Incidental Mutation 'IGL02867:Zfp629'
ID |
362384 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp629
|
Ensembl Gene |
ENSMUSG00000045639 |
Gene Name |
zinc finger protein 629 |
Synonyms |
9330199A09Rik |
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.277)
|
Stock # |
IGL02867
|
Quality Score |
|
Status
|
|
Chromosome |
7 |
Chromosomal Location |
127206203-127214969 bp(-) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
T to G
at 127209203 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000114772
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000058038]
[ENSMUST00000084564]
[ENSMUST00000122066]
[ENSMUST00000128731]
[ENSMUST00000131318]
[ENSMUST00000132524]
[ENSMUST00000134446]
[ENSMUST00000151107]
[ENSMUST00000152315]
|
AlphaFold |
Q6A085 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000058038
|
SMART Domains |
Protein: ENSMUSP00000053760 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
43 |
N/A |
INTRINSIC |
low complexity region
|
93 |
104 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
4.01e-5 |
SMART |
ZnF_C2H2
|
177 |
199 |
2.09e-3 |
SMART |
ZnF_C2H2
|
205 |
227 |
6.08e-5 |
SMART |
ZnF_C2H2
|
233 |
255 |
2.99e-4 |
SMART |
ZnF_C2H2
|
261 |
283 |
1.45e-2 |
SMART |
ZnF_C2H2
|
289 |
311 |
1.13e-4 |
SMART |
ZnF_C2H2
|
317 |
339 |
9.88e-5 |
SMART |
ZnF_C2H2
|
345 |
367 |
9.73e-4 |
SMART |
ZnF_C2H2
|
373 |
395 |
9.22e-5 |
SMART |
ZnF_C2H2
|
401 |
423 |
6.08e-5 |
SMART |
ZnF_C2H2
|
429 |
451 |
7.78e-3 |
SMART |
ZnF_C2H2
|
457 |
479 |
3.95e-4 |
SMART |
ZnF_C2H2
|
485 |
507 |
1.15e-5 |
SMART |
ZnF_C2H2
|
513 |
535 |
2.91e-2 |
SMART |
ZnF_C2H2
|
568 |
590 |
9.58e-3 |
SMART |
ZnF_C2H2
|
661 |
683 |
3.16e-3 |
SMART |
ZnF_C2H2
|
713 |
735 |
9.73e-4 |
SMART |
low complexity region
|
737 |
754 |
N/A |
INTRINSIC |
ZnF_C2H2
|
766 |
788 |
2.57e-3 |
SMART |
ZnF_C2H2
|
840 |
862 |
1.14e0 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000084564
|
SMART Domains |
Protein: ENSMUSP00000081612 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
43 |
N/A |
INTRINSIC |
low complexity region
|
93 |
104 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
4.01e-5 |
SMART |
ZnF_C2H2
|
177 |
199 |
2.09e-3 |
SMART |
ZnF_C2H2
|
205 |
227 |
6.08e-5 |
SMART |
ZnF_C2H2
|
233 |
255 |
2.99e-4 |
SMART |
ZnF_C2H2
|
261 |
283 |
1.45e-2 |
SMART |
ZnF_C2H2
|
289 |
311 |
1.13e-4 |
SMART |
ZnF_C2H2
|
317 |
339 |
9.88e-5 |
SMART |
ZnF_C2H2
|
345 |
367 |
9.73e-4 |
SMART |
ZnF_C2H2
|
373 |
395 |
9.22e-5 |
SMART |
ZnF_C2H2
|
401 |
423 |
6.08e-5 |
SMART |
ZnF_C2H2
|
429 |
451 |
7.78e-3 |
SMART |
ZnF_C2H2
|
457 |
479 |
3.95e-4 |
SMART |
ZnF_C2H2
|
485 |
507 |
1.15e-5 |
SMART |
ZnF_C2H2
|
513 |
535 |
2.91e-2 |
SMART |
ZnF_C2H2
|
568 |
590 |
9.58e-3 |
SMART |
ZnF_C2H2
|
661 |
683 |
3.16e-3 |
SMART |
ZnF_C2H2
|
713 |
735 |
9.73e-4 |
SMART |
low complexity region
|
737 |
754 |
N/A |
INTRINSIC |
ZnF_C2H2
|
766 |
788 |
2.57e-3 |
SMART |
ZnF_C2H2
|
840 |
862 |
1.14e0 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000122066
|
SMART Domains |
Protein: ENSMUSP00000113903 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
43 |
N/A |
INTRINSIC |
low complexity region
|
93 |
104 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
4.01e-5 |
SMART |
ZnF_C2H2
|
177 |
199 |
2.09e-3 |
SMART |
ZnF_C2H2
|
205 |
227 |
6.08e-5 |
SMART |
ZnF_C2H2
|
233 |
255 |
2.99e-4 |
SMART |
ZnF_C2H2
|
261 |
283 |
1.45e-2 |
SMART |
ZnF_C2H2
|
289 |
311 |
1.13e-4 |
SMART |
ZnF_C2H2
|
317 |
339 |
9.88e-5 |
SMART |
ZnF_C2H2
|
345 |
367 |
9.73e-4 |
SMART |
ZnF_C2H2
|
373 |
395 |
9.22e-5 |
SMART |
ZnF_C2H2
|
401 |
423 |
6.08e-5 |
SMART |
ZnF_C2H2
|
429 |
451 |
7.78e-3 |
SMART |
ZnF_C2H2
|
457 |
479 |
3.95e-4 |
SMART |
ZnF_C2H2
|
485 |
507 |
1.15e-5 |
SMART |
ZnF_C2H2
|
513 |
535 |
2.91e-2 |
SMART |
ZnF_C2H2
|
568 |
590 |
9.58e-3 |
SMART |
