Incidental Mutation 'R9710:Cachd1'
ID |
730050 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cachd1
|
Ensembl Gene |
ENSMUSG00000028532 |
Gene Name |
cache domain containing 1 |
Synonyms |
Vwcd1, 1190007F10Rik, B430218L07Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.274)
|
Stock # |
R9710 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
4 |
Chromosomal Location |
100633870-100861741 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 100832092 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Asparagine to Lysine
at position 751
(N751K)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000030257
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000030257]
[ENSMUST00000097955]
|
AlphaFold |
Q6PDJ1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000030257
AA Change: N751K
PolyPhen 2
Score 0.342 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000030257 Gene: ENSMUSG00000028532 AA Change: N751K
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
24 |
N/A |
INTRINSIC |
Pfam:VWA_N
|
103 |
218 |
9.4e-22 |
PFAM |
VWA
|
240 |
438 |
2.8e-1 |
SMART |
Pfam:Cache_1
|
467 |
543 |
2.4e-12 |
PFAM |
Pfam:Cache_1
|
786 |
871 |
1.5e-7 |
PFAM |
low complexity region
|
981 |
996 |
N/A |
INTRINSIC |
transmembrane domain
|
1109 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1159 |
1173 |
N/A |
INTRINSIC |
low complexity region
|
1240 |
1246 |
N/A |
INTRINSIC |
low complexity region
|
1260 |
1274 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000097955
AA Change: N751K
PolyPhen 2
Score 0.342 (Sensitivity: 0.90; Specificity: 0.89)
|
SMART Domains |
Protein: ENSMUSP00000095568 Gene: ENSMUSG00000028532 AA Change: N751K
Domain | Start | End | E-Value | Type |
low complexity region
|
11 |
24 |
N/A |
INTRINSIC |
Pfam:VWA_N
|
103 |
218 |
6.7e-32 |
PFAM |
VWA
|
240 |
438 |
2.8e-1 |
SMART |
Pfam:Cache_1
|
467 |
543 |
1.7e-12 |
PFAM |
low complexity region
|
801 |
818 |
N/A |
INTRINSIC |
low complexity region
|
981 |
996 |
N/A |
INTRINSIC |
transmembrane domain
|
1109 |
1131 |
N/A |
INTRINSIC |
low complexity region
|
1159 |
1173 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.7%
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
T |
C |
15: 81,946,852 (GRCm39) |
S250P |
probably benign |
Het |
Ahcyl1 |
T |
A |
3: 107,578,494 (GRCm39) |
I248F |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,482,646 (GRCm39) |
E454V |
probably damaging |
Het |
Ank3 |
A |
T |
10: 69,829,070 (GRCm39) |
T2580S |
|
Het |
Anks1 |
G |
A |
17: 28,128,571 (GRCm39) |
G46R |
possibly damaging |
Het |
Arhgap45 |
A |
G |
10: 79,857,635 (GRCm39) |
E322G |
probably damaging |
Het |
Arhgef2 |
T |
C |
3: 88,528,576 (GRCm39) |
I4T |
probably benign |
Het |
C1qtnf4 |
T |
C |
2: 90,720,351 (GRCm39) |
I208T |
probably damaging |
Het |
Cacna1a |
G |
T |
8: 85,320,808 (GRCm39) |
V1589F |
possibly damaging |
Het |
Cacnb1 |
T |
C |
11: 97,902,197 (GRCm39) |
H205R |
probably benign |
Het |
Castor1 |
A |
G |
11: 4,169,015 (GRCm39) |
K61E |
probably benign |
Het |
Ccdc9b |
G |
T |
2: 118,591,077 (GRCm39) |
A152E |
probably benign |
Het |
Clvs2 |
C |
A |
10: 33,389,307 (GRCm39) |
R311L |
probably benign |
Het |
Crim1 |
G |
T |
17: 78,610,504 (GRCm39) |
G320* |
probably null |
Het |
Crtam |
A |
T |
9: 40,895,671 (GRCm39) |
D218E |
probably benign |
Het |
