Homo sapiens (human): 83636
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Entry
83636 CDS
T01001
Symbol
C19orf12, MPAN, NBIA3, NBIA4, SPG43
Name
(RefSeq) chromosome 19 open reading frame 12
KO
K23168
protein MPAN
Organism
hsa
Homo sapiens (human)
Disease
H00266
Hereditary spastic paraplegia
H00833
Neurodegeneration with brain iron accumulation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
83636 (C19orf12)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitophagy factors
Other mitophagy factors
83636 (C19orf12)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
C19orf12
DUF5862
Motif
Other DBs
NCBI-GeneID:
83636
NCBI-ProteinID:
NP_001026896
OMIM:
614297
HGNC:
25443
Ensembl:
ENSG00000131943
UniProt:
Q9NSK7
LinkDB
All DBs
Position
19:complement(29698886..29715789)
Genome browser
AA seq
141 aa
AA seq
DB search
MTIMVEDIMKLLCSLSGERKMKAAVKHSGKGALVTGAMAFVGGLVGGPPGLAVGGAVGGL
LGAWMTSGQFKPVPQILMELPPAEQQRLFNEAAAIIRHLEWTDAVQLTALVMGSEALQQQ
LLAMLVNYVTKELRAEIQYDD
NT seq
426 nt
NT seq
+upstream
nt +downstream
nt
atgactatcatggtggaggacatcatgaagctgctgtgctccctttctggggagaggaag
atgaaggcggctgtcaagcactctgggaagggtgccctggtcacaggggccatggccttc
gtcgggggtttggtgggcggcccaccgggactcgccgttgggggggctgtcggggggctg
ttaggtgcctggatgacaagtggacagtttaagccggttcctcagatcctaatggagctg
ccccctgccgagcaacagaggctctttaacgaagccgcagccatcatcaggcacctggag
tggacggacgccgtgcagctgaccgcgctggtcatgggcagcgaggccctgcagcagcag
ctgctggccatgctggtgaactacgtcaccaaggagctgcgggccgagatccagtatgat
gactag
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integrated database retrieval system