User:Julialturner/RELN

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RELN for testing infobox gene

RELN
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
AliasesRELN, LIS2, PRO1598, RL, reelin, ETL7
External IDsOMIM: 600514 HomoloGene: 3699 GeneCards: RELN
Genetically Related Diseases
Alzheimer's disease, otosclerosis, multiple sclerosis, schizophrenia, Norman–Roberts syndrome, familial temporal lobe epilepsy 7[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_173054
NM_005045

n/a

RefSeq (protein)

NP_005036
NP_774959

n/a

Location (UCSC)Chr 7: 103.47 – 103.99 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Reference test[edit]

This is the text that you are going to verify with a reference.[3]

References[edit]

  1. ^ "Diseases that are genetically associated with RELN view/edit references on wikidata".
  2. ^ "Human PubMed Reference:".
  3. ^ "Daylight"."Yaylight".