Mutagenetix > Incidental Mutation

Incidental Mutation 'R1466:Dido1'

201141

Institutional Source

Beutler Lab

Gene Symbol

Dido1

Ensembl Gene

ENSMUSG00000038914

Gene Name

death inducer-obliterator 1

Synonyms

6720461J16Rik, DIO-1, Datf1, D130048F08Rik

Accession Numbers

Essential gene?

Probably essential (E-score: 0.960) question?

Stock #

R1466 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

180657964-180709999 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 180662328 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Proline to Leucine at position 1261 (P1261L)

Ref Sequence

ENSEMBL: ENSMUSP00000084794 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087517]

AlphaFold

Q8C9B9

Predicted Effect

probably damaging
Transcript: ENSMUST00000087517
AA Change: P1261L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000084794
Gene: ENSMUSG00000038914
AA Change: P1261L

Domain	Start	End	E-Value	Type
low complexity region	134	155	N/A	INTRINSIC
PHD	267	317	1.19e-11	SMART
low complexity region	430	446	N/A	INTRINSIC
TFS2M	669	770	1.16e-45	SMART
low complexity region	937	962	N/A	INTRINSIC
low complexity region	1023	1037	N/A	INTRINSIC
Pfam:SPOC	1052	1158	1e-22	PFAM
low complexity region	1253	1267	N/A	INTRINSIC
low complexity region	1279	1308	N/A	INTRINSIC
low complexity region	1372	1391	N/A	INTRINSIC
coiled coil region	1458	1502	N/A	INTRINSIC
low complexity region	1649	1680	N/A	INTRINSIC
low complexity region	1748	1766	N/A	INTRINSIC
low complexity region	1780	1792	N/A	INTRINSIC
low complexity region	1804	1815	N/A	INTRINSIC
internal_repeat_2	1816	1852	3.9e-5	PROSPERO
internal_repeat_1	1819	1859	6.92e-7	PROSPERO
internal_repeat_2	1926	1964	3.9e-5	PROSPERO
internal_repeat_1	1940	1982	6.92e-7	PROSPERO
low complexity region	2025	2045	N/A	INTRINSIC
low complexity region	2123	2160	N/A	INTRINSIC
low complexity region	2163	2177	N/A	INTRINSIC
low complexity region	2182	2239	N/A	INTRINSIC

Meta Mutation Damage Score

0.0822

Coding Region Coverage

1x: 97.4%
3x: 96.7%
10x: 94.7%
20x: 90.4%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a transcription factor involved in apoptosis. The encoded protein functions in cell cycle progression and plays a role in chromosomal stability. This protein regulates the self-renewal of embryonic stem cells. Disruption of this gene in mice causes symptoms similar to myelodysplastic/myeloproliferative diseases in humans. Mice lacking this gene show severely reduced fertility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit severely reduced fertility; about one-half develop a transplantable disease characterized by anomalies in spleen, bone marrow, and peripheral blood and including anemia and various symptoms typical of myeloid dysplasia or myeloid proliferation. [provided by MGI curators]

Allele List at MGI

All alleles(245) : Targeted, knock-out(1) Gene trapped(244)

