Incidental Mutation 'R7300:Gm4779'
ID 566948
Institutional Source Beutler Lab
Gene Symbol Gm4779
Ensembl Gene ENSMUSG00000045010
Gene Name predicted gene 4779
Synonyms
MMRRC Submission 045404-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R7300 (G1)
Quality Score 214.458
Status Not validated
Chromosome X
Chromosomal Location 100833938-100838074 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) TCGGGGCCGGGGCCGGGGCCG to TCGGGGCCGGGGCCGGGGCCGGGGCCG at 100837777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130455 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056225] [ENSMUST00000124577] [ENSMUST00000147742] [ENSMUST00000151231] [ENSMUST00000163399]
AlphaFold A0A1B0GR91
Predicted Effect probably benign
Transcript: ENSMUST00000056225
Predicted Effect probably benign
Transcript: ENSMUST00000124577
Predicted Effect probably benign
Transcript: ENSMUST00000147742
Predicted Effect probably benign
Transcript: ENSMUST00000151231
SMART Domains Protein: ENSMUSP00000133189
Gene: ENSMUSG00000046774

DomainStartEndE-ValueType
Pfam:DUF4641 101 552 3.2e-163 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000163399
SMART Domains Protein: ENSMUSP00000130455
Gene: ENSMUSG00000046774

DomainStartEndE-ValueType
Pfam:DUF4641 102 545 1.6e-182 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 94% (45/48)
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actmap G A 7: 26,900,548 (GRCm39) A176T probably damaging Het
Adgrd1 T C 5: 129,174,411 (GRCm39) probably null Het
Atr T C 9: 95,747,423 (GRCm39) I235T probably benign Het
Bpifb5 A G 2: 154,070,066 (GRCm39) E172G possibly damaging Het
Btbd2 A T 10: 80,480,100 (GRCm39) I420N probably damaging Het
Ccdc141 G A 2: 76,845,038 (GRCm39) T1343I probably benign Het
Cd59b A T 2: 103,914,795 (GRCm39) K64N possibly damaging Het
Cd63 A G 10: 128,748,034 (GRCm39) N144S probably benign Het
Cip2a A G 16: 48,834,217 (GRCm39) K631E probably damaging Het
Col4a4 C T 1: 82,464,361 (GRCm39) R989Q unknown Het
Cyp4a31 A G 4: 115,427,468 (GRCm39) T225A probably benign Het
Dnah1 T G 14: 30,991,798 (GRCm39) E3068A probably benign Het
Fpgt C T 3: 154,792,612 (GRCm39) V472I probably damaging Het
Homer3 T C 8: 70,737,953 (GRCm39) M1T probably null Het
Ighv1-4 T C 12: 114,450,908 (GRCm39) I67V probably benign Het
Il17ra A G 6: 120,459,063 (GRCm39) D738G probably benign Het
Il2ra A G 2: 11,681,721 (GRCm39) T109A not run Het
Itgb6 T C 2: 60,435,650 (GRCm39) D700G probably benign Het
Krt31 T C 11: 99,938,612 (GRCm39) E327G probably damaging Het
Large1 A C 8: 73,564,224 (GRCm39) L514R probably damaging Het
Map3k8 C T 18: 4,349,076 (GRCm39) V81M probably damaging Het
Mstn T C 1: 53,103,239 (GRCm39) S192P probably benign Het
Olfml3 T C 3: 103,643,176 (GRCm39) K402E probably damaging Het
Or13a27 A T 7: 139,925,268 (GRCm39) N211K probably damaging Het
Or2n1c A C 17: 38,519,588 (GRCm39) T151P possibly damaging Het
Or2y1c C T 11: 49,361,473 (GRCm39) T165I probably benign Het
Or52i2 A G 7: 102,319,417 (GRCm39) S97G probably benign Het
Or7g17 T C 9: 18,768,530 (GRCm39) I194T not run Het
Or8k25 T C 2: 86,244,330 (GRCm39) E22G probably null Het
Pde4a T C 9: 21,117,618 (GRCm39) S627P probably damaging Het
Pdxdc1 A G 16: 13,697,374 (GRCm39) I102T probably damaging Het
Phldb2 A G 16: 45,645,925 (GRCm39) S174P probably damaging Het
Pla2g4e C T 2: 120,021,680 (GRCm39) V143I probably damaging Het
Pou4f2 C T 8: 79,162,735 (GRCm39) probably null Het
Ppl C T 16: 4,920,235 (GRCm39) V387M possibly damaging Het
Pramel43 A T 5: 94,760,655 (GRCm39) D340E probably benign Het
Rarg A T 15: 102,160,852 (GRCm39) probably null Het
Ryr1 T C 7: 28,758,936 (GRCm39) Y3414C probably damaging Het
Serpinb8 T A 1: 107,535,053 (GRCm39) *375K probably null Het
Sim1 C T 10: 50,785,614 (GRCm39) H228Y probably benign Het
Spag4 A T 2: 155,907,541 (GRCm39) H87L probably benign Het
Ttc17 A T 2: 94,205,479 (GRCm39) L289Q probably damaging Het
Ubac2 T C 14: 122,142,586 (GRCm39) L28P probably damaging Het
Vmn2r31 C A 7: 7,387,775 (GRCm39) A599S possibly damaging Het
Vps13c T C 9: 67,847,826 (GRCm39) V2196A probably benign Het
Zswim5 A T 4: 116,833,102 (GRCm39) I612F probably damaging Het
Zzef1 T A 11: 72,765,830 (GRCm39) H1452Q probably benign Het
Other mutations in Gm4779
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2971:Gm4779 UTSW X 100,836,568 (GRCm39) missense possibly damaging 0.56
R7126:Gm4779 UTSW X 100,837,777 (GRCm39) unclassified probably benign
R7298:Gm4779 UTSW X 100,837,777 (GRCm39) unclassified probably benign
R7301:Gm4779 UTSW X 100,837,777 (GRCm39) unclassified probably benign
R8258:Gm4779 UTSW X 100,837,390 (GRCm39) missense possibly damaging 0.71
R8259:Gm4779 UTSW X 100,837,390 (GRCm39) missense possibly damaging 0.71
R8260:Gm4779 UTSW X 100,837,390 (GRCm39) missense possibly damaging 0.71
R9253:Gm4779 UTSW X 100,836,917 (GRCm39) unclassified probably benign
Z1176:Gm4779 UTSW X 100,835,792 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- TTGTACCCTCGATGGCTAGCTG -3'
(R):5'- AACAATAGGCGCCCTGGTTG -3'

Sequencing Primer
(F):5'- ATGGCTAGCTGCTGTACAAAGTCC -3'
(R):5'- TCGCGAGACTTGACCGGAAG -3'
Posted On 2019-06-26