Incidental Mutation 'R1365:Zfp979'
ID |
155997 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zfp979
|
Ensembl Gene |
ENSMUSG00000066000 |
Gene Name |
zinc finger protein 979 |
Synonyms |
Ssm1, 2610305D13Rik |
MMRRC Submission |
039430-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.190)
|
Stock # |
R1365 (G1)
|
Quality Score |
206 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
147696394-147726970 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 147697681 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 343
(Y343N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101345
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000037565]
[ENSMUST00000105720]
[ENSMUST00000133006]
|
AlphaFold |
A2A799 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000037565
AA Change: Y343N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000038153 Gene: ENSMUSG00000066000 AA Change: Y343N
Domain | Start | End | E-Value | Type |
KRAB
|
28 |
88 |
2.06e-16 |
SMART |
ZnF_C2H2
|
257 |
279 |
2.06e1 |
SMART |
ZnF_C2H2
|
285 |
307 |
2.53e-2 |
SMART |
ZnF_C2H2
|
313 |
335 |
1.95e-3 |
SMART |
ZnF_C2H2
|
341 |
363 |
1.4e1 |
SMART |
ZnF_C2H2
|
369 |
391 |
9.08e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000105720
AA Change: Y343N
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000101345 Gene: ENSMUSG00000066000 AA Change: Y343N
Domain | Start | End | E-Value | Type |
KRAB
|
28 |
88 |
2.06e-16 |
SMART |
ZnF_C2H2
|
257 |
279 |
2.06e1 |
SMART |
ZnF_C2H2
|
285 |
307 |
2.53e-2 |
SMART |
ZnF_C2H2
|
313 |
335 |
1.95e-3 |
SMART |
ZnF_C2H2
|
341 |
363 |
1.4e1 |
SMART |
ZnF_C2H2
|
369 |
391 |
9.08e-4 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000133006
|
SMART Domains |
Protein: ENSMUSP00000114677 Gene: ENSMUSG00000066000
Domain | Start | End | E-Value | Type |
KRAB
|
28 |
88 |
2.06e-16 |
SMART |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.6%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef28 |
G |
A |
13: 98,211,632 (GRCm39) |
T117M |
probably damaging |
Het |
Asb15 |
T |
C |
6: 24,567,269 (GRCm39) |
I530T |
possibly damaging |
Het |
Brca1 |
T |
C |
11: 101,392,822 (GRCm39) |
N1673S |
probably benign |
Het |
Cd48 |
A |
T |
1: 171,527,129 (GRCm39) |
Q185L |
probably damaging |
Het |
Cog2 |
A |
T |
8: 125,267,713 (GRCm39) |
K343I |
probably damaging |
Het |
Dars2 |
G |
A |
1: 160,872,564 (GRCm39) |
Q546* |
probably null |
Het |
Dst |
A |
G |
1: 34,227,275 (GRCm39) |
K1623E |
probably benign |
Het |
Epn1 |
G |
A |
7: 5,096,369 (GRCm39) |
R221Q |
probably benign |
Het |
Gtf2b |
T |
C |
3: 142,477,227 (GRCm39) |
I33T |
probably damaging |
Het |
Hsf4 |
G |
T |
8: 105,997,726 (GRCm39) |
R156L |
probably damaging |
Het |
Itch |
A |
G |
2: 155,054,951 (GRCm39) |
N752D |
probably benign |
Het |
Kif28 |
G |
A |
1: 179,567,552 (GRCm39) |
Q73* |
probably null |
Het |
Mamdc4 |
T |
C |
2: 25,456,036 (GRCm39) |
Y790C |
probably damaging |
Het |
Med1 |
T |
C |
11: 98,046,821 (GRCm39) |
|
probably benign |
Het |
Mfsd13a |
C |
T |
19: 46,354,943 (GRCm39) |
T40I |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,438,711 (GRCm39) |
|
probably null |
Het |
Oxct2b |
G |
A |
4: 123,011,162 (GRCm39) |
V361I |
probably benign |
Het |
Pid1 |
T |
C |
1: 84,015,862 (GRCm39) |
M168V |
probably damaging |
Het |
Plk1 |
A |
G |
7: 121,767,852 (GRCm39) |
D419G |
probably damaging |
Het |
Rasl10b |
G |
A |
11: 83,308,665 (GRCm39) |
|
probably null |
Het |
Rps24 |
A |
G |
