RBM10 - RNA binding motif protein 10 Gene

Also Known as S1-1; TARPS; GPATC9; ZRANB5; GPATCH9; DXS8237E; MINAS-60

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8241

About RBM10

Cytogenetic location: Xp11.3 Genomic coordinates (GRCh38): X:47,145,221-47,186,813 (from NCBI)

This gene has 6 transcripts (splice variants), 186 orthologues, 2 paralogues and is associated with 102 phenotypes. Ubiquitous expression in ovary (RPKM 15.6), spleen (RPKM 12.3) and 25 other tissues.

Summary

This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]

RBM10 Products (5)

mRNA Protein Name
NM_001204466.2 NP_001191395.1 RNA-binding protein 10 isoform 3
NM_001204467.2 NP_001191396.1 RNA-binding protein 10 isoform 4
NM_001204468.2 NP_001191397.1 RNA-binding protein 10 isoform 5
NM_005676.5 NP_005667.2 RNA-binding protein 10 isoform 1
NM_152856.3 NP_690595.1 RNA-binding protein 10 isoform 2
Molecular Function GO Annotation Evidence References Source
enables identical protein binding IPI
IPI: Inferred from physical interaction
22365833 GOA
enables miRNA binding IDA
IDA: Inferred from direct assay
28431233 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22365833 GOA
Biological Process GO Annotation Evidence References Source
involved in negative regulation of ribosomal large subunit export from nucleus IDA
IDA: Inferred from direct assay
35393574 GOA
Cellular Component GO Annotation Evidence References Source
is active in nucleolus IDA
IDA: Inferred from direct assay
35393574 GOA
located in nucleus IDA
IDA: Inferred from direct assay
28091594 GOA
part of protein-containing complex IPI
IPI: Inferred from physical interaction
17707232 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

RBM10 Protein Structure

(131 - 201)

zf-RanBP

zf-RanBP: Zn-finger in Ran binding protein and others (215 - 241)

(302 - 378)

G-patch

G-patch: G-patch domain (859 - 902)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 930 a.a.
Protein Preferred Names Protein Names

