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- Gene Symbol
- CRIP2
- Assay Reference Genome
Location
Chr.14:105479026 on build GRCh38- Cytoband
- 14q32.33
Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 1397 |
Gene Name: | cysteine rich protein 2 |
Gene Aliases: |
CRIP, CRP2, ESP1 |
Location: |
Chr.14:105472938-105480170 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 7 - Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CRIP2 | NM_001270837.1 | NP_001257766.1 | ||
| NM_001270841.1 | NP_001257770.1 | |||
| NM_001312.3 | NP_001303.1 | |||
| NR_073081.1 | ||||
| NR_073082.1 | ||||
| NR_073083.1 | ||||
| NR_073084.1 | ||||
| NR_073085.1 | ||||
| AK057837.1 | ||||
| AK091845.1 | ||||
| AK223251.1 | BAD96971.1 | |||
| AK300092.1 | ||||
| AK311402.1 | ||||
| AK315757.1 | ||||
| BC000434.2 | AAH00434.1 | |||
| BC001931.1 | AAH01931.1 | |||
| BC034151.1 | AAH34151.1 | |||
| BC128101.1 | ||||
| BE271979.1 | ||||
| BT019911.1 | AAV38714.1 | |||
| CN367966.1 | ||||
| D42123.1 | BAA07703.1 | |||
| HY078632.1 | ||||
| HY161884.1 | ||||
| U36190.1 | AAB03194.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv3996n54 | Chr.14:105474226 - 105488519 on Build GRCh38 | Gain |
 CRIP2
CRIP1
|
| nsv566204 | Chr.14:105376842 - 105479048 on Build GRCh38 | Gain |
CRIP2
TEX22
PACS2
LOC100507437
MTA1
|
| nsv817647 | Chr.14:105382554 - 105480505 on Build GRCh38 | Gain |
CRIP2
TEX22
PACS2
LOC100507437
MTA1
|
| dgv3998n54 | Chr.14:105474495 - 105770768 on Build GRCh38 | Loss |
LOC107987211
TMEM121
ELK2AP
IGHG1
IGHA1
IGHG3
IGH
IGHG2
MIR8071-2
CRIP2
C14orf80
IGHA2
IGHG4
LOC105370697
CRIP1
MIR8071-1
|
| nsv566229 | Chr.14:105474172 - 105483783 on Build GRCh38 | Loss |
CRIP2
|
| nsv1160204 | Chr.14:105291411 - 105483783 on Build GRCh38 | Duplication |
BRF1
CRIP2
TEX22
PACS2
LOC100507437
MTA1
|
| nsv566206 | Chr.14:105439736 - 105543235 on Build GRCh38 | Loss |
CRIP2
C14orf80
TMEM121
LOC105370697
CRIP1
MTA1
|
| nsv832890 | Chr.14:105304955 - 105483089 on Build GRCh38 | Loss |
BRF1
CRIP2
TEX22
PACS2
LOC100507437
MTA1
|
| nsv1440 | Chr.14:105473170 - 105479862 on Build GRCh38 | Insertion |
CRIP2
|
| esv1004211 | Chr.14:105477270 - 105479324 on Build GRCh38 | Insertion |
CRIP2
|
| nsv566210 | Chr.14:105465248 - 105488368 on Build GRCh38 | Gain |
CRIP2
CRIP1
MTA1
|
| nsv9177 | Chr.14:105476516 - 105485998 on Build GRCh38 | Gain |
CRIP2
|
| nsv827088 | Chr.14:105454469 - 105498549 on Build GRCh38 | Gain |
CRIP2
C14orf80
CRIP1
MTA1
|
| nsv952282 | Chr.14:105363764 - 105510163 on Build GRCh38 | Deletion |
CRIP2
C14orf80
TEX22
CRIP1
PACS2
LOC100507437
MTA1
|
| dgv3999n54 | Chr.14:105474867 - 105487998 on Build GRCh38 | Loss |
CRIP2
CRIP1
|
| esv2760014 | Chr.14:105047009 - 105483089 on Build GRCh38 | Loss |
GPR132
BRF1
CRIP2
JAG2
BTBD6
TEX22
PACS2
LOC100507437
MIR6765
MTA1
NUDT14
LOC102723354
|
| dgv3987n54 | Chr.14:105461599 - 105499970 on Build GRCh38 | Loss |
CRIP2
C14orf80
CRIP1
MTA1
|
| nsv470679 | Chr.14:105124547 - 105605978 on Build GRCh38 | Loss |
JAG2
TMEM121
BTBD6
TEX22
IGH
MTA1
NUDT14
BRF1
CRIP2
C14orf80
IGHA2
LOC105370697
CRIP1
PACS2
LOC100507437
MIR6765
|
| nsv566265 | Chr.14:105474766 - 105479048 on Build GRCh38 | Loss |
CRIP2
|
| esv3635645 | Chr.14:105473682 - 105484540 on Build GRCh38 | Gain |
CRIP2
|
| nsv1054190 | Chr.14:105246882 - 105701138 on Build GRCh38 | Gain |
TMEM121
BTBD6
TEX22
ELK2AP
IGH
MTA1
IGHG2
MIR8071-2
BRF1
CRIP2
C14orf80
IGHA2
IGHG4
LOC105370697
CRIP1
PACS2
LOC100507437
MIR8071-1
|
| dgv3991n54 | Chr.14:105472502 - 105480505 on Build GRCh38 | Loss |
CRIP2
|
| nsv517055 | Chr.14:105136282 - 106779068 on Build GRCh38 | Gain+Loss |
BTBD6
MIR4538
IGHD
IGHG3
IGH
KIAA0125
MTA1
ADAM6
LINC00221
MIR8071-2
CRIP2
IGHV1-69
IGHG4
LOC105370697
MIR4539
MIR6765
IGHV3-71
LOC107987211
IGHV3-41
JAG2
IGHV3-30
TMEM121
TEX22
MIR4537
ELK2AP
IGHG1
IGHA1
IGHV3-69-1
IGHV3-23
NUDT14
IGHG2
IGHM
BRF1
IGHV4-55
IGHV4-31
C14orf80
IGHA2
MIR4507
CRIP1
PACS2
LINC00226
IGHV3-48
LOC100507437
MIR8071-1
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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