Incidental Mutation 'R7858:Gm9821'
ID 607324
Institutional Source Beutler Lab
Gene Symbol Gm9821
Ensembl Gene ENSMUSG00000095332
Gene Name predicted gene 9821
Synonyms
MMRRC Submission 045911-MU
Accession Numbers
Essential gene? Not available question?
Stock # R7858 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 91776048-91779033 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 91776351 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 101 (H101L)
Ref Sequence ENSEMBL: ENSMUSP00000136804 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028667] [ENSMUST00000099709] [ENSMUST00000111303] [ENSMUST00000128152] [ENSMUST00000142090] [ENSMUST00000142231] [ENSMUST00000178895]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000028667
SMART Domains Protein: ENSMUSP00000028667
Gene: ENSMUSG00000040479

DomainStartEndE-ValueType
low complexity region 3 30 N/A INTRINSIC
low complexity region 66 75 N/A INTRINSIC
C1 96 153 2.67e-1 SMART
C1 173 231 8.18e-7 SMART
low complexity region 257 274 N/A INTRINSIC
DAGKc 296 420 4.61e-65 SMART
DAGKa 447 604 2.75e-95 SMART
low complexity region 762 780 N/A INTRINSIC
ANK 823 853 8.52e-4 SMART
ANK 858 887 2.18e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000099709
SMART Domains Protein: ENSMUSP00000106937
Gene: ENSMUSG00000040479

DomainStartEndE-ValueType
low complexity region 2 38 N/A INTRINSIC
low complexity region 83 92 N/A INTRINSIC
C1 113 170 2.67e-1 SMART
C1 190 248 8.18e-7 SMART
low complexity region 274 291 N/A INTRINSIC
DAGKc 313 437 4.61e-65 SMART
DAGKa 464 621 2.75e-95 SMART
low complexity region 779 797 N/A INTRINSIC
ANK 840 870 8.52e-4 SMART
ANK 875 904 2.18e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000111303
SMART Domains Protein: ENSMUSP00000106934
Gene: ENSMUSG00000040479

DomainStartEndE-ValueType
low complexity region 39 58 N/A INTRINSIC
low complexity region 66 81 N/A INTRINSIC
low complexity region 100 113 N/A INTRINSIC
low complexity region 118 133 N/A INTRINSIC
low complexity region 200 214 N/A INTRINSIC
low complexity region 260 269 N/A INTRINSIC
C1 290 347 2.67e-1 SMART
C1 367 425 8.18e-7 SMART
low complexity region 451 468 N/A INTRINSIC
DAGKc 490 614 4.61e-65 SMART
DAGKa 641 798 2.75e-95 SMART
low complexity region 956 974 N/A INTRINSIC
ANK 1017 1047 8.52e-4 SMART
ANK 1052 1081 2.18e-1 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000128152
SMART Domains Protein: ENSMUSP00000118684
Gene: ENSMUSG00000040479

DomainStartEndE-ValueType
low complexity region 32 41 N/A INTRINSIC
Blast:C1 62 114 9e-33 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000142090
Predicted Effect probably benign
Transcript: ENSMUST00000142231
SMART Domains Protein: ENSMUSP00000114740
Gene: ENSMUSG00000040479

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000178895
AA Change: H101L
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 100% (32/32)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acadl T C 1: 66,877,483 (GRCm39) E356G probably benign Het
Adamtsl3 T C 7: 82,099,371 (GRCm39) L175P probably damaging Het
Apon T C 10: 128,090,328 (GRCm39) I2T probably benign Het
Ccny T A 18: 9,386,782 (GRCm39) D61V probably damaging Het
Cp A G 3: 20,025,219 (GRCm39) T393A probably benign Het
Cspg5 T C 9: 110,080,134 (GRCm39) L434P probably damaging Het
Cyld T A 8: 89,436,616 (GRCm39) I302N probably damaging Het
Ercc4 T C 16: 12,943,169 (GRCm39) S283P probably damaging Het
Frem3 T A 8: 81,338,350 (GRCm39) Y214* probably null Het
Gm1123 T C 9: 98,896,107 (GRCm39) N258D possibly damaging Het
Il36b T A 2: 24,044,626 (GRCm39) C9S probably benign Het
Kti12 A C 4: 108,705,443 (GRCm39) E119A probably benign Het
Kti12 G T 4: 108,705,444 (GRCm39) E119D probably benign Het
Mansc1 T C 6: 134,587,377 (GRCm39) T267A probably benign Het
Mtor A G 4: 148,539,103 (GRCm39) D200G probably damaging Het
Muc5ac G C 7: 141,357,166 (GRCm39) V1148L possibly damaging Het
Mycbp2 C A 14: 103,393,741 (GRCm39) R2940L probably damaging Het
Myh7 A G 14: 55,227,500 (GRCm39) F312L probably benign Het
Or4c31 G A 2: 88,292,056 (GRCm39) C143Y probably damaging Het
Prkdc T A 16: 15,507,141 (GRCm39) S874T probably benign Het
Prmt7 T G 8: 106,971,320 (GRCm39) I452S possibly damaging Het
Setx A C 2: 29,051,562 (GRCm39) D2038A probably damaging Het
Spen A T 4: 141,215,442 (GRCm39) probably null Het
Sycp1 T C 3: 102,806,273 (GRCm39) K473E probably benign Het
Uggt1 A G 1: 36,195,339 (GRCm39) F1290S probably damaging Het
Unc13b T G 4: 43,176,285 (GRCm39) V2371G unknown Het
Vmn2r4 C T 3: 64,317,226 (GRCm39) V171I probably benign Het
Zfp35 T C 18: 24,136,897 (GRCm39) C414R probably damaging Het
Zfp704 A G 3: 9,509,217 (GRCm39) probably null Het
Zfp758 A G 17: 22,594,359 (GRCm39) T282A probably benign Het
Zfp961 T C 8: 72,704,949 (GRCm39) V4A unknown Het
Predicted Primers PCR Primer
(F):5'- AAAACAGCCCTGGAGCTGTG -3'
(R):5'- GTCCTTTAGGCTCAGATCTCTGTTG -3'

Sequencing Primer
(F):5'- CTCTGGGCCAGTGAAGAGGAC -3'
(R):5'- AGGCTCAGATCTCTGTTGTTTCTG -3'
Posted On 2019-12-20