Incidental Mutation 'R8944:4933427D14Rik'
| ID |
700887 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
4933427D14Rik
|
| Ensembl Gene |
ENSMUSG00000020807 |
| Gene Name |
RIKEN cDNA 4933427D14 gene |
| Synonyms |
Gm43951 |
| MMRRC Submission |
068783-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8944 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
72044755-72098308 bp(-) (GRCm39) |
| Type of Mutation |
splice site |
| DNA Base Change (assembly) |
A to T
at 72049851 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000115276
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108506]
[ENSMUST00000131546]
[ENSMUST00000142530]
|
| AlphaFold |
no structure available at present |
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
100% (88/88) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| A830018L16Rik |
A |
T |
1: 11,484,706 (GRCm39) |
|
probably benign |
Het |
| Acox1 |
C |
T |
11: 116,066,040 (GRCm39) |
R454H |
probably damaging |
Het |
| Acte1 |
G |
T |
7: 143,434,902 (GRCm39) |
|
probably null |
Het |
| Adam18 |
A |
G |
8: 25,164,703 (GRCm39) |
L4P |
probably damaging |
Het |
| AI182371 |
A |
C |
2: 34,990,622 (GRCm39) |
L25R |
probably damaging |
Het |
| Ankrd12 |
A |
C |
17: 66,277,195 (GRCm39) |
Y2026* |
probably null |
Het |
| Atad5 |
C |
T |
11: 79,986,524 (GRCm39) |
T537M |
possibly damaging |
Het |
| Atosa |
A |
G |
9: 74,911,562 (GRCm39) |
Y11C |
probably damaging |
Het |
| Avil |
G |
T |
10: 126,846,455 (GRCm39) |
G420V |
probably damaging |
Het |
| Bche |
A |
T |
3: 73,608,008 (GRCm39) |
F473I |
probably damaging |
Het |
| Borcs5 |
T |
C |
6: 134,621,437 (GRCm39) |
|
probably null |
Het |
| C4b |
T |
C |
17: 34,961,913 (GRCm39) |
Q111R |
probably benign |
Het |
| Carmil2 |
T |
A |
8: 106,417,437 (GRCm39) |
I565N |
probably damaging |
Het |
| Cd74 |
T |
C |
18: 60,943,127 (GRCm39) |
M155T |
probably damaging |
Het |
| Chrnd |
G |
T |
1: 87,119,997 (GRCm39) |
R105L |
probably damaging |
Het |
| Clpp |
G |
T |
17: 57,300,553 (GRCm39) |
E217* |
probably null |
Het |
| Cpq |
T |
A |
15: 33,594,269 (GRCm39) |
Y427N |
probably damaging |
Het |
| Crxos |
G |
A |
7: 15,636,900 (GRCm39) |
E54K |
possibly damaging |
Het |
| Dcaf13 |
A |
G |
15: 39,001,612 (GRCm39) |
R307G |
possibly damaging |
Het |
| Ddx55 |
A |
G |
5: 124,706,788 (GRCm39) |
D595G |
probably damaging |
Het |
| Dld |
T |
A |
12: 31,390,868 (GRCm39) |
I193F |
possibly damaging |
Het |
| Dnah11 |
T |
G |
12: 118,091,381 (GRCm39) |
E917A |
possibly damaging |
Het |
| Dnai2 |
T |
A |
11: 114,641,302 (GRCm39) |
Y376N |
possibly damaging |
Het |
| Dock7 |
A |
G |
4: 98,829,243 (GRCm39) |
Y2078H |
probably damaging |
Het |
