Incidental Mutation 'R5814:Ep400'
ID 508682
Institutional Source Beutler Lab
Gene Symbol Ep400
Ensembl Gene ENSMUSG00000029505
Gene Name E1A binding protein p400
Synonyms mDomino, 1700020J09Rik, p400
MMRRC Submission 043396-MU
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # R5814 (G1)
Quality Score 21
Status Validated
Chromosome 5
Chromosomal Location 110664373-110770717 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) C to A at 110695578 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000108055 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041558] [ENSMUST00000041558] [ENSMUST00000112435] [ENSMUST00000112436] [ENSMUST00000112436]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000041558
SMART Domains Protein: ENSMUSP00000049038
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
Pfam:EP400_N 1 461 1.6e-232 PFAM
low complexity region 519 532 N/A INTRINSIC
low complexity region 550 561 N/A INTRINSIC
low complexity region 598 620 N/A INTRINSIC
low complexity region 631 645 N/A INTRINSIC
low complexity region 658 686 N/A INTRINSIC
HSA 762 833 1.31e-31 SMART
low complexity region 908 925 N/A INTRINSIC
DEXDc 1049 1238 2.76e-15 SMART
Blast:DEXDc 1276 1317 2e-15 BLAST
low complexity region 1407 1417 N/A INTRINSIC
HELICc 1807 1893 1.17e-4 SMART
low complexity region 2006 2019 N/A INTRINSIC
low complexity region 2080 2100 N/A INTRINSIC
low complexity region 2214 2223 N/A INTRINSIC
SANT 2243 2310 3.57e-1 SMART
low complexity region 2402 2489 N/A INTRINSIC
low complexity region 2596 2608 N/A INTRINSIC
low complexity region 2644 2679 N/A INTRINSIC
low complexity region 2694 2738 N/A INTRINSIC
low complexity region 2769 2806 N/A INTRINSIC
low complexity region 2846 2883 N/A INTRINSIC
low complexity region 2933 2947 N/A INTRINSIC
low complexity region 2974 2986 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000041558
SMART Domains Protein: ENSMUSP00000049038
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
Pfam:EP400_N 1 461 1.6e-232 PFAM
low complexity region 519 532 N/A INTRINSIC
low complexity region 550 561 N/A INTRINSIC
low complexity region 598 620 N/A INTRINSIC
low complexity region 631 645 N/A INTRINSIC
low complexity region 658 686 N/A INTRINSIC
HSA 762 833 1.31e-31 SMART
low complexity region 908 925 N/A INTRINSIC
DEXDc 1049 1238 2.76e-15 SMART
Blast:DEXDc 1276 1317 2e-15 BLAST
low complexity region 1407 1417 N/A INTRINSIC
HELICc 1807 1893 1.17e-4 SMART
low complexity region 2006 2019 N/A INTRINSIC
low complexity region 2080 2100 N/A INTRINSIC
low complexity region 2214 2223 N/A INTRINSIC
SANT 2243 2310 3.57e-1 SMART
low complexity region 2402 2489 N/A INTRINSIC
low complexity region 2596 2608 N/A INTRINSIC
low complexity region 2644 2679 N/A INTRINSIC
low complexity region 2694 2738 N/A INTRINSIC
low complexity region 2769 2806 N/A INTRINSIC
low complexity region 2846 2883 N/A INTRINSIC
low complexity region 2933 2947 N/A INTRINSIC
low complexity region 2974 2986 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000104066
Predicted Effect probably null
