Incidental Mutation 'R1803:Lamb2'
| ID |
203300 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Lamb2
|
| Ensembl Gene |
ENSMUSG00000052911 |
| Gene Name |
laminin, beta 2 |
| Synonyms |
Lams, npht, Lamb-2 |
| MMRRC Submission |
039833-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.854)
|
| Stock # |
R1803 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
9 |
| Chromosomal Location |
108357080-108367729 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 108365298 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Arginine
at position 1318
(H1318R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000069087
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000006854]
[ENSMUST00000065014]
[ENSMUST00000085044]
[ENSMUST00000166103]
[ENSMUST00000178075]
[ENSMUST00000193678]
|
| AlphaFold |
Q61292 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000006854
|
| SMART Domains |
Protein: ENSMUSP00000006854
Gene: ENSMUSG00000006676
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CS
|
55 |
129 |
1.3e-6 |
PFAM |
|
low complexity region
|
257 |
268 |
N/A |
INTRINSIC |
|
Pfam:CS
|
326 |
414 |
7.1e-19 |
PFAM |
|
Pfam:USP19_linker
|
415 |
537 |
2.2e-61 |
PFAM |
|
Pfam:UCH
|
538 |
1253 |
1.2e-77 |
PFAM |
|
Pfam:UCH_1
|
539 |
874 |
8.6e-11 |
PFAM |
|
Pfam:zf-MYND
|
833 |
875 |
9.9e-11 |
PFAM |
|
Pfam:UCH_1
|
1021 |
1235 |
7.1e-10 |
PFAM |
|
low complexity region
|
1278 |
1287 |
N/A |
INTRINSIC |
|
low complexity region
|
1301 |
1312 |
N/A |
INTRINSIC |
|
transmembrane domain
|
1333 |
1355 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000065014
AA Change: H1318R
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000069087
Gene: ENSMUSG00000052911
AA Change: H1318R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
35 |
N/A |
INTRINSIC |
|
LamNT
|
44 |
284 |
1.9e-102 |
SMART |
|
EGF_Lam
|
286 |
347 |
1.34e-6 |
SMART |
|
EGF_Lam
|
350 |
410 |
6.1e-10 |
SMART |
|
EGF_Lam
|
413 |
470 |
2.98e-13 |
SMART |
|
EGF_Lam
|
473 |
522 |
7.93e-9 |
SMART |
|
EGF_Lam
|
525 |
569 |
1.01e-10 |
SMART |
|
EGF_Lam
|
784 |
829 |
3.42e-13 |
SMART |
|
EGF_Lam
|
832 |
875 |
6.54e-10 |
SMART |
|
EGF_Lam
|
878 |
925 |
1.34e-6 |
SMART |
|
EGF_Lam
|
928 |
984 |
4.74e-7 |
SMART |
|
EGF_Lam
|
987 |
1036 |
1.53e-10 |
SMART |
|
EGF_Lam
|
1039 |
1093 |
6.29e-12 |
SMART |
|
EGF_Lam
|
1096 |
1141 |
1.79e-7 |
SMART |
|
EGF_Lam
|
1144 |
1188 |
6.64e-11 |
SMART |
|
coiled coil region
|
1261 |
1299 |
N/A |
INTRINSIC |
|
low complexity region
|
1445 |
1458 |
N/A |
INTRINSIC |
|
coiled coil region
|
1473 |
1527 |
N/A |
INTRINSIC |
|
low complexity region
|
1609 |
1625 |
N/A |
INTRINSIC |
|
SCOP:d1eq1a_
|
1632 |
1786 |
5e-17 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000085044
|
| SMART Domains |
Protein: ENSMUSP00000082119
Gene: ENSMUSG00000006676
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CS
|
55 |
129 |
4.7e-7 |
PFAM |
|
low complexity region
|
257 |
268 |
N/A |
INTRINSIC |
|
Pfam:CS
|
326 |
414 |
2.5e-15 |
PFAM |
|
low complexity region
|
449 |
460 |
N/A |
INTRINSIC |
|
low complexity region
|
524 |
530 |
N/A |
INTRINSIC |
|
Pfam:UCH
|
538 |
1253 |
