Incidental Mutation 'R7512:Ubap2l'
ID |
582132 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Ubap2l
|
Ensembl Gene |
ENSMUSG00000042520 |
Gene Name |
ubiquitin-associated protein 2-like |
Synonyms |
4932431F02Rik, A430103N23Rik, NICE-4, 3110083O19Rik |
MMRRC Submission |
045585-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R7512 (G1)
|
Quality Score |
225.009 |
Status
|
Validated
|
Chromosome |
3 |
Chromosomal Location |
89907447-89959935 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 89917803 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Phenylalanine to Leucine
at position 864
(F864L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000066138
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029553]
[ENSMUST00000064639]
[ENSMUST00000090908]
[ENSMUST00000195995]
[ENSMUST00000196843]
[ENSMUST00000198322]
[ENSMUST00000199834]
|
AlphaFold |
Q80X50 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000029553
AA Change: F859L
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000029553 Gene: ENSMUSG00000042520 AA Change: F859L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
152 |
N/A |
INTRINSIC |
low complexity region
|
162 |
190 |
N/A |
INTRINSIC |
low complexity region
|
213 |
226 |
N/A |
INTRINSIC |
low complexity region
|
389 |
398 |
N/A |
INTRINSIC |
low complexity region
|
400 |
409 |
N/A |
INTRINSIC |
low complexity region
|
459 |
484 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
514 |
546 |
4e-22 |
PFAM |
low complexity region
|
554 |
589 |
N/A |
INTRINSIC |
low complexity region
|
665 |
675 |
N/A |
INTRINSIC |
low complexity region
|
714 |
745 |
N/A |
INTRINSIC |
low complexity region
|
748 |
804 |
N/A |
INTRINSIC |
low complexity region
|
808 |
822 |
N/A |
INTRINSIC |
low complexity region
|
893 |
916 |
N/A |
INTRINSIC |
low complexity region
|
1038 |
1051 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000064639
AA Change: F864L
|
SMART Domains |
Protein: ENSMUSP00000066138 Gene: ENSMUSG00000042520 AA Change: F864L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
152 |
N/A |
INTRINSIC |
low complexity region
|
162 |
190 |
N/A |
INTRINSIC |
low complexity region
|
213 |
226 |
N/A |
INTRINSIC |
low complexity region
|
394 |
403 |
N/A |
INTRINSIC |
low complexity region
|
405 |
414 |
N/A |
INTRINSIC |
low complexity region
|
464 |
489 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
520 |
551 |
4.1e-18 |
PFAM |
low complexity region
|
559 |
594 |
N/A |
INTRINSIC |
low complexity region
|
670 |
680 |
N/A |
INTRINSIC |
low complexity region
|
719 |
750 |
N/A |
INTRINSIC |
low complexity region
|
753 |
809 |
N/A |
INTRINSIC |
low complexity region
|
813 |
827 |
N/A |
INTRINSIC |
low complexity region
|
898 |
921 |
N/A |
INTRINSIC |
low complexity region
|
1043 |
1056 |
N/A |
INTRINSIC |
low complexity region
|
1077 |
1092 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000090908
AA Change: F839L
PolyPhen 2
Score 0.973 (Sensitivity: 0.76; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000088424 Gene: ENSMUSG00000042520 AA Change: F839L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
148 |
N/A |
INTRINSIC |
low complexity region
|
173 |
201 |
N/A |
INTRINSIC |
low complexity region
|
224 |
237 |
N/A |
INTRINSIC |
low complexity region
|
400 |
409 |
N/A |
INTRINSIC |
low complexity region
|
411 |
420 |
N/A |
INTRINSIC |
low complexity region
|
470 |
