Homo sapiens (human): 493856
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Entry
493856 CDS
T01001
Symbol
CISD2, ERIS, Miner1, NAF-1, WFS2, ZCD2
Name
(RefSeq) CDGSH iron sulfur domain 2
KO
K23882
CDGSH iron-sulfur domain-containing protein 2
Organism
hsa
Homo sapiens (human)
Network
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06536
Mitophagy
Element
N01137
PINK-Parkin-mediated autophagosome formation
N01138
Mutation-inactivated OPTN to PINK-Parkin-mediated autophagosome formation
N01139
Mutation-inactivated p62 to PINK-Parkin-mediated autophagosome formation
N01756
PINK-Parkin-independent ubiquitin-mediated mitophagy
N01757
PINK-Parkin-independent ubiquitin-mediated mitophagy, ubiquitin E3 ligase
Disease
H00854
Wolfram syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
493856 (CISD2)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Other autophagy associated proteins
Others
493856 (CISD2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
MitoNEET_N
zf-CDGSH
PGA2
Motif
Other DBs
NCBI-GeneID:
493856
NCBI-ProteinID:
NP_001008389
OMIM:
611507
HGNC:
24212
Ensembl:
ENSG00000145354
UniProt:
Q8N5K1
Structure
PDB
LinkDB
All DBs
Position
4:102868992..102892807
Genome browser
AA seq
135 aa
AA seq
DB search
MVLESVARIVKVQLPAYLKRLPVPESITGFARLTVSEWLRLLPFLGVLALLGYLAVRPFL
PKKKQQKDSLINLKIQKENPKVVNEINIEDLCLTKAAYCRCWRSKTFPACDGSHNKHNEL
TGDNVGPLILKKKEV
NT seq
408 nt
NT seq
+upstream
nt +downstream
nt
atggtgctggagagcgtggcccgtatcgtgaaggtgcagctccctgcatatctgaagcgg
ctcccagtccctgaaagcattaccgggttcgctaggctcacagtttcagaatggcttcgg
ttattgcctttccttggtgtactcgcacttcttggctaccttgcagttcgtccattcctc
ccgaagaagaaacaacagaaggatagcttgattaatcttaaaatacaaaaggaaaatccg
aaagtagtgaatgaaataaacattgaagatttgtgtcttactaaagcagcttattgtagg
tgttggcgttctaaaacgtttcctgcctgcgatggttcacataataaacacaatgaattg
acaggagataatgtgggtccactaatactgaagaagaaagaagtataa
DBGET
integrated database retrieval system