RNA-binding protein 10

  • G-patch domain containing 9

RBM10 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RBM10 P98175 BEND7 Homo sapiens Q8N7W2-2 32296183
Intra
RBM10 P98175 BEND7 Homo sapiens Q8N7W2-2 32296183
Intra
RBM10 P98175 BEND7 Homo sapiens Q8N7W2-2 32296183
Intra
RBM10 P98175 SF3A1 Homo sapiens Q15459 22365833
Intra
RBM10 P98175 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
RBM10 P98175 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
RBM10 P98175 PATZ1 Homo sapiens Q9HBE1-4 32296183
Intra
RBM10 P98175 ZNF526 Homo sapiens Q8TF50 32296183
Intra
RBM10 P98175 ZNF526 Homo sapiens Q8TF50 32296183
Intra
RBM10 P98175 ZNF526 Homo sapiens Q8TF50 32296183
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 32296183
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 26871637
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 32296183
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 26871637
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 32296183
Intra
RBM10 P98175 CPSF7 Homo sapiens Q8N684-3 26871637
Intra
RBM10 P98175 ZNF317 Homo sapiens Q96PQ6 32296183
Intra
RBM10 P98175 ZNF317 Homo sapiens Q96PQ6 32296183
Intra
RBM10 P98175 ZNF317 Homo sapiens Q96PQ6 32296183
Intra
RBM10 P98175 PTBP2 Homo sapiens Q9UKA9-2 26871637
Intra
RBM10 P98175 PTBP2 Homo sapiens Q9UKA9-2 26871637
Intra
RBM10 P98175 PTBP2 Homo sapiens Q9UKA9-2 26871637
Intra
RBM10 P98175 DHX15 Homo sapiens O43143
Y2H
22365833
Intra
RBM10 P98175 DHX15 Homo sapiens O43143 22365833
Intra
RBM10 P98175 PRR20E Homo sapiens P86478 26871637
Intra
RBM10 P98175 PRR20E Homo sapiens P86478 26871637
Intra
RBM10 P98175 PRR20E Homo sapiens P86478 26871637
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599-3 26871637
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599-3 26871637
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599-3 26871637
Intra
RBM10 P98175 MEOX2 Homo sapiens Q6FHY5 26871637
Intra
RBM10 P98175 MEOX2 Homo sapiens Q6FHY5 26871637
Intra
RBM10 P98175 MEOX2 Homo sapiens Q6FHY5 26871637
Intra
RBM10 P98175 ZNF275 Homo sapiens Q9NSD4 32296183
Intra
RBM10 P98175 ZNF275 Homo sapiens Q9NSD4 32296183
Intra
RBM10 P98175 ZNF275 Homo sapiens Q9NSD4 32296183
Intra
RBM10 P98175 SUGP1 Homo sapiens Q8IWZ8
Y2H
22365833
Intra
RBM10 P98175 CBLL1 Homo sapiens Q75N03 26871637
Intra
RBM10 P98175 CBLL1 Homo sapiens Q75N03 26871637
Intra
RBM10 P98175 CBLL1 Homo sapiens Q75N03 26871637
Intra
RBM10 P98175 U2SURP Homo sapiens O15042 22365833
Intra
RBM10 P98175 U2SURP Homo sapiens O15042
Y2H
22365833
Intra
RBM10 P98175 ZNF408 Homo sapiens Q9H9D4 32296183
Intra
RBM10 P98175 ZNF408 Homo sapiens Q9H9D4 32296183
Intra
RBM10 P98175 ZNF408 Homo sapiens Q9H9D4 32296183
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427
Y2H
22365833
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 26871637
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 32296183
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 26871637
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 26871637
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 32296183
Intra
RBM10 P98175 SF3B4 Homo sapiens Q15427 32296183
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599 26871637
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599 26871637
Intra
RBM10 P98175 PTBP1 Homo sapiens P26599 26871637
Intra
RBM10 P98175 CCAR1 Homo sapiens Q8IX12
Y2H
22365833
Intra
RBM10 P98175 CCAR1 Homo sapiens Q8IX12 35271311
Intra
RBM10 P98175 TARDBP Homo sapiens Q13148 32814053
