Incidental Mutation 'R4885:Wscd1'
ID 375653
Institutional Source Beutler Lab
Gene Symbol Wscd1
Ensembl Gene ENSMUSG00000020811
Gene Name WSC domain containing 1
Synonyms
MMRRC Submission 042851-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R4885 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 71640746-71680473 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 71650972 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Cysteine at position 100 (R100C)
Ref Sequence ENSEMBL: ENSMUSP00000104151 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021168] [ENSMUST00000108510] [ENSMUST00000108511] [ENSMUST00000150531]
AlphaFold Q80XH4
Predicted Effect probably damaging
Transcript: ENSMUST00000021168
AA Change: R100C

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000021168
Gene: ENSMUSG00000020811
AA Change: R100C

DomainStartEndE-ValueType
transmembrane domain 17 36 N/A INTRINSIC
low complexity region 100 114 N/A INTRINSIC
WSC 139 231 8.72e-40 SMART
WSC 242 337 2.09e-28 SMART
Pfam:Sulfotransfer_1 413 525 1.6e-9 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000108510
AA Change: R100C

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000104150
Gene: ENSMUSG00000020811
AA Change: R100C

DomainStartEndE-ValueType
transmembrane domain 17 36 N/A INTRINSIC
low complexity region 100 114 N/A INTRINSIC
WSC 139 231 8.72e-40 SMART
WSC 242 337 2.09e-28 SMART
Pfam:Sulfotransfer_1 413 525 1.6e-9 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000108511
AA Change: R100C

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000104151
Gene: ENSMUSG00000020811
AA Change: R100C

DomainStartEndE-ValueType
transmembrane domain 17 36 N/A INTRINSIC
low complexity region 100 114 N/A INTRINSIC
WSC 139 231 8.72e-40 SMART
WSC 242 337 2.09e-28 SMART
Pfam:Sulfotransfer_1 413 525 1.6e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138339
Predicted Effect probably benign
Transcript: ENSMUST00000150531
SMART Domains Protein: ENSMUSP00000123659
Gene: ENSMUSG00000020811

