Incidental Mutation 'R9368:Fgfr3'
ID |
709111 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Fgfr3
|
Ensembl Gene |
ENSMUSG00000054252 |
Gene Name |
fibroblast growth factor receptor 3 |
Synonyms |
sam3, Fgfr-3, HBGFR |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.364)
|
Stock # |
R9368 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
33879068-33894412 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 33885216 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Glutamine
at position 110
(R110Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000070998
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000067150]
[ENSMUST00000087820]
[ENSMUST00000114411]
[ENSMUST00000155002]
[ENSMUST00000164207]
[ENSMUST00000169212]
[ENSMUST00000171509]
[ENSMUST00000201295]
[ENSMUST00000201437]
[ENSMUST00000202138]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably benign
Transcript: ENSMUST00000067150
AA Change: R110Q
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000070998 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
low complexity region
|
125 |
144 |
N/A |
INTRINSIC |
IGc2
|
161 |
229 |
1.2e-15 |
SMART |
IGc2
|
260 |
340 |
3.28e-8 |
SMART |
transmembrane domain
|
367 |
389 |
N/A |
INTRINSIC |
TyrKc
|
466 |
742 |
3.14e-153 |
SMART |
low complexity region
|
765 |
781 |
N/A |
INTRINSIC |
low complexity region
|
789 |
798 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000087820
AA Change: R110Q
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000085122 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
IGc2
|
143 |
211 |
1.2e-15 |
SMART |
IGc2
|
242 |
322 |
3.28e-8 |
SMART |
transmembrane domain
|
349 |
371 |
N/A |
INTRINSIC |
TyrKc
|
448 |
724 |
3.14e-153 |
SMART |
low complexity region
|
747 |
763 |
N/A |
INTRINSIC |
low complexity region
|
771 |
780 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000114411
AA Change: R110Q
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000110053 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
low complexity region
|
125 |
144 |
N/A |
INTRINSIC |
IGc2
|
161 |
229 |
1.2e-15 |
SMART |
IGc2
|
260 |
339 |
2.77e-6 |
SMART |
transmembrane domain
|
369 |
391 |
N/A |
INTRINSIC |
TyrKc
|
468 |
744 |
3.14e-153 |
SMART |
low complexity region
|
767 |
783 |
N/A |
INTRINSIC |
low complexity region
|
791 |
800 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000155002
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000164207
AA Change: R110Q
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000133064 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
low complexity region
|
125 |
144 |
N/A |
INTRINSIC |
IGc2
|
161 |
229 |
1.2e-15 |
SMART |
IGc2
|
260 |
340 |
3.28e-8 |
SMART |
transmembrane domain
|
367 |
389 |
N/A |
INTRINSIC |
TyrKc
|
467 |
743 |
3.14e-153 |
SMART |
low complexity region
|
766 |
782 |
N/A |
INTRINSIC |
low complexity region
|
790 |
799 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000169212
AA Change: R110Q
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000130856 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
low complexity region
|
125 |
144 |
N/A |
INTRINSIC |
IGc2
|
161 |
229 |
1.2e-15 |
SMART |
IGc2
|
260 |
340 |
3.28e-8 |
SMART |
transmembrane domain
|
367 |
389 |
N/A |
INTRINSIC |
TyrKc
|
466 |
742 |
3.14e-153 |
SMART |
low complexity region
|
765 |
781 |
N/A |
INTRINSIC |
low complexity region
|
789 |
798 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000171509
AA Change: R110Q
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
SMART Domains |
Protein: ENSMUSP00000131845 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
low complexity region
|
125 |
144 |
N/A |
INTRINSIC |
IGc2
|
161 |
229 |
1.2e-15 |
SMART |
IGc2
|
260 |
339 |
2.77e-6 |
SMART |
