Homo sapiens (human): 51025
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Entry
51025 CDS
T01001
Symbol
PAM16, CGI-136, MAGMAS, SMDMDM, TIM16, TIMM16
Name
(RefSeq) presequence translocase associated motor 16
KO
K17805
mitochondrial import inner membrane translocase subunit TIM16
Organism
hsa
Homo sapiens (human)
Disease
H01830
Spondylometaphyseal dysplasia, Megarbane-Dagher-Melki type
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
51025 (PAM16)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Matrix
MMC/PAM proteins
51025 (PAM16)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Pam16
SLAIN
PASTA
Motif
Other DBs
NCBI-GeneID:
51025
NCBI-ProteinID:
NP_057153
OMIM:
614336
HGNC:
29679
Ensembl:
ENSG00000217930
UniProt:
Q9Y3D7
LinkDB
All DBs
Position
16:complement(4340251..4351321)
Genome browser
AA seq
125 aa
AA seq
DB search
MAKYLAQIIVMGVQVVGRAFARALRQEFAASRAAADARGRAGHRSAAASNLSGLSLQEAQ
QILNVSKLSPEEVQKNYEHLFKVNDKSVGGSFYLQSKVVRAKERLDEELKIQAQEDREKG
QMPHT
NT seq
378 nt
NT seq
+upstream
nt +downstream
nt
atggccaagtacctggcccagatcattgtgatgggcgtgcaggtggtgggcagggccttt
gcacgggccttgcggcaggagtttgcagccagccgggccgcagctgatgcccgaggacgc
gctggacaccggtctgcagccgcttccaacctctccggcctcagcctccaggaggcacag
cagattctcaacgtgtccaagctgagccctgaggaggtccagaagaactatgaacactta
tttaaggtgaatgataaatccgtgggtggctccttctacctgcagtcaaaggtggtccgc
gcaaaggagcgcctggatgaggaactcaaaatccaggcccaggaggacagagaaaaaggg
cagatgccccatacgtga
DBGET
integrated database retrieval system
