Incidental Mutation 'R9745:Pcdh7'
| ID |
732035 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Pcdh7
|
| Ensembl Gene |
ENSMUSG00000029108 |
| Gene Name |
protocadherin 7 |
| Synonyms |
BH-protocadherin |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.119)
|
| Stock # |
R9745 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
5 |
| Chromosomal Location |
57875309-58290572 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
T to C
at 57879622 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142319
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000068110]
[ENSMUST00000094783]
[ENSMUST00000191837]
[ENSMUST00000199310]
|
| AlphaFold |
A0A0A6YY83 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000068110
|
| SMART Domains |
Protein: ENSMUSP00000066306
Gene: ENSMUSG00000029108
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
30 |
N/A |
INTRINSIC |
|
CA
|
48 |
141 |
7.29e-4 |
SMART |
|
CA
|
165 |
306 |
1.13e-18 |
SMART |
|
CA
|
330 |
413 |
2.12e-23 |
SMART |
|
CA
|
445 |
533 |
1.53e-20 |
SMART |
|
CA
|
557 |
637 |
1.36e-26 |
SMART |
|
CA
|
661 |
740 |
2.38e-26 |
SMART |
|
CA
|
766 |
847 |
2.01e-15 |
SMART |
|
transmembrane domain
|
878 |
900 |
N/A |
INTRINSIC |
|
low complexity region
|
929 |
944 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000094783
|
| SMART Domains |
Protein: ENSMUSP00000092376
Gene: ENSMUSG00000029108
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
30 |
N/A |
INTRINSIC |
|
CA
|
48 |
141 |
7.29e-4 |
SMART |
|
CA
|
165 |
306 |
1.13e-18 |
SMART |
|
CA
|
330 |
413 |
2.12e-23 |
SMART |
|
CA
|
445 |
533 |
1.53e-20 |
SMART |
|
CA
|
557 |
637 |
1.36e-26 |
SMART |
|
CA
|
661 |
740 |
2.38e-26 |
SMART |
|
CA
|
766 |
847 |
2.01e-15 |
SMART |
|
transmembrane domain
|
878 |
900 |
N/A |
INTRINSIC |
|
low complexity region
|
929 |
944 |
N/A |
INTRINSIC |
|
low complexity region
|
1088 |
1099 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000191837
|
| SMART Domains |
Protein: ENSMUSP00000142319
Gene: ENSMUSG00000029108
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
30 |
N/A |
INTRINSIC |
|
CA
|
48 |
141 |
7.29e-4 |
SMART |
|
CA
|
165 |
306 |
1.13e-18 |
SMART |
|
CA
|
330 |
413 |
2.12e-23 |
SMART |
|
CA
|
445 |
533 |
1.53e-20 |
SMART |
|
CA
|
557 |
637 |
1.36e-26 |
SMART |
|
CA
|
661 |
740 |
2.38e-26 |
SMART |
|
CA
|
766 |
847 |
2.01e-15 |
SMART |
|
transmembrane domain
|
878 |
900 |
N/A |
INTRINSIC |
|
low complexity region
|
929 |
944 |
N/A |
INTRINSIC |
|
low complexity region
|
1088 |
1099 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192048
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000192287
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195156
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000199310
|
| SMART Domains |
Protein: ENSMUSP00000143387
Gene: ENSMUSG00000029108
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Protocadherin
|
1 |
79 |
5.1e-40 |
PFAM |
|
low complexity region
|
112 |
123 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.6%
- 10x: 99.1%
- 20x: 97.9%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The gene encodes a protein with an extracellular domain containing 7 cadherin repeats. The gene product is an integral membrane protein that is thought to function in cell-cell recognition and adhesion. Alternative splicing yields isoforms with unique cytoplasmic tails. [provided by RefSeq, Jul 2008]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Agap2 |
