PEX26 - peroxisomal biogenesis factor 26 Gene

Also Known as PBD7A; PBD7B; PEX26M1T; Pex26pM1T

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 55670

About PEX26

Cytogenetic location: 22q11.21 Genomic coordinates (GRCh38): 22:18,077,990-18,105,396 (from NCBI)

This gene has 3 transcripts (splice variants), 179 orthologues and is associated with 7 phenotypes. Ubiquitous expression in colon (RPKM 17.4), small intestine (RPKM 11.2) and 25 other tissues.

Summary

This gene belongs to the peroxin-26 gene family. It is probably required for protein import into peroxisomes. It anchors PEX1 and PEX6 to peroxisome membranes, possibly to form heteromeric AAA ATPase complexes required for the import of proteins into peroxisomes. Defects in this gene are the cause of peroxisome biogenesis disorder complementation group 8 (PBD-CG8). PBD refers to a group of peroxisomal disorders arising from a failure of protein import into the peroxisomal membrane or matrix. The PBD group is comprised of four disorders: Zellweger syndrome (ZWS), neonatal adrenoleukodystrophy (NALD), infantile Refsum disease (IRD), and classical rhizomelic chondrodysplasia punctata (RCDP). Alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Dec 2010]

PEX26 Products (3)

mRNA	Protein	Name
NM_001127649.3	NP_001121121.1	peroxisome assembly protein 26 isoform a
NM_001199319.2	NP_001186248.1	peroxisome assembly protein 26 isoform b
NM_017929.6	NP_060399.1	peroxisome assembly protein 26 isoform a

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	References	Source
enables ATPase binding	IPI IPI: Inferred from physical interaction	16257970	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	15713480	GOA
enables protein-containing complex binding	IDA IDA: Inferred from direct assay	16854980	GOA
enables protein-membrane adaptor activity	IDA IDA: Inferred from direct assay	12717447	GOA

Biological Process GO Annotation	Evidence	References	Source
involved in protein import into peroxisome matrix	IDA IDA: Inferred from direct assay	12717447	GOA
involved in protein import into peroxisome matrix	IMP IMP: Inferred from mutant phenotype	15858711	GOA
involved in protein to membrane docking	IDA IDA: Inferred from direct assay	12717447	GOA

Cellular Component GO Annotation	Evidence	References	Source
is active in peroxisomal membrane	IDA IDA: Inferred from direct assay	12717447	GOA
located in peroxisome	IDA IDA: Inferred from direct assay	15858711	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PEX26 Protein Structure

Pex26

0
100
200
305 a.a.

