Human Gene RBM25 (ENST00000261973.12) from GENCODE V44
  Description: Homo sapiens RNA binding motif protein 25 (RBM25), mRNA. (from RefSeq NM_021239)
Gencode Transcript: ENST00000261973.12
Gencode Gene: ENSG00000119707.14
Transcript (Including UTRs)
   Position: hg38 chr14:73,058,534-73,123,899 Size: 65,366 Total Exon Count: 19 Strand: +
Coding Region
   Position: hg38 chr14:73,071,642-73,119,805 Size: 48,164 Coding Exon Count: 18 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
RNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther SpeciesGO Annotations
mRNA DescriptionsPathwaysOther NamesMethods
Data last updated at UCSC: 2023-08-18 00:09:47

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr14:73,058,534-73,123,899)mRNA (may differ from genome)Protein (843 aa)
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-  Comments and Description Text from UniProtKB
  ID: RBM25_HUMAN
DESCRIPTION: RecName: Full=RNA-binding protein 25; AltName: Full=Arg/Glu/Asp-rich protein of 120 kDa; Short=RED120; AltName: Full=Protein S164; AltName: Full=RNA-binding motif protein 25; AltName: Full=RNA-binding region-containing protein 7;
FUNCTION: RNA-binding protein that acts as a regulator of alternative pre-mRNA splicing. Involved in apoptotic cell death through the regulation of the apoptotic factor BCL2L1 isoform expression. Modulates the ratio of proapoptotic BCL2L1 isoform S to antiapoptotic BCL2L1 isoform L mRNA expression. When overexpressed, stimulates proapoptotic BCL2L1 isoform S 5'-splice site (5'-ss) selection, whereas its depletion caused the accumulation of antiapoptotic BCL2L1 isoform L. Promotes BCL2L1 isoform S 5'-ss usage through the 5'-CGGGCA-3' RNA sequence. Its association with LUC7L3 promotes U1 snRNP binding to a weak 5' ss in a 5'-CGGGCA-3'-dependent manner. Binds to the exonic splicing enhancer 5'-CGGGCA-3' RNA sequence located within exon 2 of the BCL2L1 pre-mRNA.
SUBUNIT: Interacts with LUC7L3 and SRRM1. Specifically associates with functional splicing complexes, including Sm proteins and U1, U2, U4, U5 and U6 snRNAs. Associates with exon junction complex (EJC) proteins, including APEX1, BAT1, NCBP1, RBM8A and RNPS1. Interaction with NCBP1 is RNA-dependent.
SUBCELLULAR LOCATION: Nucleus speckle. Cytoplasm. Note=Colocalizes predominantly, with SFRS2 and LUC7L3 splicing factors, in nuclear speckles. Cytoplasmic localization is faint.
PTM: Sumoylated.
SIMILARITY: Contains 1 PWI domain.
SIMILARITY: Contains 1 RRM (RNA recognition motif) domain.
SEQUENCE CAUTION: Sequence=AAH62440.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=AAH62440.1; Type=Miscellaneous discrepancy; Note=Contaminating sequence. Potential poly-A sequence; Sequence=AAH83496.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Sequence=BAG52915.1; Type=Erroneous translation; Note=Wrong choice of CDS;

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
Click here to open Exonprimer with this transcript

To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: RBM25
Diseases sorted by gene-association score: early-onset familial alzheimer disease (2)

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 49.70 RPKM in Brain - Cerebellum
Total median expression: 1351.26 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -72.50187-0.388 Picture PostScript Text
3' UTR -960.104094-0.235 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR012677 - Nucleotide-bd_a/b_plait
IPR002483 - PWI
IPR000504 - RRM_dom

Pfam Domains:
PF01480 - PWI domain
PF00076 - RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain)

ModBase Predicted Comparative 3D Structure on P49756
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
Genome BrowserGenome BrowserGenome BrowserGenome BrowserGenome BrowserNo ortholog
Gene Details     
Gene Sorter     
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Protein SequenceProtein SequenceProtein SequenceProtein SequenceProtein Sequence 
AlignmentAlignmentAlignmentAlignmentAlignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0003676 nucleic acid binding
GO:0003723 RNA binding
GO:0003729 mRNA binding
GO:0005515 protein binding

