Incidental Mutation 'R7988:Zcwpw1'
ID 651583
Institutional Source Beutler Lab
Gene Symbol Zcwpw1
Ensembl Gene ENSMUSG00000037108
Gene Name zinc finger, CW type with PWWP domain 1
Synonyms LOC381678
MMRRC Submission 046029-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # R7988 (G1)
Quality Score 225.009
Status Validated
Chromosome 5
Chromosomal Location 137786060-137820883 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 137815753 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Aspartic acid at position 419 (Y419D)
Ref Sequence ENSEMBL: ENSMUSP00000048730 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000035852] [ENSMUST00000058897]
AlphaFold Q6IR42
Predicted Effect possibly damaging
Transcript: ENSMUST00000035852
AA Change: Y419D

PolyPhen 2 Score 0.688 (Sensitivity: 0.86; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000048730
Gene: ENSMUSG00000037108
AA Change: Y419D

DomainStartEndE-ValueType
Pfam:zf-CW 246 293 7.3e-18 PFAM
Pfam:PWWP 306 401 6.9e-22 PFAM
coiled coil region 440 462 N/A INTRINSIC
low complexity region 587 598 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000058897
SMART Domains Protein: ENSMUSP00000050313
Gene: ENSMUSG00000046245

DomainStartEndE-ValueType
signal peptide 1 31 N/A INTRINSIC
Blast:IG 45 155 3e-69 BLAST
low complexity region 156 176 N/A INTRINSIC
transmembrane domain 197 219 N/A INTRINSIC
Predicted Effect
SMART Domains Protein: ENSMUSP00000120909
Gene: ENSMUSG00000037108
AA Change: Y105D

