Incidental Mutation 'R5120:Zmym1'
ID |
392913 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Zmym1
|
Ensembl Gene |
ENSMUSG00000043872 |
Gene Name |
zinc finger, MYM domain containing 1 |
Synonyms |
5830412B09Rik |
MMRRC Submission |
042708-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.211)
|
Stock # |
R5120 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
4 |
Chromosomal Location |
126940887-126954945 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
T to C
at 126945230 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101708
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000055013]
[ENSMUST00000055013]
[ENSMUST00000055013]
[ENSMUST00000055013]
[ENSMUST00000055013]
[ENSMUST00000106099]
[ENSMUST00000106099]
[ENSMUST00000106099]
[ENSMUST00000106099]
[ENSMUST00000106099]
[ENSMUST00000106102]
[ENSMUST00000106102]
[ENSMUST00000106102]
[ENSMUST00000106102]
[ENSMUST00000136186]
|
AlphaFold |
Q3TJB1 |
Predicted Effect |
probably null
Transcript: ENSMUST00000055013
|
SMART Domains |
Protein: ENSMUSP00000050669 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
2.4e-8 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
4.9e-55 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
5.1e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000055013
|
SMART Domains |
Protein: ENSMUSP00000050669 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
2.4e-8 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
4.9e-55 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
5.1e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000055013
|
SMART Domains |
Protein: ENSMUSP00000050669 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
2.4e-8 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
4.9e-55 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
5.1e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000055013
|
SMART Domains |
Protein: ENSMUSP00000050669 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
2.4e-8 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
4.9e-55 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
5.1e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000055013
|
SMART Domains |
Protein: ENSMUSP00000050669 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
2.4e-8 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
4.9e-55 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
5.1e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106099
|
SMART Domains |
Protein: ENSMUSP00000101705 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
3.3e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
4.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
237 |
471 |
2.8e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
772 |
861 |
5.3e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106099
|
SMART Domains |
Protein: ENSMUSP00000101705 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
3.3e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
4.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
237 |
471 |
2.8e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
772 |
861 |
5.3e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106099
|
SMART Domains |
Protein: ENSMUSP00000101705 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
3.3e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
4.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
237 |
471 |
2.8e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
772 |
861 |
5.3e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106099
|
SMART Domains |
Protein: ENSMUSP00000101705 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
3.3e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
4.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
237 |
471 |
2.8e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
772 |
861 |
5.3e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106099
|
SMART Domains |
Protein: ENSMUSP00000101705 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
3.3e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
4.6e-10 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
237 |
471 |
