Incidental Mutation 'R9629:Ylpm1'
| ID |
725379 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ylpm1
|
| Ensembl Gene |
ENSMUSG00000021244 |
| Gene Name |
YLP motif containing 1 |
| Synonyms |
A930013E17Rik, Zap3, ZAP |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9629 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
12 |
| Chromosomal Location |
85043095-85117289 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to G
at 85044036 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Serine
at position 258
(I258S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000021670
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021670]
[ENSMUST00000101202]
[ENSMUST00000168977]
|
| AlphaFold |
Q9R0I7 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000021670
AA Change: I258S
|
| SMART Domains |
Protein: ENSMUSP00000021670
Gene: ENSMUSG00000021244
AA Change: I258S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
26 |
N/A |
INTRINSIC |
|
low complexity region
|
31 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
78 |
N/A |
INTRINSIC |
|
low complexity region
|
79 |
91 |
N/A |
INTRINSIC |
|
low complexity region
|
94 |
114 |
N/A |
INTRINSIC |
|
low complexity region
|
139 |
225 |
N/A |
INTRINSIC |
|
low complexity region
|
226 |
253 |
N/A |
INTRINSIC |
|
low complexity region
|
341 |
382 |
N/A |
INTRINSIC |
|
low complexity region
|
389 |
407 |
N/A |
INTRINSIC |
|
low complexity region
|
422 |
435 |
N/A |
INTRINSIC |
|
low complexity region
|
455 |
464 |
N/A |
INTRINSIC |
|
low complexity region
|
538 |
654 |
N/A |
INTRINSIC |
|
low complexity region
|
688 |
696 |
N/A |
INTRINSIC |
|
low complexity region
|
751 |
763 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
771 |
840 |
4.03e-5 |
PROSPERO |
|
low complexity region
|
841 |
854 |
N/A |
INTRINSIC |
|
low complexity region
|
966 |
972 |
N/A |
INTRINSIC |
|
internal_repeat_1
|
1062 |
1124 |
4.03e-5 |
PROSPERO |
|
low complexity region
|
1252 |
1266 |
N/A |
INTRINSIC |
|
low complexity region
|
1275 |
1293 |
N/A |
INTRINSIC |
|
low complexity region
|
1326 |
1338 |
N/A |
INTRINSIC |
|
low complexity region
|
1339 |
1353 |
N/A |
INTRINSIC |
|
low complexity region
|
1408 |
1425 |
N/A |
INTRINSIC |
|
coiled coil region
|
1447 |
1474 |
N/A |
INTRINSIC |
|
low complexity region
|
1494 |
1517 |
N/A |
INTRINSIC |
|
low complexity region
|
1518 |
1532 |
N/A |
INTRINSIC |
|
low complexity region
|
1536 |
1557 |
N/A |
INTRINSIC |
|
low complexity region
|
1598 |
1630 |
N/A |
INTRINSIC |
|
low complexity region
|
1678 |
1694 |
N/A |
INTRINSIC |
|
low complexity region
|
1705 |
1717 |
N/A |
INTRINSIC |
|
low complexity region
|
1720 |
1736 |
N/A |
INTRINSIC |
|
low complexity region
|
1797 |
1808 |
N/A |
INTRINSIC |
|
Pfam:AAA_33
|
1829 |
1990 |
7.8e-11 |
PFAM |
|
coiled coil region
|
1995 |
2032 |
N/A |
INTRINSIC |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000101202
AA Change: I211S
|
| SMART Domains |
Protein: ENSMUSP00000098763
Gene: ENSMUSG00000021244
AA Change: I211S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
26 |
N/A |
INTRINSIC |
|
low complexity region
|
31 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
78 |
N/A |
INTRINSIC |
|
low complexity region
|
79 |
91 |
N/A |
INTRINSIC |
|
low complexity region
|
94 |
114 |
N/A |
INTRINSIC |
|
low complexity region
|
139 |
206 |
N/A |
INTRINSIC |
|
low complexity region
|
294 |
335 |
N/A |
INTRINSIC |