DomainStartEndE-ValueType
transmembrane domain 15 35 N/A INTRINSIC
Meta Mutation Damage Score 0.1828 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 99% (77/78)
Allele List at MGI
Other mutations in this stock
Total: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf3 A G 16: 20,370,425 (GRCm39) T317A probably benign Het
Adck1 G A 12: 88,407,865 (GRCm39) A199T probably benign Het
Adgrb1 A T 15: 74,444,011 (GRCm39) M1038L probably benign Het
Anapc10 C T 8: 80,455,779 (GRCm39) T76I probably benign Het
Atosa T C 9: 74,913,649 (GRCm39) L94P probably damaging Het
Bptf C T 11: 106,965,474 (GRCm39) S1177N probably benign Het
Bsn A T 9: 107,984,726 (GRCm39) Y337* probably null Het
Ccl20 T A 1: 83,095,580 (GRCm39) V48E possibly damaging Het
Ccnl1 C T 3: 65,864,320 (GRCm39) D122N probably damaging Het
Chat C G 14: 32,176,567 (GRCm39) G69A probably damaging Het
Cr2 T A 1: 194,841,039 (GRCm39) I418F possibly damaging Het
Dmxl1 G C 18: 50,011,862 (GRCm39) A1340P probably damaging Het
Eef2k G A 7: 120,491,155 (GRCm39) R547Q probably benign Het
Eml2 G A 7: 18,937,935 (GRCm39) S793N probably benign Het
Enox1 T A 14: 77,958,290 (GRCm39) L632Q probably damaging Het
Fabp9 T C 3: 10,259,738 (GRCm39) K92E probably damaging Het
Fam234a T C 17: 26,432,559 (GRCm39) H530R probably benign Het
Fancm C T 12: 65,149,417 (GRCm39) Q728* probably null Het
Fgd3 G A 13: 49,417,465 (GRCm39) T666M possibly damaging Het
Foxs1 T C 2: 152,774,301 (GRCm39) M251V probably benign Het
Fsip2 A T 2: 82,818,438 (GRCm39) M4724L probably benign Het
Gemin6 G A 17: 80,535,327 (GRCm39) E96K probably damaging Het
Gfi1 C A 5: 107,871,152 (GRCm39) V80F probably damaging Het
H3c13 G T 3: 96,176,277 (GRCm39) V90F possibly damaging Het
Hectd1 A G 12: 51,847,505 (GRCm39) V442A probably damaging Het
Ift80 A G 3: 68,857,829 (GRCm39) I272T probably damaging Het
Impact C G 18: 13,119,430 (GRCm39) A214G probably damaging Het
Insl6 C T 19: 29,302,556 (GRCm39) E54K probably benign Het
Irak3 T A 10: 120,018,586 (GRCm39) D54V probably damaging Het
Itk C T 11: 46,227,171 (GRCm39) probably null Het
Ivl A T 3: 92,479,718 (GRCm39) C116S probably benign Het
Kcnq4 G A 4: 120,570,260 (GRCm39) A361V probably benign Het
L1td1 C T 4: 98,625,548 (GRCm39) P581L probably benign Het
Lrp1b T C 2: 41,358,905 (GRCm39) E656G probably benign Het
Macrod2 A G 2: 140,261,985 (GRCm39) T89A possibly damaging Het
Mettl13 T C 1: 162,364,837 (GRCm39) D514G probably damaging Het
Mfsd13b A T 7: 120,590,711 (GRCm39) I151F possibly damaging Het
Mical3 G A 6: 120,912,214 (GRCm39) P1882S probably damaging Het
Mycbp2 T C 14: 103,383,382 (GRCm39) E394G possibly damaging Het
Myo16 T A 8: 10,488,892 (GRCm39) S688T probably damaging Het
Neb T C 2: 52,176,058 (GRCm39) Y1467C probably damaging Het
Nhsl3 C T 4: 129,118,238 (GRCm39) R214Q probably damaging Het
Nkx6-3 C A 8: 23,643,914 (GRCm39) P105Q possibly damaging Het
Nlrp1b T C 11: 71,108,710 (GRCm39) T264A possibly damaging Het
Nnat G A 2: 157,403,678 (GRCm39) C122Y probably damaging Het
Notch3 G A 17: 32,360,351 (GRCm39) R1527C probably damaging Het
Or2y16 C T 11: 49,335,449 (GRCm39) T257I probably damaging Het
Or5an1c T G 19: 12,218,082 (GRCm39) probably null Het
Or5h18 A G 16: 58,847,518 (GRCm39) Y251H probably damaging Het
Pds5b C T 5: 150,639,927 (GRCm39) T14I probably benign Het
Phf19 A T 2: 34,789,718 (GRCm39) I334N probably damaging Het
Pik3ap1 T C 19: 41,364,365 (GRCm39) D118G probably benign Het
Pkhd1 T A 1: 20,140,712 (GRCm39) E3886V possibly damaging Het
