Incidental Mutation 'R6267:4933427D14Rik'
| ID |
507089 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
4933427D14Rik
|
| Ensembl Gene |
ENSMUSG00000020807 |
| Gene Name |
RIKEN cDNA 4933427D14 gene |
| Synonyms |
Gm43951 |
| MMRRC Submission |
044405-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R6267 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
72044755-72098308 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 72086580 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Arginine
at position 277
(K277R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000104145
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108505]
[ENSMUST00000108506]
[ENSMUST00000131546]
[ENSMUST00000142530]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108505
AA Change: K277R
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000104145
Gene: ENSMUSG00000020807
AA Change: K277R
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
84 |
93 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
231 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108506
|
| SMART Domains |
Protein: ENSMUSP00000104146
Gene: ENSMUSG00000020807
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF4673
|
1 |
954 |
N/A |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000131546
|
| SMART Domains |
Protein: ENSMUSP00000122273
Gene: ENSMUSG00000020807
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
84 |
93 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
231 |
N/A |
INTRINSIC |
|
coiled coil region
|
256 |
279 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
305 |
N/A |
INTRINSIC |
|
low complexity region
|
360 |
377 |
N/A |
INTRINSIC |
|
low complexity region
|
545 |
559 |
N/A |
INTRINSIC |
|
coiled coil region
|
625 |
653 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000142530
|
| SMART Domains |
Protein: ENSMUSP00000115276
Gene: ENSMUSG00000020807
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
84 |
93 |
N/A |
INTRINSIC |
|
coiled coil region
|
210 |
231 |
N/A |
INTRINSIC |
|
coiled coil region
|
256 |
279 |
N/A |
INTRINSIC |
|
low complexity region
|
291 |
305 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000144553
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154093
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.7%
- 10x: 98.6%
- 20x: 96.4%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aatf |
T |
C |
11: 84,363,926 (GRCm39) |
Y267C |
probably benign |
Het |
| Abi3bp |
A |
G |
16: 56,414,860 (GRCm39) |
T341A |
probably damaging |
Het |
| Acer2 |
T |
C |
4: 86,792,823 (GRCm39) |
F33S |
probably damaging |
Het |
| Actr1b |
A |
G |
1: 36,740,244 (GRCm39) |
V299A |
possibly damaging |
Het |
| Ampd3 |
T |
A |
7: 110,390,387 (GRCm39) |
|
probably null |
Het |
| Atm |
A |
C |
9: 53,355,300 (GRCm39) |
I2898R |
probably damaging |
Het |
| Bpifb6 |
G |
C |
2: 153,748,812 (GRCm39) |
K269N |
possibly damaging |
Het |
| Cacna1c |
T |
C |
6: 118,575,684 (GRCm39) |
E1927G |
possibly damaging |
Het |
| Cacna1c |
T |
A |
6: 118,629,675 (GRCm39) |
T1249S |
probably benign |
Het |
| Cars2 |
TCCCC |
TCCC |
8: 11,579,599 (GRCm39) |
|
probably null |
Het |
| Cbll1 |
A |
G |
12: 31,537,507 (GRCm39) |
V415A |
probably benign |
Het |
| Cd300lf |
C |
T |
11: 115,015,195 (GRCm39) |
V132I |
probably benign |
Het |
| Chd2 |
T |
C |
7: 73,113,419 (GRCm39) |
E1187G |
probably damaging |
Het |
| Cntrl |
T |
C |
2: 35,019,805 (GRCm39) |
L544P |
probably damaging |
Het |
| Cryga |
A |
C |
1: 65,142,169 (GRCm39) |
S75A |
probably benign |
Het |
| Dcbld1 |
T |
A |
10: 52,195,576 (GRCm39) |
Y261* |
probably null |
Het |
| Ddx11 |
G |
A |
17: 66,457,724 (GRCm39) |
|
probably null |
Het |