Protein Preferred Names	Protein Names
peroxisome assembly protein 26	peroxin-26

PEX26 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	PEX26	Q7Z412	ARL16	Homo sapiens	Q0P5N6	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	ARL16	Homo sapiens	Q0P5N6	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ARL16	Homo sapiens	Q0P5N6	Y2H Array	32814053
Intra	PEX26	Q7Z412	FOXR1	Homo sapiens	Q6PIV2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	FOXR1	Homo sapiens	Q6PIV2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	FOXR1	Homo sapiens	Q6PIV2	Y2H Array	32814053
Intra	PEX26	Q7Z412	ASCL4	Homo sapiens	Q6XD76	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ASCL4	Homo sapiens	Q6XD76	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	ASCL4	Homo sapiens	Q6XD76	Y2H Array	32814053
Intra	PEX26	Q7Z412	KRTAP8-1	Homo sapiens	Q8IUC2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	KRTAP8-1	Homo sapiens	Q8IUC2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	KRTAP8-1	Homo sapiens	Q8IUC2	Y2H Array	32814053
Intra	PEX26	Q7Z412	AP2B1	Homo sapiens	P63010-2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	AP2B1	Homo sapiens	P63010-2	Y2H Array	32814053
Intra	PEX26	Q7Z412	AP2B1	Homo sapiens	P63010-2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	KCTD15	Homo sapiens	Q96SI1-2	Y2H Array	32814053
Intra	PEX26	Q7Z412	KCTD15	Homo sapiens	Q96SI1-2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	KCTD15	Homo sapiens	Q96SI1-2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	KRTAP19-1	Homo sapiens	Q8IUB9	Validated Y2H	32814053
Intra	PEX26	Q7Z412	KRTAP19-1	Homo sapiens	Q8IUB9	Y2H Array	32814053
Intra	PEX26	Q7Z412	KRTAP19-1	Homo sapiens	Q8IUB9	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	SASS6	Homo sapiens	Q6UVJ0	Y2H Array	32814053
Intra	PEX26	Q7Z412	SASS6	Homo sapiens	Q6UVJ0	Validated Y2H	32814053
Intra	PEX26	Q7Z412	SASS6	Homo sapiens	Q6UVJ0	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	KLC3	Homo sapiens	Q6P597	Validated Y2H	32814053
Intra	PEX26	Q7Z412	KLC3	Homo sapiens	Q6P597	Y2H Array	32814053
Intra	PEX26	Q7Z412	KLC3	Homo sapiens	Q6P597	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	MKL1	Homo sapiens	A4FUJ8	Validated Y2H	32814053
Intra	PEX26	Q7Z412	MKL1	Homo sapiens	A4FUJ8	Y2H Array	32814053
Intra	PEX26	Q7Z412	MKL1	Homo sapiens	A4FUJ8	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	IQSEC1	Homo sapiens	Q6DN90-2	Y2H Array	32814053
Intra	PEX26	Q7Z412	IQSEC1	Homo sapiens	Q6DN90-2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	IQSEC1	Homo sapiens	Q6DN90-2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ABHD17C	Homo sapiens	Q6PCB6	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ABHD17C	Homo sapiens	Q6PCB6	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	ABHD17C	Homo sapiens	Q6PCB6	Y2H Array	32814053
Intra	PEX26	Q7Z412	MKRN3	Homo sapiens	Q13064	Y2H Array	32814053
Intra	PEX26	Q7Z412	MKRN3	Homo sapiens	Q13064	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	MKRN3	Homo sapiens	Q13064	Validated Y2H	32814053
Intra	PEX26	Q7Z412	RNF112	Homo sapiens	Q9ULX5	Validated Y2H	32814053
Intra	PEX26	Q7Z412	RNF112	Homo sapiens	Q9ULX5	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	RNF112	Homo sapiens	Q9ULX5	Y2H Array	32814053
Intra	PEX26	Q7Z412	LOC642947	Homo sapiens	Q6ZP95	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	LOC642947	Homo sapiens	Q6ZP95	Validated Y2H	32814053
Intra	PEX26	Q7Z412	LOC642947	Homo sapiens	Q6ZP95	Y2H Array	32814053
Intra	PEX26	Q7Z412	LHX5	Homo sapiens	Q9H2C1	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	LHX5	Homo sapiens	Q9H2C1	Validated Y2H	32814053
