Incidental Mutation 'IGL02934:Themis2'
ID 364247
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Themis2
Ensembl Gene ENSMUSG00000037731
Gene Name thymocyte selection associated family member 2
Synonyms ICB-1, BC013712
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02934
Quality Score
Status
Chromosome 4
Chromosomal Location 132781843-132796387 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to A at 132789551 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 213 (M213L)
Ref Sequence ENSEMBL: ENSMUSP00000036945 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045154]
AlphaFold Q91YX0
Predicted Effect probably damaging
Transcript: ENSMUST00000045154
AA Change: M213L

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000036945
Gene: ENSMUSG00000037731
AA Change: M213L

DomainStartEndE-ValueType
Pfam:CABIT 18 242 1.1e-23 PFAM
Pfam:CABIT 267 524 5.3e-50 PFAM
low complexity region 648 659 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele exhibit normal B cell development, activation, and antibody responses. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 A T 3: 122,162,359 R716* probably null Het
Abca8a A T 11: 110,040,588 N1246K probably damaging Het
Acadl A G 1: 66,836,975 Y396H probably benign Het
Apol7c A T 15: 77,526,118 S209R possibly damaging Het
Atp1a1 A T 3: 101,576,992 C990* probably null Het
Cachd1 C T 4: 100,968,098 S583L probably damaging Het
Cbfa2t3 T C 8: 122,647,758 T48A probably benign Het
Ccdc138 G T 10: 58,573,580 probably benign Het
Cenpe A G 3: 135,264,351 E2231G probably damaging Het
Cog3 T C 14: 75,741,689 I206V probably damaging Het
Cr2 A G 1: 195,154,325 probably benign Het
Ctdspl2 T C 2: 121,979,009 V147A probably damaging Het
Cyp4f13 A G 17: 32,929,871 V300A probably damaging Het
Dkk3 A T 7: 112,150,747 M72K probably damaging Het
Dock3 A T 9: 107,023,745 F340L probably benign Het
Fut1 A G 7: 45,618,703 H27R possibly damaging Het
Igkv4-80 A G 6: 69,016,856 V17A probably benign Het
Igkv9-123 G A 6: 67,954,396 P62L possibly damaging Het
Kmt2e T C 5: 23,497,884 S1021P probably damaging Het
Krt13 A C 11: 100,119,084 L320R probably damaging Het
Ldhal6b T C 17: 5,417,544 T372A probably benign Het
Manba T C 3: 135,544,749 V379A probably benign Het
Map1b C T 13: 99,435,131 V361I probably benign Het
Map4k1 A G 7: 28,994,106 S399G probably benign Het
Mff G A 1: 82,747,094 R229H probably damaging Het
Naga T C 15: 82,330,200 N370S possibly damaging Het
Ncor2 A T 5: 125,025,557 M2045K probably benign Het
Nipal1 T C 5: 72,647,907 L7P probably damaging Het
Olfr9 T A 10: 128,990,089 M59K probably damaging Het
Pcmt1 A T 10: 7,640,727 M187K probably benign Het
Perp A T 10: 18,855,772 T160S probably damaging Het
Rapgef6 G A 11: 54,625,864 D169N probably damaging Het
Sel1l G A 12: 91,809,936 Q711* probably null Het
Sept5 T C 16: 18,629,831 Y7C probably damaging Het
Spdya A T 17: 71,556,400 N48I probably benign Het
Stard6 T A 18: 70,496,104 probably benign Het
Sytl2 T C 7: 90,375,992 V396A probably benign Het
Tcaf3 T G 6: 42,593,898 M307L probably benign Het
Tdrd6 T C 17: 43,627,887 N757D probably benign Het
Tgm1 T A 14: 55,709,989 D305V probably damaging Het
Tmem184c A G 8: 77,597,820 V347A probably damaging Het
Tmem214 A G 5: 30,871,544 E159G probably benign Het
Trim58 C T 11: 58,640,466 probably benign Het
Tshz1 A T 18: 84,013,090 S1064R probably damaging Het
Ubr2 C T 17: 46,957,340 E983K possibly damaging Het
Vmn1r23 A T 6: 57,925,929 I288N probably benign Het
Vmn2r97 T C 17: 18,929,685 V445A probably benign Het
Whrn G A 4: 63,416,105 T813M probably damaging Het
Xirp2 C T 2: 67,515,676 H2754Y probably benign Het
Other mutations in Themis2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02009:Themis2 APN 4 132785442 missense probably damaging 1.00
IGL02192:Themis2 APN 4 132783347 critical splice donor site probably null
IGL02743:Themis2 APN 4 132783484 missense probably benign 0.37
R0111:Themis2 UTSW 4 132789925 missense probably benign 0.17
R0598:Themis2 UTSW 4 132789683 missense possibly damaging 0.93
R1445:Themis2 UTSW 4 132782901 missense possibly damaging 0.53
R1484:Themis2 UTSW 4 132792485 missense possibly damaging 0.94
R1719:Themis2 UTSW 4 132789649 missense possibly damaging 0.95
R2076:Themis2 UTSW 4 132785802 missense probably damaging 1.00
R3522:Themis2 UTSW 4 132785595 missense probably damaging 1.00
R4620:Themis2 UTSW 4 132786022 missense probably damaging 1.00
R4653:Themis2 UTSW 4 132782976 missense probably benign 0.40
R4891:Themis2 UTSW 4 132783357 missense probably benign 0.14
R5331:Themis2 UTSW 4 132782933 missense possibly damaging 0.85
R5660:Themis2 UTSW 4 132796256 splice site probably null
R6014:Themis2 UTSW 4 132785980 missense probably benign 0.01
R6747:Themis2 UTSW 4 132796262 missense possibly damaging 0.80
R6863:Themis2 UTSW 4 132789596 missense probably damaging 1.00
R7380:Themis2 UTSW 4 132786217 missense possibly damaging 0.93
R7890:Themis2 UTSW 4 132789643 missense probably damaging 1.00
R7998:Themis2 UTSW 4 132792564 missense probably damaging 0.99
R8847:Themis2 UTSW 4 132786198 missense probably damaging 1.00
R9503:Themis2 UTSW 4 132783346 critical splice donor site probably null
R9642:Themis2 UTSW 4 132785736 missense possibly damaging 0.96
Posted On 2015-12-18