14: 24,541,830 (GRCm39) |
T6A |
probably damaging |
Het |
Sem1 |
T |
C |
6: 6,560,501 (GRCm39) |
D26G |
possibly damaging |
Het |
Sin3a |
C |
T |
9: 57,032,487 (GRCm39) |
R1141* |
probably null |
Het |
Slf1 |
C |
T |
13: 77,274,490 (GRCm39) |
A68T |
probably damaging |
Het |
Trmo |
A |
G |
4: 46,380,278 (GRCm39) |
S364P |
probably damaging |
Het |
Uchl3 |
A |
G |
14: 101,891,528 (GRCm39) |
E10G |
probably damaging |
Het |
Usp14 |
C |
T |
18: 10,000,490 (GRCm39) |
|
probably null |
Het |
Vmn1r203 |
T |
A |
13: 22,708,756 (GRCm39) |
M179K |
probably benign |
Het |
Vps13a |
A |
G |
19: 16,596,810 (GRCm39) |
Y3103H |
probably damaging |
Het |
Zfp804a |
T |
C |
2: 82,087,590 (GRCm39) |
L473P |
probably benign |
Het |
|
Other mutations in Zfp979 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01285:Zfp979
|
APN |
4 |
147,699,853 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01865:Zfp979
|
APN |
4 |
147,699,774 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02336:Zfp979
|
APN |
4 |
147,699,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R0336:Zfp979
|
UTSW |
4 |
147,697,592 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1440:Zfp979
|
UTSW |
4 |
147,698,493 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1714:Zfp979
|
UTSW |
4 |
147,698,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Zfp979
|
UTSW |
4 |
147,697,740 (GRCm39) |
missense |
probably damaging |
0.99 |
R2155:Zfp979
|
UTSW |
4 |
147,697,915 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3735:Zfp979
|
UTSW |
4 |
147,697,939 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3963:Zfp979
|
UTSW |
4 |
147,697,588 (GRCm39) |
missense |
probably benign |
0.34 |
R3972:Zfp979
|
UTSW |
4 |
147,702,876 (GRCm39) |
nonsense |
probably null |
|
R4471:Zfp979
|
UTSW |
4 |
147,697,913 (GRCm39) |
nonsense |
probably null |
|
R4983:Zfp979
|
UTSW |
4 |
147,698,371 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5310:Zfp979
|
UTSW |
4 |
147,698,375 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5805:Zfp979
|
UTSW |
4 |
147,698,067 (GRCm39) |
missense |
probably damaging |
0.99 |
R5861:Zfp979
|
UTSW |
4 |
147,697,966 (GRCm39) |
nonsense |
probably null |
|
R6598:Zfp979
|
UTSW |
4 |
147,698,223 (GRCm39) |
missense |
probably damaging |
0.99 |
R6599:Zfp979
|
UTSW |
4 |
147,698,083 (GRCm39) |
missense |
probably benign |
0.40 |
R6925:Zfp979
|
UTSW |
4 |
147,697,999 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7684:Zfp979
|
UTSW |
4 |
147,697,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R7801:Zfp979
|
UTSW |
4 |
147,698,435 (GRCm39) |
missense |
probably damaging |
0.96 |
R8035:Zfp979
|
UTSW |
4 |
147,697,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8086:Zfp979
|
UTSW |
4 |
147,698,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R8244:Zfp979
|
UTSW |
4 |
147,697,933 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8369:Zfp979
|
UTSW |
4 |
147,697,548 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8880:Zfp979
|
UTSW |
4 |
147,697,836 (GRCm39) |
missense |
probably benign |
0.00 |
R8887:Zfp979
|
UTSW |
4 |
147,698,219 (GRCm39) |
missense |
probably damaging |
0.96 |
R8988:Zfp979
|
UTSW |
4 |
147,697,984 (GRCm39) |
missense |
probably benign |
|
R9016:Zfp979
|
UTSW |
4 |
147,697,504 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9356:Zfp979
|
UTSW |
4 |
147,698,358 (GRCm39) |
missense |
probably damaging |
0.96 |
|
Predicted Primers |
|
Posted On |
2014-02-11 |