Incidental Mutation 'R1713:Ash1l'
ID 190748
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 039746-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R1713 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 88857929-88986682 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 88983531 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 2911 (E2911G)
Ref Sequence ENSEMBL: ENSMUSP00000140251 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090933] [ENSMUST00000186583]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000090933
AA Change: E2911G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000088451
Gene: ENSMUSG00000028053
AA Change: E2911G

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 damaging
Transcript: ENSMUST00000186583
AA Change: E2911G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000140251
Gene: ENSMUSG00000028053
AA Change: E2911G

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
Meta Mutation Damage Score 0.1025 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 98% (96/98)
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: 90 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921539E11Rik T A 4: 103,127,964 (GRCm39) I54F possibly damaging Het
Ackr1 A T 1: 173,159,916 (GRCm39) H134Q probably benign Het
Agtr1b A T 3: 20,370,473 (GRCm39) F44L probably benign Het
Ahnak G A 19: 8,989,173 (GRCm39) D3486N possibly damaging Het
Akap9 T C 5: 4,089,345 (GRCm39) probably null Het
Anks6 T A 4: 47,039,726 (GRCm39) Q495L probably benign Het
Arpp21 A G 9: 111,896,237 (GRCm39) S684P probably damaging Het
Avpi1 C T 19: 42,113,248 (GRCm39) E70K probably damaging Het
Btbd17 G T 11: 114,686,650 (GRCm39) P9T probably benign Het
C4b A G 17: 34,948,245 (GRCm39) probably benign Het
Carm1 T C 9: 21,497,785 (GRCm39) V385A probably damaging Het
Casd1 A G 6: 4,624,104 (GRCm39) D299G probably damaging Het
Clca3a1 T A 3: 144,730,307 (GRCm39) K179N probably benign Het
Col1a2 T C 6: 4,538,691 (GRCm39) S1204P unknown Het
Col24a1 C T 3: 145,072,624 (GRCm39) Q780* probably null Het
Cxadr C A 16: 78,131,133 (GRCm39) N216K probably damaging Het
Daam1 C T 12: 71,942,656 (GRCm39) T40I unknown Het
Dab2 C T 15: 6,459,182 (GRCm39) P365S possibly damaging Het
Dnah1 A T 14: 31,001,139 (GRCm39) I2402N probably damaging Het
Dscaml1 T A 9: 45,663,988 (GRCm39) S1954R possibly damaging Het
Dync2h1 T C 9: 7,131,891 (GRCm39) T1639A probably benign Het
Ebf1 A T 11: 44,815,393 (GRCm39) I336F probably damaging Het
Ebna1bp2 A G 4: 118,482,881 (GRCm39) N290S possibly damaging Het
Gabra2 A G 5: 71,171,906 (GRCm39) I110T probably benign Het
Galk2 A G 2: 125,773,210 (GRCm39) N203S probably benign Het
Gria4 T C 9: 4,424,448 (GRCm39) T806A probably benign Het
Impg2 A G 16: 56,080,889 (GRCm39) T789A probably benign Het
Itga6 A G 2: 71,617,546 (GRCm39) T22A probably benign Het
Itgb4 T A 11: 115,894,315 (GRCm39) I1312N probably damaging Het
Kdm4c A G 4: 74,216,721 (GRCm39) D160G probably benign Het
Kdr A G 5: 76,129,127 (GRCm39) V173A probably benign Het
Kif14 T C 1: 136,455,202 (GRCm39) S1575P probably benign Het
Lcp1 G A 14: 75,436,884 (GRCm39) probably null Het
Lipe C A 7: 25,084,750 (GRCm39) S516I probably damaging Het
Lrrc61 G A 6: 48,545,708 (GRCm39) R177Q possibly damaging Het
Macf1 A G 4: 123,272,487 (GRCm39) I6429T probably damaging Het
Map3k4 C T 17: 12,468,458 (GRCm39) E1012K probably benign Het
Map3k5 T C 10: 19,986,593 (GRCm39) F936L possibly damaging Het
Mllt3 A T 4: 87,701,901 (GRCm39) N497K probably damaging Het
