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154197 PNLDC1

154197

PNLDC1

PARN like, ribonuclease domain containing 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition PARN like, ribonuclease domain containing 1

研究结论

Date Results Publications
2017-09-23 13:31:00 we describe the identification of a structural genetic variant segregating with affective psychosis in a family with multiple members suffering from bipolar I disorder. Using whole-genome sequencing, we delineated the translocation breakpoints as corresponding intragenic events disrupting BCL2L10 and PNLDC1. These data warrant further consideration for BCL2L10 and PNLDC1 as novel candidates for affective psychosis. 27260655
2010-04-07 21:40:00 Observational study of gene-disease association. (HuGE Navigator) 19724895
2010-04-07 21:40:00 Observational study of gene-disease association. (HuGE Navigator) 20198315
2009-12-02 21:41:00 Observational study of gene-disease association. (HuGE Navigator) 19851296

名称对应

Type IDs
Synonymous HsPNLDC1
Gene
UniProtKB-ID: PNDC1_HUMAN
UniprotKB: Q8NA58
UniParc: UPI00000717EB, UPI000006E4CF
EMBL: AK097559, CH471051, AK093139, AL139045, BC112246
Ensembl: ENSG00000146453
KO: hsa:154197
Nucleutide sequences
EMBL-CDS: EAW47612.1, BAC04070.1, BAC05101.1, EAW47613.1, AAI12247.1
Ensembl_TRS: ENST00000610273, ENST00000392167
Protein sequencees
Ensembl_PRO: ENSP00000476448, ENSP00000376007
RefSeq: NP_001258791.1, XP_016865805.1, XP_016865801.1, XP_016865803.1, XP_016865802.1, XP_011533793.1, XP_024302107.1, XP_011533795.1, NP_775787.1, XP_016865804.1
Others
UniRef100: UniRef100_Q8NA58
UniRef90: UniRef90_Q8NA58
UniRef50: UniRef50_Q8NA58
UniGene: Hs.349077
CCDS: CCDS5271.2, CCDS64561.1

全选

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研究热度

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