Incidental Mutation 'R9537:Gm5767'
ID 719756
Institutional Source Beutler Lab
Gene Symbol Gm5767
Ensembl Gene ENSMUSG00000107252
Gene Name predicted gene 5767
Synonyms
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.155) question?
Stock # R9537 (G1)
Quality Score 225.009
Status Not validated
Chromosome 16
Chromosomal Location 8680770-8683911 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) G to T at 8683313 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Cysteine to Phenylalanine at position 11 (C11F)
Ref Sequence ENSEMBL: ENSMUSP00000143858 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000201722] [ENSMUST00000202157]
AlphaFold A0A0J9YTU8
Predicted Effect
SMART Domains Protein: ENSMUSP00000143858
Gene: ENSMUSG00000107252
AA Change: C11F

DomainStartEndE-ValueType
low complexity region 18 38 N/A INTRINSIC
LITAF 57 126 9.88e-18 SMART
Predicted Effect unknown
Transcript: ENSMUST00000202157
AA Change: C11F
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310007B03Rik T C 1: 93,153,162 K341E possibly damaging Het
Adgra3 A G 5: 49,960,865 Y1114H possibly damaging Het
Atp5j A G 16: 84,828,470 Y82H probably damaging Het
Bcl2a1d T G 9: 88,731,473 I83L probably benign Het
Bean1 CT C 8: 104,182,032 probably null Het
Bglap3 T C 3: 88,368,832 D71G probably benign Het
Bnip3l G A 14: 67,008,765 P7L possibly damaging Het
Chmp2b T C 16: 65,551,046 K15E probably benign Het
Chrm3 A T 13: 9,877,426 W525R probably damaging Het
Col7a1 A T 9: 108,955,352 K143* probably null Het
D6Ertd527e G C 6: 87,111,857 S334T unknown Het
Dnaic1 A G 4: 41,629,790 probably null Het
Dnhd1 G A 7: 105,695,533 G2028D probably damaging Het
Esyt3 C T 9: 99,317,239 R773Q probably damaging Het
Ffar1 T C 7: 30,860,600 T291A probably benign Het
Golga2 G T 2: 32,288,301 probably benign Het
Hapln2 T A 3: 88,024,473 probably null Het
Ing1 T C 8: 11,561,889 L203P probably benign Het
Med1 T C 11: 98,171,760 T171A possibly damaging Het
Mib2 A T 4: 155,657,495 L387H probably damaging Het
Mier1 A G 4: 103,162,561 N494S probably benign Het
Myof A G 19: 37,907,606 L1847P probably damaging Het
Ndst3 A T 3: 123,671,513 V270D Het
Nup160 T C 2: 90,729,744 L1271S possibly damaging Het
Osgep A T 14: 50,924,662 probably null Het
Ptgfr G T 3: 151,835,808 T21N possibly damaging Het
Ptgs1 T C 2: 36,230,727 S23P unknown Het
Rsf1 CGGCGGCGG CGGCGGCGGGGGCGGCGG 7: 97,579,914 probably benign Het
Smu1 A G 4: 40,755,671 S65P probably benign Het
Spef2 T C 15: 9,601,799 Y1459C unknown Het
Spen A G 4: 141,471,704 V3204A probably benign Het
Spen TTGCTGCTGCTGCTGCTGCTGCTGCTG TTGCTGCTGCTGCTGCTGCTGCTG 4: 141,516,845 probably benign Het
Timm44 G A 8: 4,260,576 T392I possibly damaging Het
Tnc A T 4: 63,966,584 I1818N probably damaging Het
Trpm1 G T 7: 64,153,868 probably benign Het
Ttc14 A G 3: 33,803,198 Y231C probably damaging Het
Ube3b A G 5: 114,387,184 R23G probably damaging Het
Usp40 T C 1: 88,007,395 Y10C probably benign Het
Vmn2r107 C A 17: 20,374,887 S567R probably benign Het
Zfp112 T C 7: 24,127,087 Y831H probably damaging Het
Zfy2 T A Y: 2,108,596 T355S Het
Other mutations in Gm5767
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4801:Gm5767 UTSW 16 8683345 missense unknown
R6877:Gm5767 UTSW 16 8683309 missense unknown
R7637:Gm5767 UTSW 16 8683646 missense unknown
R7904:Gm5767 UTSW 16 8683817 missense
R9190:Gm5767 UTSW 16 8683783 missense
Predicted Primers PCR Primer
(F):5'- GGTGCCATACCTAGAGTTTCTG -3'
(R):5'- ATTGTTTCAGCCACCCAGC -3'

Sequencing Primer
(F):5'- GCCATACCTAGAGTTTCTGAGATATC -3'
(R):5'- ATTGTTTCAGCCACCCAGCTAGAG -3'
Posted On 2022-07-18