transmembrane domain
|
369 |
391 |
N/A |
INTRINSIC |
TyrKc
|
468 |
744 |
3.14e-153 |
SMART |
low complexity region
|
767 |
783 |
N/A |
INTRINSIC |
low complexity region
|
791 |
800 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000181298
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201295
|
SMART Domains |
Protein: ENSMUSP00000144104 Gene: ENSMUSG00000054252
Domain | Start | End | E-Value | Type |
IG
|
11 |
71 |
1.9e-3 |
SMART |
transmembrane domain
|
90 |
112 |
N/A |
INTRINSIC |
PDB:2PSQ|B
|
126 |
223 |
2e-30 |
PDB |
Blast:IG_like
|
140 |
223 |
2e-51 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201437
AA Change: R110Q
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000144379 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
2e-6 |
SMART |
Pfam:Ig_3
|
144 |
194 |
2.1e-3 |
PFAM |
Pfam:I-set
|
153 |
194 |
9.2e-6 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202138
AA Change: R110Q
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
SMART Domains |
Protein: ENSMUSP00000143945 Gene: ENSMUSG00000054252 AA Change: R110Q
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
IGc2
|
50 |
114 |
5.01e-4 |
SMART |
IGc2
|
143 |
211 |
1.2e-15 |
SMART |
IGc2
|
242 |
322 |
3.28e-8 |
SMART |
transmembrane domain
|
349 |
371 |
N/A |
INTRINSIC |
TyrKc
|
448 |
724 |
3.14e-153 |
SMART |
low complexity region
|
747 |
763 |
N/A |
INTRINSIC |
low complexity region
|
771 |
780 |
N/A |
INTRINSIC |
|
Predicted Effect |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: This gene encodes a member of the fibroblast growth factor receptor family. Members of this family are highly conserved proteins that differ from one another in their ligand affinities and tissue distribution. A representative protein consists of an extracellular region composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment, and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This family member binds acidic and basic fibroblast growth hormone and plays a role in bone development and maintenance. Mutations in this gene may be associated with craniosynostosis and multiple types of skeletal dysplasia. A pseudogene of this gene is located on chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Apr 2011] PHENOTYPE: Mutant alleles generally cause skeletal deformities, with some causing decreased body size, premature death, or hearing loss due to developmental defects of the ear. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,640,251 (GRCm39) |
L79H |
probably damaging |
Het |
Alb |
A |
G |
5: 90,623,143 (GRCm39) |
T601A |
probably benign |
Het |
Aldh1l2 |
A |
T |
10: 83,331,816 (GRCm39) |
L776* |
probably null |
Het |
Ank3 |
A |
G |
10: 69,823,329 (GRCm39) |
K666R |
|
Het |
Ankrd17 |
T |
C |
5: 90,391,986 (GRCm39) |
T1895A |
possibly damaging |
Het |
Ankrd17 |
C |
T |
5: 90,416,508 (GRCm39) |
R1108Q |
probably damaging |
Het |
Ap2a2 |
T |
C |
7: 141,207,815 (GRCm39) |
F738L |
probably benign |
Het |
Ap4m1 |
T |
A |
5: 138,175,445 (GRCm39) |
C319* |
probably null |
Het |
Arsj |
C |
T |
3: 126,232,745 (GRCm39) |
T497M |
probably damaging |
Het |
Begain |
G |
T |
12: 108,999,918 (GRCm39) |
S284R |
probably damaging |
Het |
Bicc1 |
A |
T |
10: 70,785,917 (GRCm39) |
N408K |
probably benign |
Het |
Cacybp |
T |
C |
1: 160,031,208 (GRCm39) |
M207V |
possibly damaging |
Het |
Cct8l1 |
A |
G |
5: 25,721,336 (GRCm39) |
D17G |
probably benign |
Het |
Cd1d1 |
C |
A |
3: 86,905,939 (GRCm39) |
|
probably null |
Het |
Chd3 |
C |
T |
11: 69,251,200 (GRCm39) |
C554Y |
probably damaging |
Het |
Chsy1 |
A |
G |
7: 65,821,499 (GRCm39) |
D578G |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,663,300 (GRCm39) |
Q79R |
possibly damaging |
Het |
Cpne4 |
A |
T |
9: 104,563,738 (GRCm39) |
R38S |
probably damaging |
Het |
Cyp3a57 |