ZnF_C2H2
|
661 |
683 |
3.16e-3 |
SMART |
ZnF_C2H2
|
713 |
735 |
9.73e-4 |
SMART |
low complexity region
|
737 |
754 |
N/A |
INTRINSIC |
ZnF_C2H2
|
766 |
788 |
2.57e-3 |
SMART |
ZnF_C2H2
|
840 |
862 |
1.14e0 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128731
|
SMART Domains |
Protein: ENSMUSP00000140505 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
78 |
90 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000131318
|
SMART Domains |
Protein: ENSMUSP00000116375 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
43 |
N/A |
INTRINSIC |
low complexity region
|
93 |
104 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
4.01e-5 |
SMART |
ZnF_C2H2
|
177 |
199 |
2.09e-3 |
SMART |
ZnF_C2H2
|
205 |
227 |
6.08e-5 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000132524
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134446
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151107
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000152315
|
SMART Domains |
Protein: ENSMUSP00000114772 Gene: ENSMUSG00000045639
Domain | Start | End | E-Value | Type |
low complexity region
|
27 |
43 |
N/A |
INTRINSIC |
low complexity region
|
93 |
104 |
N/A |
INTRINSIC |
ZnF_C2H2
|
149 |
171 |
4.01e-5 |
SMART |
ZnF_C2H2
|
177 |
195 |
1.24e2 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf2 |
T |
A |
5: 24,776,149 (GRCm39) |
Y310F |
probably benign |
Het |
Adarb1 |
C |
T |
10: 77,149,375 (GRCm39) |
V371I |
probably benign |
Het |
Antxr2 |
G |
T |
5: 98,125,509 (GRCm39) |
H249Q |
probably benign |
Het |
Arel1 |
A |
T |
12: 84,981,097 (GRCm39) |
N303K |
probably benign |
Het |
Bloc1s6 |
T |
C |
2: 122,584,604 (GRCm39) |
Y60H |
probably damaging |
Het |
Ccdc125 |
A |
T |
13: 100,820,790 (GRCm39) |
|
probably benign |
Het |
Cxcl16 |
A |
T |
11: 70,349,892 (GRCm39) |
Y45N |
possibly damaging |
Het |
Dnajb3 |
T |
A |
1: 88,133,249 (GRCm39) |
Q51L |
probably benign |
Het |
Ear10 |
A |
G |
14: 44,160,726 (GRCm39) |
F34L |
probably damaging |
Het |
Fgf11 |
A |
G |
11: 69,690,498 (GRCm39) |
S100P |
possibly damaging |
Het |
Fpgs |
G |
A |
2: 32,575,891 (GRCm39) |
|
probably benign |
Het |
Fyb1 |
A |
T |
15: 6,609,527 (GRCm39) |
Q33H |
probably damaging |
Het |
Ints3 |
G |
T |
3: 90,300,143 (GRCm39) |
H925N |
probably damaging |
Het |
Krt16 |
T |
C |
11: 100,138,402 (GRCm39) |
K249E |
probably damaging |
Het |
Lrp2 |
A |
T |
2: 69,382,794 (GRCm39) |
S30R |
possibly damaging |
Het |
Naa35 |
T |
C |
13: 59,756,668 (GRCm39) |
|
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,770,970 (GRCm39) |
I34V |
probably benign |
Het |
Or1e22 |
A |
G |
11: 73,376,817 (GRCm39) |
Y278H |
probably damaging |
Het |
Or8g2b |
A |
G |
9: 39,751,533 (GRCm39) |
M268V |
probably benign |
Het |
Osbpl6 |
A |
G |
2: 76,426,214 (GRCm39) |
|
probably benign |
Het |
Pramel6 |
A |
T |
2: 87,340,736 (GRCm39) |
Q356L |
probably damaging |
Het |
Prima1 |
A |
G |
12: 103,163,575 (GRCm39) |
V132A |
probably benign |
Het |
Psme1 |
A |
G |
14: 55,817,383 (GRCm39) |
|
probably benign |
Het |
Rdh11 |
A |
G |
12: 79,235,828 (GRCm39) |
V40A |
possibly damaging |
Het |
Rin1 |
C |
T |
19: 5,103,198 (GRCm39) |
R485C |
probably damaging |
Het |
Rnf40 |
C |
A |
7: 127,190,601 (GRCm39) |
S255* |
probably null |
Het |
Spata24 |
C |
A |
18: 35,789,805 (GRCm39) |
R194L |
probably benign |
Het |
Spata31h1 |
C |
T |
10: 82,119,654 (GRCm39) |
S482N |
probably damaging |
Het |
Tas1r1 |
A |
T |
4: 152,112,735 (GRCm39) |
S773T |
probably damaging |
Het |
Trdv5 |
G |
T |
14: 54,386,429 (GRCm39) |
|
probably benign |
Het |
Trpc3 |
A |
C |
3: 36,694,850 (GRCm39) |
D701E |
probably benign |
Het |
Vim |
A |
G |
2: 13,585,491 (GRCm39) |
R424G |
probably damaging |
Het |
Vmn1r216 |
A |
C |
13: 23,283,649 (GRCm39) |
T111P |
probably damaging |
Het |
Zbtb26 |
A |
C |