Transcript: ENSMUST00000112435
SMART Domains Protein: ENSMUSP00000108054
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
low complexity region 28 53 N/A INTRINSIC
low complexity region 121 145 N/A INTRINSIC
low complexity region 262 287 N/A INTRINSIC
low complexity region 298 308 N/A INTRINSIC
low complexity region 313 329 N/A INTRINSIC
coiled coil region 418 447 N/A INTRINSIC
low complexity region 471 485 N/A INTRINSIC
low complexity region 556 569 N/A INTRINSIC
low complexity region 587 598 N/A INTRINSIC
low complexity region 635 657 N/A INTRINSIC
low complexity region 668 682 N/A INTRINSIC
low complexity region 695 723 N/A INTRINSIC
HSA 799 870 1.31e-31 SMART
low complexity region 945 962 N/A INTRINSIC
DEXDc 1086 1275 2.76e-15 SMART
Blast:DEXDc 1313 1354 2e-15 BLAST
low complexity region 1444 1454 N/A INTRINSIC
internal_repeat_1 1556 1646 6.82e-5 PROSPERO
low complexity region 1887 1900 N/A INTRINSIC
low complexity region 1961 1981 N/A INTRINSIC
low complexity region 2095 2104 N/A INTRINSIC
SANT 2124 2191 3.57e-1 SMART
low complexity region 2283 2370 N/A INTRINSIC
internal_repeat_1 2371 2463 6.82e-5 PROSPERO
low complexity region 2477 2489 N/A INTRINSIC
low complexity region 2525 2560 N/A INTRINSIC
low complexity region 2575 2619 N/A INTRINSIC
low complexity region 2645 2659 N/A INTRINSIC
low complexity region 2660 2680 N/A INTRINSIC
low complexity region 2720 2757 N/A INTRINSIC
low complexity region 2807 2821 N/A INTRINSIC
low complexity region 2848 2860 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000112436
SMART Domains Protein: ENSMUSP00000108055
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
low complexity region 28 53 N/A INTRINSIC
low complexity region 121 145 N/A INTRINSIC
low complexity region 262 287 N/A INTRINSIC
low complexity region 298 308 N/A INTRINSIC
low complexity region 313 329 N/A INTRINSIC
coiled coil region 418 449 N/A INTRINSIC
low complexity region 472 482 N/A INTRINSIC
low complexity region 483 496 N/A INTRINSIC
low complexity region 514 525 N/A INTRINSIC
low complexity region 562 584 N/A INTRINSIC
low complexity region 595 609 N/A INTRINSIC
low complexity region 622 650 N/A INTRINSIC
HSA 726 797 1.31e-31 SMART
low complexity region 872 889 N/A INTRINSIC
DEXDc 1013 1202 2.76e-15 SMART
Blast:DEXDc 1240 1281 2e-15 BLAST
low complexity region 1371 1381 N/A INTRINSIC
internal_repeat_1 1483 1573 6.76e-5 PROSPERO
HELICc 1771 1857 1.17e-4 SMART
low complexity region 1970 1983 N/A INTRINSIC
low complexity region 2044 2064 N/A INTRINSIC
low complexity region 2178 2187 N/A INTRINSIC
SANT 2207 2274 3.57e-1 SMART
low complexity region 2366 2453 N/A INTRINSIC
internal_repeat_1 2454 2546 6.76e-5 PROSPERO
low complexity region 2560 2572 N/A INTRINSIC
low complexity region 2608 2643 N/A INTRINSIC
low complexity region 2658 2702 N/A INTRINSIC
low complexity region 2733 2770 N/A INTRINSIC
low complexity region 2810 2847 N/A INTRINSIC
low complexity region 2897 2911 N/A INTRINSIC
low complexity region 2938 2950 N/A INTRINSIC
Predicted Effect probably null