Cwc27 |
G |
A |
13: 104,943,158 (GRCm39) |
T128I |
probably damaging |
Het |
Cyp4a14 |
T |
A |
4: 115,349,347 (GRCm39) |
I238F |
probably benign |
Het |
D930020B18Rik |
A |
C |
10: 121,503,563 (GRCm39) |
E246A |
probably benign |
Het |
Dsg1c |
T |
A |
18: 20,410,044 (GRCm39) |
V504E |
probably benign |
Het |
Enpp6 |
T |
A |
8: 47,518,948 (GRCm39) |
S239T |
probably damaging |
Het |
Eri2 |
A |
T |
7: 119,384,824 (GRCm39) |
I559N |
probably benign |
Het |
Fbxo34 |
T |
C |
14: 47,768,724 (GRCm39) |
Y746H |
probably damaging |
Het |
Galr1 |
A |
T |
18: 82,424,103 (GRCm39) |
L58Q |
probably damaging |
Het |
Ghdc |
A |
G |
11: 100,658,863 (GRCm39) |
V423A |
probably benign |
Het |
Glt28d2 |
T |
C |
3: 85,779,059 (GRCm39) |
D138G |
probably benign |
Het |
Gm266 |
A |
T |
12: 111,451,763 (GRCm39) |
C148S |
probably benign |
Het |
Gnas |
C |
T |
2: 174,141,132 (GRCm39) |
T493M |
unknown |
Het |
Hivep2 |
T |
C |
10: 14,015,203 (GRCm39) |
I1790T |
probably damaging |
Het |
Impg1 |
A |
G |
9: 80,287,276 (GRCm39) |
V390A |
probably benign |
Het |
Isy1 |
A |
G |
6: 87,796,574 (GRCm39) |
F239L |
possibly damaging |
Het |
Itgb5 |
A |
G |
16: 33,685,917 (GRCm39) |
T86A |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,382,481 (GRCm39) |
C1458R |
possibly damaging |
Het |
Krt28 |
T |
C |
11: 99,255,921 (GRCm39) |
E446G |
probably damaging |
Het |
Lama1 |
A |
T |
17: 68,129,404 (GRCm39) |
Q3071L |
|
Het |
Lasp1 |
A |
G |
11: 97,697,593 (GRCm39) |
|
probably benign |
Het |
Lmf2 |
T |
C |
15: 89,237,419 (GRCm39) |
K348E |
probably benign |
Het |
Lrch3 |
G |
T |
16: 32,796,108 (GRCm39) |
E331* |
probably null |
Het |
Lzic |
T |
A |
4: 149,573,141 (GRCm39) |
F98I |
probably damaging |
Het |
Map7d1 |
C |
A |
4: 126,127,440 (GRCm39) |
|
probably null |
Het |
Marchf8 |
C |
T |
6: 116,378,405 (GRCm39) |
T113I |
possibly damaging |
Het |
Mgrn1 |
A |
T |
16: 4,745,740 (GRCm39) |
K423* |
probably null |
Het |
Muc20 |
G |
A |
16: 32,615,266 (GRCm39) |
T37I |
possibly damaging |
Het |
Myh15 |
A |
G |
16: 48,959,044 (GRCm39) |
E972G |
probably damaging |
Het |
Myocd |
T |
A |
11: 65,087,167 (GRCm39) |
K253N |
probably damaging |
Het |
Myod1 |
T |
G |
7: 46,026,575 (GRCm39) |
L160R |
probably damaging |
Het |
Nanog |
T |
C |
6: 122,684,799 (GRCm39) |
S20P |
probably benign |
Het |
Nat8f2 |
A |
T |
6: 85,844,683 (GRCm39) |
Y226* |
probably null |
Het |
Nsmf |
A |
G |
2: 24,949,077 (GRCm39) |
K277R |
probably null |
Het |
Nsrp1 |
C |
T |
11: 76,967,503 (GRCm39) |
G30R |
probably damaging |
Het |
Nsun6 |
C |
A |
2: 15,003,009 (GRCm39) |
R389L |
probably benign |
Het |
Obscn |
G |
A |
11: 58,943,397 (GRCm39) |
R4251C |
probably benign |
Het |
Or10g9 |
A |
T |
9: 39,912,172 (GRCm39) |
M117K |
probably damaging |
Het |
Or11h4 |
C |
T |
14: 50,974,199 (GRCm39) |
C140Y |
probably benign |
Het |
Or51h1 |
A |
G |
7: 102,308,441 (GRCm39) |
T138A |
probably damaging |
Het |
Or5w20 |
G |
A |
2: 87,726,902 (GRCm39) |
D120N |
probably damaging |
Het |
Pgm1 |
T |
C |
4: 99,843,918 (GRCm39) |
L567P |
probably damaging |
Het |
Polrmt |
G |
T |
10: 79,576,535 (GRCm39) |
H474N |
probably benign |
Het |
Ppfia2 |
A |
G |
10: 106,664,885 (GRCm39) |
I374V |
probably benign |
Het |
Pramel5 |
T |
A |
4: 143,999,545 (GRCm39) |
I181F |
probably benign |
Het |
Prpf4b |
T |
A |
13: 35,083,870 (GRCm39) |
