Entry - *400023 - CYTOKINE RECEPTOR-LIKE FACTOR 2, Y-LINKED; CRLF2Y - OMIM

 
 
* 400023

CYTOKINE RECEPTOR-LIKE FACTOR 2, Y-LINKED; CRLF2Y


HGNC Approved Gene Symbol: CRLF2

Cytogenetic location: Yp11.2   Genomic coordinates (GRCh38) : Y:1,190,490-1,212,649 (from NCBI)


▼ TEXT

Tonozuka et al. (2001) isolated a CRLF2 clone from a human T lymphocyte cDNA library. By FISH, they mapped the CRLF2 gene to Xp22.3 and Yp11.3 in the pseudoautosomal region. See 300357 for a discussion of the X-linked copy of this gene.


▼ REFERENCES

  1. Tonozuka, Y., Fujio, K., Sugiyama, T., Nosaka, T., Hirai, M., Kitamura, T. Molecular cloning of a human novel type I cytokine receptor related to delta-1/TSLPR. Cytogenet. Cell Genet. 93: 23-25, 2001. [PubMed: 11474172, related citations] [Full Text]


Creation Date:
Ada Hamosh : 8/29/2001
Edit History:
joanna : 09/05/2001
carol : 8/29/2001

* 400023

CYTOKINE RECEPTOR-LIKE FACTOR 2, Y-LINKED; CRLF2Y


HGNC Approved Gene Symbol: CRLF2

Cytogenetic location: Yp11.2   Genomic coordinates (GRCh38) : Y:1,190,490-1,212,649 (from NCBI)


TEXT

Tonozuka et al. (2001) isolated a CRLF2 clone from a human T lymphocyte cDNA library. By FISH, they mapped the CRLF2 gene to Xp22.3 and Yp11.3 in the pseudoautosomal region. See 300357 for a discussion of the X-linked copy of this gene.


REFERENCES

  1. Tonozuka, Y., Fujio, K., Sugiyama, T., Nosaka, T., Hirai, M., Kitamura, T. Molecular cloning of a human novel type I cytokine receptor related to delta-1/TSLPR. Cytogenet. Cell Genet. 93: 23-25, 2001. [PubMed: 11474172] [Full Text: https://doi.org/10.1159/000056941]


Creation Date:
Ada Hamosh : 8/29/2001

Edit History:
joanna : 09/05/2001
carol : 8/29/2001



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2025 Johns Hopkins University.
Printed: March 6, 2025