Incidental Mutation 'R7288:Ash1l'
ID 566143
Institutional Source Beutler Lab
Gene Symbol Ash1l
Ensembl Gene ENSMUSG00000028053
Gene Name ASH1 like histone lysine methyltransferase
Synonyms E430018P19Rik, 8030453L17Rik, KMT2H, chromatin remodeling factor
MMRRC Submission 045395-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R7288 (G1)
Quality Score 225.009
Status Not validated
Chromosome 3
Chromosomal Location 88857929-88986682 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to A at 88873199 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140251 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090933] [ENSMUST00000186583]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000090933
SMART Domains Protein: ENSMUSP00000088451
Gene: ENSMUSG00000028053

DomainStartEndE-ValueType
low complexity region 36 46 N/A INTRINSIC
low complexity region 226 237 N/A INTRINSIC
internal_repeat_1 238 306 6.88e-12 PROSPERO
internal_repeat_1 306 406 6.88e-12 PROSPERO
low complexity region 552 571 N/A INTRINSIC
low complexity region 706 717 N/A INTRINSIC
low complexity region 745 753 N/A INTRINSIC
low complexity region 777 791 N/A INTRINSIC
AT_hook 823 835 3.06e2 SMART
low complexity region 859 873 N/A INTRINSIC
AT_hook 885 897 9.15e0 SMART
low complexity region 938 948 N/A INTRINSIC
low complexity region 1086 1105 N/A INTRINSIC
low complexity region 1107 1121 N/A INTRINSIC
low complexity region 1159 1173 N/A INTRINSIC
low complexity region 1262 1273 N/A INTRINSIC
low complexity region 1288 1301 N/A INTRINSIC
AT_hook 1345 1357 3.09e-1 SMART
low complexity region 1377 1388 N/A INTRINSIC
low complexity region 1395 1424 N/A INTRINSIC
low complexity region 1478 1491 N/A INTRINSIC
low complexity region 1678 1692 N/A INTRINSIC
AT_hook 1843 1855 1.03e1 SMART
low complexity region 1971 1983 N/A INTRINSIC
AWS 2081 2133 3.95e-26 SMART
SET 2135 2257 8.04e-45 SMART
PostSET 2259 2275 6.38e-2 SMART
low complexity region 2296 2316 N/A INTRINSIC
BROMO 2431 2541 8.29e-23 SMART
low complexity region 2549 2563 N/A INTRINSIC
PHD 2576 2618 8.25e-6 SMART
BAH 2650 2787 1.18e-23 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000186583
SMART Domains Protein: ENSMUSP00000140251
Gene: ENSMUSG00000028053

DomainStartEndE-ValueType
low complexity region 36 46 N/A INTRINSIC
low complexity region 226 237 N/A INTRINSIC
internal_repeat_1 238 306 6.88e-12 PROSPERO
internal_repeat_1 306 406 6.88e-12 PROSPERO
low complexity region 552 571 N/A INTRINSIC
low complexity region 706 717 N/A INTRINSIC
low complexity region 745 753 N/A INTRINSIC
low complexity region 777 791 N/A INTRINSIC
AT_hook 823 835 3.06e2 SMART
low complexity region 859 873 N/A INTRINSIC
AT_hook 885 897 9.15e0 SMART
low complexity region 938 948 N/A INTRINSIC
low complexity region 1086 1105 N/A INTRINSIC
low complexity region 1107 1121 N/A INTRINSIC
low complexity region 1159 1173 N/A INTRINSIC
low complexity region 1262 1273 N/A INTRINSIC
low complexity region 1288 1301 N/A INTRINSIC
