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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RASL11B ENSG00000128045

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Description

RAS-like, family 11, member B [Source:HGNC Symbol;Acc:23804]

Location

Chromosome 4: 53,728,457-53,733,000 forward strand.

GRCh37:CM000666.1

About this gene

This gene has 3 transcripts (splice variants) and 6 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000248706.3	RASL11B-001	1993	248aa	ENSP00000248706.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS3490	Q9BPW5	NM_023940.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000505041.1	RASL11B-002	1733	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000515677.1	RASL11B-003	661	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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