Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23351
Gene name Gene Name - the full gene name approved by the HGNC.
KH and NYN domain containing
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
KHNYN
Synonyms (NCBI Gene) Gene synonyms aliases
KIAA0323
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q12
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein containing a ribonuclease NYN domain. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT030433 hsa-miR-24-3p Microarray 19748357
MIRT049771 hsa-miR-92a-3p CLASH 23622248
MIRT037179 hsa-miR-877-3p CLASH 23622248
MIRT712452 hsa-miR-3690 HITS-CLIP 19536157
MIRT712451 hsa-miR-4254 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:0003674 Function Molecular_function ND
GO:0003729 Function MRNA binding IBA 21873635
GO:0004521 Function Endoribonuclease activity IBA 21873635
GO:0005515 Function Protein binding IPI 30659753, 32296183
GO:0005575 Component Cellular_component ND
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619579 20166 ENSG00000100441
Protein
UniProt ID O15037
Protein name Protein KHNYN (KH and NYN domain-containing protein)
PDB 2N5M , 2N7K , 8WZC , 9BGL , 9CS9 , 9HTS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF11977 RNase_Zc3h12a 436 589 Zc3h12a-like Ribonuclease NYN domain Domain
Sequence
MPTWGARPASPDRFAVSAEAENKVREQQPHVERIFSVGVSVLPKDCPDNPHIWLQLEGPK
ENASRAKEYLKGLCSPELQDEIHYPPKLHCIFLGAQGFFLDCLAWSTSAHLVPRAPGSLM
ISGLTEAFVMAQSRVEELAERLSWDFTPGPSSGASQCTGVLRDFSALLQSPGDAHREALL
QLPLAVQEELLSLVQEASSGQGPGALASWEGRSSALLGAQCQGVRAPPSDGRESLDTGSM
GPGDCRGARGDTYAVEKEGGKQGGPREMDWGWKELPGEEAWEREVALRPQSVGGGARESA
PLKGKALGKEEIALGGGGFCVHREPPGAHGSCHRAAQSRGASLLQRLHNGNASPPRVPSP
PPAPEPPWHCGDRGDCGDRGDVGDRGDKQQGMARGRGPQWKRGARGGNLVTGTQRFKEAL
QDPFTLCLANVPGQPDLRHIVIDGSNVAMVHGLQHYFSSRGIAIAVQYFWDRGHRDITVF
VPQWRFSKDAKVRESHFLQKLYSLSLLSLTPSRVMDGKRISSYDDRFMVKLAEETDGIIV
SNDQFRDLAEESEKWMAIIRERLLPFTFVGNLFMVPDDPLGRNGPTLDE
FLKKPARTQGS
SKAQHPSRGFAEHGKQQQGREEEKGSGGIRKTRETERLRRQLLEVFWGQDHKVDFILQRE
PYCRDINQLSEALLSLNF
Sequence length 678
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