Incidental Mutation 'R7831:Pald1'
ID 605636
Institutional Source Beutler Lab
Gene Symbol Pald1
Ensembl Gene ENSMUSG00000020092
Gene Name phosphatase domain containing, paladin 1
Synonyms paladin, X99384
MMRRC Submission 045885-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.114) question?
Stock # R7831 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 61155435-61219309 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 61191593 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 65 (T65K)
Ref Sequence ENSEMBL: ENSMUSP00000020289 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020289]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000020289
AA Change: T65K

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000020289
Gene: ENSMUSG00000020092
AA Change: T65K

DomainStartEndE-ValueType
low complexity region 2 37 N/A INTRINSIC
PTPlike_phytase 164 333 4.33e-53 SMART
low complexity region 428 441 N/A INTRINSIC
PTPlike_phytase 548 682 5.37e-49 SMART
low complexity region 757 768 N/A INTRINSIC
Meta Mutation Damage Score 0.3232 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (87/87)
Allele List at MGI
Other mutations in this stock
Total: 85 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 G A 11: 9,247,404 (GRCm39) V2384I possibly damaging Het
Acsl1 A G 8: 46,972,043 (GRCm39) D297G probably benign Het
Ap2a1 C A 7: 44,550,436 (GRCm39) R944L probably damaging Het
Apbb1ip A G 2: 22,756,933 (GRCm39) Y398C probably damaging Het
Atp8a2 A T 14: 60,011,202 (GRCm39) V968D probably damaging Het
Becn1 T C 11: 101,181,279 (GRCm39) T341A probably benign Het
Card11 G T 5: 140,859,167 (GRCm39) S1126R possibly damaging Het
Ccdc51 T C 9: 108,921,058 (GRCm39) L315S probably damaging Het
Cdk12 T C 11: 98,140,653 (GRCm39) L1298P unknown Het
Cep170b A T 12: 112,711,234 (GRCm39) D1538V probably benign Het
Cfap52 A T 11: 67,826,782 (GRCm39) F348I possibly damaging Het
Clip1 A T 5: 123,751,342 (GRCm39) M813K Het
Col19a1 G A 1: 24,565,563 (GRCm39) T256I unknown Het
Col6a3 A T 1: 90,724,268 (GRCm39) C2027* probably null Het
Crisp4 A T 1: 18,199,013 (GRCm39) N140K probably benign Het
Crocc2 G T 1: 93,143,195 (GRCm39) A1266S probably benign Het
Cyfip2 G A 11: 46,087,273 (GRCm39) R1206C probably damaging Het
Cyp24a1 T A 2: 170,327,860 (GRCm39) M461L probably damaging Het
Cyp2a5 C T 7: 26,534,940 (GRCm39) T51I possibly damaging Het
Cyp2b19 C T 7: 26,466,565 (GRCm39) H398Y possibly damaging Het
Cyp4a29 G A 4: 115,107,367 (GRCm39) V234I probably benign Het
Dicer1 T G 12: 104,675,059 (GRCm39) K734N probably damaging Het
Dnai1 T C 4: 41,614,695 (GRCm39) probably null Het
Entpd3 G A 9: 120,373,025 (GRCm39) G14D probably damaging Het
Entrep3 G A 3: 89,091,520 (GRCm39) probably null Het
Ermp1 T C 19: 29,595,367 (GRCm39) T634A probably benign Het
Evc C T 5: 37,476,427 (GRCm39) G374D probably damaging Het
Fcgbp C A 7: 27,806,404 (GRCm39) T2124K probably damaging Het
Fgf8 G A 19: 45,730,876 (GRCm39) P50S probably benign Het
Fmnl1 C T 11: 103,088,999 (GRCm39) R1074W unknown Het
Galnt18 C T 7: 111,155,665 (GRCm39) V223M possibly damaging Het
