Homo sapiens (human): 145957
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Entry
145957 CDS
T01001
Symbol
NRG4, HRG4
Name
(RefSeq) neuregulin 4
KO
K05458
neuregulin 4
Organism
hsa
Homo sapiens (human)
Pathway
hsa04012
ErbB signaling pathway
hsa05014
Amyotrophic lateral sclerosis
Network
nt06464
Amyotrophic lateral sclerosis
nt06530
PI3K signaling
Element
N01163
NRG-ERBB4-PI3K signaling pathway
N01164
Mutation-inactivated ERBB4 to NRG-ERBB4-PI3K signaling pathway
N01656
GF-RTK-PI3K signaling pathway
N01658
GF-RTK-RAS-PI3K signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04012 ErbB signaling pathway
145957 (NRG4)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
145957 (NRG4)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04052 Cytokines and neuropeptides [BR:
hsa04052
]
145957 (NRG4)
Cytokines and neuropeptides [BR:
hsa04052
]
Cytokines
Growth factors (RTK binding)
145957 (NRG4)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EGF
EGF_2
Motif
Other DBs
NCBI-GeneID:
145957
NCBI-ProteinID:
NP_612640
OMIM:
610894
HGNC:
29862
Ensembl:
ENSG00000169752
UniProt:
Q8WWG1
LinkDB
All DBs
Position
15:complement(75935393..76060240)
Genome browser
AA seq
115 aa
AA seq
DB search
MPTDHEEPCGPSHKSFCLNGGLCYVIPTIPSPFCRCVENYTGARCEEVFLPGSSIQTKSN
LFEAFVALAVLVTLIIGAFYFLCRKGHFQRASSVQYDINLVETSSTSAHHSHEQH
NT seq
348 nt
NT seq
+upstream
nt +downstream
nt
atgccaacagatcacgaagagccctgtggtcccagtcacaagtcgttttgcctgaatggg
gggctttgttatgtgatacctactattcccagcccattttgtaggtgcgttgaaaactat
acaggagctcgttgtgaagaggtttttctcccaggctccagcatccaaactaaaagtaac
ctgtttgaagcttttgtggcattggcggtcctagtaacacttatcattggagccttctac
ttcctttgcaggaaaggccactttcagagagccagttcagtccagtatgatatcaacctg
gtagagacgagcagtaccagtgcccaccacagtcatgaacaacactga
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integrated database retrieval system