T |
A |
10: 126,919,380 (GRCm39) |
H488Q |
unknown |
Het |
| Ces1b |
T |
C |
8: 93,790,625 (GRCm39) |
D388G |
probably benign |
Het |
| Ces1f |
T |
C |
8: 93,989,740 (GRCm39) |
D392G |
probably benign |
Het |
| Ces5a |
A |
G |
8: 94,228,814 (GRCm39) |
V472A |
probably damaging |
Het |
| Chst1 |
A |
G |
2: 92,444,047 (GRCm39) |
D173G |
possibly damaging |
Het |
| Cngb1 |
T |
G |
8: 95,967,919 (GRCm39) |
E1294A |
unknown |
Het |
| Cnmd |
T |
C |
14: 79,887,850 (GRCm39) |
I124V |
possibly damaging |
Het |
| Cntnap2 |
A |
T |
6: 46,211,100 (GRCm39) |
M505L |
probably benign |
Het |
| Cntnap4 |
T |
A |
8: 113,391,808 (GRCm39) |
M91K |
possibly damaging |
Het |
| Cstad |
A |
G |
2: 30,498,197 (GRCm39) |
T11A |
unknown |
Het |
| Cyp2j6 |
A |
T |
4: 96,441,621 (GRCm39) |
V23E |
possibly damaging |
Het |
| Dapk3 |
C |
A |
10: 81,028,594 (GRCm39) |
T388K |
unknown |
Het |
| Dennd6a |
G |
A |
14: 26,320,818 (GRCm39) |
G120R |
possibly damaging |
Het |
| Disp1 |
A |
C |
1: 182,869,310 (GRCm39) |
S1037A |
probably damaging |
Het |
| Dpcd |
A |
T |
19: 45,560,881 (GRCm39) |
Q103L |
probably benign |
Het |
| Egfem1 |
A |
T |
3: 29,716,532 (GRCm39) |
D334V |
probably damaging |
Het |
| Egflam |
C |
T |
15: 7,333,419 (GRCm39) |
V178M |
probably benign |
Het |
| Ehbp1 |
T |
C |
11: 22,096,692 (GRCm39) |
T291A |
probably benign |
Het |
| Eif5b |
G |
T |
1: 38,084,729 (GRCm39) |
V859F |
probably damaging |
Het |
| Fam161a |
A |
T |
11: 22,973,495 (GRCm39) |
Q459L |
possibly damaging |
Het |
| Fcgrt |
A |
C |
7: 44,742,754 (GRCm39) |
D342E |
probably damaging |
Het |
| Fchsd1 |
A |
C |
18: 38,102,425 (GRCm39) |
D34E |
probably benign |
Het |
| Foxo4 |
G |
A |
X: 100,301,955 (GRCm39) |
S209N |
probably benign |
Het |
| Galt |
A |
T |
4: 41,758,185 (GRCm39) |
M317L |
possibly damaging |
Het |
| Gfm1 |
A |
G |
3: 67,358,657 (GRCm39) |
D416G |
possibly damaging |
Het |
| Glcci1 |
A |
T |
6: 8,573,278 (GRCm39) |
I256L |
probably benign |
Het |
| Ibtk |
C |
T |
9: 85,613,280 (GRCm39) |
G228S |
probably benign |
Het |
| Ift70b |
T |
C |
2: 75,768,261 (GRCm39) |
Y164C |
probably benign |
Het |
| Il2rb |
T |
A |
15: 78,372,399 (GRCm39) |
D106V |
probably benign |
Het |
| Map3k6 |
A |
T |
4: 132,979,783 (GRCm39) |
I1261F |
probably damaging |
Het |
| Mast2 |
A |
G |
4: 116,167,815 (GRCm39) |
L1014P |
probably benign |
Het |
| Mcm2 |
G |
A |
6: 88,868,729 (GRCm39) |
Q343* |
probably null |
Het |
| Megf8 |
A |
G |
7: 25,058,133 (GRCm39) |
T2136A |
possibly damaging |
Het |
| Mmp28 |
G |
A |
11: 83,342,283 (GRCm39) |
T103I |
probably benign |
Het |
| Mtif2 |
G |
A |
11: 29,476,587 (GRCm39) |
|
probably benign |
Het |
| Mtus2 |
A |
T |
5: 148,013,311 (GRCm39) |
T35S |
possibly damaging |
Het |
| Ncoa2 |
A |
T |
1: 13,245,192 (GRCm39) |
I502N |
probably benign |
Het |
| Nek5 |
A |
C |
8: 22,573,479 (GRCm39) |
D492E |
probably benign |
Het |
| Nin |
T |
C |
12: 70,089,899 (GRCm39) |
E1172G |
|
Het |
| Nsmaf |
T |
A |
4: 6,416,662 (GRCm39) |
I544F |
possibly damaging |
Het |
| Oas3 |
T |
C |
5: 120,899,284 (GRCm39) |
D763G |
unknown |
Het |
| Or2a20 |
G |
A |
6: 43,194,258 (GRCm39) |
W137* |
probably null |
Het |
| Or4s2 |
T |
A |
2: 88,473,310 (GRCm39) |
