Description

special AT-rich sequence binding protein 1 [Source:MGI Symbol;Acc:MGI:105084]

Location
INSDC coordinates

chromosome:GRCm38:CM001010.2:51736187:51833290:1

Transcripts



This gene has 14 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Satb1-001ENSMUST000001443316243764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
Q60611
NM_009122
NP_033148
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-201ENSMUST000001694806194764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
Q60611
NM_001163631
NP_001157103
TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-002ENSMUST000001528305993764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
Q60611
NM_001163630
NP_001157102
TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-012ENSMUST000001766694407764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
Q60611
-TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-005ENSMUST000001335743461764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
Q60611
NM_001163632
NP_001157104
TSL:1

TSL1: All splice junctions of the transcript are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-003ENSMUST000001296672896764 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS28876D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9Q535 F8WHG2
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CI3APPRIS candidate principal isoform (CCDS) [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-004ENSMUST000001409793748795 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YU76 D3YZD1 D3Z4F8
D3Z7K4 E9PVB7
-TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS CIAPPRIS candidate principal isoform [04-09-2014]
Glossary entry for APPRIS
APPRIS website
Satb1-011ENSMUST00000129205813154 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YU76 D3YZD1 D3Z4F8
-CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:3

TSL3:The only support for this transcript is from a single EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-010ENSMUST0000014855957021 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YU76 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:3

TSL3:The only support for this transcript is from a single EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-008ENSMUST0000012422246974 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YU76 D3Z4F8 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.TSL:5

TSL5: No single transcript (mRNA or EST) supports this transcript model's structure.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-013ENSMUST00000140727625No protein
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
---TSL:3

TSL3:The only support for this transcript is from a single EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-007ENSMUST000001560514857No protein
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---TSL:NA

TSL:NA:The transcript was not analyzed for one of the following reasons:

  • Pseudogene annotation, including transcribed pseudogenes
  • Human leukocyte antigen (HLA) transcript
  • Immunoglobin gene transcript
  • T-cell receptor transcript
  • Single-exon transcript (will be included in a future version)

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-006ENSMUST000001464143840No protein
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---TSL:NA

TSL:NA:The transcript was not analyzed for one of the following reasons:

  • Pseudogene annotation, including transcribed pseudogenes
  • Human leukocyte antigen (HLA) transcript
  • Immunoglobin gene transcript
  • T-cell receptor transcript
  • Single-exon transcript (will be included in a future version)

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Satb1-009ENSMUST00000137697646No protein
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
---TSL:2

TSL2: The best supporting mRNA is flagged as suspect or the support is from multiple ESTs.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

Gene-based displays