Incidental Mutation 'R1472:Dido1'
ID |
164971 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dido1
|
Ensembl Gene |
ENSMUSG00000038914 |
Gene Name |
death inducer-obliterator 1 |
Synonyms |
D130048F08Rik, Datf1, 6720461J16Rik, dido, DIO-1, C130092D22Rik |
MMRRC Submission |
039525-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.960)
|
Stock # |
R1472 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
2 |
Chromosomal Location |
180299757-180351792 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 180302513 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Serine
at position 1797
(N1797S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000084794
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000087517]
|
AlphaFold |
Q8C9B9 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000087517
AA Change: N1797S
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
SMART Domains |
Protein: ENSMUSP00000084794 Gene: ENSMUSG00000038914 AA Change: N1797S
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 |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 96.0%
- 20x: 92.0%
|
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: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,773,313 (GRCm39) |
T834M |
possibly damaging |
Het |
Ak1 |
T |
C |
2: 32,520,313 (GRCm39) |
L32P |
probably damaging |
Het |
Ankrd24 |
A |
G |
10: 81,470,754 (GRCm39) |
D61G |
probably damaging |
Het |
Atp13a2 |
T |
C |
4: 140,721,113 (GRCm39) |
S99P |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Bmp10 |
A |
G |
6: 87,410,779 (GRCm39) |
I191V |
probably benign |
Het |
C2cd6 |
A |
T |
1: 59,106,944 (GRCm39) |
S294T |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,962,743 (GRCm39) |
K20* |
probably null |
Het |
Caps2 |
C |
T |
10: 112,015,377 (GRCm39) |
T139I |
probably benign |
Het |
Cdc25a |
T |
C |
9: 109,705,157 (GRCm39) |
S34P |
probably benign |
Het |
Cenpv |
T |
C |
11: 62,427,121 (GRCm39) |
I146V |
probably benign |
Het |
Cep57 |
A |
T |
9: 13,732,850 (GRCm39) |
F32I |
probably benign |
Het |
Cep85 |
A |
G |
4: 133,894,711 (GRCm39) |
W32R |
probably damaging |
Het |
Cntrl |
T |
C |
2: 35,059,329 (GRCm39) |
|
probably null |
Het |
Cpd |
A |
G |
11: 76,675,224 (GRCm39) |
V1299A |
probably damaging |
Het |
Cpne6 |
T |
C |
14: 55,752,092 (GRCm39) |
V283A |
probably benign |
Het |
Crot |
A |
G |
5: 9,016,941 (GRCm39) |
C584R |
probably damaging |
Het |
Ctsc |
A |
C |
7: 87,930,670 (GRCm39) |
H83P |
possibly damaging |
Het |
Dlgap4 |
C |
T |
2: 156,602,821 (GRCm39) |
Q148* |
probably null |
Het |
Dnah3 |
T |
C |
7: 119,670,181 (GRCm39) |
D688G |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,843,472 (GRCm39) |
E138G |
probably benign |
Het |
Edc4 |
T |
A |
8: 106,619,460 (GRCm39) |
M1396K |
probably damaging |
Het |
Haao |
T |
A |
17: 84,146,267 (GRCm39) |
Q69L |
probably benign |
Het |
Hsd3b6 |
A |
T |
3: 98,715,255 (GRCm39) |
|
probably null |
Het |
Itpr3 |
T |
A |
17: 27,333,199 (GRCm39) |
I1937N |
probably benign |
Het |
Kcnk15 |
C |
A |
2: 163,700,127 (GRCm39) |
T103K |
probably damaging |
Het |
Kifc3 |
A |
G |
8: 95,864,541 (GRCm39) |
|
probably null |
Het |
Lama3 |
T |
A |
18: 12,615,102 (GRCm39) |
F1342Y |
probably benign |
Het |
Lilra6 |
A |
T |
7: 3,915,718 (GRCm39) |
M98K |
probably damaging |
Het |
Map3k21 |
T |
C |
8: 126,668,417 (GRCm39) |
S668P |
probably benign |
Het |
Mcpt8 |
T |
C |
14: 56,319,791 (GRCm39) |
T220A |
probably benign |
Het |
Mettl13 |
C |
T |
1: 162,364,736 (GRCm39) |
V548I |
possibly damaging |
Het |
Mfsd4b4 |
A |
G |
10: 39,767,860 (GRCm39) |
M411T |
probably benign |
Het |
Mrfap1 |
A |
G |
5: 36,953,817 (GRCm39) |
S41P |
possibly damaging |
Het |
Mroh2b |
A |
G |
15: 4,978,137 (GRCm39) |
