Incidental Mutation 'R0834:Cluh'
| ID |
77742 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Cluh
|
| Ensembl Gene |
ENSMUSG00000020741 |
| Gene Name |
clustered mitochondria homolog |
| Synonyms |
1300001I01Rik |
| MMRRC Submission |
039013-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.205)
|
| Stock # |
R0834 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
74540321-74561673 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 74554631 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 737
(V737A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000113371
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000092915]
[ENSMUST00000117818]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000092915
AA Change: V737A
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000090593
Gene: ENSMUSG00000020741
AA Change: V737A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CLU_N
|
104 |
177 |
3.1e-28 |
PFAM |
|
Pfam:CLU
|
394 |
614 |
3.4e-89 |
PFAM |
|
Pfam:eIF3_p135
|
806 |
988 |
1.3e-58 |
PFAM |
|
Pfam:TPR_10
|
1059 |
1100 |
2.9e-7 |
PFAM |
|
low complexity region
|
1114 |
1125 |
N/A |
INTRINSIC |
|
Pfam:TPR_12
|
1140 |
1218 |
1.7e-10 |
PFAM |
|
low complexity region
|
1316 |
1334 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000117818
AA Change: V737A
PolyPhen 2
Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000113371
Gene: ENSMUSG00000020741
AA Change: V737A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CLU_N
|
102 |
177 |
9.8e-30 |
PFAM |
|
Pfam:CLU
|
394 |
615 |
5.3e-92 |
PFAM |
|
Pfam:eIF3_p135
|
796 |
938 |
2.9e-38 |
PFAM |
|
Pfam:TPR_10
|
1008 |
1049 |
9.5e-7 |
PFAM |
|
low complexity region
|
1063 |
1074 |
N/A |
INTRINSIC |
|
Pfam:TPR_12
|
1089 |
1167 |
1.1e-9 |
PFAM |
|
low complexity region
|
1265 |
1283 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128155
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000155558
|
| Meta Mutation Damage Score |
0.1257 |
| Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.7%
- 20x: 95.7%
|
| Validation Efficiency |
100% (86/86) |
| MGI Phenotype |
PHENOTYPE: Constitutive homozygous KO affects liver mitochondrial function and leads to neonatal lethality. Conditional homozygous KO in the adult liver affects cellular respiration under energy stress conditions. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Add2 |
A |
T |
6: 86,063,899 (GRCm39) |
E66V |
probably damaging |
Het |
| Aldh1a3 |
T |
C |
7: 66,062,658 (GRCm39) |
I156V |
probably benign |
Het |
| Ang4 |
T |
A |
14: 52,001,725 (GRCm39) |
K74N |
probably benign |
Het |
| Arcn1 |
A |
T |
9: 44,670,172 (GRCm39) |
|
probably benign |
Het |
| Arhgef33 |
T |
A |
17: 80,655,026 (GRCm39) |
|
probably benign |
Het |
| Atn1 |
A |
G |
6: 124,720,188 (GRCm39) |
|
probably benign |
Het |
| Bmal2 |
A |
G |
6: 146,724,185 (GRCm39) |
H359R |
probably damaging |
Het |
| Bmerb1 |
T |
C |
16: 13,911,795 (GRCm39) |
L47P |
probably damaging |
Het |
| Brip1 |
T |
C |
11: 86,083,653 (GRCm39) |
T123A |
probably benign |
Het |
| Camkv |
A |
G |
9: 107,823,045 (GRCm39) |
Y95C |
probably damaging |
Het |
| Cdk12 |
T |
A |
11: 98,095,211 (GRCm39) |
S340T |
probably benign |
Het |
| Ckap2l |
G |
A |
2: 129,138,224 (GRCm39) |
|
probably benign |
Het |
| Clmn |
A |
T |
12: 104,738,085 (GRCm39) |
L1042Q |
probably damaging |
Het |
| Clmn |
G |
T |
12: 104,738,086 (GRCm39) |
L1042M |
probably damaging |
Het |
| Cpne8 |
A |
G |
15: 90,424,462 (GRCm39) |
V309A |
probably benign |
Het |
| Cpxm2 |
T |
A |
7: 131,756,342 (GRCm39) |
|
probably benign |
Het |
| Csmd3 |
A |
T |
15: 47,747,073 (GRCm39) |
|
probably benign |
Het |
| Ctr9 |
T |
A |
7: 110,650,159 (GRCm39) |
S818T |
probably benign |
Het |
| Cyp26a1 |
C |
T |
19: 37,688,405 (GRCm39) |
A309V |
probably damaging |
Het |
| Dbndd2 |
C |
T |
2: 164,332,122 (GRCm39) |
T115I |
possibly damaging |
Het |
| Dhcr7 |
A |
G |
7: 143,394,964 (GRCm39) |
N157S |
