Incidental Mutation 'R7340:Asb15'
ID 569762
Institutional Source Beutler Lab
Gene Symbol Asb15
Ensembl Gene ENSMUSG00000029685
Gene Name ankyrin repeat and SOCS box-containing 15
Synonyms 4930400E23Rik
MMRRC Submission 045430-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7340 (G1)
Quality Score 225.009
Status Validated
Chromosome 6
Chromosomal Location 24528143-24573163 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 24558513 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glutamic Acid at position 38 (V38E)
Ref Sequence ENSEMBL: ENSMUSP00000031696 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000031696] [ENSMUST00000117688]
AlphaFold Q8VHS6
Predicted Effect probably benign
Transcript: ENSMUST00000031696
AA Change: V38E

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000031696
Gene: ENSMUSG00000029685
AA Change: V38E

DomainStartEndE-ValueType
ANK 110 139 1.59e-3 SMART
ANK 143 172 2.97e-3 SMART
ANK 176 205 1.93e-2 SMART
ANK 209 238 2.1e-3 SMART
ANK 242 273 5.01e-1 SMART
ANK 275 304 2.63e2 SMART
ANK 307 336 1.99e-4 SMART
ANK 349 378 5.24e-4 SMART
ANK 379 408 1.27e-2 SMART
ANK 417 444 2.35e3 SMART
SOCS_box 534 576 2.34e-11 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000117688
AA Change: V38E

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000112965
Gene: ENSMUSG00000029685
AA Change: V38E