AT_hook 1345 1357 3.09e-1 SMART
low complexity region 1377 1388 N/A INTRINSIC
low complexity region 1395 1424 N/A INTRINSIC
low complexity region 1478 1491 N/A INTRINSIC
low complexity region 1678 1692 N/A INTRINSIC
AT_hook 1843 1855 1.03e1 SMART
low complexity region 1971 1983 N/A INTRINSIC
AWS 2081 2133 3.95e-26 SMART
SET 2135 2257 8.04e-45 SMART
PostSET 2259 2275 6.38e-2 SMART
low complexity region 2296 2316 N/A INTRINSIC
BROMO 2431 2541 8.29e-23 SMART
low complexity region 2549 2563 N/A INTRINSIC
PHD 2576 2618 8.25e-6 SMART
BAH 2650 2787 1.18e-23 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.2%
Validation Efficiency
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 trithorax group of transcriptional activators. The protein contains four AT hooks, a SET domain, a PHD-finger motif, and a bromodomain. It is localized to many small speckles in the nucleus, and also to cell-cell tight junctions. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygotes for a transposon-induced allele are more susceptible to endotoxin shock, sepsis, and autoimmune disease. Homozygotes for a hypomorphic allele show reduced growth and postnatal lethality; surviving adults lack Meibomian glands and show vertebral, reproductive organ, and fertility defects. [provided by MGI curators]
Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik T A 11: 58,771,131 (GRCm39) D204E probably benign Het
Adh1 T G 3: 137,988,493 (GRCm39) D155E probably benign Het
Akt1s1 T C 7: 44,498,571 (GRCm39) L2P unknown Het
Bend7 C T 2: 4,757,641 (GRCm39) P228S probably damaging Het
Bpifc T C 10: 85,824,585 (GRCm39) E218G possibly damaging Het
Cdk6 T A 5: 3,479,001 (GRCm39) F127Y probably benign Het
Cgnl1 A T 9: 71,632,846 (GRCm39) H168Q possibly damaging Het
Chd7 C T 4: 8,847,093 (GRCm39) T1612I possibly damaging Het
Col4a4 A T 1: 82,470,184 (GRCm39) C782S unknown Het
Copg2 T A 6: 30,801,341 (GRCm39) I364L probably damaging Het
Crygb A G 1: 65,121,084 (GRCm39) L81P probably benign Het
Cyp4f18 A T 8: 72,747,017 (GRCm39) M326K probably damaging Het
Dhx34 A G 7: 15,949,361 (GRCm39) S356P probably benign Het
Dmbt1 C T 7: 130,685,519 (GRCm39) Q855* probably null Het
Dnai3 T C 3: 145,787,007 (GRCm39) T343A probably damaging Het
Dnph1 A G 17: 46,809,938 (GRCm39) N160S probably benign Het
Esrra A T 19: 6,890,139 (GRCm39) C228* probably null Het
Evpl T C 11: 116,114,775 (GRCm39) N972D probably benign Het
Fat3 T C 9: 15,909,888 (GRCm39) D2038G probably damaging Het
Fhit T A 14: 9,763,784 (GRCm38) R102W probably damaging Het
Gal3st1 A T 11: 3,948,609 (GRCm39) D272V probably damaging Het
Gal3st1 T A 11: 3,948,651 (GRCm39) V286D probably damaging Het
Gemin4 A T 11: 76,104,206 (GRCm39) M185K possibly damaging Het
Hecw1 T C 13: 14,490,821 (GRCm39) I311V probably benign Het
Ift172 T C 5: 31,442,630 (GRCm39) Y179C probably damaging Het
Ighv7-3 C T 12: 114,116,963 (GRCm39) W66* probably null Het
Iqgap3 T A 3: 88,016,142 (GRCm39) I975N probably damaging Het
