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

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Gene: RP1L1 ENSG00000183638

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Description

retinitis pigmentosa 1-like 1 [Source:HGNC Symbol;Acc:15946]

Gene Synonyms

DCDC4B

Location

Chromosome 8: 10,463,859-10,569,697 reverse strand.

GRCh37:CM000670.1

About this gene

This gene has 2 transcripts (splice variants), 1 paralogue and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000382483.3	RP1L1-001	7973	2400aa	ENSP00000371923.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS43708	A6NKC6	NM_178857.5	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000329335.3	RP1L1-002	1536	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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