Incidental Mutation 'R9396:Ibsp'
| ID |
710823 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ibsp
|
| Ensembl Gene |
ENSMUSG00000029306 |
| Gene Name |
integrin binding sialoprotein |
| Synonyms |
Bsp2, bone sialoprotein, BSP, Bsp |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.084)
|
| Stock # |
R9396 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
5 |
| Chromosomal Location |
104447153-104459338 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 104458297 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 278
(Y278C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000031246
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000031246]
|
| AlphaFold |
Q61711 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000031246
AA Change: Y278C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000031246
Gene: ENSMUSG00000029306
AA Change: Y278C
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
16 |
N/A |
INTRINSIC |
|
Pfam:BSP_II
|
17 |
321 |
2.8e-127 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.2%
|
| Validation Efficiency |
98% (56/57) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a major structural protein of the bone matrix. It constitutes approximately 12% of the noncollagenous proteins in human bone and is synthesized by skeletal-associated cell types, including hypertrophic chondrocytes, osteoblasts, osteocytes, and osteoclasts. The only extraskeletal site of its synthesis is the trophoblast. This protein binds to calcium and hydroxyapatite via its acidic amino acid clusters, and mediates cell attachment through an RGD sequence that recognizes the vitronectin receptor. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele show reduced body weight/size, delayed long bone growth and mineralization with low bone turn over due to reduced osteoclast formation, delayed intramembranous ossification, progressive periodontal breakdown, and severe alveolar and mandibular bone loss. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(3) : Targeted, knock-out(1) Targeted, other(2)
|
| Other mutations in this stock |
Total: 57 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcg8 |
T |
A |
17: 85,000,282 (GRCm39) |
F281I |
probably damaging |
Het |
| Acad8 |
A |
G |
9: 26,887,041 (GRCm39) |
M402T |
probably damaging |
Het |
| Apcdd1 |
C |
T |
18: 63,055,731 (GRCm39) |
|
probably benign |
Het |
| Apol7a |
T |
C |
15: 77,273,925 (GRCm39) |
E179G |
possibly damaging |
Het |
| Asmt |
A |
G |
X: 169,110,141 (GRCm39) |
T217A |
probably benign |
Het |
| Cadm2 |
T |
C |
16: 66,544,102 (GRCm39) |
Y318C |
probably damaging |
Het |
| Cckar |
G |
A |
5: 53,864,623 (GRCm39) |
T26M |
probably damaging |
Het |
| Cd300ld |
G |
A |
11: 114,878,230 (GRCm39) |
T94I |
probably damaging |
Het |
| Cdk5rap2 |
A |
G |
4: 70,172,903 (GRCm39) |
Y1390H |
possibly damaging |
Het |
| Cdk5rap2 |
C |
T |
4: 70,182,895 (GRCm39) |
S1268N |
probably damaging |
Het |
| Csrnp3 |
C |
T |
2: 65,832,841 (GRCm39) |
R127C |
probably damaging |
Het |
| Dsc2 |
T |
A |
18: 20,174,773 (GRCm39) |
R501* |
probably null |
Het |
| Dusp2 |
C |
T |
2: 127,179,638 (GRCm39) |
R294C |
probably damaging |
Het |
| Edrf1 |
A |
G |
7: 133,261,838 (GRCm39) |
K878E |
possibly damaging |