495 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
525 |
557 |
3.6e-22 |
PFAM |
low complexity region
|
565 |
600 |
N/A |
INTRINSIC |
low complexity region
|
676 |
686 |
N/A |
INTRINSIC |
low complexity region
|
725 |
756 |
N/A |
INTRINSIC |
low complexity region
|
759 |
815 |
N/A |
INTRINSIC |
low complexity region
|
819 |
833 |
N/A |
INTRINSIC |
low complexity region
|
904 |
927 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000195995
AA Change: F870L
|
SMART Domains |
Protein: ENSMUSP00000143638 Gene: ENSMUSG00000042520 AA Change: F870L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
148 |
N/A |
INTRINSIC |
low complexity region
|
173 |
201 |
N/A |
INTRINSIC |
low complexity region
|
224 |
237 |
N/A |
INTRINSIC |
low complexity region
|
400 |
409 |
N/A |
INTRINSIC |
low complexity region
|
411 |
420 |
N/A |
INTRINSIC |
low complexity region
|
470 |
495 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
526 |
557 |
3.7e-18 |
PFAM |
low complexity region
|
565 |
600 |
N/A |
INTRINSIC |
low complexity region
|
676 |
686 |
N/A |
INTRINSIC |
low complexity region
|
725 |
756 |
N/A |
INTRINSIC |
low complexity region
|
759 |
815 |
N/A |
INTRINSIC |
low complexity region
|
819 |
833 |
N/A |
INTRINSIC |
low complexity region
|
904 |
927 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000196843
AA Change: F859L
|
SMART Domains |
Protein: ENSMUSP00000143459 Gene: ENSMUSG00000042520 AA Change: F859L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
152 |
N/A |
INTRINSIC |
low complexity region
|
162 |
190 |
N/A |
INTRINSIC |
low complexity region
|
213 |
226 |
N/A |
INTRINSIC |
low complexity region
|
389 |
398 |
N/A |
INTRINSIC |
low complexity region
|
400 |
409 |
N/A |
INTRINSIC |
low complexity region
|
459 |
484 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
514 |
546 |
4e-22 |
PFAM |
low complexity region
|
554 |
589 |
N/A |
INTRINSIC |
low complexity region
|
665 |
675 |
N/A |
INTRINSIC |
low complexity region
|
714 |
745 |
N/A |
INTRINSIC |
low complexity region
|
748 |
804 |
N/A |
INTRINSIC |
low complexity region
|
808 |
822 |
N/A |
INTRINSIC |
low complexity region
|
893 |
916 |
N/A |
INTRINSIC |
low complexity region
|
1038 |
1051 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1087 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000198322
AA Change: F839L
|
SMART Domains |
Protein: ENSMUSP00000142524 Gene: ENSMUSG00000042520 AA Change: F839L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
152 |
N/A |
INTRINSIC |
low complexity region
|
162 |
190 |
N/A |
INTRINSIC |
low complexity region
|
213 |
226 |
N/A |
INTRINSIC |
low complexity region
|
369 |
378 |
N/A |
INTRINSIC |
low complexity region
|
380 |
389 |
N/A |
INTRINSIC |
low complexity region
|
439 |
464 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
494 |
526 |
4.1e-22 |
PFAM |
low complexity region
|
534 |
569 |
N/A |
INTRINSIC |
low complexity region
|
645 |
655 |
N/A |
INTRINSIC |
low complexity region
|
694 |
725 |
N/A |
INTRINSIC |
low complexity region
|
728 |
784 |
N/A |
INTRINSIC |
low complexity region
|
788 |
802 |
N/A |
INTRINSIC |
low complexity region
|
873 |
896 |
N/A |
INTRINSIC |
low complexity region
|
1017 |
1030 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000199834
AA Change: F870L
|
SMART Domains |
Protein: ENSMUSP00000143254 Gene: ENSMUSG00000042520 AA Change: F870L
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