Other mutations in this stock

Total: 134 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110012J17Rik	T	A	17: 66,380,435 (GRCm38)	D492V	probably damaging	Het
Abca13	T	C	11: 9,570,536 (GRCm38)		probably benign	Het
Abcg8	G	C	17: 84,686,727 (GRCm38)		probably benign	Het
Abhd15	C	T	11: 77,515,410 (GRCm38)	A71V	probably damaging	Het
AC167973.1	A	T	9: 43,265,352 (GRCm38)		noncoding transcript	Het
Adamts12	T	C	15: 11,311,359 (GRCm38)	F1234S	probably benign	Het
Ahnak	A	G	19: 9,015,875 (GRCm38)	D4841G	probably damaging	Het
Akap13	T	C	7: 75,729,049 (GRCm38)	S2095P	possibly damaging	Het
Ampd2	T	C	3: 108,080,337 (GRCm38)		probably null	Het
Arhgef17	G	T	7: 100,929,659 (GRCm38)	P694Q	possibly damaging	Het
Arrdc1	T	C	2: 24,925,795 (GRCm38)	I398V	probably benign	Het
Ash1l	T	C	3: 89,052,065 (GRCm38)	Y2250H	probably damaging	Het
Aspg	A	G	12: 112,121,852 (GRCm38)	N385D	probably benign	Het
Atxn3	G	A	12: 101,926,499 (GRCm38)	R319C	possibly damaging	Het
Brca2	G	A	5: 150,552,258 (GRCm38)	A2478T	probably damaging	Het
Btrc	T	A	19: 45,513,382 (GRCm38)		probably benign	Het
C1s1	C	T	6: 124,531,131 (GRCm38)	C633Y	probably damaging	Het
C8g	C	T	2: 25,500,216 (GRCm38)	A6T	probably benign	Het
Capza2	T	C	6: 17,657,159 (GRCm38)		probably benign	Het
Cbl	A	T	9: 44,154,244 (GRCm38)	V706E	probably benign	Het
Ccdc121rt3	C	T	5: 112,354,764 (GRCm38)	G358D	probably benign	Het
Cenatac	A	T	9: 44,413,680 (GRCm38)		probably benign	Het
Cfhr1	C	T	1: 139,557,574 (GRCm38)	E45K	probably benign	Het
Chd7	G	A	4: 8,840,561 (GRCm38)		probably null	Het
Chek1	G	T	9: 36,725,857 (GRCm38)	A2E	probably damaging	Het
Clcn2	G	A	16: 20,712,552 (GRCm38)		probably benign	Het
Cndp2	G	A	18: 84,677,315 (GRCm38)		probably benign	Het
Cntnap1	C	A	11: 101,180,360 (GRCm38)	F366L	probably damaging	Het
Col5a1	G	T	2: 28,003,846 (GRCm38)		probably benign	Het
Corin	C	T	5: 72,302,790 (GRCm38)		probably null	Het
Crb2	T	C	2: 37,783,388 (GRCm38)	Y99H	probably damaging	Het
Csf3r	T	A	4: 126,031,932 (GRCm38)		probably benign	Het
Ctdspl2	G	A	2: 122,003,929 (GRCm38)	R332K	probably benign	Het
Ctnnbl1	C	T	2: 157,799,417 (GRCm38)		probably benign	Het
Cym	G	A	3: 107,213,458 (GRCm38)	T277I	probably damaging	Het
Cyp2d11	C	T	15: 82,391,735 (GRCm38)	C215Y	probably benign	Het
Dnah10	T	A	5: 124,763,096 (GRCm38)	Y1265N	probably benign	Het
Dtx3l	G	A	16: 35,932,728 (GRCm38)	L503F	probably damaging	Het
Eda	T	A	X: 100,392,392 (GRCm38)		probably benign	Homo
Efhb	A	G	17: 53,437,178 (GRCm38)	F462L	probably damaging	Het
Enpep	T	A	3: 129,319,448 (GRCm38)	T203S	probably damaging	Het
Exd1	G	A	2: 119,520,734 (GRCm38)		probably benign	Het
Fam184b	G	A	5: 45,580,509 (GRCm38)		probably benign	Het
Fam20b	T	C	1: 156,686,188 (GRCm38)		probably benign	Het