Het |
| Evc |
T |
C |
5: 37,476,434 (GRCm39) |
T372A |
possibly damaging |
Het |
| Fcgr1 |
T |
A |
3: 96,194,390 (GRCm39) |
K166* |
probably null |
Het |
| Fstl4 |
C |
A |
11: 52,664,778 (GRCm39) |
P36Q |
probably benign |
Het |
| Gas2l2 |
A |
T |
11: 83,313,659 (GRCm39) |
I551N |
probably benign |
Het |
| Hc |
G |
T |
2: 34,927,615 (GRCm39) |
S333* |
probably null |
Het |
| Ifitm10 |
A |
T |
7: 141,924,704 (GRCm39) |
V45D |
probably damaging |
Het |
| Kcnc3 |
T |
C |
7: 44,240,937 (GRCm39) |
S210P |
possibly damaging |
Het |
| Klhl3 |
T |
G |
13: 58,161,662 (GRCm39) |
T531P |
probably damaging |
Het |
| Mapt |
C |
A |
11: 104,189,555 (GRCm39) |
P191Q |
possibly damaging |
Het |
| Myh9 |
T |
C |
15: 77,647,496 (GRCm39) |
T1840A |
probably benign |
Het |
| Myof |
A |
T |
19: 37,923,294 (GRCm39) |
C1320S |
probably damaging |
Het |
| Myom3 |
G |
T |
4: 135,513,199 (GRCm39) |
V626L |
probably benign |
Het |
| Nalf2 |
C |
T |
X: 98,889,097 (GRCm39) |
R321W |
probably damaging |
Het |
| Ndor1 |
A |
G |
2: 25,138,921 (GRCm39) |
L321P |
probably benign |
Het |
| Nhsl1 |
T |
A |
10: 18,399,749 (GRCm39) |
M291K |
probably damaging |
Het |
| Nubp2 |
C |
T |
17: 25,103,476 (GRCm39) |
V134I |
probably benign |
Het |
| Nuf2 |
T |
C |
1: 169,337,917 (GRCm39) |
I287V |
probably benign |
Het |
| Or1d2 |
T |
A |
11: 74,256,089 (GRCm39) |
M198K |
probably benign |
Het |
| Or2n1 |
T |
A |
17: 38,486,421 (GRCm39) |
W149R |
probably damaging |
Het |
| Or4k42 |
A |
G |
2: 111,319,864 (GRCm39) |
L213P |
probably benign |
Het |
| Or51i2 |
A |
G |
7: 103,689,720 (GRCm39) |
N239S |
probably benign |
Het |
| Or55b4 |
A |
C |
7: 102,134,180 (GRCm39) |
V49G |
possibly damaging |
Het |
| Or5k3 |
G |
A |
16: 58,969,302 (GRCm39) |
V30M |
probably damaging |
Het |
| Or8k28 |
A |
T |
2: 86,285,845 (GRCm39) |
C257S |
probably benign |
Het |
| Pals1 |
G |
T |
12: 78,871,521 (GRCm39) |
R367L |
possibly damaging |
Het |
| Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
| Ppp1r12a |
A |
G |
10: 108,100,571 (GRCm39) |
E863G |
probably damaging |
Het |
| Pskh1 |
C |
T |
8: 106,640,091 (GRCm39) |
T257M |
possibly damaging |
Het |
| Rasgef1b |
T |
C |
5: 99,377,188 (GRCm39) |
I334V |
probably benign |
Het |
| Rnf180 |
T |
A |
13: 105,318,027 (GRCm39) |
K462* |
probably null |
Het |
| Sin3a |
A |
G |
9: 57,008,445 (GRCm39) |
D455G |
probably benign |
Het |
| Slc15a4 |
A |
G |
5: 127,694,463 (GRCm39) |
|
probably benign |
Het |
| Slc2a13 |
T |
C |
15: 91,227,915 (GRCm39) |
T426A |
probably benign |
Het |
| Smarca5 |
T |
C |
8: 81,463,358 (GRCm39) |
K70R |
probably benign |
Het |
| Smg1 |
A |
G |
7: 117,807,303 (GRCm39) |
V182A |
unknown |
Het |
| Stim1 |
G |
A |
7: 102,064,592 (GRCm39) |
V221I |
possibly damaging |
Het |
| Tbx18 |
T |
C |
9: 87,609,432 (GRCm39) |
D201G |
probably damaging |
Het |
| Tcf25 |
A |
G |
8: 124,127,831 (GRCm39) |
E630G |
probably benign |
Het |
| Tm7sf3 |
T |
C |
6: 146,523,472 (GRCm39) |
N135S |
possibly damaging |
Het |
| Togaram1 |
A |
G |
12: 65,014,429 (GRCm39) |
N560S |
probably damaging |
Het |
| Unc13d |
A |
G |
11: 115,966,529 (GRCm39) |
|
probably null |
Het |
| Zfp445 |
A |
C |
9: 122,681,581 (GRCm39) |
S787A |
probably benign |
Het |
| Zfp949 |
T |
C |
