PAXX - PAXX non-homologous end joining factor Gene

Homo sapiens

Also known as XLS; C9orf142

Gene ID: 286257 | Gene type: protein coding

About PAXX

Cytogenetic location: 9q34.3 Genomic coordinates (GRCh38): 9:136,992,422-136,993,976 (from NCBI)

This gene has 8 transcripts (splice variants) and 135 orthologues. Ubiquitous expression in spleen (RPKM 25.7), lymph node (RPKM 14.9) and 25 other tissues.

Summary

The protein encoded by this gene plays a role in the nonhomologous end joining (NHEJ) pathway of DNA double-strand break repair. The encoded protein may function to stabilize the Ku70/Ku80 heterodimer to facilitate the assembly and maintain the stability of the NHEJ complex. [provided by RefSeq, Jul 2016]

PAXX Products(2)

mRNA	Protein	Name
NM_001329678.2	NP_001316607.1	protein PAXX isoform 1
NM_183241.3	NP_899064.1	protein PAXX isoform 2

PAXX Protein Structure

PAXX

0
100
204 a.a.

Protein Preferred Names

Protein Names

protein PAXX

XRCC4-like small protein

Related Diseases

Diseases

Alias

Severe Combined Immunodeficiency With Sensitivity To Ionizing Radiation

Severe Combined Immunodeficiency, Athabascan Type	Severe Combined Immunodeficiency Due To Dclre1c Deficiency
Rs-Scid	Scid, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Positive, With Sensitivity To Ionizing Radiation
Scid Due To Artemis Deficiency	Scid Due To Dclre1c Deficiency
Scid, Athabascan Type	Scid, Athabaskan Type
Severe Combined Immunodeficiency Due To Artemis Deficiency	Severe Combined Immunodeficiency, Athabaskan Type
SCIDA	Severe Combined Immunodeficiency, Athabascan-Type
Artemis Deficiency	Severe Combined Immunodeficiency Athabaskan Type
Severe Combined Immunodeficiency Autosomal Recessive T-Cell-Negative/B-Cell-Negative/Nk-Cell-Positive With Sensitivity To Ionizing Radiation	RSSCID
Athabascan Scid	Immunodeficiency, Severe Combined, Athabascan Type
Severe Combined Immunodeficiency, Athabaskan-Type

Lig4 Syndrome

Dna Ligase Iv Deficiency	Ligase 4 Syndrome
LIG4S

Developmental And Epileptic Encephalopathy 54

DEE54	Epileptic Encephalopathy, Early Infantile, 54
Eiee54	Developmental And Epileptic Encephalopathy, 54
Early Infantile Epileptic Encephalopathy 54	Encephalopathy, Epileptic, Early Infantile, Type 54

Immunodeficiency With Hyper-Igm, Type 5

HIGM5	Hyper-Igm Syndrome 5
Immunodeficiency With Hyper Igm Type 5	Hyper-Igm Syndrome Type 5
Hyper-Igm Syndrome Due To Ung Deficiency	Hyper-Igm Syndrome Due To Uracil N-Glycosylase
Immunodeficiency With Hyper Igm, Type 5	Hyper Igm Syndrome 5
Immunodeficiency With Hyper-Igm 5	Hyper-Igm Immunodeficiency Type 5
Immunodeficiency, With Hyper Igm, Type 5	Hyper-Igm Immunodeficiency Syndrome, Type 5

Seckel Syndrome

Microcephalic Primordial Dwarfism	Bird-Headed Dwarfism
Harper'S Syndrome	Virchow-Seckel Dwarfism
Nanocephalic Dwarfism	Sckl
Seckel-Type Dwarfism

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS10099	PAXX Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	PAXX	RGD	RGD:1306215
Canis familiaris	PAXX	VGNC	VGNC:44283
Bos taurus	PAXX	VGNC	VGNC:32603
Macaca mulatta	PAXX	VGNC	VGNC:75686
Mus musculus	PAXX	MGD	MGI:2442831
Felis catus	PAXX	VGNC	VGNC:64052