| Dusp4 |
A |
T |
8: 35,274,941 (GRCm39) |
N20I |
probably benign |
Het |
| Dzank1 |
A |
G |
2: 144,333,729 (GRCm39) |
L367P |
probably benign |
Het |
| Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
| Erich3 |
G |
C |
3: 154,462,692 (GRCm39) |
R742S |
|
Het |
| Erich6 |
C |
T |
3: 58,537,275 (GRCm39) |
M246I |
probably benign |
Het |
| Galnt16 |
T |
G |
12: 80,623,314 (GRCm39) |
I158S |
probably damaging |
Het |
| Gm28363 |
A |
G |
1: 117,655,080 (GRCm39) |
T100A |
possibly damaging |
Het |
| Gm8257 |
A |
T |
14: 44,893,849 (GRCm39) |
Y36N |
probably damaging |
Het |
| Gmpr2 |
T |
C |
14: 55,913,149 (GRCm39) |
V142A |
possibly damaging |
Het |
| Grid2ip |
T |
C |
5: 143,366,260 (GRCm39) |
|
probably null |
Het |
| Hamp2 |
A |
G |
7: 30,622,001 (GRCm39) |
F63L |
possibly damaging |
Het |
| Hmga2 |
T |
C |
10: 120,309,159 (GRCm39) |
K66E |
probably damaging |
Het |
| Hspa1a |
T |
C |
17: 35,190,019 (GRCm39) |
T295A |
probably benign |
Het |
| Ift74 |
G |
A |
4: 94,510,128 (GRCm39) |
G53D |
probably damaging |
Het |
| Ighv6-7 |
T |
C |
12: 114,419,703 (GRCm39) |
M1V |
probably null |
Het |
| Ints4 |
T |
A |
7: 97,183,593 (GRCm39) |
D769E |
probably benign |
Het |
| Kif7 |
G |
A |
7: 79,360,005 (GRCm39) |
R411C |
probably damaging |
Het |
| Klhl30 |
T |
A |
1: 91,287,174 (GRCm39) |
Y487N |
probably damaging |
Het |
| Kras |
T |
C |
6: 145,170,853 (GRCm39) |
E174G |
probably benign |
Het |
| Krt84 |
T |
C |
15: 101,437,183 (GRCm39) |
I327V |
probably benign |
Het |
| Lamb3 |
T |
A |
1: 193,014,525 (GRCm39) |
C561* |
probably null |
Het |
| Lmbrd1 |
A |
G |
1: 24,767,407 (GRCm39) |
|
probably benign |
Het |
| Lmnb1 |
T |
A |
18: 56,876,331 (GRCm39) |
S480T |
probably benign |
Het |
| Lrp2 |
C |
T |
2: 69,341,348 (GRCm39) |
G944D |
probably damaging |
Het |
| Mta3 |
G |
A |
17: 84,083,146 (GRCm39) |
E280K |
probably damaging |
Het |
| Muc5b |
A |
T |
7: 141,421,115 (GRCm39) |
I4236F |
|
Het |
| Myh9 |
T |
C |
15: 77,655,432 (GRCm39) |
T1175A |
probably benign |
Het |
| Myt1l |
T |
A |
12: 29,861,564 (GRCm39) |
D115E |
unknown |
Het |
| Naa25 |
A |
G |
5: 121,552,573 (GRCm39) |
N167D |
probably benign |
Het |
| Ncam1 |
G |
A |
9: 49,431,493 (GRCm39) |
P648L |
probably damaging |
Het |
| Or2t26 |
T |
C |
11: 49,039,266 (GRCm39) |
Y61H |
probably damaging |
Het |
| Or2t44 |
A |
T |
11: 58,677,519 (GRCm39) |
D153V |
probably damaging |
Het |
| P3h3 |
G |
T |
6: 124,832,196 (GRCm39) |
A230E |
possibly damaging |
Het |
| Pacs2 |
A |
G |
12: 113,020,476 (GRCm39) |
E253G |
probably damaging |
Het |
| Pbld1 |
A |
T |
10: 62,901,648 (GRCm39) |
D57V |
probably benign |
Het |
| Pcsk5 |
T |
C |
19: 17,452,275 (GRCm39) |
T1077A |
