Incidental Mutation 'R7943:Wasl'
ID612563
Institutional Source Beutler Lab
Gene Symbol Wasl
Ensembl Gene ENSMUSG00000029684
Gene NameWiskott-Aldrich syndrome-like (human)
SynonymsN-WASP, 3110031I02Rik, 2900021I12Rik
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #R7943 (G1)
Quality Score225.009
Status Not validated
Chromosome6
Chromosomal Location24613805-24665009 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 24619397 bp
ZygosityHeterozygous
Amino Acid Change Proline to Serine at position 375 (P375S)
Ref Sequence ENSEMBL: ENSMUSP00000031695 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031695]
PDB Structure
Structure of a Longitudinal Actin Dimer Assembled by Tandem W Domains [X-RAY DIFFRACTION]
Predicted Effect unknown
Transcript: ENSMUST00000031695
AA Change: P375S
SMART Domains Protein: ENSMUSP00000031695
Gene: ENSMUSG00000029684
AA Change: P375S

DomainStartEndE-ValueType
WH1 31 135 5.14e-49 SMART
low complexity region 183 197 N/A INTRINSIC
PBD 200 236 1.28e-11 SMART
low complexity region 273 388 N/A INTRINSIC
WH2 401 418 3.71e-4 SMART
WH2 429 446 1.43e-5 SMART
low complexity region 482 501 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.3%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutants exhibit developmental retardation, fail to undergo turning, show abnormal differentiation of intra- and extra-embryonal mesoderm, and die around midgestation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930590J08Rik A G 6: 91,928,726 T493A probably damaging Het
Aars A G 8: 111,049,861 K650E probably benign Het
Abcb1b C T 5: 8,832,258 S793F probably benign Het
Adamts18 T A 8: 113,775,276 I318F probably damaging Het
Adcy8 A G 15: 64,699,473 I1137T probably damaging Het
Ambra1 T A 2: 91,773,493 F607L probably benign Het
Ankrd46 A T 15: 36,479,420 V175D possibly damaging Het
Arhgap28 C A 17: 67,901,282 E114* probably null Het
Arrdc1 C T 2: 24,926,146 G282S probably damaging Het
Atp1a3 A T 7: 24,981,791 L790Q probably damaging Het
Bend5 T A 4: 111,415,209 V12D probably damaging Het
Bod1l C T 5: 41,819,265 E1569K probably damaging Het
Cdc123 T A 2: 5,803,964 I234L probably benign Het
Cep126 T G 9: 8,120,748 E91D probably damaging Het
Cep89 T A 7: 35,414,145 D199E possibly damaging Het
Ces1d T C 8: 93,171,137 T442A probably benign Het
Chsy3 C T 18: 59,409,227 A479V probably benign Het
Clcn4 C A 7: 7,293,061 G261C probably damaging Het
Clhc1 A T 11: 29,557,651 probably null Het
Cnot3 T A 7: 3,655,566 probably null Het
Col9a1 C A 1: 24,237,180 P723H probably damaging Het
Crybg3 A T 16: 59,555,242 M169K probably benign Het
Cxxc4 A G 3: 134,258,053 R353G probably benign Het
Dennd3 A T 15: 73,540,808 I440F probably damaging Het
Elmo3 G T 8: 105,309,017 S553I probably damaging Het
Elovl2 A G 13: 41,187,467 Y198H probably benign Het
Epm2aip1 A G 9: 111,272,037 Y26C probably damaging Het
Ext1 A C 15: 53,089,939 C510G possibly damaging Het
Extl3 A T 14: 65,077,489 D81E probably benign Het
Fbxl5 T A 5: 43,758,676 T465S probably benign Het
Gabrr2 A T 4: 33,081,470 K169* probably null Het
Gm10436 A T 12: 88,176,352 N360K possibly damaging Het
Haus4 A G 14: 54,542,145 Y341H probably damaging Het
Itgae A T 11: 73,120,273 probably null Het
Jmjd7 C T 2: 120,030,515 H149Y possibly damaging Het
Kcnh2 C T 5: 24,324,563 C725Y probably damaging Het
