Interleukin-1 receptor accessory protein-like 1

Summary
UniProt ID
Q9NZN1
Gene Symbol
  • IL1RAPL1
  • OPHN4
Organism
Homo sapiens (human)
External Links
PubChem
Q9NZN1
The Human Metabolome Database
HMDBP12406
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Cell projection
  • Cytoplasm
  • Disulfide bond
  • Glycoprotein
  • Hydrolase
  • Immunoglobulin domain
  • Intellectual disability
  • NAD
  • Receptor
  • Reference proteome
  • Repeat
  • Signal
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MKAPIPHLILLYATFTQSLKVVTKRGSADGCTDWSIDIKKYQVLVGEPVRIKCALFYGYIRTNYSLAQSAGLSLMWYKSSGPGDFEEPIAFDGSRMSKEEDSIWFRPTLLQDSGLYACVIRNSTYCMKVSISLTVGENDTGLCYNSKMKYFEKAELSKSKEISCRDIEDFLLPTREPEILWYKECRTKTWRPSIVFKRDTLLIREVREDDIGNYTCELKYGGFVVRRTTELTVTAPLTDKPPKLLYPMESKLTIQETQLGDSANLTCRAFFGYSGDVSPLIYWMKGEKFIEDLDENRVWESDIRILKEHLGEQEVSISLIVDSVEEGDLGNYSCYVENGNGRRHASVLLHKRELMYTVELAGGLGAILLLLVCLVTIYKCYKIEIMLFYRNHFGAEELDGDNKDYDAYLSYTKVDPDQWNQETGEEERFALEILPDMLEKHYGYKLFIPDRDLIPTGTYIEDVARCVDQSKRLIIVMTPNYVVRRGWSIFELETRLRNMLVTGEIKVILIECSELRGIMNYQEVEALKHTIKLLTVIKWHGPKCNKLNSKFWKRLQYEMPFKRIEPITHEQALDVSEQGPFGELQTVSAISMAAATSTALATAHPDLRSTFHNTYHSQMRQKHYYRSYEYDVPPTGTLPLTSIGNQHTYCNIPMTLINGQRPQTKSSREQNPDEAHTNSAILPLLPRETSISSVIW
Glycosylation Sites
Displaying all 6 entries
Position Description PubMed ID GlyTouCan ID Source
63 N-linked (GlcNAc...) asparagine
122 N-linked (GlcNAc...) asparagine
138 N-linked (GlcNAc...) asparagine
213 N-linked (GlcNAc...) asparagine
264 N-linked (GlcNAc...) asparagine
331 N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 2 entries
Pathway Name Organism
Interleukin-38 signaling Homo sapiens
Receptor-type tyrosine-protein phosphatases Homo sapiens
Disease
Displaying entries 1 - 10 of 46 in total
DO ID Disease Name Source
DOID:0050745 diffuse large B-cell lymphoma
DOID:0050776 non-syndromic X-linked intellectual disability
DOID:0060041 autism spectrum disorder
DOID:0060427 chromosome Xp21 deletion syndrome
DOID:0060823 syndromic X-linked intellectual disability 94
DOID:0080156 X-linked adrenal hypoplasia congenita
DOID:1059 intellectual disability
DOID:1094 attention deficit hyperactivity disorder
DOID:114 heart disease
DOID:11665 Patau syndrome

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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