Incidental Mutation 'PIT4515001:Phldb1'
ID |
556326 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Phldb1
|
Ensembl Gene |
ENSMUSG00000048537 |
Gene Name |
pleckstrin homology like domain, family B, member 1 |
Synonyms |
D330037A14Rik, LL5A |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.104)
|
Stock # |
PIT4515001 (G1)
|
Quality Score |
189.009 |
Status
|
Not validated
|
Chromosome |
9 |
Chromosomal Location |
44597601-44646495 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to G
at 44627257 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 396
(I396T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000034611
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034611]
[ENSMUST00000123406]
[ENSMUST00000134465]
[ENSMUST00000138356]
[ENSMUST00000144251]
[ENSMUST00000147495]
[ENSMUST00000148929]
[ENSMUST00000156918]
|
AlphaFold |
Q6PDH0 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034611
AA Change: I396T
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000034611 Gene: ENSMUSG00000048537 AA Change: I396T
Domain | Start | End | E-Value | Type |
PDB:2EH0|A
|
40 |
139 |
3e-10 |
PDB |
Blast:FHA
|
63 |
110 |
6e-21 |
BLAST |
low complexity region
|
181 |
192 |
N/A |
INTRINSIC |
low complexity region
|
252 |
273 |
N/A |
INTRINSIC |
low complexity region
|
296 |
316 |
N/A |
INTRINSIC |
internal_repeat_1
|
321 |
354 |
5.01e-5 |
PROSPERO |
internal_repeat_1
|
401 |
449 |
5.01e-5 |
PROSPERO |
low complexity region
|
459 |
477 |
N/A |
INTRINSIC |
low complexity region
|
590 |
617 |
N/A |
INTRINSIC |
low complexity region
|
694 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
715 |
798 |
N/A |
INTRINSIC |
low complexity region
|
819 |
829 |
N/A |
INTRINSIC |
coiled coil region
|
865 |
904 |
N/A |
INTRINSIC |
low complexity region
|
943 |
961 |
N/A |
INTRINSIC |
low complexity region
|
976 |
997 |
N/A |
INTRINSIC |
low complexity region
|
1055 |
1069 |
N/A |
INTRINSIC |
low complexity region
|
1103 |
1111 |
N/A |
INTRINSIC |
coiled coil region
|
1150 |
1219 |
N/A |
INTRINSIC |
PH
|
1262 |
1366 |
1.31e-17 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123406
|
SMART Domains |
Protein: ENSMUSP00000114257 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
low complexity region
|
61 |
72 |
N/A |
INTRINSIC |
low complexity region
|
132 |
153 |
N/A |
INTRINSIC |
low complexity region
|
176 |
196 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000128326
|
SMART Domains |
Protein: ENSMUSP00000119966 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
12 |
N/A |
INTRINSIC |
low complexity region
|
83 |
110 |
N/A |
INTRINSIC |
low complexity region
|
187 |
200 |
N/A |
INTRINSIC |
coiled coil region
|
207 |
290 |
N/A |
INTRINSIC |
low complexity region
|
312 |
322 |
N/A |
INTRINSIC |
coiled coil region
|
357 |
396 |
N/A |
INTRINSIC |
low complexity region
|
422 |
443 |
N/A |
INTRINSIC |
low complexity region
|
493 |
506 |
N/A |
INTRINSIC |
low complexity region
|
516 |
530 |
N/A |
INTRINSIC |
low complexity region
|
564 |
572 |
N/A |
INTRINSIC |
coiled coil region
|
610 |
679 |
N/A |
INTRINSIC |
PH
|
723 |
827 |
1.31e-17 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134465
AA Change: I396T
PolyPhen 2
Score 0.326 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000117395 Gene: ENSMUSG00000048537 AA Change: I396T
