Incidental Mutation 'IGL01871:Stmnd1'
ID 178726
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stmnd1
Ensembl Gene ENSMUSG00000063529
Gene Name stathmin domain containing 1
Synonyms Gm1574, LOC380842
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # IGL01871
Quality Score
Status
Chromosome 13
Chromosomal Location 46427197-46453591 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 46443189 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 107 (E107G)
Ref Sequence ENSEMBL: ENSMUSP00000075923 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076622]
AlphaFold Q6P3A1
Predicted Effect probably damaging
Transcript: ENSMUST00000076622
AA Change: E107G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000075923
Gene: ENSMUSG00000063529
AA Change: E107G

DomainStartEndE-ValueType
Pfam:Stathmin 128 199 4.5e-9 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrv1 A T 13: 81,620,513 (GRCm39) probably null Het
Aqp7 G A 4: 41,045,321 (GRCm39) R20* probably null Het
Asxl2 G T 12: 3,552,112 (GRCm39) V1285L probably benign Het
Bdp1 A T 13: 100,202,561 (GRCm39) S688T probably benign Het
Cc2d2a A T 5: 43,846,311 (GRCm39) I357F probably damaging Het
Clasp1 A T 1: 118,498,619 (GRCm39) I884F probably damaging Het
Cpne4 T G 9: 104,802,956 (GRCm39) M200R possibly damaging Het
Cyp2d10 T A 15: 82,288,086 (GRCm39) D180V probably damaging Het
Dicer1 A T 12: 104,670,439 (GRCm39) V1042D probably damaging Het
Dlc1 G A 8: 37,317,334 (GRCm39) T447I probably damaging Het
Efl1 T C 7: 82,412,527 (GRCm39) M972T possibly damaging Het
Erbin A G 13: 103,971,274 (GRCm39) S781P probably damaging Het
Galnt4 G A 10: 98,945,103 (GRCm39) G276D probably damaging Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gmppa A G 1: 75,413,661 (GRCm39) I41V probably damaging Het
Golga1 C T 2: 38,940,210 (GRCm39) probably benign Het
H2-Ob G T 17: 34,461,519 (GRCm39) W86L probably damaging Het
Hnrnpr G A 4: 136,066,885 (GRCm39) R482H unknown Het
L2hgdh T C 12: 69,768,869 (GRCm39) E81G probably damaging Het
Mre11a T C 9: 14,723,193 (GRCm39) V389A possibly damaging Het
Mxra8 A G 4: 155,927,258 (GRCm39) T372A probably benign Het
Ncapg T A 5: 45,845,923 (GRCm39) S593R probably benign Het
Ndufaf1 C T 2: 119,488,768 (GRCm39) W250* probably null Het
Neb T C 2: 52,043,081 (GRCm39) E6783G probably damaging Het
Nmt2 T C 2: 3,313,711 (GRCm39) Y175H probably damaging Het
Olfml2b T C 1: 170,489,924 (GRCm39) probably benign Het
Pitpnm3 T A 11: 71,946,964 (GRCm39) M812L probably damaging Het
Pou2f3 A G 9: 43,045,768 (GRCm39) probably benign Het
Prkdc A G 16: 15,600,951 (GRCm39) T2871A probably benign Het
Rapgef4 A G 2: 72,028,704 (GRCm39) T392A possibly damaging Het
Rhov G T 2: 119,101,219 (GRCm39) Q71K probably benign Het
Slc22a15 T C 3: 101,768,110 (GRCm39) probably benign Het
Spaca1 T A 4: 34,040,894 (GRCm39) N22Y probably damaging Het
Tent5b A G 4: 133,213,620 (GRCm39) I164V possibly damaging Het
Timm22 T C 11: 76,298,263 (GRCm39) V78A probably damaging Het
Usp47 T C 7: 111,676,993 (GRCm39) probably benign Het
Utp4 A C 8: 107,638,949 (GRCm39) K419T probably benign Het
Zfp410 T C 12: 84,372,565 (GRCm39) probably null Het
Other mutations in Stmnd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01413:Stmnd1 APN 13 46,453,157 (GRCm39) missense probably benign 0.39
IGL02369:Stmnd1 APN 13 46,439,029 (GRCm39) missense probably benign 0.25
R0117:Stmnd1 UTSW 13 46,438,962 (GRCm39) missense possibly damaging 0.56
R1674:Stmnd1 UTSW 13 46,453,097 (GRCm39) missense possibly damaging 0.54
R5127:Stmnd1 UTSW 13 46,453,071 (GRCm39) missense probably benign 0.04
R5290:Stmnd1 UTSW 13 46,453,074 (GRCm39) missense probably benign 0.44
R6924:Stmnd1 UTSW 13 46,452,969 (GRCm39) missense probably benign
R6957:Stmnd1 UTSW 13 46,427,375 (GRCm39) missense probably benign 0.09
R7745:Stmnd1 UTSW 13 46,453,077 (GRCm39) missense possibly damaging 0.52
R8346:Stmnd1 UTSW 13 46,452,936 (GRCm39) missense probably benign 0.00
R9026:Stmnd1 UTSW 13 46,452,983 (GRCm39) missense probably benign
R9339:Stmnd1 UTSW 13 46,453,079 (GRCm39) missense probably benign 0.00
R9696:Stmnd1 UTSW 13 46,443,224 (GRCm39) missense probably damaging 1.00
Posted On 2014-05-07