Incidental Mutation 'IGL02148:Phldb1'
ID |
281835 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
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 # |
IGL02148
|
Quality Score |
|
Status
|
|
Chromosome |
9 |
Chromosomal Location |
44597601-44646495 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 44607369 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Lysine to Glutamic Acid
at position 1279
(K1279E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000120208
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034611]
[ENSMUST00000123310]
[ENSMUST00000134465]
[ENSMUST00000135436]
[ENSMUST00000138356]
[ENSMUST00000144251]
[ENSMUST00000147495]
[ENSMUST00000156918]
[ENSMUST00000154723]
|
AlphaFold |
Q6PDH0 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000034611
AA Change: K1212E
PolyPhen 2
Score 0.834 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000034611 Gene: ENSMUSG00000048537 AA Change: K1212E
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: ENSMUST00000123310
|
SMART Domains |
Protein: ENSMUSP00000122374 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
coiled coil region
|
1 |
33 |
N/A |
INTRINSIC |
low complexity region
|
58 |
79 |
N/A |
INTRINSIC |
low complexity region
|
137 |
151 |
N/A |
INTRINSIC |
low complexity region
|
185 |
193 |
N/A |
INTRINSIC |
coiled coil region
|
232 |
259 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000128326
AA Change: K672E
PolyPhen 2
Score 0.768 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000119966 Gene: ENSMUSG00000048537 AA Change: K672E
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 |
noncoding transcript
Transcript: ENSMUST00000129806
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133312
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000134465
AA Change: K1165E
PolyPhen 2
Score 0.074 (Sensitivity: 0.93; Specificity: 0.85)
|
SMART Domains |
Protein: ENSMUSP00000117395 Gene: ENSMUSG00000048537 AA Change: K1165E
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 benign
Transcript: ENSMUST00000135436
AA Change: K336E
PolyPhen 2
Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000120023 Gene: ENSMUSG00000048537 AA Change: K336E
Domain | Start | End | E-Value | Type |
low complexity region
|
67 |
85 |
N/A |
INTRINSIC |
low complexity region
|
100 |
121 |
N/A |
INTRINSIC |
low complexity region
|
179 |
193 |
N/A |
INTRINSIC |
low complexity region
|
227 |
235 |
N/A |
INTRINSIC |
coiled coil region
|
274 |
343 |
N/A |
INTRINSIC |
PH
|
386 |
490 |
1.31e-17 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000148344
AA Change: K971E
PolyPhen 2
Score 0.815 (Sensitivity: 0.84; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000121809 Gene: ENSMUSG00000048537 AA Change: K971E
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 damaging
Transcript: ENSMUST00000138356
AA Change: K1279E
PolyPhen 2
Score 0.991 (Sensitivity: 0.71; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000120208 Gene: ENSMUSG00000048537 AA Change: K1279E
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
AA Change: K525E
PolyPhen 2
Score 0.068 (Sensitivity: 0.94; Specificity: 0.84)
|
SMART Domains |
Protein: ENSMUSP00000114773 Gene: ENSMUSG00000048537 AA Change: K525E
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: K1212E
PolyPhen 2
Score 0.299 (Sensitivity: 0.91; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000122661 Gene: ENSMUSG00000048537 AA Change: K1212E
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 |
probably benign
Transcript: ENSMUST00000156918
AA Change: K482E
PolyPhen 2
Score 0.031 (Sensitivity: 0.95; Specificity: 0.82)
|
SMART Domains |
Protein: ENSMUSP00000120092 Gene: ENSMUSG00000048537 AA Change: K482E
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 |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000154723
|
SMART Domains |
Protein: ENSMUSP00000116987 Gene: ENSMUSG00000048537
Domain | Start | End | E-Value | Type |
coiled coil region
|
39 |
67 |
N/A |
INTRINSIC |
low complexity region
|
72 |
82 |
N/A |
INTRINSIC |
coiled coil region
|
118 |
157 |
N/A |
INTRINSIC |
low complexity region
|
197 |
212 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akna |
C |
T |
4: 63,300,716 (GRCm39) |
|
probably benign |
Het |
AU040320 |
T |
C |
4: 126,733,469 (GRCm39) |
V663A |
possibly damaging |
Het |
Cdh13 |
A |
G |
8: 119,925,697 (GRCm39) |
D355G |
probably damaging |
Het |
Cdyl2 |
A |
G |
8: 117,315,983 (GRCm39) |
|
probably benign |
Het |
Csnk1g3 |
C |
T |
18: 54,086,360 (GRCm39) |
R422C |
probably benign |
Het |
Dclk1 |
T |
A |
3: 55,407,520 (GRCm39) |
V233D |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,361,565 (GRCm39) |
S477P |
probably damaging |
Het |
Epb41l1 |
A |
T |
2: 156,353,748 (GRCm39) |
|
probably benign |
Het |
Epha2 |
T |
C |
4: 141,045,835 (GRCm39) |
L453P |
probably damaging |
Het |
Esco2 |
T |
C |
14: 66,064,044 (GRCm39) |
H380R |
probably benign |
Het |
Fbxo38 |
T |
C |
18: 62,669,298 (GRCm39) |
M51V |
probably benign |
Het |
Fgb |
T |
C |
3: 82,950,594 (GRCm39) |
M387V |
probably damaging |
Het |
Fryl |
A |
G |
5: 73,233,302 (GRCm39) |
L1522S |
probably benign |
Het |
Gdf9 |
T |
A |
11: 53,327,569 (GRCm39) |
M175K |
probably benign |
Het |
Gm20547 |
C |
T |
17: 35,079,524 (GRCm39) |
D243N |
probably benign |
Het |
Gramd1b |
T |
A |
9: 40,227,060 (GRCm39) |
D299V |
probably damaging |
Het |
Gsg1l |
G |
T |
7: 125,522,671 (GRCm39) |
Q186K |
possibly damaging |
Het |
H2bl1 |
A |
T |
13: 99,120,691 (GRCm39) |
F112I |
probably damaging |
Het |
Katnip |
A |
T |
7: 125,472,648 (GRCm39) |
|
probably null |
Het |
Kcnh5 |
A |
G |
12: 74,944,426 (GRCm39) |
L941P |
possibly damaging |
Het |
Lrrc8d |
A |
G |
5: 105,960,253 (GRCm39) |
D221G |
possibly damaging |
Het |
Med19 |
T |
C |
2: 84,515,603 (GRCm39) |
F96L |
probably damaging |
Het |
Mei1 |
C |
A |
15: 81,976,912 (GRCm39) |
S589* |
probably null |
Het |
Myh15 |
G |
T |
16: 48,936,678 (GRCm39) |
D708Y |
probably damaging |
Het |
Naca |
C |
T |
10: 127,879,753 (GRCm39) |
|
probably benign |
Het |
Or5d43 |
A |
T |
2: 88,104,566 (GRCm39) |
Y276N |
possibly damaging |
Het |
Otog |
G |
A |
7: 45,950,011 (GRCm39) |
C306Y |
probably damaging |
Het |
Pkd1 |
C |
T |
17: 24,798,810 (GRCm39) |
T369I |
probably damaging |
Het |
Plekha8 |
A |
G |
6: 54,592,271 (GRCm39) |
S32G |
probably damaging |
Het |
Pramel25 |
T |
A |
4: 143,519,304 (GRCm39) |
Y22N |
probably benign |
Het |
Sema4g |
A |
G |
19: 44,984,908 (GRCm39) |
T113A |
probably damaging |
Het |
Setdb2 |
C |
T |
14: 59,639,764 (GRCm39) |
R709Q |
probably damaging |
Het |
Sh3rf3 |
T |
C |
10: 58,922,562 (GRCm39) |
M546T |
probably benign |
Het |
Slc27a5 |
A |
G |
7: 12,728,878 (GRCm39) |
V328A |
probably damaging |
Het |
Spef1 |
T |
C |
2: 131,014,688 (GRCm39) |
N78S |
probably benign |
Het |
Tln1 |
T |
C |
4: 43,555,388 (GRCm39) |
T179A |
probably damaging |
Het |
Tmc5 |
T |
C |
7: 118,244,547 (GRCm39) |
I475T |
probably damaging |
Het |
Top2b |
A |
G |
14: 16,400,488 (GRCm38) |
Y621C |
probably damaging |
Het |
Ttf1 |
T |
C |
2: 28,969,438 (GRCm39) |
F727L |
probably benign |
Het |
Tufm |
T |
C |
7: 126,088,332 (GRCm39) |
L75P |
probably damaging |
Het |
Ugt1a2 |
T |
A |
1: 88,128,796 (GRCm39) |
D146E |
probably damaging |
Het |
Usp15 |
G |
A |
10: 122,963,742 (GRCm39) |
T533I |
probably damaging |
Het |
Vmn1r113 |
A |
G |
7: 20,521,747 (GRCm39) |
T180A |
probably benign |
Het |
Vmn1r205 |
G |
T |
13: 22,776,395 (GRCm39) |
P236T |
probably damaging |
Het |
Vmn2r112 |
T |
G |
17: 22,838,013 (GRCm39) |
C825G |
probably damaging |
Het |
Zfp712 |
T |
A |
13: 67,190,222 (GRCm39) |
I102F |
probably damaging |
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 |
|
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 |
PIT4515001:Phldb1
|
UTSW |
9 |
44,627,257 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
Posted On |
2015-04-16 |