Domain | Start | End | E-Value | Type |
PDB:2EH0|A
|
40 |
139 |
3e-10 |
PDB |
Blast:FHA
|
63 |
110 |
8e-21 |
BLAST |
low complexity region
|
181 |
192 |
N/A |
INTRINSIC |
low complexity region
|
252 |
273 |
N/A |
INTRINSIC |
low complexity region
|
296 |
316 |
N/A |
INTRINSIC |
internal_repeat_1
|
321 |
354 |
6.75e-5 |
PROSPERO |
internal_repeat_1
|
401 |
449 |
6.75e-5 |
PROSPERO |
low complexity region
|
459 |
477 |
N/A |
INTRINSIC |
low complexity region
|
590 |
617 |
N/A |
INTRINSIC |
low complexity region
|
694 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
715 |
798 |
N/A |
INTRINSIC |
low complexity region
|
819 |
829 |
N/A |
INTRINSIC |
coiled coil region
|
865 |
904 |
N/A |
INTRINSIC |
low complexity region
|
929 |
950 |
N/A |
INTRINSIC |
low complexity region
|
1008 |
1022 |
N/A |
INTRINSIC |
low complexity region
|
1056 |
1064 |
N/A |
INTRINSIC |
coiled coil region
|
1103 |
1172 |
N/A |
INTRINSIC |
PH
|
1215 |
1319 |
1.31e-17 |
SMART |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000138356
AA Change: I396T
PolyPhen 2
Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000120208 Gene: ENSMUSG00000048537 AA Change: I396T
Domain | Start | End | E-Value | Type |
PDB:2EH0|A
|
40 |
139 |
4e-10 |
PDB |
Blast:FHA
|
63 |
110 |
6e-21 |
BLAST |
low complexity region
|
181 |
192 |
N/A |
INTRINSIC |
low complexity region
|
252 |
273 |
N/A |
INTRINSIC |
low complexity region
|
296 |
316 |
N/A |
INTRINSIC |
internal_repeat_1
|
321 |
354 |
4.93e-5 |
PROSPERO |
internal_repeat_1
|
401 |
449 |
4.93e-5 |
PROSPERO |
low complexity region
|
459 |
477 |
N/A |
INTRINSIC |
low complexity region
|
590 |
617 |
N/A |
INTRINSIC |
low complexity region
|
694 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
715 |
798 |
N/A |
INTRINSIC |
low complexity region
|
819 |
829 |
N/A |
INTRINSIC |
coiled coil region
|
865 |
904 |
N/A |
INTRINSIC |
low complexity region
|
931 |
948 |
N/A |
INTRINSIC |
low complexity region
|
999 |
1017 |
N/A |
INTRINSIC |
low complexity region
|
1032 |
1053 |
N/A |
INTRINSIC |
low complexity region
|
1111 |
1125 |
N/A |
INTRINSIC |
low complexity region
|
1159 |
1167 |
N/A |
INTRINSIC |
coiled coil region
|
1206 |
1286 |
N/A |
INTRINSIC |
PH
|
1329 |
1444 |
6.01e-17 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000144251
|
SMART Domains |
Protein: ENSMUSP00000114773 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
24 |
N/A |
INTRINSIC |
coiled coil region
|
32 |
115 |
N/A |
INTRINSIC |
coiled coil region
|
146 |
174 |
N/A |
INTRINSIC |
low complexity region
|
179 |
189 |
N/A |
INTRINSIC |
coiled coil region
|
225 |
264 |
N/A |
INTRINSIC |
low complexity region
|
289 |
310 |
N/A |
INTRINSIC |
low complexity region
|
368 |
382 |
N/A |
INTRINSIC |
low complexity region
|
416 |
424 |
N/A |
INTRINSIC |
coiled coil region
|
463 |
532 |
N/A |
INTRINSIC |
PH
|
575 |
679 |
1.31e-17 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000147495
AA Change: I396T
PolyPhen 2
Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
|
SMART Domains |
Protein: ENSMUSP00000122661 Gene: ENSMUSG00000048537 AA Change: I396T
Domain | Start | End | E-Value | Type |
PDB:2EH0|A
|
40 |
139 |
4e-10 |
PDB |
Blast:FHA
|
63 |
110 |
6e-21 |
BLAST |
low complexity region
|
181 |
192 |
N/A |
