Description

laminin, beta 3 [Source:HGNC Symbol;Acc:HGNC:6490]

Synonyms

BM600-125kDa, kalinin-140kDa, LAMNB1, nicein-125kDa

INSDC coordinates

chromosome:GRCh38:CM000663.2:209614870:209652466:1

Transcripts



This gene has 5 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDbpProteinBiotypeCCDSUniProtRefSeqFlags
LAMB3-201ENST0000039191143051172 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS1487Q13751 Q5THA1 X1WI29
NM_001017402
NP_001017402
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 [01-09-2014]
Glossary entry for APPRIS
APPRIS website
LAMB3-001ENST0000035608240551172 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS1487Q13751 Q5THA1 X1WI29
NM_000228
NP_000219
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 [01-09-2014]
Glossary entry for APPRIS
APPRIS website
LAMB3-002ENST0000036703039311172 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS1487Q13751 Q5THA1 X1WI29
NM_001127641
NP_001121113
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 [01-09-2014]
Glossary entry for APPRIS
APPRIS website
LAMB3-003ENST00000415782908188 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q5THA1 -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.

LAMB3-004ENST00000455193710160 aa
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-X1WI29 -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.

Stable ID

ENSG00000196878.10

Status

Current

Latest Version

ENSG00000196878.10

Release: 77 (current)

Assembly: GRCh38

Database: homo_sapiens_core_77_38

Associated archived IDs for this stable ID version

No associated IDs found

Gene-based displays