Incidental Mutation 'R3086:Stk-ps2'
ID 265617
Institutional Source Beutler Lab
Gene Symbol Stk-ps2
Ensembl Gene ENSMUSG00000044457
Gene Name serine/threonine kinase 2
Synonyms Gm4776
MMRRC Submission 040575-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R3086 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 46059575-46069597 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to C at 46068236 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
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.8%
Validation Efficiency 100% (42/42)
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310039H08Rik T C 17: 47,083,881 (GRCm39) L48P probably damaging Het
Adgra3 A T 5: 50,170,733 (GRCm39) probably null Het
Alms1 A G 6: 85,655,122 (GRCm39) R3223G probably benign Het
Bltp1 A G 3: 37,065,852 (GRCm39) D3483G possibly damaging Het
Cabyr T C 18: 12,884,023 (GRCm39) V170A probably damaging Het
Ces2b A T 8: 105,559,401 (GRCm39) D89V possibly damaging Het
Dhrs2 G T 14: 55,477,301 (GRCm39) V179L probably benign Het
Dlg5 T C 14: 24,216,258 (GRCm39) T595A probably damaging Het
Dock10 T C 1: 80,510,074 (GRCm39) N1585D possibly damaging Het
Dock4 T C 12: 40,781,862 (GRCm39) I689T probably benign Het
Fgfr4 G T 13: 55,315,205 (GRCm39) probably benign Het
Frk G A 10: 34,483,950 (GRCm39) G437D probably damaging Het
Frzb T G 2: 80,248,858 (GRCm39) I199L possibly damaging Het
Gsg1l C T 7: 125,490,852 (GRCm39) R284H probably benign Het
Helq A G 5: 100,921,858 (GRCm39) L782S probably benign Het
Kif20b T C 19: 34,907,115 (GRCm39) F128S probably damaging Het
Kifc2 T C 15: 76,551,452 (GRCm39) F725L probably benign Het
Lekr1 A G 3: 65,634,581 (GRCm39) noncoding transcript Het
Macf1 T A 4: 123,328,901 (GRCm39) M2490L probably benign Het
Megf8 T A 7: 25,048,444 (GRCm39) Y1706N probably damaging Het
N4bp2 A G 5: 65,948,396 (GRCm39) Y342C probably damaging Het
Nf1 T C 11: 79,437,812 (GRCm39) C2057R probably damaging Het
Or4f60 C A 2: 111,902,320 (GRCm39) G203* probably null Het
Or4k36 A G 2: 111,146,461 (GRCm39) I212M probably benign Het
Or6c88 G A 10: 129,407,276 (GRCm39) G251S probably damaging Het
Orc4 G A 2: 48,827,501 (GRCm39) P31S probably benign Het
Pcdha1 G C 18: 37,064,001 (GRCm39) E222Q possibly damaging Het
Prune2 A T 19: 17,098,777 (GRCm39) D1427V possibly damaging Het
Rnps1 C T 17: 24,631,393 (GRCm39) probably benign Het
Rsph4a G C 10: 33,785,198 (GRCm39) V370L probably damaging Het
Sema5b T A 16: 35,443,093 (GRCm39) S33T probably benign Het
Tep1 A T 14: 51,064,511 (GRCm39) probably null Het
Tet1 T C 10: 62,715,400 (GRCm39) K132E probably benign Het
Tiam2 A G 17: 3,471,857 (GRCm39) K500E probably damaging Het
Tmem131l G T 3: 83,839,046 (GRCm39) R635S probably benign Het
Tmem68 T C 4: 3,569,594 (GRCm39) E32G possibly damaging Het
Vmn2r101 T A 17: 19,809,077 (GRCm39) probably null Het
Zfp780b A G 7: 27,663,055 (GRCm39) I500T probably damaging Het
Zfyve26 G T 12: 79,312,457 (GRCm39) probably benign 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
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
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
Predicted Primers PCR Primer
(F):5'- GCAAGCCCTGATTCTCTTGC -3'
(R):5'- TCTATCATCTCAGCCAAGCCTG -3'

Sequencing Primer
(F):5'- GCTCATTCTCTTGAAGCGGCTG -3'
(R):5'- ATCTCAGCCAAGCCTGTGGATC -3'
Posted On 2015-02-05