I1302V |
probably benign |
Het |
Mrpl45 |
C |
T |
11: 97,214,681 (GRCm39) |
R123* |
probably null |
Het |
Mstn |
T |
A |
1: 53,101,157 (GRCm39) |
I78K |
probably damaging |
Het |
Mtdh |
T |
C |
15: 34,114,191 (GRCm39) |
S168P |
possibly damaging |
Het |
Muc15 |
G |
T |
2: 110,561,905 (GRCm39) |
V114F |
probably damaging |
Het |
Muc6 |
T |
C |
7: 141,238,144 (GRCm39) |
E112G |
probably benign |
Het |
Myocd |
G |
T |
11: 65,078,330 (GRCm39) |
H360Q |
probably benign |
Het |
Naip2 |
C |
T |
13: 100,298,368 (GRCm39) |
G556D |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,563,802 (GRCm39) |
E1627G |
probably damaging |
Het |
Nlrp14 |
T |
C |
7: 106,781,910 (GRCm39) |
L369P |
probably benign |
Het |
Nlrp6 |
A |
G |
7: 140,503,408 (GRCm39) |
T505A |
probably damaging |
Het |
Npbwr1 |
T |
C |
1: 5,986,900 (GRCm39) |
S205G |
probably damaging |
Het |
Nsmaf |
G |
A |
4: 6,423,448 (GRCm39) |
R307* |
probably null |
Het |
Or5h19 |
A |
T |
16: 58,856,920 (GRCm39) |
L60Q |
probably damaging |
Het |
Or9i1b |
T |
C |
19: 13,897,208 (GRCm39) |
S275P |
probably damaging |
Het |
Parp9 |
T |
G |
16: 35,774,050 (GRCm39) |
S341A |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,289,533 (GRCm39) |
N346S |
probably benign |
Het |
Pikfyve |
T |
A |
1: 65,263,360 (GRCm39) |
F503Y |
probably damaging |
Het |
Polr1e |
G |
T |
4: 45,028,026 (GRCm39) |
A290S |
probably damaging |
Het |
Ppp1r21 |
A |
T |
17: 88,866,033 (GRCm39) |
H305L |
probably damaging |
Het |
Prss47 |
A |
G |
13: 65,197,103 (GRCm39) |
L117P |
probably damaging |
Het |
Psmb2 |
A |
G |
4: 126,580,825 (GRCm39) |
Y73C |
probably damaging |
Het |
Rcn2 |
C |
T |
9: 55,963,537 (GRCm39) |
P222L |
probably benign |
Het |
Rnf144b |
T |
C |
13: 47,396,361 (GRCm39) |
Y233H |
probably damaging |
Het |
Rnf17 |
T |
C |
14: 56,665,436 (GRCm39) |
L196P |
probably damaging |
Het |
Sik2 |
A |
G |
9: 50,920,111 (GRCm39) |
I22T |
probably damaging |
Het |
Sis |
A |
G |
3: 72,796,360 (GRCm39) |
V1807A |
probably benign |
Het |
Slc1a2 |
T |
A |
2: 102,568,254 (GRCm39) |
I88N |
probably damaging |
Het |
Slc22a22 |
A |
G |
15: 57,110,916 (GRCm39) |
F437S |
probably benign |
Het |
Slc39a13 |
A |
T |
2: 90,899,050 (GRCm39) |
C20* |
probably null |
Het |
Sos2 |
C |
T |
12: 69,632,090 (GRCm39) |
|
probably null |
Het |
Sst |
A |
G |
16: 23,709,448 (GRCm39) |
V16A |
probably benign |
Het |
Stab1 |
C |
T |
14: 30,863,543 (GRCm39) |
G2073D |
probably benign |
Het |
Stxbp1 |
A |
T |
2: 32,684,648 (GRCm39) |
S594T |
probably benign |
Het |
Sugct |
A |
T |
13: 17,627,131 (GRCm39) |
C241S |
probably benign |
Het |
Svil |
T |
A |
18: 5,048,950 (GRCm39) |
C76S |
probably benign |
Het |
Tcaf1 |
A |
G |
6: 42,663,382 (GRCm39) |
V166A |
possibly damaging |
Het |
Tmem131 |
A |
T |
1: 36,855,322 (GRCm39) |
N801K |
possibly damaging |
Het |
Tox3 |
T |
C |
8: 90,980,973 (GRCm39) |
N277S |
probably damaging |
Het |
Tril |
G |
T |
6: 53,795,012 (GRCm39) |
R737S |
probably damaging |
Het |
Trpm2 |
C |
A |
10: 77,801,841 (GRCm39) |
V75L |
probably damaging |
Het |
Tshz1 |
A |
C |
18: 84,031,930 (GRCm39) |
L826R |
possibly damaging |
Het |
Ttn |
C |
T |
2: 76,597,196 (GRCm39) |
V19906I |
probably damaging |
Het |
Wnt5a |
C |
T |
14: 28,240,461 (GRCm39) |
R184* |
probably null |
Het |
Wnt5b |
G |
A |
6: 119,410,442 (GRCm39) |
R333C |
probably damaging |
Het |
Zbtb6 |
T |
C |
2: 37,319,356 (GRCm39) |
T191A |
probably benign |
Het |
Zc3h4 |
A |
G |
7: 16,168,695 (GRCm39) |
N935D |
unknown |
Het |
Zc3h7a |
C |
T |
16: 10,978,890 (GRCm39) |
R95H |
probably damaging |
Het |
Zfp110 |
T |
C |
7: 12,582,468 (GRCm39) |
V372A |
possibly damaging |
Het |
Zmym2 |
C |
T |
14: 57,148,640 (GRCm39) |
S318L |
probably benign |
Het |
|
