| Gene Symbol |
Definition |
Felxi PID |
Halo PID |
Nluc-N PID |
Nluc-C PID |
| POLD3 |
polymerase (DNA-directed), delta 3, accessory subunit, transcript variant 1 |
FXC00381
|
FHC00381
|
FNC00381N
|
FNC00381C
|
| POLD2 |
polymerase (DNA directed), delta 2, accessory subunit, transcript variant 1 |
FXC02177
|
FHC02177
|
FNC02177N
|
FNC02177C
|
| POLDIP2 |
polymerase (DNA-directed), delta interacting protein 2, transcript variant 1 |
FXC02930
|
FHC02930
|
FNC02930N
|
FNC02930C
|
| SSB |
Sjogren syndrome antigen B (autoantigen La), transcript variant 1 |
FXC03583
|
FHC03583
|
FNC03583N
|
FNC03583C
|
| RAD54B |
RAD54 homolog B (S. cerevisiae), transcript variant 1 |
FXC03788
|
FHC03788
|
FNC03788N
|
FNC03788C
|
| MRE11A |
MRE11 homolog A, double strand break repair nuclease, transcript variant 1 |
FXC03974
|
FHC03974
|
FNC03974N
|
FNC03974C
|
| RAD51D |
RAD51 paralog D, transcript variant 1 |
FXC06580
|
FHC06580
|
FNC06580N
|
FNC06580C
|
| RPA3 |
replication protein A3, 14kDa |
FXC06678
|
FHC06678
|
FNC06678N
|
FNC06678C
|
| POLD1 |
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant 2 |
FXC08396
|
FHC08396
|
FNC08396N
|
FNC08396C
|
| RAD51B |
RAD51 paralog B, transcript variant 3 |
FXC09320
|
FHC09320
|
FNC09320N
|
FNC09320C
|
| RAD52 |
RAD52 homolog, DNA repair protein, transcript variant 1 |
FXC10450
|
FHC10450
|
FNC10450N
|
FNC10450C
|
| NBN |
nibrin |
FXC10451
|
FHC10451
|
FNC10451N
|
FNC10451C
|
| RAD51 |
RAD51 recombinase, transcript variant 1 |
FXC10574
|
FHC10574
|
FNC10574N
|
FNC10574C
|
| RAD51C |
RAD51 paralog C, transcript variant 1 |
FXC10591
|
FHC10591
|
FNC10591N
|
FNC10591C
|
| XRCC3 |
X-ray repair complementing defective repair in Chinese hamster cells 3, transcript variant 2 |
FXC11674
|
FHC11674
|
FNC11674N
|
FNC11674C
|
| ATRX |
alpha thalassemia/mental retardation syndrome X-linked, transcript variant 1 |
FXC12303
|
FHC12303
|
FNC12303N
|
FNC12303C
|
| TOP3A |
topoisomerase (DNA) III alpha |
FXC12713
|
FHC12713
|
FNC12713N
|
FNC12713C
|
| EME1 |
essential meiotic structure-specific endonuclease 1, transcript variant 1 |
FXC15815
|
FHC15815
|
FNC15815N
|
FNC15815C
|
| SHFM1 |
split hand/foot malformation (ectrodactyly) type 1 |
FXC22989
|
FHC22989
|
FNC22989N
|
FNC22989C
|
| XRCC2 |
X-ray repair complementing defective repair in Chinese hamster cells 2 |
FXC23160
|
FHC23160
|
FNC23160N
|
FNC23160C
|
| SYCP3 |
synaptonemal complex protein 3, transcript variant 2 |
FXC24855
|
FHC24855
|
FNC24855N
|
FNC24855C
|
| BRCA2 |
BRCA2, DNA repair associated |
FXC24976
|
FHC24976
|
FNC24976N
|
FNC24976C
|
| BLM |
Bloom syndrome RecQ like helicase, transcript variant 1 |
FXC25506
|
FHC25506
|
FNC25506N
|
FNC25506C
|
| RPA4 |
replication protein A4, 30kDa |
FXC29457
|
FHC29457
|
FNC29457N
|
FNC29457C
|
