DIPK2A
| DIPK2A | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | DIPK2A, DIA1, GoPro49, HASF, chromosome 3 open reading frame 58, C3orf58, divergent protein kinase domain 2A | |||||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 612200; MGI: 1916111; GeneCards: DIPK2A | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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| chromosome 3 open reading frame 58 | |
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| Identifiers | |
| Symbol | C3orf58 |
| NCBI gene | 205428 |
| HGNC | 28490 |
| RefSeq | NM_173552 |
| Other data | |
| Locus | Chr. 3 q24 |
Divergent protein kinase domain 2A is a protein encoded in humans by the DIPK2A gene. It was highlighted in a screen for genes possibly related to autism. The authors propose that the gene should be renamed Deleted in autism-1 (DIA1). Experiments in a rat neuronal cell culture model suggested that this gene may be regulated directly or indirectly by MEF2 site binding proteins.[5]
See also
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000181744 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000045414 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Morrow EM, Yoo SY, Flavell SW, et al. (2008). "Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry". Science. 321 (5886): 218–223. Bibcode:2008Sci...321..218M. doi:10.1126/science.1157657. PMC 2586171. PMID 18621663.
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