| Dgke |
C |
T |
11: 88,931,575 (GRCm39) |
V560I |
probably benign |
Het |
| Dst |
A |
C |
1: 34,267,753 (GRCm39) |
D5065A |
probably damaging |
Het |
| Dusp16 |
C |
A |
6: 134,697,456 (GRCm39) |
|
probably null |
Het |
| Eif4enif1 |
T |
A |
11: 3,177,793 (GRCm39) |
V395E |
probably damaging |
Het |
| Enox1 |
A |
G |
14: 77,815,204 (GRCm39) |
T121A |
probably damaging |
Het |
| Enpp4 |
G |
T |
17: 44,413,371 (GRCm39) |
N54K |
probably benign |
Het |
| Erc2 |
A |
T |
14: 27,802,112 (GRCm39) |
K764M |
probably damaging |
Het |
| Ercc6 |
G |
T |
14: 32,248,360 (GRCm39) |
E304* |
probably null |
Het |
| Fam117a |
T |
A |
11: 95,254,971 (GRCm39) |
C115S |
possibly damaging |
Het |
| Fcrl5 |
G |
A |
3: 87,355,631 (GRCm39) |
G448E |
probably damaging |
Het |
| Galntl5 |
T |
C |
5: 25,391,163 (GRCm39) |
S21P |
probably benign |
Het |
| Garnl3 |
T |
C |
2: 32,994,892 (GRCm39) |
D39G |
probably benign |
Het |
| Gm14295 |
C |
T |
2: 176,500,782 (GRCm39) |
Q91* |
probably null |
Het |
| Grb10 |
T |
A |
11: 11,920,639 (GRCm39) |
|
probably benign |
Het |
| Grip1 |
C |
T |
10: 119,911,369 (GRCm39) |
Q696* |
probably null |
Het |
| Herc2 |
T |
A |
7: 55,802,914 (GRCm39) |
C2112* |
probably null |
Het |
| Herc2 |
T |
G |
7: 55,854,466 (GRCm39) |
L3797R |
possibly damaging |
Het |
| Ighm |
T |
C |
12: 113,385,187 (GRCm39) |
I258V |
unknown |
Het |
| Jarid2 |
T |
A |
13: 45,056,539 (GRCm39) |
Y443N |
possibly damaging |
Het |
| Kif13b |
A |
G |
14: 64,976,083 (GRCm39) |
Y466C |
probably damaging |
Het |
| Krtap4-6 |
T |
A |
11: 99,556,245 (GRCm39) |
R161* |
probably null |
Het |
| Lingo4 |
G |
A |
3: 94,310,697 (GRCm39) |
G545E |
probably benign |
Het |
| Lmo2 |
T |
G |
2: 103,800,946 (GRCm39) |
V39G |
possibly damaging |
Het |
| Loricrin |
C |
A |
3: 91,989,119 (GRCm39) |
G56* |
probably null |
Het |
| Lrfn1 |
A |
G |
7: 28,159,169 (GRCm39) |
R363G |
probably benign |
Het |
| Lrp1b |
T |
C |
2: 40,547,537 (GRCm39) |
D446G |
probably benign |
Het |
| Ltbp1 |
G |
T |
17: 75,312,984 (GRCm39) |
G35V |
possibly damaging |
Het |
| Magel2 |
G |
A |
7: 62,028,427 (GRCm39) |
V444M |
probably damaging |
Het |
| Mkx |
A |
T |
18: 7,000,591 (GRCm39) |
|
probably null |
Het |
| Ms4a7 |
A |
T |
19: 11,310,659 (GRCm39) |
I20N |
possibly damaging |
Het |
| Myo5b |
A |
G |
18: 74,750,062 (GRCm39) |
Y173C |
probably damaging |
Het |
| Nek1 |
C |
T |
8: 61,525,343 (GRCm39) |
Q594* |
probably null |
Het |
| Nipbl |
T |
C |
15: 8,330,379 (GRCm39) |
M2349V |
possibly damaging |
Het |
| Nmnat2 |
A |
T |
1: 152,952,717 (GRCm39) |
H102L |
probably damaging |
Het |
| Nup155 |
T |
A |
15: 8,182,639 (GRCm39) |
C1201S |
probably damaging |
Het |
| Or2y8 |
C |
A |
11: 52,035,423 (GRCm39) |
R311S |
probably benign |
Het |
| Or4a76 |
G |
A |
2: 89,460,975 (GRCm39) |
T89I |
probably damaging |
Het |
| Or52x1 |
G |
A |
7: 104,852,599 (GRCm39) |
T317I |
probably damaging |
Het |
| Osbpl1a |
A |
G |
18: 12,952,560 (GRCm39) |
|
probably null |
Het |
| Pcnt |
A |
G |
10: 76,221,632 (GRCm39) |
V1998A |
probably benign |
Het |
| Pitpnc1 |
T |
C |
11: 107,117,092 (GRCm39) |
H193R |
probably damaging |
Het |
| Pitpnm1 |
T |
C |
19: 4,160,522 (GRCm39) |
L781P |
probably damaging |
Het |
| Prdm14 |
A |
T |
1: 13,189,160 (GRCm39) |
C395S |
probably damaging |
Het |
| Prmt8 |
A |
G |
6: 127,688,767 (GRCm39) |
I201T |
probably damaging |
Het |
| Pter |
T |
C |
2: 12,983,352 (GRCm39) |
V119A |
probably damaging |
Het |
| Rab11fip4 |
T |
C |
11: 79,581,655 (GRCm39) |
|
probably null |
Het |
| Rgs9 |
T |
C |
11: 109,159,813 (GRCm39) |
N173S |
probably benign |
Het |
| Rorb |
C |
A |
19: 18,955,221 (GRCm39) |
V47L |
possibly damaging |
Het |
| Rtn4r |
A |
G |
