Incidental Mutation 'IGL01838:Thbs3'
| ID |
155019 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Thbs3
|
| Ensembl Gene |
ENSMUSG00000028047 |
| Gene Name |
thrombospondin 3 |
| Synonyms |
TSP3, Thbs-3 |
| Accession Numbers |
|
| Essential gene? |
Possibly essential
(E-score: 0.558)
|
| Stock # |
IGL01838
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
3 |
| Chromosomal Location |
89122487-89134144 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
A to T
at 89126365 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Lysine to Stop codon
at position 229
(K229*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112912
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000029682]
[ENSMUST00000073572]
[ENSMUST00000118964]
[ENSMUST00000119084]
[ENSMUST00000142051]
[ENSMUST00000174126]
|
| AlphaFold |
Q05895 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000029682
AA Change: K229*
|
| SMART Domains |
Protein: ENSMUSP00000029682
Gene: ENSMUSG00000028047
AA Change: K229*
| Domain | Start | End | E-Value | Type |
|---|
|
TSPN
|
21 |
193 |
4.71e-56 |
SMART |
|
Pfam:COMP
|
226 |
270 |
2.5e-22 |
PFAM |
|
EGF
|
277 |
315 |
8.19e-2 |
SMART |
|
EGF_CA
|
316 |
369 |
6.91e-9 |
SMART |
|
EGF_CA
|
370 |
413 |
1.38e-8 |
SMART |
|
EGF
|
417 |
456 |
1.99e0 |
SMART |
|
Pfam:TSP_3
|
492 |
527 |
1e-12 |
PFAM |
|
Pfam:TSP_3
|
551 |
586 |
2.2e-16 |
PFAM |
|
Pfam:TSP_3
|
586 |
609 |
6.6e-7 |
PFAM |
|
Pfam:TSP_3
|
610 |
647 |
2.6e-14 |
PFAM |
|
Pfam:TSP_3
|
648 |
687 |
2.4e-10 |
PFAM |
|
Pfam:TSP_3
|
688 |
723 |
4.2e-15 |
PFAM |
|
Pfam:TSP_C
|
741 |
938 |
3.3e-99 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000073572
|
| SMART Domains |
Protein: ENSMUSP00000073261
Gene: ENSMUSG00000064068
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
94 |
109 |
N/A |
INTRINSIC |
|
Pfam:Tom37
|
151 |
219 |
4.2e-21 |
PFAM |
|
Pfam:Tom37_C
|
239 |
317 |
8.1e-24 |
PFAM |
|
Pfam:GST_C_3
|
267 |
383 |
1.7e-11 |
PFAM |
|
Pfam:GST_C_2
|
270 |
377 |
2.7e-8 |
PFAM |
|
Pfam:Tom37_C
|
300 |
369 |
1.1e-14 |
PFAM |
|
low complexity region
|
396 |
415 |
N/A |
INTRINSIC |
|
transmembrane domain
|
416 |
438 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000118964
|
| SMART Domains |
Protein: ENSMUSP00000114009
Gene: ENSMUSG00000064068
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
94 |
109 |
N/A |
INTRINSIC |
|
Pfam:Tom37
|
151 |
219 |
5.9e-21 |
PFAM |
|
Pfam:Tom37_C
|
216 |
287 |
6.3e-19 |
PFAM |
|
Pfam:GST_C_3
|
216 |
352 |
5.1e-11 |
PFAM |
|
Pfam:GST_C_2
|
238 |
344 |
1.9e-8 |
PFAM |
|
Pfam:Tom37_C
|
269 |
338 |
9.5e-15 |
PFAM |
|
low complexity region
|
365 |
384 |
N/A |
INTRINSIC |
|
transmembrane domain
|
385 |
407 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000119084
AA Change: K229*
|
| SMART Domains |
Protein: ENSMUSP00000112912
Gene: ENSMUSG00000028047
AA Change: K229*
| Domain | Start | End | E-Value | Type |
|---|
|
TSPN
|
21 |
193 |
4.71e-56 |
SMART |
|
Pfam:COMP
|
226 |
270 |
8.2e-26 |
PFAM |
|
EGF
|
277 |
315 |
8.19e-2 |
SMART |
|
EGF_CA
|
316 |
369 |
6.91e-9 |
SMART |
|
EGF_CA
|
370 |
413 |
1.38e-8 |
SMART |
|
Pfam:TSP_3
|
455 |
490 |
4.4e-13 |
PFAM |
|
Pfam:TSP_3
|
514 |
549 |
9.3e-17 |
PFAM |
|
Pfam:TSP_3
|
549 |
572 |
2.8e-7 |
PFAM |
|
