protein dispatched homolog 1 isoform 1 [Homo sapiens]

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DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations. [Genet Med. 2024]
DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Lavillaureix A, Rollier P, Kim A, Panasenkava V, De Tayrac M, Carré W, Guyodo H, Faoucher M, Poirel E, Akloul L, et al. Genet Med. 2024 Jul; 26(7):101126. Epub 2024 Mar 24.
Conserved cholesterol-related activities of Dispatched 1 drive Sonic hedgehog shedding from the cell membrane. [J Cell Sci. 2022]
Conserved cholesterol-related activities of Dispatched 1 drive Sonic hedgehog shedding from the cell membrane.
Ehring K, Manikowski D, Goretzko J, Froese J, Gude F, Jakobs P, Rescher U, Kirchhefer U, Grobe K. J Cell Sci. 2022 Mar 1; 135(5). Epub 2021 Aug 19.
Structure of human Dispatched-1 provides insights into Hedgehog ligand biogenesis. [Life Sci Alliance. 2020]
Structure of human Dispatched-1 provides insights into Hedgehog ligand biogenesis.
Chen H, Liu Y, Li X. Life Sci Alliance. 2020 Aug; 3(8). Epub 2020 Jul 9.

RefSeq genomic sequence
See the genomic reference sequence for the DISP1 gene (NG_009243.2).
RefSeq mRNA
See reference mRNA sequence for the DISP1 gene (NM_001377229.1).

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protein dispatched homolog 1 isoform 1 [Homo sapiens]
protein dispatched homolog 1 isoform 1 [Homo sapiens]
gi|1785916246|ref|NP_001364158.1|

Protein
Homo sapiens dispatched RND transporter family member 1 (DISP1), transcript vari...
Homo sapiens dispatched RND transporter family member 1 (DISP1), transcript variant 32, non-coding RNA
gi|1785916256|ref|NR_165135.1|

Nucleotide
Homo sapiens dispatched RND transporter family member 1 (DISP1), transcript vari...
Homo sapiens dispatched RND transporter family member 1 (DISP1), transcript variant 43, non-coding RNA
gi|1785916724|ref|NR_165146.1|

Nucleotide

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Protein