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Protein-coding gene in the species Homo sapiens
ATP-dependent RNA helicase PRP16 is an enzyme that in humans is encoded by the DHX38 gene. DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp
DHX38
Birth defect of the eye
BCOR BMP4 BMP7 C12orf57 CC2D2A CHD7 CLDN19 COX7B CRIM1 CRYAA CRYBA4 CRYBB2 DHX38 DPYD ERCC1 ERCC5 FADD FAM111A FNBP4 FOXL2 FRAS1 FREM1 FREM2 FZD5 GDF3 GDF6
Microphthalmia
Gradual retinal degeneration leading to progressive sight loss
ARL2BP Retinitis pigmentosa-82 618173 ARL3 Retinitis pigmentosa-83 618220 DHX38 Retinitis pigmentosa-84 618345 AHR Retinitis pigmentosa-85 618613 KIAA1549
Retinitis_pigmentosa
Human chromosome
Chromosome 16p13.3 deletion syndrome (Rubinstein-Taybi deletion syndrome) DHX38: DEAH-box helicase 38 DUP16p13.3, C16DUPq13.3: Chromosome 16p13.3 duplication
Chromosome_16
Q9H5Z1 4256 DHX36 HGNC:14410; Q9H2U1 4257 DHX37 HGNC:17210; Q8IY37 4258 DHX38 HGNC:17211; Q92620 4259 DHX40 HGNC:18018; Q8IX18 4260 DHX57 HGNC:20086;
List of human protein-coding genes 2
List_of_human_protein-coding_genes_2
DHX38
DHX38
DHX38
DHX38
DHX38
DHX38
DHX38
DHX38
DHX38