Pfam:TSP_3
|
573 |
610 |
1.1e-14 |
PFAM |
|
Pfam:TSP_3
|
611 |
650 |
1e-10 |
PFAM |
|
Pfam:TSP_3
|
651 |
686 |
1.8e-15 |
PFAM |
|
Pfam:TSP_C
|
704 |
904 |
7.9e-108 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126315
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126700
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000142051
|
| SMART Domains |
Protein: ENSMUSP00000116136
Gene: ENSMUSG00000028047
| Domain | Start | End | E-Value | Type |
|---|
|
TSPN
|
1 |
124 |
2.52e-6 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000146435
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174126
|
| SMART Domains |
Protein: ENSMUSP00000133291
Gene: ENSMUSG00000064068
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Tom37_C
|
1 |
74 |
7.6e-23 |
PFAM |
|
Pfam:GST_C_3
|
7 |
143 |
7.3e-12 |
PFAM |
|
Pfam:GST_C_2
|
26 |
137 |
2.8e-9 |
PFAM |
|
Pfam:Tom37_C
|
61 |
129 |
6.2e-15 |
PFAM |
|
low complexity region
|
159 |
169 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the thrombospondin family. Thrombospondin family members are adhesive glycoproteins that mediate cell-to-cell and cell-to-matrix interactions. This protein forms a pentameric molecule linked by a single disulfide bond. This gene shares a common promoter with metaxin 1. Alternate splicing results in coding and non-coding transcript variants. [provided by RefSeq, Nov 2011]
PHENOTYPE: Homozygous null mice at a young age are heavier and exhibit femurs with increased periosteal and endocortical diameters, greater moments of inertia and increased bending strength and failure loads, with these defects no longer detected in older mice. Femoral heads show accelerated bone ossification. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 24 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Akr1c6 |
T |
C |
13: 4,499,035 (GRCm39) |
S208P |
probably benign |
Het |
| Cpe |
G |
T |
8: 65,047,998 (GRCm39) |
T422K |
possibly damaging |
Het |
| Dis3l |
C |
A |
9: 64,215,581 (GRCm39) |
V888L |
probably benign |
Het |
| Dnah7b |
T |
A |
1: 46,397,297 (GRCm39) |
Y3909* |
probably null |
Het |
| Dnajb8 |
G |
A |
6: 88,200,033 (GRCm39) |
V190M |
possibly damaging |
Het |
| Grip2 |
A |
G |
6: 91,741,744 (GRCm39) |
V927A |
possibly damaging |
Het |
| Hyal3 |
C |
T |
9: 107,463,786 (GRCm39) |
R304C |
possibly damaging |
Het |
| Igkv8-21 |
A |
G |
6: 70,292,009 (GRCm39) |
S78P |
probably damaging |
Het |
| Lrrc7 |
A |
G |
3: 157,891,100 (GRCm39) |
S356P |
probably damaging |
Het |
| Meiob |
T |
C |
17: 25,042,643 (GRCm39) |
V157A |
possibly damaging |
Het |
| Mrpl48 |
C |
T |
7: 100,201,860 (GRCm39) |
V35M |
probably damaging |
Het |
| Myo9b |
T |
C |
8: 71,787,034 (GRCm39) |
Y739H |
probably damaging |
Het |
| Nfyb |
A |
G |
10: 82,586,642 (GRCm39) |
L174S |
probably benign |
Het |
| Prm2 |
T |
C |
16: 10,609,672 (GRCm39) |
|
probably benign |
Het |
| Prss50 |
T |
C |
9: 110,693,560 (GRCm39) |
L432P |
probably benign |
Het |
| Raly |
T |
A |
2: 154,701,590 (GRCm39) |
|
probably benign |
Het |
| Scn11a |
A |
T |
9: 119,587,649 (GRCm39) |
M1365K |
probably damaging |
Het |
| Slc28a2b |
C |
A |
2: 122,348,464 (GRCm39) |
F270L |
possibly damaging |
Het |
| Spred1 |
T |
G |
2: 117,008,062 (GRCm39) |
S323A |
