Incidental Mutation 'R8954:Idh2'
ID |
681833 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Idh2
|
Ensembl Gene |
ENSMUSG00000030541 |
Gene Name |
isocitrate dehydrogenase 2 (NADP+), mitochondrial |
Synonyms |
Idh-2, IDPm |
MMRRC Submission |
068790-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R8954 (G1)
|
Quality Score |
217.468 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
79744594-79765140 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
TCCCAGG to T
at 79748079 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000146084
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000107384]
[ENSMUST00000125542]
[ENSMUST00000134328]
[ENSMUST00000164056]
[ENSMUST00000206714]
|
AlphaFold |
P54071 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000107384
|
SMART Domains |
Protein: ENSMUSP00000103007 Gene: ENSMUSG00000030541
Domain | Start | End | E-Value | Type |
Iso_dh
|
49 |
441 |
5.32e-135 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000125542
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000134070
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134328
|
SMART Domains |
Protein: ENSMUSP00000118184 Gene: ENSMUSG00000030541
Domain | Start | End | E-Value | Type |
Iso_dh
|
49 |
284 |
1.59e-8 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000139178
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156761
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000164056
|
SMART Domains |
Protein: ENSMUSP00000132361 Gene: ENSMUSG00000048897
Domain | Start | End | E-Value | Type |
low complexity region
|
13 |
28 |
N/A |
INTRINSIC |
low complexity region
|
76 |
88 |
N/A |
INTRINSIC |
low complexity region
|
106 |
127 |
N/A |
INTRINSIC |
low complexity region
|
169 |
181 |
N/A |
INTRINSIC |
low complexity region
|
187 |
201 |
N/A |
INTRINSIC |
ZnF_C2H2
|
297 |
319 |
2.71e-2 |
SMART |
ZnF_C2H2
|
325 |
347 |
1.92e-2 |
SMART |
ZnF_C2H2
|
353 |
375 |
2.71e-2 |
SMART |
ZnF_C2H2
|
381 |
403 |
1.18e-2 |
SMART |
ZnF_C2H2
|
409 |
431 |
1.67e-2 |
SMART |
ZnF_C2H2
|
437 |
459 |
4.87e-4 |
SMART |
ZnF_C2H2
|
465 |
487 |
3.83e-2 |
SMART |
ZnF_C2H2
|
493 |
515 |
2.12e-4 |
SMART |
ZnF_C2H2
|
521 |
543 |
3.63e-3 |
SMART |
ZnF_C2H2
|
549 |
571 |
1.58e-3 |
SMART |
ZnF_C2H2
|
577 |
600 |
3.69e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000206714
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer. The protein encoded by this gene is the NADP(+)-dependent isocitrate dehydrogenase found in the mitochondria. It plays a role in intermediary metabolism and energy production. This protein may tightly associate or interact with the pyruvate dehydrogenase complex. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014] PHENOTYPE: Mice homozygous for a knock-out allele exhibit suppression of tumorigenesis from B16F10 melanoma cells. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
T |
A |
2: 93,688,299 (GRCm39) |
Y445F |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,594,583 (GRCm39) |
D815G |
probably damaging |
Het |
Adam4 |
T |
C |
12: 81,467,146 (GRCm39) |
S492G |
possibly damaging |
Het |
Anapc2 |
A |
G |
2: 25,170,490 (GRCm39) |
K643E |
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,641,317 (GRCm39) |
I630K |
possibly damaging |
Het |
Arhgap24 |
A |
G |
5: 103,040,136 (GRCm39) |
T361A |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,066,141 (GRCm39) |
M1571V |
probably benign |
Het |
Arid5b |
A |
C |
10: 67,937,810 (GRCm39) |
V196G |
possibly damaging |
Het |
Art2b |
C |
A |
7: 101,229,110 (GRCm39) |
|
probably null |
Het |
Asxl3 |
G |
A |
18: 22,650,807 (GRCm39) |
R932H |
probably damaging |
Het |
B3galnt1 |
T |
C |
3: 69,482,673 (GRCm39) |
N196S |
possibly damaging |
Het |
Brd10 |
A |
T |
19: 29,696,126 (GRCm39) |
N1122K |
possibly damaging |
Het |
C5ar2 |
C |
A |
7: 15,971,733 (GRCm39) |
V65F |
possibly damaging |
Het |
Cfap54 |
A |
T |
10: 92,879,255 (GRCm39) |
L403Q |
probably damaging |
Het |
Cfap74 |