Transcript: ENSMUST00000112436
SMART Domains Protein: ENSMUSP00000108055
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
low complexity region 28 53 N/A INTRINSIC
low complexity region 121 145 N/A INTRINSIC
low complexity region 262 287 N/A INTRINSIC
low complexity region 298 308 N/A INTRINSIC
low complexity region 313 329 N/A INTRINSIC
coiled coil region 418 449 N/A INTRINSIC
low complexity region 472 482 N/A INTRINSIC
low complexity region 483 496 N/A INTRINSIC
low complexity region 514 525 N/A INTRINSIC
low complexity region 562 584 N/A INTRINSIC
low complexity region 595 609 N/A INTRINSIC
low complexity region 622 650 N/A INTRINSIC
HSA 726 797 1.31e-31 SMART
low complexity region 872 889 N/A INTRINSIC
DEXDc 1013 1202 2.76e-15 SMART
Blast:DEXDc 1240 1281 2e-15 BLAST
low complexity region 1371 1381 N/A INTRINSIC
internal_repeat_1 1483 1573 6.76e-5 PROSPERO
HELICc 1771 1857 1.17e-4 SMART
low complexity region 1970 1983 N/A INTRINSIC
low complexity region 2044 2064 N/A INTRINSIC
low complexity region 2178 2187 N/A INTRINSIC
SANT 2207 2274 3.57e-1 SMART
low complexity region 2366 2453 N/A INTRINSIC
internal_repeat_1 2454 2546 6.76e-5 PROSPERO
low complexity region 2560 2572 N/A INTRINSIC
low complexity region 2608 2643 N/A INTRINSIC
low complexity region 2658 2702 N/A INTRINSIC
low complexity region 2733 2770 N/A INTRINSIC
low complexity region 2810 2847 N/A INTRINSIC
low complexity region 2897 2911 N/A INTRINSIC
low complexity region 2938 2950 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000125325
SMART Domains Protein: ENSMUSP00000116137
Gene: ENSMUSG00000029505

DomainStartEndE-ValueType
low complexity region 107 117 N/A INTRINSIC
low complexity region 223 239 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000129884
Predicted Effect noncoding transcript
Transcript: ENSMUST00000141986
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.8%
Validation Efficiency 91% (52/57)
MGI Phenotype PHENOTYPE: Mice homozygous for a knock-out allele die at E11.5 and display severe defects in yolk sac erythropoiesis, anemia, and a slight deformity of the neural tube. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933402N03Rik T C 7: 131,139,082 (GRCm38) D135G probably benign Het
Arrdc3 G T 13: 80,890,579 (GRCm38) R220L possibly damaging Het
Bace1 A G 9: 45,860,264 (GRCm38) D458G probably damaging Het
Cacna1s A G 1: 136,107,142 (GRCm38) Y1360C probably benign Het
Ccnb1-ps T C 7: 42,107,098 (GRCm38) noncoding transcript Het
Cd209b T C 8: 3,923,348 (GRCm38) E112G probably damaging Het
Cit T A 5: 115,979,419 (GRCm38) L1176Q probably damaging Het
Clcn3 T C 8: 60,934,573 (GRCm38) Y214C probably damaging Het
Clvs2 G T 10: 33,528,507 (GRCm38) Q238K probably benign Het
Creb3l3 C T 10: 81,085,662 (GRCm38) V350M probably benign Het
Crot A C 5: 8,973,996 (GRCm38) D373E probably damaging Het
Cyp4a12b T A 4: 115,432,497 (GRCm38) I187N probably damaging Het
Degs1l G A 1: 181,055,098 (GRCm38) V142I probably damaging Het
Dnhd1 C A 7: 105,719,895 (GRCm38) A4291D possibly damaging Het