Galnt2 A G 8: 125,058,817 (GRCm39) N295S probably benign Het
Grip1 T G 10: 119,854,011 (GRCm39) V600G probably damaging Het
Insm2 T A 12: 55,647,323 (GRCm39) C356S probably damaging Het
Itpr2 T A 6: 146,193,082 (GRCm39) I1672F probably benign Het
Kdm1b T G 13: 47,204,098 (GRCm39) N76K probably benign Het
Khnyn T A 14: 56,125,303 (GRCm39) probably null Het
Kidins220 C T 12: 25,111,230 (GRCm39) A1167V possibly damaging Het
Krt40 T C 11: 99,432,087 (GRCm39) D208G probably benign Het
Lars1 T A 18: 42,350,627 (GRCm39) D894V probably benign Het
Lmx1a A T 1: 167,668,521 (GRCm39) N266I probably benign Het
Mrgprb5 T A 7: 47,817,997 (GRCm39) K246M probably benign Het
Mrpl2 G A 17: 46,959,598 (GRCm39) G176R possibly damaging Het
Muc21 T A 17: 35,929,651 (GRCm39) T1512S unknown Het
Nell1 T A 7: 49,632,548 (GRCm39) F60L possibly damaging Het
Nnt G A 13: 119,506,630 (GRCm39) A453V possibly damaging Het
Opa1 A G 16: 29,467,755 (GRCm39) K940R probably benign Het
Opn5 A C 17: 42,891,510 (GRCm39) I309S probably null Het
Or1af1 C T 2: 37,109,723 (GRCm39) T74I probably damaging Het
Or1r1 A C 11: 73,875,257 (GRCm39) M59R probably damaging Het
Or2ag15 T A 7: 106,340,620 (GRCm39) I174F probably damaging Het
P3h3 T G 6: 124,832,118 (GRCm39) E256A possibly damaging Het
Pcnx3 T C 19: 5,735,989 (GRCm39) Y279C probably damaging Het
Pik3c2b G A 1: 132,998,980 (GRCm39) S367N possibly damaging Het
Pik3cb T C 9: 98,970,666 (GRCm39) T342A probably benign Het
Pkd1l3 A T 8: 110,357,990 (GRCm39) E837D possibly damaging Het
Ppp2r2b T A 18: 42,834,597 (GRCm39) Y191F probably benign Het
Ppp4r4 G A 12: 103,557,080 (GRCm39) E439K possibly damaging Het
Ptprk A G 10: 28,444,404 (GRCm39) I946V possibly damaging Het
Ror1 A G 4: 100,298,295 (GRCm39) N556S probably benign Het
Ryr3 C T 2: 112,757,183 (GRCm39) A391T possibly damaging Het
Selp G A 1: 163,972,584 (GRCm39) probably null Het
Setx T A 2: 29,069,866 (GRCm39) V2557E possibly damaging Het
Setx T C 2: 29,047,120 (GRCm39) L1866S probably damaging Het
Slc66a3 T A 12: 17,047,632 (GRCm39) probably null Het
Slit2 A G 5: 48,402,025 (GRCm39) T805A probably benign Het
Sorbs3 T G 14: 70,440,481 (GRCm39) N89T possibly damaging Het
Sorl1 C A 9: 42,001,257 (GRCm39) V248L probably benign Het
Srebf2 T A 15: 82,066,288 (GRCm39) V612E probably damaging Het
Sv2c T A 13: 96,113,200 (GRCm39) Y583F probably damaging Het
Tada1 G T 1: 166,217,442 (GRCm39) R193I probably damaging Het
Tnrc6b C G 15: 80,764,580 (GRCm39) A694G possibly damaging Het
Ttll3 CAAAGTAA CAAAGTAAAGTAA 6: 113,376,118 (GRCm39) probably null Het
Ttn C T 2: 76,711,425 (GRCm39) G8372D unknown Het
Ube2g2 A G 10: 77,470,576 (GRCm39) T68A Het
Ubl7 T G 9: 57,821,918 (GRCm39) V89G possibly damaging Het
Ush2a T A 1: 188,492,038 (GRCm39) I3109N probably damaging Het
Utp20 T A 10: 88,598,632 (GRCm39) K115* probably null Het
Vmn2r26 T A 6: 124,016,758 (GRCm39) Y407* probably null Het
Yod1 G T 1: 130,646,986 (GRCm39) V288F probably damaging Het
Zbed5 A C 5: 129,930,798 (GRCm39) N249T possibly damaging Het
Zbtb5 T C 4: 44,995,244 (GRCm39) T47A probably damaging Het
Zcchc14 T C 8: 122,331,984 (GRCm39) T460A not run Het