Fat3	A	C	9: 16,375,482 (GRCm38)	V915G	probably damaging	Het
Fbln7	A	G	2: 128,877,429 (GRCm38)	T49A	probably benign	Het
Fcho1	C	T	8: 71,712,560 (GRCm38)	A418T	probably benign	Het
Fgf14	T	A	14: 124,676,539 (GRCm38)	K60M	probably benign	Het
Galnt4	A	G	10: 99,108,709 (GRCm38)	R99G	probably benign	Het
Gimap4	C	A	6: 48,691,282 (GRCm38)	Q196K	probably benign	Het
Glcci1	C	T	6: 8,537,964 (GRCm38)	T6I	probably damaging	Het
Gm10110	A	T	14: 89,898,075 (GRCm38)		noncoding transcript	Het
Gm4884	A	G	7: 41,043,128 (GRCm38)	K174E	probably damaging	Het
Grip2	A	T	6: 91,788,443 (GRCm38)	D19E	probably damaging	Het
Grk4	T	C	5: 34,694,750 (GRCm38)	S113P	probably benign	Het
Hectd3	G	A	4: 116,996,566 (GRCm38)	E220K	probably damaging	Het
Helz2	G	A	2: 181,236,297 (GRCm38)	P903S	probably damaging	Het
Hydin	T	A	8: 110,532,953 (GRCm38)	V2519E	possibly damaging	Het
Igf2r	A	T	17: 12,717,269 (GRCm38)		probably benign	Het
Ints11	G	A	4: 155,888,110 (GRCm38)		probably null	Het
Kif1a	A	G	1: 93,054,929 (GRCm38)	W718R	possibly damaging	Het
Kif1b	A	T	4: 149,223,252 (GRCm38)	Y839N	probably damaging	Het
Kif20b	T	A	19: 34,950,599 (GRCm38)	V1047D	probably benign	Het
Klhl23	T	C	2: 69,833,888 (GRCm38)	I527T	probably damaging	Het
Klra10	T	A	6: 130,279,315 (GRCm38)	R125S	probably damaging	Het
Klra10	T	C	6: 130,279,431 (GRCm38)	N87D	probably damaging	Het
Lars1	G	A	18: 42,210,050 (GRCm38)	R1101C	probably damaging	Het
Lcn4	G	A	2: 26,668,576 (GRCm38)	P166L	probably damaging	Het
Letmd1	T	A	15: 100,472,542 (GRCm38)		probably null	Het
Lrrc27	A	G	7: 139,230,308 (GRCm38)		probably benign	Het
Map4k2	G	T	19: 6,341,917 (GRCm38)	W87L	probably damaging	Het
Mccc1	A	G	3: 35,974,286 (GRCm38)	V457A	probably benign	Het
Mdn1	T	A	4: 32,730,788 (GRCm38)	S2886T	probably benign	Het
Mgat4a	A	T	1: 37,464,406 (GRCm38)		probably benign	Het
Mmp1b	A	T	9: 7,384,779 (GRCm38)		probably benign	Het
Mroh2b	G	T	15: 4,925,684 (GRCm38)	D720Y	probably damaging	Het
Mrpl24	T	A	3: 87,921,928 (GRCm38)	Y21*	probably null	Het
Mrps35	C	T	6: 147,055,984 (GRCm38)	T169M	probably damaging	Het
Muc2	A	G	7: 141,748,974 (GRCm38)	Y457C	probably damaging	Het
Muc4	G	A	16: 32,753,595 (GRCm38)	G1157D	probably benign	Het
Myg1	T	A	15: 102,337,390 (GRCm38)	L275Q	probably damaging	Het
Naga	T	A	15: 82,334,788 (GRCm38)	M237L	probably null	Het
Nek1	C	T	8: 61,125,136 (GRCm38)		probably benign	Het
Oc90	T	A	15: 65,897,720 (GRCm38)	Y96F	probably damaging	Het
Or12d13	A	T	17: 37,336,956 (GRCm38)	L92H	probably benign	Het
Or13a18	A	G	7: 140,610,969 (GRCm38)	I268V	probably benign	Het
Or4a80	C	T	2: 89,752,267 (GRCm38)	C187Y	probably damaging	Het
Or5m11b	T	A	2: 85,975,995 (GRCm38)	F251I	probably damaging	Het
Or6ae1	A	G	7: 140,162,203 (GRCm38)	V249A	probably damaging	Het
