AutismKB 2.0

Evidence Details for CCDC19


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Basic Information Top
Gene Symbol:CCDC19 ( NESG1 )
Gene Full Name: coiled-coil domain containing 19
Band: 1q22
Quick LinksEntrez ID:25790; OMIM: 605152; Uniprot ID:CCD19_HUMAN; ENSEMBL ID: ENSG00000213085; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>CCDC19|25790|nucleotide
ATGCCACTAAGCACAGCTGGCATCCTGAGCTCCTCTTCTGCCGCTTCCAACAGGTCAAGGAATAAGGCTCGCTATCGGACCAAAGCCGTGAGCTCTGAGGTGGAT
GAGAGCCTCTTTGGAGATATCAAGTCCCCAGCCCAGGGCCAGAGCGACAGCCCCATTGTGCTGCTCCGAGATAAGCATACCCTTCAAAAAACTCTCACTGCTTTG
GGCTTGGATCGCAAGCCAGAGACCATCCAGCTCATCACCCGGGACATGGTCCGAGAACTCATTGTTCCCACAGAGGATCCCTCCGGGGAGTCCCTAATCATCAGC
CCTGAGGAGTTTGAGCGAATCAAATGGGCATCCCATGTCCTGACCAGAGAAGAACTTGAGGCCAGGGACCAGGCCTTCAAGAAGGAGAAGGAAGCCACCATGGAT
GCAGTGATGACACGAAAGAAGATCATGAAACAGAAGGAGATGGTGTGGAACAACAACAAGAAGCTCAGTGACCTGGAGGAGGTGGCCAAGGAACGGGCCCAGAAC
CTCCTGCAGAGAGCCAACAAGCTGCGGATGGAGCAGGAGGAGGAGCTCAAGGACATGAGCAAGATTATCCTCAATGCTAAGTGCCATGCCATCCGGGATGCCCAA
ATCCTGGAGAAGCAGCAGATCCAAAAAGAACTGGACACAGAAGAGAAGCGGTTGGATCAGATGATGGAAGTGGAGCGGCAGAAATCCATTCAAAGGCAGGAGGAA
CTGGAGAGGAAGAGGAGGGAGGAAAGAATTAGAGGAAGGCGGCAAATTGTGGAACAGATGGAAAAGAACCAGGAGGAGCGATCGCTGCTTGCTGAGCAGCGGGAG
CAGGAGAAGGAGCAGATGCTGGAATATATGGAACAGCTCCAAGAGGAAGATCTAAAGGACATGGAACGAAGGCAGCAACAAAAACTGAAGATGCAAGCTGAGATT
AAGCGCATCAATGATGAAAACCAGAAACAGAAAGCAGAACTGCTGGCTCAGGAGAAGCTGGCAGACCAGATGGTGATGGAGTTTACCAAGAAGAAGATGGCTCGA
GAAGCAGAGTTTGAGGCTGAGCAGGAGAGAATCCGGAGGGAGAAAGAGAAGGAGATCGCACGCTTGAGGGCCATGCAGGAGAAGGCCCAGGATTACCAGGCAGAA
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>CCDC19|25790|protein
MPLSTAGILSSSSAASNRSRNKARYRTKAVSSEVDESLFGDIKSPAQGQSDSPIVLLRDKHTLQKTLTALGLDRKPETIQLITRDMVRELIVPTEDPSGESLIIS
PEEFERIKWASHVLTREELEARDQAFKKEKEATMDAVMTRKKIMKQKEMVWNNNKKLSDLEEVAKERAQNLLQRANKLRMEQEEELKDMSKIILNAKCHAIRDAQ
ILEKQQIQKELDTEEKRLDQMMEVERQKSIQRQEELERKRREERIRGRRQIVEQMEKNQEERSLLAEQREQEKEQMLEYMEQLQEEDLKDMERRQQQKLKMQAEI
KRINDENQKQKAELLAQEKLADQMVMEFTKKKMAREAEFEAEQERIRREKEKEIARLRAMQEKAQDYQAEQDALRAKRNQEVADREWRRKEKENARKKMETEAEL
RKSRLEQVAFKEHALAVQVQRDRDEFERILRAQREQIEKERLEEEKKATGRLQHANELRRQVRENQQKEVQNRIATFEEGRRLKEEAQKRRERIDEIKRKKLEEL
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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) 1 (1) 0 (0) 0 (0) 0 (2) 0 (0) 0 (0) 0 (0) 2 (3)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top