Entry - *614835 - ACTIN, BETA-LIKE, 2; ACTBL2 - OMIM

 
 
* 614835

ACTIN, BETA-LIKE, 2; ACTBL2


HGNC Approved Gene Symbol: ACTBL2

Cytogenetic location: 5q11.2     Genomic coordinates (GRCh38): 5:57,480,018-57,482,811 (from NCBI)


TEXT

▼ Cloning and Expression

Using RT-PCR to amplify actin-like transcripts from hepatocellular carcinomas, Chang et al. (2006) obtained a partial cDNA for ACTBL2.


▼ Mapping

Hartz (2012) mapped the ACTBL2 gene to chromosome 5q11.2 based on an alignment of the ACTBL2 sequence (GenBank AY970384) with the genomic sequence (GRCh37).

▼ REFERENCES

  1. Chang, K.-W., Yang, P.-Y., Lai, H.-Y., Yeh, T.-S., Chen, T.-C., Yeh, C.-T. Identification of a novel actin isoform in hepatocellular carcinoma. Hepatol. Res. 36: 33-39, 2006. [PubMed: 16824795, related citations] [Full Text]

  2. Hartz, P. A. Personal Communication. Baltimore, Md. 9/21/2012.


Creation Date:
Patricia A. Hartz : 9/26/2012
Edit History:
mgross : 09/26/2012

* 614835

ACTIN, BETA-LIKE, 2; ACTBL2


HGNC Approved Gene Symbol: ACTBL2

Cytogenetic location: 5q11.2     Genomic coordinates (GRCh38): 5:57,480,018-57,482,811 (from NCBI)


TEXT

Cloning and Expression

Using RT-PCR to amplify actin-like transcripts from hepatocellular carcinomas, Chang et al. (2006) obtained a partial cDNA for ACTBL2.


Mapping

Hartz (2012) mapped the ACTBL2 gene to chromosome 5q11.2 based on an alignment of the ACTBL2 sequence (GenBank AY970384) with the genomic sequence (GRCh37).

REFERENCES

  1. Chang, K.-W., Yang, P.-Y., Lai, H.-Y., Yeh, T.-S., Chen, T.-C., Yeh, C.-T. Identification of a novel actin isoform in hepatocellular carcinoma. Hepatol. Res. 36: 33-39, 2006. [PubMed: 16824795] [Full Text: https://doi.org/10.1016/j.hepres.2006.05.003]

  2. Hartz, P. A. Personal Communication. Baltimore, Md. 9/21/2012.


Creation Date:
Patricia A. Hartz : 9/26/2012

Edit History:
mgross : 09/26/2012



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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: May 21, 2024