Incidental Mutation 'IGL01558:Stk33'
ID 90786
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Stk33
Ensembl Gene ENSMUSG00000031027
Gene Name serine/threonine kinase 33
Synonyms 4921505G21Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # IGL01558
Quality Score
Status
Chromosome 7
Chromosomal Location 108878430-109038288 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 108940491 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147147 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090414] [ENSMUST00000106745] [ENSMUST00000121378] [ENSMUST00000121748] [ENSMUST00000141210]
AlphaFold Q924X7
Predicted Effect probably benign
Transcript: ENSMUST00000090414
SMART Domains Protein: ENSMUSP00000087897
Gene: ENSMUSG00000031027

DomainStartEndE-ValueType
S_TKc 111 377 4.7e-102 SMART
low complexity region 399 414 N/A INTRINSIC
low complexity region 445 467 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000106745
SMART Domains Protein: ENSMUSP00000102356
Gene: ENSMUSG00000031027

DomainStartEndE-ValueType
S_TKc 111 377 4.7e-102 SMART
low complexity region 399 414 N/A INTRINSIC
low complexity region 445 467 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000121378
SMART Domains Protein: ENSMUSP00000112560
Gene: ENSMUSG00000031027

DomainStartEndE-ValueType
S_TKc 2 254 1.01e-83 SMART
low complexity region 276 291 N/A INTRINSIC
low complexity region 322 344 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000121748
SMART Domains Protein: ENSMUSP00000112515
Gene: ENSMUSG00000031027

DomainStartEndE-ValueType
S_TKc 111 377 4.8e-102 SMART
low complexity region 399 414 N/A INTRINSIC
low complexity region 445 467 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000141210
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aasdh T C 5: 77,036,464 (GRCm39) E359G possibly damaging Het
Agtr1b T C 3: 20,370,424 (GRCm39) T61A probably damaging Het
Casd1 T A 6: 4,624,143 (GRCm39) I312N possibly damaging Het
Cebpz A T 17: 79,242,734 (GRCm39) F307I probably damaging Het
Dhx33 T C 11: 70,890,579 (GRCm39) R207G probably benign Het
G0s2 T C 1: 192,955,003 (GRCm39) Y27C probably damaging Het
Glg1 A T 8: 111,914,362 (GRCm39) M474K probably benign Het
Macf1 T C 4: 123,346,798 (GRCm39) N2490S probably benign Het
Mpdz C A 4: 81,213,767 (GRCm39) E1565* probably null Het
Mthfsl A G 9: 88,570,870 (GRCm39) I126T possibly damaging Het
Nectin4 A G 1: 171,212,257 (GRCm39) D285G probably benign Het
Neurod1 T C 2: 79,284,363 (GRCm39) H340R possibly damaging Het
Nop53 G A 7: 15,679,751 (GRCm39) probably benign Het
Siglec1 A G 2: 130,920,419 (GRCm39) L795P probably damaging Het
Sntg1 A T 1: 8,533,612 (GRCm39) probably benign Het
Stox1 C T 10: 62,503,651 (GRCm39) V135M probably damaging Het
Sult2a8 C A 7: 14,159,377 (GRCm39) E81* probably null Het
Tdrd6 A G 17: 43,936,659 (GRCm39) V1463A probably damaging Het
Tdrd6 C T 17: 43,935,657 (GRCm39) G1797D probably benign Het
Trmt2b C A X: 133,139,305 (GRCm39) R389I possibly damaging Het
Ttc28 G T 5: 111,431,828 (GRCm39) V1903L probably damaging Het
Other mutations in Stk33
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01137:Stk33 APN 7 108,928,775 (GRCm39) missense probably benign 0.02
IGL01467:Stk33 APN 7 108,928,796 (GRCm39) missense probably damaging 0.99
IGL01775:Stk33 APN 7 108,911,574 (GRCm39) missense possibly damaging 0.92
R0052:Stk33 UTSW 7 108,878,876 (GRCm39) missense possibly damaging 0.46
R0336:Stk33 UTSW 7 108,930,681 (GRCm39) missense probably benign 0.01
R0394:Stk33 UTSW 7 108,940,696 (GRCm39) missense probably benign
R0579:Stk33 UTSW 7 108,924,904 (GRCm39) missense probably damaging 0.99
R0727:Stk33 UTSW 7 108,920,725 (GRCm39) missense probably damaging 0.96
R1363:Stk33 UTSW 7 108,879,028 (GRCm39) missense probably benign 0.06
R1574:Stk33 UTSW 7 108,879,027 (GRCm39) missense probably benign 0.01
R1574:Stk33 UTSW 7 108,879,027 (GRCm39) missense probably benign 0.01
R2153:Stk33 UTSW 7 108,940,527 (GRCm39) missense probably benign 0.01
R4366:Stk33 UTSW 7 108,879,002 (GRCm39) missense probably benign 0.06
R4896:Stk33 UTSW 7 108,926,802 (GRCm39) missense probably damaging 1.00
R4994:Stk33 UTSW 7 108,939,605 (GRCm39) missense probably benign 0.08
R5283:Stk33 UTSW 7 108,935,334 (GRCm39) missense possibly damaging 0.69
R6339:Stk33 UTSW 7 108,920,672 (GRCm39) missense probably benign 0.03
R6547:Stk33 UTSW 7 108,920,042 (GRCm39) missense possibly damaging 0.73
R6717:Stk33 UTSW 7 108,926,823 (GRCm39) missense possibly damaging 0.51
R6894:Stk33 UTSW 7 108,935,269 (GRCm39) missense possibly damaging 0.70
R8975:Stk33 UTSW 7 108,935,280 (GRCm39) missense probably damaging 1.00
R9168:Stk33 UTSW 7 108,928,747 (GRCm39) missense probably damaging 0.99
R9175:Stk33 UTSW 7 108,920,724 (GRCm39) missense probably damaging 1.00
R9204:Stk33 UTSW 7 108,940,686 (GRCm39) missense probably benign 0.00
R9416:Stk33 UTSW 7 108,940,689 (GRCm39) missense probably benign 0.39
Z1176:Stk33 UTSW 7 108,935,266 (GRCm39) missense possibly damaging 0.51
Posted On 2013-12-09