|
low complexity region
|
342 |
360 |
N/A |
INTRINSIC |
|
low complexity region
|
375 |
388 |
N/A |
INTRINSIC |
|
low complexity region
|
408 |
417 |
N/A |
INTRINSIC |
|
low complexity region
|
491 |
607 |
N/A |
INTRINSIC |
|
low complexity region
|
641 |
649 |
N/A |
INTRINSIC |
|
low complexity region
|
741 |
764 |
N/A |
INTRINSIC |
|
low complexity region
|
765 |
779 |
N/A |
INTRINSIC |
|
low complexity region
|
783 |
804 |
N/A |
INTRINSIC |
|
low complexity region
|
845 |
877 |
N/A |
INTRINSIC |
|
low complexity region
|
925 |
941 |
N/A |
INTRINSIC |
|
low complexity region
|
952 |
964 |
N/A |
INTRINSIC |
|
low complexity region
|
967 |
983 |
N/A |
INTRINSIC |
|
low complexity region
|
1044 |
1055 |
N/A |
INTRINSIC |
|
Pfam:AAA_33
|
1076 |
1265 |
4.9e-11 |
PFAM |
|
| Predicted Effect |
unknown
Transcript: ENSMUST00000168977
AA Change: I258S
|
| SMART Domains |
Protein: ENSMUSP00000128962
Gene: ENSMUSG00000021244
AA Change: I258S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
15 |
26 |
N/A |
INTRINSIC |
|
low complexity region
|
31 |
50 |
N/A |
INTRINSIC |
|
low complexity region
|
57 |
78 |
N/A |
INTRINSIC |
|
low complexity region
|
79 |
91 |
N/A |
INTRINSIC |
|
low complexity region
|
94 |
114 |
N/A |
INTRINSIC |
|
low complexity region
|
139 |
225 |
N/A |
INTRINSIC |
|
low complexity region
|
226 |
253 |
N/A |
INTRINSIC |
|
low complexity region
|
341 |
382 |
N/A |
INTRINSIC |
|
low complexity region
|
389 |
407 |
N/A |
INTRINSIC |
|
low complexity region
|
422 |
435 |
N/A |
INTRINSIC |
|
low complexity region
|
455 |
464 |
N/A |
INTRINSIC |
|
low complexity region
|
538 |
654 |
N/A |
INTRINSIC |
|
low complexity region
|
688 |
696 |
N/A |
INTRINSIC |
|
low complexity region
|
788 |
811 |
N/A |
INTRINSIC |
|
low complexity region
|
812 |
826 |
N/A |
INTRINSIC |
|
low complexity region
|
830 |
851 |
N/A |
INTRINSIC |
|
low complexity region
|
892 |
924 |
N/A |
INTRINSIC |
|
low complexity region
|
972 |
988 |
N/A |
INTRINSIC |
|
low complexity region
|
999 |
1011 |
N/A |
INTRINSIC |
|
low complexity region
|
1014 |
1030 |
N/A |
INTRINSIC |
|
low complexity region
|
1091 |
1102 |
N/A |
INTRINSIC |
|
Pfam:AAA_33
|
1123 |
1311 |
4.5e-11 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 84 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930596D02Rik |
T |
C |
14: 35,532,134 (GRCm39) |
E147G |
probably damaging |
Het |
| Agrn |
G |
A |
4: 156,257,094 (GRCm39) |
Q1217* |
probably null |
Het |
| Ankrd13c |
G |
C |
3: 157,653,313 (GRCm39) |
K50N |
probably benign |
Het |
| Anks3 |
C |
T |
16: 4,775,565 (GRCm39) |
S144N |
probably damaging |
Het |
| Apob |
A |
T |
12: 8,059,054 (GRCm39) |
D2512V |
probably damaging |
Het |
| Arhgap45 |
A |
G |
10: 79,863,694 (GRCm39) |
K815E |
probably damaging |
Het |
| Atr |
T |
A |
9: 95,747,098 (GRCm39) |
C127S |
probably benign |
Het |
| B4galnt4 |
A |
G |
7: 140,648,575 (GRCm39) |
D697G |
probably damaging |
Het |
| C2cd3 |
C |
T |
7: 100,029,249 (GRCm39) |
L134F |
probably damaging |
Het |
| Celsr2 |
C |
T |
3: 108,308,915 (GRCm39) |
G1697D |
probably damaging |
Het |
| Cep170 |
A |
G |
1: 176,583,821 (GRCm39) |
S88P |
possibly damaging |
Het |
| Cnot1 |
A |
G |
8: 96,455,874 (GRCm39) |
V1961A |
probably damaging |
Het |
| Cntnap4 |
A |
G |
8: 113,568,349 (GRCm39) |
N795S |
probably damaging |
Het |
| Cog2 |
T |
A |
8: 125,260,125 (GRCm39) |
V256D |
possibly damaging |
Het |
| Col14a1 |
A |