Zfp712 A C 13: 67,200,483 (GRCm39) probably null Het
Zfyve16 A T 13: 92,658,836 (GRCm39) H358Q probably benign Het
Other mutations in Pald1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02183:Pald1 APN 10 61,182,920 (GRCm39) splice site probably benign
IGL03068:Pald1 APN 10 61,156,963 (GRCm39) missense possibly damaging 0.94
IGL03106:Pald1 APN 10 61,182,884 (GRCm39) missense probably benign 0.41
R0331:Pald1 UTSW 10 61,176,708 (GRCm39) critical splice donor site probably null
R0497:Pald1 UTSW 10 61,177,094 (GRCm39) missense probably damaging 0.99
R1181:Pald1 UTSW 10 61,183,366 (GRCm39) splice site probably benign
R1437:Pald1 UTSW 10 61,177,064 (GRCm39) missense possibly damaging 0.63
R1466:Pald1 UTSW 10 61,184,304 (GRCm39) splice site probably benign
R1827:Pald1 UTSW 10 61,191,701 (GRCm39) small deletion probably benign
R2129:Pald1 UTSW 10 61,184,085 (GRCm39) critical splice donor site probably null
R2184:Pald1 UTSW 10 61,182,915 (GRCm39) missense possibly damaging 0.46
R2260:Pald1 UTSW 10 61,188,750 (GRCm39) missense probably damaging 1.00
R3051:Pald1 UTSW 10 61,182,542 (GRCm39) nonsense probably null
R3690:Pald1 UTSW 10 61,191,587 (GRCm39) splice site probably null
R3713:Pald1 UTSW 10 61,178,144 (GRCm39) missense possibly damaging 0.67
R3876:Pald1 UTSW 10 61,183,266 (GRCm39) missense probably damaging 0.97
R4261:Pald1 UTSW 10 61,179,471 (GRCm39) missense probably damaging 1.00
R4600:Pald1 UTSW 10 61,184,395 (GRCm39) missense probably benign 0.00
R4603:Pald1 UTSW 10 61,184,395 (GRCm39) missense probably benign 0.00
R5069:Pald1 UTSW 10 61,177,025 (GRCm39) missense possibly damaging 0.50
R5354:Pald1 UTSW 10 61,184,440 (GRCm39) missense probably damaging 1.00
R5590:Pald1 UTSW 10 61,179,489 (GRCm39) missense probably damaging 1.00
R5705:Pald1 UTSW 10 61,159,076 (GRCm39) missense possibly damaging 0.90
R5780:Pald1 UTSW 10 61,174,997 (GRCm39) missense probably damaging 1.00
R6239:Pald1 UTSW 10 61,156,910 (GRCm39) missense possibly damaging 0.59
R6380:Pald1 UTSW 10 61,186,714 (GRCm39) missense possibly damaging 0.86
R6812:Pald1 UTSW 10 61,178,701 (GRCm39) missense possibly damaging 0.53
R6891:Pald1 UTSW 10 61,184,311 (GRCm39) critical splice donor site probably null
R6949:Pald1 UTSW 10 61,156,996 (GRCm39) missense probably benign 0.23
R7038:Pald1 UTSW 10 61,175,078 (GRCm39) missense probably benign
R7051:Pald1 UTSW 10 61,159,125 (GRCm39) missense probably benign 0.26
R7188:Pald1 UTSW 10 61,182,845 (GRCm39) missense probably damaging 0.99
R7339:Pald1 UTSW 10 61,159,110 (GRCm39) missense possibly damaging 0.60
R8000:Pald1 UTSW 10 61,183,218 (GRCm39) missense probably benign 0.00
R8710:Pald1 UTSW 10 61,183,232 (GRCm39) missense probably benign 0.03
R8903:Pald1 UTSW 10 61,182,815 (GRCm39) critical splice donor site probably null
R9255:Pald1 UTSW 10 61,176,989 (GRCm39) critical splice donor site probably null
R9414:Pald1 UTSW 10 61,178,932 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GCCCTGCTGCTTATTTGCTG -3'
(R):5'- CACAGCAGACAGTCTCGG -3'

Sequencing Primer
(F):5'- TAATGGGCTGAACCTCTGAACCTG -3'
(R):5'- AGACAGTCTCGGCTGGCAC -3'
Posted On 2019-12-20