Incidental Mutation 'IGL02674:Zfp263'
ID |
303067 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp263
|
Ensembl Gene |
ENSMUSG00000022529 |
Gene Name |
zinc finger protein 263 |
Synonyms |
mFPM315, NT2, 1200014J04Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.121)
|
Stock # |
IGL02674
|
Quality Score |
|
Status
|
|
Chromosome |
16 |
Chromosomal Location |
3561957-3568654 bp(+) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
T to C
at 3564629 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000124433
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000023176]
[ENSMUST00000161630]
[ENSMUST00000162207]
|
AlphaFold |
Q8CF60 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000023176
|
SMART Domains |
Protein: ENSMUSP00000023176 Gene: ENSMUSG00000022529
Domain | Start | End | E-Value | Type |
SCAN
|
39 |
151 |
5.15e-71 |
SMART |
KRAB
|
219 |
279 |
1.86e-9 |
SMART |
ZnF_C2H2
|
378 |
400 |
1.45e-2 |
SMART |
ZnF_C2H2
|
434 |
456 |
3.11e-2 |
SMART |
ZnF_C2H2
|
462 |
484 |
1.2e-3 |
SMART |
ZnF_C2H2
|
490 |
512 |
6.52e-5 |
SMART |
ZnF_C2H2
|
518 |
540 |
1.98e-4 |
SMART |
ZnF_C2H2
|
572 |
594 |
2.4e-3 |
SMART |
ZnF_C2H2
|
600 |
622 |
4.87e-4 |
SMART |
ZnF_C2H2
|
628 |
650 |
1.1e-2 |
SMART |
ZnF_C2H2
|
656 |
678 |
1.72e-4 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159060
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159425
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159469
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000160923
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000161630
|
SMART Domains |
Protein: ENSMUSP00000123725 Gene: ENSMUSG00000022529
Domain | Start | End | E-Value | Type |
SCAN
|
39 |
143 |
1.61e-63 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162207
|
SMART Domains |
Protein: ENSMUSP00000124433 Gene: ENSMUSG00000022529
Domain | Start | End | E-Value | Type |
ZnF_C2H2
|
90 |
112 |
1.45e-2 |
SMART |
ZnF_C2H2
|
146 |
168 |
3.11e-2 |
SMART |
ZnF_C2H2
|
174 |
196 |
1.2e-3 |
SMART |
ZnF_C2H2
|
202 |
224 |
6.52e-5 |
SMART |
ZnF_C2H2
|
230 |
252 |
1.98e-4 |
SMART |
ZnF_C2H2
|
284 |
306 |
2.4e-3 |
SMART |
ZnF_C2H2
|
312 |
334 |
4.87e-4 |
SMART |
ZnF_C2H2
|
340 |
362 |
1.1e-2 |
SMART |
ZnF_C2H2
|
368 |
390 |
1.72e-4 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago2 |
T |
C |
15: 72,983,643 (GRCm39) |
R689G |
probably damaging |
Het |
Agrn |
C |
T |
4: 156,259,018 (GRCm39) |
|
probably benign |
Het |
Akna |
A |
T |
4: 63,289,181 (GRCm39) |
C1247* |
probably null |
Het |
Appl1 |
T |
G |
14: 26,671,418 (GRCm39) |
T345P |
possibly damaging |
Het |
Chga |
A |
G |
12: 102,529,160 (GRCm39) |
D379G |
probably damaging |
Het |
Chrna6 |
C |
T |
8: 27,896,879 (GRCm39) |
A333T |
probably benign |
Het |
Col14a1 |
G |
A |
15: 55,282,178 (GRCm39) |
G813E |
unknown |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,370,688 (GRCm39) |
Q4656R |
probably benign |
Het |
Dock9 |
A |
C |
14: 121,833,023 (GRCm39) |
|
probably null |
Het |
Fat4 |
A |
G |
3: 39,037,486 (GRCm39) |
N3713D |
probably benign |
Het |
Fsd1 |
A |
T |
17: 56,303,483 (GRCm39) |
T452S |
probably benign |
Het |
G6pc2 |
A |
G |
2: 69,056,910 (GRCm39) |
|
probably null |
Het |
Gfus |
T |
C |
15: 75,798,238 (GRCm39) |
D178G |
probably damaging |
Het |
Itprid1 |
A |
G |
6: 55,874,913 (GRCm39) |
T288A |
probably benign |
Het |
Kcnh4 |
C |
A |
11: 100,637,720 (GRCm39) |
V646L |
possibly damaging |
Het |
Kcnk1 |
T |
C |
8: 126,751,753 (GRCm39) |
Y120H |
probably damaging |
Het |
L3mbtl3 |
C |
T |
10: 26,158,711 (GRCm39) |
E646K |
unknown |
Het |
Lrrc4c |
T |
C |
2: 97,460,120 (GRCm39) |
W249R |
probably damaging |
Het |
Meox1 |
A |
T |
11: 101,784,767 (GRCm39) |
L22H |
probably damaging |
Het |
Mrgpra4 |
C |
T |
7: 47,630,690 (GRCm39) |
V304M |
probably benign |
Het |
Ncaph |
T |
C |
2: 126,955,496 (GRCm39) |
