Homo sapiens (human): 7873
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Entry
7873 CDS
T01001
Symbol
MANF, ARMET, ARP, DDDS
Name
(RefSeq) mesencephalic astrocyte derived neurotrophic factor
KO
K22556
mesencephalic astrocyte-derived neurotrophic factor
Organism
hsa
Homo sapiens (human)
Disease
H02685
Developmental delay with neuropsychiatric disorders
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
7873 (MANF)
Membrane trafficking [BR:
hsa04131
]
Endoplasmic reticulum (ER) - Golgi transport
Others
Others
7873 (MANF)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ARMET_N
ARMET_C
CheZ
TMCO5
SAP
RNF34L-like_3rd
Motif
Other DBs
NCBI-GeneID:
7873
NCBI-ProteinID:
NP_006001
OMIM:
601916
HGNC:
15461
Ensembl:
ENSG00000145050
UniProt:
P55145
A8K878
Structure
PDB
PDBj
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All DBs
Position
3:51385291..51389397
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AA seq
182 aa
AA seq
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MRRMWATQGLAVALALSVLPGSRALRPGDCEVCISYLGRFYQDLKDRDVTFSPATIENEL
IKFCREARGKENRLCYYIGATDDAATKIINEVSKPLAHHIPVEKICEKLKKKDSQICELK
YDKQIDLSTVDLKKLRVKELKKILDDWGETCKGCAEKSDYIRKINELMPKYAPKAASART
DL
NT seq
549 nt
NT seq
+upstream
nt +downstream
nt
atgaggaggatgtgggccacgcaggggctggcggtggcgctggctctgagcgtgctgccg
ggcagccgggcgctgcggccgggcgactgcgaagtttgtatttcttatctgggaagattt
taccaggacctcaaagacagagatgtcacattctcaccagccactattgaaaacgaactt
ataaagttctgccgggaagcaagaggcaaagagaatcggttgtgctactatatcggggcc
acagatgatgcagccaccaaaatcatcaatgaggtatcaaagcctctggcccaccacatc
cctgtggagaagatctgtgagaagcttaagaagaaggacagccagatatgtgagcttaag
tatgacaagcagatcgacctgagcacagtggacctgaagaagctccgagttaaagagctg
aagaagattctggatgactggggggagacatgcaaaggctgtgcagaaaagtctgactac
atccggaagataaatgaactgatgcctaaatatgcccccaaggcagccagtgcacggacc
gatttgtag
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integrated database retrieval system