A |
G |
5: 145,318,159 (GRCm39) |
D380G |
probably benign |
Het |
Dnah6 |
A |
T |
6: 72,998,261 (GRCm39) |
S4054T |
probably benign |
Het |
Emb |
G |
T |
13: 117,357,096 (GRCm39) |
|
probably benign |
Het |
Eml5 |
T |
C |
12: 98,762,837 (GRCm39) |
R1648G |
probably benign |
Het |
Fam117b |
A |
T |
1: 60,020,740 (GRCm39) |
M537L |
probably benign |
Het |
Fcrl2 |
C |
T |
3: 87,164,906 (GRCm39) |
V207I |
possibly damaging |
Het |
Ffar1 |
A |
G |
7: 30,560,457 (GRCm39) |
S147P |
probably benign |
Het |
Frmd6 |
T |
A |
12: 70,933,865 (GRCm39) |
|
probably null |
Het |
Fry |
A |
G |
5: 150,401,403 (GRCm39) |
R356G |
|
Het |
Fsip2 |
A |
G |
2: 82,811,039 (GRCm39) |
R2453G |
possibly damaging |
Het |
Glipr1l3 |
G |
A |
10: 111,983,923 (GRCm39) |
T181I |
probably benign |
Het |
Hoxc10 |
A |
G |
15: 102,879,382 (GRCm39) |
I301V |
possibly damaging |
Het |
Igf2bp2 |
T |
A |
16: 21,883,895 (GRCm39) |
D463V |
probably damaging |
Het |
Ints13 |
T |
C |
6: 146,467,129 (GRCm39) |
D194G |
probably null |
Het |
Kif5c |
A |
T |
2: 49,622,792 (GRCm39) |
E548V |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,357,979 (GRCm39) |
D350G |
probably damaging |
Het |
Lrrc61 |
T |
C |
6: 48,545,245 (GRCm39) |
S23P |
possibly damaging |
Het |
Mcpt4 |
T |
C |
14: 56,299,134 (GRCm39) |
M35V |
probably damaging |
Het |
Mical1 |
T |
A |
10: 41,357,302 (GRCm39) |
M369K |
possibly damaging |
Het |
Mre11a |
T |
A |
9: 14,736,514 (GRCm39) |
F548L |
probably benign |
Het |
Muc20 |
C |
T |
16: 32,614,471 (GRCm39) |
C302Y |
possibly damaging |
Het |
Nlgn1 |
T |
C |
3: 25,488,622 (GRCm39) |
D571G |
probably damaging |
Het |
Nup88 |
T |
C |
11: 70,858,756 (GRCm39) |
K131E |
probably damaging |
Het |
Nwd2 |
A |
G |
5: 63,962,306 (GRCm39) |
D630G |
probably damaging |
Het |
Or3a1 |
A |
G |
11: 74,225,193 (GRCm39) |
L288P |
probably damaging |
Het |
Or5h19 |
C |
T |
16: 58,856,678 (GRCm39) |
V141M |
probably benign |
Het |
Or6c212 |
A |
T |
10: 129,558,881 (GRCm39) |
C177* |
probably null |
Het |
Pdzd8 |
A |
T |
19: 59,289,219 (GRCm39) |
L727* |
probably null |
Het |
Pi16 |
T |
A |
17: 29,546,852 (GRCm39) |
N475K |
probably benign |
Het |
Pikfyve |
G |
A |
1: 65,307,901 (GRCm39) |
A1826T |
probably damaging |
Het |
Plxna1 |
A |
T |
6: 89,314,138 (GRCm39) |
S768T |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,700,599 (GRCm39) |
R656* |
probably null |
Het |
Poglut1 |
A |
G |
16: 38,349,850 (GRCm39) |
W308R |
probably damaging |
Het |
Prmt9 |
T |
G |
8: 78,285,663 (GRCm39) |
V165G |
probably benign |
Het |
Ptch2 |
A |
G |
4: 116,961,969 (GRCm39) |
E102G |
probably damaging |
Het |
Rpn2 |
G |
T |
2: 157,141,500 (GRCm39) |
A303S |
possibly damaging |
Het |
Rttn |
A |
C |
18: 89,078,576 (GRCm39) |
H1334P |
probably damaging |
Het |
Septin3 |
A |
T |
15: 82,163,739 (GRCm39) |
D32V |
probably damaging |
Het |
Sftpa1 |
G |
T |
14: 40,854,417 (GRCm39) |
M1I |
probably null |
Het |
Slc15a2 |
G |
A |
16: 36,574,080 (GRCm39) |
T591I |
probably benign |
Het |
Slc18a2 |
C |
T |
19: 59,262,791 (GRCm39) |
T252I |
probably benign |
Het |
Smchd1 |
A |
G |
17: 71,694,071 (GRCm39) |
F1225L |
probably damaging |
Het |
Sppl2c |
G |
A |
11: 104,078,561 (GRCm39) |
G454S |
probably damaging |
Het |
Swt1 |
A |
G |
1: 151,286,767 (GRCm39) |
S242P |
possibly damaging |
Het |
Tcaim |
C |
A |
9: 122,647,928 (GRCm39) |
H148N |
probably damaging |
Het |
Tgfbr3l |
T |
C |
8: 4,299,640 (GRCm39) |
V141A |
probably damaging |
Het |
Ticrr |
A |
G |
7: 79,330,735 (GRCm39) |
D711G |
probably damaging |
Het |
Trim45 |
A |
T |
3: 100,832,319 (GRCm39) |
Q184L |
possibly damaging |
Het |
Tyw1 |
G |
A |
5: 130,298,065 (GRCm39) |
R202Q |
probably damaging |
Het |
Usp25 |
G |
A |
16: 76,904,843 (GRCm39) |
R803H |
probably damaging |
Het |
Vmn2r71 |
T |
A |
7: 85,273,442 (GRCm39) |
