Incidental Mutation 'R7938:Gm11568'
ID612333
Institutional Source Beutler Lab
Gene Symbol Gm11568
Ensembl Gene ENSMUSG00000069717
Gene Namepredicted gene 11568
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.102) question?
Stock #R7938 (G1)
Quality Score225.009
Status Not validated
Chromosome11
Chromosomal Location99857917-99859061 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 99858184 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Serine at position 72 (T72S)
Ref Sequence ENSEMBL: ENSMUSP00000103057 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000107434]
Predicted Effect unknown
Transcript: ENSMUST00000107434
AA Change: T72S
SMART Domains Protein: ENSMUSP00000103057
Gene: ENSMUSG00000069717
AA Change: T72S

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 84 129 1.7e-9 PFAM
Pfam:Keratin_B2_2 103 147 7.7e-10 PFAM
Pfam:Keratin_B2_2 118 168 2.4e-6 PFAM
Pfam:Keratin_B2_2 147 189 3.8e-8 PFAM
low complexity region 195 206 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700081O15Rik T A 19: 7,422,256 I456N probably damaging Het
Abca6 A T 11: 110,191,628 V1173D probably benign Het
Ace A T 11: 105,972,379 M327L probably benign Het
Bcl2l2 C T 14: 54,884,379 probably benign Het
Bicdl2 C T 17: 23,666,017 Q231* probably null Het
Brms1l A T 12: 55,866,053 D277V possibly damaging Het
Cd38 C A 5: 43,901,448 L135M probably damaging Het
Col6a3 G T 1: 90,810,621 P1059T possibly damaging Het
Coro1c A T 5: 113,848,597 M262K probably benign Het
Cpxm2 G T 7: 132,057,695 P481Q possibly damaging Het
Dnah12 G T 14: 26,829,329 V2543F probably benign Het
Dock2 A C 11: 34,273,698 D1145E probably damaging Het
Elf3 G A 1: 135,254,352 R364W probably damaging Het
Epha3 A G 16: 63,773,560 I55T probably damaging Het
Fam69c G A 18: 84,730,046 probably benign Het
Gfer C A 17: 24,694,285 D198Y probably damaging Het
Gm10436 A T 12: 88,176,083 I450N probably benign Het
Gm13723 C A 2: 86,873,262 V154L probably benign Het
Gm21994 C T 2: 150,255,146 R121Q probably benign Het
Gm5415 A C 1: 32,546,033 I265M probably damaging Het
Igkv3-1 C T 6: 70,704,069 A84V probably benign Het
Il1rl2 A C 1: 40,343,119 Y197S probably damaging Het
Il2ra T C 2: 11,680,336 I161T possibly damaging Het
Itgb8 C T 12: 119,166,772 R667H probably benign Het
Kcnh7 G A 2: 62,837,194 Q334* probably null Het
Lctl A C 9: 64,133,216 R480S possibly damaging Het
Lrba T G 3: 86,315,430 I617S possibly damaging Het
Marf1 G T 16: 14,114,201 H1651N probably benign Het
Mitf T A 6: 97,993,196 Y142N probably damaging Het
Nup160 T A 2: 90,702,711 probably null Het
Olfr569 A G 7: 102,887,628 V175A probably benign Het
Olfr620 T A 7: 103,611,772 I194F possibly damaging Het
Pecam1 A G 11: 106,671,750 V708A probably benign Het
Pinlyp C T 7: 24,542,440 probably null Het
Polh G A 17: 46,175,248 R382W probably damaging Het
Prdm10 A G 9: 31,327,474 I221V probably benign Het
Pskh1 G T 8: 105,913,090 R134L probably benign Het
Ptpre A G 7: 135,651,995 N6D probably benign Het
Rasgrp4 C T 7: 29,150,610 P58L unknown Het
Rhbdf2 G T 11: 116,602,240 C393* probably null Het
Rlf T C 4: 121,182,691 I174M possibly damaging Het
Ryr2 T A 13: 11,706,623 R2641* probably null Het
Simc1 A G 13: 54,524,832 H331R probably benign Het
Skp2 A G 15: 9,122,241 S256P probably benign Het
Smarcd2 T C 11: 106,267,566 R10G probably benign Het
Spef2 A G 15: 9,687,895 L480P possibly damaging Het
Tenm4 A G 7: 96,873,874 H1541R probably damaging Het
Top1 T A 2: 160,714,088 L489Q probably damaging Het
Ttll13 C T 7: 80,254,097 H258Y probably damaging Het
Unc80 A G 1: 66,483,349 R237G possibly damaging Het
Vmn1r55 A G 7: 5,146,624 F267L probably benign Het
Vmn2r96 T A 17: 18,597,868 M761K possibly damaging Het
Vps33a G A 5: 123,570,979 H58Y possibly damaging Het
Zfp354c TCACACTCGGCACA TCACA 11: 50,815,240 probably benign Het
Zfp467 T C 6: 48,439,181 Q179R probably damaging Het
Zfp729a A T 13: 67,619,948 S721T possibly damaging Het
Other mutations in Gm11568
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0483:Gm11568 UTSW 11 99858383 missense unknown
R0558:Gm11568 UTSW 11 99858046 missense unknown
R1053:Gm11568 UTSW 11 99858061 missense unknown
R2273:Gm11568 UTSW 11 99858244 missense unknown
R2274:Gm11568 UTSW 11 99858244 missense unknown
R2275:Gm11568 UTSW 11 99858244 missense unknown
R4436:Gm11568 UTSW 11 99858595 missense unknown
R4985:Gm11568 UTSW 11 99858448 missense unknown
R5078:Gm11568 UTSW 11 99858355 missense unknown
R5083:Gm11568 UTSW 11 99857972 start codon destroyed probably null
R6879:Gm11568 UTSW 11 99858227 missense unknown
R7486:Gm11568 UTSW 11 99858466 missense unknown
R7855:Gm11568 UTSW 11 99858184 missense unknown
Predicted Primers PCR Primer
(F):5'- ACCATGACCAACTCCTGCTG -3'
(R):5'- CTGACAGCAGCTGGAGATAC -3'

Sequencing Primer
(F):5'- TTGCTGCCAGCCCACCTG -3'
(R):5'- AGATACAGCACCTGGGCTGAC -3'
Posted On2019-12-27