G |
15: 55,382,545 (GRCm39) |
Y515C |
|
Het |
| Cox7a1 |
A |
G |
7: 29,884,583 (GRCm39) |
Q30R |
probably damaging |
Het |
| Cs |
T |
C |
10: 128,196,885 (GRCm39) |
S427P |
probably damaging |
Het |
| Dbr1 |
T |
A |
9: 99,464,523 (GRCm39) |
C101S |
|
Het |
| Dhcr7 |
C |
A |
7: 143,401,212 (GRCm39) |
Y461* |
probably null |
Het |
| Dis3l2 |
T |
A |
1: 86,974,784 (GRCm39) |
M691K |
probably benign |
Het |
| Dnah17 |
T |
C |
11: 117,979,804 (GRCm39) |
D1751G |
probably damaging |
Het |
| Dock10 |
A |
T |
1: 80,481,389 (GRCm39) |
I536K |
|
Het |
| Dok6 |
G |
T |
18: 89,491,988 (GRCm39) |
F196L |
possibly damaging |
Het |
| Epx |
C |
T |
11: 87,755,651 (GRCm39) |
D678N |
probably damaging |
Het |
| Fcrlb |
G |
C |
1: 170,739,735 (GRCm39) |
P56A |
probably benign |
Het |
| Flrt3 |
T |
C |
2: 140,502,816 (GRCm39) |
R271G |
possibly damaging |
Het |
| Galnt15 |
T |
A |
14: 31,774,301 (GRCm39) |
L479Q |
probably damaging |
Het |
| Gfy |
G |
A |
7: 44,827,785 (GRCm39) |
L104F |
probably benign |
Het |
| Gltp |
C |
T |
5: 114,814,382 (GRCm39) |
M80I |
probably benign |
Het |
| Gm21560 |
G |
A |
14: 6,218,250 (GRCm38) |
T76I |
probably benign |
Het |
| Gm5150 |
A |
G |
3: 16,044,829 (GRCm39) |
I132T |
probably benign |
Het |
| Hdac9 |
T |
C |
12: 34,439,389 (GRCm39) |
H437R |
probably damaging |
Het |
| Hpgd |
C |
A |
8: 56,751,419 (GRCm39) |
F82L |
|
Het |
| Ifi207 |
GAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGACTATTGGATGGTGTTGATAGAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGAT |
GAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGACTATTGGATGGTGTTGATAGAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATGAAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGTTGTTGATAGAGTTGCATGTGGAGCCAGGAGGTTGCTAGATGCTGTTGATACAGTTGCTTGTGGAGCCAGGAGGTTGCTAGATGCTGTTGAT |
1: 173,556,561 (GRCm39) |
|
probably benign |
Het |
| Ilrun |
A |
T |
17: 28,012,913 (GRCm39) |
F95I |
probably damaging |
Het |
| Itgb5 |
C |
T |
16: 33,696,295 (GRCm39) |
T162I |
probably damaging |
Het |
| Jakmip3 |
G |
A |
7: 138,625,118 (GRCm39) |
|
probably null |
Het |
| Kctd1 |
A |
T |
18: 15,196,611 (GRCm39) |
M4K |
unknown |
Het |
| Kirrel1 |
C |
A |
3: 87,003,025 (GRCm39) |
E123* |
probably null |
Het |
| Krt87 |
G |
C |
15: 101,389,048 (GRCm39) |
P95A |
probably benign |
Het |
| Man1a |
A |
T |
10: 53,796,158 (GRCm39) |
H511Q |
probably damaging |
Het |
| Megf8 |
A |
G |
7: 25,043,194 (GRCm39) |
D1372G |
possibly damaging |
Het |
| Mrgprd |
A |
G |
7: 144,875,189 (GRCm39) |
D20G |
probably benign |
Het |
| Mrpl54 |
C |
T |
10: 81,101,528 (GRCm39) |
G78S |
probably damaging |
Het |
| Myl1 |
T |
A |
1: 66,969,448 (GRCm39) |
E61D |
probably benign |
Het |
| Myo7a |
G |
T |
7: 97,712,937 (GRCm39) |
H1679Q |
probably benign |
Het |
| Naca |
A |
G |
10: 127,878,226 (GRCm39) |
E1086G |
unknown |
Het |
| Nagpa |
C |
G |
16: 5,017,829 (GRCm39) |
D258H |
probably damaging |
Het |
| Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
| Nr2f6 |
G |
A |
8: 71,827,171 (GRCm39) |
L377F |
probably damaging |
Het |
| Ntsr1 |
G |
A |
2: 180,183,274 (GRCm39) |
R328H |
probably damaging |
Het |
| Nup93 |
G |
A |
8: 95,033,267 (GRCm39) |
S592N |
probably damaging |
Het |
| Or10a2 |
A |
T |
7: 106,673,164 (GRCm39) |
N43I |
probably damaging |
Het |
| Or4k40 |
T |
A |
2: 111,251,137 (GRCm39) |
H53L |
probably benign |
Het |
| Or8g36 |
T |
C |
9: 39,422,497 (GRCm39) |
D173G |
probably benign |
