Incidental Mutation 'IGL01124:Ldb3'
| ID |
52710 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Ldb3
|
| Ensembl Gene |
ENSMUSG00000021798 |
| Gene Name |
LIM domain binding 3 |
| Synonyms |
ZASP, cypher |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL01124
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
14 |
| Chromosomal Location |
34248560-34310639 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 34266157 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Aspartic acid
at position 417
(E417D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000022328
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022327]
[ENSMUST00000022328]
[ENSMUST00000064098]
[ENSMUST00000090040]
[ENSMUST00000228044]
|
| AlphaFold |
Q9JKS4 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000022327
AA Change: E479D
PolyPhen 2
Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000022327
Gene: ENSMUSG00000021798
AA Change: E479D
| Domain | Start | End | E-Value | Type |
|---|
|
PDZ
|
11 |
84 |
1.68e-16 |
SMART |
|
low complexity region
|
138 |
147 |
N/A |
INTRINSIC |
|
ZM
|
186 |
211 |
1.33e-8 |
SMART |
|
low complexity region
|
214 |
229 |
N/A |
INTRINSIC |
|
low complexity region
|
309 |
353 |
N/A |
INTRINSIC |
|
low complexity region
|
359 |
376 |
N/A |
INTRINSIC |
|
low complexity region
|
418 |
473 |
N/A |
INTRINSIC |
|
LIM
|
546 |
597 |
2.72e-16 |
SMART |
|
LIM
|
605 |
656 |
2.65e-19 |
SMART |
|
LIM
|
664 |
717 |
1.04e-17 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000022328
AA Change: E417D
PolyPhen 2
Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
|
| SMART Domains |
Protein: ENSMUSP00000022328
Gene: ENSMUSG00000021798
AA Change: E417D
| Domain | Start | End | E-Value | Type |
|---|
|
PDZ
|
11 |
84 |
1.68e-16 |
SMART |
|
low complexity region
|
138 |
147 |
N/A |
INTRINSIC |
|
ZM
|
186 |
211 |
1.33e-8 |
SMART |
|
low complexity region
|
214 |
229 |
N/A |
INTRINSIC |
|
low complexity region
|
297 |
314 |
N/A |
INTRINSIC |
|
low complexity region
|
356 |
411 |
N/A |
INTRINSIC |
|
LIM
|
484 |
535 |
2.72e-16 |
SMART |
|
LIM
|
543 |
594 |
2.65e-19 |
SMART |
|
LIM
|
602 |
655 |
1.04e-17 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000064098
AA Change: E435D
PolyPhen 2
Score 0.389 (Sensitivity: 0.90; Specificity: 0.89)
|
| SMART Domains |
Protein: ENSMUSP00000066784
Gene: ENSMUSG00000021798
AA Change: E435D
| Domain | Start | End | E-Value | Type |
|---|
|
PDZ
|
11 |
84 |
1.68e-16 |
SMART |
|
ZM
|
148 |
173 |
5.18e-11 |
SMART |
|
low complexity region
|
265 |
309 |
N/A |
INTRINSIC |
|
low complexity region
|
315 |
332 |
N/A |
INTRINSIC |
|
low complexity region
|
374 |
429 |
N/A |
INTRINSIC |
|
LIM
|
502 |
553 |
2.72e-16 |
SMART |
|
LIM
|
561 |
612 |
2.65e-19 |
SMART |
|
LIM
|
620 |
673 |
1.04e-17 |
SMART |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000090040
AA Change: E440D
PolyPhen 2
Score 0.455 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000087494
Gene: ENSMUSG00000021798
AA Change: E440D
| Domain | Start | End | E-Value | Type |
|---|
|
PDZ
|
11 |
84 |
1.68e-16 |
SMART |
|
ZM
|
148 |
173 |
5.18e-11 |
SMART |
|
low complexity region
|
270 |
314 |
N/A |
INTRINSIC |
|
low complexity region
|
320 |
337 |
N/A |
INTRINSIC |
|
low complexity region
|
379 |
434 |
N/A |
INTRINSIC |
|
LIM
|
507 |
558 |
2.72e-16 |
SMART |
|
LIM
|
566 |
617 |
2.65e-19 |
SMART |
|
LIM
|
625 |
678 |
1.04e-17 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000228044
AA Change: E378D
PolyPhen 2
Score 0.179 (Sensitivity: 0.92; Specificity: 0.87)