2.8e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
772 |
861 |
5.3e-18 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106102
|
SMART Domains |
Protein: ENSMUSP00000101708 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
7.8e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.1e-9 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
7.4e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
1.7e-17 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106102
|
SMART Domains |
Protein: ENSMUSP00000101708 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
7.8e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.1e-9 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
7.4e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
1.7e-17 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106102
|
SMART Domains |
Protein: ENSMUSP00000101708 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
7.8e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.1e-9 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
7.4e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
1.7e-17 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000106102
|
SMART Domains |
Protein: ENSMUSP00000101708 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
7.8e-9 |
PFAM |
Pfam:zf-FCS
|
53 |
96 |
1.1e-9 |
PFAM |
low complexity region
|
155 |
168 |
N/A |
INTRINSIC |
low complexity region
|
229 |
243 |
N/A |
INTRINSIC |
Pfam:DUF4371
|
335 |
569 |
7.4e-52 |
PFAM |
Pfam:Dimer_Tnp_hAT
|
870 |
959 |
1.7e-17 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000117934
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000119262
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124429
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152607
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140605
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000137236
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136186
|
SMART Domains |
Protein: ENSMUSP00000120772 Gene: ENSMUSG00000043872
Domain | Start | End | E-Value | Type |
Pfam:zf-FCS
|
6 |
46 |
1.5e-10 |
PFAM |
|
Meta Mutation Damage Score |
0.9755 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.2%
- 10x: 95.8%
- 20x: 90.6%
|
Validation Efficiency |
100% (97/97) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,101,061 (GRCm39) |
H225R |
probably benign |
Het |
Abcc9 |
T |
A |
6: 142,602,344 (GRCm39) |
I690F |
probably benign |
Het |
Acp4 |
A |
T |
7: 43,906,395 (GRCm39) |
D52E |
probably damaging |
Het |
Adam17 |
T |
C |
12: 21,393,020 (GRCm39) |
|
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,832,872 (GRCm39) |
E221G |
probably damaging |
Het |
Aoc2 |
A |
G |
11: 101,216,540 (GRCm39) |
T208A |
probably benign |
Het |
Apoa4 |
T |
G |
9: 46,154,035 (GRCm39) |
I212S |
probably damaging |
Het |
Bptf |
A |
T |
11: 106,964,211 (GRCm39) |
M1598K |
probably damaging |
Het |
Camsap3 |
G |
A |
8: 3,650,680 (GRCm39) |
R209Q |
probably damaging |
Het |
Ccdc171 |
C |
A |
4: 83,476,763 (GRCm39) |
|
probably benign |
Het |
Celsr2 |
G |
C |
3: 108,300,436 (GRCm39) |
P2875A |
probably benign |
Het |
Cenpb |
A |
G |
2: 131,021,738 (GRCm39) |
V20A |
probably benign |
Het |
Cfap61 |
A |
T |
2: 145,985,080 (GRCm39) |
K975* |
probably null |
Het |
Cfhr4 |
T |
C |
1: 139,680,841 (GRCm39) |
S226G |
probably benign |
Het |
Col9a2 |
G |
T |
4: 120,896,969 (GRCm39) |
A20S |
unknown |
Het |
Crnn |
A |
T |
3: 93,056,203 (GRCm39) |
I330F |
probably benign |
Het |
Csf3r |
C |
A |
4: 125,929,620 (GRCm39) |
P381Q |
probably benign |
Het |
Csmd3 |
G |
A |
15: 48,536,891 (GRCm39) |
Q104* |
probably null |
Het |
Ctnna1 |
G |
A |
18: 35,315,607 (GRCm39) |
|
probably null |
Het |
Cwf19l2 |
C |
T |
9: 3,418,761 (GRCm39) |
Q183* |
probably null |
Het |
Ddx60 |
T |
C |
8: 62,398,940 (GRCm39) |
Y220H |
probably benign |
Het |
Dhh |
T |
C |
15: 98,796,038 (GRCm39) |
Q39R |
probably benign |
Het |
Dynlrb2 |
T |
A |
8: 117,242,437 (GRCm39) |
I89N |
possibly damaging |
Het |
Dytn |
T |
C |
1: 63,662,202 (GRCm39) |
E645G |
probably benign |
Het |
Efcab7 |
A |
G |
4: 99,754,688 (GRCm39) |
T287A |
probably damaging |
Het |
Eogt |
A |
G |
6: 97,111,276 (GRCm39) |
V195A |
