Genomic Map
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Target Gene Details
Entrez Gene ID: | 9715 |
Gene Name: | family with sequence similarity 131 member B |
Gene Aliases: |
- |
Location: |
Chr.7:143353400-143382304 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM131B | NM_001031690.2 | 7 | 1429 | NP_001026860.2 |
| NM_001278297.1 | 6 | 1335 | NP_001265226.1 | |
| NM_014690.4 | 7 | 1322 | NP_055505.3 | |
| XM_005250073.3 | 7 | 1643 | XP_005250130.1 | |
| XM_006716186.2 | 7 | 1421 | XP_006716249.1 | |
| AB018316.1 | 6 | 1217 | ||
| AK124557.1 | 7 | 1377 | ||
| AL832579.2 | 6 | 2910 | CAD89938.1 | |
| BC045611.1 | 7 | 1434 | AAH45611.2 | |
| BC050543.1 | 7 | 1297 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv949966 | Chr.7:143351408 - 143357207 on Build GRCh38 | Deletion |
 CLCN1
FAM131B
|
| nsv517520 | Chr.7:143352880 - 143400007 on Build GRCh38 | Loss |
ZYX
LOC100507507
EPHA1
MIR6892
FAM131B
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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