Incidental Mutation 'IGL02457:Phldb1'
ID |
294464 |
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 # |
IGL02457
|
Quality Score |
|
Status
|
|
Chromosome |
9 |
Chromosomal Location |
44597601-44646495 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 44627771 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Methionine to Valine
at position 225
(M225V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000117395
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000034611]
[ENSMUST00000123406]
[ENSMUST00000134465]
[ENSMUST00000138356]
[ENSMUST00000148929]
[ENSMUST00000147495]
[ENSMUST00000156918]
[ENSMUST00000144251]
|
AlphaFold |
Q6PDH0 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000034611
AA Change: M225V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000034611 Gene: ENSMUSG00000048537 AA Change: M225V
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
AA Change: M105V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000114257 Gene: ENSMUSG00000048537 AA Change: M105V
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: M225V
PolyPhen 2
Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)
|
SMART Domains |
Protein: ENSMUSP00000117395 Gene: ENSMUSG00000048537 AA Change: M225V
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: ENSMUST00000138356
AA Change: M225V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000120208 Gene: ENSMUSG00000048537 AA Change: M225V
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: ENSMUST00000148929
AA Change: M105V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000114533 Gene: ENSMUSG00000048537 AA Change: M105V
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: ENSMUST00000147495
AA Change: M225V
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000122661 Gene: ENSMUSG00000048537 AA Change: M225V
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: ENSMUST00000148344
|
SMART Domains |
Protein: ENSMUSP00000121809 Gene: ENSMUSG00000048537
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 |
noncoding transcript
Transcript: ENSMUST00000214717
|
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 |
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd16b |
A |
G |
2: 181,136,127 (GRCm39) |
D343G |
probably benign |
Het |
Acot10 |
T |
C |
15: 20,666,229 (GRCm39) |
S171G |
possibly damaging |
Het |
Actr3b |
T |
C |
5: 26,054,160 (GRCm39) |
|
probably null |
Het |
Adamts17 |
T |
C |
7: 66,677,562 (GRCm39) |
M492T |
probably damaging |
Het |
Akap4 |
A |
C |
X: 6,943,707 (GRCm39) |
N670T |
probably benign |
Het |
Atrip |
A |
G |
9: 108,894,299 (GRCm39) |
S55P |
possibly damaging |
Het |
Bend3 |
A |
T |
10: 43,385,946 (GRCm39) |
E113V |
probably damaging |
Het |
Ccdc158 |
A |
C |
5: 92,797,907 (GRCm39) |
I411S |
probably damaging |
Het |
Cfap97 |
G |
T |
8: 46,623,315 (GRCm39) |
C235F |
possibly damaging |
Het |
Chil4 |
T |
C |
3: 106,121,715 (GRCm39) |
N45D |
probably benign |
Het |
Cripto |
C |
T |
9: 110,771,691 (GRCm39) |
C32Y |
probably damaging |
Het |
D430041D05Rik |
A |
G |
2: 104,079,690 (GRCm39) |
V1131A |
probably damaging |
Het |
Defb38 |
T |
C |
8: 19,076,552 (GRCm39) |
|
probably benign |
Het |
Dnah10 |
T |
A |
5: 124,866,860 (GRCm39) |
W2260R |
