Entry - *620037 - FAMILY WITH SEQUENCE SIMILARITY 193, MEMBER A; FAM193A - OMIM

 
 
* 620037

FAMILY WITH SEQUENCE SIMILARITY 193, MEMBER A; FAM193A


Alternative titles; symbols

RES4-22


HGNC Approved Gene Symbol: FAM193A

Cytogenetic location: 4p16.3     Genomic coordinates (GRCh38): 4:2,535,375-2,732,573 (from NCBI)


TEXT

▼ Gene Function

Hadano et al. (1998) cloned human FAM193A, which they called RES4-22. They identified several putative FAM193A splice variants encoding predicted isoforms of 1,265 amino acids, 1,224 amino acids, and 792 amino acids.


▼ Gene Structure

Hadano et al. (1998) determined that the FAM193A gene contains at least 21 exons and spans 100 kb.


▼ Mapping

By genomic sequence analysis, Hadano et al. (1998) mapped the FAM193A gene to chromosome 4p16.3.


▼ REFERENCES

  1. Hadano, S., Ishida, Y., Ikeda, J. E. The primary structure and genomic organization of five novel transcripts located close to the Huntington's disease gene on human chromosome 4p16.3. DNA Res. 5: 177-186, 1998. [PubMed: 9734812, related citations] [Full Text]


Creation Date:
Bao Lige : 09/13/2022
Edit History:
mgross : 09/13/2022

* 620037

FAMILY WITH SEQUENCE SIMILARITY 193, MEMBER A; FAM193A


Alternative titles; symbols

RES4-22


HGNC Approved Gene Symbol: FAM193A

Cytogenetic location: 4p16.3     Genomic coordinates (GRCh38): 4:2,535,375-2,732,573 (from NCBI)


TEXT

Gene Function

Hadano et al. (1998) cloned human FAM193A, which they called RES4-22. They identified several putative FAM193A splice variants encoding predicted isoforms of 1,265 amino acids, 1,224 amino acids, and 792 amino acids.


Gene Structure

Hadano et al. (1998) determined that the FAM193A gene contains at least 21 exons and spans 100 kb.


Mapping

By genomic sequence analysis, Hadano et al. (1998) mapped the FAM193A gene to chromosome 4p16.3.


REFERENCES

  1. Hadano, S., Ishida, Y., Ikeda, J. E. The primary structure and genomic organization of five novel transcripts located close to the Huntington's disease gene on human chromosome 4p16.3. DNA Res. 5: 177-186, 1998. [PubMed: 9734812] [Full Text: https://doi.org/10.1093/dnares/5.3.177]


Creation Date:
Bao Lige : 09/13/2022

Edit History:
mgross : 09/13/2022



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OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 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® 1966-2024 Johns Hopkins University.
Printed: June 11, 2024