KEGG   Homo sapiens (human): 125988
Entry
125988            CDS       T01001                                 
Symbol
MICOS13, C19orf70, MIC12, MIC13, P117, QIL1
Name
(RefSeq) mitochondrial contact site and cristae organizing system subunit 13
  KO
K24624  MICOS complex subunit MIC13
Organism
hsa  Homo sapiens (human)
Disease
H00891  Combined oxidative phosphorylation deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    125988 (MICOS13)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial protein import machinery
  Inner mambrane
   MICOS complex
    125988 (MICOS13)
SSDB
Motif
Pfam: QIL1
Other DBs
NCBI-GeneID: 125988
NCBI-ProteinID: NP_991330
OMIM: 616658
HGNC: 33702
Ensembl: ENSG00000174917
UniProt: Q5XKP0
LinkDB
Position
19:complement(5678422..5680516)
AA seq 118 aa
MVARVWSLMRFLIKGSVAGGAVYLVYDQELLGPSDKSQAALQKAGEVVPPAMYQFSQYVC
QQTGLQIPQLPAPPKIYFPIRDSWNAGIMTVMSALSVAPSKAREYSKEGWEYVKARTK
NT seq 357 nt   +upstreamnt  +downstreamnt
atggtggcccgggtgtggtcgctgatgaggttcctcatcaagggaagtgtggctgggggc
gccgtctacctggtgtacgaccaggagctgctggggcccagcgacaagagccaggcagcc
ctacagaaggctggggaggtggtcccccccgccatgtaccagttcagccagtacgtgtgt
cagcagacaggcctgcagataccccagctcccagcccctccaaagatttactttcccatc
cgtgactcctggaatgcaggcatcatgacggtgatgtcagctctgtcggtggccccctcc
aaggcccgcgagtactccaaggagggctgggagtatgtgaaggcgcgcaccaagtag

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