INTRINSIC |
low complexity region
|
252 |
273 |
N/A |
INTRINSIC |
low complexity region
|
296 |
316 |
N/A |
INTRINSIC |
internal_repeat_1
|
321 |
354 |
5e-5 |
PROSPERO |
internal_repeat_1
|
401 |
449 |
5e-5 |
PROSPERO |
low complexity region
|
459 |
477 |
N/A |
INTRINSIC |
low complexity region
|
590 |
617 |
N/A |
INTRINSIC |
low complexity region
|
694 |
707 |
N/A |
INTRINSIC |
coiled coil region
|
715 |
798 |
N/A |
INTRINSIC |
low complexity region
|
819 |
829 |
N/A |
INTRINSIC |
coiled coil region
|
865 |
904 |
N/A |
INTRINSIC |
low complexity region
|
943 |
961 |
N/A |
INTRINSIC |
low complexity region
|
976 |
997 |
N/A |
INTRINSIC |
low complexity region
|
1055 |
1069 |
N/A |
INTRINSIC |
low complexity region
|
1103 |
1111 |
N/A |
INTRINSIC |
coiled coil region
|
1150 |
1219 |
N/A |
INTRINSIC |
PH
|
1262 |
1377 |
6.01e-17 |
SMART |
|
Predicted Effect |
|
SMART Domains |
Protein: ENSMUSP00000121809 Gene: ENSMUSG00000048537 AA Change: I140T
Domain | Start | End | E-Value | Type |
low complexity region
|
4 |
19 |
N/A |
INTRINSIC |
low complexity region
|
41 |
61 |
N/A |
INTRINSIC |
internal_repeat_1
|
66 |
99 |
6.7e-6 |
PROSPERO |
internal_repeat_1
|
146 |
194 |
6.7e-6 |
PROSPERO |
low complexity region
|
204 |
222 |
N/A |
INTRINSIC |
low complexity region
|
335 |
362 |
N/A |
INTRINSIC |
low complexity region
|
439 |
452 |
N/A |
INTRINSIC |
coiled coil region
|
459 |
542 |
N/A |
INTRINSIC |
low complexity region
|
564 |
574 |
N/A |
INTRINSIC |
coiled coil region
|
609 |
648 |
N/A |
INTRINSIC |
low complexity region
|
688 |
706 |
N/A |
INTRINSIC |
low complexity region
|
721 |
742 |
N/A |
INTRINSIC |
low complexity region
|
792 |
805 |
N/A |
INTRINSIC |
low complexity region
|
815 |
829 |
N/A |
INTRINSIC |
low complexity region
|
863 |
871 |
N/A |
INTRINSIC |
coiled coil region
|
909 |
978 |
N/A |
INTRINSIC |
PH
|
1022 |
1126 |
1.31e-17 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000148929
|
SMART Domains |
Protein: ENSMUSP00000114533 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
low complexity region
|
61 |
72 |
N/A |
INTRINSIC |
low complexity region
|
132 |
153 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000156918
|
SMART Domains |
Protein: ENSMUSP00000120092 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
24 |
N/A |
INTRINSIC |
coiled coil region
|
32 |
115 |
N/A |
INTRINSIC |
low complexity region
|
136 |
146 |
N/A |
INTRINSIC |
coiled coil region
|
182 |
221 |
N/A |
INTRINSIC |
low complexity region
|
246 |
267 |
N/A |
INTRINSIC |
low complexity region
|
325 |
339 |
N/A |
INTRINSIC |
low complexity region
|
373 |
381 |
N/A |
INTRINSIC |
coiled coil region
|
420 |
489 |
N/A |
INTRINSIC |
PH
|
532 |
636 |
1.31e-17 |
SMART |
|
Coding Region Coverage |
- 1x: 93.4%
- 3x: 91.0%
- 10x: 86.0%
- 20x: 75.1%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
A |
14: 32,383,068 (GRCm39) |
R966* |
probably null |
Het |
Adam32 |
A |
T |
8: 25,404,342 (GRCm39) |
I221K |
possibly damaging |
Het |
Adcy6 |
T |
C |
15: 98,493,027 (GRCm39) |
T880A |
probably benign |
Het |
Agpat5 |
T |
A |
8: 18,896,657 (GRCm39) |
Y28N |
probably damaging |
Het |
Atg2a |
A |
G |
19: 6,303,615 (GRCm39) |
I1125V |
probably damaging |
Het |
B4galt6 |
A |
G |
18: 20,821,524 (GRCm39) |
Y335H |
probably benign |
Het |
Bend3 |
A |
