Gene Gene information from NCBI Gene database.
Entrez ID 285600
Gene name KIAA0825
Gene symbol KIAA0825
Synonyms (NCBI Gene)
C5orf36PAPA10
Chromosome 5
Chromosome location 5q15
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs956457873 T>A Pathogenic Stop gained, genic downstream transcript variant, coding sequence variant, non coding transcript variant
rs1562587032 T>-,TT Pathogenic Non coding transcript variant, frameshift variant, coding sequence variant, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
414
miRTarBase ID miRNA Experiments Reference
MIRT018655 hsa-miR-335-5p Microarray 18185580
MIRT1088095 hsa-let-7a CLIP-seq
MIRT1088096 hsa-let-7b CLIP-seq
MIRT1088097 hsa-let-7c CLIP-seq
MIRT1088098 hsa-let-7d CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183, 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617266 28532 ENSG00000185261
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8IV33
Protein name Uncharacterized protein KIAA0825
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14906 DUF4495 515 832 Domain of unknown function (DUF4495) Family
Sequence
MDWDDEYSHNSFDLHCLLNSFPGDLEFEQIFSDIDEKIEQNAASIKHCIKEIQSEINKQC
PGVQLQTTTDCFEWLTNYNYSTSESSFISHGDLIKFFKTLQDLLKNEQNQEEMTLDLLWD
LSCHSSVSFPSTLSGTSFHFLSRTSLHSVEDNSSMDVKSMWDDIRLHLRRFLVSKLQSHN
EINNSQQKILLKKQCLQQLLFLYPESEVIIKYQNIQNKLLANLLWNCFPSYNRDSNLDVI
AHGYQSTMLKLYSVIKEDFNTLCEILAPSSMVKFIKETYLDTVTEEMAKFLENFCELQFR
ENAVRVVKTSKSSSKHRGAVHALVTTECPQKGRNFSLPLDKVEFLSQLIKSFMKLEKGVQ
ELFDEILLSLKITRDTSGILEKSDREVVMEKPRANETNIPSEQSLPGKEATLLDFGWRSA
FKEVSLPMAHCVVTAIEGFSTKILQQEQNERSSAVSYAMNLVNVQQVWQDSHMFPEEEQP
KKIGKFCSDIMEKLDTMLPLALACRDDSFQEIRANLVEACCKVATAVLQRLQERAKEVPS
KAPLKNLHTYLSTAVYVFQHFKRYDNLMKEMTKKPIFLVLVQRYQEFINTLQFQVTNYCV
RVCATSILQDAESHHWDDYKAFYEGERCSFSIQMWHYFCWSLHYDLWTILPPKLAQEILV
EVLEKSLSLLASRYARAHPSRKRTPQLRLDVTTILICTENMLWSVCTSVQKLLNPHQHTD
DKIFKIHTHCNNLFTTLVILTSPLTELYKTFQHGLDESASDSLKSFFKQPLYWVSCISHF
YPSLLRTPSAGGLKAEGQLKLLLSQPRCNWNLLLETLLHHDGLLLRILLKSS
KQVSDTEN
NLNQGPSLMEAIFKILYHCSFSPQTFANVFVSYMEEEQLWDFLYNIPVSTCVEYELEVIR
CLRLALTDAIKDTVQQIVSVMSSRRNCETNLNKHIVPDCLLESMPKEWNYSPKETNRKES
CKSFTRLTAQAVSIVISKLPTVIACLPPPVKYFFFLSERKMSKKFVELKKAGLLVWNLIV
IICRIFEDGNTVELLTGASLDRWSKEKLGLICMCLKSIMGDQTSIHNQMIQKVIQSIEQQ
KPNWIERQLLKARKLSTECAFMTIEKSTALQEGDVALELTEQKINTMVLDLCHKPGGREY
LRQIYHIMQLNEEYLKEQLFSMNSSEEKPLPIRPLKTTLRSIEDQPSAFNPFHVYKAFSE
NMLDQSAITKWNWNWAKLLPNYLRLDKMTFSVLLKNRWEMKKDETLEEEEKAILEHLKQI
CTPQNSSASDNIEEQ
Sequence length 1275
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
65
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autosomal recessive nonsyndromic postaxial polydactyly Likely pathogenic; Pathogenic rs1562587032 RCV001261806
Familial pancreatic carcinoma Pathogenic rs766167375 RCV005870119
Polydactyly, postaxial, type A1 Likely pathogenic; Pathogenic rs1562587032 RCV000787313
Polydactyly, postaxial, type a10 Pathogenic; Likely pathogenic rs1239940017, rs766167375, rs201212314, rs1562587032 RCV003152436
RCV003224934
RCV003224935
RCV000787050
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs2044909, rs62364586 RCV005935449
RCV005938586
Cervical cancer Benign rs2044909 RCV005935452
Cholangiocarcinoma Benign; Uncertain significance rs2044909, rs143278447 RCV005935456
RCV005937534
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign rs62364586 RCV005938593
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Diabetes Mellitus Type 2 Associate 27863428
Hearing Loss Associate 27381092