Dnmt3b A T 2: 153,672,497 (GRCm38) E403D probably benign Het
Ect2l A T 10: 18,200,009 (GRCm38) I43K probably damaging Het
Erp27 A T 6: 136,911,566 (GRCm38) V138E possibly damaging Het
Gbp4 G A 5: 105,119,919 (GRCm38) A487V probably benign Het
Gm10142 C A 10: 77,716,123 (GRCm38) T106N probably damaging Het
Gm11639 T A 11: 104,736,114 (GRCm38) probably benign Het
Gxylt2 C A 6: 100,733,235 (GRCm38) H112Q probably damaging Het
Hexim2 G A 11: 103,138,383 (GRCm38) R87Q probably damaging Het
Hgf A G 5: 16,602,307 (GRCm38) N399S probably benign Het
Ikbke T A 1: 131,271,779 (GRCm38) I302F probably damaging Het
Itgb4 C T 11: 115,984,157 (GRCm38) R447W probably benign Het
Kdm1b A G 13: 47,063,146 (GRCm38) probably null Het
Krtap19-9a T C 16: 88,924,114 (GRCm38) noncoding transcript Het
Lin9 T A 1: 180,669,198 (GRCm38) L351I probably benign Het
Mmp10 G A 9: 7,503,620 (GRCm38) A164T possibly damaging Het
Myrip G A 9: 120,424,668 (GRCm38) G269D probably benign Het
Or1e16 AGCGGTCGTAGGC AGC 11: 73,395,654 (GRCm38) probably null Het
Paxbp1 G T 16: 91,030,496 (GRCm38) R420S probably damaging Het
Pcbp2 T A 15: 102,483,162 (GRCm38) S38R probably damaging Het
Pcf11 A G 7: 92,657,714 (GRCm38) V1082A probably benign Het
Pkhd1 T C 1: 20,199,405 (GRCm38) E3305G probably damaging Het
Pla2g4c T A 7: 13,340,618 (GRCm38) W250R probably damaging Het
Prune2 A G 19: 17,016,361 (GRCm38) probably null Het
Rpsa A G 9: 120,128,485 (GRCm38) probably benign Het
Sema3e A G 5: 14,225,666 (GRCm38) I262V probably benign Het
Setd2 T A 9: 110,567,758 (GRCm38) L1663* probably null Het
Sh3d19 G A 3: 86,126,604 (GRCm38) V755I probably benign Het
Spag9 T A 11: 94,082,828 (GRCm38) V14E possibly damaging Het
Srsf11 C T 3: 158,023,344 (GRCm38) probably benign Het
Sspo A T 6: 48,451,884 (GRCm38) Q411L probably damaging Het
Sycp1 A C 3: 102,895,897 (GRCm38) S532R probably benign Het
Taf6l C A 19: 8,774,846 (GRCm38) A493S probably benign Het
Tsnaxip1 A G 8: 105,843,971 (GRCm38) D574G probably benign Het
Ttll10 T A 4: 156,047,627 (GRCm38) K117N possibly damaging Het
Uqcc5 A G 14: 31,124,520 (GRCm38) probably null Het
Utp4 T A 8: 106,912,275 (GRCm38) I405K probably damaging Het
Vmn2r45 T A 7: 8,471,476 (GRCm38) Y851F probably benign Het
Vps33a T C 5: 123,565,056 (GRCm38) D168G probably damaging Het
Other mutations in Ep400
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:Ep400 APN 5 110,687,841 (GRCm38) missense unknown
IGL00585:Ep400 APN 5 110,755,905 (GRCm38) missense possibly damaging 0.70
IGL00586:Ep400 APN 5 110,739,594 (GRCm38) missense probably damaging 1.00
IGL00816:Ep400 APN 5 110,735,490 (GRCm38) unclassified probably benign
IGL01066:Ep400 APN 5 110,668,199 (GRCm38) splice site probably benign
IGL01302:Ep400 APN 5 110,742,048 (GRCm38) missense probably benign 0.00
IGL01568:Ep400 APN 5 110,719,495 (GRCm38) missense unknown
IGL01833:Ep400 APN 5 110,680,008 (GRCm38) missense unknown
IGL02086:Ep400 APN 5 110,676,943 (GRCm38) splice site probably benign
IGL02266:Ep400 APN 5 110,695,297 (GRCm38) unclassified probably benign
IGL02288:Ep400 APN 5 110,683,836 (GRCm38) splice site probably benign
