Human (GRCh37.p13)
Description

serine/arginine-rich splicing factor 2 [Source:HGNC Symbol;Acc:10783]

Gene Synonyms

MIRN636, PR264, SC-35, SC35, SFRS2, SFRS2A, SRp30b, hsa-mir-636

Location

Chromosome 17: 74,730,197-74,733,456 reverse strand.

GRCh37:CM000679.1

About this gene

This gene has 11 transcripts (splice variants), 4 paralogues and is associated with 59 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000392485.2SRSF2-0032885221aaENSP00000376276.2
 
Protein coding
CCDS11749B3KUY1 Q01130 NM_003016.4GENCODE basic
ENST00000359995.5SRSF2-0011927221aaENSP00000353089.5
 
Protein coding
CCDS11749B3KUY1 Q01130 NM_001195427.1GENCODE basic
ENST00000508921.3SRSF2-0021390209aaENSP00000441780.2
 
Protein coding
B4DN89 -GENCODE basic
ENST00000358156.6SRSF2-007572133aaENSP00000350877.6
 
Protein coding
J3KP15 -CDS 3' incomplete
ENST00000583836.1SRSF2-008561130aaENSP00000463317.1
 
Protein coding
J3QL05 -CDS 3' incomplete
ENST00000585202.1SRSF2-0041359221aaENSP00000462425.1
 
Nonsense mediated decay
CCDS11749B3KUY1 Q01130 --
ENST00000452355.3SRSF2-0051357221aaENSP00000391278.3
 
Nonsense mediated decay
CCDS11749B3KUY1 Q01130 --
ENST00000582449.1SRSF2-0061518No protein-
 
Retained intron
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ENST00000586778.1SRSF2-0161001No protein-
 
Retained intron
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ENST00000589919.1SRSF2-017595No protein-
 
Retained intron
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ENST00000592676.1SRSF2-015559No protein-
 
Retained intron
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