Incidental Mutation 'IGL01949:Stk-ps2'
ID 181012
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: 0.083) question?
Stock # IGL01949
Quality Score
Status
Chromosome 1
Chromosomal Location 46059575-46069597 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 46069148 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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts20 C A 15: 94,223,987 (GRCm39) R1247L probably benign Het
Atp2a3 T A 11: 72,872,723 (GRCm39) M757K probably damaging Het
Dusp5 T C 19: 53,525,904 (GRCm39) I182T probably damaging Het
Fuca1 T A 4: 135,650,420 (GRCm39) probably benign Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm10718 A T 9: 3,025,118 (GRCm39) Y194F probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Hap1 G T 11: 100,239,588 (GRCm39) D610E probably damaging Het
Hoxa6 T A 6: 52,183,511 (GRCm39) Y178F possibly damaging Het
Ighmbp2 A C 19: 3,315,538 (GRCm39) D627E probably benign Het
Itgae T C 11: 73,009,010 (GRCm39) I497T probably benign Het
Katnip G A 7: 125,361,014 (GRCm39) W108* probably null Het
Kbtbd3 A G 9: 4,331,066 (GRCm39) D480G possibly damaging Het
Kmt2b A T 7: 30,276,586 (GRCm39) probably null Het
Krt5 T A 15: 101,619,048 (GRCm39) M278L probably benign Het
Krtap4-9 G A 11: 99,676,391 (GRCm39) probably benign Het
Myl12a T C 17: 71,303,709 (GRCm39) D56G probably benign Het
Or2g25 T C 17: 37,970,357 (GRCm39) Y289C probably damaging Het
Pdgfra C A 5: 75,331,326 (GRCm39) H310Q probably damaging Het
Pglyrp2 G T 17: 32,635,080 (GRCm39) probably null Het
Polk C T 13: 96,620,046 (GRCm39) S718N probably benign Het
Ppip5k1 T A 2: 121,168,341 (GRCm39) H687L probably benign Het
Pram1 A T 17: 33,860,309 (GRCm39) Q292L probably damaging Het
Prodh2 A G 7: 30,209,190 (GRCm39) probably null Het
Rgs9 A T 11: 109,150,660 (GRCm39) probably null Het
Sp140l2 A G 1: 85,231,907 (GRCm39) probably benign Het
Svep1 C T 4: 58,176,006 (GRCm39) G298R probably damaging Het
Troap T C 15: 98,979,102 (GRCm39) S341P probably benign Het
Ugt3a1 T C 15: 9,335,815 (GRCm39) F12S probably damaging Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Zfp236 G T 18: 82,642,521 (GRCm39) T1123K probably damaging Het
Other mutations in Stk-ps2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01088:Stk-ps2 APN 1 46,069,010 (GRCm39) exon noncoding transcript
IGL01662:Stk-ps2 APN 1 46,068,522 (GRCm39) unclassified noncoding transcript
IGL01859:Stk-ps2 APN 1 46,069,202 (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 2014-05-07