Pkp1 A G 1: 135,846,690 (GRCm39) S21P possibly damaging Het
Pramel32 T A 4: 88,546,219 (GRCm39) L374F possibly damaging Het
Rack1 C A 11: 48,696,463 (GRCm39) A290E probably damaging Het
Rbm15 A G 3: 107,239,570 (GRCm39) V276A probably benign Het
Rnf216 A T 5: 143,076,335 (GRCm39) L183* probably null Het
Sc5d T C 9: 42,166,922 (GRCm39) I206V probably benign Het
Scpep1 A G 11: 88,826,737 (GRCm39) I233T probably benign Het
Sh3pxd2a A G 19: 47,257,132 (GRCm39) Y529H probably damaging Het
Slc1a4 A C 11: 20,254,384 (GRCm39) V494G probably damaging Het
Slc38a7 T C 8: 96,575,230 (GRCm39) T17A probably benign Het
Smg6 T C 11: 74,932,744 (GRCm39) S73P probably damaging Het
Stk32b T C 5: 37,624,141 (GRCm39) Y202C probably damaging Het
Tas2r140 A G 6: 40,468,334 (GRCm39) S55G probably damaging Het
Tcf12 C T 9: 71,766,122 (GRCm39) G504S probably null Het
Ttc3 G C 16: 94,227,690 (GRCm39) probably null Het
Ttc3 T C 16: 94,220,324 (GRCm39) I568T probably damaging Het
Ttc41 T G 10: 86,594,966 (GRCm39) N913K possibly damaging Het
Vrk1 G A 12: 106,024,231 (GRCm39) V236M probably damaging Het
Zc3h18 C T 8: 123,128,445 (GRCm39) probably benign Het
Other mutations in Wscd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00980:Wscd1 APN 11 71,679,768 (GRCm39) missense possibly damaging 0.89
IGL01982:Wscd1 APN 11 71,657,699 (GRCm39) missense possibly damaging 0.94
IGL01991:Wscd1 APN 11 71,678,549 (GRCm39) nonsense probably null
IGL02211:Wscd1 APN 11 71,679,801 (GRCm39) missense probably damaging 1.00
R0011:Wscd1 UTSW 11 71,679,654 (GRCm39) missense probably damaging 1.00
R0011:Wscd1 UTSW 11 71,679,654 (GRCm39) missense probably damaging 1.00
R0359:Wscd1 UTSW 11 71,657,692 (GRCm39) missense probably damaging 1.00
R0371:Wscd1 UTSW 11 71,679,549 (GRCm39) missense probably damaging 1.00
R1340:Wscd1 UTSW 11 71,659,586 (GRCm39) missense probably benign 0.01
R1429:Wscd1 UTSW 11 71,651,000 (GRCm39) missense probably damaging 0.99
R1511:Wscd1 UTSW 11 71,679,501 (GRCm39) missense probably damaging 1.00
R1823:Wscd1 UTSW 11 71,651,044 (GRCm39) missense probably benign 0.05
R4772:Wscd1 UTSW 11 71,662,802 (GRCm39) critical splice donor site probably null
R5221:Wscd1 UTSW 11 71,659,501 (GRCm39) missense possibly damaging 0.53
R5714:Wscd1 UTSW 11 71,675,261 (GRCm39) critical splice donor site probably null
R6351:Wscd1 UTSW 11 71,650,709 (GRCm39) missense probably damaging 1.00
R7181:Wscd1 UTSW 11 71,650,709 (GRCm39) missense probably damaging 1.00
R7184:Wscd1 UTSW 11 71,679,543 (GRCm39) missense probably damaging 1.00
R7461:Wscd1 UTSW 11 71,650,799 (GRCm39) missense possibly damaging 0.95
R7613:Wscd1 UTSW 11 71,650,799 (GRCm39) missense possibly damaging 0.95
R7754:Wscd1 UTSW 11 71,675,191 (GRCm39) missense probably damaging 1.00
R7875:Wscd1 UTSW 11 71,679,560 (GRCm39) missense probably damaging 1.00
R8804:Wscd1 UTSW 11 71,675,161 (GRCm39) missense probably damaging 1.00
R9103:Wscd1 UTSW 11 71,674,245 (GRCm39) critical splice donor site probably null
R9220:Wscd1 UTSW 11 71,662,750 (GRCm39) missense probably benign 0.01
R9359:Wscd1 UTSW 11 71,650,799 (GRCm39) missense possibly damaging 0.95
R9473:Wscd1 UTSW 11 71,679,644 (GRCm39) missense probably damaging 1.00
Z1177:Wscd1 UTSW 11 71,679,811 (GRCm39) missense probably damaging 0.98
Z1177:Wscd1 UTSW 11 71,679,626 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- TTTCTCCGCAGAACACAGTTC -3'
(R):5'- CATACTCTTCAGCTACCGCAG -3'

Sequencing Primer
(F):5'- GCAGAACACAGTTCCTGCTACTC -3'
(R):5'- CAGGGCCAAGAAAAGAGACAATAC -3'
Posted On 2016-03-17