Incidental Mutation 'R5323:Pum2'
ID |
404981 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pum2
|
Ensembl Gene |
ENSMUSG00000020594 |
Gene Name |
pumilio RNA-binding family member 2 |
Synonyms |
Pumm2, 5730503J23Rik |
MMRRC Submission |
042906-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5323 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
12 |
Chromosomal Location |
8724134-8802581 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 8794706 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 737
(I737N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000137020
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000020915]
[ENSMUST00000111122]
[ENSMUST00000111123]
[ENSMUST00000163569]
[ENSMUST00000165293]
[ENSMUST00000168361]
[ENSMUST00000169089]
[ENSMUST00000178015]
|
AlphaFold |
Q80U58 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000020915
AA Change: I732N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000020915 Gene: ENSMUSG00000020594 AA Change: I732N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
319 |
336 |
N/A |
INTRINSIC |
low complexity region
|
353 |
378 |
N/A |
INTRINSIC |
low complexity region
|
464 |
490 |
N/A |
INTRINSIC |
low complexity region
|
498 |
509 |
N/A |
INTRINSIC |
low complexity region
|
521 |
535 |
N/A |
INTRINSIC |
low complexity region
|
542 |
576 |
N/A |
INTRINSIC |
low complexity region
|
591 |
609 |
N/A |
INTRINSIC |
Pumilio
|
642 |
677 |
2.35e-7 |
SMART |
Pumilio
|
678 |
713 |
6.54e-6 |
SMART |
Pumilio
|
714 |
749 |
2.89e-7 |
SMART |
Pumilio
|
750 |
785 |
3.37e-8 |
SMART |
Pumilio
|
786 |
821 |
4.84e-9 |
SMART |
Pumilio
|
822 |
857 |
3.2e-9 |
SMART |
Pumilio
|
858 |
893 |
5.78e-7 |
SMART |
Pumilio
|
901 |
936 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111122
AA Change: I816N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106751 Gene: ENSMUSG00000020594 AA Change: I816N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
602 |
N/A |
INTRINSIC |
low complexity region
|
630 |
660 |
N/A |
INTRINSIC |
low complexity region
|
675 |
693 |
N/A |
INTRINSIC |
Pumilio
|
726 |
761 |
2.35e-7 |
SMART |
Pumilio
|
762 |
797 |
6.54e-6 |
SMART |
Pumilio
|
798 |
833 |
2.89e-7 |
SMART |
Pumilio
|
834 |
869 |
3.37e-8 |
SMART |
Pumilio
|
870 |
905 |
4.84e-9 |
SMART |
Pumilio
|
906 |
941 |
3.2e-9 |
SMART |
Pumilio
|
942 |
977 |
5.78e-7 |
SMART |
Pumilio
|
985 |
1020 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111123
AA Change: I816N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000106752 Gene: ENSMUSG00000020594 AA Change: I816N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
602 |
N/A |
INTRINSIC |
low complexity region
|
630 |
660 |
N/A |
INTRINSIC |
low complexity region
|
675 |
693 |
N/A |
INTRINSIC |
Pumilio
|
726 |
761 |
2.35e-7 |
SMART |
Pumilio
|
762 |
797 |
6.54e-6 |
SMART |
Pumilio
|
798 |
833 |
2.89e-7 |
SMART |
Pumilio
|
834 |
869 |
3.37e-8 |
SMART |
Pumilio
|
870 |
905 |
4.84e-9 |
SMART |
Pumilio
|
906 |
941 |
3.2e-9 |
SMART |
Pumilio
|
942 |
977 |
5.78e-7 |
SMART |
Pumilio
|
985 |
1020 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000163569
