Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
388650
Gene name Gene Name - the full gene name approved by the HGNC.
Divergent protein kinase domain 1A
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DIPK1A
Synonyms (NCBI Gene) Gene synonyms aliases
FAM69A
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p22.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. Alternatively spliced transcript variants encoding multiple isof
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005789 Component Endoplasmic reticulum membrane IEA
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614542 32213 ENSG00000154511
Protein
UniProt ID Q5T7M9
Protein name Divergent protein kinase domain 1A (Protein FAM69A)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14875 PIP49_N 19 176 N-term cysteine-rich ER, FAM69 Domain
PF12260 PIP49_C 194 396 Protein-kinase domain of FAM69 Family
Sequence
Sequence length 428
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Anemia Anemia, Diamond-Blackfan rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966
View all (89 more)
19061985, 23718193, 19773262
Aplastic anemia Aplastic Anemia rs113993991, rs113993993, rs864309668, rs121908974, rs199422265, rs199422270, rs104894176, rs104894180, rs28933973, rs104894182, rs28933376, rs771552960, rs786205093, rs193302876, rs113993992
View all (104 more)
Atrial septal defect Atrial Septal Defects rs137852951, rs137852953, rs137852955, rs267607106, rs104893900, rs104893901, rs104893903, rs606231358, rs606231359, rs137852683, rs606231360, rs104893907, rs104894073, rs1585703301, rs104894074
View all (25 more)
Diamond-blackfan anemia Diamond-Blackfan Anemia 1 rs121434389, rs1570566590, rs151155897, rs143951267, rs267607023, rs786200892, rs148622862, rs397507554, rs121434405, rs1571026775, rs142156224, rs267607021, rs1581931541, rs267607022, rs61762293
View all (76 more)
Unknown
Disease term Disease name Evidence References Source
Multiple Sclerosis Multiple Sclerosis GWAS
Prostate cancer Prostate cancer Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Multiple Sclerosis Associate 20087403
Myasthenia Gravis Associate 30696470
Neurologic Manifestations Associate 23840464
Ophthalmoplegia Associate 30696470