Incidental Mutation 'R0579:4921517D22Rik'
ID |
56364 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
4921517D22Rik
|
Ensembl Gene |
ENSMUSG00000049902 |
Gene Name |
RIKEN cDNA 4921517D22 gene |
Synonyms |
|
MMRRC Submission |
038769-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.073)
|
Stock # |
R0579 (G1)
|
Quality Score |
212 |
Status
|
Validated
|
Chromosome |
13 |
Chromosomal Location |
59835216-59841917 bp(-) (GRCm39) |
Type of Mutation |
frame shift |
DNA Base Change (assembly) |
GCC to GC
at 59839412 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000153380
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000061597]
[ENSMUST00000225373]
|
AlphaFold |
Q8CET0 |
Predicted Effect |
probably null
Transcript: ENSMUST00000061597
|
Predicted Effect |
probably null
Transcript: ENSMUST00000225373
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000225788
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.4%
- 20x: 94.7%
|
Validation Efficiency |
89% (34/38) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
G |
A |
16: 20,369,398 (GRCm39) |
R260Q |
probably benign |
Het |
Abcg3 |
A |
G |
5: 105,121,969 (GRCm39) |
V136A |
probably damaging |
Het |
Acr |
C |
G |
15: 89,453,678 (GRCm39) |
H72Q |
probably damaging |
Het |
Ambra1 |
A |
G |
2: 91,654,810 (GRCm39) |
N783S |
possibly damaging |
Het |
Cd300ld2 |
A |
G |
11: 114,903,125 (GRCm39) |
F240S |
probably benign |
Het |
Cep83 |
A |
G |
10: 94,584,915 (GRCm39) |
D340G |
possibly damaging |
Het |
Crybg2 |
T |
A |
4: 133,800,049 (GRCm39) |
I403N |
probably damaging |
Het |
Dnah14 |
T |
A |
1: 181,572,312 (GRCm39) |
M2881K |
possibly damaging |
Het |
Erbb4 |
T |
C |
1: 68,081,621 (GRCm39) |
M1138V |
probably benign |
Het |
Evi5 |
A |
G |
5: 107,969,575 (GRCm39) |
V112A |
probably benign |
Het |
F2r |
A |
G |
13: 95,754,857 (GRCm39) |
V9A |
probably benign |
Het |
Flot1 |
C |
A |
17: 36,141,900 (GRCm39) |
S337R |
probably benign |
Het |
Glt28d2 |
G |
A |
3: 85,779,440 (GRCm39) |
T11I |
probably damaging |
Het |
Gm19345 |
A |
G |
7: 19,588,901 (GRCm39) |
|
probably benign |
Het |
Gm6605 |
C |
A |
7: 38,147,699 (GRCm39) |
|
noncoding transcript |
Het |
Hmgcs2 |
A |
T |
3: 98,198,264 (GRCm39) |
I56F |
probably damaging |
Het |
Ifna9 |
T |
A |
4: 88,510,508 (GRCm39) |
T39S |
possibly damaging |
Het |
Il21 |
T |
G |
3: 37,281,923 (GRCm39) |
K74Q |
possibly damaging |
Het |
Itpripl1 |
G |
T |
2: 126,983,011 (GRCm39) |
Y370* |
probably null |
Het |
Kif24 |
G |
A |
4: 41,393,706 (GRCm39) |
P1056S |
probably damaging |
Het |
L2hgdh |
A |
T |
12: 69,748,046 (GRCm39) |
|
probably benign |
Het |
Lipo2 |
A |
T |
19: 33,724,298 (GRCm39) |
L156Q |
probably damaging |
Het |
Nlrp4c |
T |
A |
7: 6,063,844 (GRCm39) |
M84K |
probably benign |
Het |
Npy4r |
G |
A |
14: 33,868,640 (GRCm39) |
T216I |
probably benign |
Het |
Or12d17 |
T |
C |
17: 37,777,238 (GRCm39) |
V47A |
probably benign |
Het |
Or2h2c |
G |
C |
17: 37,422,347 (GRCm39) |
L176V |
probably benign |
Het |
Or6c1 |
A |
T |
10: 129,518,106 (GRCm39) |
C167* |
probably null |
Het |
Pafah1b2 |
T |
C |
9: 45,880,011 (GRCm39) |
E222G |
probably benign |
Het |
Pop1 |
T |
A |
15: 34,510,115 (GRCm39) |
D406E |
possibly damaging |
Het |
Proser1 |
A |
G |
3: 53,374,572 (GRCm39) |
Y32C |
probably damaging |
Het |
Ptprj |
C |
A |
2: 90,266,913 (GRCm39) |
|
probably null |
Het |
Slc1a3 |
T |
A |
15: 8,717,793 (GRCm39) |
I100F |
probably damaging |
Het |
Slc25a22 |
T |
C |
7: 141,011,272 (GRCm39) |
D176G |
probably damaging |
Het |
Stard7 |
T |
C |
2: 127,126,473 (GRCm39) |
