Incidental Mutation 'R6549:Gm9922'
ID 521461
Institutional Source Beutler Lab
Gene Symbol Gm9922
Ensembl Gene ENSMUSG00000053821
Gene Name predicted gene 9922
Synonyms
MMRRC Submission 044674-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.138) question?
Stock # R6549 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 101965036-101967164 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 101966893 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000097910 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066461] [ENSMUST00000100337]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000066461
AA Change: A120S
Predicted Effect probably benign
Transcript: ENSMUST00000100337
SMART Domains Protein: ENSMUSP00000097910
Gene: ENSMUSG00000033060

DomainStartEndE-ValueType
CH 14 124 2.57e-13 SMART
low complexity region 200 211 N/A INTRINSIC
Pfam:DUF4757 242 348 2.2e-14 PFAM
low complexity region 448 462 N/A INTRINSIC
Pfam:DUF4757 568 735 1.8e-46 PFAM
low complexity region 861 879 N/A INTRINSIC
low complexity region 979 991 N/A INTRINSIC
low complexity region 1003 1015 N/A INTRINSIC
PDZ 1047 1119 1.05e-8 SMART
coiled coil region 1222 1275 N/A INTRINSIC
coiled coil region 1319 1411 N/A INTRINSIC
low complexity region 1585 1596 N/A INTRINSIC
low complexity region 1599 1617 N/A INTRINSIC
LIM 1629 1687 6.54e-10 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 25 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atm T C 9: 53,404,477 (GRCm39) D1288G probably benign Het
Atxn7 T C 14: 14,013,087 (GRCm38) S2P probably damaging Het
C1rl T A 6: 124,485,487 (GRCm39) I286N probably benign Het
Ccdc54 T C 16: 50,410,388 (GRCm39) R293G possibly damaging Het
Cndp1 A T 18: 84,654,309 (GRCm39) I85K probably benign Het
Col25a1 A G 3: 129,976,444 (GRCm39) T110A probably benign Het
Defb8 G T 8: 19,497,560 (GRCm39) P17Q probably damaging Het
Dnah1 A T 14: 30,991,340 (GRCm39) L3146Q probably damaging Het
Espn A T 4: 152,215,525 (GRCm39) M1K probably null Het
Hycc2 T C 1: 58,578,759 (GRCm39) I264V probably benign Het
Ldb3 A G 14: 34,263,854 (GRCm39) M545T probably damaging Het
Or8k30 A T 2: 86,339,726 (GRCm39) I308L probably benign Het
Piezo1 G A 8: 123,227,002 (GRCm39) H420Y Het
Primpol A T 8: 47,058,185 (GRCm39) L115I probably damaging Het
Pus10 G A 11: 23,679,075 (GRCm39) probably null Het
Rictor C G 15: 6,825,656 (GRCm39) A1689G probably damaging Het
Scn2a A G 2: 65,595,018 (GRCm39) N1956D probably benign Het
Scn4a T C 11: 106,234,791 (GRCm39) D384G probably damaging Het
Sell A G 1: 163,893,198 (GRCm39) D138G probably damaging Het
Slc4a7 T A 14: 14,748,564 (GRCm38) F327L probably damaging Het
Sox6 A G 7: 115,085,927 (GRCm39) I680T possibly damaging Het
Synj1 A G 16: 90,735,565 (GRCm39) S1463P probably benign Het
Vmn1r31 A T 6: 58,449,648 (GRCm39) N72K possibly damaging Het
Vmn2r77 A G 7: 86,450,065 (GRCm39) I104V probably benign Het
Zfp988 G A 4: 147,416,310 (GRCm39) C248Y probably benign Het
Other mutations in Gm9922
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0271:Gm9922 UTSW 14 101,966,989 (GRCm39) unclassified probably benign
R0309:Gm9922 UTSW 14 101,967,129 (GRCm39) unclassified probably benign
R1809:Gm9922 UTSW 14 101,966,841 (GRCm39) unclassified probably benign
R2173:Gm9922 UTSW 14 101,967,012 (GRCm39) unclassified probably benign
R7298:Gm9922 UTSW 14 101,966,961 (GRCm39) missense unknown
R9241:Gm9922 UTSW 14 101,967,220 (GRCm39) missense unknown
R9712:Gm9922 UTSW 14 101,966,893 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ACCACGAAGGGTACAGGTTTTG -3'
(R):5'- CAGGAATAGCTGCACACAATTG -3'

Sequencing Primer
(F):5'- CACGAAGGGTACAGGTTTTGATTCTC -3'
(R):5'- TTTCCGGGCCAAGAAACTTC -3'
Posted On 2018-06-06