Incidental Mutation 'R9672:Wdr97'
ID 728118
Institutional Source Beutler Lab
Gene Symbol Wdr97
Ensembl Gene ENSMUSG00000109179
Gene Name WD repeat domain 97
Synonyms Gm35339
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.122) question?
Stock # R9672 (G1)
Quality Score 225.009
Status Not validated
Chromosome 15
Chromosomal Location 76238649-76249141 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 76240377 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 355 (V355E)
Ref Sequence ENSEMBL: ENSMUSP00000146420 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023212] [ENSMUST00000160172] [ENSMUST00000160853] [ENSMUST00000160914] [ENSMUST00000161527] [ENSMUST00000208833]
AlphaFold A0A140LHH9
Predicted Effect probably benign
Transcript: ENSMUST00000023212
SMART Domains Protein: ENSMUSP00000023212
Gene: ENSMUSG00000022553

DomainStartEndE-ValueType
Pfam:Maf1 24 202 2.8e-69 PFAM
low complexity region 215 244 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000160172
SMART Domains Protein: ENSMUSP00000124242
Gene: ENSMUSG00000022553

DomainStartEndE-ValueType
Pfam:Maf1 24 202 2.7e-70 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000160853
SMART Domains Protein: ENSMUSP00000124893
Gene: ENSMUSG00000022553

DomainStartEndE-ValueType
Pfam:Maf1 25 202 4.6e-67 PFAM
low complexity region 215 244 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000160914
SMART Domains Protein: ENSMUSP00000124110
Gene: ENSMUSG00000022553

DomainStartEndE-ValueType
low complexity region 33 48 N/A INTRINSIC
Pfam:Maf1 84 202 4.3e-37 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000161527
SMART Domains Protein: ENSMUSP00000125387
Gene: ENSMUSG00000022553

