Homo sapiens (human): 55847
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Entry
55847 CDS
T01001
Symbol
CISD1, C10orf70, MDS029, ZCD1, mitoNEET
Name
(RefSeq) CDGSH iron sulfur domain 1
KO
K23885
CDGSH iron-sulfur domain-containing protein 1
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
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99977 Transport
55847 (CISD1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-CDGSH
MitoNEET_N
Motif
Other DBs
NCBI-GeneID:
55847
NCBI-ProteinID:
NP_060934
OMIM:
611932
HGNC:
30880
Ensembl:
ENSG00000122873
UniProt:
Q9NZ45
Structure
PDB
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All DBs
Position
10:58269162..58289586
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AA seq
108 aa
AA seq
DB search
MSLTSSSSVRVEWIAAVTIAAGTAAIGYLAYKRFYVKDHRNKAMINLHIQKDNPKIVHAF
DMEDLGDKAVYCRCWRSKKFPFCDGAHTKHNEETGDNVGPLIIKKKET
NT seq
327 nt
NT seq
+upstream
nt +downstream
nt
atgagtctgacttccagttccagcgtacgagttgaatggatcgcagcagttaccattgct
gctgggacagctgcaattggttatctagcttacaaaagattttatgttaaagatcatcga
aataaagctatgataaaccttcacatccagaaagacaaccccaagatagtacatgctttt
gacatggaggatttgggagataaagctgtgtactgccgttgttggaggtccaaaaagttc
ccattctgtgatggggctcacacaaaacataacgaagagactggagacaatgtgggccct
ctgatcatcaagaaaaaagaaacttaa
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integrated database retrieval system