Mroh1 C T 15: 76,447,332 P1252L probably benign Het
Ms4a14 A G 19: 11,302,944 F750S probably benign Het
Naf1 T A 8: 66,860,513 D49E unknown Het
Notch3 T C 17: 32,122,773 T2002A possibly damaging Het
Olfr1413 G A 1: 92,574,088 D306N probably benign Het
Olfr1495 T A 19: 13,768,352 D3E probably benign Het
Olfr168 A T 16: 19,530,417 C168S probably damaging Het
Olfr301 A G 7: 86,407,911 probably benign Het
Olfr393 A T 11: 73,847,507 I206N probably benign Het
Olfr709-ps1 A T 7: 106,926,570 D296E probably benign Het
Olfr869 A T 9: 20,137,575 N153I probably benign Het
Pck1 A G 2: 173,155,950 T271A possibly damaging Het
Penk A G 4: 4,133,976 W224R possibly damaging Het
Per2 C A 1: 91,444,759 V198F probably damaging Het
Phf11d A G 14: 59,361,831 M23T probably damaging Het
Pla2g4d A G 2: 120,266,730 V796A probably benign Het
Prdx6 A T 1: 161,241,858 probably null Het
Prep A T 10: 45,091,012 N47I probably damaging Het
Prss38 G T 11: 59,375,170 H96N probably damaging Het
Rab11a C A 9: 64,728,331 E47* probably null Het
Rad18 C T 6: 112,649,837 G369D probably benign Het
Rragc T C 4: 123,929,924 V330A probably damaging Het
Serpina9 A T 12: 104,001,421 H238Q probably benign Het
Serpinb3b T A 1: 107,157,737 K91N probably damaging Het
Slc16a12 T G 19: 34,675,330 S139R probably benign Het
Slc22a27 T A 19: 7,910,107 probably null Het
Slc25a11 A G 11: 70,645,179 V243A probably benign Het
Slc38a9 A T 13: 112,731,614 I545F probably benign Het
Slc39a8 A T 3: 135,884,396 H349L probably damaging Het
Slk C T 19: 47,642,071 T1227I possibly damaging Het
Spdye4b A G 5: 143,194,854 E25G possibly damaging Het
St3gal1 A G 15: 67,111,265 V214A probably benign Het
St7l T A 3: 104,926,577 M550K probably benign Het
Tbk1 A C 10: 121,552,246 F638C possibly damaging Het
Tex101 A T 7: 24,669,765 C114S probably damaging Het
Ttll13 A G 7: 80,255,387 M384V probably benign Het
Ugt2b37 A T 5: 87,254,330 D147E probably damaging Het
Vmn1r10 A T 6: 57,113,701 T93S probably benign Het
Wdr63 A G 3: 146,066,920 L457P probably damaging Het
Zfp236 C A 18: 82,674,356 E165* probably null Het
Zfp839 A T 12: 110,855,626 R291S probably damaging Het
Other mutations in Wasl
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02262:Wasl APN 6 24619187 missense unknown
IGL02550:Wasl APN 6 24633884 missense probably damaging 1.00
R0211:Wasl UTSW 6 24633893 missense probably damaging 1.00
R0211:Wasl UTSW 6 24633893 missense probably damaging 1.00
R2012:Wasl UTSW 6 24624361 missense probably damaging 1.00
R2103:Wasl UTSW 6 24618378 missense unknown
R2762:Wasl UTSW 6 24619501 missense unknown
R4629:Wasl UTSW 6 24637681 missense probably damaging 1.00
R4726:Wasl UTSW 6 24633111 missense probably benign 0.04
R6001:Wasl UTSW 6 24619574 missense unknown
R7109:Wasl UTSW 6 24633187 missense probably benign 0.08
R7336:Wasl UTSW 6 24619687 missense unknown
R7539:Wasl UTSW 6 24619198 missense unknown
R7849:Wasl UTSW 6 24633923 missense possibly damaging 0.52
R7860:Wasl UTSW 6 24619397 missense unknown
R7932:Wasl UTSW 6 24633923 missense possibly damaging 0.52
R8016:Wasl UTSW 6 24634595 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTTCAATTGAATGCCCTGTCG -3'
(R):5'- TTCAAGAGCTCCTACTGCTGC -3'

Sequencing Primer
(F):5'- GTCGTATCTGGTCTAAAAGCGCATC -3'
(R):5'- GAGCTCCTACTGCTGCACCTC -3'
Posted On2019-12-27