Biological Process:
GO:0000381 regulation of alternative mRNA splicing, via spliceosome
GO:0006397 mRNA processing
GO:0008380 RNA splicing
GO:0042981 regulation of apoptotic process

Cellular Component:
GO:0005634 nucleus
GO:0005681 spliceosomal complex
GO:0005737 cytoplasm
GO:0016607 nuclear speck


-  Descriptions from all associated GenBank mRNAs
  BC062440 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone IMAGE:4248893), partial cds.
AK026107 - Homo sapiens cDNA: FLJ22454 fis, clone HRC09703.
AL832314 - Homo sapiens mRNA; cDNA DKFZp667O2119 (from clone DKFZp667O2119).
BC033664 - Homo sapiens cDNA clone IMAGE:4993741, containing frame-shift errors.
BC083496 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone IMAGE:6474335), complete cds.
BC111066 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone IMAGE:5768319), complete cds.
BX647116 - Homo sapiens mRNA; cDNA DKFZp686M06144 (from clone DKFZp686M06144).
JD474092 - Sequence 455116 from Patent EP1572962.
BC136775 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone MGC:168388 IMAGE:9020765), complete cds.
BC136776 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone MGC:168389 IMAGE:9020766), complete cds.
BC144407 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone MGC:177945 IMAGE:9052928), complete cds.
AK094697 - Homo sapiens cDNA FLJ37378 fis, clone BRAMY2025230, highly similar to Probable RNA-binding protein 25.
KJ894474 - Synthetic construct Homo sapiens clone ccsbBroadEn_03868 RBM25 gene, encodes complete protein.
JD321692 - Sequence 302716 from Patent EP1572962.
BC113391 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone IMAGE:8322443), partial cds.
BC113389 - Homo sapiens RNA binding motif protein 25, mRNA (cDNA clone IMAGE:8322441), partial cds.
JD370093 - Sequence 351117 from Patent EP1572962.
JD085805 - Sequence 66829 from Patent EP1572962.
JD297456 - Sequence 278480 from Patent EP1572962.
JD093886 - Sequence 74910 from Patent EP1572962.
JD534016 - Sequence 515040 from Patent EP1572962.
JD560340 - Sequence 541364 from Patent EP1572962.
AK125513 - Homo sapiens cDNA FLJ43525 fis, clone PLACE5000372, highly similar to Homo sapiens U1 small ribonucleoprotein 1SNRP.
S67071 - U1 small nuclear ribonucleoprotein 1SNRP homolog [human, thyroid associated ophthalmopathy patient, mRNA Partial, 255 nt].
AL833497 - Homo sapiens mRNA; cDNA DKFZp686O1329 (from clone DKFZp686O1329).
L40392 - Homo sapiens hypothetical protein mRNA, partial cds.
JD267238 - Sequence 248262 from Patent EP1572962.
JD082975 - Sequence 63999 from Patent EP1572962.
JD099422 - Sequence 80446 from Patent EP1572962.
JD513971 - Sequence 494995 from Patent EP1572962.
JD415020 - Sequence 396044 from Patent EP1572962.
JD415021 - Sequence 396045 from Patent EP1572962.
JD080204 - Sequence 61228 from Patent EP1572962.
JD415022 - Sequence 396046 from Patent EP1572962.
JD120604 - Sequence 101628 from Patent EP1572962.
JD120605 - Sequence 101629 from Patent EP1572962.
JD379770 - Sequence 360794 from Patent EP1572962.
JD379772 - Sequence 360796 from Patent EP1572962.
JD312246 - Sequence 293270 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa03040 - Spliceosome

-  Other Names for This Gene
  Alternate Gene Symbols: A0PJL9, B2RNA8, B3KT03, ENST00000261973.1, ENST00000261973.10, ENST00000261973.11, ENST00000261973.2, ENST00000261973.3, ENST00000261973.4, ENST00000261973.5, ENST00000261973.6, ENST00000261973.7, ENST00000261973.8, ENST00000261973.9, NM_021239, P49756, Q2TA72, Q5XJ17, Q6P665, Q9H6A1, Q9UEQ5, Q9UIE9, RBM25_HUMAN, RNPC7, uc001xno.1, uc001xno.2, uc001xno.3, uc001xno.4, uc001xno.5
UCSC ID: ENST00000261973.12
RefSeq Accession: NM_021239
Protein: P49756 (aka RBM25_HUMAN)
CCDS: CCDS32113.1

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.