Intra
RBM10 P98175 TARDBP Homo sapiens Q13148 32814053
Intra
RBM10 P98175 TARDBP Homo sapiens Q13148 32814053
Intra
RBM10 P98175 PRPF19 Homo sapiens Q9UMS4 22365833
Intra
RBM10 P98175 PRPF19 Homo sapiens Q9UMS4
Y2H
22365833
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 26871637
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 26871637
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 26871637
Intra
RBM10 P98175 PRDM14 Homo sapiens Q9GZV8 32296183
Intra
RBM10 P98175 ZFP64 Homo sapiens Q9NTW7 26871637
Intra
RBM10 P98175 ZFP64 Homo sapiens Q9NTW7 26871637
Intra
RBM10 P98175 ZFP64 Homo sapiens Q9NTW7 26871637
Intra
RBM10 P98175 TLE5 Homo sapiens Q08117 25416956
Intra
RBM10 P98175 MBD6 Homo sapiens Q96DN6 32296183
Intra
RBM10 P98175 MBD6 Homo sapiens Q96DN6 32296183
Intra
RBM10 P98175 MBD6 Homo sapiens Q96DN6 32296183
Intra
RBM10 P98175 ccsb orf id: 2129 Homo sapiens EBI-16432778 32296183
Intra
RBM10 P98175 ccsb orf id: 2129 Homo sapiens EBI-16432778 26871637
Intra
RBM10 P98175 ccsb orf id: 2129 Homo sapiens EBI-16432778 26871637
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 26871637
Intra
RBM10 P98175 ccsb orf id: 2129 Homo sapiens EBI-16432778 32296183
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 26871637
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 26871637
Intra
RBM10 P98175 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
RBM10 P98175 ccsb orf id: 2129 Homo sapiens EBI-16432778 26871637
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 26871637
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 32296183
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 26871637
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 32296183
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 26871637
Intra
RBM10 P98175 THAP1 Homo sapiens Q9NVV9 32296183
Intra
RBM10 P98175 U2AF2 Homo sapiens P26368
Y2H
22365833
Intra
RBM10 P98175 BAHD1 Homo sapiens Q8TBE0 32296183
Intra
RBM10 P98175 BAHD1 Homo sapiens Q8TBE0 32296183
Intra
RBM10 P98175 BAHD1 Homo sapiens Q8TBE0 32296183
Intra
RBM10 P98175 KHDRBS2 Homo sapiens Q5VWX1 26871637
Intra
RBM10 P98175 KHDRBS2 Homo sapiens Q5VWX1 26871637
Intra
RBM10 P98175 KHDRBS2 Homo sapiens Q5VWX1 26871637
Intra
RBM10 P98175 ZBTB24 Homo sapiens O43167 26871637
Intra
RBM10 P98175 ZBTB24 Homo sapiens O43167 26871637
Intra
RBM10 P98175 ZBTB24 Homo sapiens O43167 26871637
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 26871637
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 32296183
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 26871637
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 32296183
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 26871637
Intra
RBM10 P98175 DDX17 Homo sapiens Q92841 32296183
Intra
RBM10 P98175 GPKOW Homo sapiens Q92917
Y2H
22365833
Intra
RBM10 P98175 ZNF473 Homo sapiens Q8WTR7 26871637
Intra
RBM10 P98175 ZNF473 Homo sapiens Q8WTR7 26871637
Intra
RBM10 P98175 ZNF473 Homo sapiens Q8WTR7 26871637
Intra
RBM10 P98175 SNRPC Homo sapiens P09234
Y2H
22365833
Intra
RBM10 P98175 KLF1 Homo sapiens Q13351 32296183
Intra
RBM10 P98175 KLF1 Homo sapiens Q13351 32296183
Intra
RBM10 P98175 KLF1 Homo sapiens Q13351 32296183
Intra
RBM10 P98175 RBMY1F Homo sapiens Q15415 26871637
Intra
RBM10 P98175 RBMY1F Homo sapiens Q15415 26871637
Intra
RBM10 P98175 RBMY1F Homo sapiens Q15415 26871637
Intra
RBM10 P98175 TBC1D22B Homo sapiens Q9NU19 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

