Homo sapiens (human): 7555
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Entry
7555 CDS
T01001
Symbol
CNBP, CNBP1, DM2, PROMM, RNF163, ZCCHC22, ZNF9
Name
(RefSeq) CCHC-type zinc finger nucleic acid binding protein
KO
K09250
cellular nucleic acid-binding protein
Organism
hsa
Homo sapiens (human)
Disease
H00568
Myotonic dystrophy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
7555 (CNBP)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Other zinc fingers
7555 (CNBP)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-CCHC
zf-CCHC_5
zf-CCHC_4
zf-CCHC_3
zf-CCHC_2
Motif
Other DBs
NCBI-GeneID:
7555
NCBI-ProteinID:
NP_003409
OMIM:
116955
HGNC:
13164
Ensembl:
ENSG00000169714
UniProt:
P62633
A0A0S2Z4K2
LinkDB
All DBs
Position
3:complement(129167827..129183896)
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AA seq
177 aa
AA seq
DB search
MSSNECFKCGRSGHWARECPTGGGRGRGMRSRGRGGFTSDRGFQFVSSSLPDICYRCGES
GHLAKDCDLQEDACYNCGRGGHIAKDCKEPKREREQCCYNCGKPGHLARDCDHADEQKCY
SCGEFGHIQKDCTKVKCYRCGETGHVAINCSKTSEVNCYRCGESGHLARECTIEATA
NT seq
534 nt
NT seq
+upstream
nt +downstream
nt
atgagcagcaatgagtgcttcaagtgtggacgatctggccactgggcccgggaatgtcct
actggtggaggccgtggtcgtggaatgagaagccgtggcagaggtggttttacctcggat
agaggtttccagtttgtttcctcgtctcttccagacatttgttatcgctgtggtgagtct
ggtcatcttgccaaggattgtgatcttcaggaggatgcctgctataactgcggtagaggt
ggccacattgccaaggactgcaaggagcccaagagagagcgagagcaatgctgctacaac
tgtggcaaaccaggccatctggctcgtgactgcgaccatgcagatgagcagaaatgctat
tcttgtggagaattcggacacattcaaaaagactgcaccaaagtgaagtgctataggtgt
ggtgaaactggtcatgtagccatcaactgcagcaagacaagtgaagtcaactgttaccgc
tgtggcgagtcagggcaccttgcacgggaatgcacaattgaggctacagcctaa
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integrated database retrieval system