M752K |
probably damaging |
Het |
Wdr35 |
G |
A |
12: 9,071,826 (GRCm39) |
V893I |
probably benign |
Het |
Zdhhc7 |
G |
T |
8: 120,814,494 (GRCm39) |
P105Q |
probably damaging |
Het |
Zfp316 |
A |
G |
5: 143,250,046 (GRCm39) |
|
probably null |
Het |
Zfp454 |
G |
C |
11: 50,764,537 (GRCm39) |
N298K |
possibly damaging |
Het |
Zfp7 |
TGCGGGAAAGGTTTCCACCTGAGCG |
TGCG |
15: 76,774,800 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Fgfr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00705:Fgfr3
|
APN |
5 |
33,892,484 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL01585:Fgfr3
|
APN |
5 |
33,891,305 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03266:Fgfr3
|
APN |
5 |
33,891,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03285:Fgfr3
|
APN |
5 |
33,892,557 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4280001:Fgfr3
|
UTSW |
5 |
33,889,576 (GRCm39) |
missense |
probably benign |
0.13 |
R0543:Fgfr3
|
UTSW |
5 |
33,887,054 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R0604:Fgfr3
|
UTSW |
5 |
33,890,126 (GRCm39) |
missense |
probably damaging |
0.99 |
R1496:Fgfr3
|
UTSW |
5 |
33,887,094 (GRCm39) |
missense |
probably damaging |
0.96 |
R1861:Fgfr3
|
UTSW |
5 |
33,887,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Fgfr3
|
UTSW |
5 |
33,891,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R2920:Fgfr3
|
UTSW |
5 |
33,891,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4361:Fgfr3
|
UTSW |
5 |
33,880,676 (GRCm39) |
intron |
probably benign |
|
R4506:Fgfr3
|
UTSW |
5 |
33,887,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R4513:Fgfr3
|
UTSW |
5 |
33,880,460 (GRCm39) |
intron |
probably benign |
|
R4647:Fgfr3
|
UTSW |
5 |
33,892,330 (GRCm39) |
unclassified |
probably benign |
|
R5240:Fgfr3
|
UTSW |
5 |
33,887,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R5251:Fgfr3
|
UTSW |
5 |
33,892,900 (GRCm39) |
unclassified |
probably benign |
|
R5454:Fgfr3
|
UTSW |
5 |
33,880,642 (GRCm39) |
intron |
probably benign |
|
R5595:Fgfr3
|
UTSW |
5 |
33,887,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Fgfr3
|
UTSW |
5 |
33,887,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Fgfr3
|
UTSW |
5 |
33,889,503 (GRCm39) |
missense |
probably benign |
0.35 |
R6985:Fgfr3
|
UTSW |
5 |
33,892,785 (GRCm39) |
missense |
probably null |
1.00 |
R7106:Fgfr3
|
UTSW |
5 |
33,888,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Fgfr3
|
UTSW |
5 |
33,890,092 (GRCm39) |
frame shift |
probably null |
|
R7319:Fgfr3
|
UTSW |
5 |
33,885,146 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7373:Fgfr3
|
UTSW |
5 |
33,885,034 (GRCm39) |
missense |
probably benign |
0.00 |
R7497:Fgfr3
|
UTSW |
5 |
33,892,766 (GRCm39) |
frame shift |
probably null |
|
R7498:Fgfr3
|
UTSW |
5 |
33,892,766 (GRCm39) |
frame shift |
probably null |
|
R7499:Fgfr3
|
UTSW |
5 |
33,892,766 (GRCm39) |
frame shift |
probably null |
|
R7883:Fgfr3
|
UTSW |
5 |
33,891,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Fgfr3
|
UTSW |
5 |
33,891,250 (GRCm39) |
missense |
probably damaging |
0.98 |
R8179:Fgfr3
|
UTSW |
5 |
33,885,099 (GRCm39) |
missense |
probably benign |
0.00 |
R8422:Fgfr3
|
UTSW |
5 |
33,892,249 (GRCm39) |
nonsense |
probably null |
|
R8935:Fgfr3
|
UTSW |
5 |
33,892,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R9179:Fgfr3
|
UTSW |
5 |
33,887,316 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9414:Fgfr3
|
UTSW |
5 |
33,887,298 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9689:Fgfr3
|
UTSW |
5 |
33,892,248 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Predicted Primers |
PCR Primer
(F):5'- TTTACTCCACAGAGGTTCCAGG -3'
(R):5'- GCCATTCATTCAGATGGCACC -3'
Sequencing Primer
(F):5'- TTCCAGGGCCTGAACCTAG -3'
(R):5'- TCATTCAGATGGCACCTACTTAGGG -3'
|
Posted On |
2022-04-18 |