Incidental Mutation 'IGL00428:Zfp984'
ID |
332400 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp984
|
Ensembl Gene |
ENSMUSG00000078495 |
Gene Name |
zinc finger protein 984 |
Synonyms |
Gm13157 |
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.501)
|
Stock # |
IGL00428
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
147838431-147894245 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 147839343 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glycine to Serine
at position 503
(G503S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000114023
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000105734]
[ENSMUST00000122309]
|
AlphaFold |
A2A7A2 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000105734
AA Change: G503S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000101360 Gene: ENSMUSG00000078495 AA Change: G503S
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
72 |
5.24e-18 |
SMART |
ZnF_C2H2
|
238 |
260 |
1.69e-3 |
SMART |
ZnF_C2H2
|
266 |
288 |
1.18e-2 |
SMART |
ZnF_C2H2
|
294 |
316 |
1.38e-3 |
SMART |
ZnF_C2H2
|
322 |
344 |
1.58e-3 |
SMART |
ZnF_C2H2
|
350 |
372 |
4.24e-4 |
SMART |
ZnF_C2H2
|
378 |
400 |
3.69e-4 |
SMART |
ZnF_C2H2
|
406 |
428 |
1.58e-3 |
SMART |
ZnF_C2H2
|
434 |
456 |
3.39e-3 |
SMART |
ZnF_C2H2
|
462 |
484 |
1.3e-4 |
SMART |
ZnF_C2H2
|
490 |
512 |
1.4e-4 |
SMART |
ZnF_C2H2
|
518 |
540 |
4.79e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000122309
AA Change: G503S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000114023 Gene: ENSMUSG00000078495 AA Change: G503S
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
72 |
5.24e-18 |
SMART |
ZnF_C2H2
|
238 |
260 |
1.69e-3 |
SMART |
ZnF_C2H2
|
266 |
288 |
1.18e-2 |
SMART |
ZnF_C2H2
|
294 |
316 |
1.38e-3 |
SMART |
ZnF_C2H2
|
322 |
344 |
1.58e-3 |
SMART |
ZnF_C2H2
|
350 |
372 |
4.24e-4 |
SMART |
ZnF_C2H2
|
378 |
400 |
3.69e-4 |
SMART |
ZnF_C2H2
|
406 |
428 |
1.58e-3 |
SMART |
ZnF_C2H2
|
434 |
456 |
3.39e-3 |
SMART |
ZnF_C2H2
|
462 |
484 |
1.3e-4 |
SMART |
ZnF_C2H2
|
490 |
512 |
1.4e-4 |
SMART |
ZnF_C2H2
|
518 |
540 |
4.79e-3 |
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 |
Adgrg6 |
G |
A |
10: 14,343,119 (GRCm39) |
P276L |
probably benign |
Het |
Asap1 |
G |
A |
15: 63,991,803 (GRCm39) |
|
probably benign |
Het |
Axl |
T |
C |
7: 25,460,297 (GRCm39) |
T723A |
probably damaging |
Het |
Barhl2 |
C |
T |
5: 106,603,365 (GRCm39) |
A265T |
possibly damaging |
Het |
Bltp1 |
A |
G |
3: 37,065,876 (GRCm39) |
N3491S |
probably benign |
Het |
Capn7 |
A |
G |
14: 31,085,535 (GRCm39) |
K503E |
probably benign |
Het |
Cbln4 |
A |
G |
2: 171,880,970 (GRCm39) |
V108A |
probably benign |
Het |
Ccdc71 |
C |
T |
9: 108,341,354 (GRCm39) |
T389M |
probably damaging |
Het |
Ccdc91 |
A |
G |
6: 147,508,452 (GRCm39) |
T393A |
unknown |
Het |
Cdh20 |
A |
T |
1: 104,881,612 (GRCm39) |
H359L |
probably benign |
Het |
Cfap119 |
A |
T |
7: 127,184,210 (GRCm39) |
S229T |
probably damaging |
Het |
Coro7 |
C |
T |
16: 4,452,500 (GRCm39) |
V364M |
possibly damaging |
Het |
Ctsq |
A |
T |
13: 61,185,528 (GRCm39) |
N204K |
probably damaging |
Het |
Dnaja3 |
C |
T |
16: 4,512,309 (GRCm39) |
R238C |
probably damaging |
Het |
Dynlt1a |
C |
T |
17: 6,362,062 (GRCm39) |
V39I |
possibly damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,478 (GRCm39) |
|
probably benign |
Het |
Gtf3c3 |