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a PDZ domain-containing protein. PDZ motifs are modular protein-protein interaction domains consisting of 80-120 amino acid residues. PDZ domain-containing proteins interact with each other in cytoskeletal assembly or with other proteins involved in targeting and clustering of membrane proteins. The protein encoded by this gene interacts with alpha-actinin-2 through its N-terminal PDZ domain and with protein kinase C via its C-terminal LIM domains. The LIM domain is a cysteine-rich motif defined by 50-60 amino acids containing two zinc-binding modules. This protein also interacts with all three members of the myozenin family. Mutations in this gene have been associated with myofibrillar myopathy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding different isoforms have been identified; all isoforms have N-terminal PDZ domains while only longer isoforms (1, 2 and 5) have C-terminal LIM domains. [provided by RefSeq, Jan 2010]
PHENOTYPE: Homozygous mutation of this gene results in lethality within a few days after birth from muscle abnormalities. Mutant mice exhibit myopathy, dysphagia, heart vascular congestion, dilated heart ventricles, cyanosis, and respiratory distress. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ascc3 |
T |
C |
10: 50,608,569 (GRCm39) |
I1477T |
probably damaging |
Het |
| Baat |
A |
G |
4: 49,490,391 (GRCm39) |
I231T |
possibly damaging |
Het |
| Cactin |
T |
C |
10: 81,160,184 (GRCm39) |
S426P |
possibly damaging |
Het |
| Cfh |
A |
T |
1: 140,110,999 (GRCm39) |
F6I |
probably benign |
Het |
| Clec4a2 |
C |
T |
6: 123,116,037 (GRCm39) |
|
probably benign |
Het |
| Col12a1 |
A |
G |
9: 79,611,129 (GRCm39) |
S148P |
probably damaging |
Het |
| Cubn |
G |
T |
2: 13,482,904 (GRCm39) |
Q281K |
possibly damaging |
Het |
| Cyp2c65 |
T |
A |
19: 39,081,954 (GRCm39) |
|
probably benign |
Het |
| Dennd4b |
A |
T |
3: 90,176,381 (GRCm39) |
T243S |
possibly damaging |
Het |
| Epha8 |
C |
T |
4: 136,663,394 (GRCm39) |
G518D |
probably damaging |
Het |
| Fmo3 |
G |
A |
1: 162,785,830 (GRCm39) |
R387C |
probably damaging |
Het |
| Foxo6 |
T |
C |
4: 120,126,349 (GRCm39) |
T149A |
probably benign |
Het |
| Fthl17d |
T |
C |
X: 8,852,827 (GRCm39) |
E3G |
probably benign |
Het |
| Gm10521 |
A |
G |
1: 171,724,010 (GRCm39) |
Y107C |
unknown |
Het |
| Ipo8 |
T |
A |
6: 148,678,874 (GRCm39) |
E908V |
probably benign |
Het |
| Kcnd2 |
T |
C |
6: 21,217,216 (GRCm39) |
S307P |
probably damaging |
Het |
| Klf3 |
A |
G |
5: 64,974,123 (GRCm39) |
M3V |
possibly damaging |
Het |
| Lrch1 |
A |
T |
14: 74,994,503 (GRCm39) |
D673E |
probably benign |
Het |
| Map3k4 |
T |
C |
17: 12,474,087 (GRCm39) |
K865E |
probably benign |
Het |
| Muc4 |
G |
A |
16: 32,589,104 (GRCm39) |
V754I |
possibly damaging |
Het |
| Nek4 |
A |
G |
14: 30,692,219 (GRCm39) |
N223D |
probably benign |
Het |
| Nell2 |
G |
A |
15: 95,194,060 (GRCm39) |
T551M |
probably damaging |
Het |
| Nup155 |
T |
A |
15: 8,183,163 (GRCm39) |
M1241K |
probably damaging |
Het |
| Or2t49 |
A |
T |
11: 58,393,020 (GRCm39) |
S121T |
possibly damaging |
Het |
| Or5i1 |
T |
C |
2: 87,613,720 (GRCm39) |
F279L |
probably benign |
Het |
| Orc1 |
T |
C |
4: 108,445,984 (GRCm39) |
|
probably benign |
Het |
| Pclo |
T |
C |
5: 14,764,343 (GRCm39) |
I4272T |
unknown |
Het |
| Ppp1r12c |
A |
G |
7: 4,500,344 (GRCm39) |
|
probably benign |
Het |
| Prcp |
A |
G |
7: 92,559,416 (GRCm39) |
E160G |
probably benign |
Het |
| Prl3d3 |
G |
A |
13: 27,343,090 (GRCm39) |
R92Q |
possibly damaging |
Het |
| Prl6a1 |
T |
A |
13: 27,500,347 (GRCm39) |
M106K |
possibly damaging |
Het |
| Slc22a1 |
T |
A |
17: 12,869,749 (GRCm39) |
|
probably benign |
Het |
| Slco3a1 |
A |
G |
7: 73,934,295 (GRCm39) |