probably benign |
Het |
Ep400 |
G |
T |
5: 110,904,224 (GRCm39) |
P125Q |
probably damaging |
Het |
Fasn |
A |
G |
11: 120,702,217 (GRCm39) |
V1815A |
probably benign |
Het |
Gm5866 |
T |
C |
5: 52,740,224 (GRCm39) |
|
noncoding transcript |
Het |
Gm8674 |
C |
A |
13: 50,055,984 (GRCm39) |
|
noncoding transcript |
Het |
Gpat4 |
G |
T |
8: 23,670,218 (GRCm39) |
H270Q |
possibly damaging |
Het |
Grik5 |
A |
G |
7: 24,710,065 (GRCm39) |
L890P |
probably damaging |
Het |
Gsap |
A |
G |
5: 21,474,934 (GRCm39) |
N500S |
probably damaging |
Het |
H2-M10.1 |
T |
C |
17: 36,636,048 (GRCm39) |
D173G |
probably benign |
Het |
Igfn1 |
T |
A |
1: 135,901,240 (GRCm39) |
I413F |
possibly damaging |
Het |
Ighv1-52 |
G |
T |
12: 115,109,406 (GRCm39) |
H17N |
probably benign |
Het |
Kcnu1 |
T |
A |
8: 26,424,516 (GRCm39) |
D270E |
possibly damaging |
Het |
Kif16b |
A |
C |
2: 142,690,259 (GRCm39) |
N274K |
probably damaging |
Het |
Klk1b11 |
C |
T |
7: 43,648,446 (GRCm39) |
T151I |
probably benign |
Het |
Krtap13 |
A |
G |
16: 88,548,458 (GRCm39) |
F10S |
probably damaging |
Het |
Large1 |
A |
T |
8: 73,585,969 (GRCm39) |
I379N |
probably damaging |
Het |
Lhx8 |
T |
C |
3: 154,017,332 (GRCm39) |
H301R |
probably damaging |
Het |
Lrriq3 |
T |
C |
3: 154,835,021 (GRCm39) |
V252A |
probably benign |
Het |
Lysmd3 |
T |
A |
13: 81,817,311 (GRCm39) |
I96N |
probably damaging |
Het |
Mpeg1 |
C |
T |
19: 12,438,793 (GRCm39) |
Q84* |
probably null |
Het |
Myoz1 |
C |
T |
14: 20,700,722 (GRCm39) |
G165D |
probably benign |
Het |
Myt1 |
G |
A |
2: 181,439,413 (GRCm39) |
V312I |
probably benign |
Het |
Ndufb7 |
T |
C |
8: 84,293,606 (GRCm39) |
|
probably benign |
Het |
Numa1 |
C |
T |
7: 101,626,644 (GRCm39) |
T10M |
probably damaging |
Het |
Or10d1b |
T |
A |
9: 39,613,366 (GRCm39) |
H233L |
probably benign |
Het |
Or1e30 |
A |
C |
11: 73,677,790 (GRCm39) |
I9L |
probably benign |
Het |
Or2g7 |
A |
T |
17: 38,378,157 (GRCm39) |
I32F |
probably damaging |
Het |
Or4f14d |
A |
T |
2: 111,960,903 (GRCm39) |
D84E |
probably damaging |
Het |
Or4k39 |
T |
C |
2: 111,239,585 (GRCm39) |
|
noncoding transcript |
Het |
Osmr |
A |
T |
15: 6,856,756 (GRCm39) |
S464T |
probably benign |
Het |
Pak5 |
G |
A |
2: 135,925,149 (GRCm39) |
H718Y |
probably damaging |
Het |
Pan2 |
T |
A |
10: 128,150,864 (GRCm39) |
|
probably null |
Het |
Pik3r4 |
T |
C |
9: 105,546,208 (GRCm39) |
S853P |
probably benign |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Polr3gl |
T |
A |
3: 96,485,795 (GRCm39) |
|
probably benign |
Het |
Psd2 |
G |
A |
18: 36,112,863 (GRCm39) |
R186Q |
possibly damaging |
Het |
Psd4 |
T |
C |
2: 24,295,450 (GRCm39) |
V868A |
probably benign |
Het |
Ralgapa2 |
G |
T |
2: 146,254,004 (GRCm39) |
T852K |
probably benign |
Het |
Rbm43 |
T |
C |
2: 51,822,435 (GRCm39) |
|
probably benign |
Het |
Rps6kl1 |
C |
A |
12: 85,186,122 (GRCm39) |
G329C |
probably damaging |
Het |
Scaf11 |
T |
C |
15: 96,317,423 (GRCm39) |
T714A |
probably benign |
Het |
Selenoo |
C |
A |
15: 88,978,508 (GRCm39) |
N310K |
possibly damaging |
Het |
Sepsecs |
T |
C |
5: 52,818,003 (GRCm39) |
Q258R |
probably damaging |
Het |
Sgcz |
T |
C |
8: 37,993,420 (GRCm39) |
S226G |
probably benign |
Het |
Slfn5 |
A |
G |
11: 82,851,754 (GRCm39) |
K627E |
probably damaging |
Het |
Sos1 |
A |
T |
17: 80,715,677 (GRCm39) |
F1027I |
probably damaging |
Het |
Ssh1 |
C |
G |
5: 114,095,459 (GRCm39) |
V228L |
possibly damaging |
Het |
Sugp1 |
C |
A |
8: 70,501,317 (GRCm39) |
P65T |
probably benign |
Het |
Tas2r106 |
T |
A |
6: 131,655,779 (GRCm39) |
N24I |
probably damaging |
Het |
Tex10 |
T |
C |
4: 48,459,272 (GRCm39) |
E534G |
possibly damaging |
Het |
Tmem182 |
C |
T |
1: 40,894,061 (GRCm39) |
T192I |
possibly damaging |
Het |
Traf7 |
T |
A |
17: 24,737,718 (GRCm39) |
K51* |
probably null |
Het |
Trap1 |
C |
A |
16: 3,861,952 (GRCm39) |
R604L |
probably damaging |
Het |
Trim6 |
T |
A |
7: 103,877,447 (GRCm39) |
L179Q |
probably damaging |
Het |
Ubfd1 |
T |
C |
7: 121,670,973 (GRCm39) |
S264P |
probably damaging |
Het |
Upk3bl |
T |
C |
5: 136,093,045 (GRCm39) |
|
probably benign |
Het |
Wdfy3 |
T |
A |
5: 102,015,972 (GRCm39) |
Q2601L |