16: 17,969,046 (GRCm39) |
Y158C |
probably damaging |
Het |
| Sdr16c5 |
C |
T |
4: 4,016,162 (GRCm39) |
G88E |
probably damaging |
Het |
| Sfxn1 |
C |
T |
13: 54,247,899 (GRCm39) |
T208I |
probably benign |
Het |
| Sgo2b |
C |
T |
8: 64,380,827 (GRCm39) |
M668I |
probably benign |
Het |
| Slc52a3 |
G |
T |
2: 151,849,529 (GRCm39) |
|
probably null |
Het |
| Smco1 |
A |
T |
16: 32,092,832 (GRCm39) |
M168L |
probably benign |
Het |
| Spata31d1d |
G |
A |
13: 59,876,278 (GRCm39) |
T419I |
possibly damaging |
Het |
| Spata31d1e |
T |
C |
13: 59,890,497 (GRCm39) |
D441G |
probably benign |
Het |
| Spink5 |
T |
C |
18: 44,147,824 (GRCm39) |
S857P |
probably damaging |
Het |
| Stk35 |
T |
A |
2: 129,652,808 (GRCm39) |
Y436* |
probably null |
Het |
| Tmem225 |
T |
A |
9: 40,059,731 (GRCm39) |
I37N |
probably damaging |
Het |
| Unkl |
T |
C |
17: 25,450,839 (GRCm39) |
*232R |
probably null |
Het |
| Usp16 |
A |
G |
16: 87,280,079 (GRCm39) |
N813S |
probably benign |
Het |
| Vmn1r128 |
A |
T |
7: 21,084,221 (GRCm39) |
*308C |
probably null |
Het |
| Vmn2r45 |
A |
G |
7: 8,475,207 (GRCm39) |
V607A |
probably benign |
Het |
| Vmn2r63 |
A |
T |
7: 42,578,059 (GRCm39) |
|
probably null |
Het |
| Wnk4 |
A |
T |
11: 101,164,824 (GRCm39) |
N718Y |
probably damaging |
Het |
| Zfp503 |
G |
C |
14: 22,035,868 (GRCm39) |
Y349* |
probably null |
Het |
| Zfp990 |
T |
A |
4: 145,264,673 (GRCm39) |
F557Y |
possibly damaging |
Het |
|
| Other mutations in 4933427D14Rik |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00707:4933427D14Rik
|
APN |
11 |
72,069,330 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01643:4933427D14Rik
|
APN |
11 |
72,082,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02004:4933427D14Rik
|
APN |
11 |
72,082,423 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL02308:4933427D14Rik
|
APN |
11 |
72,093,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02378:4933427D14Rik
|
APN |
11 |
72,080,424 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02715:4933427D14Rik
|
APN |
11 |
72,089,714 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03330:4933427D14Rik
|
APN |
11 |
72,050,254 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03384:4933427D14Rik
|
APN |
11 |
72,086,673 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
BB002:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
BB012:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
IGL03047:4933427D14Rik
|
UTSW |
11 |
72,057,552 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R0114:4933427D14Rik
|
UTSW |
11 |
72,086,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0526:4933427D14Rik
|
UTSW |
11 |
72,060,609 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0653:4933427D14Rik
|
UTSW |
11 |
72,066,371 (GRCm39) |
nonsense |
probably null |
|
|
R0669:4933427D14Rik
|
UTSW |
11 |
72,089,671 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R0729:4933427D14Rik
|
UTSW |
11 |
72,050,281 (GRCm39) |
missense |
probably benign |
0.07 |
|
R1797:4933427D14Rik
|
UTSW |
11 |
72,089,285 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R3973:4933427D14Rik
|
UTSW |
11 |
72,089,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4744:4933427D14Rik
|
UTSW |
11 |
72,066,365 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4897:4933427D14Rik
|
UTSW |
11 |
72,082,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5023:4933427D14Rik
|
UTSW |
11 |
72,057,581 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5057:4933427D14Rik
|
UTSW |
11 |
72,057,581 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5100:4933427D14Rik
|
UTSW |
11 |
72,057,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5497:4933427D14Rik
|
UTSW |
