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RANBP9

RANBP9

Protein-coding gene in the species Homo sapiens

Ran-binding protein 9 is a protein that in humans is encoded by the RANBP9 gene. This gene encodes a protein that binds RAN, a small GTP binding protein

RANBP9

Androgen receptor

Mammalian protein found in humans

NCOA6, NCOR2, NONO, p300, PA2G4, PAK6, PATZ1, PIAS2, PRPF6, PTEN, RAD9A, RANBP9, RCHY1, Retinoblastoma protein, RNF14, RNF4, SART3, SIRT1, SMAD3, Small

Androgen receptor

Androgen_receptor

Skraban–Deardorff syndrome

Rare genetic disorder

helps stabilize a protein called Ran-binding protein 9 (RANBP9; green components in the image). RANBP9 brings the CTLH complex to DNA regions (chromatin),

Skraban–Deardorff syndrome

Skraban–Deardorff_syndrome

Glucocorticoid receptor

Receptor to which cortisol and other glucocorticoids bind

Mineralocorticoid receptor, NRIP1, NCOR1, NCOA1, NCOA2, NCOA3, POU2F1, RANBP9, RELA, SMAD3, SMARCD1, SMARCA4 STAT3, STAT5B, Thioredoxin, TRIM28, and YWHAH

Glucocorticoid receptor

Glucocorticoid_receptor

Hepatocyte growth factor receptor

Mammalian protein found in Homo sapiens

with: CDH1, Cbl gene, GLMN, Grb2, Hepatocyte growth factor, PTPmu, and RANBP9 c-Met inhibitors Tpr-met fusion protein GRCh38: Ensembl release 89: ENSG00000105976

Hepatocyte growth factor receptor

Hepatocyte_growth_factor_receptor

S100A7

Protein-coding gene in the species Homo sapiens

interact with COP9 constitutive photomorphogenic homolog subunit 5, FABP5 and RANBP9. S100A7 interacts with RAGE (receptor of advanced glycated end products)

S100A7

USP11

Protein-coding gene in the species Homo sapiens

gene cluster on chromosome Xp11.23 USP11 has been shown to interact with RANBP9. GRCh38: Ensembl release 89: ENSG00000102226 – Ensembl, May 2017 GRCm38:

USP11

List of human protein-coding genes 6

Q9H6Z4 13401 RANBP3L HGNC:26353; Q86VV4 13402 RANBP6 HGNC:9851; O60518 13403 RANBP9 HGNC:13727; Q96S59 13404 RANBP10 HGNC:29285; Q6VN20 13405 RANBP17 HGNC:14428;

List of human protein-coding genes 6

List_of_human_protein-coding_genes_6

DYRK1B

Protein-coding gene in the species Homo sapiens

the catalytic domain. DYRK1B has been shown to interact with: PCBD1 and RANBP9. One lone missense mutation in Dyrk1B gene (R102C) was found associated

DYRK1B

DISC1

Protein-coding gene in the species Homo sapiens

locus for schizophrenia. Other interactions include: ACTN2, CEP63, EIF3A, RANBP9, and SPTBN4. Aberrations of DISC1 are considered a generalized risk factor

DISC1