SENCR - smooth muscle and endothelial cell enriched migration/differentiation-associated lncRNA Gene

Homo sapiens

Also known as lncRNA9; FLI1-AS1

Gene ID: 100507392 | Gene type: ncRNA

About SENCR

Cytogenetic location: 11q24.3 Genomic coordinates (GRCh38): 11:128,691,672-128,696,023 (from NCBI)

This gene has 3 transcripts (splice variants). Broad expression in spleen (RPKM 2.6), placenta (RPKM 0.7) and 16 other tissues.

Diseases

Alias

Jacobsen Syndrome

Chromosome 11q Deletion Syndrome	Partial 11q Monosomy Syndrome
Jacobsen Distal 11q Deletion Syndrome	JBS
11q Partial Monosomy Syndrome	Chromosome 11q Deletion
11q Deletion	11q Monosomy
Deletion 11q	Monosomy 11q
Partial Monosomy 11q	11q Deletion Disorder
11q Deletion Syndrome	11q Terminal Deletion Disorder
11q- Deletion Syndrome	11q23 Deletion Disorder
Jacobsen Thrombocytopenia	11q Terminal Deletion Syndrome
Del(11)(Q23.3)	Del(11)(Qter)
Distal Deletion 11q	Distal Monosomy 11q
Monosomy 11qter	Telomeric Deletion 11q
Paris-Trousseau Thrombocytopenia

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