Moxd1 G A 10: 24,157,394 (GRCm39) G342D probably damaging Het
Mtdh A C 15: 34,114,985 (GRCm39) Q202H possibly damaging Het
Nav1 A G 1: 135,522,972 (GRCm39) probably benign Het
Nop56 T C 2: 130,119,886 (GRCm39) V109A possibly damaging Het
Obscn T C 11: 58,970,712 (GRCm39) D2540G probably damaging Het
Omg T C 11: 79,393,679 (GRCm39) I60V probably benign Het
Or10q12 A T 19: 13,746,659 (GRCm39) T318S probably benign Het
Or12e9 A T 2: 87,202,290 (GRCm39) Y138F probably damaging Het
Osbpl5 G A 7: 143,248,110 (GRCm39) H652Y probably damaging Het
Parvb T C 15: 84,182,192 (GRCm39) probably benign Het
Pcdhb3 A C 18: 37,436,375 (GRCm39) E780D probably benign Het
Pik3c3 A G 18: 30,456,639 (GRCm39) D723G possibly damaging Het
Prkdc T C 16: 15,612,958 (GRCm39) V3172A probably benign Het
Psme4 G T 11: 30,756,310 (GRCm39) W272L probably damaging Het
Rem1 G A 2: 152,476,455 (GRCm39) V238M probably damaging Het
Rhobtb1 A C 10: 69,108,601 (GRCm39) S434R probably benign Het
Rhobtb1 G C 10: 69,108,602 (GRCm39) S434T possibly damaging Het
Rnf8 T C 17: 29,853,735 (GRCm39) F413S probably damaging Het
Rpn2 A G 2: 157,156,888 (GRCm39) N497S probably damaging Het
Rsbn1l G T 5: 21,156,488 (GRCm39) P99Q probably benign Het
Serpinb3b A T 1: 107,083,164 (GRCm39) M246K probably benign Het
Sgsm2 T C 11: 74,787,652 (GRCm39) E19G probably null Het
Shank1 A G 7: 43,969,161 (GRCm39) H352R unknown Het
Slc17a7 A G 7: 44,819,728 (GRCm39) I177V probably benign Het
Slc28a2 T A 2: 122,281,494 (GRCm39) F228I probably damaging Het
Slc35b4 C T 6: 34,147,484 (GRCm39) V35I probably benign Het
Slc38a1 T C 15: 96,476,641 (GRCm39) I407V probably damaging Het
Slc39a13 A G 2: 90,893,442 (GRCm39) V326A probably damaging Het
Slc44a5 T C 3: 153,944,743 (GRCm39) L120P probably damaging Het
Slfn3 T C 11: 83,104,140 (GRCm39) I214T probably damaging Het
Slitrk3 A C 3: 72,957,024 (GRCm39) S583A probably benign Het
Snx14 T C 9: 88,297,728 (GRCm39) Y180C probably damaging Het
Sorl1 T A 9: 41,907,538 (GRCm39) K1483I probably benign Het
Ssrp1 C A 2: 84,871,104 (GRCm39) H247N probably damaging Het
Stk39 A T 2: 68,137,460 (GRCm39) probably benign Het
Syde1 C T 10: 78,421,530 (GRCm39) G674R probably damaging Het
Tent4a A T 13: 69,651,170 (GRCm39) I565N probably benign Het
Themis3 G A 17: 66,862,848 (GRCm39) S370L probably benign Het
Tll1 T A 8: 64,554,907 (GRCm39) N259Y probably damaging Het
Tnip2 T G 5: 34,661,175 (GRCm39) probably benign Het
Top2b T C 14: 16,409,823 (GRCm38) V830A probably benign Het
Trpm8 T A 1: 88,292,802 (GRCm39) N934K probably damaging Het
Ttc14 A G 3: 33,857,069 (GRCm39) Y179C probably damaging Het
Ttn T G 2: 76,573,965 (GRCm39) I17316L possibly damaging Het
Tufm T C 7: 126,086,871 (GRCm39) V52A probably benign Het
Vamp8 T A 6: 72,365,270 (GRCm39) N20I probably benign Het
Vmn1r170 A T 7: 23,306,288 (GRCm39) H230L probably benign Het
Vmn2r50 T G 7: 9,771,731 (GRCm39) T657P probably damaging Het
Xirp2 G A 2: 67,342,762 (GRCm39) G1668R probably benign Het
Zik1 C A 7: 10,224,311 (GRCm39) R262L possibly damaging Het
Zscan25 T G 5: 145,220,501 (GRCm39) Y99D 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
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
R7288:Ash1l UTSW 3 88,873,199 (GRCm39) start gained probably benign
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'- GCTTTGCCCTTGATTGAAGAGGTACTG -3'
(R):5'- GACACCATCTGATCTTAGCATCACTCC -3'

Sequencing Primer
(F):5'- GACATTGGGGACGCTGAAAA -3'
(R):5'- cagacacacacacatagacacac -3'
Posted On 2014-05-14