Genomic Map
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Target Gene Details
Entrez Gene ID: | 1675 |
Gene Name: | complement factor D |
Gene Aliases: |
ADIPSIN, ADN, DF, PFD |
Location: |
Chr.19:859659-863569 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 4 - Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CFD | NM_001317335.1 | NP_001304264.1 | ||
| NM_001928.3 | NP_001919.2 | |||
| AJ313463.1 | CAC48304.1 | |||
| AK300963.1 | ||||
| BC034529.1 | AAH34529.1 | |||
| BC040146.1 | AAH40146.1 | |||
| BC051001.1 | AAH51001.1 | |||
| BC057807.1 | AAH57807.1 | |||
| CR536575.1 | CAG38812.1 | |||
| DQ884409.1 | ||||
| HY281047.1 | ||||
| M84526.1 | AAA35527.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv134n111 | Chr.19:607984 - 967584 on Build GRCh38 | Deletion |
 RNU6-9
ELANE
FSTL3
MISP
FGF22
PRTN3
AZU1
MIR4745
KISS1R
PRSS57
MED16
POLRMT
PALM
HCN2
PTBP1
MIR3187
RNF126
R3HDM4
LOC101928450
ARID3A
PLPPR3
CFD
|
| nsv1072293 | Chr.19:860899 - 862600 on Build GRCh38 | Deletion |
CFD
|
| nsv2385 | Chr.19:858907 - 894070 on Build GRCh38 | Insertion |
RNU6-9
MED16
CFD
|
| nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
POLR2E
ELANE
FSTL3
MISP
GZMM
TPGS1
CDC34
MIR4745
GRIN3B
KISS1R
CNN2
ODF3L2
THEG
MED16
WDR18
GPX4
ARHGAP45
RNF126
LOC101928450
SHC2
ARID3A
BSG
PLPPR3
CFD
RNU6-9
C2CD4C
FGF22
PRTN3
AZU1
ABCA7
MADCAM1
PRSS57
LOC105372235
POLRMT
PALM
HCN2
PTBP1
RNU6-2
MIR3187
R3HDM4
TMEM259
|
| nsv470101 | Chr.19:401714 - 1008505 on Build GRCh38 | Loss |
ELANE
FSTL3
MISP
GZMM
TPGS1
CDC34
MIR4745
GRIN3B
KISS1R
ODF3L2
MED16
WDR18
RNF126
LOC101928450
SHC2
ARID3A
BSG
PLPPR3
CFD
RNU6-9
C2CD4C
FGF22
PRTN3
AZU1
MADCAM1
PRSS57
LOC105372235
POLRMT
PALM
HCN2
PTBP1
MIR3187
R3HDM4
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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