Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
158405
Gene name Gene Name - the full gene name approved by the HGNC.
KIAA1958
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KIAA1958
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
9
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q32
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT026952 hsa-miR-192-5p Microarray 19074876
MIRT718166 hsa-miR-6812-3p HITS-CLIP 19536157
MIRT718165 hsa-miR-4434 HITS-CLIP 19536157
MIRT718164 hsa-miR-4516 HITS-CLIP 19536157
MIRT718163 hsa-miR-5703 HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 31515488, 32296183
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
617390 23427 ENSG00000165185
Protein
UniProt ID Q8N8K9
Protein name Uncharacterized protein KIAA1958
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12012 DUF3504 532 687 Domain of unknown function (DUF3504) Family
Sequence
MEDCLHTSSENLSKLVSWAHSHGTICSLIPNLKHLLSEGSHGNLTAMWGCSAGHAYHWPL
TATCRAGSQERVCFQDNRSFNSDSPSIIGVPSETQTSPVERYPGRPVKAKLDCNRTRDSC
DFSYCSEPSELDETVEEYEDENTLFDMVCESSVTDEDSDFEPQTQRPQSIARKRPGVVPS
SLHSSSQTQMVDECSNDVIIKKIKQEIPEDYYIVANAELTGGVDGPALSLTQMAKPKPQT
HAGPSCVGSAKLIPHVTSAISTELDPHGMSASPSVISRPIVQKTARVSLASPNRGPPGTH
GTNQQVAMQMPVSTSHPNKQISIPLSALQLPGQDEQVASEEFLSHLPSQVSSCEVALSPS
VNTEPEVSSSQQQPPVAPAITTEATAQCIPAYSTKLNKFPVFNINDDLNDLCTSAVSPNT
TKATRYALNVWRYWCMTNGLKDHTDITKIPAVKLNELLENFYVTVKKSDGSDFLATSLHA
IRRGLDRILKNAGVGFSITSSTFSSSTKKLKEKLWVLSKAGMSGARSRNIVYFSLSDEEE
MWQAGCLGDDSPITLLSTVVKYNSQYLNMRTLQEHADLMYGDIELLKDPQNQPYFARTDS
VKRESRSGSTRVCHGKIYHEHSRGHKQCPYCLLYKYMYIHRPPTQMEAKSPFYLTARKEA
TDMGSVWYEEQRMGLRSLRGIVPNLAK
KVKLENCENFTFVSFTQVSRRLGSHSCCQ
Sequence length 716
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Asthma Childhood asthma, Asthma 30373671 ClinVar, GWAS