Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23288 |
Gene nameGene Name - the full gene name approved by the HGNC.
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IQ motif containing E |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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IQCE |
SynonymsGene synonyms aliases
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1700028P05Rik, PAPA7 |
ChromosomeChromosome number
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7 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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7p22.3 |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs753670589 |
C>T |
Likely-pathogenic |
Stop gained, coding sequence variant |
rs755938967 |
G>A |
Pathogenic |
Genic upstream transcript variant, splice acceptor variant |
rs760694987 |
AGAG>- |
Pathogenic |
Coding sequence variant, splice acceptor variant |
rs773701437 |
CGGAGTGTCC>- |
Pathogenic |
Coding sequence variant, frameshift variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
Q6IPM2 |
Protein name |
IQ domain-containing protein E |
Protein function |
Component of the EvC complex that positively regulates ciliary Hedgehog (Hh) signaling (By similarity). Required for proper limb morphogenesis (PubMed:28488682). |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00612 |
IQ |
543 → 563 |
IQ calmodulin-binding motif |
Motif |
PF00612 |
IQ |
602 → 622 |
IQ calmodulin-binding motif |
Motif |
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Sequence |
MFLGTGEPALDTGDDSLSAVTFDSDVETKAKRKAFHKPPPTSPKSPYLSKPRKVASWRSL RTAGSMPLGGRASLTPQKLWLGTAKPGSLTQALNSPLTWEHAWTGVPGGTPDCLTDTFRV KRPHLRRSASNGHVPGTPVYREKEDMYDEIIELKKSLHVQKSDVDLMRTKLRRLEEENSR KDRQIEQLLDPSRGTDFVRTLAEKRPDASWVINGLKQRILKLEQQCKEKDGTISKLQTDM KTTNLEEMRIAMETYYEEVHRLQTLLASSETTGKKPLGEKKTGAKRQKKMGSALLSLSRS VQELTEENQSLKEDLDRVLSTSPTISKTQGYVEWSKPRLLRRIVELEKKLSVMESSKSHA AEPVRSHPPACLASSSALHRQPRGDRNKDHERLRGAVRDLKEERTALQEQLLQRDLEVKQ LLQAKADLEKELECAREGEEERREREEVLREEIQTLTSKLQELQEMKKEEKEDCPEVPHK AQELPAPTPSSRHCEQDWPPDSSEEGLPRPRSPCSDGRRDAAARVLQAQWKVYKHKKKKA VLDEAAVVLQAAFRGHLTRTKLLASKAHGSEPPSVPGLPDQSSPVPRVPSPIAQATGSPV QEEAIVIIQSALRAHLARARHSATGKRTTTAASTRRRSASATHGDASSPPFLAALPDPSP SGPQALAPLPGDDVNSDDSDDIVIAPSLPTKNFPV
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Sequence length |
695 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Multiple congenital anomalies |
Multiple congenital anomalies |
rs1057517732 |
22981989, 18799693, 19810119, 25348401, 28224613, 3719536, 9399901, 28488682, 24582806, 23719536, 27626380, 22495311 |
Polydactyly |
POLYDACTYLY, POSTAXIAL, Postaxial polydactyly type A, POLYDACTYLY, POSTAXIAL, TYPE A7 |
rs1583729398, rs121917709, rs1583734240, rs121917714, rs397507422, rs398122899, rs587776959, rs386833752, rs1057518698, rs1060499558, rs755938967, rs1375768446, rs1309855392, rs1565601979, rs748321474, rs368652620, rs1562587032, rs760694987 |
26394607, 28488682, 28488682 |
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