Intra	PEX26	Q7Z412	LHX5	Homo sapiens	Q9H2C1	Y2H Array	32814053
Intra	PEX26	Q7Z412	ZMAT2	Homo sapiens	Q96NC0	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ZMAT2	Homo sapiens	Q96NC0	Y2H Array	32814053
Intra	PEX26	Q7Z412	ZMAT2	Homo sapiens	Q96NC0	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	MEOX1	Homo sapiens	P50221	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	MEOX1	Homo sapiens	P50221	Validated Y2H	32814053
Intra	PEX26	Q7Z412	MEOX1	Homo sapiens	P50221	Y2H Array	32814053
Intra	PEX26	Q7Z412	NEBL	Homo sapiens	O76041	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	NEBL	Homo sapiens	O76041	Validated Y2H	32814053
Intra	PEX26	Q7Z412	NEBL	Homo sapiens	O76041	Y2H Array	32814053
Intra	PEX26	Q7Z412	HDAC10	Homo sapiens	Q969S8	Validated Y2H	32814053
Intra	PEX26	Q7Z412	HDAC10	Homo sapiens	Q969S8	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	HDAC10	Homo sapiens	Q969S8	Y2H Array	32814053
Intra	PEX26	Q7Z412	COPS3	Homo sapiens	Q9UNS2	Y2H Array	32814053
Intra	PEX26	Q7Z412	COPS3	Homo sapiens	Q9UNS2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	COPS3	Homo sapiens	Q9UNS2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	PFDN5	Homo sapiens	Q99471	Validated Y2H	32814053
Intra	PEX26	Q7Z412	PFDN5	Homo sapiens	Q99471	Y2H Array	32814053
Intra	PEX26	Q7Z412	PFDN5	Homo sapiens	Q99471	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	SKIC8	Homo sapiens	Q9GZS3	Validated Y2H	32814053
Intra	PEX26	Q7Z412	SKIC8	Homo sapiens	Q9GZS3	Y2H Array	32814053
Intra	PEX26	Q7Z412	SKIC8	Homo sapiens	Q9GZS3	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	TP53	Homo sapiens	P04637	Validated Y2H	32814053
Intra	PEX26	Q7Z412	TP53	Homo sapiens	P04637	Y2H Array	32814053
Intra	PEX26	Q7Z412	TP53	Homo sapiens	P04637	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	BMF	Homo sapiens	Q96LC9	Y2H Array	32814053
Intra	PEX26	Q7Z412	BMF	Homo sapiens	Q96LC9	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	BMF	Homo sapiens	Q96LC9	Validated Y2H	32814053
Intra	PEX26	Q7Z412	BIRC5	Homo sapiens	O15392	Validated Y2H	32814053
Intra	PEX26	Q7Z412	BIRC5	Homo sapiens	O15392	Y2H Array	32814053
Intra	PEX26	Q7Z412	BIRC5	Homo sapiens	O15392	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	PEX19	Homo sapiens	P40855	Y2H Prey Pooling	32296183
Intra	PEX26	Q7Z412	PEX19	Homo sapiens	P40855	Y2H Array	32296183
Intra	PEX26	Q7Z412	ZNG1C	Homo sapiens	Q5JTY5	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	ZNG1C	Homo sapiens	Q5JTY5	Validated Y2H	32814053
Intra	PEX26	Q7Z412	ZNG1C	Homo sapiens	Q5JTY5	Y2H Array	32814053
Intra	PEX26	Q7Z412	SUFU	Homo sapiens	Q9UMX1	Pull Down	16189514
Intra	PEX26	Q7Z412	BBLN	Homo sapiens	Q9BUW7	Y2H Array	32814053
Intra	PEX26	Q7Z412	BBLN	Homo sapiens	Q9BUW7	Validated Y2H	32814053
Intra	PEX26	Q7Z412	BBLN	Homo sapiens	Q9BUW7	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	DAXX	Homo sapiens	Q9UER7	Y2H Array	32814053
Intra	PEX26	Q7Z412	DAXX	Homo sapiens	Q9UER7	Validated Y2H	32814053
Intra	PEX26	Q7Z412	DAXX	Homo sapiens	Q9UER7	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	E2F8	Homo sapiens	A0AVK6	Validated Y2H	32814053
Intra	PEX26	Q7Z412	E2F8	Homo sapiens	A0AVK6	Y2H Array	32814053
Intra	PEX26	Q7Z412	E2F8	Homo sapiens	A0AVK6	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	q7z783_human	Homo sapiens	Q7Z783	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	q7z783_human	Homo sapiens	Q7Z783	Validated Y2H	32814053
Intra	PEX26	Q7Z412	q7z783_human	Homo sapiens	Q7Z783	Y2H Array	32814053
Intra	PEX26	Q7Z412	MSRB2	Homo sapiens	Q9Y3D2	Validated Y2H	32814053
Intra	PEX26	Q7Z412	MSRB2	Homo sapiens	Q9Y3D2	Y2H Pooling	32814053
Intra	PEX26	Q7Z412	MSRB2	Homo sapiens	Q9Y3D2	Y2H Array	32814053

