Peromyscus leucopus (white-footed mouse): 114694642
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Entry
114694642 CDS
T07241
Symbol
Wdr41
Name
(RefSeq) WD repeat-containing protein 41 isoform X1
KO
K23610
WD repeat-containing protein 41
Organism
pleu
Peromyscus leucopus (white-footed mouse)
Pathway
pleu04140
Autophagy - animal
pleu05014
Amyotrophic lateral sclerosis
pleu05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
pleu00001
]
09140 Cellular Processes
09141 Transport and catabolism
04140 Autophagy - animal
114694642 (Wdr41)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
114694642 (Wdr41)
05022 Pathways of neurodegeneration - multiple diseases
114694642 (Wdr41)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
pleu04131
]
114694642 (Wdr41)
Membrane trafficking [BR:
pleu04131
]
Autophagy
Other autophagy associated proteins
Rab associated proteins
114694642 (Wdr41)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
WD40
WD40_Prp19
Beta-prop_TEP1_2nd
WDR55
WD40_WDHD1_1st
Beta-prop_TEP1_C
WD40_CDC20-Fz
Beta-prop_EML_2
Beta-prop_CAF1B_HIR1
EIF3I
Beta-prop_WDR90_POC16_2nd
Beta-prop_EML
WD40_MABP1-WDR62_2nd
Beta-prop_RIG_2nd
Beta-prop_EIPR1
WDR90_beta-prop_4th
Beta-prop_WDR75_1st
Beta-prop_IFT122_1st
Beta-prop_Nup120_160
Beta-prop_Vps41
Beta-prop_SPT8
Beta-prop_SCAP
Beta-prop_IP5PC_F
PorZ_N_b_propeller
Motif
Other DBs
NCBI-GeneID:
114694642
NCBI-ProteinID:
XP_028727492
LinkDB
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Position
11:complement(53715538..53765876)
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AA seq
459 aa
AA seq
DB search
MLRWLIGGGREPQGLAEKAALQTIGEDQSQNPYTELLVLKGHHDIVRFLVQLDDHRFASA
GDDGIIVVWNVQTGEKLLELRGHTQKLTAIIAFPPLDSCEEGSQLILTASADRTVCVWDC
DTGRQIQRVSCLQSTVKCLTVLRRLDVWLSGGNDLGVWNRKLDLLCKTDHLSETGISALV
EIPRNCVVAAVGKELIIFRLLAPTEDLQEWDIVEVKRLLDHQDNILSLVNINDTSFATGS
HVGELIIWDALDWTVQACERSFWNPSSQLDAQQEIKLCQKQNDISINHVTCDEENIFAAV
GRGLYVYNLQSKRVIACQKTAHDSNILHIDKLPNRQLISCSEDGSVRIWEVREKQQLAAE
PVPTGFFNMWGFGRVNKQTSQPVKKQQENGTTCSLELTGDLIGHSSSVEMFLYFEDHGLV
TCSADHLIILWKNGERESGFRSIKLFQKLEEDGDLYPAV
NT seq
1380 nt
NT seq
+upstream
nt +downstream
nt
atgctgcgctggctgatcgggggaggccgcgagccgcagggcctggccgagaaagctgct
ttgcagacgataggagaagaccaaagtcagaacccctacactgagctgctggttctgaaa
ggccatcatgacattgtccggttcctggtgcagctggatgaccacagatttgcatctgct
ggcgatgatggaatcatagttgtgtggaatgtccagacaggagagaagctcctggaactc
agaggacacacccagaagctaacggccatcattgcatttccccctctggactcctgtgag
gagggcagtcagctcatcttgacggcctcggctgacaggaccgtctgtgtttgggactgc
gataccggcagacaaatccagagagtctcctgtttgcagtctacagtaaagtgcctaact
gtcctgcggagactagatgtttggctctcgggtggtaatgacttaggtgtgtggaaccga
aaactagatctgctgtgtaagaccgaccatctttctgagacagggatcagtgctttggtt
gaaatccctaggaattgtgttgtagcagcagttggcaaagaactgataatttttaggtta
ctagcacccacagaagatttgcaggaatgggatatcgttgaagttaaacgccttcttgat
caccaggataatattttgtcattggtcaatatcaatgatacgagtttcgccactggctcc
catgttggagagctgatcatctgggatgccctggactggactgtgcaagcttgtgagcgc
agcttctggaacccatcttcacagctggatgcccagcaggaaataaaactctgccagaaa
caaaatgacatttctattaatcatgtcacctgtgatgaagagaatatatttgctgcagtt
ggaagggggctgtatgtgtataacctacaatcgaagcgtgtgattgcctgccagaaaact
gcgcatgactccaacatcctacacatcgacaaacttcccaacaggcagttaatctcatgc
tcagaagatggcagtgtacgcatttgggaggtccgagaaaaacagcagctggcagctgaa
cctgtcccaacagggttttttaatatgtggggatttggacgagtgaacaagcaaaccagc
cagcctgttaaaaaacagcaagaaaacggcactacgtgttccctggagctcactggagat
ctgatcgggcactcgtcctccgtggagatgtttctgtacttcgaagatcatggactggta
acatgctctgcagatcatctcattattttgtggaaaaacggagagcgggaatctggattc
cgaagtatcaagttatttcagaagttagaagaagacggtgacttataccctgctgtctag
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