DomainStartEndE-ValueType
Pfam:PWWP 21 109 8.2e-19 PFAM
coiled coil region 126 148 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (59/59)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610030E20Rik C T 6: 72,324,635 (GRCm39) T56M probably damaging Het
Adamtsl5 C T 10: 80,181,372 (GRCm39) S36N probably benign Het
Adgrf5 A T 17: 43,750,704 (GRCm39) probably benign Het
Ago1 A G 4: 126,354,210 (GRCm39) F200S probably damaging Het
Akr1cl T C 1: 65,063,865 (GRCm39) D108G possibly damaging Het
Aopep A G 13: 63,208,954 (GRCm39) D357G probably benign Het
Arhgef3 A T 14: 27,123,743 (GRCm39) D468V probably benign Het
Aspn T C 13: 49,705,353 (GRCm39) C72R possibly damaging Het
Baz2b T C 2: 59,792,485 (GRCm39) T548A possibly damaging Het
Birc6 G A 17: 74,906,368 (GRCm39) probably null Het
Btnl2 A T 17: 34,577,249 (GRCm39) T135S possibly damaging Het
Ccnl1 T A 3: 65,865,282 (GRCm39) I90F possibly damaging Het
Ccnt1 T C 15: 98,463,024 (GRCm39) probably null Het
Cemip C A 7: 83,652,616 (GRCm39) probably benign Het
Cfap45 A G 1: 172,357,501 (GRCm39) D85G probably damaging Het
Cfap54 T A 10: 92,737,941 (GRCm39) D2319V unknown Het
Cma1 T C 14: 56,181,989 (GRCm39) M14V possibly damaging Het
Cmtm1 T C 8: 105,036,774 (GRCm39) probably benign Het
Col27a1 A G 4: 63,249,559 (GRCm39) H1738R unknown Het
Colq T A 14: 31,275,794 (GRCm39) D41V probably damaging Het
Cubn T C 2: 13,337,166 (GRCm39) T2437A probably benign Het
Dnah14 A G 1: 181,611,139 (GRCm39) D3755G probably damaging Het
Eprs1 A G 1: 185,150,545 (GRCm39) Y1349C probably damaging Het
Eps8 C T 6: 137,505,569 (GRCm39) R53Q possibly damaging Het
Fbf1 T C 11: 116,043,594 (GRCm39) D405G probably benign Het
Fen1 C T 19: 10,177,674 (GRCm39) E257K possibly damaging Het
Gstm7 A T 3: 107,834,271 (GRCm39) M198K possibly damaging Het
Hook3 A T 8: 26,563,675 (GRCm39) S190T probably benign Het
Htra4 A C 8: 25,520,526 (GRCm39) probably null Het
Ighv1-15 T C 12: 114,621,116 (GRCm39) I70V probably benign Het
Ikzf4 T A 10: 128,470,324 (GRCm39) N452Y probably damaging Het
Insyn2a T G 7: 134,519,427 (GRCm39) K368Q probably damaging Het
Iqcf5 T A 9: 106,393,020 (GRCm39) N92K possibly damaging Het
Itk A G 11: 46,246,661 (GRCm39) Y186H probably damaging Het
Klhdc10 T C 6: 30,446,690 (GRCm39) S282P probably benign Het
Klhl18 T A 9: 110,305,577 (GRCm39) E29V possibly damaging Het
Ky T C 9: 102,402,614 (GRCm39) S140P probably damaging Het
Lmntd2 T C 7: 140,793,550 (GRCm39) E112G unknown Het
Lrrc36 C A 8: 106,178,718 (GRCm39) D304E possibly damaging Het
Macf1 A T 4: 123,400,273 (GRCm39) F674Y probably damaging Het
Notch1 C T 2: 26,361,013 (GRCm39) D1111N probably benign Het
Osbpl8 T G 10: 111,107,941 (GRCm39) N312K possibly damaging Het
Otogl C T 10: 107,731,637 (GRCm39) C168Y probably damaging Het
Phldb2 T G 16: 45,645,934 (GRCm39) T171P probably benign Het
Ppef2 A T 5: 92,386,841 (GRCm39) F365L probably benign Het
Repin1 G T 6: 48,574,279 (GRCm39) E403* probably null Het
Ryr1 G A 7: 28,795,596 (GRCm39) T1105I probably benign Het
Sclt1 T A 3: 41,617,889 (GRCm39) *29L probably null Het
Scn11a T C 9: 119,594,503 (GRCm39) K1297E probably damaging Het
Serpinb9c T A 13: 33,334,262 (GRCm39) Y288F probably benign Het
Setd1a T A 7: 127,385,366 (GRCm39) M691K probably benign Het
Sftpc T C 14: 70,760,059 (GRCm39) E66G probably damaging Het
Spata31h1 T C 10: 82,131,934 (GRCm39) I359V probably benign Het
Thnsl2 T C 6: 71,118,303 (GRCm39) T42A probably benign Het
Tram1 T C 1: 13,640,199 (GRCm39) D285G probably benign Het
Ttn G A 2: 76,675,374 (GRCm39) P11137L unknown Het
Ttn C A 2: 76,727,103 (GRCm39) V5821F unknown Het
Ttn A T 2: 76,566,584 (GRCm39) I28103K probably damaging Het
Usp38 T A 8: 81,740,945 (GRCm39) M41L probably benign Het
Zfp407 G A 18: 84,577,525 (GRCm39) A1196V possibly damaging Het
Zfp446 T A 7: 12,712,970 (GRCm39) S103T possibly damaging Het
Other mutations in Zcwpw1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01296:Zcwpw1 APN 5 137,795,061 (GRCm39) missense probably benign 0.42
IGL02316:Zcwpw1 APN 5 137,808,272 (GRCm39) unclassified probably benign
IGL02336:Zcwpw1 APN 5 137,808,376 (GRCm39) missense probably damaging 0.96
R0103:Zcwpw1 UTSW 5 137,808,375 (GRCm39) nonsense probably null
R0103:Zcwpw1 UTSW 5 137,808,375 (GRCm39) nonsense probably null
R0295:Zcwpw1 UTSW 5 137,815,734 (GRCm39) missense probably damaging 1.00
R0514:Zcwpw1 UTSW 5 137,794,945 (GRCm39) missense probably benign 0.26
R0685:Zcwpw1 UTSW 5 137,797,854 (GRCm39) missense probably benign 0.00
R0698:Zcwpw1 UTSW 5 137,815,783 (GRCm39) missense probably benign
R0727:Zcwpw1 UTSW 5 137,809,069 (GRCm39) unclassified probably benign
R1677:Zcwpw1 UTSW 5 137,795,022 (GRCm39) missense probably damaging 0.99
R1780:Zcwpw1 UTSW 5 137,794,914 (GRCm39) missense probably damaging 0.98
R1938:Zcwpw1 UTSW 5 137,809,884 (GRCm39) missense probably damaging 0.99
R2875:Zcwpw1 UTSW 5 137,808,304 (GRCm39) missense probably damaging 1.00
R4177:Zcwpw1 UTSW 5 137,798,395 (GRCm39) missense probably damaging 0.99
R5073:Zcwpw1 UTSW 5 137,793,781 (GRCm39) start codon destroyed probably null 0.81
R5913:Zcwpw1 UTSW 5 137,798,269 (GRCm39) missense probably benign 0.31
R6224:Zcwpw1 UTSW 5 137,810,298 (GRCm39) missense possibly damaging 0.63
R6542:Zcwpw1 UTSW 5 137,810,282 (GRCm39) missense probably damaging 0.98
R7204:Zcwpw1 UTSW 5 137,810,346 (GRCm39) missense probably damaging 0.98
R7542:Zcwpw1 UTSW 5 137,817,785 (GRCm39) missense probably benign 0.00
R7600:Zcwpw1 UTSW 5 137,798,396 (GRCm39) nonsense probably null
R7911:Zcwpw1 UTSW 5 137,795,032 (GRCm39) missense probably null 1.00
R7972:Zcwpw1 UTSW 5 137,799,323 (GRCm39) missense probably benign 0.13
R8174:Zcwpw1 UTSW 5 137,817,839 (GRCm39) critical splice donor site probably null
R8713:Zcwpw1 UTSW 5 137,797,794 (GRCm39) missense probably benign 0.06
R8851:Zcwpw1 UTSW 5 137,820,626 (GRCm39) missense probably damaging 1.00
R9016:Zcwpw1 UTSW 5 137,798,340 (GRCm39) missense probably damaging 0.98
R9131:Zcwpw1 UTSW 5 137,809,182 (GRCm39) missense probably damaging 1.00
R9337:Zcwpw1 UTSW 5 137,799,274 (GRCm39) missense probably benign 0.37
X0021:Zcwpw1 UTSW 5 137,809,869 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAGTGACATGTGAGTTTCTCTTTCC -3'
(R):5'- ACGTCACCATGGTCCTACAG -3'

Sequencing Primer
(F):5'- GTCATTTGTTCCATCATGAATCAAC -3'
(R):5'- TGGTCCTACAGATCATGACTCAC -3'
Posted On 2020-09-15