2: 37,326,261 (GRCm39) |
N247K |
probably benign |
Het |
|
Other mutations in Zfp629 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00957:Zfp629
|
APN |
7 |
127,211,896 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01541:Zfp629
|
APN |
7 |
127,211,917 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02116:Zfp629
|
APN |
7 |
127,211,890 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02134:Zfp629
|
APN |
7 |
127,211,042 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02547:Zfp629
|
APN |
7 |
127,210,846 (GRCm39) |
splice site |
probably null |
|
IGL02858:Zfp629
|
APN |
7 |
127,209,484 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02889:Zfp629
|
APN |
7 |
127,209,203 (GRCm39) |
unclassified |
probably benign |
|
R6768_Zfp629_044
|
UTSW |
7 |
127,209,997 (GRCm39) |
missense |
probably benign |
0.03 |
R0020:Zfp629
|
UTSW |
7 |
127,210,341 (GRCm39) |
missense |
probably benign |
0.02 |
R0137:Zfp629
|
UTSW |
7 |
127,210,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Zfp629
|
UTSW |
7 |
127,211,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Zfp629
|
UTSW |
7 |
127,211,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R1182:Zfp629
|
UTSW |
7 |
127,209,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1187:Zfp629
|
UTSW |
7 |
127,209,401 (GRCm39) |
missense |
probably benign |
|
R1187:Zfp629
|
UTSW |
7 |
127,211,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Zfp629
|
UTSW |
7 |
127,211,916 (GRCm39) |
start gained |
probably benign |
|
R1507:Zfp629
|
UTSW |
7 |
127,211,033 (GRCm39) |
nonsense |
probably null |
|
R1526:Zfp629
|
UTSW |
7 |
127,209,931 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1622:Zfp629
|
UTSW |
7 |
127,211,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R1704:Zfp629
|
UTSW |
7 |
127,210,036 (GRCm39) |
missense |
probably benign |
0.06 |
R1918:Zfp629
|
UTSW |
7 |
127,211,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R2147:Zfp629
|
UTSW |
7 |
127,209,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R2156:Zfp629
|
UTSW |
7 |
127,211,551 (GRCm39) |
missense |
probably benign |
0.00 |
R2258:Zfp629
|
UTSW |
7 |
127,210,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R2994:Zfp629
|
UTSW |
7 |
127,210,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R3735:Zfp629
|
UTSW |
7 |
127,211,950 (GRCm39) |
splice site |
probably benign |
|
R4287:Zfp629
|
UTSW |
7 |
127,211,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Zfp629
|
UTSW |
7 |
127,211,492 (GRCm39) |
missense |
probably benign |
0.26 |
R4758:Zfp629
|
UTSW |
7 |
127,209,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Zfp629
|
UTSW |
7 |
127,210,190 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4922:Zfp629
|
UTSW |
7 |
127,211,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5414:Zfp629
|
UTSW |
7 |
127,210,454 (GRCm39) |
missense |
probably damaging |
0.97 |
R5772:Zfp629
|
UTSW |
7 |
127,210,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R5907:Zfp629
|
UTSW |
7 |
127,209,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768:Zfp629
|
UTSW |
7 |
127,209,997 (GRCm39) |
missense |
probably benign |
0.03 |
R7122:Zfp629
|
UTSW |
7 |
127,210,484 (GRCm39) |
missense |
probably damaging |
0.99 |
R7156:Zfp629
|
UTSW |
7 |
127,211,463 (GRCm39) |
nonsense |
probably null |
|
R7407:Zfp629
|
UTSW |
7 |
127,209,415 (GRCm39) |
missense |
probably benign |
|
R7446:Zfp629
|
UTSW |
7 |
127,210,201 (GRCm39) |
missense |
probably benign |
0.00 |
R7780:Zfp629
|
UTSW |
7 |
127,211,601 (GRCm39) |
missense |
probably benign |
0.12 |
R7871:Zfp629
|
UTSW |
7 |
127,211,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:Zfp629
|
UTSW |
7 |
127,210,364 (GRCm39) |
nonsense |
probably null |
|
R9095:Zfp629
|
UTSW |
7 |
127,209,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-12-18 |