Y880N |
probably damaging |
Het |
Ptpn3 |
G |
A |
4: 57,249,957 (GRCm39) |
Q180* |
probably null |
Het |
Ptprc |
T |
C |
1: 138,008,627 (GRCm39) |
R687G |
probably damaging |
Het |
Rnaseh2a |
T |
C |
8: 85,684,638 (GRCm39) |
T241A |
probably damaging |
Het |
Rnf148 |
T |
A |
6: 23,654,802 (GRCm39) |
I65F |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,331,831 (GRCm39) |
I2348V |
|
Het |
Rttn |
A |
G |
18: 89,035,334 (GRCm39) |
N736S |
possibly damaging |
Het |
Ryr3 |
A |
C |
2: 112,633,534 (GRCm39) |
V2093G |
probably damaging |
Het |
Selenof |
T |
A |
3: 144,283,370 (GRCm39) |
F33L |
probably benign |
Het |
Sh2d3c |
C |
T |
2: 32,635,889 (GRCm39) |
R238* |
probably null |
Het |
Slc23a4 |
T |
C |
6: 34,923,235 (GRCm39) |
K543R |
probably benign |
Het |
Smn1 |
A |
T |
13: 100,272,210 (GRCm39) |
N278I |
possibly damaging |
Het |
Sox7 |
G |
A |
14: 64,185,509 (GRCm39) |
A182T |
probably benign |
Het |
Spata31e5 |
T |
A |
1: 28,817,120 (GRCm39) |
Y304F |
probably benign |
Het |
Sptlc2 |
A |
T |
12: 87,359,533 (GRCm39) |
I501N |
probably benign |
Het |
Srf |
T |
C |
17: 46,866,271 (GRCm39) |
T162A |
probably benign |
Het |
Srm |
C |
T |
4: 148,676,039 (GRCm39) |
|
probably benign |
Het |
Stim1 |
CAGCGCCTGACGGAGC |
CAGC |
7: 102,080,118 (GRCm39) |
|
probably benign |
Het |
Taar8a |
T |
C |
10: 23,952,714 (GRCm39) |
L106P |
probably damaging |
Het |
Tcte1 |
A |
G |
17: 45,850,798 (GRCm39) |
H358R |
possibly damaging |
Het |
Tmem205 |
A |
G |
9: 21,837,587 (GRCm39) |
S20P |
probably damaging |
Het |
Trav16 |
T |
A |
14: 53,980,910 (GRCm39) |
V33E |
possibly damaging |
Het |
Trf |
T |
A |
9: 103,103,217 (GRCm39) |
I149F |
probably damaging |
Het |
Trmt2a |
C |
T |
16: 18,070,041 (GRCm39) |
Q419* |
probably null |
Het |
Ttc19 |
A |
G |
11: 62,203,997 (GRCm39) |
I319M |
probably benign |
Het |
Txndc16 |
T |
C |
14: 45,400,467 (GRCm39) |
I345V |
probably benign |
Het |
Ube3b |
T |
C |
5: 114,553,370 (GRCm39) |
I914T |
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,727,957 (GRCm39) |
F107L |
possibly damaging |
Het |
Vmn1r73 |
T |
C |
7: 11,490,407 (GRCm39) |
F75S |
possibly damaging |
Het |
Vmn2r54 |
A |
T |
7: 12,363,753 (GRCm39) |
M380K |
possibly damaging |
Het |
Wdr7 |
T |
A |
18: 63,927,317 (GRCm39) |
M989K |
possibly damaging |
Het |
Zcchc3 |
A |
G |
2: 152,256,385 (GRCm39) |
S105P |
probably benign |
Het |
Zfp735 |
T |
A |
11: 73,601,806 (GRCm39) |
V250E |
possibly damaging |
Het |
|
Other mutations in Cachd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00922:Cachd1
|
APN |
4 |
100,824,163 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01531:Cachd1
|
APN |
4 |
100,810,231 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01705:Cachd1
|
APN |
4 |
100,840,736 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01843:Cachd1
|
APN |
4 |
100,850,069 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01938:Cachd1
|
APN |
4 |
100,831,325 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02268:Cachd1
|
APN |
4 |
100,809,294 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02934:Cachd1
|
APN |
4 |
100,825,295 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03019:Cachd1
|
APN |
4 |
100,809,282 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03084:Cachd1
|
APN |
4 |
100,860,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R0366:Cachd1