F66L |
probably benign |
Het |
| Or51r1 |
A |
T |
7: 102,227,861 (GRCm39) |
D53V |
probably damaging |
Het |
| Or5al6 |
C |
T |
2: 85,976,251 (GRCm39) |
V276M |
probably damaging |
Het |
| Or5aq1 |
T |
A |
2: 86,965,783 (GRCm39) |
N294I |
probably damaging |
Het |
| Or5k15 |
A |
T |
16: 58,710,265 (GRCm39) |
L106Q |
probably damaging |
Het |
| Or5t17 |
T |
C |
2: 86,832,487 (GRCm39) |
V58A |
probably benign |
Het |
| Pitx3 |
A |
G |
19: 46,124,660 (GRCm39) |
S236P |
possibly damaging |
Het |
| Plscr5 |
T |
A |
9: 92,087,502 (GRCm39) |
I157N |
probably damaging |
Het |
| Potefam1 |
T |
C |
2: 111,000,008 (GRCm39) |
M201V |
unknown |
Het |
| Preb |
T |
C |
5: 31,116,732 (GRCm39) |
N54D |
probably benign |
Het |
| Pskh1 |
C |
T |
8: 106,656,404 (GRCm39) |
A360V |
possibly damaging |
Het |
| Ptprk |
T |
C |
10: 28,139,608 (GRCm39) |
L111S |
possibly damaging |
Het |
| Reln |
T |
A |
5: 22,152,525 (GRCm39) |
I2314F |
probably damaging |
Het |
| Siglecg |
A |
G |
7: 43,067,476 (GRCm39) |
D681G |
probably damaging |
Het |
| Snx5 |
A |
G |
2: 144,096,716 (GRCm39) |
V283A |
probably benign |
Het |
| Srpk2 |
C |
A |
5: 23,880,874 (GRCm39) |
|
probably benign |
Het |
| Tacr1 |
T |
C |
6: 82,469,619 (GRCm39) |
Y168H |
possibly damaging |
Het |
| Tal1 |
G |
T |
4: 114,920,557 (GRCm39) |
R77L |
probably benign |
Het |
| Tdrd12 |
T |
C |
7: 35,185,964 (GRCm39) |
|
probably null |
Het |
| Tdrd7 |
A |
T |
4: 45,994,310 (GRCm39) |
N236I |
possibly damaging |
Het |
| Tdrd9 |
T |
C |
12: 112,009,130 (GRCm39) |
F1012S |
probably damaging |
Het |
| Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
| Tert |
T |
A |
13: 73,784,609 (GRCm39) |
L685Q |
probably damaging |
Het |
| Th |
T |
G |
7: 142,448,851 (GRCm39) |
D342A |
probably damaging |
Het |
| Tpsg1 |
G |
T |
17: 25,591,492 (GRCm39) |
V31L |
probably damaging |
Het |
| Traf3ip1 |
C |
G |
1: 91,439,095 (GRCm39) |
S337* |
probably null |
Het |
| Trpv6 |
A |
G |
6: 41,600,003 (GRCm39) |
F551S |
probably damaging |
Het |
| Urah |
A |
G |
7: 140,415,531 (GRCm39) |
N23D |
probably benign |
Het |
| Vangl1 |
A |
C |
3: 102,072,669 (GRCm39) |
|
probably null |
Het |
| Zc3h6 |
A |
G |
2: 128,859,155 (GRCm39) |
E1062G |
probably benign |
Het |
| Zfp37 |
A |
T |
4: 62,110,644 (GRCm39) |
V181E |
possibly damaging |
Het |
| Zfp638 |
T |
A |
6: 83,921,795 (GRCm39) |
S641T |
probably benign |
Het |
| Zkscan16 |
A |
T |
4: 58,957,473 (GRCm39) |
H585L |
possibly damaging |
Het |
|
| Other mutations in Pcdh7 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00790:Pcdh7
|
APN |
5 |
57,878,806 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00920:Pcdh7
|
APN |
5 |
57,877,473 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL00990:Pcdh7
|
APN |
5 |
57,877,806 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL01367:Pcdh7
|
APN |
5 |
58,286,566 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
IGL01388:Pcdh7
|
APN |
5 |
57,877,546 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01543:Pcdh7
|
APN |
5 |
57,878,107 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01750:Pcdh7
|
APN |
5 |
57,877,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02010:Pcdh7
|
APN |
5 |
58,286,597 (GRCm39) |
missense |
probably benign |
|
|
IGL02014:Pcdh7
|
APN |
5 |
57,877,045 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL02269:Pcdh7
