Incidental Mutation 'R5020:Zfp219'
ID |
389165 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp219
|
Ensembl Gene |
ENSMUSG00000049295 |
Gene Name |
zinc finger protein 219 |
Synonyms |
2010302A17Rik |
MMRRC Submission |
042611-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5020 (G1)
|
Quality Score |
188 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
52243534-52258190 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 52247112 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Histidine
at position 5
(R5H)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000154768
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000067549]
[ENSMUST00000093813]
[ENSMUST00000100639]
[ENSMUST00000166169]
[ENSMUST00000182061]
[ENSMUST00000226554]
[ENSMUST00000226527]
[ENSMUST00000226522]
[ENSMUST00000182909]
[ENSMUST00000182905]
[ENSMUST00000182760]
[ENSMUST00000183208]
[ENSMUST00000228162]
[ENSMUST00000226605]
[ENSMUST00000226964]
[ENSMUST00000228051]
[ENSMUST00000228747]
[ENSMUST00000228580]
|
AlphaFold |
Q6IQX8 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000067549
AA Change: R5H
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000068184 Gene: ENSMUSG00000049295 AA Change: R5H
Domain | Start | End | E-Value | Type |
low complexity region
|
30 |
47 |
N/A |
INTRINSIC |
ZnF_C2H2
|
61 |
83 |
6.23e-2 |
SMART |
ZnF_C2H2
|
89 |
111 |
4.17e-3 |
SMART |
low complexity region
|
113 |
146 |
N/A |
INTRINSIC |
ZnF_C2H2
|
167 |
190 |
3.07e-1 |
SMART |
ZnF_C2H2
|
193 |
216 |
1.51e0 |
SMART |
low complexity region
|
229 |
276 |
N/A |
INTRINSIC |
ZnF_C2H2
|
277 |
299 |
8.47e-4 |
SMART |
ZnF_C2H2
|
305 |
327 |
1.38e-3 |
SMART |
low complexity region
|
331 |
350 |
N/A |
INTRINSIC |
low complexity region
|
354 |
379 |
N/A |
INTRINSIC |
low complexity region
|
427 |
441 |
N/A |
INTRINSIC |
ZnF_C2H2
|
501 |
523 |
3.63e-3 |
SMART |
ZnF_C2H2
|
529 |
551 |
1.58e-3 |
SMART |
low complexity region
|
560 |
570 |
N/A |
INTRINSIC |
low complexity region
|
594 |
611 |
N/A |
INTRINSIC |
low complexity region
|
637 |
648 |
N/A |
INTRINSIC |
ZnF_C2H2
|
650 |
672 |
2.82e0 |
SMART |
low complexity region
|
675 |
684 |
N/A |
INTRINSIC |
low complexity region
|
695 |
714 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000093813
|
SMART Domains |
Protein: ENSMUSP00000091331 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
773 |
792 |
N/A |
INTRINSIC |
low complexity region
|
885 |
914 |
N/A |
INTRINSIC |
low complexity region
|
958 |
996 |
N/A |
INTRINSIC |
Pfam:RhoGEF
|
1087 |
1246 |
6.1e-9 |
PFAM |
PH
|
1264 |
1372 |
3.97e-8 |
SMART |
low complexity region
|
1403 |
1424 |
N/A |
INTRINSIC |
low complexity region
|
1478 |
1491 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000100639
|
SMART Domains |
Protein: ENSMUSP00000098204 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
773 |
792 |
N/A |
INTRINSIC |
low complexity region
|
885 |
914 |
N/A |
INTRINSIC |
low complexity region
|
958 |
996 |
N/A |
INTRINSIC |
Pfam:RhoGEF
|
1087 |
1246 |
5.9e-9 |
PFAM |
PH
|
1264 |
1372 |
3.97e-8 |
SMART |
low complexity region
|
1430 |
1443 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000166169
AA Change: R5H
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000126854 Gene: ENSMUSG00000049295 AA Change: R5H
Domain | Start | End | E-Value | Type |
low complexity region
|
30 |
47 |
N/A |
INTRINSIC |
ZnF_C2H2
|
61 |
83 |
6.23e-2 |
SMART |
ZnF_C2H2
|
89 |
111 |
4.17e-3 |
SMART |
low complexity region
|
113 |
146 |
N/A |
INTRINSIC |
ZnF_C2H2
|
167 |
190 |
3.07e-1 |
SMART |
ZnF_C2H2
|
193 |
216 |
1.51e0 |
SMART |
low complexity region
|
229 |
276 |
N/A |
INTRINSIC |
ZnF_C2H2
|
277 |
299 |
8.47e-4 |
SMART |
ZnF_C2H2
|
305 |
327 |
1.38e-3 |
SMART |
low complexity region
|
331 |
350 |
N/A |
INTRINSIC |
