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 (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
26
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Autosomal recessive nonsyndromic postaxial polydactyly Likely pathogenic; Pathogenic rs1562587032 RCV001261806
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Familial pancreatic carcinoma Pathogenic rs766167375 RCV005870119
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Polydactyly, postaxial, type A1 Likely pathogenic; Pathogenic rs1562587032 RCV000787313
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Polydactyly, postaxial, type a10 Pathogenic; Likely pathogenic rs1239940017, rs766167375, rs201212314, rs1562587032 RCV003152436
RCV003224934
RCV003224935
RCV000787050
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Acute myeloid leukemia Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cholangiocarcinoma Benign; Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Chronic lymphocytic leukemia/small lymphocytic lymphoma Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Diabetes Mellitus Type 2 Diabetes mellitus, type 2 Pubtator 27863428 Associate
★☆☆☆☆
Found in Text Mining only
Diabetic Retinopathy Diabetic Retinopathy GWASDB_DG 21310492
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Diabetic Retinopathy Diabetic Retinopathy GWASCAT_DG 21310492
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Hearing Loss Hearing loss Pubtator 27381092 Associate
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm GWASCAT_DG 29299148
★☆☆☆☆
Found in Text Mining only
POLYDACTYLY, POSTAXIAL Polydactyly BEFREE 30982135
★☆☆☆☆
Found in Text Mining only
Postaxial foot polydactyly Foot Polydactyly HPO_DG
★☆☆☆☆
Found in Text Mining only
Postaxial polydactyly type A Polydactyly ORPHANET_DG 30982135
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Postaxial polydactyly type A Polydactyly HPO_DG
★★☆☆☆
Found in Text Mining + Unknown/Other Associations