Other mutations in Dido1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Dido1
|
APN |
2 |
180,325,782 (GRCm39) |
missense |
probably benign |
|
IGL00834:Dido1
|
APN |
2 |
180,331,319 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01317:Dido1
|
APN |
2 |
180,313,550 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01588:Dido1
|
APN |
2 |
180,330,668 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01834:Dido1
|
APN |
2 |
180,325,824 (GRCm39) |
splice site |
probably benign |
|
IGL02102:Dido1
|
APN |
2 |
180,304,040 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL02556:Dido1
|
APN |
2 |
180,331,128 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02756:Dido1
|
APN |
2 |
180,303,716 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02826:Dido1
|
APN |
2 |
180,325,751 (GRCm39) |
missense |
probably benign |
|
IGL02970:Dido1
|
APN |
2 |
180,331,208 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03110:Dido1
|
APN |
2 |
180,331,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03116:Dido1
|
APN |
2 |
180,312,772 (GRCm39) |
missense |
probably damaging |
1.00 |
3370:Dido1
|
UTSW |
2 |
180,313,335 (GRCm39) |
missense |
probably benign |
|
A4554:Dido1
|
UTSW |
2 |
180,317,164 (GRCm39) |
missense |
probably damaging |
1.00 |
H8441:Dido1
|
UTSW |
2 |
180,330,807 (GRCm39) |
missense |
probably benign |
0.12 |
R0044:Dido1
|
UTSW |
2 |
180,303,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Dido1
|
UTSW |
2 |
180,303,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R0054:Dido1
|
UTSW |
2 |
180,303,267 (GRCm39) |
missense |
probably benign |
0.00 |
R0054:Dido1
|
UTSW |
2 |
180,303,267 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Dido1
|
UTSW |
2 |
180,313,617 (GRCm39) |
missense |
probably benign |
0.01 |
R0620:Dido1
|
UTSW |
2 |
180,301,644 (GRCm39) |
missense |
probably benign |
0.26 |
R0734:Dido1
|
UTSW |
2 |
180,301,835 (GRCm39) |
missense |
probably benign |
0.01 |
R1390:Dido1
|
UTSW |
2 |
180,326,917 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1445:Dido1
|
UTSW |
2 |
180,313,263 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1466:Dido1
|
UTSW |
2 |
180,304,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Dido1
|
UTSW |
2 |
180,304,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1538:Dido1
|
UTSW |
2 |
180,326,763 (GRCm39) |
missense |
possibly damaging |
0.49 |
R1584:Dido1
|
UTSW |
2 |
180,304,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Dido1
|
UTSW |
2 |
180,301,378 (GRCm39) |
missense |
unknown |
|
R2025:Dido1
|
UTSW |
2 |
180,330,974 (GRCm39) |
nonsense |
probably null |
|
R2026:Dido1
|
UTSW |
2 |
180,330,974 (GRCm39) |
nonsense |
probably null |
|
R2027:Dido1
|
UTSW |
2 |
180,330,974 (GRCm39) |
nonsense |
probably null |
|
R2089:Dido1
|
UTSW |
2 |
180,303,677 (GRCm39) |
missense |
probably benign |
0.29 |
R2091:Dido1
|
UTSW |
2 |
180,303,677 (GRCm39) |
missense |
probably benign |
0.29 |
R2091:Dido1
|
UTSW |
2 |
180,303,677 (GRCm39) |
missense |
probably benign |
0.29 |
R2495:Dido1
|
UTSW |
2 |
180,331,181 (GRCm39) |
missense |
probably benign |
0.00 |
R2931:Dido1
|
UTSW |
2 |
180,303,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Dido1
|
UTSW |
2 |
180,302,728 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3735:Dido1
|
UTSW |
2 |
180,325,829 (GRCm39) |
splice site |
probably benign |
|
R4523:Dido1
|
UTSW |
2 |
180,314,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4674:Dido1
|
UTSW |
2 |
180,329,352 (GRCm39) |
missense |
probably damaging |
0.97 |
R4729:Dido1
|
UTSW |
2 |
180,329,443 (GRCm39) |
missense |
probably benign |
0.00 |
R4762:Dido1
|
UTSW |
2 |
180,331,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Dido1
|
UTSW |