Khdrbs3 A G 15: 68,921,262 (GRCm39) E281G possibly damaging Het
Lamb2 A T 9: 108,365,523 (GRCm39) T1369S probably benign Het
Mettl8 A T 2: 70,812,382 (GRCm39) D84E probably benign Het
Mrgprb3 C A 7: 48,293,059 (GRCm39) C164F probably damaging Het
Mtg2 A G 2: 179,725,180 (GRCm39) Y131C probably damaging Het
Nacc1 C T 8: 85,403,174 (GRCm39) A234T probably benign Het
Nsmaf C T 4: 6,416,641 (GRCm39) V551I probably benign Het
Or13a26 T A 7: 140,284,942 (GRCm39) C259* probably null Het
Or7e175 T A 9: 20,048,737 (GRCm39) Y108* probably null Het
Oxr1 C T 15: 41,677,004 (GRCm39) P187L not run Het
Pcdhb12 T A 18: 37,569,068 (GRCm39) D71E probably benign Het
Pigt CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT 2: 164,341,589 (GRCm39) probably null Het
Pkm A G 9: 59,576,196 (GRCm39) S127G probably benign Het
Plxna2 T A 1: 194,479,227 (GRCm39) L1296H probably damaging Het
Ppil6 C G 10: 41,374,524 (GRCm39) T135R probably benign Het
Ppp2r3d T C 9: 101,004,203 (GRCm39) Y378C probably damaging Het
Rabep2 C T 7: 126,043,377 (GRCm39) R426C probably damaging Het
Rad21 A T 15: 51,845,976 (GRCm39) H31Q possibly damaging Het
Rad50 G T 11: 53,545,776 (GRCm39) Y1182* probably null Het
Serpinb9c C T 13: 33,335,883 (GRCm39) A218T possibly damaging Het
Slc34a1 C A 13: 24,003,095 (GRCm39) H248Q probably benign Het
Slc45a4 C A 15: 73,458,785 (GRCm39) E255* probably null Het
Slc8a3 T A 12: 81,263,598 (GRCm39) K596N possibly damaging Het
Tbc1d32 A C 10: 55,927,483 (GRCm39) probably null Het
Tbl2 T A 5: 135,183,253 (GRCm39) I112N possibly damaging Het
Tchp A C 5: 114,853,630 (GRCm39) K238T probably damaging Het
Tfap2d G A 1: 19,189,207 (GRCm39) G251D probably damaging Het
Thrb T A 14: 18,030,186 (GRCm38) M324K probably damaging Het
Tmem259 A T 10: 79,814,300 (GRCm39) L328Q probably damaging Het
Tmtc2 T C 10: 105,249,469 (GRCm39) H88R probably damaging Het
Tnfrsf21 A G 17: 43,348,709 (GRCm39) H107R possibly damaging Het
Trib1 T C 15: 59,526,471 (GRCm39) V347A probably benign Het
Ung T A 5: 114,269,315 (GRCm39) L9* probably null Het
Vmn1r195 G T 13: 22,463,174 (GRCm39) V215F probably damaging Het
Wdr90 A G 17: 26,065,286 (GRCm39) S1657P probably benign Het
Wdsub1 A T 2: 59,708,487 (GRCm39) Y129N possibly damaging Het
Zfp369 T G 13: 65,432,832 (GRCm39) probably null Het
Zfp770 G T 2: 114,026,142 (GRCm39) C642* probably null Het
Zfp981 C T 4: 146,622,100 (GRCm39) R342C probably benign Het
Zhx3 A C 2: 160,623,042 (GRCm39) V375G probably damaging Het
Other mutations in Ash1l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Ash1l APN 3 88,889,019 (GRCm39) missense probably benign 0.19
IGL00819:Ash1l APN 3 88,915,043 (GRCm39) missense possibly damaging 0.68
IGL00939:Ash1l APN 3 88,942,543 (GRCm39) missense probably damaging 0.99
IGL01064:Ash1l APN 3 88,979,791 (GRCm39) missense probably damaging 1.00
IGL01066:Ash1l APN 3 88,891,942 (GRCm39) missense probably damaging 1.00
IGL01087:Ash1l APN 3 88,971,209 (GRCm39) missense probably damaging 1.00
