Genomic Map
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Target Gene Details
Entrez Gene ID: | 51306 |
Gene Name: | family with sequence similarity 13 member B |
Gene Aliases: |
ARHGAP49, C5orf5, FAM13B1, KHCHP, N61 |
Location: |
Chr.5:137937909-138051961 on Build GRCh38 |
Assay Gene Location: | Within Exon 30 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM13B | NM_001101800.2 | 22 | 4788 | NP_001095270.1 |
| NM_001101801.2 | 22 | 4662 | NP_001095271.1 | |
| NM_016603.3 | 23 | 4872 | NP_057687.2 | |
| XM_005272007.1 | 23 | 4854 | XP_005272064.1 | |
| XM_006714647.1 | 24 | 4938 | XP_006714710.1 | |
| XM_006714648.1 | 24 | 4690 | XP_006714711.1 | |
| XM_006714649.1 | 23 | 4746 | XP_006714712.1 | |
| XM_011543448.1 | 25 | 4731 | XP_011541750.1 | |
| XM_011543449.1 | 25 | 5035 | XP_011541751.1 | |
| XM_011543450.1 | 24 | 4647 | XP_011541752.1 | |
| XM_017009549.1 | 23 | 4897 | XP_016865038.1 | |
| XM_017009550.1 | 23 | 4581 | XP_016865039.1 | |
| XM_017009551.1 | 22 | 4680 | XP_016865040.1 | |
| AF157316.1 | 5 | 2158 | AAF67482.1 | |
| AF251038.1 | 23 | 4791 | AAF63764.1 | |
| AL833699.1 | 9 | 2812 | ||
| BC056887.1 | AAH56887.1 |
Target Gene Details
Entrez Gene ID: | 27039 |
Gene Name: | polycystin 2 like 2, transient receptor potential cation channel |
Gene Aliases: |
TRPP5 |
Location: |
Chr.5:137889420-137942747 on Build GRCh38 |
Assay Gene Location: | Within Intron 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PKD2L2 | NM_001258448.1 | NP_001245377.1 | ||
| NM_001258449.1 | NP_001245378.1 | |||
| NM_001300921.1 | NP_001287850.1 | |||
| NM_014386.3 | NP_055201.2 | |||
| XM_017009343.1 | XP_016864832.1 | |||
| AF118125.1 | AAD46478.1 | |||
| AF182034.1 | AAF65622.1 | |||
| AK301924.1 | ||||
| BC044581.1 | AAH44581.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv830501 | Chr.5:137788777 - 137977035 on Build GRCh38 | Gain |
 MYOT
FAM13B
PKD2L2
NPY6R
|
| nsv830502 | Chr.5:137909039 - 138106588 on Build GRCh38 | Gain |
FAM13B
PKD2L2
LOC100130172
WNT8A
|
| esv3606913 | Chr.5:137856857 - 138124533 on Build GRCh38 | Gain |
NME5
MYOT
FAM13B
PKD2L2
LOC100130172
WNT8A
|
| esv3606915 | Chr.5:137917640 - 137950572 on Build GRCh38 | Gain |
FAM13B
PKD2L2
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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