IGL02301:Ep400 APN 5 110,674,960 (GRCm38) missense probably damaging 1.00
IGL02377:Ep400 APN 5 110,720,825 (GRCm38) missense unknown
IGL02382:Ep400 APN 5 110,701,728 (GRCm38) missense unknown
IGL02419:Ep400 APN 5 110,697,376 (GRCm38) splice site probably null
IGL02591:Ep400 APN 5 110,733,772 (GRCm38) unclassified probably benign
IGL02981:Ep400 APN 5 110,691,610 (GRCm38) splice site probably benign
IGL02981:Ep400 APN 5 110,756,103 (GRCm38) missense possibly damaging 0.79
IGL03173:Ep400 APN 5 110,708,871 (GRCm38) unclassified probably benign
IGL03244:Ep400 APN 5 110,727,563 (GRCm38) missense unknown
IGL03333:Ep400 APN 5 110,703,566 (GRCm38) missense unknown
santol UTSW 5 110,701,671 (GRCm38) missense unknown
PIT4243001:Ep400 UTSW 5 110,735,580 (GRCm38) missense unknown
PIT4260001:Ep400 UTSW 5 110,693,171 (GRCm38) nonsense probably null
R0017:Ep400 UTSW 5 110,673,529 (GRCm38) missense probably damaging 1.00
R0179:Ep400 UTSW 5 110,668,649 (GRCm38) missense probably damaging 0.99
R0243:Ep400 UTSW 5 110,724,407 (GRCm38) splice site probably benign
R0366:Ep400 UTSW 5 110,701,671 (GRCm38) missense unknown
R0508:Ep400 UTSW 5 110,739,508 (GRCm38) missense probably benign 0.00
R0541:Ep400 UTSW 5 110,705,016 (GRCm38) missense unknown
R0558:Ep400 UTSW 5 110,685,067 (GRCm38) splice site probably benign
R0576:Ep400 UTSW 5 110,711,093 (GRCm38) unclassified probably benign
R0595:Ep400 UTSW 5 110,703,542 (GRCm38) missense unknown
R0671:Ep400 UTSW 5 110,688,196 (GRCm38) missense unknown
R0763:Ep400 UTSW 5 110,665,837 (GRCm38) missense probably damaging 1.00
R1078:Ep400 UTSW 5 110,735,522 (GRCm38) unclassified probably benign
R1300:Ep400 UTSW 5 110,673,560 (GRCm38) missense probably damaging 1.00
R1439:Ep400 UTSW 5 110,685,478 (GRCm38) missense unknown
R1520:Ep400 UTSW 5 110,691,778 (GRCm38) intron probably benign
R1529:Ep400 UTSW 5 110,739,445 (GRCm38) missense probably benign 0.00
R1535:Ep400 UTSW 5 110,708,166 (GRCm38) unclassified probably benign
R1560:Ep400 UTSW 5 110,671,106 (GRCm38) splice site probably null
R1587:Ep400 UTSW 5 110,726,902 (GRCm38) missense probably benign 0.23
R1596:Ep400 UTSW 5 110,708,861 (GRCm38) unclassified probably benign
R1653:Ep400 UTSW 5 110,693,174 (GRCm38) nonsense probably null
R1711:Ep400 UTSW 5 110,693,308 (GRCm38) unclassified probably benign
R1774:Ep400 UTSW 5 110,685,491 (GRCm38) missense unknown
R1836:Ep400 UTSW 5 110,705,054 (GRCm38) missense unknown
R1905:Ep400 UTSW 5 110,670,948 (GRCm38) missense probably damaging 1.00
R1917:Ep400 UTSW 5 110,703,575 (GRCm38) missense unknown
R2064:Ep400 UTSW 5 110,735,404 (GRCm38) unclassified probably benign
R2122:Ep400 UTSW 5 110,708,850 (GRCm38) unclassified probably benign
R2144:Ep400 UTSW 5 110,703,518 (GRCm38) missense unknown
R2215:Ep400 UTSW 5 110,693,555 (GRCm38) unclassified probably benign
R2252:Ep400 UTSW 5 110,719,091 (GRCm38) missense unknown
R2253:Ep400 UTSW 5 110,719,091 (GRCm38) missense unknown
R2483:Ep400 UTSW 5 110,719,236 (GRCm38) missense unknown
R2504:Ep400 UTSW 5 110,668,645 (GRCm38) missense probably damaging 1.00