7.4e-84 |
PFAM |
|
Pfam:UCH_1
|
539 |
879 |
2.3e-13 |
PFAM |
|
Pfam:zf-MYND
|
833 |
875 |
2.4e-10 |
PFAM |
|
Pfam:UCH_1
|
1020 |
1235 |
2.9e-11 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000166103
|
| SMART Domains |
Protein: ENSMUSP00000128573
Gene: ENSMUSG00000006676
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CS
|
55 |
129 |
2.6e-7 |
PFAM |
|
low complexity region
|
257 |
268 |
N/A |
INTRINSIC |
|
Pfam:CS
|
326 |
390 |
3.9e-9 |
PFAM |
|
low complexity region
|
425 |
436 |
N/A |
INTRINSIC |
|
low complexity region
|
500 |
506 |
N/A |
INTRINSIC |
|
Pfam:UCH
|
514 |
1229 |
1.8e-84 |
PFAM |
|
Pfam:UCH_1
|
515 |
855 |
5.5e-14 |
PFAM |
|
Pfam:zf-MYND
|
809 |
851 |
1.7e-10 |
PFAM |
|
Pfam:UCH_1
|
996 |
1211 |
6.9e-12 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000178075
|
| SMART Domains |
Protein: ENSMUSP00000135930
Gene: ENSMUSG00000006676
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CS
|
55 |
129 |
1e-6 |
PFAM |
|
low complexity region
|
258 |
269 |
N/A |
INTRINSIC |
|
Pfam:CS
|
327 |
415 |
5.4e-15 |
PFAM |
|
low complexity region
|
450 |
461 |
N/A |
INTRINSIC |
|
low complexity region
|
525 |
531 |
N/A |
INTRINSIC |
|
Pfam:UCH
|
539 |
1254 |
4.9e-84 |
PFAM |
|
Pfam:UCH_1
|
540 |
880 |
1.4e-13 |
PFAM |
|
Pfam:zf-MYND
|
834 |
876 |
5.2e-10 |
PFAM |
|
Pfam:UCH_1
|
1021 |
1236 |
1.8e-11 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000192854
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000193301
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000194421
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000193678
|
| SMART Domains |
Protein: ENSMUSP00000141738
Gene: ENSMUSG00000006676
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:CS
|
55 |
129 |
6.8e-7 |
PFAM |
|
low complexity region
|
258 |
269 |
N/A |
INTRINSIC |
|
Pfam:CS
|
327 |
415 |
3.6e-15 |
PFAM |
|
low complexity region
|
448 |
459 |
N/A |
INTRINSIC |
|
low complexity region
|
523 |
529 |
N/A |
INTRINSIC |
|
Pfam:UCH
|
537 |
1252 |
3.8e-84 |
PFAM |
|
Pfam:UCH_1
|
538 |
878 |
1.1e-13 |
PFAM |
|
Pfam:zf-MYND
|
832 |
874 |
5.1e-10 |
PFAM |
|
Pfam:UCH_1
|
1019 |
1234 |
1.4e-11 |
PFAM |
|
| Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.0%
- 20x: 91.6%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Laminins, a family of extracellular matrix glycoproteins, are the major noncollagenous constituent of basement membranes. They have been implicated in a wide variety of biological processes including cell adhesion, differentiation, migration, signaling, neurite outgrowth and metastasis. Laminins, composed of 3 non identical chains: laminin alpha, beta and gamma (formerly A, B1, and B2, respectively), form a cruciform structure consisting of 3 short arms, each formed by a different chain, and a long arm composed of all 3 chains. Each laminin chain is a multidomain protein encoded by a distinct gene. Several isoforms of each chain have been described. Different alpha, beta and gamma chain isomers combine to give rise to different heterotrimeric laminin isoforms which are designated by Arabic numerals in the order of their