Het |
| Pard3 |
T |
C |
8: 128,136,153 (GRCm39) |
V842A |
possibly damaging |
Het |
| Phospho2 |
T |
A |
2: 69,626,295 (GRCm39) |
N150K |
probably damaging |
Het |
| Piwil1 |
T |
C |
5: 128,831,051 (GRCm39) |
S791P |
probably damaging |
Het |
| Pkhd1 |
A |
G |
1: 20,462,437 (GRCm39) |
V2039A |
possibly damaging |
Het |
| Ppp1r3c |
A |
G |
19: 36,711,404 (GRCm39) |
I122T |
probably benign |
Het |
| Prrc2c |
A |
G |
1: 162,519,959 (GRCm39) |
Y2131H |
possibly damaging |
Het |
| Qtrt2 |
T |
C |
16: 43,683,540 (GRCm39) |
M311V |
possibly damaging |
Het |
| Rbbp4 |
T |
C |
4: 129,212,243 (GRCm39) |
D346G |
probably damaging |
Het |
| Slc13a5 |
A |
G |
11: 72,138,578 (GRCm39) |
I455T |
probably damaging |
Het |
| Slc28a3 |
A |
T |
13: 58,717,187 (GRCm39) |
Y366* |
probably null |
Het |
| Srgap1 |
T |
A |
10: 121,705,746 (GRCm39) |
Q226L |
probably benign |
Het |
| Syt17 |
A |
G |
7: 118,007,379 (GRCm39) |
V362A |
probably damaging |
Het |
| Tas2r117 |
T |
C |
6: 132,780,374 (GRCm39) |
S171P |
probably benign |
Het |
| Tfap2b |
A |
T |
1: 19,289,468 (GRCm39) |
I198F |
probably damaging |
Het |
| Tg |
A |
T |
15: 66,555,587 (GRCm39) |
I760F |
possibly damaging |
Het |
| Tmem123 |
T |
C |
9: 7,790,984 (GRCm39) |
V95A |
possibly damaging |
Het |
| Tmem198b |
C |
A |
10: 128,638,386 (GRCm39) |
G59V |
probably damaging |
Het |
| Tmem30c |
T |
G |
16: 57,096,585 (GRCm39) |
I179L |
probably benign |
Het |
| Tmprss2 |
A |
T |
16: 97,369,702 (GRCm39) |
D357E |
probably benign |
Het |
| Tns3 |
G |
A |
11: 8,401,142 (GRCm39) |
T1052M |
possibly damaging |
Het |
| Trex1 |
A |
T |
9: 108,887,632 (GRCm39) |
C120S |
probably damaging |
Het |
| Ttc8 |
A |
G |
12: 98,886,965 (GRCm39) |
S13G |
possibly damaging |
Het |
| Ttll7 |
T |
C |
3: 146,621,487 (GRCm39) |
I362T |
probably damaging |
Het |
| Usp34 |
A |
T |
11: 23,314,364 (GRCm39) |
T769S |
|
Het |
| Vmn1r185 |
G |
T |
7: 26,311,439 (GRCm39) |
T22K |
probably damaging |
Het |
| Vmn1r39 |
T |
G |
6: 66,781,578 (GRCm39) |
M247L |
probably benign |
Het |
| Vmn2r96 |
A |
G |
17: 18,803,257 (GRCm39) |
D389G |
probably benign |
Het |
| Xirp1 |
C |
T |
9: 119,846,379 (GRCm39) |
V835I |
probably benign |
Het |
| Zfp971 |
A |
T |
2: 177,675,417 (GRCm39) |
S339C |
probably damaging |
Het |
|
| Other mutations in Ylpm1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00539:Ylpm1
|
APN |
12 |
85,075,728 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL00809:Ylpm1
|
APN |
12 |
85,095,968 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01508:Ylpm1
|
APN |
12 |
85,062,229 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
IGL02199:Ylpm1
|
APN |
12 |
85,080,779 (GRCm39) |
nonsense |
probably null |
|
|
IGL02392:Ylpm1
|
APN |
12 |
85,061,731 (GRCm39) |
missense |
unknown |
|
|
IGL02455:Ylpm1
|
APN |
12 |
85,077,037 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02506:Ylpm1
|
APN |
12 |
85,095,965 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03102:Ylpm1
|
APN |
12 |
85,096,032 (GRCm39) |
splice site |
probably benign |
|
|
I1329:Ylpm1
|
UTSW |
12 |
85,087,654 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02799:Ylpm1
|
UTSW |
12 |
85,091,258 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0010:Ylpm1
|
UTSW |
12 |
85,075,800 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R0090:Ylpm1
|
UTSW |
12 |
85,075,814 (GRCm39) |
intron |
probably benign |
|
|
R0149:Ylpm1
|
UTSW |
12 |
