KEGG   Homo sapiens (human): 7802
Entry
7802              CDS       T01001                                 
Symbol
DNALI1, P28, SPGF83, dJ423B22.5, hp28
Name
(RefSeq) dynein axonemal light intermediate chain 1
  KO
K10410  dynein axonemal light intermediate chain 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04814  Motor proteins
hsa05014  Amyotrophic lateral sclerosis
hsa05016  Huntington disease
hsa05022  Pathways of neurodegeneration - multiple diseases
Network
nt06461  Huntington disease
nt06463  Parkinson disease
nt06464  Amyotrophic lateral sclerosis
nt06466  Pathways of neurodegeneration
  Element
N00976  Retrograde axonal transport
N00977  Mutation-caused aberrant Htt to retrograde axonal transport
N01159  Mutation-caused aberrant TUBA4A to retrograde axonal transport
N01160  Mutation-caused aberrant SOD1 to retrograde axonal transport
Disease
H01282  Spermatogenic failure
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09142 Cell motility
   04814 Motor proteins
    7802 (DNALI1)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    7802 (DNALI1)
   05016 Huntington disease
    7802 (DNALI1)
   05022 Pathways of neurodegeneration - multiple diseases
    7802 (DNALI1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    7802 (DNALI1)
   04812 Cytoskeleton proteins [BR:hsa04812]
    7802 (DNALI1)
Cilium and associated proteins [BR:hsa03037]
 Motile cilia and associated proteins
  Dynein arm
   7802 (DNALI1)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Microtubules
   Tubulin-binding proteins
    Dyneins
     7802 (DNALI1)
SSDB
Motif
Pfam: Ax_dynein_light RIB43A FapA
Other DBs
NCBI-GeneID: 7802
NCBI-ProteinID: NP_003453
OMIM: 602135
HGNC: 14353
Ensembl: ENSG00000163879
UniProt: O14645 A0A499FIY3
Structure
LinkDB
Position
1:37556940..37566857
AA seq 258 aa
MIPPADSLLKYDTPVLVSRNTEKRSPKARLLKVSPQQPGPSGSAPQPPKTKLPSTPCVPD
PTKQAEEILNAILPPREWVEDTQLWIQQVSSTPSTRMDVVHLQEQLDLKLQQRQARETGI
CPVRRELYSQCFDELIREVTINCAERGLLLLRVRDEIRMTIAAYQTLYESSVAFGMRKAL
QAEQGKSDMERKIAELETEKRDLERQVNEQKAKCEATEKRESERRQVEEKKHNEEIQFLK
RTNQQLKAQLEGIIAPKK
NT seq 777 nt   +upstreamnt  +downstreamnt
atgattccgcccgcagactctttgctcaagtacgacaccccagtgctggtgagccggaac
acggagaaacggagccccaaggctcggctactgaaagtcagcccccagcagcctggacct
tcaggttcagccccacagccacccaagaccaagctcccctcaactccctgtgtcccagat
cctacaaagcaggcagaagaaatcttgaatgccatactacccccaagggagtgggtggaa
gacacgcagctatggatccagcaggtgtccagcacccctagcaccaggatggacgtggtg
cacctccaggagcagttagacttaaagctgcagcagcggcaggccagggaaacaggcatc
tgccctgtccgcagggaactctactcacagtgttttgatgagttgatccgggaggtcacc
atcaactgtgcggagagggggctgctgctgctgcgagtccgggacgagatccgcatgacc
atcgctgcctaccagaccctgtacgagagcagcgtggcgtttggcatgaggaaggcactg
caggctgagcaggggaagtcagacatggagaggaaaatcgcagaattggagacggaaaag
agagacctggagaggcaagtgaacgagcagaaggcaaaatgtgaagccactgagaagcgg
gagagcgagaggcggcaggtggaggagaagaagcacaatgaggagattcagttcctgaag
cgaacaaatcagcagctgaaggcccaactggaaggcattattgcaccaaagaagtga

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