R2512:Ep400 UTSW 5 110,708,915 (GRCm38) unclassified probably benign
R2842:Ep400 UTSW 5 110,698,815 (GRCm38) nonsense probably null
R2920:Ep400 UTSW 5 110,755,914 (GRCm38) missense probably damaging 1.00
R3082:Ep400 UTSW 5 110,693,230 (GRCm38) unclassified probably benign
R3151:Ep400 UTSW 5 110,703,569 (GRCm38) missense unknown
R3552:Ep400 UTSW 5 110,729,287 (GRCm38) missense unknown
R3623:Ep400 UTSW 5 110,719,236 (GRCm38) missense unknown
R3779:Ep400 UTSW 5 110,691,649 (GRCm38) missense unknown
R3923:Ep400 UTSW 5 110,756,523 (GRCm38) missense possibly damaging 0.55
R4062:Ep400 UTSW 5 110,741,981 (GRCm38) missense probably benign 0.10
R4508:Ep400 UTSW 5 110,703,615 (GRCm38) missense unknown
R4584:Ep400 UTSW 5 110,733,897 (GRCm38) unclassified probably benign
R4585:Ep400 UTSW 5 110,753,859 (GRCm38) missense probably damaging 1.00
R4586:Ep400 UTSW 5 110,753,859 (GRCm38) missense probably damaging 1.00
R4807:Ep400 UTSW 5 110,695,578 (GRCm38) splice site probably null
R4921:Ep400 UTSW 5 110,665,810 (GRCm38) missense probably damaging 1.00
R4976:Ep400 UTSW 5 110,720,756 (GRCm38) missense unknown
R4976:Ep400 UTSW 5 110,698,812 (GRCm38) missense unknown
R5075:Ep400 UTSW 5 110,685,485 (GRCm38) missense unknown
R5120:Ep400 UTSW 5 110,756,358 (GRCm38) missense probably damaging 1.00
R5122:Ep400 UTSW 5 110,668,170 (GRCm38) missense probably damaging 1.00
R5223:Ep400 UTSW 5 110,668,630 (GRCm38) missense probably damaging 1.00
R5284:Ep400 UTSW 5 110,668,124 (GRCm38) missense probably damaging 1.00
R5388:Ep400 UTSW 5 110,701,728 (GRCm38) missense unknown
R5401:Ep400 UTSW 5 110,683,171 (GRCm38) missense unknown
R5431:Ep400 UTSW 5 110,676,554 (GRCm38) missense unknown
R5461:Ep400 UTSW 5 110,676,684 (GRCm38) nonsense probably null
R5568:Ep400 UTSW 5 110,756,205 (GRCm38) missense probably damaging 1.00
R5650:Ep400 UTSW 5 110,695,952 (GRCm38) critical splice donor site probably null
R5778:Ep400 UTSW 5 110,719,584 (GRCm38) missense unknown
R5806:Ep400 UTSW 5 110,755,554 (GRCm38) nonsense probably null
R5830:Ep400 UTSW 5 110,683,996 (GRCm38) missense unknown
R5882:Ep400 UTSW 5 110,755,587 (GRCm38) missense probably benign 0.00
R5931:Ep400 UTSW 5 110,735,520 (GRCm38) unclassified probably benign
R5945:Ep400 UTSW 5 110,682,866 (GRCm38) missense unknown
R5966:Ep400 UTSW 5 110,676,900 (GRCm38) missense unknown
R5973:Ep400 UTSW 5 110,729,831 (GRCm38) missense unknown
R5980:Ep400 UTSW 5 110,733,729 (GRCm38) unclassified probably benign
R6000:Ep400 UTSW 5 110,683,201 (GRCm38) missense unknown
R6006:Ep400 UTSW 5 110,704,959 (GRCm38) missense unknown
R6053:Ep400 UTSW 5 110,755,795 (GRCm38) missense probably benign 0.22
R6145:Ep400 UTSW 5 110,756,703 (GRCm38) missense possibly damaging 0.95
R6154:Ep400 UTSW 5 110,755,933 (GRCm38) missense probably damaging 0.97
R6169:Ep400 UTSW 5 110,741,997 (GRCm38) missense possibly damaging 0.83
R6228:Ep400 UTSW 5 110,670,942 (GRCm38) missense probably damaging 1.00
R6295:Ep400 UTSW 5 110,753,809 (GRCm38) missense probably benign 0.00
