Incidental Mutation 'IGL01088:Stk-ps2'
ID 50228
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stk-ps2
Ensembl Gene ENSMUSG00000044457
Gene Name serine/threonine kinase 2
Synonyms Gm4776
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL01088
Quality Score
Status
Chromosome 1
Chromosomal Location 46059575-46069597 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 46069010 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000051224
SMART Domains Protein: ENSMUSP00000054781
Gene: ENSMUSG00000044457

DomainStartEndE-ValueType
S_TKc 14 262 5.9e-85 SMART
UBA 276 313 8.44e-4 SMART
low complexity region 335 349 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000167676
SMART Domains Protein: ENSMUSP00000133145
Gene: ENSMUSG00000044457

DomainStartEndE-ValueType
S_TKc 14 262 5.9e-85 SMART
UBA 276 313 8.44e-4 SMART
low complexity region 335 349 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000171707
SMART Domains Protein: ENSMUSP00000125766
Gene: ENSMUSG00000044457

DomainStartEndE-ValueType
S_TKc 14 262 5.9e-85 SMART
UBA 276 313 8.44e-4 SMART
low complexity region 335 349 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187808
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr6 C T 10: 89,561,703 (GRCm39) V148I probably damaging Het
Aspn G T 13: 49,720,029 (GRCm39) K348N probably benign Het
C1qtnf9 T C 14: 61,017,205 (GRCm39) V245A probably benign Het
Cfhr4 T C 1: 139,625,823 (GRCm39) probably benign Het
Chd4 T C 6: 125,099,431 (GRCm39) probably benign Het
Clcn3 A T 8: 61,390,381 (GRCm39) C187S probably damaging Het
Dcxr T C 11: 120,616,993 (GRCm39) I123M possibly damaging Het
Fstl1 T C 16: 37,647,175 (GRCm39) Y182H probably damaging Het
Ghrhr T C 6: 55,356,178 (GRCm39) probably null Het
Gpr179 T C 11: 97,228,627 (GRCm39) E1176G probably damaging Het
H2-T22 A G 17: 36,352,811 (GRCm39) S99P probably damaging Het
Igkv4-79 T A 6: 69,020,110 (GRCm39) K68N probably damaging Het
Kpna6 C T 4: 129,549,276 (GRCm39) V169I probably damaging Het
Krit1 G T 5: 3,862,844 (GRCm39) V278F probably damaging Het
Mrpl4 T C 9: 20,914,627 (GRCm39) S68P probably damaging Het
Mylk3 A C 8: 86,078,586 (GRCm39) probably null Het
Nfasc A T 1: 132,570,514 (GRCm39) probably benign Het
Ntsr1 T C 2: 180,184,335 (GRCm39) F346S probably damaging Het
Or10ak11 A G 4: 118,686,989 (GRCm39) V216A probably benign Het
Or5b107 T C 19: 13,142,735 (GRCm39) M119T probably damaging Het
Phox2a T C 7: 101,470,942 (GRCm39) F145L probably damaging Het
Rbm7 A G 9: 48,402,149 (GRCm39) V146A probably damaging Het
Sall3 A T 18: 81,016,447 (GRCm39) Y494N probably damaging Het
Ssbp1 T A 6: 40,455,004 (GRCm39) probably benign Het
Stard7 T C 2: 127,112,746 (GRCm39) L4P probably damaging Het
Tmem67 G A 4: 12,063,126 (GRCm39) R507C probably damaging Het
Unc13c A T 9: 73,839,563 (GRCm39) D429E possibly damaging Het
Unc93b1 A G 19: 3,985,356 (GRCm39) probably null Het
Vmn1r171 T C 7: 23,332,252 (GRCm39) V159A probably damaging Het
Zfp608 T C 18: 55,031,159 (GRCm39) E927G probably benign Het
Zfp820 T A 17: 22,040,162 (GRCm39) K16* probably null Het
Zgrf1 T C 3: 127,381,790 (GRCm39) probably benign Het
Other mutations in Stk-ps2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01662:Stk-ps2 APN 1 46,068,522 (GRCm39) unclassified noncoding transcript
IGL01859:Stk-ps2 APN 1 46,069,202 (GRCm39) exon noncoding transcript
IGL01949:Stk-ps2 APN 1 46,069,148 (GRCm39) exon noncoding transcript
IGL02338:Stk-ps2 APN 1 46,069,337 (GRCm39) exon noncoding transcript
R0087:Stk-ps2 UTSW 1 46,069,049 (GRCm39) exon noncoding transcript
R0139:Stk-ps2 UTSW 1 46,068,955 (GRCm39) exon noncoding transcript
R0627:Stk-ps2 UTSW 1 46,068,851 (GRCm39) exon noncoding transcript
R3086:Stk-ps2 UTSW 1 46,068,236 (GRCm39) unclassified noncoding transcript
R3763:Stk-ps2 UTSW 1 46,069,081 (GRCm39) exon noncoding transcript
R4817:Stk-ps2 UTSW 1 46,068,125 (GRCm39) unclassified noncoding transcript
R4951:Stk-ps2 UTSW 1 46,068,602 (GRCm39) unclassified noncoding transcript
Posted On 2013-06-21