Klotho

Summary
UniProt ID
Q9UEF7
Gene Symbol
  • KL
Organism
Homo sapiens (human)
External Links
GlyConnect
GlyGen
Q9UEF7
PubChem
Q9UEF7
The Human Metabolome Database
HMDBP07765
Sequence
MPASAPPRRPRPPPPSLSLLLVLLGLGGRRLRAEPGDGAQTWARFSRPPAPEAAGLFQGTFPDGFLWAVGSAAYQTEGGWQQHGKGASIWDTFTHHPLAPPGDSRNASLPLGAPSPLQPATGDVASDSYNNVFRDTEALRELGVTHYRFSISWARVLPNGSAGVPNREGLRYYRRLLERLRELGVQPVVTLYHWDLPQRLQDAYGGWANRALADHFRDYAELCFRHFGGQVKYWITIDNPYVVAWHGYATGRLAPGIRGSPRLGYLVAHNLLLAHAKVWHLYNTSFRPTQGGQVSIALSSHWINPRRMTDHSIKECQKSLDFVLGWFAKPVFIDGDYPESMKNNLSSILPDFTESEKKFIKGTADFFALCFGPTLSFQLLDPHMKFRQLESPNLRQLLSWIDLEFNHPQIFIVENGWFVSGTTKRDDAKYMYYLKKFIMETLKAIKLDGVDVIGYTAWSLMDGFEWHRGYSIRRGLFYVDFLSQDKMLLPKSSALFYQKLIEKNGFPPLPENQPLEGTFPCDFAWGVVDNYIQVDTTLSQFTDLNVYLWDVHHSKRLIKVDGVVTKKRKSYCVDFAAIQPQIALLQEMHVTHFRFSLDWALILPLGNQSQVNHTILQYYRCMASELVRVNITPVVALWQPMAPNQGLPRLLARQGAWENPYTALAFAEYARLCFQELGHHVKLWITMNEPYTRNMTYSAGHNLLKAHALAWHVYNEKFRHAQNGKISIALQADWIEPACPFSQKDKEVAERVLEFDIGWLAEPIFGSGDYPWVMRDWLNQRNNFLLPYFTEDEKKLIQGTFDFLALSHYTTILVDSEKEDPIKYNDYLEVQEMTDITWLNSPSQVAVVPWGLRKVLNWLKFKYGDLPMYIISNGIDDGLHAEDDQLRVYYMQNYINEALKAHILDGINLCGYFAYSFNDRTAPRFGLYRYAADQFEPKASMKHYRKIIDSNGFPGPETLERFCPEEFTVCTECSFFHTRKSLLAFIAFLFFASIISLSLIFYYSKKGRRSYK
Glycosylation Sites
Displaying all 9 entries
Position Description PubMed ID GlyTouCan ID Source
106 N-linked (GlcNAc...) asparagine
115
159 N-linked (GlcNAc...) asparagine
283 N-linked (GlcNAc...) asparagine
344 N-linked (GlcNAc...) asparagine
607 N-linked (GlcNAc...) asparagine
612 N-linked (GlcNAc...) asparagine
630
694 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Disease
Displaying entries 31 - 40 of 343 in total
DO ID Disease Name Source
DOID:0060585 Noonan syndrome 7
DOID:0060586 Noonan syndrome 8
DOID:0060587 Noonan syndrome 9
DOID:0060588 Noonan syndrome 10
DOID:0060608 microcephalic osteodysplastic primordial dwarfism type I
DOID:0060609 microcephalic osteodysplastic primordial dwarfism type II
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome
DOID:0060764 autosomal recessive Robinow syndrome
DOID:0060765 autosomal dominant Robinow syndrome 2
DOID:0060766 autosomal dominant Robinow syndrome 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024