R6486:Ep400 UTSW 5 110,697,218 (GRCm38) unclassified probably benign
R6504:Ep400 UTSW 5 110,708,837 (GRCm38) unclassified probably benign
R6607:Ep400 UTSW 5 110,683,314 (GRCm38) missense unknown
R6657:Ep400 UTSW 5 110,693,545 (GRCm38) unclassified probably benign
R6660:Ep400 UTSW 5 110,719,447 (GRCm38) nonsense probably null
R6741:Ep400 UTSW 5 110,676,895 (GRCm38) missense unknown
R6933:Ep400 UTSW 5 110,665,862 (GRCm38) missense probably damaging 1.00
R6937:Ep400 UTSW 5 110,711,152 (GRCm38) unclassified probably benign
R7069:Ep400 UTSW 5 110,668,124 (GRCm38) missense probably damaging 1.00
R7103:Ep400 UTSW 5 110,733,785 (GRCm38) missense unknown
R7156:Ep400 UTSW 5 110,685,363 (GRCm38) missense unknown
R7272:Ep400 UTSW 5 110,755,645 (GRCm38) nonsense probably null
R7365:Ep400 UTSW 5 110,719,614 (GRCm38) missense unknown
R7581:Ep400 UTSW 5 110,756,025 (GRCm38) missense unknown
R7684:Ep400 UTSW 5 110,697,352 (GRCm38) missense unknown
R7699:Ep400 UTSW 5 110,696,032 (GRCm38) missense unknown
R7700:Ep400 UTSW 5 110,696,032 (GRCm38) missense unknown
R7856:Ep400 UTSW 5 110,666,584 (GRCm38) missense probably damaging 0.99
R7954:Ep400 UTSW 5 110,668,733 (GRCm38) missense possibly damaging 0.46
R8098:Ep400 UTSW 5 110,693,251 (GRCm38) missense unknown
R8108:Ep400 UTSW 5 110,687,883 (GRCm38) missense unknown
R8260:Ep400 UTSW 5 110,755,612 (GRCm38) nonsense probably null
R8293:Ep400 UTSW 5 110,708,892 (GRCm38) missense unknown
R8314:Ep400 UTSW 5 110,755,753 (GRCm38) missense unknown
R8351:Ep400 UTSW 5 110,739,334 (GRCm38) missense probably damaging 1.00
R8424:Ep400 UTSW 5 110,693,278 (GRCm38) missense unknown
R8459:Ep400 UTSW 5 110,708,891 (GRCm38) missense unknown
R8529:Ep400 UTSW 5 110,719,236 (GRCm38) missense unknown
R8688:Ep400 UTSW 5 110,720,819 (GRCm38) missense unknown
R8744:Ep400 UTSW 5 110,742,059 (GRCm38) missense unknown
R8923:Ep400 UTSW 5 110,683,998 (GRCm38) missense unknown
R9005:Ep400 UTSW 5 110,711,093 (GRCm38) missense unknown
R9087:Ep400 UTSW 5 110,667,564 (GRCm38) nonsense probably null
R9146:Ep400 UTSW 5 110,701,769 (GRCm38) nonsense probably null
R9383:Ep400 UTSW 5 110,685,485 (GRCm38) missense unknown
R9479:Ep400 UTSW 5 110,729,864 (GRCm38) missense unknown
R9496:Ep400 UTSW 5 110,707,987 (GRCm38) missense unknown
R9582:Ep400 UTSW 5 110,676,449 (GRCm38) critical splice donor site probably null
R9607:Ep400 UTSW 5 110,683,939 (GRCm38) missense unknown
R9712:Ep400 UTSW 5 110,756,643 (GRCm38) missense unknown
R9746:Ep400 UTSW 5 110,742,006 (GRCm38) missense unknown
X0012:Ep400 UTSW 5 110,673,196 (GRCm38) small deletion probably benign
X0021:Ep400 UTSW 5 110,682,864 (GRCm38) missense unknown
Z1176:Ep400 UTSW 5 110,756,635 (GRCm38) missense unknown
Z1177:Ep400 UTSW 5 110,733,743 (GRCm38) missense unknown
Z1177:Ep400 UTSW 5 110,683,364 (GRCm38) missense unknown
Z1188:Ep400 UTSW 5 110,755,683 (GRCm38) missense unknown
Predicted Primers PCR Primer
(F):5'- AGCACAAAGGCCTCTTCCTTC -3'
(R):5'- TGCAGACATTGTGGTCTTTACTC -3'

Sequencing Primer
(F):5'- TTCTTCCAGGAAGGGAACAAATC -3'
(R):5'- CATAGAAGTAGGCTGTGGATG -3'
Posted On 2018-03-29