Homo sapiens chromosome 11, GRCh38.p14 Primary Assembly

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Assembly
Assembly
BioProject
Related BioProject entry
Protein
Protein sequence from Nucleotide coding region
PubMed
PubMed articles cited by Nucleotide sequence record
Taxonomy
Taxonomy sequences associated with Nucleotide record
Components (Core)
Links to Core components
Full text in PMC
Free full text articles in PMC
Gene
Link to related Genes
Identical GenBank Sequence
Links from RefSeq assemblies to source GenBank records.
OMIM
OMIM records associated with Nucleotide sequence
PubMed (Weighted)
Links to pubmed
RNA
RNA sequence records that are annotated on the current genomic nucleotide sequences. The RNA records represent aligned or predicted transcripts of the current records.

Alstrom Syndrome
Alstrom Syndrome
Rare autosomal recessive disease characterized by multiple organ dysfunction. The key clinical features include retinal degeneration (NYSTAGMUS, PATHOLOGIC; RETINITIS PIGMENTO...<br/>Year introduced: 2010

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Nucleotide