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Rabbit Anti-SLC22A18AS antibody
SLC22A18AS (Solute Carrier Family 22 Member 18 Antisense) is a Protein Coding gene. Diseases associated with SLC22A18AS include Beckwith-Wiedemann Syndrome.
Tissue Specificity:
Most abundantly expressed in gastrointestinal tissues. Expressed at lower levels in kidney and placenta. Expressed in fetal brain, liver, placenta, kidney and lung.
SWISS:
Q8N1D0
Gene ID:
5003
Database links:
Entrez Gene: 5003 Human
Omim: 60348 Human
SwissProt: Q8N1D0 Human
Unigene: 300076 Human
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