discovery, i.e. alpha1beta1gamma1 heterotrimer is laminin 1. The biological functions of the different chains and trimer molecules are largely unknown, but some of the chains have been shown to differ with respect to their tissue distribution, presumably reflecting diverse functions in vivo. This gene encodes the beta chain isoform laminin, beta 2. The beta 2 chain contains the 7 structural domains typical of beta chains of laminin, including the short alpha region. However, unlike beta 1 chain, beta 2 has a more restricted tissue distribution. It is enriched in the basement membrane of muscles at the neuromuscular junctions, kidney glomerulus and vascular smooth muscle. Transgenic mice in which the beta 2 chain gene was inactivated by homologous recombination, showed defects in the maturation of neuromuscular junctions and impairment of glomerular filtration. Alternative splicing involving a non consensus 5' splice site (gc) in the 5' UTR of this gene has been reported. It was suggested that inefficient splicing of this first intron, which does not change the protein sequence, results in a greater abundance of the unspliced form of the transcript than the spliced form. The full-length nature of the spliced transcript is not known. [provided by RefSeq, Aug 2011]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit small size, severe proteinuria due to a defect in glomerular filtration, abnormalities of the retina and skeletal neuromuscular synapses, and lethality by 30 days of age. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(5) : Targeted, knock-out(2) Gene trapped(3)
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4921513D11Rik |
A |
T |
17: 79,935,095 (GRCm39) |
|
probably benign |
Het |
| Adgrl3 |
C |
T |
5: 81,919,464 (GRCm39) |
R586* |
probably null |
Het |
| Arpp21 |
T |
C |
9: 111,956,466 (GRCm39) |
T471A |
possibly damaging |
Het |
| Blnk |
T |
C |
19: 40,940,821 (GRCm39) |
E194G |
probably damaging |
Het |
| Cd44 |
G |
A |
2: 102,664,597 (GRCm39) |
P332S |
probably damaging |
Het |
| Cd47 |
T |
C |
16: 49,688,169 (GRCm39) |
F30L |
possibly damaging |
Het |
| Cdh23 |
T |
C |
10: 60,167,060 (GRCm39) |
E1861G |
probably damaging |
Het |
| Cdkal1 |
T |
A |
13: 29,701,454 (GRCm39) |
M332L |
probably damaging |
Het |
| Cul9 |
A |
G |
17: 46,814,023 (GRCm39) |
S2284P |
probably damaging |
Het |
| Cyp2a5 |
G |
T |
7: 26,534,971 (GRCm39) |
|
probably null |
Het |
| Dcp2 |
T |
C |
18: 44,528,984 (GRCm39) |
I33T |
probably damaging |
Het |
| Ddx52 |
A |
T |
11: 83,836,958 (GRCm39) |
I150L |
probably damaging |
Het |
| Dennd5a |
T |
A |
7: 109,497,820 (GRCm39) |
T1067S |
probably benign |
Het |
| Dnpep |
A |
T |
1: 75,286,058 (GRCm39) |
L419* |
probably null |
Het |
| Dock8 |
A |
G |
19: 25,109,599 (GRCm39) |
K927R |
probably benign |
Het |
| Dpy19l4 |
A |
T |
4: 11,281,020 (GRCm39) |
V475E |
possibly damaging |
Het |
| Edf1 |
C |
T |
2: 25,450,206 (GRCm39) |
S41F |
probably damaging |
Het |
| Elapor2 |
A |
G |
5: 9,477,832 (GRCm39) |
H410R |
probably benign |
Het |
| Emilin1 |
C |
T |
5: 31,075,082 (GRCm39) |
P441L |
possibly damaging |
Het |
| Epha3 |
T |
