Description

neuromedin B [Source:HGNC Symbol;Acc:HGNC:7842]

Synonyms

MGC17211, MGC2277, MGC3936

Location
About this transcript

This transcript has 3 exons, is annotated with 6 domains and features, is associated with 42 variations and maps to 11 oligo probes.

Gene
NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
NMB-002ENST000003945881017154aaENSP00000378089
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS42076P08949 NM_205858
NP_995580
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 ALT2APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species
Glossary entry for APPRIS
APPRIS website
NMB-001ENST000003604761007121aaENSP00000353664
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS10332P08949 NM_021077
NP_066563
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

Protein domains for ENSP00000378089.3

Transcript-based displays