00000221829
Pharos:
O15287
(Tbio)
UniProt:
O15287
Q53XM5
Structure
PDB
PDBj
LinkDB
All DBs
Position
9:complement(35073839..35079942)
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AA seq
622 aa
AA seq
DB search
MSRQTTSVGSSCLDLWREKNDRLVRQAKVAQNSGLTLRRQQLAQDALEGLRGLLHSLQGL
PAAVPVLPLELTVTCNFIILRASLAQGFTEDQAQDIQRSLERVLETQEQQGPRLEQGLRE
LWDSVLRASCLLPELLSALHRLVGLQAALWLSADRLGDLALLLETLNGSQSGASKDLLLL
LKTWSPPAEELDAPLTLQDAQGLKDVLLTAFAYRQGLQELITGNPDKALSSLHEAASGLC
PRPVLVQVYTALGSCHRKMGNPQRALLYLVAALKEGSAWGPPLLEASRLYQQLGDTTAEL
ESLELLVEALNVPCSSKAPQFLIEVELLLPPPDLASPLHCGTQSQTKHILASRCLQTGRA
GDAAEHYLDLLALLLDSSEPRFSPPPSPPGPCMPEVFLEAAVALIQAGRAQDALTLCEEL
LSRTSSLLPKMSRLWEDARKGTKELPYCPLWVSATHLLQGQAWVQLGAQKVAISEFSRCL
ELLFRATPEEKEQGAAFNCEQGCKSDAALQQLRAAALISRGLEWVASGQDTKALQDFLLS
VQMCPGNRDTYFHLLQTLKRLDRRDEATALWWRLEAQTKGSHEDALWSLPLYLESYLSWI
RPSDRDAFLEEFRTSLPKSCDL
NT seq
1869 nt
NT seq
+upstream
nt +downstream
nt
atgtcccgccagaccacctctgtgggctccagctgcctggacctgtggagggaaaagaat
gaccggctcgttcgacaggccaaggtggctcagaactccggtctgactctgaggcgacag
cagttggctcaggatgcactggaagggctcagagggctcctccatagtctgcaagggctc
cctgcagctgttcctgttcttcccttggagctgactgtcacctgcaacttcattatcctg
agggcaagcttggcccagggtttcacagaggatcaggcccaggatatccagcggagccta
gagagagtgctggagacacaggagcagcaggggcccaggttggaacaggggctcagggag
ctgtgggactctgtccttcgtgcttcctgccttctgccggagctgctgtctgccctgcac
cgcctggttggcctgcaggctgccctctggttgagtgctgaccgtcttggggacctggcc
ttgttactagagaccctgaatggcagccagagtggagcctctaaggatctgctgttactt
ctgaaaacttggagtcccccagctgaggaattagatgctccattgaccctgcaggatgcc
cagggattgaaggatgtcctcctgacagcatttgcctaccgccaaggtctccaggagctg
atcacagggaacccagacaaggcactaagcagccttcatgaagcggcctcaggcctgtgt
ccacggcctgtgttggtccaggtgtacacagcactggggtcctgtcaccgtaagatggga
aatccacagagagcactgttgtacttggttgcagccctgaaagagggatcagcctggggt
cctccacttctggaggcctctaggctctatcagcaactgggggacacaacagcagagctg
gagagtctggagctgctagttgaggccttgaatgtcccatgcagttccaaagccccgcag
tttctcattgaggtagaattactactgccaccacctgacctagcctcaccccttcattgt
ggcactcagagccagaccaagcacatactagcaagcaggtgcctacagacggggagggca
ggagacgctgcagagcattacttggacctgctggccctgttgctggatagctcggagcca
aggttctccccacccccctcccctccagggccctgtatgcctgaggtgtttttggaggca
gcggtagcactgatccaggcaggcagagcccaagatgccttgactctatgtgaggagttg
ctcagccgcacatcatctctgctacccaagatgtcccggctgtgggaagatgccagaaaa
ggaaccaaggaactgccatactgcccactctgggtctctgccacccacctgcttcagggc
caggcctgggttcaactgggtgcccaaaaagtggcaattagtgaatttagcaggtgcctc
gagctgctcttccgggccacacctgaggaaaaagaacaaggggcagctttcaactgtgag
cagggatgtaagtcagatgcggcactgcagcagcttcgggcagccgccctaattagtcgt
ggactggaatgggtagccagcggccaggataccaaagccttacaggacttcctcctcagt
gtgcagatgtgcccaggtaatcgagacacttactttcacctgcttcagactctgaagagg
ctagatcggagggatgaggccactgcactctggtggaggctggaggcccaaactaagggg
tcacatgaagatgctctgtggtctctccccctgtacctagaaagctatttgagctggatc
cgtccctctgatcgtgacgccttccttgaagaatttcggacatctctgccaaagtcttgt
gacctgtag
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