G |
A |
4: 155,521,187 (GRCm39) |
E620K |
|
Het |
Chac1 |
C |
T |
2: 119,183,836 (GRCm39) |
A146V |
probably damaging |
Het |
Cpne2 |
T |
A |
8: 95,284,774 (GRCm39) |
S317T |
probably damaging |
Het |
Cux1 |
T |
A |
5: 136,402,203 (GRCm39) |
K138* |
probably null |
Het |
Cwc22 |
T |
A |
2: 77,754,937 (GRCm39) |
Y214F |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,525,197 (GRCm39) |
T167S |
probably benign |
Het |
Cyp4a12a |
T |
A |
4: 115,185,935 (GRCm39) |
Y414* |
probably null |
Het |
Dap3 |
A |
T |
3: 88,835,570 (GRCm39) |
D256E |
probably damaging |
Het |
Dmxl2 |
C |
T |
9: 54,381,156 (GRCm39) |
S110N |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,343,986 (GRCm39) |
I1777L |
probably benign |
Het |
Ecel1 |
G |
A |
1: 87,076,349 (GRCm39) |
Q717* |
probably null |
Het |
Efcab3 |
T |
G |
11: 104,909,525 (GRCm39) |
|
probably null |
Het |
Eif3j2 |
G |
A |
18: 43,610,699 (GRCm39) |
T38M |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 16,287,864 (GRCm39) |
H553R |
probably benign |
Het |
Fcho2 |
T |
C |
13: 98,913,985 (GRCm39) |
D204G |
probably benign |
Het |
Frmpd1 |
A |
T |
4: 45,284,702 (GRCm39) |
E1174D |
probably benign |
Het |
Gabra6 |
T |
A |
11: 42,205,959 (GRCm39) |
Y299F |
probably damaging |
Het |
Gak |
G |
A |
5: 108,777,518 (GRCm39) |
|
probably benign |
Het |
Gapdhs |
T |
A |
7: 30,432,591 (GRCm39) |
H214L |
probably damaging |
Het |
Gapvd1 |
T |
C |
2: 34,568,110 (GRCm39) |
Y1418C |
probably damaging |
Het |
Gk5 |
C |
A |
9: 96,059,562 (GRCm39) |
D471E |
probably benign |
Het |
Glg1 |
A |
G |
8: 111,914,527 (GRCm39) |
M419T |
probably damaging |
Het |
H2ac25 |
T |
A |
11: 58,845,785 (GRCm39) |
N74K |
possibly damaging |
Het |
Ice1 |
T |
C |
13: 70,758,697 (GRCm39) |
N215S |
probably damaging |
Het |
Ifitm10 |
T |
C |
7: 141,882,300 (GRCm39) |
N157D |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,676,545 (GRCm39) |
D911G |
possibly damaging |
Het |
Kcnt1 |
A |
G |
2: 25,784,338 (GRCm39) |
N247S |
probably benign |
Het |
Kirrel1 |
T |
C |
3: 86,997,173 (GRCm39) |
T265A |
probably benign |
Het |
Klhl29 |
A |
T |
12: 5,187,542 (GRCm39) |
L274H |
possibly damaging |
Het |
Kmt2b |
T |
G |
7: 30,273,640 (GRCm39) |
T2326P |
probably damaging |
Het |
Lcn11 |
A |
G |
2: 25,669,265 (GRCm39) |
S141G |
probably benign |
Het |
Ldb3 |
T |
C |
14: 34,277,301 (GRCm39) |
R358G |
probably null |
Het |
Ldlr |
G |
A |
9: 21,650,828 (GRCm39) |
D446N |
possibly damaging |
Het |
Lipt2 |
T |
C |
7: 99,809,449 (GRCm39) |
F179L |
probably damaging |
Het |
Lmbrd1 |
G |
T |
1: 24,745,121 (GRCm39) |
V154F |
possibly damaging |
Het |
Malrd1 |
A |
G |
2: 15,556,178 (GRCm39) |
I99V |
|
Het |
Map1b |
T |
A |
13: 99,570,735 (GRCm39) |
E662V |
unknown |
Het |
Mfsd11 |
T |
C |
11: 116,750,162 (GRCm39) |
S100P |
probably damaging |
Het |
Mgst1 |
C |
T |
6: 138,119,967 (GRCm39) |
|
probably benign |
Het |
Mtf1 |
T |
A |
4: 124,698,649 (GRCm39) |
V49D |
probably damaging |
Het |
Mtss1 |
T |
C |
15: 58,826,986 (GRCm39) |
D236G |
probably damaging |
Het |
Myct1 |
C |
T |
10: 5,554,208 (GRCm39) |
T25I |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,143,806 (GRCm39) |
F1089I |
possibly damaging |
Het |
Nrxn1 |
A |
T |
17: 90,897,615 (GRCm39) |
I835K |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,163,394 (GRCm39) |
S595T |
probably damaging |
Het |
Nt5c2 |
A |
T |
19: 46,877,361 (GRCm39) |
S527T |
probably damaging |
Het |
Or52m1 |
T |
C |
7: 102,289,882 (GRCm39) |
V143A |
probably benign |
Het |
Or56b2 |
T |
A |
7: 104,337,900 (GRCm39) |
L226* |
probably null |
Het |
Or5k3 |
T |
A |
16: 58,969,319 (GRCm39) |
Y35* |
probably null |
Het |
Or7e175 |
A |
T |
9: 20,048,664 (GRCm39) |
D84V |
probably damaging |
Het |
Or8k28 |
C |
A |
2: 86,285,892 (GRCm39) |
C241F |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,108,053 (GRCm39) |
S350G |
probably benign |
Het |
Otoa |
G |
A |
7: 120,744,741 (GRCm39) |
W833* |
probably null |
Het |
Pcdhga6 |
T |
G |