Y626H |
probably damaging |
Het |
| Smtn |
A |
G |
11: 3,476,326 (GRCm39) |
|
probably null |
Het |
| Snx30 |
T |
C |
4: 59,886,404 (GRCm39) |
|
probably benign |
Het |
| Spock2 |
A |
G |
10: 59,967,209 (GRCm39) |
D393G |
unknown |
Het |
| Trem3 |
T |
G |
17: 48,556,829 (GRCm39) |
L100R |
probably damaging |
Het |
| Trpm2 |
A |
T |
10: 77,781,659 (GRCm39) |
|
probably benign |
Het |
| Ubr1 |
T |
C |
2: 120,745,386 (GRCm39) |
M901V |
probably benign |
Het |
| Usp28 |
T |
A |
9: 48,948,513 (GRCm39) |
S873T |
probably damaging |
Het |
| Vmn1r86 |
T |
C |
7: 12,836,856 (GRCm39) |
I7V |
probably benign |
Het |
| Xirp2 |
T |
C |
2: 67,338,959 (GRCm39) |
L400P |
probably damaging |
Het |
|
| Other mutations in Ldb3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01485:Ldb3
|
APN |
14 |
34,264,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01983:Ldb3
|
APN |
14 |
34,299,156 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0323:Ldb3
|
UTSW |
14 |
34,266,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0335:Ldb3
|
UTSW |
14 |
34,300,608 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R0483:Ldb3
|
UTSW |
14 |
34,258,541 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0920:Ldb3
|
UTSW |
14 |
34,289,460 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1524:Ldb3
|
UTSW |
14 |
34,277,313 (GRCm39) |
missense |
probably benign |
0.01 |
|
R2161:Ldb3
|
UTSW |
14 |
34,289,353 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2246:Ldb3
|
UTSW |
14 |
34,251,432 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2865:Ldb3
|
UTSW |
14 |
34,251,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3113:Ldb3
|
UTSW |
14 |
34,251,418 (GRCm39) |
makesense |
probably null |
|
|
R3765:Ldb3
|
UTSW |
14 |
34,300,639 (GRCm39) |
splice site |
probably null |
|
|
R3870:Ldb3
|
UTSW |
14 |
34,289,440 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4018:Ldb3
|
UTSW |
14 |
34,274,128 (GRCm39) |
splice site |
probably benign |
|
|
R4797:Ldb3
|
UTSW |
14 |
34,277,470 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4963:Ldb3
|
UTSW |
14 |
34,288,815 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5705:Ldb3
|
UTSW |
14 |
34,298,986 (GRCm39) |
missense |
probably null |
0.01 |
|
R6401:Ldb3
|
UTSW |
14 |
34,299,291 (GRCm39) |
missense |
probably benign |
0.33 |
|
R6549:Ldb3
|
UTSW |
14 |
34,263,854 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6682:Ldb3
|
UTSW |
14 |
34,274,221 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R6917:Ldb3
|
UTSW |
14 |
34,277,321 (GRCm39) |
missense |
probably null |
0.03 |
|
R7132:Ldb3
|
UTSW |
14 |
34,298,992 (GRCm39) |
missense |
probably benign |
0.25 |
|
R7327:Ldb3
|
UTSW |
14 |
34,293,759 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7488:Ldb3
|
UTSW |
14 |
34,289,402 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7760:Ldb3
|
UTSW |
14 |
34,264,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8755:Ldb3
|
UTSW |
14 |
34,299,256 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8845:Ldb3
|
UTSW |
14 |
34,258,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8954:Ldb3
|
UTSW |
14 |
34,277,301 (GRCm39) |
missense |
probably null |
0.17 |
|
R9179:Ldb3
|
UTSW |
14 |
34,277,312 (GRCm39) |
missense |
probably benign |
|
|
R9321:Ldb3
|
UTSW |
14 |
34,266,099 (GRCm39) |
nonsense |
probably null |
|
|
R9702:Ldb3
|
UTSW |
14 |
34,299,090 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1176:Ldb3
|
UTSW |
14 |
34,277,322 (GRCm39) |
missense |
probably benign |
0.21 |
|
Z1177:Ldb3
|
UTSW |
14 |
34,266,060 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Posted On |
2013-06-21 |
Incidental Mutation