Evidence Details for ZFYVE28
Basic Information Top
Gene Symbol: | ZFYVE28 ( LYST2,MGC43699,MGC61592 ) |
---|---|
Gene Full Name: | zinc finger, FYVE domain containing 28 |
Band: | 4p16.3 |
Quick Links | Entrez ID:57732; OMIM: NA; Uniprot ID:LST2_HUMAN; ENSEMBL ID: ENSG00000159733; HGNC ID: 29334 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ZFYVE28|57732|nucleotide
ATGATGAACAGGTTCCGAAAGTGGCTCTACAAACCCAAGAGGTCGGATCCGCAGCTGCTTGCCCGGTTCTACTATGCCGACGAGGAGCTGAACCAGGTGGCCGCG
GAGCTGGACAGCCTGGATGGGCGGAAGGACCCCCAGCGGTGCACGCTGCTGGTCAGCCAGTTCCGCTCCTGTCAGGACAATGTGTTGAACATCATTAACCAGATC
ATGGATGAGTGCATCCCCCAGGACCGCGCCCCCAGAGATTTCTGCGTCAAGTTCCCTGAGGAGATCCGGCACGACAACCTGGCCGGCCAGCTGTGGTTCGGTGCC
GAGTGCCTGGCCGCCGGCTCCATCATCATGAACCGGGAGCTGGAGAGCATGGCCATGCGCCCGCTGGCCAAGGAGCTGACGCGCAGCCTGGAGGACGTGCGGGGC
GCCCTCCGTGACCAGGCGCTGCGGGACCTGAACACCTACACAGAGAAGATGAGGGAAGCGCTGAGGCACTTCGACGTCCTGTTCGCAGAGTTTGAGCTCAGCTAC
GTCTCGGCCATGGTGCCTGTGAAGTCCCCCAGGGAGTACTACGTGCAGCAGGAGGTCATCGTGCTCTTCTGCGAGACGGTGGAGAGTGGCCTCGTGGTCTATGCG
GACGGACCTCTGAACTTGGACCGCAAGGTGGAAGACATGTCCGAGCTGTTCCGGCCCTTCCACACGTTGCTGCGGAAAATAAGGGATTTGCTGCAGACGCTGACG
GAGGAGGAGCTGCACACGCTGGAACGGAACCTCTGCATTTCCCAAGACGTGGAGTTCCCCATCCGCGCAGACGTGCAGGGACCCGCTGCCCTGGCGCCTGCCCTC
TCTGCCCCTCTCCCCCCTGAGGGGCCACTCTCAGCTAAGGCCAAAGACCCGGATGCAGAGCTGGCCTGCTCCATGCAGTACGACGACCAGGAGCTGGAGCAGCTC
AGCCGCATGGTCCACAGGGCGGGGGACGAGATGTCCTCTTTGCTTTCACCGCCCATTGCCTGCCAGTCCCCAGCTCACAGGCCAGGAGCGGAGGGCAGCCCAGGC
GGGGAGGCCTCTCCAGGTAGACCGCGCCTGCGGTCAGGCAGTGACGAGGAGGAGCGCGTGTTCTTCATGGATGACGTGGAGGGGACGGCAGAAGCCCTGGCCAGG
Show »
ATGATGAACAGGTTCCGAAAGTGGCTCTACAAACCCAAGAGGTCGGATCCGCAGCTGCTTGCCCGGTTCTACTATGCCGACGAGGAGCTGAACCAGGTGGCCGCG
GAGCTGGACAGCCTGGATGGGCGGAAGGACCCCCAGCGGTGCACGCTGCTGGTCAGCCAGTTCCGCTCCTGTCAGGACAATGTGTTGAACATCATTAACCAGATC
ATGGATGAGTGCATCCCCCAGGACCGCGCCCCCAGAGATTTCTGCGTCAAGTTCCCTGAGGAGATCCGGCACGACAACCTGGCCGGCCAGCTGTGGTTCGGTGCC
GAGTGCCTGGCCGCCGGCTCCATCATCATGAACCGGGAGCTGGAGAGCATGGCCATGCGCCCGCTGGCCAAGGAGCTGACGCGCAGCCTGGAGGACGTGCGGGGC
GCCCTCCGTGACCAGGCGCTGCGGGACCTGAACACCTACACAGAGAAGATGAGGGAAGCGCTGAGGCACTTCGACGTCCTGTTCGCAGAGTTTGAGCTCAGCTAC
GTCTCGGCCATGGTGCCTGTGAAGTCCCCCAGGGAGTACTACGTGCAGCAGGAGGTCATCGTGCTCTTCTGCGAGACGGTGGAGAGTGGCCTCGTGGTCTATGCG