11 |
72,056,360 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5556:4933427D14Rik
|
UTSW |
11 |
72,066,026 (GRCm39) |
splice site |
probably null |
|
|
R5631:4933427D14Rik
|
UTSW |
11 |
72,067,590 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R5683:4933427D14Rik
|
UTSW |
11 |
72,093,266 (GRCm39) |
missense |
probably benign |
|
|
R5742:4933427D14Rik
|
UTSW |
11 |
72,056,379 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R6247:4933427D14Rik
|
UTSW |
11 |
72,049,768 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6296:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6860:4933427D14Rik
|
UTSW |
11 |
72,080,412 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7023:4933427D14Rik
|
UTSW |
11 |
72,069,229 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7328:4933427D14Rik
|
UTSW |
11 |
72,060,606 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7514:4933427D14Rik
|
UTSW |
11 |
72,086,628 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7544:4933427D14Rik
|
UTSW |
11 |
72,089,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7925:4933427D14Rik
|
UTSW |
11 |
72,071,327 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8204:4933427D14Rik
|
UTSW |
11 |
72,057,606 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8280:4933427D14Rik
|
UTSW |
11 |
72,086,667 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8316:4933427D14Rik
|
UTSW |
11 |
72,059,612 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R8366:4933427D14Rik
|
UTSW |
11 |
72,067,521 (GRCm39) |
nonsense |
probably null |
|
|
R8384:4933427D14Rik
|
UTSW |
11 |
72,057,591 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8722:4933427D14Rik
|
UTSW |
11 |
72,080,422 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8944:4933427D14Rik
|
UTSW |
11 |
72,049,851 (GRCm39) |
splice site |
probably benign |
|
|
R9749:4933427D14Rik
|
UTSW |
11 |
72,080,521 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0063:4933427D14Rik
|
UTSW |
11 |
72,067,595 (GRCm39) |
missense |
probably benign |
|
|
X0065:4933427D14Rik
|
UTSW |
11 |
72,080,401 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
Z1176:4933427D14Rik
|
UTSW |
11 |
72,049,826 (GRCm39) |
missense |
probably benign |
0.12 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1186:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,086,536 (GRCm39) |
frame shift |
probably null |
|
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1187:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1188:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1189:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1190:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1191:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,308 (GRCm39) |
missense |
probably benign |
0.13 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,595 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,590 (GRCm39) |
frame shift |
probably null |
|
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,569 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,086,538 (GRCm39) |
frame shift |
probably null |
|
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,080,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,067,535 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,750 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1192:4933427D14Rik
|
UTSW |
11 |
72,089,360 (GRCm39) |
missense |
probably benign |
0.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TCAGGGTCACATGTACAAGC -3'
(R):5'- TTCCTTAGTAAGACACGTCAGC -3'
Sequencing Primer
(F):5'- GGGTCACATGTACAAGCACTTTTTC -3'
(R):5'- AAGACACGTCAGCTATTAATTACTC -3'
|
| Posted On |
2018-03-15 |
Incidental Mutation