Hs04287166_cn

• Gene Symbol: ABLIM2
• Assay Reference Genome Location: Chr.4:7972142 on build GRCh38
• Cytoband: 4p16.1

Target Gene Details

• Entrez Gene ID: 84448
• Gene Name: actin binding LIM protein family member 2
• Gene Aliases: -
• Location: Chr.4:7965310-8158832 on Build GRCh38
• Assay Gene Location: Within Intron 24

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ABLIM2	NM_001130083.1			NP_001123555.1
	NM_001130084.1			NP_001123556.1
	NM_001130085.1			NP_001123557.1
	NM_001130086.1			NP_001123558.1
	NM_001130087.1			NP_001123559.1
	NM_001286688.1			NP_001273617.1
	NM_032432.4			NP_115808.3
	XM_005248014.4			XP_005248071.1
	XM_005248017.4			XP_005248074.1
	XM_005248018.4			XP_005248075.1
	XM_005248019.4			XP_005248076.1
	XM_005248020.4			XP_005248077.1
	XM_005248021.4			XP_005248078.1
	XM_005248022.4			XP_005248079.1
	XM_005248023.4			XP_005248080.1
	XM_005248024.4			XP_005248081.1
	XM_005248027.4			XP_005248084.1
	XM_005248028.4			XP_005248085.1
	XM_005248029.4			XP_005248086.1
	XM_005248030.4			XP_005248087.1
	XM_006713923.3			XP_006713986.1
	XM_006713924.3			XP_006713987.1
	XM_006713925.3			XP_006713988.1
	XM_006713927.3			XP_006713990.1
	XM_011513586.2			XP_011511888.1
	XM_017008706.1			XP_016864195.1
	XM_017008707.1			XP_016864196.1
	XM_017008708.1			XP_016864197.1
	XM_017008709.1			XP_016864198.1
	XM_017008710.1			XP_016864199.1
	XM_017008711.1			XP_016864200.1
	XM_017008712.1			XP_016864201.1
	XM_017008713.1			XP_016864202.1
	XM_017008714.1			XP_016864203.1
	XM_017008715.1			XP_016864204.1
	XM_017008716.1			XP_016864205.1
	XM_017008717.1			XP_016864206.1
	XM_017008718.1			XP_016864207.1
	XM_017008719.1			XP_016864208.1
	XM_017008720.1			XP_016864209.1
	XM_017008721.1			XP_016864210.1
	XM_017008722.1			XP_016864211.1
	XM_017008724.1			XP_016864213.1
	XM_017008726.1			XP_016864215.1
	XM_017008727.1			XP_016864216.1
	AB058711.1			BAB47437.1
	AJ748600.1			CAG38375.1
	AJ748601.1			CAG38376.1
	AK094754.1			BAC04414.1
	AK094798.1			BAC04427.1
	AK097003.1
	AK301060.1
	AL834195.1			CAD38885.2
	BC122567.1
	DQ413176.1
	DQ413177.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv34140	Chr.4:7786209 - 8170764 on Build GRCh38	Loss	LOC389199 AFAP1 MIR95 ABLIM2
nsv593622	Chr.4:7970145 - 7973020 on Build GRCh38	Loss	ABLIM2
esv3599538	Chr.4:7968979 - 7973413 on Build GRCh38	Loss	ABLIM2
esv23700	Chr.4:7969526 - 7973205 on Build GRCh38	Loss	ABLIM2
nsv469779	Chr.4:7963526 - 8175919 on Build GRCh38	Loss	MIR95 ABLIM2
nsv829851	Chr.4:7956971 - 8047333 on Build GRCh38	Loss	MIR95 ABLIM2
esv2677688	Chr.4:7968883 - 7973420 on Build GRCh38	Deletion	ABLIM2
esv3563370	Chr.4:7968772 - 7973372 on Build GRCh38	Deletion	ABLIM2

More Information

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

Panther Classification:

Molecular Function -

actin or actin-binding cytoskeletal protein

Gene Ontology Categories:

Process(es)

transcription, DNA-templated
actin cytoskeleton organization

Function(s)

actin binding
zinc ion binding