probably benign |
Het |
| Dlx2 |
C |
A |
2: 71,375,859 (GRCm39) |
V155F |
probably damaging |
Het |
| Duox1 |
A |
T |
2: 122,176,982 (GRCm39) |
I1470F |
probably damaging |
Het |
| Esrrb |
A |
T |
12: 86,517,071 (GRCm39) |
I68F |
probably benign |
Het |
| Fhod3 |
T |
A |
18: 25,248,862 (GRCm39) |
L1347* |
probably null |
Het |
| Fip1l1 |
T |
C |
5: 74,755,721 (GRCm39) |
|
probably benign |
Het |
| Frem3 |
A |
G |
8: 81,413,637 (GRCm39) |
Y1966C |
probably damaging |
Het |
| Gatd3a |
T |
C |
10: 77,998,539 (GRCm39) |
D229G |
probably damaging |
Het |
| Ggt5 |
C |
T |
10: 75,440,604 (GRCm39) |
R242C |
possibly damaging |
Het |
| Gm14496 |
G |
A |
2: 181,637,480 (GRCm39) |
V185I |
probably benign |
Het |
| Gnptab |
T |
C |
10: 88,265,814 (GRCm39) |
V409A |
probably damaging |
Het |
| Gramd1a |
A |
G |
7: 30,837,589 (GRCm39) |
F390S |
possibly damaging |
Het |
| Helz2 |
A |
G |
2: 180,872,570 (GRCm39) |
S2477P |
probably damaging |
Het |
| Hsd17b3 |
T |
C |
13: 64,236,936 (GRCm39) |
K3E |
probably benign |
Het |
| Ift172 |
T |
C |
5: 31,414,715 (GRCm39) |
H1395R |
probably benign |
Het |
| Jam2 |
T |
A |
16: 84,609,855 (GRCm39) |
C180S |
probably damaging |
Het |
| Kalrn |
A |
C |
16: 33,870,289 (GRCm39) |
S160A |
possibly damaging |
Het |
| Kcnk3 |
T |
C |
5: 30,779,979 (GRCm39) |
I343T |
probably damaging |
Het |
| Kif13a |
T |
C |
13: 46,967,712 (GRCm39) |
E334G |
probably damaging |
Het |
| Klhl41 |
A |
G |
2: 69,508,491 (GRCm39) |
K482E |
possibly damaging |
Het |
| Lig3 |
A |
G |
11: 82,689,113 (GRCm39) |
E794G |
probably damaging |
Het |
| Myh13 |
T |
C |
11: 67,240,436 (GRCm39) |
M780T |
possibly damaging |
Het |
| Ndst2 |
A |
G |
14: 20,779,761 (GRCm39) |
Y160H |
probably damaging |
Het |
| Ndufb10 |
T |
C |
17: 24,941,648 (GRCm39) |
M90V |
probably damaging |
Het |
| Obscn |
T |
C |
11: 59,024,104 (GRCm39) |
K522R |
probably benign |
Het |
| Olfml2b |
T |
C |
1: 170,475,413 (GRCm39) |
S113P |
probably benign |
Het |
| Or14a257 |
T |
A |
7: 86,138,698 (GRCm39) |
E20D |
probably benign |
Het |
| Or4a78 |
A |
G |
2: 89,497,423 (GRCm39) |
I269T |
probably benign |
Het |
| Or4d10b |
T |
A |
19: 12,036,979 (GRCm39) |
M46L |
probably benign |
Het |
| Or51v14 |
T |
C |
7: 103,261,444 (GRCm39) |
T39A |
probably benign |
Het |
| Or6k2 |
T |
A |
1: 173,986,930 (GRCm39) |
M197K |
possibly damaging |
Het |
| Parg |
T |
C |
14: 31,936,511 (GRCm39) |
|
probably benign |
Het |
| Pde7a |
C |
T |
3: 19,284,482 (GRCm39) |
C367Y |
probably damaging |
Het |
| Pigr |
T |
A |
1: 130,772,281 (GRCm39) |
C166* |
probably null |
Het |
| Pip4k2c |
A |
T |
10: 127,036,704 (GRCm39) |
|
probably benign |
Het |
| Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
| Prkd2 |
A |
T |
7: 16,599,602 (GRCm39) |
|
probably benign |
Het |
| Ptprt |
G |
T |
2: 161,654,059 (GRCm39) |
|
probably null |
Het |
| Rapgef5 |
C |
T |
12: 117,610,741 (GRCm39) |
|
probably benign |
Het |
| Retreg1 |
T |
C |
15: 25,971,756 (GRCm39) |
L356P |
probably benign |
Het |
| Rigi |
T |
A |
4: 40,239,596 (GRCm39) |
E34V |
possibly damaging |
Het |
| Rnf43 |
A |
G |
11: 87,622,077 (GRCm39) |
T393A |
probably benign |
Het |
| Samd3 |
T |
C |
10: 26,147,725 (GRCm39) |
S467P |
probably benign |
Het |
| Scarf1 |
C |
A |
11: 75,405,229 (GRCm39) |
C89* |
probably null |
Het |
| Sdk1 |
T |
C |
5: 141,227,779 (GRCm39) |
L59S |
probably benign |
Het |
| Sgca |
C |
T |
11: 94,861,512 (GRCm39) |
W244* |
probably null |
Het |
| Sh3d21 |
T |
C |
4: 126,045,065 (GRCm39) |
K538R |
probably benign |
Het |
| Smyd4 |
T |
A |
11: 75,281,958 (GRCm39) |
L477Q |
possibly damaging |
Het |
| Sra1 |
A |
G |
18: 36,801,829 (GRCm39) |
M87T |
probably benign |
Het |
| Ssh2 |
T |
C |
11: 77,328,459 (GRCm39) |
Y336H |
possibly damaging |
Het |
| Steap1 |
T |
C |
5: 5,790,357 (GRCm39) |
Y197C |
probably damaging |
Het |
| Strn3 |
A |
G |
12: 51,673,879 (GRCm39) |
|
probably benign |
Het |
| Tgm3 |
A |
G |
2: 129,868,677 (GRCm39) |
