Homo sapiens (human): 400916
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Entry
400916 CDS
T01001
Symbol
CHCHD10, C22orf16, FTDALS2, IMMD, MIX17A, N27C7-4, SMAJ
Name
(RefSeq) coiled-coil-helix-coiled-coil-helix domain containing 10
KO
K22759
coiled-coil-helix-coiled-coil-helix domain-containing protein 10
Organism
hsa
Homo sapiens (human)
Pathway
hsa05014
Amyotrophic lateral sclerosis
Disease
H02342
Frontotemporal dementia and amyotrophic lateral sclerosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
400916 (CHCHD10)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
400916 (CHCHD10)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Inner mambrane
Other inner membrane factors
400916 (CHCHD10)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CHCH
DUF2076
Gly-zipper_YMGG
Motif
Other DBs
NCBI-GeneID:
400916
NCBI-ProteinID:
NP_998885
OMIM:
615903
HGNC:
15559
Ensembl:
ENSG00000250479
Pharos:
Q8WYQ3
(Tbio)
UniProt:
Q8WYQ3
LinkDB
All DBs
Position
22:complement(23765834..23767972)
Genome browser
AA seq
142 aa
AA seq
DB search
MPRGSRSAASRPASRPAAPSAHPPAHPPPSAAAPAPAPSGQPGLMAQMATTAAGVAVGSA
VGHVMGSALTGAFSGGSSEPSQPAVQQAPTPAAPQPLQMGPCAYEIRQFLDCSTTQSDLS
LCEGFSEALKQCKYYHGLSSLP
NT seq
429 nt
NT seq
+upstream
nt +downstream
nt
atgcctcggggaagccgcagcgcggcctcccggccagccagccgcccagccgcgccctct
gcccacccgcccgcgcacccaccgccctcggcagccgccccagcccccgccccttcgggc
cagccggggctcatggctcagatggcgaccacggccgcaggggtagccgtgggctcggct
gtgggacacgtcatgggcagcgccctgaccggagccttcagcggggggagctcggagccc
tcccagcctgctgtccagcaggcccccacccccgctgccccccagcccctgcagatgggg
ccctgcgcctacgagatcaggcagttcctggactgttccaccactcagagtgacctgtcc
ctgtgtgagggcttcagcgaggccctgaagcagtgcaagtactaccatggtctgagctcc
ctgccctga
DBGET
integrated database retrieval system