possibly damaging |
Het |
Wdr89 |
A |
G |
12: 75,679,412 (GRCm39) |
Y281H |
probably damaging |
Het |
Zfp286 |
A |
T |
11: 62,671,551 (GRCm39) |
M174K |
probably benign |
Het |
|
Other mutations in Zmym1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Zmym1
|
APN |
4 |
126,943,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02326:Zmym1
|
APN |
4 |
126,941,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02392:Zmym1
|
APN |
4 |
126,942,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02431:Zmym1
|
APN |
4 |
126,941,557 (GRCm39) |
nonsense |
probably null |
|
IGL02512:Zmym1
|
APN |
4 |
126,942,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Zmym1
|
APN |
4 |
126,942,927 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Zmym1
|
UTSW |
4 |
126,944,578 (GRCm39) |
missense |
possibly damaging |
0.77 |
BB019:Zmym1
|
UTSW |
4 |
126,944,578 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0195:Zmym1
|
UTSW |
4 |
126,941,704 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0266:Zmym1
|
UTSW |
4 |
126,941,818 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0416:Zmym1
|
UTSW |
4 |
126,952,613 (GRCm39) |
missense |
probably benign |
0.00 |
R1374:Zmym1
|
UTSW |
4 |
126,943,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1480:Zmym1
|
UTSW |
4 |
126,942,405 (GRCm39) |
missense |
probably damaging |
0.99 |
R1704:Zmym1
|
UTSW |
4 |
126,942,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R1806:Zmym1
|
UTSW |
4 |
126,941,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1815:Zmym1
|
UTSW |
4 |
126,942,814 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2124:Zmym1
|
UTSW |
4 |
126,943,363 (GRCm39) |
missense |
probably benign |
0.05 |
R2169:Zmym1
|
UTSW |
4 |
126,947,996 (GRCm39) |
splice site |
probably null |
|
R4027:Zmym1
|
UTSW |
4 |
126,943,672 (GRCm39) |
missense |
probably benign |
0.08 |
R4410:Zmym1
|
UTSW |
4 |
126,941,897 (GRCm39) |
nonsense |
probably null |
|
R4572:Zmym1
|
UTSW |
4 |
126,944,628 (GRCm39) |
missense |
probably benign |
0.39 |
R4788:Zmym1
|
UTSW |
4 |
126,948,090 (GRCm39) |
missense |
probably benign |
0.10 |
R5130:Zmym1
|
UTSW |
4 |
126,942,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Zmym1
|
UTSW |
4 |
126,943,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Zmym1
|
UTSW |
4 |
126,941,677 (GRCm39) |
missense |
probably damaging |
0.99 |
R7426:Zmym1
|
UTSW |
4 |
126,943,191 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7464:Zmym1
|
UTSW |
4 |
126,952,728 (GRCm39) |
nonsense |
probably null |
|
R7540:Zmym1
|
UTSW |
4 |
126,942,550 (GRCm39) |
missense |
probably benign |
|
R7779:Zmym1
|
UTSW |
4 |
126,948,038 (GRCm39) |
missense |
probably benign |
|
R7807:Zmym1
|
UTSW |
4 |
126,941,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R7876:Zmym1
|
UTSW |
4 |
126,941,496 (GRCm39) |
missense |
probably damaging |
0.98 |
R7932:Zmym1
|
UTSW |
4 |
126,944,578 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8183:Zmym1
|
UTSW |
4 |
126,952,649 (GRCm39) |
missense |
probably benign |
0.07 |
R8276:Zmym1
|
UTSW |
4 |
126,948,051 (GRCm39) |
missense |
probably damaging |
0.99 |
R8744:Zmym1
|
UTSW |
4 |
126,945,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R8798:Zmym1
|
UTSW |
4 |
126,943,664 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9199:Zmym1
|
UTSW |
4 |
126,944,623 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9385:Zmym1
|
UTSW |
4 |
126,952,683 (GRCm39) |
missense |
probably damaging |
1.00 |
T0722:Zmym1
|
UTSW |
4 |
126,943,466 (GRCm39) |
missense |
probably benign |
0.05 |
T0722:Zmym1
|
UTSW |
4 |
126,942,043 (GRCm39) |
missense |
probably benign |
0.01 |
T0722:Zmym1
|
UTSW |
4 |
126,941,740 (GRCm39) |
missense |
probably benign |
0.00 |
T0975:Zmym1
|
UTSW |
4 |
126,943,466 (GRCm39) |
missense |
probably benign |
0.05 |
T0975:Zmym1
|
UTSW |
4 |
126,942,043 (GRCm39) |
missense |
probably benign |
0.01 |
T0975:Zmym1
|
UTSW |
4 |
126,941,740 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- GGCATTACCTGAAGGAGACTCC -3'
(R):5'- CCCAGGATCGTATGGTAGATAC -3'
Sequencing Primer
(F):5'- CTCCATCACAGCACTGTTGTATGAAG -3'
(R):5'- TGCAAGGGCTCATGTCCAAG -3'
|
Posted On |
2016-06-15 |