Homo sapiens (human): 7802
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ax_dynein_light
RIB43A
FapA
Motif
Other DBs
NCBI-GeneID:
7802
NCBI-ProteinID:
NP_003453
OMIM:
602135
HGNC:
14353
Ensembl:
ENSG00000163879
UniProt:
O14645
A0A499FIY3
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:37556940..37566857
Genome browser
AA seq
258 aa
AA seq
DB search
MIPPADSLLKYDTPVLVSRNTEKRSPKARLLKVSPQQPGPSGSAPQPPKTKLPSTPCVPD
PTKQAEEILNAILPPREWVEDTQLWIQQVSSTPSTRMDVVHLQEQLDLKLQQRQARETGI
CPVRRELYSQCFDELIREVTINCAERGLLLLRVRDEIRMTIAAYQTLYESSVAFGMRKAL
QAEQGKSDMERKIAELETEKRDLERQVNEQKAKCEATEKRESERRQVEEKKHNEEIQFLK
RTNQQLKAQLEGIIAPKK
NT seq
777 nt
NT seq
+upstream
nt +downstream
nt
atgattccgcccgcagactctttgctcaagtacgacaccccagtgctggtgagccggaac
acggagaaacggagccccaaggctcggctactgaaagtcagcccccagcagcctggacct
tcaggttcagccccacagccacccaagaccaagctcccctcaactccctgtgtcccagat
cctacaaagcaggcagaagaaatcttgaatgccatactacccccaagggagtgggtggaa
gacacgcagctatggatccagcaggtgtccagcacccctagcaccaggatggacgtggtg
cacctccaggagcagttagacttaaagctgcagcagcggcaggccagggaaacaggcatc
tgccctgtccgcagggaactctactcacagtgttttgatgagttgatccgggaggtcacc
atcaactgtgcggagagggggctgctgctgctgcgagtccgggacgagatccgcatgacc
atcgctgcctaccagaccctgtacgagagcagcgtggcgtttggcatgaggaaggcactg
caggctgagcaggggaagtcagacatggagaggaaaatcgcagaattggagacggaaaag
agagacctggagaggcaagtgaacgagcagaaggcaaaatgtgaagccactgagaagcgg
gagagcgagaggcggcaggtggaggagaagaagcacaatgaggagattcagttcctgaag
cgaacaaatcagcagctgaaggcccaactggaaggcattattgcaccaaagaagtga
DBGET
integrated database retrieval system