18: 37,841,540 (GRCm39) |
I420S |
probably damaging |
Het |
Pmfbp1 |
A |
C |
8: 110,258,433 (GRCm39) |
M666L |
probably benign |
Het |
Pola2 |
T |
G |
19: 5,998,452 (GRCm39) |
D370A |
probably damaging |
Het |
Ppip5k1 |
C |
G |
2: 121,153,701 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
A |
T |
1: 134,762,200 (GRCm39) |
D815E |
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,155,669 (GRCm39) |
V545E |
possibly damaging |
Het |
Ptpn23 |
A |
T |
9: 110,221,568 (GRCm39) |
N177K |
probably damaging |
Het |
Rad9b |
A |
T |
5: 122,482,293 (GRCm39) |
S147R |
probably benign |
Het |
Rps20 |
T |
A |
4: 3,834,617 (GRCm39) |
M82L |
probably benign |
Het |
Samd9l |
C |
T |
6: 3,374,577 (GRCm39) |
V895I |
probably damaging |
Het |
Sbf2 |
T |
A |
7: 110,038,118 (GRCm39) |
K396* |
probably null |
Het |
Sbno2 |
G |
T |
10: 79,893,796 (GRCm39) |
Q1198K |
probably damaging |
Het |
Scp2d1 |
C |
T |
2: 144,665,886 (GRCm39) |
T75I |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,433,431 (GRCm39) |
I1392N |
possibly damaging |
Het |
Sidt1 |
A |
G |
16: 44,082,390 (GRCm39) |
F532L |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,755,752 (GRCm39) |
V243D |
probably damaging |
Het |
Smg1 |
T |
C |
7: 117,806,215 (GRCm39) |
R185G |
probably damaging |
Het |
Spag16 |
C |
T |
1: 70,036,004 (GRCm39) |
S344F |
|
Het |
Spata31f3 |
G |
T |
4: 42,871,753 (GRCm39) |
D207E |
probably damaging |
Het |
Spsb3 |
A |
G |
17: 25,110,493 (GRCm39) |
D440G |
probably damaging |
Het |
Themis |
A |
C |
10: 28,665,709 (GRCm39) |
S591R |
probably benign |
Het |
Trpm1 |
G |
A |
7: 63,858,089 (GRCm39) |
V177I |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,514,143 (GRCm39) |
|
probably null |
Het |
Vmn1r171 |
C |
T |
7: 23,332,525 (GRCm39) |
T238I |
probably damaging |
Het |
Vmn2r33 |
T |
C |
7: 7,554,655 (GRCm39) |
M633V |
probably benign |
Het |
Vmn2r93 |
T |
A |
17: 18,546,252 (GRCm39) |
L708H |
probably damaging |
Het |
Vps35l |
A |
T |
7: 118,393,801 (GRCm39) |
T450S |
possibly damaging |
Het |
Wdr53 |
T |
A |
16: 32,075,473 (GRCm39) |
V226E |
probably damaging |
Het |
Wdr62 |
T |
A |
7: 29,953,454 (GRCm39) |
I193F |
probably damaging |
Het |
Zfp607b |
T |
A |
7: 27,403,387 (GRCm39) |
D614E |
probably benign |
Het |
|
Other mutations in Idh2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01529:Idh2
|
APN |
7 |
79,747,693 (GRCm39) |
missense |
probably benign |
|
IGL02281:Idh2
|
APN |
7 |
79,745,550 (GRCm39) |
splice site |
probably null |
|
IGL02874:Idh2
|
APN |
7 |
79,747,621 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02892:Idh2
|
APN |
7 |
79,745,418 (GRCm39) |
missense |
probably benign |
|
IGL02937:Idh2
|
APN |
7 |
79,748,661 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02989:Idh2
|
APN |
7 |
79,748,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Idh2
|
UTSW |
7 |
79,747,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Idh2
|
UTSW |
7 |
79,747,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Idh2
|
UTSW |
7 |
79,747,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R0322:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0386:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Idh2
|
UTSW |
7 |
79,748,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R1603:Idh2
|
UTSW |
7 |
79,748,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Idh2
|
UTSW |
7 |
79,748,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Idh2
|
UTSW |
7 |
79,748,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1844:Idh2
|
UTSW |
7 |
79,748,625 (GRCm39) |
missense |
probably benign |
0.31 |
R3700:Idh2
|
UTSW |
7 |
79,748,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Idh2
|
UTSW |
7 |
79,745,847 (GRCm39) |
missense |
probably damaging |
0.98 |
R5234:Idh2
|
UTSW |
7 |
79,745,853 (GRCm39) |
missense |
probably damaging |
0.99 |
R5387:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R5582:Idh2
|
UTSW |
7 |
79,748,087 (GRCm39) |
frame shift |
probably null |
