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Search references for PSTPIP1. Phrases containing PSTPIP1
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Enzyme found in humans
phosphatase-interacting protein 1 is an enzyme that in humans is encoded by the PSTPIP1 gene. PSTPIP1 has been shown to interact with: Abl gene BZW1 CD2 PTPN12 PTPN18
PSTPIP1
Inflammatory skin disease with painful pustules and ulcers
mutations in the proline-serine-threonine phosphatase-interacting 1 gene (PSTPIP1). Though the cause is not well understood, the disease is thought to be
Pyoderma_gangrenosum
Medical condition
NOD2 Pyogenic sterile arthritis, pyoderma gangrenosum, acne (PAPA) 604416 PSTPIP1 Deficiency of the interleukin-1–receptor antagonist (DIRA) 612852 IL1RN
Periodic_fever_syndrome
Human protein-coding gene on chromosome 9
EPHB2, GPX1, GRB10, MTOR, GRB2, MDM2, NCK1, NEDD9, NTRK1, P73, PAG1, PAK2, PSTPIP1, RAD9A, RAD51, RB1, RFX1, RYBP, SHC1, SORBS2, SPTA1, SPTAN1, TERF1, VAV1
Tyrosine-protein_kinase_ABL1
Cell adhesion molecule found on the surface of T cells and natural killer
extracellular portion. CD2 has been shown to interact with CD2BP2, Lck and PSTPIP1. GRCh38: Ensembl release 89: ENSG00000116824 – Ensembl, May 2017 GRCm38:
CD2
Mammalian protein found in humans
with: CDC42, CRKL, EGFR, FGR, FYN, Grb2, ITK ITSN2, NCK1, PIK3R1, PLCG1, PSTPIP1, Src, TRIP10, and WIPF1. Wiskott–Aldrich syndrome-like cortactin GRCh38:
Wiskott–Aldrich syndrome protein
Wiskott–Aldrich_syndrome_protein
Genetic disorder in humans
M, Mansfield E, Hull KM, Wood G, Wise CA, Kastner DL. Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome
PAPA_syndrome
Protein-coding gene in the species Homo sapiens
cytoskeleton and cell adhesion molecules, such as p130 (Cas), CAKbeta/PTK2B, PSTPIP1, and paxillin, which suggested its regulatory roles in controlling cell
PTPN12
Protein-coding gene in the species Homo sapiens
PTP has not yet been determined. PTPN18 has been shown to interact with PSTPIP1. GRCh38: Ensembl release 89: ENSG00000072135 – Ensembl, May 2017 GRCm38:
PTPN18
PPARG Köbberling–Dunnigan syndrome PRKAR1 Protein kinase A Carney complex PSTPIP1 CD2 binding protein 1 PAPA syndrome PTCH Patched Nevoid basal cell carcinoma
List of genes mutated in cutaneous conditions
List_of_genes_mutated_in_cutaneous_conditions
Protein
Wiskott-Aldrich syndrome protein acts downstream of CD2 and the CD2AP and PSTPIP1 adaptors to promote formation of the immunological synapse". Immunity.
CD2AP
Protein-coding gene in the species Homo sapiens
encephalitis are associated with BZW1. BZW1 has been shown to interact with PSTPIP1 and CDC5L. GRCh38: Ensembl release 89: ENSG00000082153 – Ensembl, May 2017
BZW1
Protein-coding gene in the species Homo sapiens
to interact with: BZW1 EIF2S2 PSTPIP1 NEK4 ORF4 SNW1 rep EIF2S2 and ORF4 work to synthesize and replicate BZW2. PSTPIP1 and NEK4 are regulatory proteins
Basic leucine zipper and W2 domain-containing protein 2
Basic_leucine_zipper_and_W2_domain-containing_protein_2
O60542 13068 PSRC1 HGNC:24472; Q6PGN9 13069 PSTK HGNC:28578; Q8IV42 13070 PSTPIP1 HGNC:9580; O43586 13071 PSTPIP2 HGNC:9581; Q9H939 13072 PTAFR HGNC:9582;
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
MYD88 Pyogenic sterile arthritis, pyoderma gangrenosum, and acne; 604416; PSTPIP1 Pyridoxamine 5'-phosphate oxidase deficiency; 610090; PNPO Pyropoikilocytosis;
List_of_OMIM_disorder_codes
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