9: 88,449,260 (GRCm39) |
W22R |
probably damaging |
Het |
|
| Other mutations in Ibsp |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00687:Ibsp
|
APN |
5 |
104,457,934 (GRCm39) |
missense |
probably benign |
0.27 |
|
IGL02317:Ibsp
|
APN |
5 |
104,450,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02539:Ibsp
|
APN |
5 |
104,450,149 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03236:Ibsp
|
APN |
5 |
104,453,871 (GRCm39) |
missense |
probably benign |
0.30 |
|
crunch
|
UTSW |
5 |
104,457,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
I2289:Ibsp
|
UTSW |
5 |
104,450,353 (GRCm39) |
missense |
possibly damaging |
0.64 |
|
PIT4445001:Ibsp
|
UTSW |
5 |
104,450,170 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R0049:Ibsp
|
UTSW |
5 |
104,450,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Ibsp
|
UTSW |
5 |
104,450,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0234:Ibsp
|
UTSW |
5 |
104,457,935 (GRCm39) |
small deletion |
probably benign |
|
|
R0610:Ibsp
|
UTSW |
5 |
104,458,000 (GRCm39) |
missense |
probably benign |
0.07 |
|
R0656:Ibsp
|
UTSW |
5 |
104,457,886 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R1168:Ibsp
|
UTSW |
5 |
104,450,018 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1440:Ibsp
|
UTSW |
5 |
104,458,405 (GRCm39) |
missense |
unknown |
|
|
R1569:Ibsp
|
UTSW |
5 |
104,458,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1921:Ibsp
|
UTSW |
5 |
104,458,078 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2172:Ibsp
|
UTSW |
5 |
104,458,296 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2879:Ibsp
|
UTSW |
5 |
104,458,260 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4399:Ibsp
|
UTSW |
5 |
104,457,148 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4517:Ibsp
|
UTSW |
5 |
104,453,863 (GRCm39) |
nonsense |
probably null |
|
|
R5417:Ibsp
|
UTSW |
5 |
104,458,335 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5575:Ibsp
|
UTSW |
5 |
104,457,925 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R6183:Ibsp
|
UTSW |
5 |
104,453,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6273:Ibsp
|
UTSW |
5 |
104,458,167 (GRCm39) |
missense |
probably benign |
0.15 |
|
R6295:Ibsp
|
UTSW |
5 |
104,449,987 (GRCm39) |
splice site |
probably null |
|
|
R7061:Ibsp
|
UTSW |
5 |
104,457,768 (GRCm39) |
splice site |
probably null |
|
|
R7133:Ibsp
|
UTSW |
5 |
104,450,172 (GRCm39) |
nonsense |
probably null |
|
|
R7202:Ibsp
|
UTSW |
5 |
104,450,027 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7205:Ibsp
|
UTSW |
5 |
104,458,297 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7769:Ibsp
|
UTSW |
5 |
104,458,050 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R7769:Ibsp
|
UTSW |
5 |
104,453,871 (GRCm39) |
missense |
probably benign |
0.15 |
|
R8506:Ibsp
|
UTSW |
5 |
104,457,947 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8840:Ibsp
|
UTSW |
5 |
104,458,006 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9431:Ibsp
|
UTSW |
5 |
104,457,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAGCGTCACTGAAGCAGGTG -3'
(R):5'- GCACCTTCCTGAGTTGAATTTTG -3'
Sequencing Primer
(F):5'- TCACTGAAGCAGGTGCAGAAG -3'
(R):5'- TGGGGAATTCAAATGGGGAAATTCC -3'
|
| Posted On |
2022-04-18 |
Incidental Mutation