ENSG00000183258
 Homo sapiens | |
Features
Gene ID: | ENSG00000183258 | | | Biological name : | DDX41 | | | Synonyms : | DDX41 / DEAD-box helicase 41 / Q9UJV9 | | | Possible biological names infered from orthology : | | | | Species: | Homo sapiens | | | Chr. number: | 5 | Strand: | -1 | Band: | q35.3 | Gene start: | 177511577 | Gene end: | 177517469 | | | Corresponding Affymetrix probe sets: | 217840_at (Human Genome U133 Plus 2.0 Array) | | | Cross references: | Ensembl peptide - ENSP00000426330 Ensembl peptide - ENSP00000487280 Ensembl peptide - ENSP00000486367 Ensembl peptide - ENSP00000427082 Ensembl peptide - ENSP00000330349 Ensembl peptide - ENSP00000421460 Ensembl peptide - ENSP00000422753 Ensembl peptide - ENSP00000425739 NCBI entrez gene - 51428
See in Manteia.
OMIM - 608170 RefSeq - NM_016222 RefSeq - NM_001321732 RefSeq - NM_001321830 RefSeq Peptide - NP_001308759 RefSeq Peptide - NP_001308661 RefSeq Peptide - NP_057306 swissprot - Q9UJV9 swissprot - D6RD33 swissprot - H0Y8L8 swissprot - H0YA06 swissprot - J3KNN5 swissprot - D6RGI7 Ensembl - ENSG00000183258
| | | Related genetic diseases (OMIM): | 616871 - {Myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to}, 616871 | See expression report in BioGPS See gene description in Wikigenes See gene description in GeneCards See co-cited genes in PubMed
Ortholog prediction (from Ensembl)
Paralog prediction (from Ensembl)
Protein motifs (from Interpro)
IPR001650 | Helicase, C-terminal | IPR011545 | DEAD/DEAH box helicase domain | IPR014001 | Helicase superfamily 1/2, ATP-binding domain | IPR014014 | RNA helicase, DEAD-box type, Q motif | IPR027417 | P-loop containing nucleoside triphosphate hydrolase |
Gene Ontology (GO)
Pathways (from Reactome)
Phenotype (from MGI, Zfin or HPO)
No match
Interacting proteins (from Reactome)
ENSG00000132109 | P19474 / TRIM21 / tripartite motif containing 21 | / complex / reaction |
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