probably damaging |
Het |
Ecsit |
A |
G |
9: 21,989,500 (GRCm39) |
S14P |
probably damaging |
Het |
Eif3l |
T |
C |
15: 78,962,296 (GRCm39) |
F106L |
probably benign |
Het |
Erich5 |
G |
T |
15: 34,470,999 (GRCm39) |
G76V |
probably damaging |
Het |
Evpl |
A |
G |
11: 116,120,939 (GRCm39) |
L432P |
possibly damaging |
Het |
Fbxw10 |
T |
C |
11: 62,765,808 (GRCm39) |
F698L |
probably damaging |
Het |
Frem2 |
A |
T |
3: 53,428,470 (GRCm39) |
S2866T |
probably damaging |
Het |
Fuca1 |
G |
A |
4: 135,662,073 (GRCm39) |
V334I |
probably benign |
Het |
Hprt1 |
T |
A |
X: 52,091,010 (GRCm39) |
H60Q |
probably benign |
Het |
Kirrel2 |
T |
C |
7: 30,152,165 (GRCm39) |
N481S |
probably damaging |
Het |
Krt16 |
A |
T |
11: 100,137,162 (GRCm39) |
|
probably benign |
Het |
Lilrb4b |
T |
A |
10: 51,357,334 (GRCm39) |
Y57N |
probably benign |
Het |
Lix1l |
A |
G |
3: 96,521,792 (GRCm39) |
Y126C |
probably damaging |
Het |
Lox |
T |
C |
18: 52,654,388 (GRCm39) |
D347G |
probably damaging |
Het |
Mak16 |
C |
T |
8: 31,654,753 (GRCm39) |
R147Q |
possibly damaging |
Het |
Ndst2 |
G |
A |
14: 20,779,622 (GRCm39) |
A206V |
possibly damaging |
Het |
Or1ak2 |
A |
T |
2: 36,827,760 (GRCm39) |
I210F |
probably damaging |
Het |
Or2q1 |
T |
A |
6: 42,795,176 (GRCm39) |
I257N |
probably damaging |
Het |
Pofut1 |
C |
T |
2: 153,090,516 (GRCm39) |
Q137* |
probably null |
Het |
Polr2a |
T |
C |
11: 69,634,076 (GRCm39) |
|
probably benign |
Het |
Prdm5 |
T |
A |
6: 65,858,100 (GRCm39) |
L388Q |
probably damaging |
Het |
Rad51c |
A |
G |
11: 87,271,681 (GRCm39) |
S344P |
possibly damaging |
Het |
Scart1 |
G |
A |
7: 139,800,308 (GRCm39) |
G30S |
probably benign |
Het |
Sdk1 |
C |
T |
5: 141,938,771 (GRCm39) |
P398L |
probably damaging |
Het |
Sec63 |
G |
A |
10: 42,677,729 (GRCm39) |
|
probably benign |
Het |
Sgo1 |
A |
T |
17: 53,983,989 (GRCm39) |
L463Q |
probably damaging |
Het |
Slc5a6 |
A |
G |
5: 31,198,002 (GRCm39) |
L291P |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,757,205 (GRCm39) |
T9A |
probably benign |
Het |
Sp3 |
A |
G |
2: 72,801,813 (GRCm39) |
W67R |
probably damaging |
Het |
Ssxb9 |
A |
C |
X: 21,041,234 (GRCm39) |
S23A |
probably benign |
Het |
Syne1 |
A |
G |
10: 5,292,167 (GRCm39) |
L1367S |
probably damaging |
Het |
Tbc1d23 |
T |
A |
16: 56,990,754 (GRCm39) |
I690F |
probably damaging |
Het |
Tmed5 |
A |
T |
5: 108,272,416 (GRCm39) |
S227R |
probably benign |
Het |
Tnrc6c |
T |
A |
11: 117,613,803 (GRCm39) |
S814T |
probably benign |
Het |
Trbv2 |
C |
T |
6: 41,024,905 (GRCm39) |
T107I |
probably benign |
Het |
Trpm6 |
T |
C |
19: 18,803,155 (GRCm39) |
V866A |
probably damaging |
Het |
Trpm6 |
A |
T |
19: 18,804,762 (GRCm39) |
K905* |
probably null |
Het |
Ttn |
A |
G |
2: 76,539,654 (GRCm39) |
V34444A |
probably benign |
Het |
Vmn1r86 |
C |
T |
7: 12,836,707 (GRCm39) |
M56I |
probably benign |
Het |
Vmn2r17 |
A |
C |
5: 109,601,012 (GRCm39) |
D770A |
probably damaging |
Het |
Wnk4 |
T |
C |
11: 101,160,389 (GRCm39) |
|
probably benign |
Het |
Xaf1 |
T |
C |
11: 72,194,257 (GRCm39) |
M46T |
possibly 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 |
|
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 |
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 |