DomainStartEndE-ValueType
ANK 110 139 1.59e-3 SMART
ANK 143 172 2.97e-3 SMART
ANK 176 205 1.93e-2 SMART
ANK 209 238 2.1e-3 SMART
ANK 242 273 5.01e-1 SMART
ANK 275 304 2.63e2 SMART
ANK 307 336 1.99e-4 SMART
ANK 349 378 5.24e-4 SMART
ANK 379 408 1.27e-2 SMART
ANK 417 444 2.35e3 SMART
SOCS_box 534 576 2.34e-11 SMART
Meta Mutation Damage Score 0.2543 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (83/84)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the suppressor of cytokine signaling box superfamily. The proteins in this superfamily participate in the ubiquitin-proteasome system for the degradation of proteins in the cell cycle and signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
Allele List at MGI
Other mutations in this stock
Total: 83 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb11 C T 2: 69,130,211 (GRCm39) D282N probably damaging Het
Adam30 A T 3: 98,069,637 (GRCm39) N490I probably benign Het
Ankrd55 A T 13: 112,492,497 (GRCm39) I223F probably damaging Het
Ano8 T A 8: 71,935,655 (GRCm39) E321V probably damaging Het
Apc2 A G 10: 80,149,316 (GRCm39) K1457E probably benign Het
Atp4a T C 7: 30,416,155 (GRCm39) S417P possibly damaging Het
AY358078 A G 14: 52,063,716 (GRCm39) N454S probably damaging Het
Cables2 A G 2: 179,903,450 (GRCm39) Y245H Het
Cactin CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG 10: 81,157,152 (GRCm39) probably benign Het
Camsap3 G A 8: 3,637,960 (GRCm39) probably null Het
Ccdc178 A T 18: 22,150,518 (GRCm39) V705E probably benign Het
Ccdc47 T C 11: 106,091,799 (GRCm39) Q472R possibly damaging Het
Ccdc62 A G 5: 124,089,283 (GRCm39) D307G probably damaging Het
Cdcp3 A G 7: 130,879,344 (GRCm39) T1788A unknown Het
Cdh23 A G 10: 60,366,775 (GRCm39) I235T probably benign Het
Cep89 G A 7: 35,129,353 (GRCm39) R630H probably damaging Het
Cfap65 T C 1: 74,960,742 (GRCm39) N743D probably benign Het
Cimap1b T A 15: 89,262,610 (GRCm39) T116S probably benign Het
Clec16a A G 16: 10,398,827 (GRCm39) N329S probably null Het
Col25a1 A G 3: 130,340,006 (GRCm39) probably null Het
Daam1 T G 12: 72,035,713 (GRCm39) D969E probably benign Het
Dntt A C 19: 41,047,004 (GRCm39) probably null Het
Dsel C T 1: 111,789,303 (GRCm39) G411S probably damaging Het
Dst T A 1: 34,229,810 (GRCm39) Y2468N probably benign Het
Exosc9 A G 3: 36,615,297 (GRCm39) T262A possibly damaging Het
Exph5 G A 9: 53,288,309 (GRCm39) A1797T probably damaging Het
Fbp2 A T 13: 62,985,061 (GRCm39) Y287N probably damaging Het
Fmn2 CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC 1: 174,436,769 (GRCm39) probably benign Het
Fus T A 7: 127,581,123 (GRCm39) probably null Het
Galnt9 T A 5: 110,762,054 (GRCm39) N397K probably damaging Het
Gdi1 G A X: 73,350,461 (GRCm39) R55H probably benign Het
Gga1 A G 15: 78,775,651 (GRCm39) T369A probably benign Het
Gp1ba T C 11: 70,531,119 (GRCm39) I295T unknown Het
Hk2 T C 6: 82,705,873 (GRCm39) E810G probably benign Het
Igsf10 A G 3: 59,233,189 (GRCm39) V1848A probably damaging Het
Insrr G A 3: 87,721,623 (GRCm39) probably null Het
Ip6k3 T A 17: 27,367,504 (GRCm39) M231L probably benign Het
Itgb8 T C 12: 119,155,939 (GRCm39) N171S probably benign Het
Ldlrad3 T C 2: 101,897,184 (GRCm39) probably null Het
Ltbp1 T A 17: 75,634,223 (GRCm39) C886* probably null Het
Mettl13 T C 1: 162,366,547 (GRCm39) D444G probably benign Het
Mns1 A G 9: 72,356,025 (GRCm39) Y224C probably damaging Het
Mri1 C T 8: 84,983,525 (GRCm39) R122Q probably benign Het
Ms4a6d G A 19: 11,567,437 (GRCm39) Q155* probably null Het
Myo5c A C 9: 75,196,423 (GRCm39) K1290Q probably benign Het
Nlrp12 T G 7: 3,281,755 (GRCm39) Q842H possibly damaging Het
Oga G A 19: 45,755,895 (GRCm39) Q583* probably null Het
Or14c44 T C 7: 86,061,957 (GRCm39) L129P possibly damaging Het
Or14j8 T A 17: 38,263,413 (GRCm39) R167S probably benign Het
Or2t1 A T 14: 14,328,401 (GRCm38) T97S possibly damaging Het
Or5d39 T C 2: 87,979,620 (GRCm39) T248A possibly damaging Het
Otoa A G 7: 120,729,288 (GRCm39) T554A probably benign Het
Per1 A G 11: 68,994,008 (GRCm39) D438G probably damaging Het
Phactr3 G A 2: 177,975,854 (GRCm39) R533H probably damaging Het
Phykpl T C 11: 51,490,370 (GRCm39) F417S probably damaging Het
Pole A T 5: 110,482,330 (GRCm39) T2057S probably benign Het
Polq A G 16: 36,881,288 (GRCm39) T1151A probably benign Het
Polr1g T C 7: 19,093,073 (GRCm39) T36A probably benign Het
Rbm26 A T 14: 105,389,976 (GRCm39) V216E possibly damaging Het
Ryk T C 9: 102,775,737 (GRCm39) I449T probably damaging Het
Sap25 A G 5: 137,640,935 (GRCm39) T225A probably benign Het
Sart3 A G 5: 113,882,728 (GRCm39) M864T probably benign Het
Sec31b T C 19: 44,517,161 (GRCm39) S280G probably benign Het
Sema4d A T 13: 51,877,598 (GRCm39) I78N probably damaging Het
Sgip1 G C 4: 102,778,661 (GRCm39) R419S unknown Het
