Homo sapiens (human): 55255
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Entry
55255 CDS
T01001
Symbol
WDR41, MSTP048
Name
(RefSeq) WD repeat domain 41
KO
K23610
WD repeat-containing protein 41
Organism
hsa
Homo sapiens (human)
Pathway
hsa04140
Autophagy - animal
hsa05014
Amyotrophic lateral sclerosis
hsa05022
Pathways of neurodegeneration - multiple diseases
Network
nt06464
Amyotrophic lateral sclerosis
nt06466
Pathways of neurodegeneration
nt06532
Autophagy
Element
N01142
C9orf72-mediated autophagy initiation
N01143
Mutation-inactivated C9orf72 to C9orf72-mediated autophagy initiation
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
55255 (WDR41)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
55255 (WDR41)
05022 Pathways of neurodegeneration - multiple diseases
55255 (WDR41)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
55255 (WDR41)
Membrane trafficking [BR:
hsa04131
]
Autophagy
Other autophagy associated proteins
Rab associated proteins
55255 (WDR41)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
WD40
WD40_Prp19
WDR55
WD40_WDHD1_1st
Beta-prop_EML_2
WD40_CDC20-Fz
Beta-prop_CAF1B_HIR1
Beta-prop_EML
WD40_MABP1-WDR62_2nd
Beta-prop_WD40_POC16_2nd
EIF3I
Beta-prop_EIPR1
Beta-prop_RIG_2nd
Beta-prop_WDR75_1st
WDR90_beta-prop_4th
Beta-prop_IP5PC_F
Beta-prop_SCAP
DUF5793
Motif
Other DBs
NCBI-GeneID:
55255
NCBI-ProteinID:
NP_060738
OMIM:
617502
HGNC:
25601
Ensembl:
ENSG00000164253
UniProt:
Q9HAD4
A0A0S2Z5E0
Structure
PDB
PDBj
LinkDB
All DBs
Position
5:complement(77430933..77620577)
Genome browser
AA seq
459 aa
AA seq
DB search
MLRWLIGGGREPQGLAEKSPLQTIGEEQTQNPYTELLVLKAHHDIVRFLVQLDDYRFASA
GDDGIVVVWNAQTGEKLLELNGHTQKITAIITFPSLESCEEKNQLILTASADRTVIVWDG
DTTRQVQRISCFQSTVKCLTVLQRLDVWLSGGNDLCVWNRKLDLLCKTSHLSDTGISALV
EIPKNCVVAAVGKELIIFRLVAPTEGSLEWDILEVKRLLDHQDNILSLINVNDLSFVTGS
HVGELIIWDALDWTMQAYERNFWDPSPQLDTQQEIKLCQKSNDISIHHFTCDEENVFAAV
GRGLYVYSLQMKRVIACQKTAHDSNVLHVARLPNRQLISCSEDGSVRIWELREKQQLAAE
PVPTGFFNMWGFGRVSKQASQPVKKQQENATSCSLELIGDLIGHSSSVEMFLYFEDHGLV
TCSADHLIILWKNGERESGLRSLRLFQKLEENGDLYLAV
NT seq
1380 nt
NT seq
+upstream
nt +downstream
nt
atgttgcgatggctgatcgggggaggccgagaaccgcagggactggccgagaaatctcct
ttacagacaataggtgaagaacaaacccagaatccctacactgaactgctagtactgaag
gctcatcatgatattgtacgatttctggtacagttagatgactacagatttgcatctgct
ggtgatgatggaattgtagttgtgtggaatgcccagacaggggaaaaacttttagaactg
aatggacacactcaaaagataacagctattattacatttccttccttggaatcttgtgaa
gagaaaaatcaactcatcttgacagcctctgctgatagaacagttattgtgtgggatggt
gatactaccagacaagttcagagaatatcatgcttccagtctactgtaaagtgtttaact
gttcttcagagactagatgtttggctttctggtgggaatgacctgtgtgtgtggaaccga
aaattagatctcctgtgtaagactagccacctttctgatacaggtattagtgctttggtt
gaaatacctaagaactgtgttgtggcagcagttggcaaagaactgataattttcaggttg
gtagcacccacagaaggatcactagaatgggatattcttgaagttaagcgcctccttgat
caccaggataatattctctcattgattaatgtcaatgatttgagttttgtcaccggctcc
cacgtcggagagctgatcatctgggatgccctggactggaccatgcaggcctatgaacgc
aacttctgggacccatctccacaactggacacccaacaagaaataaaactctgtcaaaaa
tcaaatgacatttctattcatcatttcacatgtgatgaagagaatgtatttgctgcagtt
ggaaggggtttatacgtgtatagccttcaaatgaagcgtgtgattgcctgccagaaaact
gcacatgactccaatgtcctgcacgttgccagacttccaaacaggcagttaatctcatgc
tcagaagatggcagtgtacgcatttgggagttaagagaaaaacagcagcttgcagctgag
cctgtaccaacaggtttttttaacatgtggggatttggaagagtcagcaaacaagccagc
caacctgttaaaaagcagcaagaaaatgctacttcatgttcactggagcttattggagat
ttgattggacactcatcatctgtggagatgtttctatactttgaagatcatggactagtg
acgtgctccgctgatcatctcattattttgtggaaaaatggagagcgagaatctggattg
cgcagtttaagattatttcaaaaattagaggagaatggtgacttataccttgctgtctag
DBGET
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