IGL01293:Ash1l APN 3 88,890,836 (GRCm39) missense probably benign 0.01
IGL01541:Ash1l APN 3 88,973,572 (GRCm39) missense probably damaging 1.00
IGL01863:Ash1l APN 3 88,892,813 (GRCm39) nonsense probably null
IGL02326:Ash1l APN 3 88,873,364 (GRCm39) missense probably benign 0.00
IGL02407:Ash1l APN 3 88,979,855 (GRCm39) missense probably damaging 1.00
IGL02419:Ash1l APN 3 88,892,872 (GRCm39) missense probably benign 0.00
IGL02422:Ash1l APN 3 88,976,386 (GRCm39) critical splice donor site probably null
IGL02494:Ash1l APN 3 88,973,525 (GRCm39) nonsense probably null
IGL02727:Ash1l APN 3 88,930,344 (GRCm39) missense probably benign
IGL02732:Ash1l APN 3 88,873,535 (GRCm39) missense probably damaging 1.00
IGL02817:Ash1l APN 3 88,892,108 (GRCm39) missense probably damaging 1.00
IGL02887:Ash1l APN 3 88,891,488 (GRCm39) missense probably benign 0.11
IGL03224:Ash1l APN 3 88,942,575 (GRCm39) splice site probably benign
IGL03253:Ash1l APN 3 88,891,981 (GRCm39) missense probably damaging 1.00
IGL03327:Ash1l APN 3 88,930,390 (GRCm39) missense probably benign 0.02
IGL03398:Ash1l APN 3 88,914,527 (GRCm39) missense probably benign 0.01
3-1:Ash1l UTSW 3 88,873,633 (GRCm39) missense probably benign
BB008:Ash1l UTSW 3 88,950,848 (GRCm39) missense probably damaging 1.00
BB018:Ash1l UTSW 3 88,950,848 (GRCm39) missense probably damaging 1.00
R0068:Ash1l UTSW 3 88,914,624 (GRCm39) missense probably benign 0.17
R0068:Ash1l UTSW 3 88,914,624 (GRCm39) missense probably benign 0.17
R0239:Ash1l UTSW 3 88,974,529 (GRCm39) missense possibly damaging 0.49
R0239:Ash1l UTSW 3 88,974,529 (GRCm39) missense possibly damaging 0.49
R0395:Ash1l UTSW 3 88,965,896 (GRCm39) missense probably damaging 1.00
R0477:Ash1l UTSW 3 88,890,766 (GRCm39) missense probably benign 0.41
R0528:Ash1l UTSW 3 88,889,584 (GRCm39) missense probably benign
R0543:Ash1l UTSW 3 88,971,085 (GRCm39) splice site probably null
R0855:Ash1l UTSW 3 88,961,761 (GRCm39) missense possibly damaging 0.82
R1147:Ash1l UTSW 3 88,892,194 (GRCm39) missense possibly damaging 0.72
R1147:Ash1l UTSW 3 88,892,194 (GRCm39) missense possibly damaging 0.72
R1163:Ash1l UTSW 3 88,942,570 (GRCm39) critical splice donor site probably null
R1196:Ash1l UTSW 3 88,890,623 (GRCm39) missense probably damaging 0.99
R1419:Ash1l UTSW 3 88,892,204 (GRCm39) missense probably damaging 0.99
R1445:Ash1l UTSW 3 88,914,659 (GRCm39) missense probably benign 0.02
R1466:Ash1l UTSW 3 88,959,372 (GRCm39) missense probably damaging 1.00
R1466:Ash1l UTSW 3 88,959,372 (GRCm39) missense probably damaging 1.00
R1480:Ash1l UTSW 3 88,892,359 (GRCm39) missense probably damaging 1.00
R1506:Ash1l UTSW 3 88,965,806 (GRCm39) missense probably damaging 0.99
R1537:Ash1l UTSW 3 88,979,783 (GRCm39) missense probably damaging 0.99
R1584:Ash1l UTSW 3 88,959,372 (GRCm39) missense probably damaging 1.00
R1669:Ash1l UTSW 3 88,974,549 (GRCm39) critical splice donor site probably null
R1713:Ash1l UTSW 3 88,983,531 (GRCm39) missense probably damaging 1.00