|
UTSW |
4 |
100,851,934 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0395:Cachd1
|
UTSW |
4 |
100,810,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R0520:Cachd1
|
UTSW |
4 |
100,754,900 (GRCm39) |
missense |
probably damaging |
0.99 |
R0578:Cachd1
|
UTSW |
4 |
100,852,039 (GRCm39) |
splice site |
probably benign |
|
R0646:Cachd1
|
UTSW |
4 |
100,845,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Cachd1
|
UTSW |
4 |
100,832,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R0962:Cachd1
|
UTSW |
4 |
100,840,498 (GRCm39) |
splice site |
probably benign |
|
R1156:Cachd1
|
UTSW |
4 |
100,845,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1157:Cachd1
|
UTSW |
4 |
100,832,037 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1314:Cachd1
|
UTSW |
4 |
100,832,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Cachd1
|
UTSW |
4 |
100,845,795 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1632:Cachd1
|
UTSW |
4 |
100,824,169 (GRCm39) |
missense |
probably benign |
0.02 |
R1774:Cachd1
|
UTSW |
4 |
100,821,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1774:Cachd1
|
UTSW |
4 |
100,824,240 (GRCm39) |
missense |
probably benign |
0.02 |
R1845:Cachd1
|
UTSW |
4 |
100,634,555 (GRCm39) |
missense |
probably benign |
0.01 |
R1869:Cachd1
|
UTSW |
4 |
100,840,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Cachd1
|
UTSW |
4 |
100,810,366 (GRCm39) |
missense |
probably damaging |
0.99 |
R2069:Cachd1
|
UTSW |
4 |
100,848,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2082:Cachd1
|
UTSW |
4 |
100,860,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R2267:Cachd1
|
UTSW |
4 |
100,806,266 (GRCm39) |
splice site |
probably benign |
|
R2517:Cachd1
|
UTSW |
4 |
100,838,079 (GRCm39) |
splice site |
probably null |
|
R2896:Cachd1
|
UTSW |
4 |
100,828,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R3729:Cachd1
|
UTSW |
4 |
100,832,077 (GRCm39) |
nonsense |
probably null |
|
R3818:Cachd1
|
UTSW |
4 |
100,848,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R3979:Cachd1
|
UTSW |
4 |
100,828,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Cachd1
|
UTSW |
4 |
100,810,327 (GRCm39) |
nonsense |
probably null |
|
R4791:Cachd1
|
UTSW |
4 |
100,775,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Cachd1
|
UTSW |
4 |
100,851,935 (GRCm39) |
missense |
probably damaging |
0.98 |
R5147:Cachd1
|
UTSW |
4 |
100,821,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Cachd1
|
UTSW |
4 |
100,823,397 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5322:Cachd1
|
UTSW |
4 |
100,809,319 (GRCm39) |
missense |
probably damaging |
0.98 |
R5335:Cachd1
|
UTSW |
4 |
100,825,282 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5390:Cachd1
|
UTSW |
4 |
100,838,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R5573:Cachd1
|
UTSW |
4 |
100,831,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R5578:Cachd1
|
UTSW |
4 |
100,722,203 (GRCm39) |
missense |
probably benign |
0.31 |
R5905:Cachd1
|
UTSW |
4 |
100,840,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R6003:Cachd1
|
UTSW |
4 |
100,809,216 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6028:Cachd1
|
UTSW |
4 |
100,840,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R6185:Cachd1
|
UTSW |
4 |
100,838,228 (GRCm39) |