Orc4	A	T	2: 48,909,494 (GRCm38)	C324S	possibly damaging	Het
Pald1	T	C	10: 61,348,525 (GRCm38)		probably benign	Het
Paox	A	G	7: 140,129,281 (GRCm38)		probably benign	Het
Pcdh10	T	G	3: 45,379,974 (GRCm38)	L241R	probably damaging	Het
Pdzrn4	T	C	15: 92,770,537 (GRCm38)	S857P	probably benign	Het
Plec	C	T	15: 76,185,908 (GRCm38)	E1000K	possibly damaging	Het
Plvap	A	T	8: 71,508,481 (GRCm38)	V149D	probably benign	Het
Ppef1	C	A	X: 160,625,674 (GRCm38)		probably null	Homo
Prkaa1	C	A	15: 5,178,798 (GRCm38)	P507T	probably benign	Het
Psmd2	A	G	16: 20,657,965 (GRCm38)		probably benign	Het
Ptch1	A	G	13: 63,524,969 (GRCm38)	Y804H	probably benign	Het
R3hdm2	A	G	10: 127,476,690 (GRCm38)	I434V	probably benign	Het
Rbm28	G	A	6: 29,155,017 (GRCm38)		probably benign	Het
Rfx5	T	A	3: 94,956,303 (GRCm38)	Y88N	probably damaging	Het
Rnase2b	A	T	14: 51,162,839 (GRCm38)	K126*	probably null	Het
Rpl3l	A	G	17: 24,730,871 (GRCm38)	I15V	probably benign	Het
Saal1	G	T	7: 46,702,545 (GRCm38)		probably null	Het
Sbpl	A	C	17: 23,953,254 (GRCm38)	D230E	unknown	Het
Scn10a	T	C	9: 119,666,490 (GRCm38)	Y322C	probably damaging	Het
Sec16a	A	T	2: 26,431,157 (GRCm38)	Y1308N	probably damaging	Het
Sis	A	T	3: 72,932,060 (GRCm38)	D824E	possibly damaging	Het
Slc25a36	A	G	9: 97,080,355 (GRCm38)	F194L	probably damaging	Het
Slc27a4	T	A	2: 29,811,190 (GRCm38)	V331E	probably damaging	Het
Slc7a11	G	T	3: 50,381,073 (GRCm38)		probably null	Het
Slco4c1	A	T	1: 96,841,172 (GRCm38)	S322T	probably damaging	Het
Smarcc2	A	T	10: 128,474,245 (GRCm38)	T376S	probably damaging	Het
Srebf1	C	T	11: 60,200,702 (GRCm38)	R999H	probably benign	Het
St3gal3	A	C	4: 118,107,662 (GRCm38)	M1R	probably null	Het
Syp	A	T	X: 7,648,705 (GRCm38)		probably benign	Homo
Tas1r2	A	G	4: 139,669,411 (GRCm38)	D687G	probably damaging	Het
Tekt4	A	T	17: 25,472,074 (GRCm38)	Q118L	probably benign	Het
Thoc2l	T	A	5: 104,518,257 (GRCm38)	I215N	probably damaging	Het
Tph2	T	C	10: 115,079,695 (GRCm38)	N480S	probably benign	Het
Tsc2	A	T	17: 24,608,973 (GRCm38)	M839K	probably damaging	Het
Ttc22	T	C	4: 106,622,780 (GRCm38)	F77S	probably damaging	Het
Uaca	C	T	9: 60,854,321 (GRCm38)	A205V	possibly damaging	Het
Ubp1	T	G	9: 113,944,835 (GRCm38)		probably benign	Het
Uhmk1	A	T	1: 170,208,653 (GRCm38)		probably null	Het
Usp17lc	A	G	7: 103,418,941 (GRCm38)	H481R	possibly damaging	Het
Vwa3a	A	G	7: 120,768,165 (GRCm38)	Y181C	probably damaging	Het
Wdr26	C	T	1: 181,185,934 (GRCm38)		probably benign	Het
Wfikkn2	G	A	11: 94,238,895 (GRCm38)	T140I	probably damaging	Het
Zfp704	G	T	3: 9,447,348 (GRCm38)	T288N	possibly damaging	Het
Zfp93	T	C	7: 24,276,096 (GRCm38)	V502A	probably damaging	Het
Zzef1	C	T	11: 72,924,679 (GRCm38)	P2942S	probably damaging	Het