T205A |
probably benign |
Het |
| Tll2 |
G |
A |
19: 41,101,512 (GRCm39) |
T374I |
probably damaging |
Het |
| Tmem63b |
C |
A |
17: 45,971,870 (GRCm39) |
D782Y |
possibly damaging |
Het |
| Trim10 |
G |
A |
17: 37,183,283 (GRCm39) |
S193N |
probably benign |
Het |
| Ttf1 |
A |
T |
2: 28,963,962 (GRCm39) |
K613* |
probably null |
Het |
| Tube1 |
T |
A |
10: 39,010,168 (GRCm39) |
|
probably null |
Het |
| Uimc1 |
T |
A |
13: 55,224,222 (GRCm39) |
|
probably null |
Het |
| Wwp2 |
G |
T |
8: 108,283,428 (GRCm39) |
|
probably benign |
Het |
| Zfp101 |
C |
T |
17: 33,601,418 (GRCm39) |
V113I |
probably benign |
Het |
| Zfp292 |
T |
C |
4: 34,809,114 (GRCm39) |
D1310G |
probably benign |
Het |
| Zfp575 |
A |
T |
7: 24,285,245 (GRCm39) |
L132H |
probably damaging |
Het |
| Zmym2 |
T |
C |
14: 57,194,420 (GRCm39) |
F1226S |
probably damaging |
Het |
| Zswim6 |
A |
C |
13: 107,862,989 (GRCm39) |
|
noncoding transcript |
Het |
|
| Other mutations in Cluh |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00095:Cluh
|
APN |
11 |
74,554,890 (GRCm39) |
missense |
probably benign |
0.28 |
|
IGL00858:Cluh
|
APN |
11 |
74,550,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL01380:Cluh
|
APN |
11 |
74,556,772 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL02402:Cluh
|
APN |
11 |
74,547,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02620:Cluh
|
APN |
11 |
74,555,893 (GRCm39) |
nonsense |
probably null |
|
|
IGL02990:Cluh
|
APN |
11 |
74,558,591 (GRCm39) |
splice site |
probably null |
|
|
IGL03163:Cluh
|
APN |
11 |
74,556,894 (GRCm39) |
missense |
probably benign |
0.44 |
|
IGL03208:Cluh
|
APN |
11 |
74,560,332 (GRCm39) |
splice site |
probably null |
|
|
IGL03293:Cluh
|
APN |
11 |
74,556,578 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL03408:Cluh
|
APN |
11 |
74,556,779 (GRCm39) |
missense |
probably benign |
0.06 |
|
spent
|
UTSW |
11 |
74,551,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4342:Cluh
|
UTSW |
11 |
74,560,352 (GRCm39) |
small insertion |
probably benign |
|
|
FR4342:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
FR4449:Cluh
|
UTSW |
11 |
74,560,358 (GRCm39) |
small insertion |
probably benign |
|
|
FR4589:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,345 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Cluh
|
UTSW |
11 |
74,560,359 (GRCm39) |
small insertion |
probably benign |
|
|
FR4976:Cluh
|
UTSW |
11 |
74,560,346 (GRCm39) |
small insertion |
probably benign |
|
|
R0147:Cluh
|
UTSW |
11 |
74,556,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0153:Cluh
|
UTSW |
11 |
74,548,176 (GRCm39) |
splice site |
probably benign |
|
|
R0506:Cluh
|
UTSW |
11 |
74,555,720 (GRCm39) |
missense |
probably benign |
0.20 |
|
R0526:Cluh
|
UTSW |
11 |
74,556,812 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1873:Cluh
|
UTSW |
11 |
74,552,902 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R1991:Cluh
|
UTSW |
11 |
74,550,355 (GRCm39) |
nonsense |
probably null |
|
|
R1992:Cluh
|
UTSW |
11 |
74,550,828 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2095:Cluh
|
UTSW |
11 |
74,552,550 (GRCm39) |
nonsense |
probably null |
|
|
R2101:Cluh
|
UTSW |
11 |
74,551,328 (GRCm39) |
splice site |
probably benign |
|
|
R2103:Cluh
|
UTSW |
11 |
74,550,355 (GRCm39) |
nonsense |
probably null |
|
|
R2220:Cluh
|
UTSW |
11 |
74,557,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3702:Cluh
|
UTSW |
11 |
74,556,182 (GRCm39) |
missense |
probably benign |
|
|
R3853:Cluh
|
UTSW |
11 |
74,547,279 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3900:Cluh
|
UTSW |
11 |
74,557,930 (GRCm39) |
missense |
probably benign |
0.29 |
|
R4891:Cluh
|
UTSW |
11 |
74,555,885 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R4895:Cluh
|
UTSW |
11 |
74,558,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5056:Cluh
|
UTSW |
11 |
74,552,772 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5089:Cluh