probably damaging |
Het |
| Pou4f2 |
T |
A |
8: 79,161,932 (GRCm39) |
M224L |
|
Het |
| Ppcdc |
C |
T |
9: 57,342,265 (GRCm39) |
R19H |
probably benign |
Het |
| Ppp1r10 |
T |
A |
17: 36,241,018 (GRCm39) |
M640K |
probably benign |
Het |
| Prdx6 |
A |
T |
1: 161,069,432 (GRCm39) |
|
probably benign |
Het |
| Rab40b |
A |
G |
11: 121,250,384 (GRCm39) |
|
probably null |
Het |
| Rassf9 |
T |
A |
10: 102,381,329 (GRCm39) |
M237K |
probably benign |
Het |
| Rbbp8nl |
G |
T |
2: 179,919,769 (GRCm39) |
Y604* |
probably null |
Het |
| Reep2 |
G |
T |
18: 34,975,929 (GRCm39) |
W42L |
possibly damaging |
Het |
| Serpinb6e |
A |
T |
13: 34,017,261 (GRCm39) |
M253K |
probably damaging |
Het |
| Shank2 |
A |
G |
7: 143,623,927 (GRCm39) |
Q304R |
probably damaging |
Het |
| Slk |
T |
C |
19: 47,600,057 (GRCm39) |
M120T |
probably damaging |
Het |
| Spata31e5 |
T |
C |
1: 28,816,155 (GRCm39) |
I626V |
probably benign |
Het |
| Sphkap |
T |
A |
1: 83,256,927 (GRCm39) |
H274L |
probably benign |
Het |
| Stc1 |
T |
G |
14: 69,269,884 (GRCm39) |
F155V |
possibly damaging |
Het |
| Tbc1d12 |
A |
G |
19: 38,899,510 (GRCm39) |
T477A |
probably damaging |
Het |
| Tmem19 |
T |
A |
10: 115,183,671 (GRCm39) |
I54F |
possibly damaging |
Het |
| Tmem62 |
G |
A |
2: 120,817,316 (GRCm39) |
|
probably null |
Het |
| Ttc6 |
A |
T |
12: 57,689,826 (GRCm39) |
R505S |
|
Het |
| Ttn |
G |
T |
2: 76,623,184 (GRCm39) |
R15418S |
probably damaging |
Het |
| Ugt2a3 |
C |
A |
5: 87,473,417 (GRCm39) |
C500F |
possibly damaging |
Het |
| Ugt2b35 |
T |
C |
5: 87,149,310 (GRCm39) |
F187S |
probably benign |
Het |
| Ung |
T |
A |
5: 114,269,456 (GRCm39) |
I56N |
probably damaging |
Het |
| Vmn1r17 |
G |
T |
6: 57,338,142 (GRCm39) |
F25L |
probably benign |
Het |
| Vmn1r29 |
C |
A |
6: 58,284,274 (GRCm39) |
|
probably benign |
Het |
| Vps26c |
T |
A |
16: 94,302,481 (GRCm39) |
I242F |
probably benign |
Het |
| Wdhd1 |
T |
C |
14: 47,504,470 (GRCm39) |
D368G |
probably benign |
Het |
| Wdr3 |
A |
T |
3: 100,057,259 (GRCm39) |
I448N |
probably damaging |
Het |
| Wdr47 |
T |
A |
3: 108,550,480 (GRCm39) |
M835K |
possibly damaging |
Het |
| Wt1 |
G |
A |
2: 104,957,584 (GRCm39) |
G10D |
possibly damaging |
Het |
| Zdhhc19 |
G |
A |
16: 32,316,500 (GRCm39) |
G85D |
probably 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 |
|
R6267:4933427D14Rik
|
UTSW |
11 |
72,086,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
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'- AATTGCTCAAACCGGCTACAG -3'
(R):5'- GGTGGGCATCAAACACTTG -3'
Sequencing Primer
(F):5'- CGGCTACAGTAAGCACCAATG -3'
(R):5'- TGCATTGTAAGGAAGCCTCC -3'
|
| Posted On |
2022-02-28 |
Incidental Mutation