T |
C |
1: 54,455,114 (GRCm39) |
Y583C |
probably damaging |
Het |
Invs |
T |
C |
4: 48,402,909 (GRCm39) |
F514S |
probably damaging |
Het |
Kif23 |
A |
T |
9: 61,833,750 (GRCm39) |
C484S |
probably benign |
Het |
Masp1 |
A |
G |
16: 23,295,062 (GRCm39) |
Y400H |
probably damaging |
Het |
Olfml3 |
G |
A |
3: 103,644,298 (GRCm39) |
|
probably null |
Het |
Pard3b |
T |
C |
1: 62,200,357 (GRCm39) |
S299P |
probably damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,611,623 (GRCm39) |
E194D |
possibly damaging |
Het |
Pip5k1c |
A |
T |
10: 81,141,545 (GRCm39) |
T78S |
probably benign |
Het |
Septin11 |
T |
C |
5: 93,304,877 (GRCm39) |
|
probably null |
Het |
Septin8 |
A |
G |
11: 53,422,823 (GRCm39) |
N11D |
probably benign |
Het |
Slc10a6 |
G |
A |
5: 103,760,362 (GRCm39) |
T211I |
probably benign |
Het |
Smim8 |
T |
C |
4: 34,769,006 (GRCm39) |
T93A |
probably benign |
Het |
Tg |
A |
G |
15: 66,645,273 (GRCm39) |
I774M |
probably benign |
Het |
Tulp4 |
A |
G |
17: 6,189,351 (GRCm39) |
T58A |
probably damaging |
Het |
Virma |
T |
C |
4: 11,519,424 (GRCm39) |
|
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,970,177 (GRCm39) |
D210G |
probably damaging |
Het |
|
Other mutations in Zfp984 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00469:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00550:Zfp984
|
APN |
4 |
147,839,343 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4791001:Zfp984
|
UTSW |
4 |
147,840,603 (GRCm39) |
missense |
probably benign |
0.15 |
R0281:Zfp984
|
UTSW |
4 |
147,839,722 (GRCm39) |
missense |
probably benign |
|
R0731:Zfp984
|
UTSW |
4 |
147,840,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Zfp984
|
UTSW |
4 |
147,840,446 (GRCm39) |
missense |
probably benign |
0.24 |
R1293:Zfp984
|
UTSW |
4 |
147,840,398 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1518:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R2041:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Zfp984
|
UTSW |
4 |
147,839,234 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5038:Zfp984
|
UTSW |
4 |
147,839,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Zfp984
|
UTSW |
4 |
147,840,362 (GRCm39) |
missense |
probably benign |
0.00 |
R6254:Zfp984
|
UTSW |
4 |
147,840,643 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6418:Zfp984
|
UTSW |
4 |
147,845,703 (GRCm39) |
missense |
probably benign |
0.00 |
R6527:Zfp984
|
UTSW |
4 |
147,840,381 (GRCm39) |
missense |
probably benign |
0.45 |
R6974:Zfp984
|
UTSW |
4 |
147,845,707 (GRCm39) |
start codon destroyed |
possibly damaging |
0.94 |
R7058:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
R7495:Zfp984
|
UTSW |
4 |
147,839,287 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7843:Zfp984
|
UTSW |
4 |
147,842,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8462:Zfp984
|
UTSW |
4 |
147,839,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R8520:Zfp984
|
UTSW |
4 |
147,840,668 (GRCm39) |
missense |
probably benign |
0.01 |
R8918:Zfp984
|
UTSW |
4 |
147,840,623 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9387:Zfp984
|
UTSW |
4 |
147,840,002 (GRCm39) |
missense |
probably benign |
|
Z1176:Zfp984
|
UTSW |
4 |
147,839,921 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Zfp984
|
UTSW |
4 |
147,840,577 (GRCm39) |
missense |
probably benign |
0.04 |
|
Posted On |
2015-08-05 |