85,075,612 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0226:Ylpm1
|
UTSW |
12 |
85,096,511 (GRCm39) |
missense |
probably benign |
0.21 |
|
R0375:Ylpm1
|
UTSW |
12 |
85,061,754 (GRCm39) |
missense |
unknown |
|
|
R0378:Ylpm1
|
UTSW |
12 |
85,043,850 (GRCm39) |
intron |
probably benign |
|
|
R0507:Ylpm1
|
UTSW |
12 |
85,075,886 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0742:Ylpm1
|
UTSW |
12 |
85,075,886 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1350:Ylpm1
|
UTSW |
12 |
85,060,856 (GRCm39) |
unclassified |
probably benign |
|
|
R1452:Ylpm1
|
UTSW |
12 |
85,077,157 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1500:Ylpm1
|
UTSW |
12 |
85,061,770 (GRCm39) |
missense |
unknown |
|
|
R1837:Ylpm1
|
UTSW |
12 |
85,076,107 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R1945:Ylpm1
|
UTSW |
12 |
85,062,192 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1971:Ylpm1
|
UTSW |
12 |
85,087,560 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2211:Ylpm1
|
UTSW |
12 |
85,091,152 (GRCm39) |
nonsense |
probably null |
|
|
R2213:Ylpm1
|
UTSW |
12 |
85,116,492 (GRCm39) |
missense |
probably benign |
0.25 |
|
R2269:Ylpm1
|
UTSW |
12 |
85,061,824 (GRCm39) |
missense |
unknown |
|
|
R2300:Ylpm1
|
UTSW |
12 |
85,107,093 (GRCm39) |
splice site |
probably null |
|
|
R2439:Ylpm1
|
UTSW |
12 |
85,060,891 (GRCm39) |
unclassified |
probably benign |
|
|
R2497:Ylpm1
|
UTSW |
12 |
85,043,535 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2890:Ylpm1
|
UTSW |
12 |
85,076,587 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R3111:Ylpm1
|
UTSW |
12 |
85,076,145 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3436:Ylpm1
|
UTSW |
12 |
85,096,644 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3437:Ylpm1
|
UTSW |
12 |
85,096,644 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4156:Ylpm1
|
UTSW |
12 |
85,104,177 (GRCm39) |
intron |
probably benign |
|
|
R4157:Ylpm1
|
UTSW |
12 |
85,104,177 (GRCm39) |
intron |
probably benign |
|
|
R4959:Ylpm1
|
UTSW |
12 |
85,096,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5014:Ylpm1
|
UTSW |
12 |
85,061,523 (GRCm39) |
missense |
unknown |
|
|
R5039:Ylpm1
|
UTSW |
12 |
85,089,013 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5039:Ylpm1
|
UTSW |
12 |
85,062,267 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5084:Ylpm1
|
UTSW |
12 |
85,076,095 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5325:Ylpm1
|
UTSW |
12 |
85,060,735 (GRCm39) |
unclassified |
probably benign |
|
|
R5378:Ylpm1
|
UTSW |
12 |
85,077,029 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5428:Ylpm1
|
UTSW |
12 |
85,077,003 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5467:Ylpm1
|
UTSW |
12 |
85,043,633 (GRCm39) |
missense |
unknown |
|
|
R5605:Ylpm1
|
UTSW |
12 |
85,075,627 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5614:Ylpm1
|
UTSW |
12 |
85,111,718 (GRCm39) |
intron |
probably benign |
|
|
R5748:Ylpm1
|
UTSW |
12 |
85,107,025 (GRCm39) |
splice site |
probably null |
|
|
R5860:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5861:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5881:Ylpm1
|
UTSW |
12 |
85,088,899 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5909:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5912:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5915:Ylpm1
|
UTSW |
12 |
85,087,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6000:Ylpm1
