Homo sapiens (human): 116028
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Entry
116028 CDS
T01001
Symbol
RMI2, BLAP18, C16orf75
Name
(RefSeq) RecQ mediated genome instability 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
Gene cluster
GFIT
Motif
Pfam:
RMI2
Motif
Other DBs
NCBI-GeneID:
116028
NCBI-ProteinID:
NP_689521
OMIM:
612426
HGNC:
28349
Ensembl:
ENSG00000175643
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