Other mutations in Dido1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00425:Dido1	APN	2	180,683,989 (GRCm38)	missense	probably benign
IGL00834:Dido1	APN	2	180,689,526 (GRCm38)	missense	possibly damaging	0.87
IGL01317:Dido1	APN	2	180,671,757 (GRCm38)	missense	probably benign	0.17
IGL01588:Dido1	APN	2	180,688,875 (GRCm38)	missense	probably benign	0.00
IGL01834:Dido1	APN	2	180,684,031 (GRCm38)	splice site	probably benign
IGL02102:Dido1	APN	2	180,662,247 (GRCm38)	missense	possibly damaging	0.58
IGL02556:Dido1	APN	2	180,689,335 (GRCm38)	missense	possibly damaging	0.69
IGL02756:Dido1	APN	2	180,661,923 (GRCm38)	missense	probably benign	0.00
IGL02826:Dido1	APN	2	180,683,958 (GRCm38)	missense	probably benign
IGL02970:Dido1	APN	2	180,689,415 (GRCm38)	missense	probably damaging	0.99
IGL03110:Dido1	APN	2	180,689,342 (GRCm38)	missense	probably damaging	1.00
IGL03116:Dido1	APN	2	180,670,979 (GRCm38)	missense	probably damaging	1.00
3370:Dido1	UTSW	2	180,671,542 (GRCm38)	missense	probably benign
A4554:Dido1	UTSW	2	180,675,371 (GRCm38)	missense	probably damaging	1.00
H8441:Dido1	UTSW	2	180,689,014 (GRCm38)	missense	probably benign	0.12
R0044:Dido1	UTSW	2	180,661,819 (GRCm38)	missense	probably damaging	1.00
R0044:Dido1	UTSW	2	180,661,819 (GRCm38)	missense	probably damaging	1.00
R0054:Dido1	UTSW	2	180,661,474 (GRCm38)	missense	probably benign	0.00
R0054:Dido1	UTSW	2	180,661,474 (GRCm38)	missense	probably benign	0.00
R0127:Dido1	UTSW	2	180,671,824 (GRCm38)	missense	probably benign	0.01
R0620:Dido1	UTSW	2	180,659,851 (GRCm38)	missense	probably benign	0.26
R0734:Dido1	UTSW	2	180,660,042 (GRCm38)	missense	probably benign	0.01
R1390:Dido1	UTSW	2	180,685,124 (GRCm38)	missense	possibly damaging	0.70
R1445:Dido1	UTSW	2	180,671,470 (GRCm38)	missense	possibly damaging	0.62
R1466:Dido1	UTSW	2	180,662,328 (GRCm38)	missense	probably damaging	1.00
R1472:Dido1	UTSW	2	180,660,720 (GRCm38)	missense	probably benign	0.02
R1538:Dido1	UTSW	2	180,684,970 (GRCm38)	missense	possibly damaging	0.49
R1584:Dido1	UTSW	2	180,662,328 (GRCm38)	missense	probably damaging	1.00
R2020:Dido1	UTSW	2	180,659,585 (GRCm38)	missense	unknown
R2025:Dido1	UTSW	2	180,689,181 (GRCm38)	nonsense	probably null
R2026:Dido1	UTSW	2	180,689,181 (GRCm38)	nonsense	probably null
R2027:Dido1	UTSW	2	180,689,181 (GRCm38)	nonsense	probably null
R2089:Dido1	UTSW	2	180,661,884 (GRCm38)	missense	probably benign	0.29
R2091:Dido1	UTSW	2	180,661,884 (GRCm38)	missense	probably benign	0.29
R2091:Dido1	UTSW	2	180,661,884 (GRCm38)	missense	probably benign	0.29
R2495:Dido1	UTSW	2	180,689,388 (GRCm38)	missense	probably benign	0.00
R2931:Dido1	UTSW	2	180,661,653 (GRCm38)	missense	probably damaging	1.00
R3418:Dido1	UTSW	2	180,660,935 (GRCm38)	missense	possibly damaging	0.84
R3735:Dido1	UTSW	2	180,684,036 (GRCm38)	splice site	probably benign
R4523:Dido1	UTSW	2	180,672,292 (GRCm38)	missense	probably damaging	1.00
R4674:Dido1	UTSW	2	180,687,559 (GRCm38)	missense	probably damaging	0.97
R4729:Dido1	UTSW	2	180,687,650 (GRCm38)	missense	probably benign	0.00
R4762:Dido1	UTSW	2	180,689,575 (GRCm38)	missense	probably damaging	1.00