|
UTSW |
12 |
85,044,030 (GRCm39) |
missense |
unknown |
|
|
R6004:Ylpm1
|
UTSW |
12 |
85,075,858 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R6007:Ylpm1
|
UTSW |
12 |
85,076,064 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6053:Ylpm1
|
UTSW |
12 |
85,043,277 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6104:Ylpm1
|
UTSW |
12 |
85,076,404 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6197:Ylpm1
|
UTSW |
12 |
85,088,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6293:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
|
R6297:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
|
R6305:Ylpm1
|
UTSW |
12 |
85,077,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6379:Ylpm1
|
UTSW |
12 |
85,077,574 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6465:Ylpm1
|
UTSW |
12 |
85,096,576 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6608:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
|
R6609:Ylpm1
|
UTSW |
12 |
85,062,051 (GRCm39) |
missense |
unknown |
|
|
R6737:Ylpm1
|
UTSW |
12 |
85,077,620 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R6794:Ylpm1
|
UTSW |
12 |
85,043,655 (GRCm39) |
missense |
unknown |
|
|
R7383:Ylpm1
|
UTSW |
12 |
85,091,242 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7514:Ylpm1
|
UTSW |
12 |
85,077,268 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7577:Ylpm1
|
UTSW |
12 |
85,043,994 (GRCm39) |
missense |
unknown |
|
|
R7709:Ylpm1
|
UTSW |
12 |
85,059,799 (GRCm39) |
missense |
unknown |
|
|
R7718:Ylpm1
|
UTSW |
12 |
85,075,896 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7736:Ylpm1
|
UTSW |
12 |
85,059,757 (GRCm39) |
missense |
unknown |
|
|
R7758:Ylpm1
|
UTSW |
12 |
85,061,796 (GRCm39) |
missense |
unknown |
|
|
R7807:Ylpm1
|
UTSW |
12 |
85,060,855 (GRCm39) |
nonsense |
probably null |
|
|
R7838:Ylpm1
|
UTSW |
12 |
85,095,640 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7846:Ylpm1
|
UTSW |
12 |
85,104,042 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8170:Ylpm1
|
UTSW |
12 |
85,080,801 (GRCm39) |
missense |
probably benign |
0.40 |
|
R8776:Ylpm1
|
UTSW |
12 |
85,077,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8776-TAIL:Ylpm1
|
UTSW |
12 |
85,077,195 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8812:Ylpm1
|
UTSW |
12 |
85,043,566 (GRCm39) |
missense |
unknown |
|
|
R8847:Ylpm1
|
UTSW |
12 |
85,061,672 (GRCm39) |
missense |
unknown |
|
|
R8874:Ylpm1
|
UTSW |
12 |
85,116,394 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9129:Ylpm1
|
UTSW |
12 |
85,104,052 (GRCm39) |
missense |
|
|
|
R9165:Ylpm1
|
UTSW |
12 |
85,077,342 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9198:Ylpm1
|
UTSW |
12 |
85,080,689 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9564:Ylpm1
|
UTSW |
12 |
85,091,176 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9797:Ylpm1
|
UTSW |
12 |
85,077,109 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
Z1088:Ylpm1
|
UTSW |
12 |
85,076,929 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Z1176:Ylpm1
|
UTSW |
12 |
85,077,058 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
Z1177:Ylpm1
|
UTSW |
12 |
85,104,057 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- ATCCCAGTCGTACATGCCTC -3'
(R):5'- GCTGTTGGAATTACGATAGGC -3'
Sequencing Primer
(F):5'- GTACATGCCTCCACCTCAG -3'
(R):5'- GCATTAGCTGGTTAAAGCCC -3'
|
| Posted On |
2022-09-12 |
Incidental Mutation