Homo sapiens (human): 51142
Help
Entry
51142 CDS
T01001
Symbol
CHCHD2, C7orf17, MIX17B, MNRR1, NS2TP, PARK22
Name
(RefSeq) coiled-coil-helix-coiled-coil-helix domain-containing protein 2 isoform 2 precursor
KO
K22758
coiled-coil-helix-coiled-coil-helix domain-containing protein 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04156
Integrated stress response (ISR) signaling pathway
Network
nt06552
Integrated stress response (ISR) signaling pathway
Element
N02051
OMA1 inhibition by CHCHD2 and CHCHD10
Disease
H00057
Parkinson disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09143 Cell growth and death
04156 Integrated stress response (ISR) signaling pathway
51142 (CHCHD2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
51142 (CHCHD2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Other transcription factors
Others
51142 (CHCHD2)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
CHCH
Phage_P22_gp16
SctB2
Motif
Other DBs
NCBI-GeneID:
51142
NCBI-ProteinID:
NP_057223
OMIM:
616244
HGNC:
21645
Ensembl:
ENSP00000378812.3
UniProt:
Q9Y6H1
Structure
PDB
PDBj
LinkDB
All DBs
Position
7:complement(56101573..56106476)
Genome browser
AA seq
151 aa
AA seq
DB search
MPRGSRSRTSRMAPPASRAPQMRAAPRPAPVAQPPAAAPPSAVGSSAAAPRQPGLMAQMA
TTAAGVAVGSAVGHTLGHAITGGFSGGSNAEPARPDITYQEPQGTQPAQQQQPCLYEIKQ
FLECAQNQGDIKLCEGFNEVLKQCRLANGLA
NT seq
456 nt
NT seq
+upstream
nt +downstream
nt
atgccgcgtggaagccgaagccgcacctcccgcatggcccctccggccagccgggcccct
cagatgagagctgcacccaggccagcaccagtcgctcagccaccagcagcggcaccccca
tctgcagttggctcttctgctgctgcgccccggcagccaggtctgatggcccagatggca
accactgcagctggcgtggctgtgggctctgctgtggggcacacattgggtcacgccatt
actgggggcttcagtggaggaagtaatgctgagcctgcgaggcctgacatcacttaccag
gagcctcagggaacccagccagcacagcagcagcagccttgcctctatgagatcaaacag
tttctggagtgtgcccagaaccagggtgacatcaagctctgtgagggtttcaatgaggtg
ctgaaacagtgccgacttgcaaacggattggcctaa
DBGET
integrated database retrieval system
