Homo sapiens (human): 7516
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Entry
7516 CDS
T01001
Symbol
XRCC2, FANCU, POF17, SPGF50
Name
(RefSeq) X-ray repair cross complementing 2
KO
K10879
DNA-repair protein XRCC2
Organism
hsa
Homo sapiens (human)
Pathway
hsa03440
Homologous recombination
Disease
H00238
Fanconi anemia
H00627
Premature ovarian failure
H01282
Spermatogenic failure
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09124 Replication and repair
03440 Homologous recombination
7516 (XRCC2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03400 DNA repair and recombination proteins [BR:
hsa03400
]
7516 (XRCC2)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
DSBR (double strand breaks repair)
HR (homologous recombination)
RecA family proteins
7516 (XRCC2)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Rad51
AAA_25
RecA
Motif
Other DBs
NCBI-GeneID:
7516
NCBI-ProteinID:
NP_005422
OMIM:
600375
HGNC:
12829
Ensembl:
ENSG00000196584
Pharos:
O43543
(Tbio)
UniProt:
O43543
A0A384MEK2
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Position
7:complement(152644776..152676141)
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AA seq
280 aa
AA seq
DB search
MCSAFHRAESGTELLARLEGRSSLKEIEPNLFADEDSPVHGDILEFHGPEGTGKTEMLYH
LTARCILPKSEGGLEVEVLFIDTDYHFDMLRLVTILEHRLSQSSEEIIKYCLGRFFLVYC
SSSTHLLLTLYSLESMFCSHPSLCLLILDSLSAFYWIDRVNGGESVNLQESTLRKCSQCL
EKLVNDYRLVLFATTQTIMQKASSSSEEPSHASRRLCDVDIDYRPYLCKAWQQLVKHRMF
FSKQDDSQSSNQFSLVSRCLKSNSLKKHFFIIGESGVEFC
NT seq
843 nt
NT seq
+upstream
nt +downstream
nt
atgtgtagtgccttccatagggctgagtctgggaccgagctccttgcccgacttgaaggt
agaagttccttgaaagaaatagaaccaaatctgtttgctgatgaagattcacctgtgcat
ggtgatattcttgaatttcatggcccagaaggaacaggaaaaacagaaatgctttatcac
ctaacagcacgatgtatacttcccaaatcagaaggtggcctggaagtagaagtcttattt
attgatacagattaccactttgatatgctccggctagttacaattcttgagcacagacta
tcccaaagctctgaagaaataatcaaatactgcctgggaagattttttttggtgtactgc
agtagtagcacccacttacttcttacactttactcactagaaagtatgttttgtagtcac
ccatctctctgccttttgattttggatagcctgtcagctttttactggatagaccgcgtc
aatggaggagaaagtgtgaacttacaggagtctactctgaggaaatgttctcagtgctta
gagaagcttgtaaatgactatcgcctggttctttttgcaacgacacaaactataatgcag
aaagcctcgagctcatcagaagaaccttctcatgcctctcgacgactgtgtgatgtggac
atagactacagaccttatctctgtaaggcatggcagcaactggtgaagcacaggatgttt
ttctccaaacaagatgattctcaaagcagcaaccaattttcattagtttcacgttgttta
aaaagtaacagtttaaaaaaacatttttttattattggagaaagtggggttgaattttgt
tga
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