AA Change: I816N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000131074 Gene: ENSMUSG00000020594 AA Change: I816N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
602 |
N/A |
INTRINSIC |
low complexity region
|
630 |
660 |
N/A |
INTRINSIC |
low complexity region
|
675 |
693 |
N/A |
INTRINSIC |
Pumilio
|
726 |
761 |
2.35e-7 |
SMART |
Pumilio
|
762 |
797 |
6.54e-6 |
SMART |
Pumilio
|
798 |
832 |
1.29e-4 |
SMART |
Pumilio
|
836 |
871 |
3.37e-8 |
SMART |
Pumilio
|
872 |
907 |
4.84e-9 |
SMART |
Pumilio
|
908 |
943 |
3.2e-9 |
SMART |
Pumilio
|
944 |
979 |
5.78e-7 |
SMART |
Pumilio
|
987 |
1022 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000164818
|
SMART Domains |
Protein: ENSMUSP00000129243 Gene: ENSMUSG00000020594
Domain | Start | End | E-Value | Type |
low complexity region
|
24 |
42 |
N/A |
INTRINSIC |
Pumilio
|
75 |
110 |
2.35e-7 |
SMART |
Pumilio
|
111 |
139 |
1.58e1 |
SMART |
Pumilio
|
140 |
175 |
3.37e-8 |
SMART |
Pumilio
|
176 |
211 |
4.84e-9 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000165293
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000168361
AA Change: I816N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000128292 Gene: ENSMUSG00000020594 AA Change: I816N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
602 |
N/A |
INTRINSIC |
low complexity region
|
630 |
660 |
N/A |
INTRINSIC |
low complexity region
|
675 |
693 |
N/A |
INTRINSIC |
Pumilio
|
726 |
761 |
2.35e-7 |
SMART |
Pumilio
|
762 |
797 |
6.54e-6 |
SMART |
Pumilio
|
798 |
832 |
1.29e-4 |
SMART |
Pumilio
|
836 |
871 |
3.37e-8 |
SMART |
Pumilio
|
872 |
907 |
4.84e-9 |
SMART |
Pumilio
|
908 |
943 |
3.2e-9 |
SMART |
Pumilio
|
944 |
979 |
5.78e-7 |
SMART |
Pumilio
|
987 |
1022 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000169089
AA Change: I737N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000132122 Gene: ENSMUSG00000020594 AA Change: I737N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
581 |
N/A |
INTRINSIC |
low complexity region
|
596 |
614 |
N/A |
INTRINSIC |
Pumilio
|
647 |
682 |
2.35e-7 |
SMART |
Pumilio
|
683 |
718 |
6.54e-6 |
SMART |
Pumilio
|
719 |
754 |
2.89e-7 |
SMART |
Pumilio
|
755 |
790 |
3.37e-8 |
SMART |
Pumilio
|
791 |
826 |
4.84e-9 |
SMART |
Pumilio
|
827 |
862 |
3.2e-9 |
SMART |
Pumilio
|
863 |
898 |
5.78e-7 |
SMART |
Pumilio
|
906 |
941 |
3.62e-8 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000178015
AA Change: I737N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000137020 Gene: ENSMUSG00000020594 AA Change: I737N
Domain | Start | End | E-Value | Type |
low complexity region
|
193 |
206 |
N/A |
INTRINSIC |
low complexity region
|
269 |
290 |
N/A |
INTRINSIC |
low complexity region
|
324 |
341 |
N/A |
INTRINSIC |
low complexity region
|
358 |
383 |
N/A |
INTRINSIC |
low complexity region
|
469 |
495 |
N/A |
INTRINSIC |
low complexity region
|
503 |
514 |
N/A |
INTRINSIC |
low complexity region
|
526 |
540 |
N/A |
INTRINSIC |
low complexity region
|
547 |
581 |
N/A |
INTRINSIC |
low complexity region
|
596 |
614 |
N/A |
INTRINSIC |
Pumilio
|
647 |
682 |
2.35e-7 |
SMART |
Pumilio
|
683 |
718 |
