Genomic Map
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Target Gene Details
Entrez Gene ID: | 9501 |
Gene Name: | rabphilin 3A-like (without C2 domains) |
Gene Aliases: |
NOC2 |
Location: |
Chr.17:212389-386254 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 13 - Exon 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RPH3AL | NM_001190411.1 | NP_001177340.1 | ||
| NM_001190412.1 | NP_001177341.1 | |||
| NM_001190413.1 | NP_001177342.1 | |||
| NM_006987.3 | NP_008918.1 | |||
| XM_011535364.2 | XP_011533666.1 | |||
| XM_011535365.2 | XP_011533667.1 | |||
| XM_011535366.2 | XP_011533668.1 | |||
| XM_011535367.2 | XP_011533669.1 | |||
| XM_011535368.2 | XP_011533670.1 | |||
| XM_011535369.2 | XP_011533671.1 | |||
| XM_017025367.1 | XP_016880856.1 | |||
| XM_017025368.1 | XP_016880857.1 | |||
| XM_017025369.1 | XP_016880858.1 | |||
| XM_017025370.1 | XP_016880859.1 | |||
| AF129812.1 | AAD45582.1 | |||
| AK000469.1 | BAA91186.1 | |||
| AK291950.1 | ||||
| BC005153.1 | AAH05153.1 | |||
| BC093776.1 | AAH93776.1 | |||
| BC113413.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3639615 | Chr.17:177867 - 302096 on Build GRCh38 | Gain |
 LOC100506371
DOC2B
RPH3AL
|
| nsv469538 | Chr.17:150208 - 266971 on Build GRCh38 | Loss |
LOC100506371
DOC2B
RPH3AL
|
| esv3639614 | Chr.17:176972 - 217320 on Build GRCh38 | Gain |
LOC100506371
DOC2B
RPH3AL
|
| dgv3071n100 | Chr.17:150721 - 853554 on Build GRCh38 | Gain |
DBIL5P
RPH3AL
LOC105371430
GEMIN4
VPS53
LOC100506371
LOC100506388
FAM101B
GLOD4
FAM57A
MRM3
DOC2B
NXN
C17orf97
|
| nsv509642 | Chr.17:191012 - 394464 on Build GRCh38 | Insertion |
LOC100506388
RPH3AL
|
| nsv573933 | Chr.17:191293 - 286907 on Build GRCh38 | Gain |
RPH3AL
|
| esv2422420 | Chr.17:210752 - 1113141 on Build GRCh38 | Duplication |
MIR3183
DBIL5P
RPH3AL
LOC105371430
GEMIN4
VPS53
LOC101927727
LOC100130876
LOC100506388
FAM101B
GLOD4
FAM57A
ABR
MRM3
NXN
C17orf97
TIMM22
|
| nsv457627 | Chr.17:201297 - 733582 on Build GRCh38 | Gain |
LOC100506388
FAM101B
FAM57A
RPH3AL
LOC105371430
C17orf97
VPS53
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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