Hs06288924_cn

• Gene Symbol: CELF1
• Assay Reference Genome Location: Chr.11:47495138 on build GRCh38
• Cytoband: 11p11.2

Target Gene Details

• Entrez Gene ID: 10658
• Gene Name: CUGBP, Elav-like family member 1
• Gene Aliases: BRUNOL2, CUG-BP, CUGBP, CUGBP1, EDEN-BP, NAB50, NAPOR, hNab50
• Location: Chr.11:47465937-47565569 on Build GRCh38
• Assay Gene Location: Within Intron 7

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CELF1	NM_001172639.1			NP_001166110.1
	NM_006560.3			NP_006551.1
	XM_011519848.2			XP_011518150.1
	XM_011519850.2			XP_011518152.2
	XM_011519852.2			XP_011518154.1
	XM_011519854.1			XP_011518156.1
	XM_011519855.1			XP_011518157.1
	XM_011519856.1			XP_011518158.1
	XM_011519857.1			XP_011518159.1
	XM_011519858.1			XP_011518160.1
	XM_011519859.1			XP_011518161.1
	XM_017017101.1			XP_016872590.1
	XM_017017102.1			XP_016872591.1
	XM_017017103.1			XP_016872592.1
	XM_017017104.1			XP_016872593.1
	XM_017017105.1			XP_016872594.1
	XM_017017106.1			XP_016872595.1
	XM_017017107.1			XP_016872596.1
	XM_017017108.1			XP_016872597.1
	XM_017017109.1			XP_016872598.1
	XM_017017110.1			XP_016872599.1
	XM_017017111.1			XP_016872600.1
	XM_017017112.1			XP_016872601.1
	XM_017017113.1			XP_016872602.1
	XM_017017114.1			XP_016872603.1
	XM_017017115.1			XP_016872604.1
	XM_017017116.1			XP_016872605.1
	XM_017017118.1			XP_016872607.1
	XM_017017119.1			XP_016872608.1
	XM_017017120.1			XP_016872609.1
	XM_017017121.1			XP_016872610.1
	XM_017017122.1			XP_016872611.1
	XM_017017123.1			XP_016872612.1
	XM_017017124.1			XP_016872613.1
	XM_017017125.1			XP_016872614.1
	XM_017017126.1			XP_016872615.1
	XM_017017127.1			XP_016872616.1
	XM_017017128.1			XP_016872617.1
	XM_017017129.1			XP_016872618.1
	XM_017017130.1			XP_016872619.1
	XM_017017131.1			XP_016872620.1
	XM_017017132.1			XP_016872621.1
	XM_017017133.1			XP_016872622.1
	XM_017017134.1			XP_016872623.1
	XM_017017135.1			XP_016872624.1
	AB210019.1
	CB960956.1
	DA217269.1
	DA320861.1
	DB162286.1
	U63289.1			AAC50895.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv832141	Chr.11:47311629 - 47499441 on Build GRCh38	Loss	SLC39A13 SPI1 RAPSN PSMC3 MADD MIR4487 CELF1 MYBPC3

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Gene Ontology Categories:

Process(es)

mRNA splice site selection
mRNA processing
germ cell development
spermatid development
embryo development
RNA interference
negative regulation of translation
positive regulation of multicellular organism growth
regulation of RNA splicing

Function(s)

nucleotide binding
translation repressor activity, nucleic acid binding
RNA binding
mRNA binding
protein binding
translation initiation factor binding
BRE binding
poly(A) RNA binding