Evidence Details for PRDM14
Basic Information Top
| Gene Symbol: | PRDM14 ( MGC59730,PFM11 ) |
|---|---|
| Gene Full Name: | PR domain containing 14 |
| Band: | 8q13.3 |
| Quick Links | Entrez ID:63978; OMIM: 611781; Uniprot ID:PRD14_HUMAN; ENSEMBL ID: ENSG00000147596; HGNC ID: 14001 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>PRDM14|63978|nucleotide
ATGGCTCTACCCCGGCCAAGTGAGGCCGTGCCTCAGGACAAGGTGTGCTACCCGCCGGAGAGCAGCCCGCAGAACCTGGCCGCGTACTACACGCCTTTCCCGTCC
TATGGACACTACAGAAACAGCCTGGCCACCGTGGAGGAAGACTTCCAACCTTTCCGGCAGCTGGAGGCCGCAGCGTCTGCTGCCCCCGCCATGCCCCCCTTCCCC
TTCCGGATGGCGCCTCCCTTGCTGAGCCCGGGTCTGGGCCTACAGAGGGAGCCTCTCTACGATCTGCCCTGGTACAGCAAGCTGCCACCGTGGTACCCAATTCCC
CACGTCCCCAGGGAAGTGCCGCCCTTCCTGAGCAGCAGCCACGAGTACGCGGGTGCCAGCAGTGAAGATCTGGGCCACCAAATCATTGGTGGCGACAACGAGAGT
GGCCCGTGTTGTGGACCTGACACTTTAATTCCACCGCCCCCTGCGGATGCTTCTCTGTTACCTGAGGGGCTGAGGACCTCCCAGTTATTACCTTGCTCACCCAGC
AAGCAGTCAGAGGATGGTCCCAAACCCTCCAACCAAGAAGGGAAGTCCCCTGCTCGGTTCCAGTTCACGGAGGAGGACCTGCACTTCGTTCTGTACGGGGTCACT
CCCAGCCTGGAGCACCCAGCCAGCCTGCACCATGCGATTTCAGGCCTCCTGGTCCCCCCAGACAGCTCTGGATCTGATTCTCTTCCTCAAACTCTGGATAAAGAC
TCCCTTCAACTTCCAGAAGGTCTATGCCTCATGCAGACGGTGTTTGGTGAAGTCCCACATTTTGGTGTGTTCTGCAGTAGTTTTATCGCCAAAGGAGTCAGGTTT
GGGCCCTTTCAAGGTAAAGTGGTCAATGCCAGTGAAGTGAAGACCTACGGAGACAATTCTGTGATGTGGGAGATCTTTGAAGATGGTCATTTGAGCCACTTTATA
GATGGAAAAGGAGGTACGGGGAACTGGATGTCCTATGTCAACTGTGCCCGCTTCCCCAAGGAGCAGAACCTAGTTGCTGTGCAGTGTCAAGGGCATATATTTTAT
GAGAGCTGCAAAGAGATCCATCAGAACCAAGAGCTCCTTGTGTGGTATGGAGACTGCTATGAGAAATTTCTGGATATTCCTGTGAGCCTTCAGGTCACAGAGCCG
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ATGGCTCTACCCCGGCCAAGTGAGGCCGTGCCTCAGGACAAGGTGTGCTACCCGCCGGAGAGCAGCCCGCAGAACCTGGCCGCGTACTACACGCCTTTCCCGTCC
TATGGACACTACAGAAACAGCCTGGCCACCGTGGAGGAAGACTTCCAACCTTTCCGGCAGCTGGAGGCCGCAGCGTCTGCTGCCCCCGCCATGCCCCCCTTCCCC
TTCCGGATGGCGCCTCCCTTGCTGAGCCCGGGTCTGGGCCTACAGAGGGAGCCTCTCTACGATCTGCCCTGGTACAGCAAGCTGCCACCGTGGTACCCAATTCCC
CACGTCCCCAGGGAAGTGCCGCCCTTCCTGAGCAGCAGCCACGAGTACGCGGGTGCCAGCAGTGAAGATCTGGGCCACCAAATCATTGGTGGCGACAACGAGAGT
GGCCCGTGTTGTGGACCTGACACTTTAATTCCACCGCCCCCTGCGGATGCTTCTCTGTTACCTGAGGGGCTGAGGACCTCCCAGTTATTACCTTGCTCACCCAGC