C |
16: 63,422,651 (GRCm39) |
K579E |
probably benign |
Het |
| Exoc1 |
A |
G |
5: 76,709,288 (GRCm39) |
N23S |
probably benign |
Het |
| Flt3 |
C |
A |
5: 147,303,865 (GRCm39) |
E358* |
probably null |
Het |
| Fzd1 |
A |
T |
5: 4,806,385 (GRCm39) |
I399K |
probably damaging |
Het |
| Gdi2 |
T |
A |
13: 3,614,547 (GRCm39) |
Y333* |
probably null |
Het |
| Gm10479 |
A |
G |
12: 20,483,654 (GRCm39) |
H91R |
probably benign |
Het |
| Gm10842 |
G |
A |
11: 105,037,867 (GRCm39) |
R50K |
unknown |
Het |
| Grin2c |
A |
T |
11: 115,151,558 (GRCm39) |
|
probably null |
Het |
| Grk2 |
C |
T |
19: 4,344,911 (GRCm39) |
V53M |
probably damaging |
Het |
| H2-M10.2 |
C |
T |
17: 36,596,763 (GRCm39) |
M104I |
probably benign |
Het |
| Hyou1 |
C |
T |
9: 44,295,479 (GRCm39) |
Q290* |
probably null |
Het |
| Inka1 |
A |
G |
9: 107,861,938 (GRCm39) |
V128A |
probably benign |
Het |
| Itgb2 |
T |
C |
10: 77,400,624 (GRCm39) |
S746P |
probably benign |
Het |
| Jmjd7 |
C |
T |
2: 119,860,589 (GRCm39) |
L39F |
probably damaging |
Het |
| Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
| Klhl2 |
T |
C |
8: 65,212,831 (GRCm39) |
E236G |
probably damaging |
Het |
| Krtap19-4 |
C |
A |
16: 88,681,879 (GRCm39) |
G26C |
unknown |
Het |
| Krtap4-16 |
G |
A |
11: 99,741,998 (GRCm39) |
T134I |
possibly damaging |
Het |
| Mab21l3 |
G |
A |
3: 101,742,446 (GRCm39) |
T38M |
probably benign |
Het |
| Mfsd10 |
A |
T |
5: 34,794,094 (GRCm39) |
D6E |
possibly damaging |
Het |
| Mnat1 |
G |
T |
12: 73,226,007 (GRCm39) |
G91* |
probably null |
Het |
| Mns1 |
A |
T |
9: 72,360,016 (GRCm39) |
I389F |
probably damaging |
Het |
| Morc1 |
A |
T |
16: 48,443,001 (GRCm39) |
T829S |
probably benign |
Het |
| Morn5 |
T |
A |
2: 35,943,089 (GRCm39) |
V63E |
probably benign |
Het |
| Mybpc1 |
T |
C |
10: 88,389,157 (GRCm39) |
T404A |
possibly damaging |
Het |
| Npc1l1 |
A |
T |
11: 6,178,846 (GRCm39) |
M188K |
probably damaging |
Het |
| Nrcam |
T |
A |
12: 44,618,991 (GRCm39) |
M846K |
probably benign |
Het |
| Nup210 |
A |
C |
6: 91,051,264 (GRCm39) |
F373C |
probably damaging |
Het |
| Or4k49 |
G |
T |
2: 111,495,099 (GRCm39) |
S176I |
probably damaging |
Het |
| Or5b111 |
A |
T |
19: 13,291,535 (GRCm39) |
V38E |
possibly damaging |
Het |
| Or7g18 |
T |
C |
9: 18,787,376 (GRCm39) |
V248A |
probably damaging |
Het |
| Osbpl8 |
T |
C |
10: 111,110,910 (GRCm39) |
S471P |
probably damaging |
Het |
| Plekhn1 |
A |
T |
4: 156,306,838 (GRCm39) |
I517N |
probably benign |
Het |
| Plin4 |
G |
T |
17: 56,411,931 (GRCm39) |
T700K |
probably damaging |
Het |
| Plxna4 |
A |
T |
6: 32,494,379 (GRCm39) |
V79D |
probably damaging |
Het |
| Prdm16 |
A |
T |
4: 154,419,718 (GRCm39) |
M897K |
probably damaging |
Het |
| Ptprg |
T |
A |
14: 12,091,410 (GRCm38) |
|
probably null |
Het |
| Rcan2 |
G |
T |
17: 44,347,924 (GRCm39) |
C211F |
probably damaging |
Het |
| Rigi |
A |
G |
4: 40,224,013 (GRCm39) |
S289P |
probably benign |
Het |
| Rxfp1 |
C |
T |
3: 79,645,076 (GRCm39) |
C9Y |
probably benign |
Het |
| Scn2a |
G |
A |
2: 65,501,111 (GRCm39) |
|
probably null |
Het |
| Scnn1a |
A |
C |
6: 125,309,157 (GRCm39) |