|
R5655:Idh2
|
UTSW |
7 |
79,747,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R6191:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6261:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R6311:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6351:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6413:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6561:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6709:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6772:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6781:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6848:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R6861:Idh2
|
UTSW |
7 |
79,747,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R6899:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7063:Idh2
|
UTSW |
7 |
79,745,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R7076:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7081:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R7090:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7254:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
frame shift |
probably null |
|
R7298:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7401:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R7560:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
frame shift |
probably null |
|
R7561:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7694:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7816:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7884:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R7919:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R7961:Idh2
|
UTSW |
7 |
79,748,001 (GRCm39) |
missense |
probably benign |
0.18 |
R8009:Idh2
|
UTSW |
7 |
79,748,001 (GRCm39) |
missense |
probably benign |
0.18 |
R8036:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8162:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R8321:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8451:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8488:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R8501:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8671:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8673:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8707:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R8725:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
frame shift |
probably null |
|
R8863:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8872:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8892:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8915:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8935:Idh2
|
UTSW |
7 |
79,764,946 (GRCm39) |
missense |
probably benign |
0.00 |
R8951:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R8985:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9101:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9111:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9138:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
frame shift |
probably null |
|
R9138:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
R9140:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9555:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9580:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9614:Idh2
|
UTSW |
7 |
79,747,925 (GRCm39) |
nonsense |
probably null |
|
R9619:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9697:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9756:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
R9790:Idh2
|
UTSW |
7 |
79,748,079 (GRCm39) |
intron |
probably benign |
|
RF030:Idh2
|
UTSW |
7 |
79,748,077 (GRCm39) |
intron |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- GAGGTTGTTACTTGTCAAAGATCTCC -3'
(R):5'- CAGTAGGCGGCTTAAACAAGC -3'
Sequencing Primer
(F):5'- GTCAAAGATCTCCTGGAAGATGTC -3'
(R):5'- GCCTGTACCAGCTATAAGGTCTAG -3'
|
Posted On |
2021-08-31 |