NEXMIF

gene product

KIAA2022, KIDLIA, MRX98, XPN

An inversion on the X chromosome which disrupts this gene and a G-protein coupled purinergic receptor gene located in the pseudoautosomal region of the X chromosome has been linked to X linked cognitive disability. [provided by RefSeq, Mar 2009]

Ensembl	UniProt	RefSeq	Entrez
ENST00000055682 ENSP00000055682	Q5QGS0.128 Q5QGS0	NP_001008537.1 NP_001008537	NEXMIF 340533
ENST00000616200 ENSP00000480284	Q5QGS0.128 Q5QGS0		NEXMIF 340533
ENST00000642681 ENSP00000495800	A0A2R8YEQ5		NEXMIF 340533

Ensembl	UniProt	RefSeq	Entrez
ENSMUST00000056502 ENSMUSP00000049716	Q5DTT1.106 Q5DTT1 Q003Y7		Nexmif 245555
ENSMUST00000087879 ENSMUSP00000085187	Q5DTT1.106 Q5DTT1	NP_001070822.2 NP_001070822	Nexmif 245555
ENSMUST00000118314 ENSMUSP00000113625	Q5DTT1.106 Q5DTT1 Q003Y7		Nexmif 245555

More gene data

Antibodies

Enhanced validation

Supportive data in Antibodypedia

Data presented on provider website

Data in Antibodypedia (inconclusive)

Recommended by provider

21 antibodies from 8 providers.

Show Additional Columns

	Antibody	Type
Biorbyt 13 antibodies
	orb312211	Polyclonal
	orb183262	Polyclonal

antibodies-online 1 antibody
	ABIN4328778	Polyclonal

Atlas Antibodies 1 antibody
	HPA000407	Polyclonal

Invitrogen Antibodies 1 antibody
	PA5-51383	Polyclonal

Novus Biologicals 1 antibody
	NBP2-14156	Polyclonal

Creative Diagnostics 2 antibodies
	DCABH-200802	Monoclonal
	DPABH-02926	Polyclonal

MilliporeSigma / Merck KGaA 1 antibody
	HPA000404	Polyclonal

Abnova Corporation 1 antibody
	H00340533-K	Monoclonal

NEXMIF

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