T |
10: 43,386,630 (GRCm39) |
E341V |
probably damaging |
Het |
Bltp1 |
T |
A |
3: 37,028,385 (GRCm39) |
Y2351N |
probably damaging |
Het |
Ccdc136 |
T |
A |
6: 29,417,225 (GRCm39) |
V682E |
probably benign |
Het |
Ccdc142 |
T |
C |
6: 83,080,238 (GRCm39) |
C394R |
probably benign |
Het |
Cfap58 |
A |
G |
19: 48,023,122 (GRCm39) |
N845D |
probably benign |
Het |
Col4a3 |
G |
A |
1: 82,660,024 (GRCm39) |
G890R |
unknown |
Het |
Cyp1a2 |
C |
A |
9: 57,589,242 (GRCm39) |
V191L |
probably benign |
Het |
Cyp51 |
A |
T |
5: 4,149,122 (GRCm39) |
|
probably null |
Het |
Diras2 |
T |
C |
13: 52,661,783 (GRCm39) |
S175G |
possibly damaging |
Het |
Dnah6 |
A |
G |
6: 73,091,565 (GRCm39) |
F2242S |
probably damaging |
Het |
Erg |
T |
A |
16: 95,210,619 (GRCm39) |
N78Y |
probably benign |
Het |
Fdft1 |
T |
A |
14: 63,402,032 (GRCm39) |
Q49L |
probably benign |
Het |
Frem1 |
G |
T |
4: 82,818,663 (GRCm39) |
H2183Q |
probably damaging |
Het |
Fut2 |
G |
A |
7: 45,299,890 (GRCm39) |
T294I |
probably damaging |
Het |
Gabrb1 |
A |
C |
5: 71,858,160 (GRCm39) |
D62A |
probably damaging |
Het |
Gbe1 |
T |
A |
16: 70,238,004 (GRCm39) |
Y263* |
probably null |
Het |
Gimap6 |
T |
C |
6: 48,679,502 (GRCm39) |
D178G |
probably benign |
Het |
Gss |
T |
A |
2: 155,420,261 (GRCm39) |
T147S |
probably damaging |
Het |
Hlcs |
A |
T |
16: 94,068,275 (GRCm39) |
V315E |
probably benign |
Het |
Hoxa3 |
C |
T |
6: 52,147,164 (GRCm39) |
G363E |
unknown |
Het |
Ift140 |
A |
G |
17: 25,305,834 (GRCm39) |
N807S |
probably damaging |
Het |
Iglc1 |
T |
G |
16: 18,880,701 (GRCm39) |
D40A |
|
Het |
Itga10 |
T |
A |
3: 96,569,948 (GRCm39) |
I1120N |
probably damaging |
Het |
Jak3 |
T |
C |
8: 72,132,286 (GRCm39) |
V217A |
probably benign |
Het |
Kank2 |
T |
G |
9: 21,706,179 (GRCm39) |
I280L |
probably benign |
Het |
Kcnk1 |
G |
T |
8: 126,752,081 (GRCm39) |
G229V |
probably damaging |
Het |
Kpna7 |
T |
C |
5: 144,941,862 (GRCm39) |
T143A |
probably benign |
Het |
Letmd1 |
C |
T |
15: 100,374,683 (GRCm39) |
R310C |
probably damaging |
Het |
Mga |
G |
A |
2: 119,746,985 (GRCm39) |
V379I |
probably damaging |
Het |
Mto1 |
T |
A |
9: 78,364,699 (GRCm39) |
Y313N |
probably damaging |
Het |
Muc5ac |
G |
A |
7: 141,361,153 (GRCm39) |
C1488Y |
probably damaging |
Het |
Nde1 |
T |
A |
16: 13,988,357 (GRCm39) |
|
probably null |
Het |
Nfatc3 |
T |
C |
8: 106,805,835 (GRCm39) |
S235P |
possibly damaging |
Het |
Nup88 |
T |
C |
11: 70,835,547 (GRCm39) |
D602G |
probably benign |
Het |
Or11g25 |
T |
A |
14: 50,723,536 (GRCm39) |
M207K |
probably benign |
Het |
Or2h1b |
A |
C |
17: 37,462,270 (GRCm39) |
S198A |
probably benign |
Het |
Pcnx1 |
G |
A |
12: 82,038,561 (GRCm39) |
C1309Y |
|
Het |
Pramel38 |
T |
C |
5: 94,368,831 (GRCm39) |
M442T |
probably benign |
Het |
Pramel41 |
A |
C |
5: 94,594,694 (GRCm39) |
K185Q |
probably benign |
Het |
Prss53 |
G |
A |
7: 127,487,963 (GRCm39) |
T173I |
probably benign |
Het |
Ptpn11 |
C |
A |
5: 121,302,617 (GRCm39) |
D156Y |
probably damaging |
Het |
Rfx8 |
A |
G |
1: 39,729,265 (GRCm39) |
Y167H |
probably benign |
Het |
Rpsa |
T |
A |
9: 119,960,214 (GRCm39) |
I259N |
probably benign |
Het |
Rrm2b |
G |
T |
15: 37,947,048 (GRCm39) |
D84E |
probably benign |
Het |
Scgb2b19 |
A |
T |
7: 32,979,036 (GRCm39) |
|
probably null |
Het |
Sik3 |
