Human (GRCh37.p13)
Description

lin-7 homolog B (C. elegans) [Source:HGNC Symbol;Acc:17788]

Gene Synonyms

LIN-7B, MALS-2, MALS2, VELI2

Location

Chromosome 19: 49,617,581-49,621,717 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 7 transcripts (splice variants), 179 orthologues and 3 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000221459.2LIN7B-001755207aaENSP00000221459.2
 
Protein coding
CCDS12757Q9HAP6 NM_022165.2Ensembl CanonicalGENCODE Basic
ENST00000391864.3LIN7B-002582137aaENSP00000375737.3
 
Protein coding
Q9HAP6 -GENCODE Basic
ENST00000486217.2LIN7B-006367115aaENSP00000474643.1
 
Protein coding
--CDS 5' incomplete
ENST00000595200.1LIN7B-007795132aaENSP00000472804.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000469137.1LIN7B-0031057No protein-
 
Retained intron
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ENST00000474252.1LIN7B-004521No protein-
 
Retained intron
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ENST00000465141.1LIN7B-005496No protein-
 
Retained intron
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