|
APN |
5 |
58,070,664 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03051:Pcdh7
|
APN |
5 |
58,286,415 (GRCm39) |
missense |
probably damaging |
0.99 |
|
floated
|
UTSW |
5 |
57,878,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
proposed
|
UTSW |
5 |
57,879,582 (GRCm39) |
missense |
probably damaging |
0.99 |
|
P0037:Pcdh7
|
UTSW |
5 |
58,070,590 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0003:Pcdh7
|
UTSW |
5 |
58,070,590 (GRCm39) |
missense |
probably benign |
0.17 |
|
R0421:Pcdh7
|
UTSW |
5 |
57,877,402 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0551:Pcdh7
|
UTSW |
5 |
57,879,336 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0562:Pcdh7
|
UTSW |
5 |
57,877,405 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0732:Pcdh7
|
UTSW |
5 |
57,878,657 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0755:Pcdh7
|
UTSW |
5 |
57,877,664 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1080:Pcdh7
|
UTSW |
5 |
57,876,768 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1381:Pcdh7
|
UTSW |
5 |
57,878,882 (GRCm39) |
nonsense |
probably null |
|
|
R1591:Pcdh7
|
UTSW |
5 |
57,877,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1891:Pcdh7
|
UTSW |
5 |
57,878,217 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2011:Pcdh7
|
UTSW |
5 |
57,876,971 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2140:Pcdh7
|
UTSW |
5 |
58,286,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2147:Pcdh7
|
UTSW |
5 |
58,286,458 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R2848:Pcdh7
|
UTSW |
5 |
57,877,618 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2867:Pcdh7
|
UTSW |
5 |
57,879,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2867:Pcdh7
|
UTSW |
5 |
57,879,236 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3719:Pcdh7
|
UTSW |
5 |
58,286,374 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4075:Pcdh7
|
UTSW |
5 |
57,879,150 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4231:Pcdh7
|
UTSW |
5 |
57,876,631 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4236:Pcdh7
|
UTSW |
5 |
57,876,631 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4352:Pcdh7
|
UTSW |
5 |
57,879,361 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R4420:Pcdh7
|
UTSW |
5 |
58,286,512 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4449:Pcdh7
|
UTSW |
5 |
57,877,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4584:Pcdh7
|
UTSW |
5 |
57,878,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4686:Pcdh7
|
UTSW |
5 |
58,286,511 (GRCm39) |
missense |
probably benign |
|
|
R4837:Pcdh7
|
UTSW |
5 |
57,877,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R4838:Pcdh7
|
UTSW |
5 |
57,878,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4947:Pcdh7
|
UTSW |
5 |
57,879,258 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5053:Pcdh7
|
UTSW |
5 |
57,878,943 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5068:Pcdh7
|
UTSW |
5 |
57,879,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5117:Pcdh7
|
UTSW |
5 |
57,879,090 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5132:Pcdh7
|
UTSW |
5 |
57,885,463 (GRCm39) |
missense |
probably benign |
|
|
R5248:Pcdh7
|
UTSW |
5 |
58,286,515 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R5294:Pcdh7
|
UTSW |
5 |
