Homo sapiens (human): 91689
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Entry
91689 CDS
T01001
Symbol
SMDT1, C22orf32, DDDD, EMRE
Name
(RefSeq) single-pass membrane protein with aspartate rich tail 1
KO
K22830
essential MCU regulator, mitochondrial
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03029 Mitochondrial biogenesis [BR:
hsa03029
]
91689 (SMDT1)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial protein import machinery
Inner mambrane
Mitochondrial calcium uniporter complex
91689 (SMDT1)
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DDDD
Motif
Other DBs
NCBI-GeneID:
91689
NCBI-ProteinID:
NP_201575
OMIM:
615588
HGNC:
25055
Ensembl:
ENSG00000183172
UniProt:
Q9H4I9
Structure
PDB
PDBj
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All DBs
Position
22:42079700..42084284
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AA seq
107 aa
AA seq
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MASGAARWLVLAPVRSGALRSGPSLRKDGDVSAAWSGSGRSLVPSRSVIVTRSGAILPKP
VKMSFGLLRVFSIVIPFLYVGTLISKNFAALLEEHDIFVPEDDDDDD
NT seq
324 nt
NT seq
+upstream
nt +downstream
nt
atggcgtccggagcggctcgctggctagtattggcacccgtcaggtccggggctctccgg
agcgggcctagcttgaggaaagatggcgatgtctccgccgcatggagcggctcaggccgg
agcctggtaccgtcgaggtcagtcatcgttacccgcagcggcgccattttgcccaaaccg
gtgaaaatgtccttcggccttctccgtgtgttctccattgtgatcccctttctctatgtc
gggacactcattagcaagaactttgctgctctacttgaggaacatgacatttttgttcca
gaggatgatgatgatgatgactaa
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