30 |
N/A |
INTRINSIC |
UBA
|
50 |
88 |
1.31e-9 |
SMART |
low complexity region
|
124 |
148 |
N/A |
INTRINSIC |
low complexity region
|
173 |
201 |
N/A |
INTRINSIC |
low complexity region
|
224 |
237 |
N/A |
INTRINSIC |
low complexity region
|
400 |
409 |
N/A |
INTRINSIC |
low complexity region
|
411 |
420 |
N/A |
INTRINSIC |
low complexity region
|
470 |
495 |
N/A |
INTRINSIC |
Pfam:DUF3697
|
525 |
557 |
3.6e-22 |
PFAM |
low complexity region
|
565 |
600 |
N/A |
INTRINSIC |
low complexity region
|
676 |
686 |
N/A |
INTRINSIC |
low complexity region
|
725 |
756 |
N/A |
INTRINSIC |
low complexity region
|
759 |
815 |
N/A |
INTRINSIC |
low complexity region
|
819 |
833 |
N/A |
INTRINSIC |
low complexity region
|
904 |
927 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.1954 |
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
100% (59/59) |
MGI Phenotype |
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit decreased female body size and reduced female fertility. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
C |
T |
11: 109,829,275 (GRCm39) |
A1395T |
probably benign |
Het |
Ank3 |
A |
G |
10: 69,826,691 (GRCm39) |
K1787E |
|
Het |
Atg2a |
C |
T |
19: 6,310,106 (GRCm39) |
A1763V |
probably damaging |
Het |
Bdp1 |
T |
C |
13: 100,187,457 (GRCm39) |
I1637V |
probably benign |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Camsap3 |
A |
G |
8: 3,648,740 (GRCm39) |
T20A |
probably benign |
Het |
Ccnt2 |
T |
A |
1: 127,730,031 (GRCm39) |
S303T |
possibly damaging |
Het |
Cdh3 |
C |
T |
8: 107,265,640 (GRCm39) |
Q228* |
probably null |
Het |
Col19a1 |
C |
T |
1: 24,356,788 (GRCm39) |
G632R |
probably damaging |
Het |
Dock2 |
A |
C |
11: 34,262,542 (GRCm39) |
C938G |
possibly damaging |
Het |
Dync1i1 |
G |
T |
6: 5,969,410 (GRCm39) |
V412L |
possibly damaging |
Het |
Eif1ad6 |
G |
T |
12: 87,668,751 (GRCm39) |
E128* |
probably null |
Het |
Entrep2 |
C |
T |
7: 64,805,918 (GRCm39) |
A52T |
probably benign |
Het |
Fam185a |
G |
A |
5: 21,652,356 (GRCm39) |
|
probably null |
Het |
Fcho1 |
A |
G |
8: 72,169,507 (GRCm39) |
L133P |
possibly damaging |
Het |
Galnt12 |
G |
A |
4: 47,108,406 (GRCm39) |
R181H |
possibly damaging |
Het |
Gen1 |
A |
G |
12: 11,310,977 (GRCm39) |
V85A |
possibly damaging |
Het |
Gm12185 |
A |
T |
11: 48,806,717 (GRCm39) |
I158K |
probably benign |
Het |
Gm5624 |
T |
C |
14: 44,799,312 (GRCm39) |
R82G |
|
Het |
Grap2 |
A |
C |
15: 80,532,754 (GRCm39) |
N307T |
probably benign |
Het |
H6pd |
A |
G |
4: 150,080,405 (GRCm39) |
F147L |
probably benign |
Het |
Haspin |
A |
T |
11: 73,027,418 (GRCm39) |
I557N |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,435,172 (GRCm39) |
K961N |
possibly damaging |
Het |
Helz2 |
A |
G |
2: 180,872,647 (GRCm39) |
M2495T |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,877,393 (GRCm39) |
|
probably null |
Het |
Impdh1 |
T |
C |
6: 29,207,168 (GRCm39) |
I59V |
probably benign |
Het |
Kcnn1 |
A |
T |
8: 71,307,293 (GRCm39) |
L200Q |
possibly damaging |
Het |
Kif5c |
T |
A |
2: 49,590,977 (GRCm39) |
H276Q |
probably damaging |
Het |
Kntc1 |
T |
C |
5: 123,929,001 (GRCm39) |
L1259P |
probably damaging |
Het |
Krtap4-1 |
A |
T |
11: 99,518,859 (GRCm39) |
C50* |
probably null |
Het |
Lat2 |
T |
A |
5: 134,634,798 (GRCm39) |
D114V |
probably damaging |
Het |
Lrrc41 |
A |
G |
4: 115,950,191 (GRCm39) |
T535A |
possibly damaging |
Het |
Ly75 |
