Homo sapiens (human): 51142
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Entry
51142 CDS
T01001
Symbol
CHCHD2, C7orf17, MIX17B, MNRR1, NS2TP, PARK22
Name
(RefSeq) coiled-coil-helix-coiled-coil-helix domain containing 2
KO
K22758
coiled-coil-helix-coiled-coil-helix domain-containing protein 2
Organism
hsa
Homo sapiens (human)
Disease
H00057
Parkinson disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CHCH
SctB2
Motif
Other DBs
NCBI-GeneID:
51142
NCBI-ProteinID:
NP_057223
OMIM:
616244
HGNC:
21645
Ensembl:
ENSG00000106153
UniProt:
Q9Y6H1
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