probably benign |
Het |
| Svep1 |
T |
C |
4: 58,121,910 (GRCm39) |
E761G |
possibly damaging |
Het |
| Thoc1 |
G |
A |
18: 9,993,386 (GRCm39) |
G582S |
possibly damaging |
Het |
| Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
| Vmn2r114 |
T |
C |
17: 23,515,956 (GRCm39) |
T512A |
probably benign |
Het |
| Wee1 |
T |
C |
7: 109,723,744 (GRCm39) |
S220P |
probably benign |
Het |
|
| Other mutations in Thbs3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL02927:Thbs3
|
APN |
3 |
89,127,514 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02980:Thbs3
|
UTSW |
3 |
89,130,451 (GRCm39) |
missense |
probably benign |
|
|
R0648:Thbs3
|
UTSW |
3 |
89,123,972 (GRCm39) |
splice site |
probably null |
|
|
R0690:Thbs3
|
UTSW |
3 |
89,127,472 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R1856:Thbs3
|
UTSW |
3 |
89,133,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1928:Thbs3
|
UTSW |
3 |
89,125,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2116:Thbs3
|
UTSW |
3 |
89,126,699 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4600:Thbs3
|
UTSW |
3 |
89,131,897 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4719:Thbs3
|
UTSW |
3 |
89,124,147 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4947:Thbs3
|
UTSW |
3 |
89,133,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4989:Thbs3
|
UTSW |
3 |
89,130,409 (GRCm39) |
intron |
probably benign |
|
|
R5134:Thbs3
|
UTSW |
3 |
89,130,409 (GRCm39) |
intron |
probably benign |
|
|
R5217:Thbs3
|
UTSW |
3 |
89,130,471 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5305:Thbs3
|
UTSW |
3 |
89,125,283 (GRCm39) |
intron |
probably benign |
|
|
R5354:Thbs3
|
UTSW |
3 |
89,128,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5444:Thbs3
|
UTSW |
3 |
89,130,692 (GRCm39) |
intron |
probably benign |
|
|
R5569:Thbs3
|
UTSW |
3 |
89,126,770 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5646:Thbs3
|
UTSW |
3 |
89,126,405 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5801:Thbs3
|
UTSW |
3 |
89,131,704 (GRCm39) |
missense |
probably benign |
0.15 |
|
R5886:Thbs3
|
UTSW |
3 |
89,127,470 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6031:Thbs3
|
UTSW |
3 |
89,125,401 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6031:Thbs3
|
UTSW |
3 |
89,125,401 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6943:Thbs3
|
UTSW |
3 |
89,132,171 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7017:Thbs3
|
UTSW |
3 |
89,131,722 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7352:Thbs3
|
UTSW |
3 |
89,132,587 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7570:Thbs3
|
UTSW |
3 |
89,126,359 (GRCm39) |
nonsense |
probably null |
|
|
R7671:Thbs3
|
UTSW |
3 |
89,124,014 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7707:Thbs3
|
UTSW |
3 |
89,132,207 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8255:Thbs3
|
UTSW |
3 |
89,132,565 (GRCm39) |
missense |
probably benign |
|
|
R8341:Thbs3
|
UTSW |
3 |
89,132,698 (GRCm39) |
missense |
probably benign |
|
|
R8769:Thbs3
|
UTSW |
3 |
89,131,937 (GRCm39) |
intron |
probably benign |
|
|
R9536:Thbs3
|
UTSW |
3 |
89,124,044 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
| Posted On |
2014-02-04 |
Incidental Mutation