A |
T |
2: 60,164,907 (GRCm39) |
V757D |
probably damaging |
Het |
Masp1 |
C |
A |
16: 23,288,874 (GRCm39) |
R642L |
probably damaging |
Het |
Morn3 |
A |
G |
5: 123,175,343 (GRCm39) |
|
probably null |
Het |
Mpl |
A |
T |
4: 118,306,089 (GRCm39) |
I384N |
|
Het |
Mtmr14 |
C |
T |
6: 113,245,652 (GRCm39) |
Q409* |
probably null |
Het |
Nek1 |
T |
A |
8: 61,583,179 (GRCm39) |
D1272E |
probably benign |
Het |
Oit3 |
T |
C |
10: 59,274,716 (GRCm39) |
Y28C |
probably damaging |
Het |
Or2z8 |
T |
A |
8: 72,812,367 (GRCm39) |
I281N |
probably damaging |
Het |
Or4x12-ps1 |
A |
G |
2: 89,916,040 (GRCm39) |
I255T |
possibly damaging |
Het |
Or5ac22 |
T |
A |
16: 59,135,390 (GRCm39) |
N127Y |
probably damaging |
Het |
Pcdh15 |
T |
C |
10: 74,477,214 (GRCm39) |
Y186H |
possibly damaging |
Het |
Pcdhgb1 |
T |
A |
18: 37,815,418 (GRCm39) |
D636E |
probably damaging |
Het |
Pdgfra |
A |
T |
5: 75,355,675 (GRCm39) |
R1062* |
probably null |
Het |
Pds5b |
T |
C |
5: 150,711,807 (GRCm39) |
F922L |
probably damaging |
Het |
Pip5k1c |
G |
A |
10: 81,150,953 (GRCm39) |
|
probably null |
Het |
Ppp2r3d |
T |
C |
9: 101,052,532 (GRCm39) |
T226A |
possibly damaging |
Het |
Ptprh |
G |
A |
7: 4,574,780 (GRCm39) |
T413I |
possibly damaging |
Het |
Rora |
C |
A |
9: 69,281,367 (GRCm39) |
D382E |
probably benign |
Het |
Sacs |
T |
A |
14: 61,441,879 (GRCm39) |
N1308K |
probably benign |
Het |
Sgce |
C |
T |
6: 4,707,192 (GRCm39) |
D218N |
possibly damaging |
Het |
Slc34a3 |
A |
T |
2: 25,122,253 (GRCm39) |
|
probably null |
Het |
Slit1 |
T |
C |
19: 41,589,074 (GRCm39) |
Y1471C |
probably damaging |
Het |
Smarca2 |
G |
T |
19: 26,661,209 (GRCm39) |
V935L |
possibly damaging |
Het |
Smchd1 |
T |
C |
17: 71,688,364 (GRCm39) |
N1298S |
possibly damaging |
Het |
Sort1 |
T |
A |
3: 108,233,323 (GRCm39) |
|
probably null |
Het |
Spata13 |
T |
C |
14: 60,989,226 (GRCm39) |
L964P |
probably damaging |
Het |
Spata31h1 |
G |
A |
10: 82,128,469 (GRCm39) |
L1514F |
probably benign |
Het |
Trav7-6 |
C |
A |
14: 53,954,552 (GRCm39) |
D47E |
probably benign |
Het |
Vmn2r102 |
C |
T |
17: 19,914,363 (GRCm39) |
P643S |
probably damaging |
Het |
Zfp112 |
T |
A |
7: 23,824,604 (GRCm39) |
C195S |
possibly damaging |
Het |
Zfp764l1 |
C |
T |
7: 126,992,496 (GRCm39) |
C38Y |
probably null |
Het |
|
Other mutations in Ubap2l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Ubap2l
|
APN |
3 |
89,916,563 (GRCm39) |
nonsense |
probably null |
|
IGL02606:Ubap2l
|
APN |
3 |
89,945,735 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02809:Ubap2l
|
APN |
3 |
89,928,553 (GRCm39) |
missense |
probably damaging |
1.00 |
Panhandle
|
UTSW |
3 |
89,938,683 (GRCm39) |
splice site |
probably benign |
|
plainview
|
UTSW |
3 |
89,946,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Ubap2l
|
UTSW |
3 |
89,946,235 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0052:Ubap2l
|
UTSW |
3 |
89,946,235 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0128:Ubap2l
|
UTSW |
3 |
89,928,680 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0130:Ubap2l
|
UTSW |
3 |
89,928,680 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0502:Ubap2l
|
UTSW |
3 |
89,916,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0619:Ubap2l
|
UTSW |
3 |
89,924,527 (GRCm39) |
missense |
probably benign |
0.01 |
R0726:Ubap2l
|
UTSW |
3 |
89,928,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Ubap2l
|