R1780:Ash1l UTSW 3 88,873,291 (GRCm39) missense probably benign
R1793:Ash1l UTSW 3 88,977,616 (GRCm39) missense probably damaging 1.00
R1881:Ash1l UTSW 3 88,888,862 (GRCm39) missense probably benign 0.00
R1909:Ash1l UTSW 3 88,891,835 (GRCm39) missense probably benign 0.29
R1938:Ash1l UTSW 3 88,891,729 (GRCm39) missense probably damaging 0.98
R2035:Ash1l UTSW 3 88,973,624 (GRCm39) missense probably benign 0.00
R2070:Ash1l UTSW 3 88,873,510 (GRCm39) missense probably damaging 1.00
R2071:Ash1l UTSW 3 88,873,510 (GRCm39) missense probably damaging 1.00
R2114:Ash1l UTSW 3 88,890,571 (GRCm39) missense probably benign 0.00
R2116:Ash1l UTSW 3 88,890,571 (GRCm39) missense probably benign 0.00
R2118:Ash1l UTSW 3 88,892,602 (GRCm39) missense possibly damaging 0.80
R2143:Ash1l UTSW 3 88,892,726 (GRCm39) missense probably benign 0.09
R2164:Ash1l UTSW 3 88,892,726 (GRCm39) missense probably benign 0.09
R2210:Ash1l UTSW 3 88,973,605 (GRCm39) missense probably damaging 1.00
R2247:Ash1l UTSW 3 88,914,674 (GRCm39) missense possibly damaging 0.77
R2303:Ash1l UTSW 3 88,933,733 (GRCm39) missense probably damaging 1.00
R2860:Ash1l UTSW 3 88,961,785 (GRCm39) missense probably damaging 1.00
R2861:Ash1l UTSW 3 88,961,785 (GRCm39) missense probably damaging 1.00
R3104:Ash1l UTSW 3 88,961,693 (GRCm39) missense probably damaging 1.00
R4133:Ash1l UTSW 3 88,889,567 (GRCm39) missense probably benign 0.00
R4164:Ash1l UTSW 3 88,889,273 (GRCm39) missense probably damaging 0.97
R4270:Ash1l UTSW 3 88,889,347 (GRCm39) missense probably benign 0.26
R4271:Ash1l UTSW 3 88,889,347 (GRCm39) missense probably benign 0.26
R4287:Ash1l UTSW 3 88,973,722 (GRCm39) missense probably damaging 0.99
R4409:Ash1l UTSW 3 88,914,506 (GRCm39) missense probably damaging 0.99
R4459:Ash1l UTSW 3 88,873,541 (GRCm39) missense probably damaging 0.99
R4487:Ash1l UTSW 3 88,892,622 (GRCm39) missense possibly damaging 0.65
R4674:Ash1l UTSW 3 88,979,783 (GRCm39) missense possibly damaging 0.80
R4739:Ash1l UTSW 3 88,890,152 (GRCm39) missense probably benign 0.19
R4927:Ash1l UTSW 3 88,892,641 (GRCm39) missense probably damaging 1.00
R5000:Ash1l UTSW 3 88,965,941 (GRCm39) missense probably damaging 1.00
R5016:Ash1l UTSW 3 88,889,630 (GRCm39) missense probably damaging 1.00
R5055:Ash1l UTSW 3 88,930,519 (GRCm39) critical splice donor site probably null
R5081:Ash1l UTSW 3 88,892,024 (GRCm39) missense probably damaging 1.00
R5082:Ash1l UTSW 3 88,873,541 (GRCm39) missense probably damaging 0.99
R5090:Ash1l UTSW 3 88,960,184 (GRCm39) missense probably damaging 1.00
R5113:Ash1l UTSW 3 88,973,582 (GRCm39) missense probably damaging 0.99
R5408:Ash1l UTSW 3 88,889,701 (GRCm39) missense probably damaging 1.00
R5452:Ash1l UTSW 3 88,892,183 (GRCm39) missense possibly damaging 0.93
R5487:Ash1l UTSW 3 88,888,733 (GRCm39) missense probably benign 0.17
R5610:Ash1l UTSW 3 88,930,492 (GRCm39) missense probably damaging 1.00
R5624:Ash1l UTSW 3 88,892,916 (GRCm39) missense probably damaging 1.00
