Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: mks1 ENSXETG00000010339

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Description

Meckel syndrome, type 1 [Source:Xenbase;Acc:XB-GENE-1221180]

Location

Primary_assembly 2: 41,735,856-41,750,447 forward strand.

UCB_Xtro_10.0:CM004444.2

About this gene

This gene has 3 transcripts (splice variants), 212 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSXETT00000065924.3	mks1-201	2219	550aa	ENSXETP00000062900.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6I8PUW1	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,
ENSXETT00000022745.5	mks1-202	2147	526aa	ENSXETP00000022745.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q28BY4	-
ENSXETT00000068904.2	mks1-203	2030	487aa	ENSXETP00000095751.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6I8SBV6	-

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Summary

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