low complexity region
|
354 |
379 |
N/A |
INTRINSIC |
low complexity region
|
427 |
441 |
N/A |
INTRINSIC |
ZnF_C2H2
|
501 |
523 |
3.63e-3 |
SMART |
ZnF_C2H2
|
529 |
551 |
1.58e-3 |
SMART |
low complexity region
|
560 |
570 |
N/A |
INTRINSIC |
low complexity region
|
594 |
611 |
N/A |
INTRINSIC |
low complexity region
|
637 |
648 |
N/A |
INTRINSIC |
ZnF_C2H2
|
650 |
672 |
2.82e0 |
SMART |
low complexity region
|
675 |
684 |
N/A |
INTRINSIC |
low complexity region
|
695 |
714 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182061
|
SMART Domains |
Protein: ENSMUSP00000138128 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
773 |
792 |
N/A |
INTRINSIC |
low complexity region
|
885 |
914 |
N/A |
INTRINSIC |
low complexity region
|
958 |
996 |
N/A |
INTRINSIC |
Pfam:RhoGEF
|
1087 |
1247 |
3.7e-9 |
PFAM |
PH
|
1264 |
1372 |
3.97e-8 |
SMART |
low complexity region
|
1430 |
1443 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182217
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182504
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182931
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000183213
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182644
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182777
|
Predicted Effect |
unknown
Transcript: ENSMUST00000226554
AA Change: R5H
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000226527
AA Change: R5H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000226522
AA Change: R5H
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182909
|
SMART Domains |
Protein: ENSMUSP00000138635 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
773 |
792 |
N/A |
INTRINSIC |
low complexity region
|
885 |
914 |
N/A |
INTRINSIC |
low complexity region
|
958 |
996 |
N/A |
INTRINSIC |
Pfam:RhoGEF
|
1087 |
1247 |
3.9e-9 |
PFAM |
PH
|
1264 |
1372 |
3.97e-8 |
SMART |
low complexity region
|
1403 |
1424 |
N/A |
INTRINSIC |
low complexity region
|
1478 |
1491 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182905
|
SMART Domains |
Protein: ENSMUSP00000138797 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
773 |
792 |
N/A |
INTRINSIC |
low complexity region
|
885 |
914 |
N/A |
INTRINSIC |
low complexity region
|
958 |
996 |
N/A |
INTRINSIC |
SCOP:d1kz7a1
|
1073 |
1162 |
4e-7 |
SMART |
Blast:RhoGEF
|
1087 |
1157 |
1e-8 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000226474
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182760
|
SMART Domains |
Protein: ENSMUSP00000138125 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
low complexity region
|
451 |
472 |
N/A |
INTRINSIC |
low complexity region
|
550 |
564 |
N/A |
INTRINSIC |
low complexity region
|
581 |
606 |
N/A |
INTRINSIC |
low complexity region
|
782 |
801 |
N/A |
INTRINSIC |
low complexity region
|
894 |
923 |
N/A |
INTRINSIC |
low complexity region
|
967 |
1005 |
N/A |
INTRINSIC |
Pfam:RhoGEF
|
1096 |
1256 |
5.9e-9 |
PFAM |
PH
|
1273 |
1381 |
3.97e-8 |
SMART |
low complexity region
|
1412 |
1433 |
N/A |
INTRINSIC |
low complexity region
|
1487 |
1500 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000183208
|
SMART Domains |
Protein: ENSMUSP00000138354 Gene: ENSMUSG00000004562
Domain | Start | End | E-Value | Type |
low complexity region
|
201 |
223 |
N/A |
INTRINSIC |
low complexity region
|
306 |
320 |
N/A |
INTRINSIC |
low complexity region
|
332 |
345 |
N/A |
INTRINSIC |
low complexity region
|
351 |
395 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182828
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000182667
|
Predicted Effect |
unknown
Transcript: ENSMUST00000228162
AA Change: R5H
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000226605
AA Change: R5H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000226964