AAGCAGTCAGAGGATGGTCCCAAACCCTCCAACCAAGAAGGGAAGTCCCCTGCTCGGTTCCAGTTCACGGAGGAGGACCTGCACTTCGTTCTGTACGGGGTCACT
CCCAGCCTGGAGCACCCAGCCAGCCTGCACCATGCGATTTCAGGCCTCCTGGTCCCCCCAGACAGCTCTGGATCTGATTCTCTTCCTCAAACTCTGGATAAAGAC
TCCCTTCAACTTCCAGAAGGTCTATGCCTCATGCAGACGGTGTTTGGTGAAGTCCCACATTTTGGTGTGTTCTGCAGTAGTTTTATCGCCAAAGGAGTCAGGTTT
GGGCCCTTTCAAGGTAAAGTGGTCAATGCCAGTGAAGTGAAGACCTACGGAGACAATTCTGTGATGTGGGAGATCTTTGAAGATGGTCATTTGAGCCACTTTATA
GATGGAAAAGGAGGTACGGGGAACTGGATGTCCTATGTCAACTGTGCCCGCTTCCCCAAGGAGCAGAACCTAGTTGCTGTGCAGTGTCAAGGGCATATATTTTAT
GAGAGCTGCAAAGAGATCCATCAGAACCAAGAGCTCCTTGTGTGGTATGGAGACTGCTATGAGAAATTTCTGGATATTCCTGTGAGCCTTCAGGTCACAGAGCCG
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>PRDM14|63978|protein
MALPRPSEAVPQDKVCYPPESSPQNLAAYYTPFPSYGHYRNSLATVEEDFQPFRQLEAAASAAPAMPPFPFRMAPPLLSPGLGLQREPLYDLPWYSKLPPWYPIP
HVPREVPPFLSSSHEYAGASSEDLGHQIIGGDNESGPCCGPDTLIPPPPADASLLPEGLRTSQLLPCSPSKQSEDGPKPSNQEGKSPARFQFTEEDLHFVLYGVT
PSLEHPASLHHAISGLLVPPDSSGSDSLPQTLDKDSLQLPEGLCLMQTVFGEVPHFGVFCSSFIAKGVRFGPFQGKVVNASEVKTYGDNSVMWEIFEDGHLSHFI
DGKGGTGNWMSYVNCARFPKEQNLVAVQCQGHIFYESCKEIHQNQELLVWYGDCYEKFLDIPVSLQVTEPGKQPSGPSEESAEGYRCERCGKVFTYKYYRDKHLK
YTPCVDKGDRKFPCSLCKRSFEKRDRLRIHILHVHEKHRPHKCSTCGKCFSQSSSLNKHMRVHSGDRPYQCVYCTKRFTASSILRTHIRQHSGEKPFKCKYCGKS
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MALPRPSEAVPQDKVCYPPESSPQNLAAYYTPFPSYGHYRNSLATVEEDFQPFRQLEAAASAAPAMPPFPFRMAPPLLSPGLGLQREPLYDLPWYSKLPPWYPIP
HVPREVPPFLSSSHEYAGASSEDLGHQIIGGDNESGPCCGPDTLIPPPPADASLLPEGLRTSQLLPCSPSKQSEDGPKPSNQEGKSPARFQFTEEDLHFVLYGVT
PSLEHPASLHHAISGLLVPPDSSGSDSLPQTLDKDSLQLPEGLCLMQTVFGEVPHFGVFCSSFIAKGVRFGPFQGKVVNASEVKTYGDNSVMWEIFEDGHLSHFI
DGKGGTGNWMSYVNCARFPKEQNLVAVQCQGHIFYESCKEIHQNQELLVWYGDCYEKFLDIPVSLQVTEPGKQPSGPSEESAEGYRCERCGKVFTYKYYRDKHLK
YTPCVDKGDRKFPCSLCKRSFEKRDRLRIHILHVHEKHRPHKCSTCGKCFSQSSSLNKHMRVHSGDRPYQCVYCTKRFTASSILRTHIRQHSGEKPFKCKYCGKS
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| Evidences | Syndromic Gene | GWAS | CNV | Linkage | Association | Expression | NGS de novo | NGS Mosaic | NGS Other | Low-Scale Gene Studies | Total |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Score (No. of Studies) | No | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top

