Description

zinc finger and BTB domain containing 7B [Source:MGI Symbol;Acc:MGI:102755]

Location
INSDC coordinates

chromosome:GRCm38:CM000996.2:89377644:89394776:1

Transcripts

This gene has 9 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
Zbtb7b-003ENSMUST000001074354333544 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17504D3YXC8 D3YZR6 D3Z0B5
D3Z2X8 Q5BJ24 Q64321
-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 PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
Zbtb7b-001ENSMUST000000296773851544 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17504D3YXC8 D3YZR6 D3Z0B5
D3Z2X8 Q5BJ24 Q64321
NM_009565
NP_033591
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 PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
Zbtb7b-004ENSMUST000001074333650544 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17504D3YXC8 D3YZR6 D3Z0B5
D3Z2X8 Q5BJ24 Q64321
-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 PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
Zbtb7b-002ENSMUST000001074323639544 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS17504D3YXC8 D3YZR6 D3Z0B5
D3Z2X8 Q5BJ24 Q64321
-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 PIAPPRIS principal isoform
Glossary entry for APPRIS
APPRIS website
Zbtb7b-006ENSMUST00000126027544124 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YXC8 D3YZR6 D3Z0B5
D3Z2X8
-CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.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.

Zbtb7b-008ENSMUST00000148361481102 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YXC8 D3Z2X8 -CDS 3' incomplete3' truncation in transcript evidence prevents annotation of the end of the CDS.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.

Zbtb7b-009ENSMUST00000142119403112 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YXC8 D3Z0B5 D3Z2X8
-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.

Zbtb7b-007ENSMUST0000012478335429 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-D3YXC8 -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.

Zbtb7b-005ENSMUST00000139094697No 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.

Gene-based displays