R264S |
probably damaging |
Het |
| Sema4g |
T |
C |
19: 44,986,459 (GRCm39) |
V345A |
probably benign |
Het |
| Sgo2b |
T |
A |
8: 64,380,426 (GRCm39) |
D802V |
probably benign |
Het |
| Slc25a21 |
G |
A |
12: 56,904,872 (GRCm39) |
T54I |
probably benign |
Het |
| Slc25a46 |
C |
T |
18: 31,727,641 (GRCm39) |
E223K |
probably damaging |
Het |
| Slc25a54 |
A |
G |
3: 109,010,013 (GRCm39) |
I171V |
probably benign |
Het |
| Slc7a6 |
T |
C |
8: 106,919,088 (GRCm39) |
V224A |
possibly damaging |
Het |
| Smchd1 |
A |
T |
17: 71,694,001 (GRCm39) |
V1248E |
probably damaging |
Het |
| Sort1 |
C |
A |
3: 108,233,015 (GRCm39) |
F196L |
probably damaging |
Het |
| Sptbn4 |
G |
A |
7: 27,118,008 (GRCm39) |
T357M |
probably damaging |
Het |
| Srrm3 |
T |
A |
5: 135,885,983 (GRCm39) |
W308R |
probably damaging |
Het |
| Stard9 |
A |
T |
2: 120,531,970 (GRCm39) |
E2742D |
probably benign |
Het |
| Tas1r1 |
T |
A |
4: 152,116,705 (GRCm39) |
I310F |
probably damaging |
Het |
| Tas1r3 |
G |
A |
4: 155,944,927 (GRCm39) |
R765C |
probably damaging |
Het |
| Tff1 |
A |
T |
17: 31,380,560 (GRCm39) |
C85* |
probably null |
Het |
| Tlr11 |
C |
T |
14: 50,598,104 (GRCm39) |
T30I |
probably benign |
Het |
| Trio |
T |
C |
15: 27,748,426 (GRCm39) |
T1265A |
probably benign |
Het |
| Ttc7b |
T |
C |
12: 100,373,261 (GRCm39) |
M338V |
possibly damaging |
Het |
| Umod |
T |
A |
7: 119,063,947 (GRCm39) |
S620C |
probably damaging |
Het |
| Ust |
C |
A |
10: 8,173,819 (GRCm39) |
|
probably null |
Het |
| Vmn1r176 |
A |
T |
7: 23,534,609 (GRCm39) |
S181R |
probably damaging |
Het |
| Vmn1r202 |
T |
C |
13: 22,686,313 (GRCm39) |
T35A |
probably benign |
Het |
| Vmn1r39 |
C |
A |
6: 66,781,895 (GRCm39) |
R104L |
probably benign |
Het |
| Vps13b |
T |
A |
15: 35,430,351 (GRCm39) |
Y286* |
probably null |
Het |
| Zfp579 |
G |
A |
7: 4,996,769 (GRCm39) |
R381C |
probably damaging |
Het |
| Zfp85 |
A |
G |
13: 67,899,747 (GRCm39) |
S71P |
probably benign |
Het |
| Zfyve16 |
A |
T |
13: 92,640,593 (GRCm39) |
V1254E |
probably damaging |
Het |
|
| Other mutations in Lamb2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01370:Lamb2
|
APN |
9 |
108,364,932 (GRCm39) |
splice site |
probably null |
|
|
IGL02072:Lamb2
|
APN |
9 |
108,359,107 (GRCm39) |
nonsense |
probably null |
|
|
IGL02079:Lamb2
|
APN |
9 |
108,359,312 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02087:Lamb2
|
APN |
9 |
108,364,318 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02193:Lamb2
|
APN |
9 |
108,366,559 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02199:Lamb2
|
APN |
9 |
108,357,824 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
IGL02201:Lamb2
|
APN |
9 |
108,364,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02468:Lamb2
|
APN |
9 |
108,364,348 (GRCm39) |
missense |
probably damaging |
1.00 |
|
F6893:Lamb2
|
UTSW |
9 |
108,359,755 (GRCm39) |
missense |
probably benign |
0.12 |
|
R0053:Lamb2
|
UTSW |
9 |
108,363,936 (GRCm39) |
nonsense |
probably null |
|
|
R0053:Lamb2
|
UTSW |
9 |
108,363,936 (GRCm39) |
nonsense |
probably null |
|
|
R0122:Lamb2
|
UTSW |
9 |
