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Search Thermo Fisher Scientific
Entrez Gene ID: | 81494 |
Gene Name: | complement factor H related 5 |
Gene Aliases: |
CFHL5, CFHR5D, FHR-5, FHR5 |
Location: |
Chr.1:196975022-197009725 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CFHR5 | NM_030787.3 | NP_110414.1 | ||
XM_011510020.2 | XP_011508322.1 | |||
AF295327.1 | AAK15619.1 | |||
AK314026.1 | ||||
BC111773.1 | AAI11774.1 |
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2676788 | Chr.1:196987254 - 197007832 on Build GRCh38 | Deletion | CFHR5 |
dgv12e55 | Chr.1:196762018 - 197042447 on Build GRCh38 | Gain | F13B CFHR1 CFHR5 CFHR4 CFHR3 CFHR2 |
esv2758990 | Chr.1:196621707 - 197200642 on Build GRCh38 | Gain+Loss | F13B ZBTB41 CFHR1 CFH CFHR5 CFHR4 CFHR3 CFHR2 ASPM |
nsv528460 | Chr.1:196573437 - 197477572 on Build GRCh38 | Gain | F13B ZBTB41 CFHR1 KCNT2 CFH CFHR5 CFHR4 CFHR3 CFHR2 MIR4735 ASPM CRB1 |
dgv72e214 | Chr.1:196987015 - 197011691 on Build GRCh38 | Loss | CFHR5 |
Set Membership: |
Intragenic Non-exonic DGV Variation |