- Diseases
- Aplasia cutis congenita
Aplasia cutis congenita
Name: |
Aplasia cutis congenita
|
Description: |
A rare skin disorder characterized by localized absence of skin that is usually located on the scalp but can occur anywhere on the body including the face, trunk and extremities. Aplasia cutis congenita (ACC) may occasionally be associated with other anomalies.
|
ORPHAcode: |
1114
|
XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
|
Changed: |
22 Jun 2023 - 16:14
|
-
Epidermolysis bullosa and bladder diseases (60 genes) - KUL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ADAMTS2 95.00 0 NM_014244.5/ interpretable range CS1>95% ATP2A2 95.00 0 NM_001681.4/ interpretable range CS1>95% ATP2C1 95.00 0 NM_014382.5/ interpretable range CS1>95% CAST 95.00 0 NM_001042440.5/ interpretable range CS1>95% CD151 95.00 0 NM_004357.5/ interpretable range CS1>95% CDSN 95.00 0 NM_001264.5/ interpretable range CS1>95% CHST14 95.00 0 NM_130468.4/ interpretable range CS1>95% CHST8 95.00 0 NM_001127896.2/ interpretable range CS1>95% COL17A1 95.00 0 NM_000494.4/ interpretable range CS1>95% COL5A1 95.00 0 NM_000093.5/ interpretable range CS1>95% COL5A2 95.00 0 NM_000393.5/ interpretable range CS1>95% COL7A1 95.00 0 NM_000094.4/ interpretable range CS1>95% CSTA 95.00 0 NM_005213.4/ interpretable range CS1>95% CSTB 95.00 0 NM_000100.4/ interpretable range CS1>95% DSC3 95.00 0 NM_024423.4/ interpretable range CS1>95% DSG1 95.00 0 NM_001942.4/ interpretable range CS1>95% DSG2 95.00 0 NM_001943.5/ interpretable range CS1>95% DSG3 95.00 0 NM_001944.3/ interpretable range CS1>95% DSG4 95.00 0 NM_177986.5/ interpretable range CS1>95% DSP 95.00 0 NM_004415.4/ interpretable range CS1>95% DST 95.00 0 NM_001723.7/ interpretable range CS1>95% EXPH5 95.00 0 NM_015065.3/ interpretable range CS1>95% FERMT1 95.00 0 NM_017671.5/ interpretable range CS1>95% FLG2 95.00 0 NM_001014342.3/ interpretable range CS1>95% GJB2 95.00 0 NM_004004.6/ interpretable range CS1>95% GRIP1 95.00 0 NM_021150.4/ interpretable range CS1>95% IKBKG 95.00 0 NM_001099857.5/ interpretable range CS1>95% ITGA3 95.00 0 NM_002204.4/ interpretable range CS1>95% ITGA6 95.00 0 NM_000210.4/ interpretable range CS1>95% ITGB4 95.00 0 NM_001005731.3/ interpretable range CS1>95% JUP 95.00 0 NM_002230.4/ interpretable range CS1>95% KLHL24 95.00 0 NM_017644.3/ interpretable range CS1>95% KRT1 95.00 0 NM_006121.4/ interpretable range CS1>95% KRT10 95.00 0 NM_000421.5/ interpretable range CS1>95% KRT14 95.00 0 NM_000526.5/ interpretable range CS1>95% KRT16 95.00 0 NM_005557.4/ interpretable range CS1>95% KRT17 95.00 0 NM_000422.3/ interpretable range CS1>95% KRT2 95.00 0 NM_000423.3/ interpretable range CS1>95% KRT5 95.00 0 NM_000424.4/ interpretable range CS1>95% KRT6A 95.00 0 NM_005554.4/ interpretable range CS1>95% KRT6B 95.00 0 NM_005555.4/ interpretable range CS1>95% KRT6C 95.00 0 NM_173086.5/ interpretable range CS1>95% KRT9 95.00 0 NM_000226.4/ interpretable range CS1>95% LAMA3 95.00 0 NM_000227.6/ interpretable range CS1>95% LAMB3 95.00 0 NM_000228.3/ interpretable range CS1>95% LAMC2 95.00 0 NM_005562.3/ interpretable range CS1>95% MMP1 95.00 0 NM_002421.4/ interpretable range CS1>95% NID1 95.00 0 NM_002508.3/ interpretable range CS1>95% PKP1 95.00 0 NM_001005337.3/ interpretable range CS1>95% PLEC 95.00 0 NM_000445.5/ interpretable range CS1>95% PLOD3 95.00 0 NM_001084.5/ interpretable range CS1>95% SERPINB8 95.00 0 NM_198833.2/ interpretable range CS1>95% SLC39A4 95.00 0 NM_130849.4/ interpretable range CS1>95% SPINK5 95.00 0 NM_006846.4/ interpretable range CS1>95% TGM5 95.00 0 NM_201631.4/ interpretable range CS1>95% TP63 95.00 0 NM_003722.5/ interpretable range CS1>95% UROD 95.00 0 NM_000374.5/ interpretable range CS1>95% UROS 95.00 0 NM_000375.3/ interpretable range CS1>95% WNT10A 95.00 0 NM_025216.3/ interpretable range CS1>95%