KEGG   Gorilla gorilla gorilla (western lowland gorilla): 101154126
Entry
101154126         CDS       T02442                                 
Symbol
TOMM40L
Name
(RefSeq) mitochondrial import receptor subunit TOM40B isoform X1
  KO
K11518  mitochondrial import receptor subunit TOM40
Organism
ggo  Gorilla gorilla gorilla (western lowland gorilla)
Pathway
ggo04137  Mitophagy - animal
ggo05014  Amyotrophic lateral sclerosis
ggo05022  Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:ggo00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04137 Mitophagy - animal
    101154126 (TOMM40L)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    101154126 (TOMM40L)
   05022 Pathways of neurodegeneration - multiple diseases
    101154126 (TOMM40L)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ggo03029]
    101154126 (TOMM40L)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ggo02000]
    101154126 (TOMM40L)
Mitochondrial biogenesis [BR:ggo03029]
 Mitochondrial protein import machinery
  Outer membrane
   Transporter outer membrane (TOM) complex
    101154126 (TOMM40L)
Transporters [BR:ggo02000]
 Other transporters
  Primary active transporters [TC:3]
   101154126 (TOMM40L)
SSDB
Motif
Pfam: Porin_3 CBP_BcsS
Other DBs
NCBI-GeneID: 101154126
NCBI-ProteinID: XP_018881285
Ensembl: ENSGGOG00000005720
UniProt: G3QSG5
LinkDB
Position
1:complement(join(95541765..95541904,95542043..95542145,95542356..95542432,95542552..95542674,95542871..95542976,95543123..95543224,95543511..95543603,95543906..95543973,95544257..95544371))
AA seq 308 aa
MGNTLGLAPMGTLPRRSPRREEPLPNPGSFDELHRLCKDVFPAQMEGVKLVVNKVLSSHF
QVAHTIHMSALGLPGYHLHAAYAGDWQLSPTEVFPTVVGDMDSSGSLNAQVLLLLAERLR
AKAVFQTQQAKFLTWQFDGEYRGDDYTATLTLGNPDLIGESVIMVAHFLQSLTHRLVLGG
ELVYHRRPGEEGAILTLAGKYSAVHWVATLNVGSGGAHASYYHRANEQVQVGVEFEANTR
LQDTTFSFGYHLTLPQANMVFRGLVDSNWCVGAVLEKKMPPLPVTLALGAFLNHWRNRFH
CGFSITVG
NT seq 927 nt   +upstreamnt  +downstreamnt
atggggaacacattgggtctggcaccaatggggactttgccccgccggagcccccgccga
gaggaacccctgcccaaccctgggagcttcgatgagctgcaccggctatgcaaagatgta
ttcccagcacagatggagggcgtgaagctcgttgtcaacaaggttctgagcagccatttc
caggtggcgcacactatacacatgagtgccctgggcttgccgggatatcacctccatgcg
gcctatgcaggggattggcagctcagtcccactgaggtgttccccactgtggtaggggat
atggacagcagtggcagcctgaacgcccaggtcttgctcctcttggcagagcggctccga
gctaaggctgtcttccagacgcagcaggccaagttcttgacatggcagtttgatggcgag
tatcggggagatgactacacagccactctgaccctaggaaatcctgacctgattggggag
tcggtgatcatggttgctcacttcctgcagagcctcactcatcggctggtgctgggagga
gagctagtttatcaccggcggccaggcgaagagggggccatcttgacactggctgggaag
tactcggctgtacactgggtagctacattgaatgtgggatcaggcggggcccatgcaagt
tactatcacagggcaaatgaacaggttcaggttggagtggagtttgaggcaaacacaagg
ctacaagacacaacattctcctttggttaccacctgactctgccccaggccaacatggta
tttagaggcttggtggatagtaactggtgtgtaggtgctgtgctggagaagaagatgccc
cctctgcctgtcaccctagcccttggagccttcctcaatcactggcgcaacagattccac
tgtggcttcagcatcactgtgggctga

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