Homo sapiens (human): 84942
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Entry
84942 CDS
T01001
Symbol
WDR73, GAMOS, GAMOS1, HSPC264
Name
(RefSeq) WD repeat domain 73
KO
K24754
WD repeat-containing protein 73
Organism
hsa
Homo sapiens (human)
Disease
H01722
Galloway-Mowat syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04990 Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
84942 (WDR73)
Domain-containing proteins not elsewhere classified [BR:
hsa04990
]
WD40 repeat (WDR) domain-containing proteins
Other WDR domain-containing proteins
84942 (WDR73)
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Other DBs
NCBI-GeneID:
84942
NCBI-ProteinID:
NP_116245
OMIM:
616144
HGNC:
25928
Ensembl:
ENSG00000177082
UniProt:
Q6P4I2
Q6PJL8
Q5RKY8
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Position
15:complement(84639285..84654283)
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AA seq
378 aa
AA seq
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MDPGDDWLVESLRLYQDFYAFDLSGATRVLEWIDDKGVFVAGYESLKKNEILHLKLPLRL
SVKENKGLFPERDFKVRHGGFSDRSIFDLKHVPHTRLLVTSGLPGCYLQVWQVAEDSDVI
KAVSTIAVHEKEESLWPRVAVFSTLAPGVLHGARLRSLQVVDLESRKTTYTSDVSDSEEL
SSLQVLDADTFAFCCASGRLGLVDTRQKWAPLENRSPGPGSGGERWCAEVGSWGQGPGPS
IASLGSDGRLCLLDPRDLCHPVSSVQCPVSVPSPDPELLRVTWAPGLKNCLAISGFDGTV
QVYDATSWDGTRSQDGTRSQVEPLFTHRGHIFLDGNGMDPAPLVTTHTWHPCRPRTLLSA
TNDASLHVWDWVDLCAPR
NT seq
1137 nt
NT seq
+upstream
nt +downstream
nt
atggatcctggggacgactggctggtggaatccttgcgcttgtaccaggatttctatgca
ttcgacctgtcaggagccactcgagtccttgaatggattgatgacaaaggagtctttgtt
gctggctatgaaagcctgaaaaagaatgaaattcttcatctgaaattacctctcagactt
tctgtaaaggaaaacaagggcttattcccagaaagagatttcaaagtgcgccatggagga
ttttcagacaggtctatctttgatctaaagcatgtgccacataccagattgctggttacc
agtggccttccaggttgttatctgcaggtgtggcaggttgcagaggacagtgatgtcatt
aaagctgtcagcaccattgctgtgcatgagaaagaggagagtctctggcctagggtggcc
gtcttctccacattggcacccggagtcctccatggggcgaggctccgaagtctgcaggtc
gttgatctggagtcccggaagaccacgtacacctcagatgtcagtgacagtgaggagctg
agtagcctgcaggtcctagatgcagacacctttgccttctgctgtgcttcaggccggctg
gggcttgttgacacccggcagaagtgggcaccgttggagaatcgcagccctggccctggg
tctggtggagagagatggtgtgctgaagttgggagctggggccagggccctgggcccagc
attgccagccttggctcagatgggcgtctttgtcttcttgacccccgggatctctgccat
cctgtgagctcagtccagtgcccagtatccgtacctagccctgacccagagctgctgcga
gtgacttgggccccaggcctgaagaattgcttggccatctcaggttttgatggtacagtc
caggtctatgatgccacatcttgggatggaacacggagccaagatggaacacggagccaa
gtagaacctctcttcactcacagaggtcacatcttcctagatggaaatgggatggaccct
gctcctttggtcaccacccacacctggcatccctgcagaccaaggactttgttatcagca
acaaatgatgcctctctgcatgtgtgggactgggtggacctttgtgccccccgctga
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