T |
C |
9: 46,120,029 (GRCm39) |
L706P |
probably damaging |
Het |
Slc4a4 |
A |
T |
5: 89,281,112 (GRCm39) |
E426D |
probably damaging |
Het |
Slc8a2 |
C |
A |
7: 15,874,504 (GRCm39) |
L251I |
possibly damaging |
Het |
Taf6 |
T |
C |
5: 138,180,504 (GRCm39) |
K287E |
probably benign |
Het |
Tiam1 |
G |
A |
16: 89,657,130 (GRCm39) |
T702I |
probably damaging |
Het |
Tle1 |
A |
T |
4: 72,117,556 (GRCm39) |
F35I |
possibly damaging |
Het |
Tle2 |
A |
G |
10: 81,422,964 (GRCm39) |
Q454R |
possibly damaging |
Het |
Tsc2 |
T |
C |
17: 24,840,121 (GRCm39) |
N425S |
probably benign |
Het |
Utp3 |
A |
G |
5: 88,702,564 (GRCm39) |
D31G |
probably benign |
Het |
Vmn1r173 |
A |
T |
7: 23,401,911 (GRCm39) |
R49* |
probably null |
Het |
Ybx2 |
T |
A |
11: 69,831,224 (GRCm39) |
V273E |
probably benign |
Het |
Zbtb22 |
G |
A |
17: 34,137,672 (GRCm39) |
A606T |
probably benign |
Het |
Zcchc8 |
A |
T |
5: 123,838,995 (GRCm39) |
D514E |
probably benign |
Het |
Zfy2 |
T |
A |
Y: 2,117,096 (GRCm39) |
I244F |
probably benign |
Het |
Zglp1 |
T |
C |
9: 20,977,485 (GRCm39) |
N110S |
probably benign |
Het |
|
Other mutations in Phldb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00549:Phldb1
|
APN |
9 |
44,622,443 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01089:Phldb1
|
APN |
9 |
44,619,184 (GRCm39) |
nonsense |
probably null |
|
IGL01374:Phldb1
|
APN |
9 |
44,607,464 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01654:Phldb1
|
APN |
9 |
44,629,654 (GRCm39) |
splice site |
probably null |
|
IGL02148:Phldb1
|
APN |
9 |
44,607,369 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02408:Phldb1
|
APN |
9 |
44,627,203 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02429:Phldb1
|
APN |
9 |
44,612,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02440:Phldb1
|
APN |
9 |
44,626,700 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02457:Phldb1
|
APN |
9 |
44,627,771 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02471:Phldb1
|
APN |
9 |
44,622,530 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Phldb1
|
APN |
9 |
44,622,223 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03335:Phldb1
|
APN |
9 |
44,639,366 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0070:Phldb1
|
UTSW |
9 |
44,619,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R0117:Phldb1
|
UTSW |
9 |
44,623,003 (GRCm39) |
start codon destroyed |
probably null |
|
R0344:Phldb1
|
UTSW |
9 |
44,612,964 (GRCm39) |
missense |
probably benign |
0.14 |
R0364:Phldb1
|
UTSW |
9 |
44,610,632 (GRCm39) |
splice site |
probably benign |
|
R0622:Phldb1
|
UTSW |
9 |
44,627,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R0737:Phldb1
|
UTSW |
9 |
44,610,933 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1449:Phldb1
|
UTSW |
9 |
44,627,930 (GRCm39) |
missense |
probably benign |
0.17 |
R1498:Phldb1
|
UTSW |
9 |
44,612,915 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1633:Phldb1
|
UTSW |
9 |
44,629,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Phldb1
|
UTSW |
9 |
44,626,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R1692:Phldb1
|
UTSW |
9 |
44,626,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R1749:Phldb1
|
UTSW |
9 |
44,627,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1797:Phldb1
|
UTSW |
9 |
44,627,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R2012:Phldb1
|
UTSW |
9 |
44,639,333 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2078:Phldb1
|
UTSW |
9 |
44,619,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R2208:Phldb1
|
UTSW |
9 |
44,607,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Phldb1
|
UTSW |
9 |
44,637,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R2696:Phldb1
|
UTSW |
9 |
44,629,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R3705:Phldb1
|
UTSW |
9 |
44,605,691 (GRCm39) |
missense |
probably damaging |
0.97 |
R4110:Phldb1
|
UTSW |
9 |
44,627,128 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4772:Phldb1
|
UTSW |
9 |
44,622,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Phldb1
|
UTSW |
9 |
44,607,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R5148:Phldb1
|
UTSW |
9 |
44,615,455 (GRCm39) |
missense |
probably benign |
0.04 |
R5651:Phldb1
|
UTSW |
9 |
44,623,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Phldb1
|
UTSW |
9 |
44,627,078 (GRCm39) |
missense |
probably damaging |
0.97 |
R5670:Phldb1
|
UTSW |
9 |
44,627,078 (GRCm39) |
missense |
probably damaging |
0.97 |
R5914:Phldb1
|
UTSW |
9 |
44,622,948 (GRCm39) |
missense |
probably damaging |
0.97 |
R6232:Phldb1
|
UTSW |
9 |
44,607,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Phldb1
|
UTSW |
9 |
44,607,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R6413:Phldb1
|
UTSW |
9 |
44,607,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6418:Phldb1
|
UTSW |
9 |
44,623,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6813:Phldb1
|
UTSW |
9 |
44,610,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6845:Phldb1
|
UTSW |
9 |
44,627,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Phldb1
|
UTSW |
9 |
44,605,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R7042:Phldb1
|
UTSW |
9 |
44,605,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R7062:Phldb1
|
UTSW |
9 |
44,607,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R7077:Phldb1
|
UTSW |
9 |
44,623,201 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7307:Phldb1
|
UTSW |
9 |
44,605,344 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7995:Phldb1
|
UTSW |
9 |
44,626,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R8108:Phldb1
|
UTSW |
9 |
44,622,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R8433:Phldb1
|
UTSW |
9 |
44,627,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R9151:Phldb1
|
UTSW |
9 |
44,619,740 (GRCm39) |
missense |
probably null |
0.01 |
R9366:Phldb1
|
UTSW |
9 |
44,622,546 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9378:Phldb1
|
UTSW |
9 |
44,615,425 (GRCm39) |
missense |
probably benign |
0.01 |
R9448:Phldb1
|
UTSW |
9 |
44,622,546 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9539:Phldb1
|
UTSW |
9 |
44,627,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Phldb1
|
UTSW |
9 |
44,627,839 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Phldb1
|
UTSW |
9 |
44,609,243 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Phldb1
|
UTSW |
9 |
44,598,974 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CTTCGAGACAGAGATGGACTC -3'
(R):5'- ACCATTTGGCTCTGCAACC -3'
Sequencing Primer
(F):5'- AGTTCCCGCATACTGTCCAGG -3'
(R):5'- ACAGTCTCGCCCAAGTGGTTC -3'
|
Posted On |
2019-06-07 |