2 |
180,312,664 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4817:Dido1
|
UTSW |
2 |
180,303,209 (GRCm39) |
missense |
probably benign |
0.02 |
R4892:Dido1
|
UTSW |
2 |
180,316,822 (GRCm39) |
nonsense |
probably null |
|
R4979:Dido1
|
UTSW |
2 |
180,302,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R5510:Dido1
|
UTSW |
2 |
180,326,966 (GRCm39) |
missense |
probably benign |
0.00 |
R5586:Dido1
|
UTSW |
2 |
180,301,445 (GRCm39) |
nonsense |
probably null |
|
R5672:Dido1
|
UTSW |
2 |
180,313,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R5863:Dido1
|
UTSW |
2 |
180,303,566 (GRCm39) |
missense |
probably benign |
0.02 |
R5943:Dido1
|
UTSW |
2 |
180,303,675 (GRCm39) |
missense |
probably benign |
0.00 |
R5974:Dido1
|
UTSW |
2 |
180,313,290 (GRCm39) |
missense |
probably benign |
0.02 |
R6123:Dido1
|
UTSW |
2 |
180,325,760 (GRCm39) |
missense |
probably benign |
0.07 |
R6214:Dido1
|
UTSW |
2 |
180,303,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6215:Dido1
|
UTSW |
2 |
180,303,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Dido1
|
UTSW |
2 |
180,302,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Dido1
|
UTSW |
2 |
180,302,940 (GRCm39) |
missense |
probably benign |
0.00 |
R6349:Dido1
|
UTSW |
2 |
180,302,494 (GRCm39) |
missense |
probably benign |
0.03 |
R6437:Dido1
|
UTSW |
2 |
180,316,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Dido1
|
UTSW |
2 |
180,302,274 (GRCm39) |
missense |
probably benign |
0.00 |
R6836:Dido1
|
UTSW |
2 |
180,304,100 (GRCm39) |
missense |
probably benign |
0.16 |
R7055:Dido1
|
UTSW |
2 |
180,303,002 (GRCm39) |
missense |
probably benign |
0.09 |
R7289:Dido1
|
UTSW |
2 |
180,301,424 (GRCm39) |
missense |
unknown |
|
R7304:Dido1
|
UTSW |
2 |
180,329,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Dido1
|
UTSW |
2 |
180,316,914 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7363:Dido1
|
UTSW |
2 |
180,304,310 (GRCm39) |
nonsense |
probably null |
|
R7429:Dido1
|
UTSW |
2 |
180,331,319 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7594:Dido1
|
UTSW |
2 |
180,316,905 (GRCm39) |
missense |
probably benign |
|
R7629:Dido1
|
UTSW |
2 |
180,303,266 (GRCm39) |
missense |
probably benign |
|
R7899:Dido1
|
UTSW |
2 |
180,313,390 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7946:Dido1
|
UTSW |
2 |
180,303,501 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7951:Dido1
|
UTSW |
2 |
180,312,674 (GRCm39) |
missense |
probably benign |
0.01 |
R8033:Dido1
|
UTSW |
2 |
180,316,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Dido1
|
UTSW |
2 |
180,302,705 (GRCm39) |
missense |
probably benign |
|
R8331:Dido1
|
UTSW |
2 |
180,302,242 (GRCm39) |
missense |
probably benign |
0.00 |
R8479:Dido1
|
UTSW |
2 |
180,315,022 (GRCm39) |
critical splice donor site |
probably null |
|
R8936:Dido1
|
UTSW |
2 |
180,303,195 (GRCm39) |
missense |
probably benign |
|
R9089:Dido1
|
UTSW |
2 |
180,303,293 (GRCm39) |
missense |
probably benign |
0.00 |
R9647:Dido1
|
UTSW |
2 |
180,315,068 (GRCm39) |
missense |
probably benign |
0.00 |
R9648:Dido1
|
UTSW |
2 |
180,302,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R9784:Dido1
|
UTSW |
2 |
180,325,354 (GRCm39) |
missense |
probably benign |
0.27 |
V1024:Dido1
|
UTSW |
2 |
180,330,807 (GRCm39) |
missense |
probably benign |
0.12 |
X0011:Dido1
|
UTSW |
2 |
180,302,627 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Dido1
|
UTSW |
2 |
180,313,365 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
Predicted Primers |
PCR Primer
(F):5'- CGTCTCTGGCCTCCAAACTGAAAG -3'
(R):5'- GTGCTCAGTCTGCTGGGAAGAATG -3'
Sequencing Primer
(F):5'- GATCTGGCCCTTCACACTGAG -3'
(R):5'- TGACAGCCCAGTAGCTGATATG -3'
|
Posted On |
2014-03-28 |