AA Change: R5H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000228051
AA Change: R5H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000228747
AA Change: R5H
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000228580
|
Meta Mutation Damage Score |
0.0996 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.9%
- 20x: 94.1%
|
Validation Efficiency |
99% (72/73) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acadsb |
A |
T |
7: 131,042,929 (GRCm39) |
|
probably null |
Het |
Actl6a |
A |
G |
3: 32,774,656 (GRCm39) |
I340V |
possibly damaging |
Het |
Alppl2 |
C |
T |
1: 87,017,431 (GRCm39) |
V19I |
probably benign |
Het |
Ankrd34c |
T |
C |
9: 89,611,759 (GRCm39) |
K194R |
probably benign |
Het |
Anpep |
T |
A |
7: 79,483,475 (GRCm39) |
M672L |
probably benign |
Het |
Arhgap31 |
T |
C |
16: 38,423,438 (GRCm39) |
D876G |
probably damaging |
Het |
Arid2 |
T |
A |
15: 96,269,869 (GRCm39) |
N1327K |
probably damaging |
Het |
Atp5f1d |
C |
A |
10: 79,981,263 (GRCm39) |
P101Q |
probably benign |
Het |
Bcl7b |
G |
A |
5: 135,200,017 (GRCm39) |
|
probably null |
Het |
Brca2 |
A |
T |
5: 150,483,901 (GRCm39) |
S2907C |
probably damaging |
Het |
Ccser2 |
T |
C |
14: 36,662,134 (GRCm39) |
E350G |
probably benign |
Het |
Cdh23 |
G |
T |
10: 60,143,811 (GRCm39) |
D2929E |
probably damaging |
Het |
Clec2i |
T |
A |
6: 128,870,621 (GRCm39) |
V78E |
probably benign |
Het |
Cpxm1 |
A |
T |
2: 130,237,897 (GRCm39) |
|
probably null |
Het |
Crybg3 |
C |
T |
16: 59,375,159 (GRCm39) |
V2032I |
possibly damaging |
Het |
Eif5b |
A |
T |
1: 38,058,150 (GRCm39) |
K151* |
probably null |
Het |
Gemin7 |
T |
A |
7: 19,299,348 (GRCm39) |
E82D |
possibly damaging |
Het |
Gm14496 |
A |
G |
2: 181,633,152 (GRCm39) |
E45G |
possibly damaging |
Het |
Gm21915 |
T |
C |
9: 40,581,966 (GRCm39) |
S20P |
probably damaging |
Het |
Gm8126 |
A |
C |
14: 43,119,026 (GRCm39) |
E165A |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,710,405 (GRCm39) |
D1047G |
probably benign |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Ikbke |
T |
A |
1: 131,201,397 (GRCm39) |
Y150F |
probably damaging |
Het |
Inhca |
T |
C |
9: 103,159,701 (GRCm39) |
D70G |
probably benign |
Het |
Itih5 |
T |
A |
2: 10,245,315 (GRCm39) |
|
probably null |
Het |
Lrig2 |
T |
C |
3: 104,365,217 (GRCm39) |
Q645R |
possibly damaging |
Het |
Map4 |
A |
G |
9: 109,897,868 (GRCm39) |
M712V |
probably benign |
Het |
Mecom |
A |
G |
3: 30,015,255 (GRCm39) |
S823P |
probably damaging |
Het |
Mettl25 |
A |
G |
10: 105,662,068 (GRCm39) |
Y301H |
possibly damaging |
Het |
Mga |
A |
T |
2: 119,781,654 (GRCm39) |
K2136* |
probably null |
Het |
Mmp24 |
A |
G |
2: 155,652,204 (GRCm39) |
E304G |
probably benign |
Het |
Mmp3 |
T |
A |
9: 7,445,984 (GRCm39) |
D29E |
probably benign |
Het |
Nbas |
T |
A |
12: 13,424,713 (GRCm39) |
I984N |
probably damaging |
Het |
Nedd9 |
A |
G |
13: 41,469,270 (GRCm39) |
Y628H |
probably damaging |
Het |
Nlrp2 |
C |
T |
7: 5,331,076 (GRCm39) |
C440Y |
probably damaging |
Het |
Or4g16 |
T |
C |
2: 111,136,637 (GRCm39) |
V29A |
probably benign |
Het |
Or6p1 |
T |
G |
1: 174,258,237 (GRCm39) |
L81R |
probably damaging |
Het |
P4ha2 |
T |
C |
11: 54,022,016 (GRCm39) |
V513A |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,161,869 (GRCm39) |
N124S |
probably benign |
Het |
Phf12 |
T |
C |
11: 77,914,622 (GRCm39) |
F139S |
probably damaging |
Het |
Phlpp2 |
T |
A |
8: 110,666,714 (GRCm39) |
L1081H |
probably damaging |
Het |
Phospho2 |
T |
A |
2: 69,626,323 (GRCm39) |
F160I |
probably damaging |
Het |
Plch2 |
T |
G |
4: 155,091,540 (GRCm39) |
D115A |
probably damaging |
Het |
Plekho1 |
A |
G |
3: 95,896,851 (GRCm39) |
F215S |
probably damaging |
Het |
Psma4 |
C |
A |
9: 54,860,056 (GRCm39) |
A47E |
probably damaging |
Het |
Rasa4 |
A |
C |
