Difference between revisions of "DSCAM-AS1"
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==Annotated Information== | ==Annotated Information== | ||
===Approved Symbol=== | ===Approved Symbol=== | ||
− | DSCAM-AS1 | + | DSCAM-AS1 (DSCAM antisense RNA 1) |
− | + | [[File:Characterization of DSCAM-AS1.jpg|right|thumb|400px|'''Characterization of DSCAM-AS1'''<ref name="ref1" />]] | |
− | |||
− | = | ||
− | |||
===Synonyms=== | ===Synonyms=== | ||
M41 | M41 | ||
Line 12: | Line 9: | ||
===RefSeq ID=== | ===RefSeq ID=== | ||
NR_038896 | NR_038896 | ||
− | |||
− | |||
===RefSeq(supplied by NCBI)=== | ===RefSeq(supplied by NCBI)=== | ||
NR_038896 | NR_038896 | ||
Line 20: | Line 15: | ||
===Disease=== | ===Disease=== | ||
breast cancer | breast cancer | ||
+ | ===Characteristics=== | ||
+ | ER preferentially binds to the DSCAM-AS1 promoter in tumours with clinical aggression.<ref name="ref1" /> | ||
+ | |||
+ | ===Function=== | ||
+ | DSCAM-AS1 mediates tumour progression and tamoxifen resistance.<ref name="ref1" /> | ||
+ | DSCAM-AS1 provides oestrogen-independent growth and a proliferative advantage when grown in oestrogen-deprived medium compared to normal serum.<ref name="ref1" /> | ||
+ | |||
+ | ===Regulation=== | ||
+ | hnRNPL is an interacting protein involved in the mechanism of DSCAM-AS1 action.<ref name="ref1" /> | ||
+ | |||
+ | ===Expression=== | ||
+ | DSCAM-AS1 expression is highly enriched in ER-positive tumours.<ref name="ref1" /> | ||
+ | |||
+ | ==Labs working on this lncRNA== | ||
+ | * Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA | ||
+ | * Department of Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan 48109, USA. | ||
+ | |||
+ | ==References== | ||
+ | <references> | ||
+ | <ref name="ref1"> | ||
+ | </ref>(1) | ||
+ | </references> |
Revision as of 02:43, 13 November 2017
Contents
Annotated Information
Approved Symbol
DSCAM-AS1 (DSCAM antisense RNA 1)
Synonyms
M41
Chromosome
21q22.2
RefSeq ID
NR_038896
RefSeq(supplied by NCBI)
NR_038896
pubmed IDs
27666543
Disease
breast cancer
Characteristics
ER preferentially binds to the DSCAM-AS1 promoter in tumours with clinical aggression.[1]
Function
DSCAM-AS1 mediates tumour progression and tamoxifen resistance.[1] DSCAM-AS1 provides oestrogen-independent growth and a proliferative advantage when grown in oestrogen-deprived medium compared to normal serum.[1]
Regulation
hnRNPL is an interacting protein involved in the mechanism of DSCAM-AS1 action.[1]
Expression
DSCAM-AS1 expression is highly enriched in ER-positive tumours.[1]
Labs working on this lncRNA
- Michigan Center for Translational Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA
- Department of Cellular and Molecular Biology, University of Michigan, Ann Arbor, Michigan 48109, USA.