6.54e-6 |
SMART |
Pumilio
|
719 |
754 |
2.89e-7 |
SMART |
Pumilio
|
755 |
790 |
3.37e-8 |
SMART |
Pumilio
|
791 |
826 |
4.84e-9 |
SMART |
Pumilio
|
827 |
862 |
3.2e-9 |
SMART |
Pumilio
|
863 |
898 |
5.78e-7 |
SMART |
Pumilio
|
906 |
941 |
3.62e-8 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000171608
|
Coding Region Coverage |
- 1x: 99.4%
- 3x: 98.9%
- 10x: 97.9%
- 20x: 96.7%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that belongs to a family of RNA-binding proteins. The encoded protein functions as a translational repressor during embryonic development and cell differentiation. This protein is also thought to be a positive regulator of cell proliferation in adipose-derived stem cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit significantly smaller testes and seminiferous tubule degeneration but are otherwise viable and fertile. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl3 |
T |
A |
7: 82,206,269 (GRCm39) |
C784S |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,745,989 (GRCm39) |
|
probably benign |
Het |
Apon |
A |
G |
10: 128,090,907 (GRCm39) |
E195G |
probably damaging |
Het |
Atxn10 |
A |
G |
15: 85,275,944 (GRCm39) |
I334V |
probably benign |
Het |
Camsap1 |
G |
T |
2: 25,855,823 (GRCm39) |
A145E |
probably damaging |
Het |
Capns1 |
G |
T |
7: 29,887,147 (GRCm39) |
F243L |
possibly damaging |
Het |
Catsper2 |
A |
T |
2: 121,237,216 (GRCm39) |
I228N |
probably damaging |
Het |
Ceacam14 |
A |
T |
7: 17,549,402 (GRCm39) |
*264C |
probably null |
Het |
Cel |
A |
C |
2: 28,450,530 (GRCm39) |
V165G |
probably damaging |
Het |
Cldnd1 |
T |
A |
16: 58,550,016 (GRCm39) |
D66E |
possibly damaging |
Het |
Cntnap5b |
T |
A |
1: 100,311,275 (GRCm39) |
C589* |
probably null |
Het |
Dnah3 |
T |
A |
7: 119,620,234 (GRCm39) |
H1554L |
probably damaging |
Het |
Fbxw25 |
T |
A |
9: 109,492,573 (GRCm39) |
M55L |
probably benign |
Het |
Fn1 |
T |
C |
1: 71,636,591 (GRCm39) |
H2187R |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,818,489 (GRCm39) |
T4741A |
possibly damaging |
Het |
Gabpa |
T |
A |
16: 84,653,934 (GRCm39) |
I272N |
possibly damaging |
Het |
Ganab |
T |
C |
19: 8,886,049 (GRCm39) |
S212P |
probably benign |
Het |
Ggt1 |
A |
G |
10: 75,421,495 (GRCm39) |
|
probably null |
Het |
Hpgds |
T |
C |
6: 65,109,169 (GRCm39) |
T81A |
probably benign |
Het |
Insr |
G |
A |
8: 3,252,902 (GRCm39) |
T419I |
probably benign |
Het |
Itgb7 |
A |
G |
15: 102,140,059 (GRCm39) |
|
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,799,289 (GRCm39) |
I951V |
possibly damaging |
Het |
Lrrc4c |
T |
A |
2: 97,460,498 (GRCm39) |
C375S |
probably damaging |
Het |
Muc17 |
G |
T |
5: 137,175,537 (GRCm39) |
C44* |
probably null |
Het |
Mycbpap |
A |
T |
11: 94,394,330 (GRCm39) |
D313E |
probably benign |
Het |
Neo1 |
A |
G |
9: 58,813,931 (GRCm39) |
|
probably null |
Het |
Ntsr2 |
C |
T |
12: 16,709,934 (GRCm39) |
S405F |
probably benign |
Het |
Nup153 |
G |
A |
13: 46,870,682 (GRCm39) |
P21S |
probably benign |
Het |
Obscn |
T |
A |
11: 58,887,703 (GRCm39) |
E7705D |
probably benign |
Het |
Ogn |
A |
G |
13: 49,762,817 (GRCm39) |
