Incidental Mutation 'R2226:Gm11555'
ID239739
Institutional Source Beutler Lab
Gene Symbol Gm11555
Ensembl Gene ENSMUSG00000078130
Gene Namepredicted gene 11555
Synonyms
MMRRC Submission 040227-MU
Accession Numbers
Is this an essential gene? Not available question?
Stock #R2226 (G1)
Quality Score225
Status Not validated
Chromosome11
Chromosomal Location99649599-99650236 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 99649759 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Serine at position 141 (R141S)
Ref Sequence ENSEMBL: ENSMUSP00000100533 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073126] [ENSMUST00000104929]
Predicted Effect unknown
Transcript: ENSMUST00000073126
AA Change: R131S
SMART Domains Protein: ENSMUSP00000131822
Gene: ENSMUSG00000078130
AA Change: R131S

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 1 43 1.4e-7 PFAM
Pfam:Keratin_B2 1 79 1.9e-9 PFAM
Pfam:Keratin_B2_2 14 58 6.4e-14 PFAM
Pfam:Keratin_B2_2 39 88 2.1e-11 PFAM
Pfam:Keratin_B2_2 79 123 1.7e-12 PFAM
Pfam:Keratin_B2_2 89 134 4.6e-8 PFAM
Pfam:Keratin_B2_2 123 164 3.3e-4 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000104929
AA Change: R141S
SMART Domains Protein: ENSMUSP00000100533
Gene: ENSMUSG00000078130
AA Change: R141S

DomainStartEndE-ValueType
Pfam:Keratin_B2_2 1 58 2.8e-9 PFAM
Pfam:Keratin_B2 1 74 4.2e-11 PFAM
Pfam:Keratin_B2_2 49 96 2.1e-11 PFAM
Pfam:Keratin_B2_2 59 117 2.6e-6 PFAM
Pfam:Keratin_B2_2 89 133 5.7e-13 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl3 A T 4: 144,463,725 V2E possibly damaging Het
Aen C A 7: 78,902,451 T15K probably benign Het
Aggf1 A G 13: 95,370,846 S144P probably damaging Het
Ar T A X: 98,151,331 M517K probably benign Het
Ascc3 A G 10: 50,754,052 T1746A probably benign Het
Atg9b A G 5: 24,386,395 V735A possibly damaging Het
Atp1b3 A G 9: 96,343,276 F113S probably damaging Het
BC005561 T A 5: 104,519,420 Y603N probably damaging Het
Cacna1h T C 17: 25,385,943 N1132S probably benign Het
Ccdc150 A G 1: 54,364,925 I943V probably null Het
Cntnap4 A G 8: 112,815,488 D751G probably damaging Het
Dgkk T A X: 6,875,248 D102E probably damaging Het
Efhb A T 17: 53,462,429 probably null Het
Elfn2 A G 15: 78,674,243 W35R probably damaging Het
Emcn T C 3: 137,404,017 I140T possibly damaging Het
Epha2 G A 4: 141,321,237 R569H probably damaging Het
Gabrg2 A T 11: 41,971,908 F116L probably damaging Het
Gm4985 T A X: 23,958,934 M1L probably null Het
Gm5415 A T 1: 32,545,853 H325Q probably damaging Het
Hectd3 T C 4: 116,995,689 I96T possibly damaging Het
Hnrnpul2 T A 19: 8,824,985 N405K probably damaging Het
Iigp1 A T 18: 60,389,888 K26I possibly damaging Het
Kirrel2 T C 7: 30,454,154 K260R probably damaging Het
Kpna1 G A 16: 36,031,221 A392T probably damaging Het
Krt19 T C 11: 100,141,575 E260G probably damaging Het
March7 A G 2: 60,229,846 R106G probably benign Het
Mthfd2l G T 5: 90,948,834 E105* probably null Het
Mtus1 C T 8: 41,082,775 V635M probably damaging Het
Ndufaf5 T C 2: 140,188,860 V222A probably benign Het
Nkpd1 A T 7: 19,519,820 Y37F probably benign Het
Nsun7 T A 5: 66,261,219 Y97* probably null Het
Nxph3 T C 11: 95,514,164 Y17C probably benign Het
Olfr1110 A C 2: 87,136,246 V25G possibly damaging Het
Olfr167 T C 16: 19,515,246 H130R probably benign Het
Olfr586 A G 7: 103,121,908 M292T probably benign Het
Olfr728 A G 14: 50,140,619 S7P probably damaging Het
Olfr832 A T 9: 18,944,881 I78F probably damaging Het
P2rx2 A G 5: 110,342,879 F26S probably damaging Het
Pank1 A T 19: 34,827,363 L131Q probably damaging Het
Pcx T C 19: 4,617,998 I516T possibly damaging Het
Pkhd1l1 T C 15: 44,512,792 I950T possibly damaging Het
Ppwd1 A G 13: 104,217,245 L335P probably damaging Het
Ptch1 A G 13: 63,513,671 S1218P probably damaging Het
Ptpn4 C T 1: 119,682,785 R664Q probably damaging Het
Sfxn1 A G 13: 54,085,517 T20A possibly damaging Het
Sgsm3 A G 15: 81,003,868 E53G probably damaging Het
Slc22a19 C T 19: 7,683,850 V320M possibly damaging Het
Slc25a33 A T 4: 149,753,849 I122N probably benign Het
Spata31d1a T A 13: 59,703,715 I200L probably benign Het
Spin2g A T X: 34,237,275 I171N possibly damaging Het
Srsf6 G A 2: 162,931,699 S10N probably damaging Het
Ttc12 A G 9: 49,441,835 probably null Het
Vmn2r100 A G 17: 19,522,372 K336R probably benign Het
Vmn2r108 A T 17: 20,481,033 Y68* probably null Het
Zfp738 A G 13: 67,670,312 F520S probably damaging Het
Other mutations in Gm11555
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0486:Gm11555 UTSW 11 99650160 missense unknown
R0531:Gm11555 UTSW 11 99650018 splice site probably benign
R3870:Gm11555 UTSW 11 99649990 nonsense probably null
Predicted Primers PCR Primer
(F):5'- GGCTTCTCATCAGACTCATAAAGCTG -3'
(R):5'- TCTGTGTGCTGCCAGTCAAG -3'

Sequencing Primer
(F):5'- GACTCATAAAGCTGAATTATGCAGC -3'
(R):5'- TGCCAGTCAAGCTGCTG -3'
Posted On2014-10-15