DomainStartEndE-ValueType
Pfam:Maf1 24 202 2.8e-69 PFAM
low complexity region 215 244 N/A INTRINSIC
Predicted Effect
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 G T 10: 79,838,563 (GRCm39) K612N probably null Het
Atrnl1 G A 19: 57,618,695 (GRCm39) A138T possibly damaging Het
Bicc1 T C 10: 70,794,666 (GRCm39) T164A probably damaging Het
Bnip3l G A 14: 67,246,214 (GRCm39) P7L possibly damaging Het
Ccdc7a A G 8: 129,671,016 (GRCm39) S497P unknown Het
Cd209d C G 8: 3,922,036 (GRCm39) G212A probably damaging Het
Cog8 A G 8: 107,780,658 (GRCm39) I200T probably damaging Het
Cuzd1 T A 7: 130,919,847 (GRCm39) I90F possibly damaging Het
Cyp4a30b T A 4: 115,316,576 (GRCm39) C401S probably benign Het
Cyp4a31 T A 4: 115,427,422 (GRCm39) N209K probably benign Het
D6Ertd527e G C 6: 87,088,839 (GRCm39) S334T unknown Het
Dcaf11 T A 14: 55,806,484 (GRCm39) Y468* probably null Het
Dennd4a A G 9: 64,800,640 (GRCm39) D926G probably benign Het
Dph7 T C 2: 24,855,606 (GRCm39) L135P probably benign Het
Fcho2 A T 13: 98,869,178 (GRCm39) C564* probably null Het
Gabrb2 G A 11: 42,312,207 (GRCm39) G11R probably benign Het
Gas6 A G 8: 13,528,273 (GRCm39) S187P probably benign Het
Gemin5 C T 11: 58,058,585 (GRCm39) V93I probably benign Het
Gldn A T 9: 54,245,780 (GRCm39) I444F probably damaging Het
Gmps T C 3: 63,897,750 (GRCm39) V234A probably damaging Het
Hand1 A G 11: 57,722,516 (GRCm39) S33P possibly damaging Het
Ice2 G A 9: 69,322,899 (GRCm39) A465T probably benign Het
Irf9 T C 14: 55,842,129 (GRCm39) S2P probably benign Het
Kpna7 C T 5: 144,944,776 (GRCm39) M21I probably benign Het
Lig4 A G 8: 10,023,213 (GRCm39) M189T probably damaging Het
Lrp1b T C 2: 40,779,291 (GRCm39) T2698A Het
Med10 A G 13: 69,963,711 (GRCm39) K104R probably benign Het
Mfsd14b A G 13: 65,260,320 (GRCm39) W38R probably benign Het
Mrgpra2a A G 7: 47,076,490 (GRCm39) F256S probably benign Het
Myo9a A G 9: 59,687,332 (GRCm39) K146E probably benign Het
Oxgr1 T A 14: 120,259,454 (GRCm39) Y251F probably damaging Het
Pabpc4 T C 4: 123,184,133 (GRCm39) probably null Het
Pde8a A G 7: 80,942,014 (GRCm39) N151S probably damaging Het
Pdilt A G 7: 119,100,824 (GRCm39) F176L possibly damaging Het
Plekhg5 C A 4: 152,187,541 (GRCm39) D115E probably benign Het
Plxnd1 C T 6: 115,940,274 (GRCm39) R1370Q possibly damaging Het
Ppp1r9a T C 6: 5,007,889 (GRCm39) C532R unknown Het
Rasa2 A G 9: 96,427,781 (GRCm39) W695R probably damaging Het
Rbpms2 A G 9: 65,538,118 (GRCm39) N3S probably benign Het
Rsph6a A G 7: 18,799,842 (GRCm39) Y491C probably damaging Het
Scel T A 14: 103,836,838 (GRCm39) N495K possibly damaging Het
Setd1a T C 7: 127,385,237 (GRCm39) L648P possibly damaging Het
Snx29 A T 16: 11,478,515 (GRCm39) R333S probably benign Het
Sppl2c A G 11: 104,077,344 (GRCm39) Y48C probably damaging Het
Uba2 A T 7: 33,856,749 (GRCm39) N230K probably benign Het
Utrn T C 10: 12,603,613 (GRCm39) Q589R possibly damaging Het
Vmn1r51 T A 6: 90,106,549 (GRCm39) L155H probably damaging Het
Vmn2r97 A G 17: 19,149,442 (GRCm39) N277D probably benign Het
Yy1 C A 12: 108,759,584 (GRCm39) H82Q unknown Het
Other mutations in Wdr97
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6006:Wdr97 UTSW 15 76,241,372 (GRCm39) missense probably damaging 1.00
R6258:Wdr97 UTSW 15 76,239,895 (GRCm39) nonsense probably null
R6464:Wdr97 UTSW 15 76,246,977 (GRCm39) missense probably benign 0.01
R6544:Wdr97 UTSW 15 76,242,478 (GRCm39) missense probably benign 0.00
R6545:Wdr97 UTSW 15 76,247,578 (GRCm39) missense probably damaging 1.00
R6554:Wdr97 UTSW 15 76,239,178 (GRCm39) missense possibly damaging 0.64
R6803:Wdr97 UTSW 15 76,240,776 (GRCm39) missense probably damaging 1.00
R6850:Wdr97 UTSW 15 76,241,996 (GRCm39) missense probably damaging 1.00
R7574:Wdr97 UTSW 15 76,241,949 (GRCm39) nonsense probably null
R7793:Wdr97 UTSW 15 76,243,307 (GRCm39) missense
R7985:Wdr97 UTSW 15 76,245,687 (GRCm39) missense
R8008:Wdr97 UTSW 15 76,244,832 (GRCm39) missense
R8170:Wdr97 UTSW 15 76,247,819 (GRCm39) missense
R8171:Wdr97 UTSW 15 76,247,819 (GRCm39) missense
R8267:Wdr97 UTSW 15 76,240,794 (GRCm39) missense
R8337:Wdr97 UTSW 15 76,245,684 (GRCm39) missense
R8478:Wdr97 UTSW 15 76,247,629 (GRCm39) splice site probably null
R8735:Wdr97 UTSW 15 76,240,775 (GRCm39) missense
R8958:Wdr97 UTSW 15 76,245,694 (GRCm39) missense
R9385:Wdr97 UTSW 15 76,240,367 (GRCm39) missense
R9440:Wdr97 UTSW 15 76,245,064 (GRCm39) missense
R9657:Wdr97 UTSW 15 76,245,476 (GRCm39) missense
R9778:Wdr97 UTSW 15 76,241,125 (GRCm39) missense
RF004:Wdr97 UTSW 15 76,247,373 (GRCm39) frame shift probably null
RF009:Wdr97 UTSW 15 76,247,367 (GRCm39) frame shift probably null
RF016:Wdr97 UTSW 15 76,240,172 (GRCm39) missense
RF030:Wdr97 UTSW 15 76,247,365 (GRCm39) frame shift probably null
Z1177:Wdr97 UTSW 15 76,247,330 (GRCm39) missense
Z1177:Wdr97 UTSW 15 76,239,130 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- ACACAGGTATGTCAGGCTGG -3'
(R):5'- ACCTGTATATGGAGCACTGGTG -3'

Sequencing Primer
(F):5'- ATGTCAGGCTGGCAGCTTTTG -3'
(R):5'- GCACACGCCATAGCTCTATG -3'
Posted On 2022-10-06