Genomic Map
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Target Gene Details
Entrez Gene ID: | 25953 |
Gene Name: | paroxysmal nonkinesigenic dyskinesia |
Gene Aliases: |
BRP17, DYT8, FKSG19, FPD1, KIPP1184, MR-1, MR1, PDC, PKND1, TAHCCP2 |
Location: |
Chr.2:218270392-218346793 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PNKD | NM_015488.4 | NP_056303.3 | ||
| XM_017003771.1 | XP_016859260.1 | |||
| AB033010.1 | BAA86498.1 | |||
| AK289867.1 | ||||
| BC036457.2 | AAH36457.1 |
Target Gene Details
Entrez Gene ID: | 64114 |
Gene Name: | transmembrane BAX inhibitor motif containing 1 |
Gene Aliases: |
LFG3, MST100, MSTP100, PP1201, RECS1 |
Location: |
Chr.2:218274192-218292577 on Build GRCh38 |
Assay Gene Location: | Within Exon 17 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMBIM1 | NM_001321427.1 | 13 | 1609 | NP_001308356.1 |
| NM_001321428.1 | 12 | 1020 | NP_001308357.1 | |
| NM_001321429.1 | 13 | 1196 | NP_001308358.1 | |
| NM_001321430.1 | 13 | 1136 | NP_001308359.1 | |
| NM_001321432.1 | 12 | 960 | NP_001308361.1 | |
| NM_001321433.1 | 13 | 1133 | NP_001308362.1 | |
| NM_001321435.1 | 13 | 1207 | NP_001308364.1 | |
| NM_001321436.1 | 13 | 1211 | NP_001308365.1 | |
| NM_001321438.1 | 11 | 970 | NP_001308367.1 | |
| NM_022152.5 | 12 | 1035 | NP_071435.2 | |
| NR_135643.1 | 11 | 793 | ||
| XM_011511627.1 | 12 | 1388 | XP_011509929.1 | |
| AB257295.1 | 12 | 1096 | ||
| AF193045.1 | 12 | 949 | AAG22473.1 | |
| AK027755.1 | 10 | 683 | BAB55346.1 | |
| AK075465.1 | 8 | 510 | BAC11636.1 | |
| AK090618.1 | 13 | 1607 | ||
| AK093911.1 | 10 | 1547 | ||
| AK130380.1 | 12 | 993 | ||
| AK130713.1 | 12 | 971 | ||
| AK298123.1 | 13 | 807 | ||
| AK298500.1 | 11 | 729 | ||
| AK300597.1 | 11 | 897 | ||
| BC007980.2 | 12 | 949 | AAH07980.1 | |
| BC013428.1 | 12 | 1013 | AAH13428.1 | |
| BC026348.1 | 12 | 970 | AAH26348.1 | |
| BC026693.2 | 12 | 981 | AAH26693.1 | |
| CA488388.1 | 2 | 148 |
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Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
non-DGV Variation
|
Gene Ontology Categories:
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