57,885,453 (GRCm39) |
splice site |
probably null |
|
|
R5420:Pcdh7
|
UTSW |
5 |
57,877,529 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5777:Pcdh7
|
UTSW |
5 |
57,876,856 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5800:Pcdh7
|
UTSW |
5 |
57,879,567 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5834:Pcdh7
|
UTSW |
5 |
57,878,970 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5870:Pcdh7
|
UTSW |
5 |
57,877,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R5917:Pcdh7
|
UTSW |
5 |
57,879,097 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6014:Pcdh7
|
UTSW |
5 |
57,878,497 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6193:Pcdh7
|
UTSW |
5 |
57,877,666 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6240:Pcdh7
|
UTSW |
5 |
57,878,704 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6335:Pcdh7
|
UTSW |
5 |
58,099,607 (GRCm39) |
splice site |
probably null |
|
|
R6418:Pcdh7
|
UTSW |
5 |
57,879,046 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6907:Pcdh7
|
UTSW |
5 |
57,876,471 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R7058:Pcdh7
|
UTSW |
5 |
57,879,582 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7069:Pcdh7
|
UTSW |
5 |
57,877,126 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7073:Pcdh7
|
UTSW |
5 |
57,878,299 (GRCm39) |
missense |
probably benign |
0.19 |
|
R7463:Pcdh7
|
UTSW |
5 |
57,878,340 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7509:Pcdh7
|
UTSW |
5 |
57,877,529 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7588:Pcdh7
|
UTSW |
5 |
57,877,246 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7707:Pcdh7
|
UTSW |
5 |
57,877,672 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7734:Pcdh7
|
UTSW |
5 |
57,876,976 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7899:Pcdh7
|
UTSW |
5 |
57,877,152 (GRCm39) |
missense |
probably benign |
|
|
R8194:Pcdh7
|
UTSW |
5 |
57,877,678 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8480:Pcdh7
|
UTSW |
5 |
58,286,407 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8890:Pcdh7
|
UTSW |
5 |
57,876,717 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8906:Pcdh7
|
UTSW |
5 |
57,879,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8990:Pcdh7
|
UTSW |
5 |
57,879,364 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9264:Pcdh7
|
UTSW |
5 |
58,286,663 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9272:Pcdh7
|
UTSW |
5 |
57,878,779 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R9294:Pcdh7
|
UTSW |
5 |
57,878,677 (GRCm39) |
missense |
probably benign |
0.39 |
|
R9518:Pcdh7
|
UTSW |
5 |
58,070,513 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R9597:Pcdh7
|
UTSW |
5 |
57,877,197 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R9642:Pcdh7
|
UTSW |
5 |
57,876,717 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0021:Pcdh7
|
UTSW |
5 |
57,878,826 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
X0026:Pcdh7
|
UTSW |
5 |
57,876,721 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Pcdh7
|
UTSW |
5 |
57,877,006 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCGATCTGTTAATGGTGGGC -3'
(R):5'- ACATCTCTATCCTATAAGGCCTCTGG -3'
Sequencing Primer
(F):5'- TGGCAAGGCATTACAAATCCAGTTC -3'
(R):5'- CTATAAGGCCTCTGGTACATCAGTG -3'
|
| Posted On |
2022-11-14 |
Incidental Mutation