Incidental Mutation 'IGL02534:Zfp263'
ID |
297445 |
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 # |
IGL02534
|
Quality Score |
|
Status
|
|
Chromosome |
16 |
Chromosomal Location |
3561957-3568654 bp(+) (GRCm39) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
T to A
at 3564279 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: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aggf1 |
C |
T |
13: 95,506,030 (GRCm39) |
E186K |
possibly damaging |
Het |
Ajm1 |
G |
T |
2: 25,467,043 (GRCm39) |
S956* |
probably null |
Het |
Anks1b |
A |
G |
10: 90,730,979 (GRCm39) |
I932V |
probably benign |
Het |
Atg2b |
A |
G |
12: 105,609,526 (GRCm39) |
Y1361H |
probably damaging |
Het |
Bcl9 |
G |
T |
3: 97,122,545 (GRCm39) |
L85M |
probably damaging |
Het |
Bcl9l |
T |
G |
9: 44,417,036 (GRCm39) |
S291R |
probably benign |
Het |
Cpa2 |
T |
A |
6: 30,550,767 (GRCm39) |
D201E |
probably benign |
Het |
Efna5 |
A |
T |
17: 62,920,384 (GRCm39) |
C164* |
probably null |
Het |
Fhip2b |
A |
T |
14: 70,823,128 (GRCm39) |
H642Q |
probably damaging |
Het |
Fhip2b |
T |
A |
14: 70,823,630 (GRCm39) |
H580L |
probably benign |
Het |
Gm6316 |
A |
G |
12: 69,967,763 (GRCm39) |
|
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,500 (GRCm39) |
S57P |
probably damaging |
Het |
Inf2 |
C |
A |
12: 112,576,930 (GRCm39) |
A968E |
unknown |
Het |
Man2a2 |
G |
A |
7: 80,009,388 (GRCm39) |
A822V |
probably damaging |
Het |
Mcm5 |
T |
A |
8: 75,840,861 (GRCm39) |
V222E |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,398,456 (GRCm39) |
Y287C |
unknown |
Het |
Or12e9 |
T |
G |
2: 87,202,598 (GRCm39) |
S241A |
probably benign |
Het |
Or13a24 |
A |
T |
7: 140,154,554 (GRCm39) |
M163L |
probably benign |
Het |
Or14c39 |
G |
A |
7: 86,343,939 (GRCm39) |
V92M |
probably benign |
Het |
Or8u10 |
A |
G |
2: 85,915,713 (GRCm39) |
M136T |
probably damaging |
Het |
Pabpc1l |
A |
G |
2: 163,869,410 (GRCm39) |
D70G |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,187,944 (GRCm39) |
I3455F |
probably damaging |
Het |
Ppp1r17 |
C |
A |
6: 56,003,445 (GRCm39) |
S86* |
probably null |
Het |
Rasd1 |
A |
G |
11: 59,855,615 (GRCm39) |
M6T |
possibly damaging |
Het |
Rsph14 |
C |
A |
10: 74,793,466 (GRCm39) |
V345F |
probably damaging |
Het |
Slc11a2 |
T |
A |
15: 100,299,207 (GRCm39) |
Q121L |
probably benign |
Het |
Smc5 |
A |
T |
19: 23,205,536 (GRCm39) |
|
probably null |
Het |
Tanc2 |
T |
C |
11: 105,725,994 (GRCm39) |
L386P |
probably damaging |
Het |
Tmem9b |
A |
T |
7: 109,336,164 (GRCm39) |
L160Q |
probably damaging |
Het |
Trim32 |
A |
G |
4: 65,532,906 (GRCm39) |
T488A |
possibly damaging |
Het |
Tubb1 |
A |
G |
2: 174,297,462 (GRCm39) |
I24V |
probably benign |
Het |
Upf1 |
A |
T |
8: 70,788,302 (GRCm39) |
|
probably null |
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 |
IGL02674:Zfp263
|
APN |
16 |
3,564,629 (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 |