Homo sapiens (human): 116028
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Entry
116028 CDS
T01001
Symbol
RMI2, BLAP18, C16orf75
Name
(RefSeq) recQ-mediated genome instability protein 2
KO
K15365
RecQ-mediated genome instability protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa03460
Fanconi anemia pathway
Network
nt06506
Double-strand break repair
Element
N01447
Double Holliday junction dissolution
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09124 Replication and repair
03460 Fanconi anemia pathway
116028 (RMI2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03400 DNA repair and recombination proteins [BR:
hsa03400
]
116028 (RMI2)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
DSBR (double strand breaks repair)
HR (homologous recombination)
Bloom's syndrome complex (BTR)
116028 (RMI2)
FA (Fanconi anemia) pathway
116028 (RMI2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
RMI2
Motif
Other DBs
NCBI-GeneID:
116028
NCBI-ProteinID:
NP_689521
OMIM:
612426
HGNC:
28349
Ensembl:
ENSP00000310356.5
UniProt:
Q96E14
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:11345459..11351760
Genome browser
AA seq
147 aa
AA seq
DB search
MAAAADSFSGGPAGVRLPRSPPLKVLAEQLRRDAEGGPGAWRLSRAAAGRGPLDLAAVWM
QGRVVMADRGEARLRDPSGDFSVRGLERVPRGRPCLVPGKYVMVMGVVQACSPEPCLQAV
KMTDLSDNPIHESMWELEVEDLHRNIP
NT seq
444 nt
NT seq
+upstream
nt +downstream
nt
atggcggcggctgcggactcgttctcaggcggccccgcgggggtgcggcttccgaggtcg
ccgccactcaaggtgctggcggagcagctgcggcgcgacgcggagggcggcccgggcgcg
tggcggctgtcacgggcggcggcgggccgcgggccgctggacctggcggccgtgtggatg
cagggcagggtagtgatggcggaccgcggcgaggctcggctgagggacccgagcggggac
ttctcggtccgcggcctggagcgggtgccgcgcgggcggccctgtctagtcccaggaaag
tatgtgatggtgatgggagtggttcaggcctgcagccctgagccctgcctgcaggctgtg
aagatgacagacctttctgataatcccatccatgaaagtatgtgggaactggaggtagaa
gatttacacaggaatattccttag
DBGET
integrated database retrieval system
