Table 2 Genes with variants detected in two families

From: Whole-exome sequencing analysis of supernumerary teeth occurrence in Japanese individuals

Gene

Presence of gene variants in familes

 

Family A

Family B

Family C

Family D

1 Absent in melanoma 1-like (AIM1L)

â—‹

 

â—‹

 

2 Agrin (AGRN)

 

â—‹

â—‹

 

3 Ataxin 1(ATXN1)

 

â—‹

â—‹

 

4 Cadherin 26 (CDH26)

â—‹

 

â—‹

 

5 Chromosome 21 open reading frame 58 (C21orf58)

 

â—‹

â—‹

 

6 Complement factor B (CFB)

 

â—‹

â—‹

 

7 EF-hand calcium binding domain 5 (EFCAB5)

â—‹

â—‹

  

8 Exocyst complex component 3 like 4 (EXOC3L4)

â—‹

 

â—‹

 

9 Family with sequence similarity 186 member A (FAM186A)

â—‹

 

â—‹

 

10 Fanconi anemia complementation group E (FANCE)

 

â—‹

â—‹

 

11 Formin like 1 (FMNL1)

 

â—‹

â—‹

 

12 FXYD domain containing ion transport regulator 4 (FXYD4)

â—‹

 

â—‹

 

13 Hemicentin 1 (HMCN1)

 

â—‹

â—‹

 

14 Immunoglobulin superfamily member 9B (IGSF9B)

 

â—‹

â—‹

 

15 KIAA1614

 

â—‹

â—‹

 

16 LOC100652824

â—‹

 

â—‹

 

17 MGA, MAX dimerization protein(MGA)

 

â—‹

â—‹

 

18 Phospholipase C eta 2 (PLCH2)

 

â—‹

â—‹

 

19 Polycystin 1 like 2 (PKD1L2)

â—‹

 

â—‹

 

20 Ring finger protein 207 (RNF207)

 

â—‹

â—‹

 

21 Testis expressed 15 (TEX15)

â—‹

â—‹

  

22 Transketolase-like 1 (TKTL1)

â—‹

 

â—‹

 

23 Tumor suppressor candidate 1 (TUSC1)

â—‹

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