D53G |
probably benign |
Het |
Or10d5j |
A |
T |
9: 39,868,125 (GRCm39) |
Y35* |
probably null |
Het |
Or14j10 |
A |
T |
17: 37,935,046 (GRCm39) |
I160K |
probably benign |
Het |
Or5k8 |
G |
A |
16: 58,645,066 (GRCm39) |
T2I |
probably benign |
Het |
Or5p5 |
T |
C |
7: 107,413,883 (GRCm39) |
F33L |
possibly damaging |
Het |
Or9i1b |
A |
T |
19: 13,896,980 (GRCm39) |
I199F |
possibly damaging |
Het |
Pde6a |
G |
A |
18: 61,365,983 (GRCm39) |
R236H |
possibly damaging |
Het |
Pigk |
T |
A |
3: 152,443,837 (GRCm39) |
M85K |
probably damaging |
Het |
Pirb |
A |
C |
7: 3,719,598 (GRCm39) |
I516S |
possibly damaging |
Het |
Polr3a |
T |
C |
14: 24,505,009 (GRCm39) |
I1084V |
possibly damaging |
Het |
Recql5 |
A |
T |
11: 115,818,215 (GRCm39) |
C159S |
probably damaging |
Het |
Rxrg |
A |
G |
1: 167,452,573 (GRCm39) |
N125S |
probably benign |
Het |
Sgip1 |
C |
A |
4: 102,823,477 (GRCm39) |
N699K |
probably damaging |
Het |
Shprh |
G |
A |
10: 11,046,041 (GRCm39) |
|
probably null |
Het |
Smcp |
C |
T |
3: 92,491,454 (GRCm39) |
G131D |
unknown |
Het |
St8sia6 |
A |
G |
2: 13,798,188 (GRCm39) |
L23P |
possibly damaging |
Het |
Stk32c |
T |
A |
7: 138,699,276 (GRCm39) |
T335S |
probably benign |
Het |
Stox1 |
G |
A |
10: 62,499,812 (GRCm39) |
A916V |
possibly damaging |
Het |
Syk |
A |
T |
13: 52,785,753 (GRCm39) |
T297S |
probably benign |
Het |
Tert |
G |
T |
13: 73,796,490 (GRCm39) |
A1074S |
probably benign |
Het |
Tex9 |
A |
T |
9: 72,385,187 (GRCm39) |
D135E |
probably damaging |
Het |
Tmem132a |
G |
A |
19: 10,841,371 (GRCm39) |
H318Y |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,738,249 (GRCm39) |
S4097P |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,553,874 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
T |
11: 118,156,020 (GRCm39) |
S586T |
probably benign |
Het |
Vsig8 |
A |
G |
1: 172,388,244 (GRCm39) |
S71G |
probably benign |
Het |
Zfp318 |
G |
A |
17: 46,697,662 (GRCm39) |
D173N |
probably damaging |
Het |
Zfp638 |
T |
A |
6: 83,939,076 (GRCm39) |
S936T |
probably damaging |
Het |
Zic2 |
A |
G |
14: 122,713,728 (GRCm39) |
Y214C |
probably damaging |
Het |
|
Other mutations in Pum2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00737:Pum2
|
APN |
12 |
8,783,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Pum2
|
APN |
12 |
8,779,117 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02185:Pum2
|
APN |
12 |
8,798,955 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02528:Pum2
|
APN |
12 |
8,778,696 (GRCm39) |
nonsense |
probably null |
|
IGL02718:Pum2
|
APN |
12 |
8,783,344 (GRCm39) |
missense |
probably benign |
0.02 |
Plumbat
|
UTSW |
12 |
8,778,779 (GRCm39) |
critical splice donor site |
probably null |
|
Pummie
|
UTSW |
12 |
8,763,906 (GRCm39) |
nonsense |
probably null |
|
Yorkshire
|
UTSW |
12 |
8,778,726 (GRCm39) |
nonsense |
probably null |
|
PIT4366001:Pum2
|
UTSW |
12 |
8,783,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R0152:Pum2
|
UTSW |
12 |
8,778,754 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0317:Pum2
|
UTSW |
12 |
8,778,754 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0357:Pum2
