RBM17 - RNA binding motif protein 17 Gene

Also Known as SPF45

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 84991

About RBM17

Cytogenetic location: 10p15.1 Genomic coordinates (GRCh38): 10:6,089,034-6,117,447 (from NCBI)

This gene has 12 transcripts (splice variants) and 225 orthologues. Ubiquitous expression in bone marrow (RPKM 17.7), lymph node (RPKM 15.8) and 25 other tissues.

Summary

This gene encodes an RNA binding protein. The encoded protein is part of the spliceosome complex and functions in the second catalytic step of mRNA splicing. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 9 and 15. [provided by RefSeq, Mar 2009]

RBM17 Products (2)

mRNA Protein Name
NM_001145547.2 NP_001139019.1 splicing factor 45
NM_032905.5 NP_116294.1 splicing factor 45
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence References Source
involved in alternative mRNA splicing, via spliceosome IMP
IMP: Inferred from mutant phenotype
17589525 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

RBM17 Protein Structure

G-patch

G-patch: G-patch domain (238 - 276)

RRM_5

RRM_5: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (328 - 386)

  • 0
  • 100
  • 200
  • 300
  • 401 a.a.
Protein Preferred Names Protein Names

splicing factor 45

  • 45 kDa-splicing factor

RBM17 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RBM17 Q96I25 FAM9B Homo sapiens Q8IZU0 25416956
Intra
RBM17 Q96I25 FAM9B Homo sapiens Q8IZU0 25416956
Intra
RBM17 Q96I25 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
RBM17 Q96I25 CCHCR1 Homo sapiens Q8TD31-3 32296183
Intra
RBM17 Q96I25 PPP1R12C Homo sapiens Q9BZL4-5 25416956
Intra
RBM17 Q96I25 PPP1R12C Homo sapiens Q9BZL4-5 25416956
Intra
RBM17 Q96I25 NEK7 Homo sapiens Q8TDX7 32814053
Intra
RBM17 Q96I25 NEK7 Homo sapiens Q8TDX7 32814053
Intra
RBM17 Q96I25 NEK7 Homo sapiens Q8TDX7 32814053
Intra
RBM17 Q96I25 SF1 Homo sapiens Q15637-4 32296183
Intra
RBM17 Q96I25 SF1 Homo sapiens Q15637-4 32296183
Intra
RBM17 Q96I25 DHX15 Homo sapiens O43143 35271311
Intra
RBM17 Q96I25 DHX15 Homo sapiens O43143 25416956
Intra
RBM17 Q96I25 DHX15 Homo sapiens O43143 25416956
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533-1 17589525
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533-1 17589525
Intra
RBM17 Q96I25 SF3A2 Homo sapiens Q15428 17332742
Intra
RBM17 Q96I25 SF3A2 Homo sapiens Q15428 33961781
Intra
RBM17 Q96I25 SF3A2 Homo sapiens Q15428 28514442
Intra
RBM17 Q96I25 SUGP1 Homo sapiens Q8IWZ8 35271311
Intra
RBM17 Q96I25 QRICH1 Homo sapiens Q2TAL8 25416956
Intra
RBM17 Q96I25 QRICH1 Homo sapiens Q2TAL8 25416956
Intra
RBM17 Q96I25 CCDC170 Homo sapiens Q8IYT3 32296183
Intra
RBM17 Q96I25 CCDC170 Homo sapiens Q8IYT3 32296183
Intra
RBM17 Q96I25 U2SURP Homo sapiens O15042 33961781
Intra
RBM17 Q96I25 U2SURP Homo sapiens O15042 35271311
Intra
RBM17 Q96I25 U2SURP Homo sapiens O15042
Y2H
22365833
Intra
RBM17 Q96I25 GOLGA2 Homo sapiens Q08379 25416956
Intra
RBM17 Q96I25 GOLGA2 Homo sapiens Q08379 32296183
Intra
RBM17 Q96I25 GOLGA2 Homo sapiens Q08379 32296183
Intra
RBM17 Q96I25 SAT1 Homo sapiens P21673
Y2H
21516116
Intra
RBM17 Q96I25 SAT1 Homo sapiens P21673 25416956
Intra
RBM17 Q96I25 HSF2BP Homo sapiens O75031 32296183
Intra
RBM17 Q96I25 HSF2BP Homo sapiens O75031 32296183
Intra
RBM17 Q96I25 PECAM1 Homo sapiens P16284 32814053
Intra
RBM17 Q96I25 PECAM1 Homo sapiens P16284 32814053
Intra
RBM17 Q96I25 PECAM1 Homo sapiens P16284 32814053
Intra
RBM17 Q96I25 WFS1 Homo sapiens O76024 32814053
Intra
RBM17 Q96I25 WFS1 Homo sapiens O76024 32814053
Intra
RBM17 Q96I25 WFS1 Homo sapiens O76024 32814053
Intra
RBM17 Q96I25 PPP1R12C Homo sapiens Q9BZL4 32296183
Intra
RBM17 Q96I25 PPP1R12C Homo sapiens Q9BZL4 32296183
Intra
RBM17 Q96I25 PPP1R12C Homo sapiens Q9BZL4 32296183
Intra
RBM17 Q96I25 U2AF2 Homo sapiens P26368 17589525
Intra
RBM17 Q96I25 SF1 Homo sapiens Q15637 26420826
Intra
RBM17 Q96I25 SF1 Homo sapiens Q15637 17589525
Intra
RBM17 Q96I25 IQCN Homo sapiens Q9H0B3 25416956
Intra
RBM17 Q96I25 IQCN Homo sapiens Q9H0B3 25416956
Intra
RBM17 Q96I25 CEP55 Homo sapiens Q53EZ4 32296183
Intra
RBM17 Q96I25 CEP55 Homo sapiens Q53EZ4 31515488
Intra
RBM17 Q96I25 CEP55 Homo sapiens Q53EZ4 32296183
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533 33961781
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533 28514442
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533 35271311
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533 37219487
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533 22365833
Intra
RBM17 Q96I25 SF3B1 Homo sapiens O75533
Y2H
22365833
Intra
RBM17 Q96I25 ATXN1 Homo sapiens P54253 18337722
Intra
RBM17 Q96I25 ATXN1 Homo sapiens P54253
Y2H
18337722
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Sickle Cell Anemia
  • Hemoglobin Sc Disease