V99A |
probably damaging |
Het |
Stk33 |
C |
T |
7: 108,924,904 (GRCm39) |
V184I |
probably damaging |
Het |
Timmdc1 |
A |
G |
16: 38,342,745 (GRCm39) |
L51P |
probably benign |
Het |
Tppp |
T |
C |
13: 74,169,352 (GRCm39) |
S31P |
probably benign |
Het |
Upf2 |
A |
T |
2: 5,993,240 (GRCm39) |
R599W |
unknown |
Het |
Vav1 |
G |
T |
17: 57,586,271 (GRCm39) |
W25L |
probably benign |
Het |
|
Other mutations in 4921517D22Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00827:4921517D22Rik
|
APN |
13 |
59,837,290 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01516:4921517D22Rik
|
APN |
13 |
59,838,548 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4677001:4921517D22Rik
|
UTSW |
13 |
59,838,305 (GRCm39) |
missense |
probably benign |
0.12 |
R0395:4921517D22Rik
|
UTSW |
13 |
59,837,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0664:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0757:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0758:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0777:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0779:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0814:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0870:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0872:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R0873:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1062:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1064:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1149:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1149:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1151:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1152:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1207:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1207:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1285:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1339:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1358:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1359:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1360:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1361:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R1679:4921517D22Rik
|
UTSW |
13 |
59,839,412 (GRCm39) |
frame shift |
probably null |
|
R4703:4921517D22Rik
|
UTSW |
13 |
59,837,342 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4785:4921517D22Rik
|
UTSW |
13 |
59,839,406 (GRCm39) |
missense |
probably benign |
|
R4823:4921517D22Rik
|
UTSW |
13 |
59,838,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R5054:4921517D22Rik
|
UTSW |
13 |
59,837,315 (GRCm39) |
missense |
probably damaging |
0.97 |
R6144:4921517D22Rik
|
UTSW |
13 |
59,837,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R6977:4921517D22Rik
|
UTSW |
13 |
59,839,394 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7009:4921517D22Rik
|
UTSW |
13 |
59,838,624 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7791:4921517D22Rik
|
UTSW |
13 |
59,838,508 (GRCm39) |
missense |
probably benign |
|
R8319:4921517D22Rik
|
UTSW |
13 |
59,838,486 (GRCm39) |
missense |
probably benign |
|
R8422:4921517D22Rik
|
UTSW |
13 |
59,839,443 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R8520:4921517D22Rik
|
UTSW |
13 |
59,838,423 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
Predicted Primers |
PCR Primer
(F):5'- ACTGAAATGAAACTCCGGTGCCC -3'
(R):5'- TCACCAATGAAATGGTCAGAGCTGC -3'
Sequencing Primer
(F):5'- TCGCCTGCATGTGGTATCAT -3'
(R):5'- GCTACTTGAAACATGATTGACTCGAC -3'
|
Posted On |
2013-07-11 |