non-syndromic X-linked intellectual disability 21

Summary
Synonym
  • MRX21
  • MRX34
  • X-linked mental retardation 21
  • X-linked mental retardation 21/34
  • X-linked mental retardation 34
Definition
A non-syndromic X-linked intellectual disability characterized by a spectrum of cognitive neurologic impairments ranging from moderate mental retardation to high-functioning autism that has_material_basis_in hemizygous mutation in the IL1RAPL1 gene on chromosome Xp21.3-p21.2.
Super Class
X-linked recessive disease non-syndromic X-linked intellectual disability
Disease Ontology
DOID:0112022
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
11141 IL1RAPL1 interleukin 1 receptor accessory protein like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
331461 Il1rapl1 interleukin 1 receptor accessory protein-like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
317553 Il1rapl1 interleukin 1 receptor accessory protein-like 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
557801 il1rapl1b interleukin 1 receptor accessory protein-like 1b
568868 il1rapl1a interleukin 1 receptor accessory protein-like 1a
The Human Phenotype Ontology
Displaying entries 1 - 10 of 19 in total
HPO ID HPO Term
HP:0000678 Dental crowding
HP:0003196 Short nose
HP:0000316 Hypertelorism
HP:0001382 Joint hypermobility
HP:0000194 Open mouth
HP:0001611 Hypernasal speech
HP:0000582 Upslanted palpebral fissure
HP:0010804 Tented upper lip vermilion
HP:0000752 Hyperactivity
HP:0000053 Macroorchidism
Displaying 1 entry
Gene ID Gene Symbol Description
11141 IL1RAPL1 interleukin 1 receptor accessory protein like 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: December 9, 2024