5: 136,130,153 (GRCm39) |
Q303P |
probably damaging |
Het |
Rbmxl2 |
C |
T |
7: 106,809,414 (GRCm39) |
P233L |
probably damaging |
Het |
Reln |
A |
T |
5: 22,239,636 (GRCm39) |
L877H |
probably damaging |
Het |
Rtel1 |
A |
G |
2: 180,964,307 (GRCm39) |
|
probably null |
Het |
Septin12 |
T |
C |
16: 4,811,620 (GRCm39) |
D116G |
probably damaging |
Het |
Son |
T |
A |
16: 91,453,263 (GRCm39) |
V670E |
probably damaging |
Het |
Spag9 |
T |
A |
11: 93,988,612 (GRCm39) |
I544N |
probably benign |
Het |
Spsb3 |
T |
G |
17: 25,106,036 (GRCm39) |
|
probably benign |
Het |
Tcstv2c |
T |
C |
13: 120,616,652 (GRCm39) |
F164L |
possibly damaging |
Het |
Tgfbr3 |
T |
C |
5: 107,362,836 (GRCm39) |
T59A |
probably damaging |
Het |
Tsc1 |
T |
A |
2: 28,566,531 (GRCm39) |
I649K |
probably damaging |
Het |
Txndc9 |
T |
C |
1: 38,034,793 (GRCm39) |
D37G |
probably benign |
Het |
Uba7 |
C |
T |
9: 107,856,113 (GRCm39) |
A496V |
probably benign |
Het |
Usf3 |
T |
A |
16: 44,035,889 (GRCm39) |
I123N |
probably damaging |
Het |
Vmn1r184 |
T |
A |
7: 25,966,955 (GRCm39) |
S234T |
possibly damaging |
Het |
Vsig10l |
C |
A |
7: 43,114,741 (GRCm39) |
S314* |
probably null |
Het |
Wdfy4 |
A |
G |
14: 32,801,892 (GRCm39) |
F1922S |
probably damaging |
Het |
Zfp946 |
G |
T |
17: 22,674,584 (GRCm39) |
C446F |
probably benign |
Het |
|
Other mutations in Zfp219 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02134:Zfp219
|
APN |
14 |
52,246,758 (GRCm39) |
missense |
probably damaging |
1.00 |
Bart
|
UTSW |
14 |
52,244,163 (GRCm39) |
missense |
probably damaging |
0.99 |
Bert
|
UTSW |
14 |
52,244,395 (GRCm39) |
missense |
probably benign |
0.02 |
R0019:Zfp219
|
UTSW |
14 |
52,246,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Zfp219
|
UTSW |
14 |
52,244,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R0811:Zfp219
|
UTSW |
14 |
52,244,395 (GRCm39) |
missense |
probably benign |
0.02 |
R0812:Zfp219
|
UTSW |
14 |
52,244,395 (GRCm39) |
missense |
probably benign |
0.02 |
R1677:Zfp219
|
UTSW |
14 |
52,246,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Zfp219
|
UTSW |
14 |
52,244,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1921:Zfp219
|
UTSW |
14 |
52,245,691 (GRCm39) |
missense |
probably benign |
0.00 |
R2929:Zfp219
|
UTSW |
14 |
52,246,436 (GRCm39) |
missense |
probably benign |
0.00 |
R3970:Zfp219
|
UTSW |
14 |
52,244,421 (GRCm39) |
missense |
probably benign |
0.05 |
R4485:Zfp219
|
UTSW |
14 |
52,244,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R5206:Zfp219
|
UTSW |
14 |
52,247,022 (GRCm39) |
missense |
probably benign |
0.40 |
R5244:Zfp219
|
UTSW |
14 |
52,245,999 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5907:Zfp219
|
UTSW |
14 |
52,244,606 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6903:Zfp219
|
UTSW |
14 |
52,244,118 (GRCm39) |
missense |
probably benign |
0.31 |
R7409:Zfp219
|
UTSW |
14 |
52,244,570 (GRCm39) |
nonsense |
probably null |
|
R8725:Zfp219
|
UTSW |
14 |
52,244,899 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8937:Zfp219
|
UTSW |
14 |
52,244,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R9135:Zfp219
|
UTSW |
14 |
52,244,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Zfp219
|
UTSW |
14 |
52,246,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R9203:Zfp219
|
UTSW |
14 |
52,246,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R9297:Zfp219
|
UTSW |
14 |
52,246,494 (GRCm39) |
missense |
probably damaging |
0.98 |
R9313:Zfp219
|
UTSW |
14 |
52,246,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R9717:Zfp219
|
UTSW |
14 |
52,247,049 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTCCGCACACAGGACAAGG -3'
(R):5'- TACGTTATTAACTTGGCCCCG -3'
Sequencing Primer
(F):5'- ACAAGGGAAGCGCCGTTC -3'
(R):5'- ATTAACTTGGCCCCGGTGTC -3'
|
Posted On |
2016-06-06 |