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Peroxisome Biogenesis Disorder 7a	PBD7A Peroxisome Biogenesis Disorder Complementation Group 8 PBD-CG8 Cg8 Pbd-Cga Peroxisome Biogenesis Disorder Complementation Group A Peroxisome Biogenesis Disorder, Type 7a
Peroxisome Biogenesis Disorder 7b	PBD7B Peroxisome Biogenesis Disorder, Type 7b
Peroxisome Biogenesis Disorder 1b	Peroxisome Biogenesis Disorder Infantile Refsum Disease Infantile Phytanic Acid Storage Disease PBD1B Refsum Disease, Infantile Adrenoleukodystrophy, Autosomal Neonatal Ird Mild Pbd-Zsd Mild Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder Pbd-Zsd Peroxisome Biogenesis Disorder Spectrum Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder Autosomal Neonatal Adrenoleukodystrophy Refsum Disease Infantile Peroxisome Biogenesis Disorders Peroxisome Biogenesis Disorder, Type 1b
Neonatal Adrenoleukodystrophy	Nald Adrenoleukodystrophy Autosomal Neonatal Form Intermediate Pbd-Zsd Intermediate Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder Adrenoleukodystrophy, Autosomal, Neonatal Form Adrenoleukodystrophy Neonatal Adrenoleukodystrophy, Neonatal
Zellweger Spectrum Disorder	Zsd Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum Zellweger Spectrum Cerebrohepatorenal Syndrome Pbd, Zss Pbd-Zsd Zellweger Syndrome Spectrum Zellweger Syndrome
Zellweger Syndrome	Cerebrohepatorenal Syndrome Zellweger Leukodystrophy Zs Congenital Iron Overload Chr Zws Severe Pbd-Zsd Severe Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder
Rhizomelic Chondrodysplasia Punctata	Chondrodysplasia Punctata, Rhizomelic Rcdp Chondrodysplasia Punctata, Rhizomelic Form Rcp Chondrodysplasia Punctata Rhizomelic
Adrenoleukodystrophy	X-Linked Adrenoleukodystrophy ALD Siemerling-Creutzfeldt Disease X-Ald X-Linked Cerebral Adrenoleukodystrophy Bronze Schilder Disease Melanodermic Leukodystrophy Addison Disease And Cerebral Sclerosis Adrenomyeloneuropathy, Adult Diffuse Sclerosis X-Cald Adrenomyeloneuropathy Encephalitis Periaxialis Concentrica Encephalitis Periaxialis, Schilder'S Sudanophilic Cerebral Sclerosis Ald Childhood Cerebral Form Adrenoleukodystrophy X-Linked Cerebral Form Adrenoleukodystrophy Childhood Cerebral Form Childhood Cerebral Ald Schilder Disease X-Linked Ald Adrenoleukodystrophy, X-Linked Amn Diffuse Cerebral Sclerosis Of Schilder Systemic Scleroderma Balo'S Concentric Sclerosis Ald - [Adrenoleukodystrophy] Addison-Schilder
Peroxisomal Biogenesis Disorder	Zellweger Spectrum Disorders Peroxisome Biogenesis Disorder-Zellweger Syndrome Spectrum Disorders Of Peroxisome Biogenesis Zellweger Spectrum Zellweger Syndrome Spectrum Peroxisomal Biogenesis Disorders Pbd, Zss Pbd-Zsd Pbd-Zss Pbd-Zellweger Spectrum Disorder Peroxisomal Biogenesis Disorders, Zellweger Syndrome Spectrum Peroxisome Biogenesis Disorder Peroxisome Biogenesis Disorder Spectrum Peroxisome Biogenesis Disorders Zellweger Spectrum Disorder Hyperpipecolic Acidaemia
Deafness, Autosomal Recessive 59	DFNB59 Autosomal Recessive Nonsyndromic Deafness 59 Autosomal Recessive Deafness 59 Deafness, Autosomal Recessive, 59 Dfnb59 Auditory Neuropathy Deafness, Autosomal Recessive, Type 59
Refsum Disease, Classic	Refsum Disease Heredopathia Atactica Polyneuritiformis Phytanic Acid Oxidase Deficiency Hmsn Iv Refsum Disease, Adult, 1 Refsum'S Disease Phytanic Acid Storage Disease Hereditary Motor And Sensory Neuropathy Iv Hmsn4 Hmsn Type Iv Hmsn 4 Adult Refsum Disease Classic Refsum Disease Hereditary Motor And Sensory Neuropathy Type Iv Refsum Syndrome Hsmn Iv Disorder Of Cornification 11 Doc 11 Hereditary Sensory And Motor Neuropathy Type 4 Hypertrophic Neuropathy Of Refsum Ard Crd Hereditary Motor And Sensory Neuropathy Type 4 Phytanic-Coa Hydroxylase Deficiency RD
