Loading…

5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia

The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes i...

Full description

Saved in:
Bibliographic Details
Published in:American journal of human genetics 1988-09, Vol.43 (3), p.331-335
Main Authors: SUTHERLAND, G. R, BAKER, E, CALLEN, D. F, HYLAND, V. J, MAY, B. K, BAWDEN, M. J, HEALY, H. M, BORTHWICK, I. A
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 335
container_issue 3
container_start_page 331
container_title American journal of human genetics
container_volume 43
creator SUTHERLAND, G. R
BAKER, E
CALLEN, D. F
HYLAND, V. J
MAY, B. K
BAWDEN, M. J
HEALY, H. M
BORTHWICK, I. A
description The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1715374</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15054482</sourcerecordid><originalsourceid>FETCH-LOGICAL-p352t-fc082d00af015123020764a20c01b60dfb45a63f00e871612665a0509429ce513</originalsourceid><addsrcrecordid>eNqFUUtLw0AQDqLUWv0Jwh7EW2D2nVyEUnxBwYuCtzDZbOxqsqnZTaH_3oih6MnTDHwPvvnmKJlTyXWqFMjjZA4ALM1Zrk-TsxDeASjNgM-SGRdUqEzPk1qmy9b5rrG7oXEeoyVh7-MGgyUuEIyEbxkl6CsSN0MgvovjYsm2dy32e1LZ2ppInCev6aj_sBUJrrJ9VzYYojOj0rYOz5OTGptgL6a5SF7ubp9XD-n66f5xtVynWy5ZTGsDGasAsAYqKePAQCuBDAzQUkFVl0Ki4jWAzTRVlCklESTkguXGSsoXyc2P73YoW1sZ62OPTTGlLTp0xV_Eu03x1u0Kqr97E6PB9WTQd5-DDbFoXTC2acY7uiEUOhNA87HE_4hc5ZqznP5LpBKkEBkbiZe_sx9CT78a8asJx2CwqXv0xoUDTWWZzqXgX1QonSA</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15054482</pqid></control><display><type>article</type><title>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</title><source>International Bibliography of the Social Sciences (IBSS)</source><source>PubMed Central</source><creator>SUTHERLAND, G. R ; BAKER, E ; CALLEN, D. F ; HYLAND, V. J ; MAY, B. K ; BAWDEN, M. J ; HEALY, H. M ; BORTHWICK, I. A</creator><creatorcontrib>SUTHERLAND, G. R ; BAKER, E ; CALLEN, D. F ; HYLAND, V. J ; MAY, B. K ; BAWDEN, M. J ; HEALY, H. M ; BORTHWICK, I. A</creatorcontrib><description>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</description><identifier>ISSN: 0002-9297</identifier><identifier>EISSN: 1537-6605</identifier><identifier>PMID: 3414687</identifier><identifier>CODEN: AJHGAG</identifier><language>eng</language><publisher>Chicago, IL: University of Chicago Press</publisher><subject>5-Aminolevulinate Synthetase - genetics ; Anemia, Sideroblastic - genetics ; Anemias. Hemoglobinopathies ; Biological and medical sciences ; Chromosome Mapping ; Chromosomes, Human, Pair 3 ; Cloning, Molecular ; Defects ; Diseases of red blood cells ; Hematologic and hematopoietic diseases ; Humans ; Medical sciences ; Nucleic Acid Hybridization</subject><ispartof>American journal of human genetics, 1988-09, Vol.43 (3), p.331-335</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715374/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1715374/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,33223,53790,53792</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=6887954$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3414687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SUTHERLAND, G. R</creatorcontrib><creatorcontrib>BAKER, E</creatorcontrib><creatorcontrib>CALLEN, D. F</creatorcontrib><creatorcontrib>HYLAND, V. J</creatorcontrib><creatorcontrib>MAY, B. K</creatorcontrib><creatorcontrib>BAWDEN, M. J</creatorcontrib><creatorcontrib>HEALY, H. M</creatorcontrib><creatorcontrib>BORTHWICK, I. A</creatorcontrib><title>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</title><title>American journal of human genetics</title><addtitle>Am J Hum Genet</addtitle><description>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</description><subject>5-Aminolevulinate Synthetase - genetics</subject><subject>Anemia, Sideroblastic - genetics</subject><subject>Anemias. Hemoglobinopathies</subject><subject>Biological and medical sciences</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 3</subject><subject>Cloning, Molecular</subject><subject>Defects</subject><subject>Diseases of red blood cells</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Nucleic Acid Hybridization</subject><issn>0002-9297</issn><issn>1537-6605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>8BJ</sourceid><recordid>eNqFUUtLw0AQDqLUWv0Jwh7EW2D2nVyEUnxBwYuCtzDZbOxqsqnZTaH_3oih6MnTDHwPvvnmKJlTyXWqFMjjZA4ALM1Zrk-TsxDeASjNgM-SGRdUqEzPk1qmy9b5rrG7oXEeoyVh7-MGgyUuEIyEbxkl6CsSN0MgvovjYsm2dy32e1LZ2ppInCev6aj_sBUJrrJ9VzYYojOj0rYOz5OTGptgL6a5SF7ubp9XD-n66f5xtVynWy5ZTGsDGasAsAYqKePAQCuBDAzQUkFVl0Ki4jWAzTRVlCklESTkguXGSsoXyc2P73YoW1sZ62OPTTGlLTp0xV_Eu03x1u0Kqr97E6PB9WTQd5-DDbFoXTC2acY7uiEUOhNA87HE_4hc5ZqznP5LpBKkEBkbiZe_sx9CT78a8asJx2CwqXv0xoUDTWWZzqXgX1QonSA</recordid><startdate>19880901</startdate><enddate>19880901</enddate><creator>SUTHERLAND, G. R</creator><creator>BAKER, E</creator><creator>CALLEN, D. F</creator><creator>HYLAND, V. J</creator><creator>MAY, B. K</creator><creator>BAWDEN, M. J</creator><creator>HEALY, H. M</creator><creator>BORTHWICK, I. A</creator><general>University