|
UTSW |
11 |
74,551,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5217:Cluh
|
UTSW |
11 |
74,550,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5346:Cluh
|
UTSW |
11 |
74,556,044 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5382:Cluh
|
UTSW |
11 |
74,555,935 (GRCm39) |
intron |
probably benign |
|
|
R5516:Cluh
|
UTSW |
11 |
74,551,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5809:Cluh
|
UTSW |
11 |
74,552,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6146:Cluh
|
UTSW |
11 |
74,558,054 (GRCm39) |
splice site |
probably null |
|
|
R6326:Cluh
|
UTSW |
11 |
74,557,068 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6541:Cluh
|
UTSW |
11 |
74,548,040 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6674:Cluh
|
UTSW |
11 |
74,557,053 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6870:Cluh
|
UTSW |
11 |
74,556,210 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6875:Cluh
|
UTSW |
11 |
74,552,744 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7086:Cluh
|
UTSW |
11 |
74,558,166 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7225:Cluh
|
UTSW |
11 |
74,557,232 (GRCm39) |
splice site |
probably null |
|
|
R7310:Cluh
|
UTSW |
11 |
74,560,285 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7317:Cluh
|
UTSW |
11 |
74,556,530 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7674:Cluh
|
UTSW |
11 |
74,558,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7941:Cluh
|
UTSW |
11 |
74,550,583 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9061:Cluh
|
UTSW |
11 |
74,551,192 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R9326:Cluh
|
UTSW |
11 |
74,554,902 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9489:Cluh
|
UTSW |
11 |
74,558,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9605:Cluh
|
UTSW |
11 |
74,558,772 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
RF020:Cluh
|
UTSW |
11 |
74,560,364 (GRCm39) |
small insertion |
probably benign |
|
|
RF032:Cluh
|
UTSW |
11 |
74,560,341 (GRCm39) |
small insertion |
probably benign |
|
|
X0028:Cluh
|
UTSW |
11 |
74,554,292 (GRCm39) |
missense |
probably benign |
0.26 |
|
Z1177:Cluh
|
UTSW |
11 |
74,558,580 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
Z1186:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
Z1186:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,342 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,346 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,347 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,350 (GRCm39) |
small insertion |
probably benign |
|
|
Z1187:Cluh
|
UTSW |
11 |
74,560,355 (GRCm39) |
small insertion |
probably benign |
|
|
Z1188:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,357 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
nonsense |
probably null |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,355 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,349 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,345 (GRCm39) |
small insertion |
probably benign |
|
|
Z1189:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,344 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1190:Cluh
|
UTSW |
11 |
74,560,358 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,349 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,340 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,356 (GRCm39) |
small insertion |
probably benign |
|
|
Z1191:Cluh
|
UTSW |
11 |
74,560,352 (GRCm39) |
small insertion |
probably benign |
|
|
Z1192:Cluh
|
UTSW |
11 |
74,560,351 (GRCm39) |
small insertion |
probably benign |
|
|
Z1192:Cluh
|
UTSW |
11 |
74,560,343 (GRCm39) |
small insertion |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- TCCTTGCTTGTTTGGAGAGCCC -3'
(R):5'- TGGCAGGACTCAGGAAATCGAACC -3'
Sequencing Primer
(F):5'- TTTGGAGAGCCCAAGCTG -3'
(R):5'- TCGAACCCCTGGGAAGGTAG -3'
|
| Posted On |
2013-10-16 |
Incidental Mutation