Linear Skin Defects With Multiple Congenital Anomalies 1	Midas Syndrome Mcops7 Mls Syndrome Microphthalmia, Syndromic 7 Microphthalmia With Linear Skin Defects Syndrome Microphthalmia With Linear Skin Defects Microphthalmia-Dermal Aplasia-Sclerocornea Syndrome Syndromic Microphthalmia Type 7 LSDMCA1 Mls Microphthalmia, Dermal Aplasia, And Sclerocornea Microphthalmia With Linear Skin Defect Syndrome Syndromic Microphthalmia 7 Linear Skin Defects With Multiple Congenital Anomalies Microphthalmia, Dermal Aplasia, Sclerocornea Syndrome Microphthalmia Dermal Aplasia And Sclerocornea Syndrome Micropthalmia Syndromic 7 Microphthalmia Syndromic 7 Microphthalmia With Linear Skin Lesions Syndrome Syndromic Microphthalmia-7 Microphthalmia, Dermal Aplasia And Sclerocornea Microphthalmia, Syndromic, 7 Midas
Peroxisomal Disease	Peroxisomal Disorder Peroxisomal Disorders Peroxisomal Defects
Deafness, Autosomal Dominant 59	DFNA59 Autosomal Dominant Nonsyndromic Deafness 59 Autosomal Dominant Deafness 59
Chondrodysplasia Punctata Syndrome	Chondrodysplasia Punctata Chondrodysplasia Punctata Congenita Toriello Higgins Miller Syndrome Chondrodysplasia Punctata, Toriello Type Toriello-Higgins-Miller Syndrome Cdp Chondrodysplasia Punctata, X-Linked Dominant Type Chondrodysplasia Punctata Group Dysplasia Punctata Epiphysis Dysplasia Punctata Dysplasia Epiphysealis Punctata Chondrodystrophy Of Punctata
Chromosome 17q12 Deletion Syndrome	17q12 Microdeletion Syndrome Del(17)(Q12) Monosomy 17q12
Albinism, Ocular, With Late-Onset Sensorineural Deafness	Ocular Albinism With Sensorineural Deafness OASD Deafness And Ocular Albinism Ocular Albinism With Late-Onset Sensorineural Deafness Albinism, Ocular, With Sensorineural Deafness Autosomal Recessive Waardenburg Syndrome Type 2 With Ocular Albinism Digenic Waardenburg Syndrome/Albinism Digenic Waardenburg Syndrome/Ocular Albinism Ws2-Oa Albinism Ocular Late Onset Sensorineural Deafness Ocular Albinism With Late-Onset Sensorineural Hearing Loss Waardenburg Syndrome/Ocular Albinism, Digenic Waardenburg Syndrome/Albinism, Digenic Ocular Albinism And Sensorineural Deafness
Alpha-Methylacyl-Coa Racemase Deficiency	Amacr Deficiency AMACRD
Fraser Syndrome 1	Fraser Syndrome Cryptophthalmos With Other Malformations Cryptophthalmos Syndrome FRASRS1 Cryptophthalmos-Syndactyly Syndrome Fraser-Francois Syndrome Cyclopism Meyer-Schwickerath'S Syndrome Ulrich-Feichtiger Syndrome Cryptophthalmos Syndactyly Syndrome Fraser'S Syndrome Meyer-Schwickerath Syndrome Ullrich-Feichtiger Syndrome
Sensorineural Hearing Loss	Sensory Hearing Loss Sensorineural Deafness Sensorineural Hearing Loss Disorder Hearing Loss, Sensorineural Central Hearing Loss High Frequency Deafness High Frequency Hearing Loss High-Frequency Hearing Loss Perceptive Deafness Perceptive Hearing Loss Perceptive Hearing Loss Or Deafness Hearing Loss Sensorineural Deafness Sensorineural Hearing Loss High-Frequency Hearing Loss, Central Hearing Loss, High-Frequency
Cornelia De Lange Syndrome 1	De Lange Syndrome CDLS1 Cdl Cdls Typus Degenerativus Amstelodamensis Brachmann-De Lange Syndrome Bdls Amstelodamensis Typus Degenerativus Cornelia De Lange Syndrome, Type 1
Cerebral Degeneration	Brain Degeneration Degenerative Brain Disorder
Leukodystrophy	Leukodystrophies
Fundus Dystrophy	Retinal Dystrophy Retinal Dystrophies Dystrophy, Retinal
Retinitis Pigmentosa	RP Rod-Cone Dystrophy Autosomal Recessive Retinitis Pigmentosa Non-Syndromic Retinitis Pigmentosa Pericentral Pigmentary Retinopathy Pigmentary Retinopathy Tapetoretinal Degeneration Rcd Retinitis Pigmentosa Autosomal Recessive ARRP Retinitis Pigmentosa, Autosomal Recessive Retinitis Pigmentosa 1

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS10349	PEX26 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	PEX26	RGD	RGD:1584998
Felis catus	PEX26	VGNC	VGNC:64115
Bos taurus	PEX26	VGNC	VGNC:32759
Mus musculus	PEX26	MGD	MGI:1921293
Canis familiaris	PEX26	VGNC	VGNC:44433
Macaca mulatta	PEX26	VGNC	VGNC:97122
Others	PEX26	NCBI