of Chicago Press</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>8BJ</scope><scope>FQK</scope><scope>JBE</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19880901</creationdate><title>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</title><author>SUTHERLAND, G. R ; BAKER, E ; CALLEN, D. F ; HYLAND, V. J ; MAY, B. K ; BAWDEN, M. J ; HEALY, H. M ; BORTHWICK, I. A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p352t-fc082d00af015123020764a20c01b60dfb45a63f00e871612665a0509429ce513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>5-Aminolevulinate Synthetase - genetics</topic><topic>Anemia, Sideroblastic - genetics</topic><topic>Anemias. Hemoglobinopathies</topic><topic>Biological and medical sciences</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Pair 3</topic><topic>Cloning, Molecular</topic><topic>Defects</topic><topic>Diseases of red blood cells</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Nucleic Acid Hybridization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SUTHERLAND, G. R</creatorcontrib><creatorcontrib>BAKER, E</creatorcontrib><creatorcontrib>CALLEN, D. F</creatorcontrib><creatorcontrib>HYLAND, V. J</creatorcontrib><creatorcontrib>MAY, B. K</creatorcontrib><creatorcontrib>BAWDEN, M. J</creatorcontrib><creatorcontrib>HEALY, H. M</creatorcontrib><creatorcontrib>BORTHWICK, I. A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>International Bibliography of the Social Sciences (IBSS)</collection><collection>International Bibliography of the Social Sciences</collection><collection>International Bibliography of the Social Sciences</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of human genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUTHERLAND, G. R</au><au>BAKER, E</au><au>CALLEN, D. F</au><au>HYLAND, V. J</au><au>MAY, B. K</au><au>BAWDEN, M. J</au><au>HEALY, H. M</au><au>BORTHWICK, I. A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia</atitle><jtitle>American journal of human genetics</jtitle><addtitle>Am J Hum Genet</addtitle><date>1988-09-01</date><risdate>1988</risdate><volume>43</volume><issue>3</issue><spage>331</spage><epage>335</epage><pages>331-335</pages><issn>0002-9297</issn><eissn>1537-6605</eissn><coden>AJHGAG</coden><abstract>The gene for 5-aminolevulinate synthase (ALAS) has been mapped to 3pter-3q13.2 by Southern blot hybridization analysis of a mouse/human hybrid cell panel. In situ hybridization maps the gene to 3p21, distal to the common fragile site at 3p14.2 (FRA3B). The mapping of this gene to an autosome makes it improbable that it is the site of the primary defect in X-linked sideroblastic anemia.</abstract><cop>Chicago, IL</cop><pub>University of Chicago Press</pub><pmid>3414687</pmid><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0002-9297
ispartof American journal of human genetics, 1988-09, Vol.43 (3), p.331-335
issn 0002-9297
1537-6605
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1715374
source International Bibliography of the Social Sciences (IBSS); PubMed Central
subjects 5-Aminolevulinate Synthetase - genetics
Anemia, Sideroblastic - genetics
Anemias. Hemoglobinopathies
Biological and medical sciences
Chromosome Mapping
Chromosomes, Human, Pair 3
Cloning, Molecular
Defects
Diseases of red blood cells
Hematologic and hematopoietic diseases
Humans
Medical sciences
Nucleic Acid Hybridization
title 5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T18%3A16%3A10IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=5-Aminolevulinate%20synthase%20is%20at%203p21%20and%20thus%20not%20the%20primary%20defect%20in%20X-linked%20sideroblastic%20anemia&rft.jtitle=American%20journal%20of%20human%20genetics&rft.au=SUTHERLAND,%20G.%20R&rft.date=1988-09-01&rft.volume=43&rft.issue=3&rft.spage=331&rft.epage=335&rft.pages=331-335&rft.issn=0002-9297&rft.eissn=1537-6605&rft.coden=AJHGAG&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E15054482%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p352t-fc082d00af015123020764a20c01b60dfb45a63f00e871612665a0509429ce513%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=15054482&rft_id=info:pmid/3414687&rfr_iscdi=true