nonsense |
probably null |
|
R6367:Cachd1
|
UTSW |
4 |
100,860,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R6492:Cachd1
|
UTSW |
4 |
100,809,315 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6591:Cachd1
|
UTSW |
4 |
100,846,683 (GRCm39) |
missense |
probably benign |
|
R6691:Cachd1
|
UTSW |
4 |
100,846,683 (GRCm39) |
missense |
probably benign |
|
R7129:Cachd1
|
UTSW |
4 |
100,775,263 (GRCm39) |
missense |
probably null |
0.99 |
R7187:Cachd1
|
UTSW |
4 |
100,833,552 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7387:Cachd1
|
UTSW |
4 |
100,634,375 (GRCm39) |
missense |
unknown |
|
R7833:Cachd1
|
UTSW |
4 |
100,832,012 (GRCm39) |
missense |
probably benign |
0.09 |
R7835:Cachd1
|
UTSW |
4 |
100,831,350 (GRCm39) |
splice site |
probably null |
|
R7838:Cachd1
|
UTSW |
4 |
100,824,211 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7867:Cachd1
|
UTSW |
4 |
100,845,759 (GRCm39) |
missense |
probably damaging |
0.97 |
R7882:Cachd1
|
UTSW |
4 |
100,824,244 (GRCm39) |
missense |
probably benign |
0.29 |
R7941:Cachd1
|
UTSW |
4 |
100,845,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R7978:Cachd1
|
UTSW |
4 |
100,832,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Cachd1
|
UTSW |
4 |
100,845,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R8153:Cachd1
|
UTSW |
4 |
100,845,835 (GRCm39) |
critical splice donor site |
probably null |
|
R8174:Cachd1
|
UTSW |
4 |
100,823,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R8219:Cachd1
|
UTSW |
4 |
100,848,159 (GRCm39) |
missense |
probably benign |
0.34 |
R8358:Cachd1
|
UTSW |
4 |
100,816,668 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8376:Cachd1
|
UTSW |
4 |
100,832,073 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Cachd1
|
UTSW |
4 |
100,845,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R8747:Cachd1
|
UTSW |
4 |
100,860,045 (GRCm39) |
intron |
probably benign |
|
R8845:Cachd1
|
UTSW |
4 |
100,810,343 (GRCm39) |
missense |
probably benign |
0.36 |
R8864:Cachd1
|
UTSW |
4 |
100,852,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R8869:Cachd1
|
UTSW |
4 |
100,809,280 (GRCm39) |
missense |
probably benign |
0.09 |
R8870:Cachd1
|
UTSW |
4 |
100,754,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R8904:Cachd1
|
UTSW |
4 |
100,810,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R8958:Cachd1
|
UTSW |
4 |
100,851,283 (GRCm39) |
missense |
probably benign |
0.11 |
R9061:Cachd1
|
UTSW |
4 |
100,809,202 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9193:Cachd1
|
UTSW |
4 |
100,634,339 (GRCm39) |
missense |
unknown |
|
R9304:Cachd1
|
UTSW |
4 |
100,824,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9358:Cachd1
|
UTSW |
4 |
100,833,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R9373:Cachd1
|
UTSW |
4 |
100,832,067 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9425:Cachd1
|
UTSW |
4 |
100,832,057 (GRCm39) |
missense |
probably benign |
|
R9632:Cachd1
|
UTSW |
4 |
100,832,092 (GRCm39) |
missense |
probably benign |
0.34 |
R9751:Cachd1
|
UTSW |
4 |
100,823,438 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
Predicted Primers |
PCR Primer
(F):5'- AGTACTTGGGCTTGGCTTCC -3'
(R):5'- GCACGGCAGTCAAAACATAG -3'
Sequencing Primer
(F):5'- TTCCCTGCGAGAGAACCTTG -3'
(R):5'- GGCAGTCAAAACATAGCCCAC -3'
|
Posted On |
2022-10-06 |