RBM10 Antibodies

Cat. No. Product Name Application Reactivity
HY-P89604 RBM10 Antibody (YA8948) WB, ICC/IF, IF-Tissue, IP, ELISA human

Related Diseases

Diseases Alias
Tarp Syndrome
  • TARPS

  • Pierre Robin Syndrome With Congenital Heart Malformation And Clubfoot

  • Pierre Robin Sequence-Congenital Heart Defect-Talipes Syndrome

  • Pierre Robin Syndrome-Congenital Heart Defect-Talipes Syndrome

  • Talipes Equinovarus-Atrial Septal Defect-Robin Sequence-Persistence Of The Left Superior Vena Cava Syndrome

  • Talipes Equinovarus, Atrial Septal Defect, Robin Sequence, And Persistence Of Left Superior Vena Cava

  • Pierre Robin Sequence - Congenital Heart Defect - Talipes

  • Pierre Robin Syndrome - Congenital Heart Defect - Talipes

  • Talipes Equinovarus - Atrial Septal Defect - Robin Sequence - Persistence Of The Left Superior Vena Cava

  • Talipes Equinovarus Atrial Septal Defect Robin Sequence And Persistence Of Left Superior Vena Cava

Pierre Robin Syndrome
  • Pierre Robin Sequence

  • Glossoptosis, Micrognathia, And Cleft Palate

  • Pierre Robin Syndrome Skeletal Dysplasia Polydactyly

  • Pierre-Robin Syndrome

  • Isolated Pierre Robin Sequence

  • Isolated Pierre-Robin Syndrome

  • PRBNS

  • Robin Sequence

  • Robin Syndrome

  • Isolated Pierre Robin Syndrome

Skin Angiosarcoma
  • Angiosarcoma Of Skin

  • Hemangiosarcoma Of The Skin

  • Haemangiosarcoma Of Skin

  • Lymphangiosarcoma Of Skin

  • Cutaneous Angiosarcoma

  • Malignant Haemangioendothelioma Of Skin

Talipes Equinovarus
  • Congenital Equinovarus

  • Congenital Talipes Equinovarus

  • Equinovarus

  • Congenital Varus Clubfoot

Treacher Collins Syndrome 1
  • Treacher Collins Syndrome

  • Mandibulofacial Dysostosis

  • Treacher Collins-Franceschetti Syndrome

  • Tcof

  • Tcs

  • Mfd1

  • Franceschetti-Klein Syndrome

  • TCS1

  • Franceschetti Syndrome

  • Franceschetti-Zwahlen-Klein Syndrome

  • Zygoauromandibular Dysplasia

  • Treacher-Collins Syndrome

  • Mandibulofacial Dysostosis Without Limb Anomalies

  • Bilateral And Symmetric Oto-Mandibular Dysplasia

Atrial Heart Septal Defect
  • Atrial Septal Defect

  • Atrial Septal Defects

  • Atrioseptal Defect

  • Auricular Septal Defect

  • Congenital Atrial Septal Defect

  • Interatrial Septal Defect

  • Interauricular Septal Defect

  • Heart Septal Defects, Atrial

  • Septal Defect, Atrial

Cleft Palate, Isolated
  • Cleft Palate

  • Isolated Cleft Palate

  • CPI

  • Cp

  • Palatoschisis

  • Cleft Palate Isolated

  • Uranostaphyloschisis

  • Congenital Fissure Of Palate

  • Cleft Of Secondary Palate

Renal Cell Carcinoma, Papillary, 1
  • Papillary Renal Cell Carcinoma

  • Hereditary Papillary Renal Cell Carcinoma

  • Papillary Renal Cell Carcinoma, Sporadic

  • Papillary Renal Cell Adenocarcinoma

  • RCCP

  • RCCP1

  • Renal Cell Carcinoma, Papillary

  • Renal Cell Carcinoma, Papillary, 1, Familial And Somatic

  • Chromophil Carcinoma Of Kidney

  • Papillary Kidney Carcinoma

  • Sporadic Papillary Renal Cell Carcinoma

  • Chromophil Renal Cell Carcinoma

  • Papillary Renal Carcinoma, Malignant -

  • Papillary Renal Cell Carcinoma, Bilateral -

  • Papillary Renal Cell Carcinoma, Familial -

  • Papillary Renal Cell Carcinoma, Multiple -

  • Papillary Renal Cell Carcinoma, Sporadic -

  • Renal Adenocarcinoma

  • Chromophil Rcc

  • Hprcc

  • Renal Cell Carcinoma Papillary

  • Chromophilic Renal Cell Carcinoma

  • Prcc

  • Carcinoma, Renal Cell, Papillary, Type 1

  • Type 1 Papillary Renal Cell Carcinoma

  • Renal Cell Carcinoma

  • Hereditary Papillary Renal Carcinoma

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

Orthologs Information

Species Symbol Source ID
Bos taurus RBM10 VGNC VGNC:33783
Macaca mulatta RBM10 VGNC VGNC:76680
Felis catus RBM10 VGNC VGNC:69262
Mus musculus RBM10 MGD MGI:2384310
Rattus norvegicus RBM10 RGD RGD:631366
Canis familiaris RBM10 VGNC VGNC:45404
Others RBM10 NCBI