GACGGACCTCTGAACTTGGACCGCAAGGTGGAAGACATGTCCGAGCTGTTCCGGCCCTTCCACACGTTGCTGCGGAAAATAAGGGATTTGCTGCAGACGCTGACG
GAGGAGGAGCTGCACACGCTGGAACGGAACCTCTGCATTTCCCAAGACGTGGAGTTCCCCATCCGCGCAGACGTGCAGGGACCCGCTGCCCTGGCGCCTGCCCTC
TCTGCCCCTCTCCCCCCTGAGGGGCCACTCTCAGCTAAGGCCAAAGACCCGGATGCAGAGCTGGCCTGCTCCATGCAGTACGACGACCAGGAGCTGGAGCAGCTC
AGCCGCATGGTCCACAGGGCGGGGGACGAGATGTCCTCTTTGCTTTCACCGCCCATTGCCTGCCAGTCCCCAGCTCACAGGCCAGGAGCGGAGGGCAGCCCAGGC
GGGGAGGCCTCTCCAGGTAGACCGCGCCTGCGGTCAGGCAGTGACGAGGAGGAGCGCGTGTTCTTCATGGATGACGTGGAGGGGACGGCAGAAGCCCTGGCCAGG
Show »
>ZFYVE28|57732|protein
MMNRFRKWLYKPKRSDPQLLARFYYADEELNQVAAELDSLDGRKDPQRCTLLVSQFRSCQDNVLNIINQIMDECIPQDRAPRDFCVKFPEEIRHDNLAGQLWFGA
ECLAAGSIIMNRELESMAMRPLAKELTRSLEDVRGALRDQALRDLNTYTEKMREALRHFDVLFAEFELSYVSAMVPVKSPREYYVQQEVIVLFCETVESGLVVYA
DGPLNLDRKVEDMSELFRPFHTLLRKIRDLLQTLTEEELHTLERNLCISQDVEFPIRADVQGPAALAPALSAPLPPEGPLSAKAKDPDAELACSMQYDDQELEQL
SRMVHRAGDEMSSLLSPPIACQSPAHRPGAEGSPGGEASPGRPRLRSGSDEEERVFFMDDVEGTAEALARPESPAGPFGWAGSTWADPQEKGQGGPGGAAGISLP
ASEKEEDLSNNNLEAEGTDGASLAGTSSCSCLDSRLHLDGWEVGADDAETAEMIAHRTGGMKLSATVIFNPKSPTSLDSAVATQEAASEPVAEGMDGGPHKLSTG
Show »
MMNRFRKWLYKPKRSDPQLLARFYYADEELNQVAAELDSLDGRKDPQRCTLLVSQFRSCQDNVLNIINQIMDECIPQDRAPRDFCVKFPEEIRHDNLAGQLWFGA
ECLAAGSIIMNRELESMAMRPLAKELTRSLEDVRGALRDQALRDLNTYTEKMREALRHFDVLFAEFELSYVSAMVPVKSPREYYVQQEVIVLFCETVESGLVVYA
DGPLNLDRKVEDMSELFRPFHTLLRKIRDLLQTLTEEELHTLERNLCISQDVEFPIRADVQGPAALAPALSAPLPPEGPLSAKAKDPDAELACSMQYDDQELEQL
SRMVHRAGDEMSSLLSPPIACQSPAHRPGAEGSPGGEASPGRPRLRSGSDEEERVFFMDDVEGTAEALARPESPAGPFGWAGSTWADPQEKGQGGPGGAAGISLP
ASEKEEDLSNNNLEAEGTDGASLAGTSSCSCLDSRLHLDGWEVGADDAETAEMIAHRTGGMKLSATVIFNPKSPTSLDSAVATQEAASEPVAEGMDGGPHKLSTG
Show »
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 (2) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (4) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Szatmari, 2007 | Europe, North America | SNP microarray | ASD | 1491 | - | - | - | - | - | 0 | ||
Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Bailey, 1998 | - | microsatellite-based genomic screen | PDD | 99 | - | 99 | - | - | - | - |
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Michaelson JJ, 2012 | - | 10 | 565 | Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.