R4786:Dido1	UTSW	2	180,670,871 (GRCm38)	missense	possibly damaging	0.85
R4817:Dido1	UTSW	2	180,661,416 (GRCm38)	missense	probably benign	0.02
R4892:Dido1	UTSW	2	180,675,029 (GRCm38)	nonsense	probably null
R4979:Dido1	UTSW	2	180,660,813 (GRCm38)	missense	probably damaging	0.98
R5510:Dido1	UTSW	2	180,685,173 (GRCm38)	missense	probably benign	0.00
R5586:Dido1	UTSW	2	180,659,652 (GRCm38)	nonsense	probably null
R5672:Dido1	UTSW	2	180,671,903 (GRCm38)	missense	probably damaging	0.99
R5863:Dido1	UTSW	2	180,661,773 (GRCm38)	missense	probably benign	0.02
R5943:Dido1	UTSW	2	180,661,882 (GRCm38)	missense	probably benign	0.00
R5974:Dido1	UTSW	2	180,671,497 (GRCm38)	missense	probably benign	0.02
R6123:Dido1	UTSW	2	180,683,967 (GRCm38)	missense	probably benign	0.07
R6214:Dido1	UTSW	2	180,662,152 (GRCm38)	missense	probably damaging	1.00
R6215:Dido1	UTSW	2	180,662,152 (GRCm38)	missense	probably damaging	1.00
R6248:Dido1	UTSW	2	180,660,255 (GRCm38)	missense	probably damaging	1.00
R6285:Dido1	UTSW	2	180,661,147 (GRCm38)	missense	probably benign	0.00
R6349:Dido1	UTSW	2	180,660,701 (GRCm38)	missense	probably benign	0.03
R6437:Dido1	UTSW	2	180,675,013 (GRCm38)	missense	probably damaging	1.00
R6477:Dido1	UTSW	2	180,660,481 (GRCm38)	missense	probably benign	0.00
R6836:Dido1	UTSW	2	180,662,307 (GRCm38)	missense	probably benign	0.16
R7055:Dido1	UTSW	2	180,661,209 (GRCm38)	missense	probably benign	0.09
R7289:Dido1	UTSW	2	180,659,631 (GRCm38)	missense	unknown
R7304:Dido1	UTSW	2	180,687,493 (GRCm38)	missense	probably damaging	1.00
R7343:Dido1	UTSW	2	180,675,121 (GRCm38)	missense	possibly damaging	0.49
R7363:Dido1	UTSW	2	180,662,517 (GRCm38)	nonsense	probably null
R7429:Dido1	UTSW	2	180,689,526 (GRCm38)	missense	possibly damaging	0.87
R7594:Dido1	UTSW	2	180,675,112 (GRCm38)	missense	probably benign
R7629:Dido1	UTSW	2	180,661,473 (GRCm38)	missense	probably benign
R7899:Dido1	UTSW	2	180,671,597 (GRCm38)	missense	possibly damaging	0.82
R7946:Dido1	UTSW	2	180,661,708 (GRCm38)	missense	possibly damaging	0.81
R7951:Dido1	UTSW	2	180,670,881 (GRCm38)	missense	probably benign	0.01
R8033:Dido1	UTSW	2	180,674,842 (GRCm38)	missense	probably damaging	1.00
R8069:Dido1	UTSW	2	180,660,912 (GRCm38)	missense	probably benign
R8331:Dido1	UTSW	2	180,660,449 (GRCm38)	missense	probably benign	0.00
R8479:Dido1	UTSW	2	180,673,229 (GRCm38)	critical splice donor site	probably null
R8936:Dido1	UTSW	2	180,661,402 (GRCm38)	missense	probably benign
R9089:Dido1	UTSW	2	180,661,500 (GRCm38)	missense	probably benign	0.00
R9647:Dido1	UTSW	2	180,673,275 (GRCm38)	missense	probably benign	0.00
R9648:Dido1	UTSW	2	180,660,675 (GRCm38)	missense	probably damaging	1.00
R9784:Dido1	UTSW	2	180,683,561 (GRCm38)	missense	probably benign	0.27
V1024:Dido1	UTSW	2	180,689,014 (GRCm38)	missense	probably benign	0.12
X0011:Dido1	UTSW	2	180,660,834 (GRCm38)	missense	probably benign	0.00
X0019:Dido1	UTSW	2	180,671,572 (GRCm38)	missense	possibly damaging	0.62

Predicted Primers

PCR Primer
(F):5'- CCTTGGCCTTGGAATCCTGATGTG -3'
(R):5'- ATGAGAAGCGGACTCGACTCCAAC -3'

Sequencing Primer
(F):5'- TCCAGACGGCTCAAATGATTTC -3'
(R):5'- GGACTCGACTCCAACAGGAAG -3'

Posted On

2014-05-23