|
UTSW |
12 |
8,771,785 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0413:Pum2
|
UTSW |
12 |
8,763,464 (GRCm39) |
missense |
probably benign |
0.00 |
R0494:Pum2
|
UTSW |
12 |
8,771,736 (GRCm39) |
nonsense |
probably null |
|
R0520:Pum2
|
UTSW |
12 |
8,771,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0727:Pum2
|
UTSW |
12 |
8,794,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R1576:Pum2
|
UTSW |
12 |
8,763,524 (GRCm39) |
missense |
probably benign |
0.01 |
R2035:Pum2
|
UTSW |
12 |
8,778,638 (GRCm39) |
nonsense |
probably null |
|
R2060:Pum2
|
UTSW |
12 |
8,778,726 (GRCm39) |
nonsense |
probably null |
|
R2422:Pum2
|
UTSW |
12 |
8,798,931 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2437:Pum2
|
UTSW |
12 |
8,794,654 (GRCm39) |
missense |
probably benign |
0.19 |
R3767:Pum2
|
UTSW |
12 |
8,769,076 (GRCm39) |
nonsense |
probably null |
|
R4715:Pum2
|
UTSW |
12 |
8,797,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5155:Pum2
|
UTSW |
12 |
8,763,572 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5226:Pum2
|
UTSW |
12 |
8,763,458 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6250:Pum2
|
UTSW |
12 |
8,794,755 (GRCm39) |
splice site |
probably null |
|
R6253:Pum2
|
UTSW |
12 |
8,798,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R6508:Pum2
|
UTSW |
12 |
8,798,861 (GRCm39) |
missense |
probably benign |
0.17 |
R6953:Pum2
|
UTSW |
12 |
8,778,779 (GRCm39) |
critical splice donor site |
probably null |
|
R7135:Pum2
|
UTSW |
12 |
8,778,952 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7355:Pum2
|
UTSW |
12 |
8,763,906 (GRCm39) |
nonsense |
probably null |
|
R7586:Pum2
|
UTSW |
12 |
8,797,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R7683:Pum2
|
UTSW |
12 |
8,778,922 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7869:Pum2
|
UTSW |
12 |
8,763,595 (GRCm39) |
missense |
probably benign |
0.00 |
R7873:Pum2
|
UTSW |
12 |
8,798,802 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7980:Pum2
|
UTSW |
12 |
8,763,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R8166:Pum2
|
UTSW |
12 |
8,771,739 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8316:Pum2
|
UTSW |
12 |
8,763,456 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8345:Pum2
|
UTSW |
12 |
8,759,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8418:Pum2
|
UTSW |
12 |
8,760,245 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8802:Pum2
|
UTSW |
12 |
8,778,726 (GRCm39) |
nonsense |
probably null |
|
R9039:Pum2
|
UTSW |
12 |
8,794,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9207:Pum2
|
UTSW |
12 |
8,763,904 (GRCm39) |
missense |
probably damaging |
0.98 |
R9366:Pum2
|
UTSW |
12 |
8,783,344 (GRCm39) |
missense |
probably benign |
0.02 |
R9700:Pum2
|
UTSW |
12 |
8,779,044 (GRCm39) |
missense |
probably damaging |
0.97 |
X0039:Pum2
|
UTSW |
12 |
8,778,944 (GRCm39) |
small deletion |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- CTAAAGTTGGGCAACAGTCAG -3'
(R):5'- CTCCATGGAGAGGCAGTGAATG -3'
Sequencing Primer
(F):5'- TTGGGCAACAGTCAGGAACC -3'
(R):5'- CAGTGAATGGATCAAAGTTCTGC -3'
|
Posted On |
2016-07-22 |