  • Anemia, Sickle Cell

  • Hbsc Disease

  • Sickle Cell-Hemoglobin C Disease Syndrome

  • Hb Ss Disease

  • Sickle Cell Trait

  • Drepanocytosis

  • Haemoglobin Sc Disease

  • Hb Sc Disease

  • Hb-S/Hb-C Disease

  • Hb-Ss Disease Without Crisis

  • Hemoglobin S Disease Without Crisis

  • Sickle Cell Anaemia

  • Sickle-Cell/Hb-C Disease Without Crisis

  • Sickle Cell - Hemoglobin C Disease

  • Hbs Disease

  • Hemoglobin S Disease

  • Sickling Disorder Due To Hemoglobin S

  • SKCA

  • Sickle Cell Disease

  • Sickle Cell-Hemoglobin C Disease

  • Sickle-Cell Disease Carrier

  • Sickle-Cell Heterozygous Disorder

  • Haemoglobin A-S Genotype

  • Hb-S - [Sickle Cell Haemoglobin] Carrier

  • Sickle Cell Haemoglobin Trait

  • As - [Sickle Cell Trait]

  • Hbas - [Sickle Cell Haemoglobin Trait]

  • Sickle-Cell Trait Haemoglobin Disease

  • Haemoglobin Sickle Cell Trait Disorder

  • Heterozygous Sickle Cell Trait

  • Hbas - [Heterozygous Haemoglobin S]

Spinocerebellar Ataxia 1
  • Spinocerebellar Ataxia Type 1

  • SCA1

  • Olivopontocerebellar Atrophy I

  • Opca1

  • Opca4

  • Menzel Type Opca

  • Schut-Haymaker Type Opca

  • Spinocerebellar Atrophy I

  • Opca I

  • Olivopontocerebellar Atrophy Iv

  • Opca Iv

  • Cerebelloparenchymal Disorder I

  • Cpd1

  • Olivopontocerebellar Atrophy 1

  • Cerebelloparenchymal Disorder 1

  • Olivopontocerebellar Atrophy 4

  • Spinocerebellar Atrophy 1

  • Type 1 Spinocerebellar Ataxia

  • Spinocerebellar Ataxia-1

  • Ataxia, Spinocerebellar, Type 1

Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

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
Canis familiaris RBM17 VGNC VGNC:45411
Mus musculus RBM17 MGD MGI:1924188
Bos taurus RBM17 VGNC VGNC:33788
Macaca mulatta RBM17 VGNC VGNC:76496
Rattus norvegicus RBM17 RGD RGD:1311208
Felis catus RBM17 VGNC VGNC:64522
Others RBM17 NCBI