108,363,713 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0452:Lamb2
|
UTSW |
9 |
108,363,553 (GRCm39) |
unclassified |
probably benign |
|
|
R0524:Lamb2
|
UTSW |
9 |
108,361,571 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0605:Lamb2
|
UTSW |
9 |
108,363,304 (GRCm39) |
unclassified |
probably benign |
|
|
R0737:Lamb2
|
UTSW |
9 |
108,360,993 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1083:Lamb2
|
UTSW |
9 |
108,360,892 (GRCm39) |
missense |
probably benign |
|
|
R1159:Lamb2
|
UTSW |
9 |
108,358,607 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1283:Lamb2
|
UTSW |
9 |
108,359,007 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R1507:Lamb2
|
UTSW |
9 |
108,367,581 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1547:Lamb2
|
UTSW |
9 |
108,359,824 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1576:Lamb2
|
UTSW |
9 |
108,357,506 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R1647:Lamb2
|
UTSW |
9 |
108,358,622 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1678:Lamb2
|
UTSW |
9 |
108,360,885 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1740:Lamb2
|
UTSW |
9 |
108,359,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1846:Lamb2
|
UTSW |
9 |
108,364,586 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1863:Lamb2
|
UTSW |
9 |
108,358,583 (GRCm39) |
missense |
probably benign |
0.13 |
|
R2184:Lamb2
|
UTSW |
9 |
108,357,752 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2262:Lamb2
|
UTSW |
9 |
108,357,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2338:Lamb2
|
UTSW |
9 |
108,359,340 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2483:Lamb2
|
UTSW |
9 |
108,357,758 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4084:Lamb2
|
UTSW |
9 |
108,365,217 (GRCm39) |
missense |
probably benign |
0.17 |
|
R4164:Lamb2
|
UTSW |
9 |
108,367,497 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4295:Lamb2
|
UTSW |
9 |
108,363,410 (GRCm39) |
missense |
probably benign |
0.42 |
|
R4422:Lamb2
|
UTSW |
9 |
108,360,754 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4497:Lamb2
|
UTSW |
9 |
108,363,997 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4880:Lamb2
|
UTSW |
9 |
108,361,226 (GRCm39) |
splice site |
probably null |
|
|
R4935:Lamb2
|
UTSW |
9 |
108,364,700 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R4977:Lamb2
|
UTSW |
9 |
108,364,846 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5152:Lamb2
|
UTSW |
9 |
108,364,937 (GRCm39) |
missense |
probably benign |
|
|
R5499:Lamb2
|
UTSW |
9 |
108,365,001 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R5724:Lamb2
|
UTSW |
9 |
108,357,950 (GRCm39) |
splice site |
probably null |
|
|
R5932:Lamb2
|
UTSW |
9 |
108,357,810 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5997:Lamb2
|
UTSW |
9 |
108,357,587 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R6052:Lamb2
|
UTSW |
9 |
108,364,811 (GRCm39) |
nonsense |
probably null |
|
|
R6142:Lamb2
|
UTSW |
9 |
108,362,817 (GRCm39) |
nonsense |
probably null |
|
|
R6245:Lamb2
|
UTSW |
9 |
108,365,398 (GRCm39) |
splice site |
probably null |
|
|
R6531:Lamb2
|
UTSW |
9 |
