Gene
dipk2b
- ID
- ZDB-GENE-110411-223
- Name
- divergent protein kinase domain 2B
- Symbol
- dipk2b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 9 Mapping Details/Browsers
- Description
- Predicted to be located in extracellular region and membrane. Is expressed in blood cell and vascular endothelium. Orthologous to human DIPK2B (divergent protein kinase domain 2B).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Cannon et al., 2013
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
| Allele | Type | Localization | Consequence | Mutagen | Supplier |
|---|---|---|---|---|---|
| sa17295 | Allele with one point mutation | Unknown | Premature Stop | ENU |
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Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Divergent protein kinase domain 2A/B | FAM69, protein-kinase domain |
|---|---|---|---|
|
UniProtKB:A0A8M3B5S2
|
359 | ||
|
UniProtKB:A0A8N7TFN4
|
417 |
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| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
dipk2b-203
(1)
|
Ensembl | 1,296 nt | ||
| mRNA |
si:ch73-147f11.1-201
(1)
|
Ensembl | 1,494 nt | ||
| mRNA |
si:ch73-147f11.1-202
(1)
|
Ensembl | 1,320 nt |
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Interactions and Pathways
No data available
Plasmids
No data available
No data available
| Relationship | Marker Type | Marker | Accession Numbers | Citations |
|---|---|---|---|---|
| Contained in | BAC | CH73-147F11 | ZFIN Curated Data |
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| Type | Accession # | Sequence | Length (nt/aa) | Analysis |
|---|---|---|---|---|
| RNA | RefSeq:XM_068223491 (1) | 1468 nt | ||
| Genomic | GenBank:CU929974 (1) | 41156 nt | ||
| Polypeptide | UniProtKB:A0A8N7TFN4 (1) | 417 aa |
- Ozantürk, A., Davis, E.E., Sabo, A., Weiss, M.M., Muzny, D., Dugan-Perez, S., Sistermans, E.A., Gibbs, R.A., Özgül, K.R., Yalnızoglu, D., Serdaroglu, E., Dursun, A., Katsanis, N. (2016) A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay. Cold Spring Harbor molecular case studies. 2:a000703
- Elkon, R., Milon, B., Morrison, L., Shah, M., Vijayakumar, S., Racherla, M., Leitch, C.C., Silipino, L., Hadi, S., Weiss-Gayet, M., Barras, E., Schmid, C.D., Ait-Lounis, A., Barnes, A., Song, Y., Eisenman, D.J., Eliyahu, E., Frolenkov, G.I., Strome, S.E., Durand, B., Zaghloul, N.A., Jones, S.M., Reith, W., Hertzano, R. (2015) RFX transcription factors are essential for hearing in mice. Nature communications. 6:8549
- Cannon, J.E., Place, E.S., Eve, A.M., Bradshaw, C.R., Sesay, A., Morrell, N.W., and Smith, J.C. (2013) Global analysis of the haematopoietic and endothelial transcriptome during zebrafish development. Mechanisms of Development. 130(2-3):122-131
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