Assay Details
Target Gene Details
Entrez Gene ID: | 26121 |
Gene Name: | pre-mRNA processing factor 31 |
Gene Aliases: |
NY-BR-99, PRP31, RP11, SNRNP61 |
Location: |
Chr.19:54115410-54131719 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PRPF31 | NM_015629.3 | NP_056444.3 | ||
XM_006723137.3 | XP_006723200.1 | |||
AB593024.1 | ||||
AB593025.1 | ||||
AF308303.1 | AAG48270.1 | |||
AK098547.1 | BAC05329.1 | |||
AK301709.1 | ||||
AL050369.1 | CAB43677.1 | |||
AY040822.1 | AAK77986.1 | |||
BC117389.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv510773 | Chr.19:54017180 - 54132236 on Build GRCh38 | Deletion | PRPF31 VSTM1 TARM1 OSCAR TFPT NDUFA3 |
nsv515623 | Chr.19:54102901 - 54179150 on Build GRCh38 | Loss | LENG1 PRPF31 MBOAT7 TFPT CNOT3 TMC4 NDUFA3 |
nsv953613 | Chr.19:54097214 - 54198733 on Build GRCh38 | Deletion | LENG1 PRPF31 MBOAT7 OSCAR TFPT CNOT3 TMC4 TSEN34 NDUFA3 |
esv2718812 | Chr.19:53184636 - 54322450 on Build GRCh38 | Deletion | MIR526A1 LILRA5 MIR525 MIR521-2 MBOAT7 MIR373 MIR526A2 MIR515-2 MIR371A DPRX MIR517C VSTM1 LILRB3 TFPT MIR520D PRKCG MIR526B PRPF31 RPS9 MIR520A MIR523 MIR516B1 MYADM MIR4752 OSCAR CACNG8 MIR371B ZNF331 LOC105372457 ZNF525 MIR517A TPM3P9 MIR520G MIR519A2 MIR518D TMC4 TSEN34 CACNG7 MIR518B ZNF765 LOC284379 MIR516B2 MIR522 VN1R2 MIR498 MIR518A1 MIR517B MIR518A2 LILRB5 LILRB2 MIR516A1 LILRA6 VN1R4 MIR520E ZNF818P MIR1323 ZNF845 CACNG6 MIR519A1 MIR524 MIR512-1 ZNF665 MIR520F MIR518C MIR520H ZNF677 CNOT3 MIR935 MIR518E MIR372 MIR518F MIR512-2 MIR521-1 MIR527 MIR519D MIR520C TARM1 MIR519E ZNF761 ZNF813 MIR515-1 LENG1 MIR1283-1 MIR1283-2 FAM90A27P BIRC8 MIR519C MIR516A2 MIR520B NDUFA3 MIR519B NLRP12 |
nsv470157 | Chr.19:54063999 - 54127773 on Build GRCh38 | Loss | PRPF31 TARM1 OSCAR TFPT NDUFA3 |
nsv2545 | Chr.19:54122949 - 54142607 on Build GRCh38 | Insertion | PRPF31 CNOT3 |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |