Incidental Mutation 'IGL02408:Phldb1'
ID |
292163 |
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 # |
IGL02408
|
Quality Score |
|
Status
|
|
Chromosome |
9 |
Chromosomal Location |
44597601-44646495 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 44627203 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Glycine
at position 414
(E414G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000120208
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034611]
[ENSMUST00000123406]
[ENSMUST00000134465]
[ENSMUST00000138356]
[ENSMUST00000144251]
[ENSMUST00000147495]
[ENSMUST00000156918]
[ENSMUST00000154723]
[ENSMUST00000148929]
|
AlphaFold |
Q6PDH0 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034611
AA Change: E414G
PolyPhen 2
Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
|
SMART Domains |
Protein: ENSMUSP00000034611 Gene: ENSMUSG00000048537 AA Change: E414G
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 |
noncoding transcript
Transcript: ENSMUST00000126818
|
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: E414G
PolyPhen 2
Score 0.113 (Sensitivity: 0.93; Specificity: 0.86)
|
SMART Domains |
Protein: ENSMUSP00000117395 Gene: ENSMUSG00000048537 AA Change: E414G
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 |
possibly damaging
Transcript: ENSMUST00000138356
AA Change: E414G
PolyPhen 2
Score 0.495 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000120208 Gene: ENSMUSG00000048537 AA Change: E414G
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: E414G
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000122661 Gene: ENSMUSG00000048537 AA Change: E414G
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 |
unknown
Transcript: ENSMUST00000148344
AA Change: E158G
|
SMART Domains |
Protein: ENSMUSP00000121809 Gene: ENSMUSG00000048537 AA Change: E158G
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: 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 |
|
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 |
|
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 |
noncoding transcript
Transcript: ENSMUST00000214717
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,621,130 (GRCm39) |
Y278C |
probably damaging |
Het |
Abcd2 |
A |
G |
15: 91,062,444 (GRCm39) |
L498P |
possibly damaging |
Het |
Acot11 |
A |
G |
4: 106,615,578 (GRCm39) |
F271S |
probably damaging |
Het |
Acr |
T |
A |
15: 89,454,217 (GRCm39) |
Y185N |
probably damaging |
Het |
Adcy10 |
C |
T |
1: 165,365,949 (GRCm39) |
R489C |
probably damaging |
Het |
Arsb |
A |
G |
13: 93,930,670 (GRCm39) |
T213A |
probably benign |
Het |
Atg2a |
T |
A |
19: 6,291,858 (GRCm39) |
C11* |
probably null |
Het |
B3galt6 |
A |
T |
4: 156,076,152 (GRCm39) |
Y308N |
probably damaging |
Het |
Cd226 |
A |
G |
18: 89,225,451 (GRCm39) |
N116S |
probably benign |
Het |
Crat |
T |
A |
2: 30,297,146 (GRCm39) |
D269V |
probably damaging |
Het |
Crim1 |
T |
A |
17: 78,623,083 (GRCm39) |
I427N |
possibly damaging |
Het |
Dock3 |
T |
C |
9: 106,790,298 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,407,776 (GRCm39) |
V374E |
probably damaging |
Het |
Dtl |
A |
G |
1: 191,273,352 (GRCm39) |
S519P |
probably benign |
Het |
Fastkd1 |
C |
T |
2: 69,532,945 (GRCm39) |
R474H |
probably benign |
Het |
Fbxo10 |
T |
C |
4: 45,058,361 (GRCm39) |
T459A |
possibly damaging |
Het |
Frmd4b |
A |
G |
6: 97,272,770 (GRCm39) |
L828P |
probably damaging |
Het |
Gc |
T |
C |
5: 89,593,255 (GRCm39) |
S55G |
probably benign |
Het |
Gm6455 |
T |
G |
5: 10,917,257 (GRCm39) |
|
noncoding transcript |
Het |
Gnai2 |
T |
C |
9: 107,493,393 (GRCm39) |
T280A |
probably benign |
Het |
Hmgn2 |
A |
G |
4: 133,693,260 (GRCm39) |
|
probably null |
Het |
Jmjd1c |
G |
T |
10: 67,062,161 (GRCm39) |
A1505S |
probably benign |
Het |
Lrriq1 |
T |
C |
10: 102,982,142 (GRCm39) |
K1393E |
probably benign |
Het |
Mcam |
A |
G |
9: 44,051,547 (GRCm39) |
N469D |
probably benign |
Het |
Mrpl47 |
A |
G |
3: 32,790,789 (GRCm39) |
|
probably null |
Het |
Mslnl |
C |
T |
17: 25,966,972 (GRCm39) |
A659V |
possibly damaging |
Het |
Nlrp1a |
A |
G |
11: 71,013,456 (GRCm39) |
V598A |
probably benign |
Het |
Npff |
A |
T |
15: 102,433,000 (GRCm39) |
L15Q |
probably null |
Het |
Obsl1 |
G |
T |
1: 75,481,890 (GRCm39) |
Q327K |
probably damaging |
Het |
Or13a18 |
T |
C |
7: 140,190,844 (GRCm39) |
V255A |
probably damaging |
Het |
Or4c58 |
T |
A |
2: 89,675,315 (GRCm39) |
M1L |
probably benign |
Het |
Or52s1b |
T |
C |
7: 102,822,658 (GRCm39) |
Y62C |
probably damaging |
Het |
Or7e165 |
A |
T |
9: 19,694,711 (GRCm39) |
Y94F |
probably benign |
Het |
Or8b50 |
G |
A |
9: 38,518,417 (GRCm39) |
G219S |
possibly damaging |
Het |
Pdzd2 |
T |
A |
15: 12,375,851 (GRCm39) |
H1428L |
probably benign |
Het |
Reln |
T |
C |
5: 22,106,617 (GRCm39) |
D3251G |
probably benign |
Het |
Secisbp2l |
G |
T |
2: 125,582,789 (GRCm39) |
S889* |
probably null |
Het |
Setx |
T |
A |
2: 29,023,942 (GRCm39) |
C133S |
probably damaging |
Het |
Slc22a29 |
A |
C |
19: 8,184,649 (GRCm39) |
S214A |
probably benign |
Het |
Slc30a5 |
A |
C |
13: 100,950,232 (GRCm39) |
L285R |
probably damaging |
Het |
Taar7a |
T |
G |
10: 23,868,500 (GRCm39) |
I294L |
probably benign |
Het |
Tfap2b |
T |
A |
1: 19,304,485 (GRCm39) |
F414I |
probably damaging |
Het |
Trpc4ap |
A |
T |
2: 155,512,989 (GRCm39) |
Y129N |
possibly damaging |
Het |
Vmn2r94 |
T |
C |
17: 18,473,523 (GRCm39) |
E501G |
probably benign |
Het |
Xpot |
T |
C |
10: 121,439,070 (GRCm39) |
H709R |
probably damaging |
Het |
Zfhx3 |
T |
A |
8: 109,682,004 (GRCm39) |
|
probably benign |
Het |
Zscan22 |
T |
G |
7: 12,640,426 (GRCm39) |
H223Q |
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 |
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 |