Slc13a3 T C 2: 165,272,210 (GRCm39) I278V probably benign Het
Slc2a5 A G 4: 150,224,439 (GRCm39) D312G probably benign Het
Slc39a2 A T 14: 52,131,660 (GRCm39) Q77L possibly damaging Het
Srbd1 A T 17: 86,443,782 (GRCm39) V148E probably benign Het
Syngr2 A G 11: 117,703,322 (GRCm39) E46G probably damaging Het
Taok1 A G 11: 77,470,643 (GRCm39) V54A possibly damaging Het
Tas2r106 T A 6: 131,655,185 (GRCm39) H222L probably damaging Het
Tcaf3 A G 6: 42,566,848 (GRCm39) I747T probably benign Het
Tmem151b G T 17: 45,856,195 (GRCm39) P415Q probably benign Het
Tmf1 T C 6: 97,145,061 (GRCm39) D659G possibly damaging Het
Tnn G T 1: 159,973,592 (GRCm39) D258E probably damaging Het
Traj33 A G 14: 54,422,862 (GRCm39) I16V unknown Het
Ttll13 G T 7: 79,906,772 (GRCm39) C480F probably damaging Het
Ttn T C 2: 76,714,415 (GRCm39) N8137S unknown Het
Vmn1r85 T C 7: 12,819,073 (GRCm39) N24D probably damaging Het
Wdr81 T C 11: 75,335,525 (GRCm39) Q649R probably null Het
Zan T C 5: 137,382,092 (GRCm39) T5152A unknown Het
Zc3h6 A G 2: 128,835,110 (GRCm39) D82G possibly damaging Het
Other mutations in Asb15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00418:Asb15 APN 6 24,558,642 (GRCm39) splice site probably benign
IGL00557:Asb15 APN 6 24,558,649 (GRCm39) missense probably benign
IGL00694:Asb15 APN 6 24,570,663 (GRCm39) missense possibly damaging 0.79
IGL01137:Asb15 APN 6 24,556,521 (GRCm39) missense probably benign
IGL01681:Asb15 APN 6 24,567,137 (GRCm39) missense probably damaging 0.98
IGL01691:Asb15 APN 6 24,567,271 (GRCm39) missense probably benign 0.02
IGL01791:Asb15 APN 6 24,567,211 (GRCm39) missense probably damaging 1.00
IGL01989:Asb15 APN 6 24,565,943 (GRCm39) missense probably damaging 1.00
IGL02480:Asb15 APN 6 24,570,745 (GRCm39) missense probably damaging 0.99
IGL02541:Asb15 APN 6 24,566,265 (GRCm39) missense probably damaging 1.00
IGL02707:Asb15 APN 6 24,558,787 (GRCm39) splice site probably benign
IGL03090:Asb15 APN 6 24,567,185 (GRCm39) missense possibly damaging 0.52
IGL03331:Asb15 APN 6 24,556,523 (GRCm39) missense possibly damaging 0.70
3-1:Asb15 UTSW 6 24,566,220 (GRCm39) missense probably benign 0.00
BB002:Asb15 UTSW 6 24,562,723 (GRCm39) missense probably benign 0.00
BB012:Asb15 UTSW 6 24,562,723 (GRCm39) missense probably benign 0.00
R0196:Asb15 UTSW 6 24,564,392 (GRCm39) missense probably damaging 0.99
R0603:Asb15 UTSW 6 24,556,556 (GRCm39) missense probably damaging 1.00
R0650:Asb15 UTSW 6 24,566,163 (GRCm39) missense probably damaging 1.00
R1114:Asb15 UTSW 6 24,567,176 (GRCm39) missense probably damaging 1.00
R1170:Asb15 UTSW 6 24,562,486 (GRCm39) splice site probably benign
R1365:Asb15 UTSW 6 24,567,269 (GRCm39) missense possibly damaging 0.95
R2323:Asb15 UTSW 6 24,556,600 (GRCm39) missense probably benign 0.01
R3147:Asb15 UTSW 6 24,566,258 (GRCm39) missense probably damaging 1.00
R3148:Asb15 UTSW 6 24,566,258 (GRCm39) missense probably damaging 1.00
R4762:Asb15 UTSW 6 24,567,236 (GRCm39) missense possibly damaging 0.81
R4771:Asb15 UTSW 6 24,570,621 (GRCm39) missense probably damaging 0.99
R4915:Asb15 UTSW 6 24,566,292 (GRCm39) missense probably damaging 0.96
R5369:Asb15 UTSW 6 24,562,563 (GRCm39) missense probably benign 0.00
R5415:Asb15 UTSW 6 24,570,690 (GRCm39) missense probably benign 0.05
R5781:Asb15 UTSW 6 24,564,377 (GRCm39) missense probably benign 0.11
R6649:Asb15 UTSW 6 24,562,632 (GRCm39) missense probably benign
R6653:Asb15 UTSW 6 24,562,632 (GRCm39) missense probably benign
R6781:Asb15 UTSW 6 24,558,674 (GRCm39) missense probably benign
R6984:Asb15 UTSW 6 24,566,336 (GRCm39) missense probably benign 0.17
R7297:Asb15 UTSW 6 24,566,462 (GRCm39) missense probably damaging 0.96
R7419:Asb15 UTSW 6 24,556,555 (GRCm39) missense probably benign 0.08
R7549:Asb15 UTSW 6 24,559,029 (GRCm39) splice site probably null
R7662:Asb15 UTSW 6 24,566,089 (GRCm39) missense probably benign 0.08
R7717:Asb15 UTSW 6 24,559,251 (GRCm39) missense probably benign
R7767:Asb15 UTSW 6 24,559,281 (GRCm39) missense probably benign
R7781:Asb15 UTSW 6 24,562,644 (GRCm39) missense probably benign 0.01
R7797:Asb15 UTSW 6 24,562,505 (GRCm39) missense probably damaging 0.98
R7847:Asb15 UTSW 6 24,564,266 (GRCm39) missense probably damaging 1.00
R7925:Asb15 UTSW 6 24,562,723 (GRCm39) missense probably benign 0.00
R8055:Asb15 UTSW 6 24,556,565 (GRCm39) missense probably benign 0.05
R8304:Asb15 UTSW 6 24,559,296 (GRCm39) missense possibly damaging 0.89
R8694:Asb15 UTSW 6 24,570,666 (GRCm39) missense probably benign 0.00
R9268:Asb15 UTSW 6 24,566,298 (GRCm39) missense probably benign
Z1176:Asb15 UTSW 6 24,566,330 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTAGTGTACTCTGTGCCTGG -3'
(R):5'- CAGCTTCATGCAATGGGAAC -3'

Sequencing Primer
(F):5'- CCTGGCTTTGGAGAAATTTTCAAG -3'
(R):5'- TCTTCCAGTGCATATTTATATTGCAC -3'
Posted On 2019-09-13