Description
serine/arginine-rich splicing factor 7 [Source:HGNC Symbol;Acc:10789]
Gene Synonyms
9G8, AAG3, HSSG1, RBM37, SFRS7, ZCCHC20, ZCRB2
Location
Chromosome 2: 38,970,741-38,978,636 reverse strand.
GRCh37:CM000664.1
About this gene
This gene has 12 transcripts (splice variants) and 6 paralogues.
Transcripts
| Transcript ID | Name | bp | Protein | Translation ID | Biotype | CCDS | UniProt Match | RefSeq | Flags |
|---|---|---|---|---|---|---|---|---|---|
| ENST00000313117.6 | SRSF7-001 | 2489 | 238aa | ENSP00000325905.6 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS33183 | Q16629 | NM_001195446.1 | A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, |
| ENST00000446327.2 | SRSF7-201 | 1169 | 226aa | ENSP00000402264.2 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | CCDS56115 | Q16629 | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, |
| ENST00000409276.1 | SRSF7-012 | 1050 | 235aa | ENSP00000386806.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | C9JAB2 | - | The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, | |
| ENST00000452806.1 | SRSF7-007 | 747 | 110aa | ENSP00000392300.1 | Gene/transcipt that contains an open reading frame (ORF).Protein coding | - | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, | |
| ENST00000425778.1 | SRSF7-002 | 2857 | 137aa | ENSP00000400246.1 | Nonsense mediated decay | - | - | - | |
| ENST00000425941.2 | SRSF7-010 | 1944 | 137aa | ENSP00000416516.2 | Nonsense mediated decay | - | - | - | |
| ENST00000443213.1 | SRSF7-003 | 1903 | 132aa | ENSP00000402544.1 | Nonsense mediated decay | Q16629 | - | - | |
| ENST00000431066.1 | SRSF7-011 | 1847 | 132aa | ENSP00000398159.1 | Nonsense mediated decay | Q16629 | - | - | |
| ENST00000415527.1 | SRSF7-004 | 1135 | 51aa | ENSP00000408868.1 | Nonsense mediated decay | F8WEA1 | - | - | |
| ENST00000432873.1 | SRSF7-008 | 603 | 70aa | ENSP00000401202.1 | Nonsense mediated decay | H7C1N1 | - | 5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete, | |
| ENST00000477635.1 | SRSF7-005 | 680 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - | - | |
| ENST00000487773.1 | SRSF7-009 | 637 | No protein | - | An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron | - | - | - |
