Incidental Mutation 'IGL00595:Zfp944'
ID |
5772 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Zfp944
|
Ensembl Gene |
ENSMUSG00000033972 |
Gene Name |
zinc finger protein 944 |
Synonyms |
6330416L07Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.223)
|
Stock # |
IGL00595
|
Quality Score |
|
Status
|
|
Chromosome |
17 |
Chromosomal Location |
22556970-22580381 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 22558186 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Glycine
at position 354
(S354G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000111197
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000115535]
|
AlphaFold |
E9PUS4 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000115535
AA Change: S354G
PolyPhen 2
Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000111197 Gene: ENSMUSG00000033972 AA Change: S354G
Domain | Start | End | E-Value | Type |
KRAB
|
13 |
76 |
2.08e-21 |
SMART |
ZnF_C2H2
|
183 |
205 |
1.01e-1 |
SMART |
ZnF_C2H2
|
211 |
233 |
1.07e0 |
SMART |
ZnF_C2H2
|
239 |
261 |
1.95e-3 |
SMART |
ZnF_C2H2
|
267 |
289 |
1.22e-4 |
SMART |
ZnF_C2H2
|
295 |
317 |
2.24e-3 |
SMART |
ZnF_C2H2
|
323 |
345 |
1.82e-3 |
SMART |
ZnF_C2H2
|
351 |
373 |
5.99e-4 |
SMART |
ZnF_C2H2
|
379 |
401 |
4.79e-3 |
SMART |
ZnF_C2H2
|
407 |
429 |
2.99e-4 |
SMART |
ZnF_C2H2
|
435 |
457 |
4.17e-3 |
SMART |
ZnF_C2H2
|
463 |
485 |
1.36e-2 |
SMART |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057J18Rik |
G |
A |
10: 28,849,954 (GRCm39) |
R161* |
probably null |
Het |
Adam20 |
T |
A |
8: 41,249,084 (GRCm39) |
F398Y |
probably benign |
Het |
Ano1 |
T |
A |
7: 144,192,250 (GRCm39) |
I374F |
probably damaging |
Het |
Apol10a |
A |
T |
15: 77,369,135 (GRCm39) |
N45Y |
probably null |
Het |
Asnsd1 |
A |
G |
1: 53,386,647 (GRCm39) |
S327P |
probably damaging |
Het |
Ccdc83 |
T |
A |
7: 89,893,252 (GRCm39) |
K168N |
probably damaging |
Het |
Chmp1b2 |
A |
G |
X: 106,831,450 (GRCm39) |
S189P |
probably damaging |
Het |
Dpysl4 |
G |
T |
7: 138,676,092 (GRCm39) |
V274F |
probably damaging |
Het |
Fxr2 |
T |
G |
11: 69,540,018 (GRCm39) |
S292A |
probably benign |
Het |
Gm15130 |
T |
A |
2: 110,969,322 (GRCm39) |
D132V |
unknown |
Het |
Gpr161 |
A |
G |
1: 165,146,372 (GRCm39) |
H436R |
probably benign |
Het |
Jaml |
C |
T |
9: 45,012,287 (GRCm39) |
|
probably benign |
Het |
Kcnc2 |
A |
T |
10: 112,297,893 (GRCm39) |
S606C |
probably damaging |
Het |
Kcnc2 |
G |
T |
10: 112,297,892 (GRCm39) |
E605D |
probably benign |
Het |
Kcnrg |
T |
C |
14: 61,845,359 (GRCm39) |
I133T |
probably damaging |
Het |
Kdm7a |
A |
G |
6: 39,121,444 (GRCm39) |
I837T |
probably benign |
Het |
Lactb2 |
A |
G |
1: 13,700,350 (GRCm39) |
L227S |
probably benign |
Het |
Lats1 |
T |
G |
10: 7,578,069 (GRCm39) |
S398A |
probably benign |
Het |
Llgl2 |
T |
A |
11: 115,725,710 (GRCm39) |
D19E |
probably benign |
Het |
Nup107 |
A |
T |
10: 117,609,257 (GRCm39) |
C365* |
probably null |
Het |
Nup107 |
T |
C |
10: 117,609,273 (GRCm39) |
|
probably null |
Het |
Plekhf2 |
T |
C |
4: 10,991,022 (GRCm39) |
K107E |
probably damaging |
Het |
Rnf139 |
A |
T |
15: 58,770,391 (GRCm39) |
I139F |
possibly damaging |
Het |
Rsbn1 |
A |
G |
3: 103,836,006 (GRCm39) |
N348S |
probably benign |
Het |
Rttn |
A |
T |
18: 88,992,464 (GRCm39) |
Q136H |
probably benign |
Het |
Syne2 |
C |
T |
12: 75,972,420 (GRCm39) |
T1052I |
possibly damaging |
Het |
Tom1l1 |
A |
T |
11: 90,565,566 (GRCm39) |
L101Q |
probably damaging |
Het |
Tubal3 |
A |
G |
13: 3,983,015 (GRCm39) |
N265S |
probably damaging |
Het |
Zfp141 |
T |
C |
7: 42,126,079 (GRCm39) |
N131S |
probably benign |
Het |
Zfp961 |
G |
A |
8: 72,722,272 (GRCm39) |
A262T |
probably damaging |
Het |
|
Other mutations in Zfp944 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00917:Zfp944
|
APN |
17 |
22,558,765 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01093:Zfp944
|
APN |
17 |
22,562,615 (GRCm39) |
splice site |
probably benign |
|
IGL02113:Zfp944
|
APN |
17 |
22,558,047 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02694:Zfp944
|
APN |
17 |
22,558,899 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03135:Zfp944
|
APN |
17 |
22,558,737 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03172:Zfp944
|
APN |
17 |
22,559,018 (GRCm39) |
missense |
probably damaging |
0.98 |
R0121:Zfp944
|
UTSW |
17 |
22,558,249 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0336:Zfp944
|
UTSW |
17 |
22,558,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R0755:Zfp944
|
UTSW |
17 |
22,558,889 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1536:Zfp944
|
UTSW |
17 |
22,558,697 (GRCm39) |
nonsense |
probably null |
|
R1708:Zfp944
|
UTSW |
17 |
22,558,026 (GRCm39) |
missense |
probably damaging |
0.98 |
R1886:Zfp944
|
UTSW |
17 |
22,558,960 (GRCm39) |
missense |
probably benign |
0.04 |
R1928:Zfp944
|
UTSW |
17 |
22,560,065 (GRCm39) |
missense |
probably damaging |
0.96 |
R1950:Zfp944
|
UTSW |
17 |
22,558,681 (GRCm39) |
missense |
probably benign |
0.16 |
R2075:Zfp944
|
UTSW |
17 |
22,558,178 (GRCm39) |
nonsense |
probably null |
|
R2101:Zfp944
|
UTSW |
17 |
22,558,809 (GRCm39) |
missense |
probably benign |
0.41 |
R2433:Zfp944
|
UTSW |
17 |
22,558,193 (GRCm39) |
nonsense |
probably null |
|
R4698:Zfp944
|
UTSW |
17 |
22,558,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R4986:Zfp944
|
UTSW |
17 |
22,558,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6451:Zfp944
|
UTSW |
17 |
22,557,846 (GRCm39) |
missense |
probably benign |
0.40 |
R6566:Zfp944
|
UTSW |
17 |
22,558,726 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6752:Zfp944
|
UTSW |
17 |
22,558,500 (GRCm39) |
missense |
probably benign |
0.01 |
R7064:Zfp944
|
UTSW |
17 |
22,558,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R8193:Zfp944
|
UTSW |
17 |
22,558,861 (GRCm39) |
nonsense |
probably null |
|
R8323:Zfp944
|
UTSW |
17 |
22,558,235 (GRCm39) |
missense |
probably benign |
|
R8328:Zfp944
|
UTSW |
17 |
22,558,705 (GRCm39) |
nonsense |
probably null |
|
R8902:Zfp944
|
UTSW |
17 |
22,558,761 (GRCm39) |
missense |
probably benign |
0.41 |
R8915:Zfp944
|
UTSW |
17 |
22,558,507 (GRCm39) |
missense |
probably benign |
0.05 |
R9130:Zfp944
|
UTSW |
17 |
22,560,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Zfp944
|
UTSW |
17 |
22,562,619 (GRCm39) |
critical splice donor site |
probably null |
|
|
Posted On |
2012-04-20 |