Description

thymopoietin [Source:MGI Symbol;Acc:MGI:106920]

Location
INSDC coordinates

chromosome:GRCm38:CM001003.2:91147571:91171582:1

About this gene

This gene has 5 transcripts (splice variants), 68 orthologues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Tmpo-201ENSMUST000000201233776693aaENSMUSP00000020123
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS24122Q61033 NM_011605
NP_035735
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 PI3APPRIS candidate principal isoform (earliest CCDS)
Glossary entry for APPRIS
APPRIS website
Tmpo-202ENSMUST000000722393533452aaENSMUSP00000072092
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36035Q3TXQ1 Q61029 NM_001080129
NM_001283048
NP_001073598
NP_001269977
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 ALT1APPRIS candidate principal isoform that is conserved in at least three tested non-primate species
Glossary entry for APPRIS
APPRIS website
Tmpo-203ENSMUST000000922193413412aaENSMUSP00000089864
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36034Q3TNH0 Q3TXQ1 Q61029
NM_001080130
NP_001073599
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).
Tmpo-204ENSMUST000000993553317380aaENSMUSP00000096956
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36033Q3TXQ1 Q61029 NM_001080131
NP_001073600
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).
Tmpo-205ENSMUST000001052933206343aaENSMUSP00000100930
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS36032Q3TXQ1 Q61029 NM_001080132
NP_001073601
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).

Gene-based displays