Y554C |
probably damaging |
Het |
Nfx1 |
T |
C |
4: 40,999,717 (GRCm39) |
|
probably null |
Het |
Or10p1 |
A |
C |
10: 129,443,939 (GRCm39) |
M137R |
possibly damaging |
Het |
Or8g37 |
A |
G |
9: 39,730,934 (GRCm39) |
|
probably null |
Het |
Otol1 |
C |
T |
3: 69,926,077 (GRCm39) |
P84L |
probably benign |
Het |
Pcdhb11 |
T |
C |
18: 37,556,667 (GRCm39) |
S666P |
probably damaging |
Het |
Pou2f3 |
T |
C |
9: 43,050,628 (GRCm39) |
K244R |
probably damaging |
Het |
Ppp6r1 |
T |
C |
7: 4,649,812 (GRCm39) |
N51S |
probably damaging |
Het |
Prdm4 |
A |
T |
10: 85,729,263 (GRCm39) |
L715M |
probably damaging |
Het |
Rgs11 |
G |
A |
17: 26,426,605 (GRCm39) |
V279I |
probably benign |
Het |
Rsc1a1 |
G |
T |
4: 141,411,406 (GRCm39) |
P502Q |
probably damaging |
Het |
Senp1 |
T |
C |
15: 97,954,840 (GRCm39) |
E448G |
probably damaging |
Het |
Shd |
A |
G |
17: 56,278,554 (GRCm39) |
D39G |
possibly damaging |
Het |
Skint5 |
A |
C |
4: 113,487,582 (GRCm39) |
|
probably benign |
Het |
Tmprss15 |
T |
G |
16: 78,798,682 (GRCm39) |
T667P |
possibly damaging |
Het |
Vps13b |
A |
T |
15: 35,640,104 (GRCm39) |
M1325L |
probably benign |
Het |
Zfp786 |
A |
G |
6: 47,797,427 (GRCm39) |
F504L |
probably benign |
Het |
|
Other mutations in Zfp263 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Zfp263
|
APN |
16 |
3,563,710 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01112:Zfp263
|
APN |
16 |
3,566,776 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02049:Zfp263
|
APN |
16 |
3,562,482 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02534:Zfp263
|
APN |
16 |
3,564,279 (GRCm39) |
unclassified |
probably benign |
|
IGL03065:Zfp263
|
APN |
16 |
3,564,344 (GRCm39) |
missense |
probably benign |
|
IGL03105:Zfp263
|
APN |
16 |
3,566,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03153:Zfp263
|
APN |
16 |
3,564,744 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02796:Zfp263
|
UTSW |
16 |
3,564,740 (GRCm39) |
missense |
probably benign |
0.03 |
R1201:Zfp263
|
UTSW |
16 |
3,567,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R1414:Zfp263
|
UTSW |
16 |
3,567,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Zfp263
|
UTSW |
16 |
3,564,323 (GRCm39) |
missense |
probably benign |
0.18 |
R3085:Zfp263
|
UTSW |
16 |
3,567,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4368:Zfp263
|
UTSW |
16 |
3,562,770 (GRCm39) |
unclassified |
probably benign |
|
R4989:Zfp263
|
UTSW |
16 |
3,566,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Zfp263
|
UTSW |
16 |
3,564,704 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5073:Zfp263
|
UTSW |
16 |
3,564,704 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5074:Zfp263
|
UTSW |
16 |
3,564,704 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5122:Zfp263
|
UTSW |
16 |
3,567,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R5705:Zfp263
|
UTSW |
16 |
3,564,318 (GRCm39) |
missense |
probably benign |
0.00 |
R6140:Zfp263
|
UTSW |
16 |
3,566,081 (GRCm39) |
missense |
probably benign |
0.10 |
R6879:Zfp263
|
UTSW |
16 |
3,567,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R7133:Zfp263
|
UTSW |
16 |
3,567,255 (GRCm39) |
nonsense |
probably null |
|
R7216:Zfp263
|
UTSW |
16 |
3,562,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R8517:Zfp263
|
UTSW |
16 |
3,564,760 (GRCm39) |
critical splice donor site |
probably null |
|
R8822:Zfp263
|
UTSW |
16 |
3,562,004 (GRCm39) |
unclassified |
probably benign |
|
R9130:Zfp263
|
UTSW |
16 |
3,567,701 (GRCm39) |
missense |
probably benign |
0.06 |
R9172:Zfp263
|
UTSW |
16 |
3,567,323 (GRCm39) |
missense |
probably benign |
0.22 |
R9512:Zfp263
|
UTSW |
16 |
3,564,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Zfp263
|
UTSW |
16 |
3,567,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Posted On |
2015-04-16 |