Homo sapiens (human): 3094
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Entry
3094 CDS
T01001
Symbol
HINT1, HINT, NMAN, PKCI-1, PRKCNH1
Name
(RefSeq) histidine triad nucleotide binding protein 1
KO
K02503
histidine triad (HIT) family protein [EC:3.9.1.-]
Organism
hsa
Homo sapiens (human)
Disease
H02390
Autosomal recessive neuromyotonia and axonal neuropathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03016 Transfer RNA biogenesis [BR:
hsa03016
]
3094 (HINT1)
09183 Protein families: signaling and cellular processes
04147 Exosome [BR:
hsa04147
]
3094 (HINT1)
Transfer RNA biogenesis [BR:
hsa03016
]
Eukaryotic type
Aminoacyl-tRNA synthetases (AARSs)
AARS associated factors
3094 (HINT1)
Exosome [BR:
hsa04147
]
Exosomal proteins
Exosomal proteins of haemopoietic cells (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
3094 (HINT1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
HIT
DcpS_C
Motif
Other DBs
NCBI-GeneID:
3094
NCBI-ProteinID:
NP_005331
OMIM:
601314
HGNC:
4912
Ensembl:
ENSG00000169567
UniProt:
P49773
A0A384NPU2
Structure
PDB
PDBj
LinkDB
All DBs
Position
5:complement(131159027..131165256)
Genome browser
AA seq
126 aa
AA seq
DB search
MADEIAKAQVARPGGDTIFGKIIRKEIPAKIIFEDDRCLAFHDISPQAPTHFLVIPKKHI
SQISVAEDDDESLLGHLMIVGKKCAADLGLNKGYRMVVNEGSDGGQSVYHVHLHVLGGRQ
MHWPPG
NT seq
381 nt
NT seq
+upstream
nt +downstream
nt
atggcagatgagattgccaaggctcaggtcgctcggcctggtggcgacacgatctttggg
aagatcatccgcaaggaaataccagccaaaatcatttttgaggatgaccggtgccttgct
ttccatgacatttcccctcaagcaccaacacattttctggtgatacccaagaaacatata
tcccagatttctgtggcagaagatgatgatgaaagtcttcttggacacttaatgattgtt
ggcaagaaatgtgctgctgatctgggcctgaataagggttatcgaatggtggtgaatgaa
ggttcagatggtggacagtctgtctatcacgttcatctccatgttcttggaggtcggcaa
atgcattggcctcctggttaa
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integrated database retrieval system