108,360,925 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R6557:Lamb2
|
UTSW |
9 |
108,365,599 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6562:Lamb2
|
UTSW |
9 |
108,364,207 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R6997:Lamb2
|
UTSW |
9 |
108,358,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7024:Lamb2
|
UTSW |
9 |
108,366,687 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7116:Lamb2
|
UTSW |
9 |
108,364,522 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7146:Lamb2
|
UTSW |
9 |
108,361,283 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7261:Lamb2
|
UTSW |
9 |
108,358,496 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7288:Lamb2
|
UTSW |
9 |
108,365,523 (GRCm39) |
missense |
probably benign |
0.20 |
|
R7404:Lamb2
|
UTSW |
9 |
108,364,782 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7456:Lamb2
|
UTSW |
9 |
108,362,979 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7472:Lamb2
|
UTSW |
9 |
108,363,347 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7623:Lamb2
|
UTSW |
9 |
108,366,423 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R8125:Lamb2
|
UTSW |
9 |
108,364,722 (GRCm39) |
missense |
probably benign |
|
|
R8153:Lamb2
|
UTSW |
9 |
108,357,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8154:Lamb2
|
UTSW |
9 |
108,357,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8155:Lamb2
|
UTSW |
9 |
108,357,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8156:Lamb2
|
UTSW |
9 |
108,357,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8157:Lamb2
|
UTSW |
9 |
108,357,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8419:Lamb2
|
UTSW |
9 |
108,365,563 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8695:Lamb2
|
UTSW |
9 |
108,363,365 (GRCm39) |
missense |
probably benign |
0.08 |
|
R8825:Lamb2
|
UTSW |
9 |
108,362,460 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9005:Lamb2
|
UTSW |
9 |
108,361,370 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9315:Lamb2
|
UTSW |
9 |
108,364,366 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9398:Lamb2
|
UTSW |
9 |
108,364,366 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R9419:Lamb2
|
UTSW |
9 |
108,356,959 (GRCm39) |
missense |
unknown |
|
|
R9450:Lamb2
|
UTSW |
9 |
108,357,760 (GRCm39) |
nonsense |
probably null |
|
|
R9495:Lamb2
|
UTSW |
9 |
108,358,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9514:Lamb2
|
UTSW |
9 |
108,358,006 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9529:Lamb2
|
UTSW |
9 |
108,363,477 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9532:Lamb2
|
UTSW |
9 |
108,365,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9534:Lamb2
|
UTSW |
9 |
108,365,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9734:Lamb2
|
UTSW |
9 |
108,365,830 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Lamb2
|
UTSW |
9 |
108,360,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AGGCTTCTCTAAACATGTCCC -3'
(R):5'- GTATCTGCTGAGTTGCTCACAG -3'
Sequencing Primer
(F):5'- CCCCATTGATACAGTCATGAAATCGG -3'
(R):5'- CTGAGTTGCTCACAGGGCTG -3'
|
| Posted On |
2014-06-23 |
Incidental Mutation