Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: nhsb ENSACLG00000018451

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Description

Nance-Horan syndrome b (congenital cataracts and dental anomalies) [Ensembl NN prediction with score 77.91%]

Location

Primary_assembly 23: 9,133,045-9,146,827 forward strand.

fAstCal1.3:LS420040.1

About this gene

This gene has 1 transcript (splice variant), 197 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSACLT00000028243.2	nhsb-201	5385	1445aa	ENSACLP00000027596.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3P8QE92	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,

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Summary

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