R5682:Ash1l UTSW 3 88,914,914 (GRCm39) missense probably damaging 0.99
R5712:Ash1l UTSW 3 88,959,297 (GRCm39) missense probably damaging 0.99
R5719:Ash1l UTSW 3 88,965,933 (GRCm39) missense probably damaging 1.00
R5719:Ash1l UTSW 3 88,961,805 (GRCm39) missense possibly damaging 0.83
R5839:Ash1l UTSW 3 88,890,658 (GRCm39) missense probably damaging 0.99
R5859:Ash1l UTSW 3 88,976,300 (GRCm39) missense probably damaging 1.00
R5877:Ash1l UTSW 3 88,888,891 (GRCm39) missense probably benign 0.00
R5940:Ash1l UTSW 3 88,891,343 (GRCm39) missense probably damaging 0.96
R6026:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6027:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6029:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6033:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6033:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6034:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6034:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6035:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6035:Ash1l UTSW 3 88,892,326 (GRCm39) missense probably damaging 1.00
R6089:Ash1l UTSW 3 88,960,450 (GRCm39) nonsense probably null
R6110:Ash1l UTSW 3 88,892,436 (GRCm39) missense probably damaging 1.00
R6168:Ash1l UTSW 3 88,960,080 (GRCm39) nonsense probably null
R6200:Ash1l UTSW 3 88,977,834 (GRCm39) missense probably damaging 1.00
R6290:Ash1l UTSW 3 88,890,068 (GRCm39) nonsense probably null
R6331:Ash1l UTSW 3 88,915,172 (GRCm39) missense probably benign 0.00
R6425:Ash1l UTSW 3 88,891,087 (GRCm39) missense probably damaging 0.99
R6540:Ash1l UTSW 3 88,892,368 (GRCm39) missense probably damaging 1.00
R6568:Ash1l UTSW 3 88,959,344 (GRCm39) missense probably benign 0.09
R6828:Ash1l UTSW 3 88,983,420 (GRCm39) missense probably benign 0.00
R6843:Ash1l UTSW 3 88,892,695 (GRCm39) missense probably damaging 1.00
R6894:Ash1l UTSW 3 88,890,298 (GRCm39) missense probably benign 0.00
R6976:Ash1l UTSW 3 88,888,964 (GRCm39) missense possibly damaging 0.77
R7038:Ash1l UTSW 3 88,889,978 (GRCm39) missense probably benign 0.00
R7073:Ash1l UTSW 3 88,892,647 (GRCm39) missense probably damaging 1.00
R7133:Ash1l UTSW 3 88,890,764 (GRCm39) frame shift probably null
R7150:Ash1l UTSW 3 88,984,381 (GRCm39) missense probably damaging 1.00
R7205:Ash1l UTSW 3 88,873,259 (GRCm39) missense probably benign 0.00
R7254:Ash1l UTSW 3 88,977,816 (GRCm39) missense probably damaging 1.00
R7272:Ash1l UTSW 3 88,961,941 (GRCm39) splice site probably null
R7319:Ash1l UTSW 3 88,888,694 (GRCm39) missense probably benign 0.19
R7341:Ash1l UTSW 3 88,889,066 (GRCm39) missense possibly damaging 0.93
R7342:Ash1l UTSW 3 88,873,304 (GRCm39) missense possibly damaging 0.94
R7454:Ash1l UTSW 3 88,891,172 (GRCm39) missense probably benign 0.16
R7677:Ash1l UTSW 3 88,950,500 (GRCm39) missense probably damaging 1.00
R7822:Ash1l UTSW 3 88,914,571 (GRCm39) missense probably benign
R7857:Ash1l UTSW 3 88,891,616 (GRCm39) nonsense probably null