UTSW |
3 |
89,955,180 (GRCm39) |
utr 5 prime |
probably benign |
|
R1172:Ubap2l
|
UTSW |
3 |
89,930,807 (GRCm39) |
missense |
probably benign |
0.24 |
R1174:Ubap2l
|
UTSW |
3 |
89,930,807 (GRCm39) |
missense |
probably benign |
0.24 |
R1175:Ubap2l
|
UTSW |
3 |
89,930,807 (GRCm39) |
missense |
probably benign |
0.24 |
R1191:Ubap2l
|
UTSW |
3 |
89,930,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R1432:Ubap2l
|
UTSW |
3 |
89,926,635 (GRCm39) |
missense |
probably benign |
0.11 |
R1582:Ubap2l
|
UTSW |
3 |
89,941,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Ubap2l
|
UTSW |
3 |
89,926,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Ubap2l
|
UTSW |
3 |
89,938,683 (GRCm39) |
splice site |
probably benign |
|
R2059:Ubap2l
|
UTSW |
3 |
89,938,683 (GRCm39) |
splice site |
probably benign |
|
R2081:Ubap2l
|
UTSW |
3 |
89,946,271 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2408:Ubap2l
|
UTSW |
3 |
89,916,439 (GRCm39) |
missense |
probably null |
0.99 |
R3404:Ubap2l
|
UTSW |
3 |
89,946,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R3551:Ubap2l
|
UTSW |
3 |
89,922,758 (GRCm39) |
missense |
unknown |
|
R4132:Ubap2l
|
UTSW |
3 |
89,916,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Ubap2l
|
UTSW |
3 |
89,928,210 (GRCm39) |
missense |
probably damaging |
0.98 |
R4798:Ubap2l
|
UTSW |
3 |
89,928,210 (GRCm39) |
missense |
probably damaging |
0.98 |
R5173:Ubap2l
|
UTSW |
3 |
89,928,337 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5274:Ubap2l
|
UTSW |
3 |
89,920,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5387:Ubap2l
|
UTSW |
3 |
89,913,903 (GRCm39) |
missense |
probably benign |
0.10 |
R6548:Ubap2l
|
UTSW |
3 |
89,930,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Ubap2l
|
UTSW |
3 |
89,946,155 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6995:Ubap2l
|
UTSW |
3 |
89,916,548 (GRCm39) |
missense |
probably damaging |
0.98 |
R7039:Ubap2l
|
UTSW |
3 |
89,909,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R7323:Ubap2l
|
UTSW |
3 |
89,922,713 (GRCm39) |
missense |
unknown |
|
R7815:Ubap2l
|
UTSW |
3 |
89,951,071 (GRCm39) |
nonsense |
probably null |
|
R7975:Ubap2l
|
UTSW |
3 |
89,946,076 (GRCm39) |
splice site |
probably null |
|
R8200:Ubap2l
|
UTSW |
3 |
89,930,933 (GRCm39) |
missense |
probably benign |
0.34 |
R8291:Ubap2l
|
UTSW |
3 |
89,915,538 (GRCm39) |
makesense |
probably null |
|
R8424:Ubap2l
|
UTSW |
3 |
89,928,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R8441:Ubap2l
|
UTSW |
3 |
89,920,007 (GRCm39) |
missense |
unknown |
|
R9098:Ubap2l
|
UTSW |
3 |
89,909,756 (GRCm39) |
missense |
unknown |
|
R9373:Ubap2l
|
UTSW |
3 |
89,915,587 (GRCm39) |
missense |
unknown |
|
R9421:Ubap2l
|
UTSW |
3 |
89,955,108 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9488:Ubap2l
|
UTSW |
3 |
89,928,656 (GRCm39) |
missense |
probably benign |
0.02 |
Z1176:Ubap2l
|
UTSW |
3 |
89,926,511 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ubap2l
|
UTSW |
3 |
89,909,124 (GRCm39) |
critical splice donor site |
probably null |
|
Z1186:Ubap2l
|
UTSW |
3 |
89,916,543 (GRCm39) |
missense |
unknown |
|
Z1191:Ubap2l
|
UTSW |
3 |
89,916,543 (GRCm39) |
missense |
unknown |
|
|
Predicted Primers |
PCR Primer
(F):5'- TCATATCCATGACAACAAGGGG -3'
(R):5'- TATTCTACTCGTGGCAGGCTG -3'
Sequencing Primer
(F):5'- CATATCCATGACAACAAGGGGTAGGG -3'
(R):5'- GGAACAGTGTATGCCAGATTAATTG -3'
|
Posted On |
2019-10-17 |