R7889:Ash1l UTSW 3 88,873,345 (GRCm39) missense probably benign 0.00
R7898:Ash1l UTSW 3 88,890,932 (GRCm39) missense possibly damaging 0.54
R7931:Ash1l UTSW 3 88,950,848 (GRCm39) missense probably damaging 1.00
R7937:Ash1l UTSW 3 88,977,624 (GRCm39) nonsense probably null
R7973:Ash1l UTSW 3 88,960,164 (GRCm39) missense probably benign
R8119:Ash1l UTSW 3 88,942,734 (GRCm39) missense probably damaging 1.00
R8157:Ash1l UTSW 3 88,971,014 (GRCm39) critical splice donor site probably null
R8162:Ash1l UTSW 3 88,977,553 (GRCm39) missense probably damaging 0.99
R8194:Ash1l UTSW 3 88,960,062 (GRCm39) missense probably damaging 1.00
R8306:Ash1l UTSW 3 88,873,259 (GRCm39) missense probably benign 0.00
R8497:Ash1l UTSW 3 88,914,951 (GRCm39) missense probably benign 0.02
R8558:Ash1l UTSW 3 88,891,713 (GRCm39) missense probably damaging 0.96
R8744:Ash1l UTSW 3 88,965,890 (GRCm39) missense possibly damaging 0.89
R8923:Ash1l UTSW 3 88,892,974 (GRCm39) missense possibly damaging 0.51
R8969:Ash1l UTSW 3 88,873,598 (GRCm39) missense possibly damaging 0.52
R8970:Ash1l UTSW 3 88,976,307 (GRCm39) missense probably benign 0.00
R9002:Ash1l UTSW 3 88,888,715 (GRCm39) missense probably benign 0.17
R9023:Ash1l UTSW 3 88,892,576 (GRCm39) missense probably damaging 1.00
R9032:Ash1l UTSW 3 88,891,529 (GRCm39) missense probably benign 0.00
R9032:Ash1l UTSW 3 88,889,294 (GRCm39) missense probably benign 0.19
R9049:Ash1l UTSW 3 88,914,671 (GRCm39) missense probably benign
R9085:Ash1l UTSW 3 88,891,529 (GRCm39) missense probably benign 0.00
R9085:Ash1l UTSW 3 88,889,294 (GRCm39) missense probably benign 0.19
R9130:Ash1l UTSW 3 88,965,848 (GRCm39) nonsense probably null
R9149:Ash1l UTSW 3 88,914,530 (GRCm39) missense probably benign
R9294:Ash1l UTSW 3 88,890,297 (GRCm39) missense possibly damaging 0.90
R9365:Ash1l UTSW 3 88,889,207 (GRCm39) missense possibly damaging 0.63
R9450:Ash1l UTSW 3 88,915,139 (GRCm39) missense possibly damaging 0.86
R9542:Ash1l UTSW 3 88,950,566 (GRCm39) missense probably damaging 1.00
R9558:Ash1l UTSW 3 88,889,521 (GRCm39) missense probably benign 0.02
R9572:Ash1l UTSW 3 88,960,188 (GRCm39) missense probably damaging 1.00
R9688:Ash1l UTSW 3 88,892,024 (GRCm39) missense probably damaging 1.00
R9736:Ash1l UTSW 3 88,891,733 (GRCm39) missense probably damaging 1.00
R9765:Ash1l UTSW 3 88,930,500 (GRCm39) missense probably damaging 1.00
R9789:Ash1l UTSW 3 88,873,373 (GRCm39) missense probably benign
X0017:Ash1l UTSW 3 88,891,892 (GRCm39) missense probably benign 0.45
X0019:Ash1l UTSW 3 88,977,863 (GRCm39) missense probably damaging 1.00
X0021:Ash1l UTSW 3 88,890,511 (GRCm39) missense probably benign 0.10
Z1088:Ash1l UTSW 3 88,890,016 (GRCm39) missense probably benign 0.00
Z1176:Ash1l UTSW 3 88,950,524 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGTGGCTTACTCATATCTACAGAAC -3'
(R):5'- GCGAGGATCCTCTTCTTCTG -3'

Sequencing Primer
(F):5'- ACTCATATCTACAGAACAATGAAAGG -3'
(R):5'- GAGGATCCTCTTCTTCTGTGGCAC -3'
Posted On 2019-06-26