Incidental Mutation 'R9609:Cad'
ID |
724087 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cad
|
Ensembl Gene |
ENSMUSG00000013629 |
Gene Name |
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase |
Synonyms |
2410008J01Rik |
MMRRC Submission |
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.968)
|
Stock # |
R9609 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
5 |
Chromosomal Location |
31212124-31235823 bp(+) (GRCm39) |
Type of Mutation |
critical splice donor site (2 bp from exon) |
DNA Base Change (assembly) |
T to C
at 31228018 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000013773
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000013773]
[ENSMUST00000013773]
[ENSMUST00000200953]
[ENSMUST00000201182]
[ENSMUST00000201838]
[ENSMUST00000202795]
[ENSMUST00000202973]
|
AlphaFold |
B2RQC6 |
Predicted Effect |
probably null
Transcript: ENSMUST00000013773
|
SMART Domains |
Protein: ENSMUSP00000013773 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.7e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.2e-15 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.8e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
1.5e-9 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
2.2e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
1.8e-23 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
3.1e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
2.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
7.4e-12 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1924 |
2065 |
1.9e-44 |
PFAM |
Pfam:OTCace
|
2071 |
2221 |
7.6e-37 |
PFAM |
|
Predicted Effect |
probably null
Transcript: ENSMUST00000013773
|
SMART Domains |
Protein: ENSMUSP00000013773 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.7e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.2e-15 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.8e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
1.5e-9 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
2.2e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
1.8e-23 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
3.1e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
2.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
7.4e-12 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1924 |
2065 |
1.9e-44 |
PFAM |
Pfam:OTCace
|
2071 |
2221 |
7.6e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000200953
|
SMART Domains |
Protein: ENSMUSP00000144307 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.5e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:CPSase_L_D2
|
514 |
616 |
1.5e-34 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
625 |
2.4e-7 |
PFAM |
Pfam:CPSase_L_D2
|
614 |
655 |
4.9e-15 |
PFAM |
CPSase_L_D3
|
735 |
858 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
981 |
1160 |
1.7e-23 |
PFAM |
Pfam:CPSase_L_D2
|
984 |
1187 |
3e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
991 |
1179 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
992 |
1159 |
2.1e-12 |
PFAM |
MGS
|
1264 |
1365 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1399 |
1667 |
7.1e-12 |
PFAM |
low complexity region
|
1757 |
1776 |
N/A |
INTRINSIC |
low complexity region
|
1801 |
1817 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1861 |
2002 |
1.8e-44 |
PFAM |
Pfam:OTCace
|
2008 |
2158 |
7.3e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201182
|
SMART Domains |
Protein: ENSMUSP00000144684 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
4.5e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.1e-15 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.7e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
1.4e-9 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
2.1e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
1.7e-23 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
3e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
2.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
2.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
7.1e-12 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1949 |
1994 |
1.4e-11 |
PFAM |
Pfam:OTCace
|
2000 |
2150 |
7.3e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000201838
|
SMART Domains |
Protein: ENSMUSP00000144127 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
6.3e-48 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
1.9e-16 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
3.7e-86 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
2.5e-10 |
PFAM |
Pfam:Dala_Dala_lig_C
|
526 |
687 |
4.2e-11 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
SCOP:d1a9xa3
|
935 |
964 |
1e-7 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202795
|
SMART Domains |
Protein: ENSMUSP00000144009 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
CPSase_sm_chain
|
1 |
139 |
8.81e-80 |
SMART |
Pfam:GATase
|
179 |
356 |
1.9e-47 |
PFAM |
low complexity region
|
397 |
407 |
N/A |
INTRINSIC |
Pfam:ATP-grasp_4
|
511 |
692 |
5.9e-16 |
PFAM |
Pfam:CPSase_L_D2
|
514 |
718 |
1.2e-85 |
PFAM |
Pfam:ATP-grasp
|
522 |
690 |
7.3e-10 |
PFAM |
Pfam:Dala_Dala_lig_C
|
527 |
687 |
1.3e-10 |
PFAM |
CPSase_L_D3
|
798 |
921 |
9.7e-59 |
SMART |
Pfam:ATP-grasp_4
|
1044 |
1223 |
8.9e-24 |
PFAM |
Pfam:CPSase_L_D2
|
1047 |
1250 |
2.1e-28 |
PFAM |
Pfam:Dala_Dala_lig_C
|
1054 |
1242 |
1.3e-7 |
PFAM |
Pfam:ATP-grasp
|
1055 |
1222 |
1.1e-12 |
PFAM |
MGS
|
1327 |
1428 |
1.35e-7 |
SMART |
Pfam:Amidohydro_1
|
1462 |
1730 |
2.5e-11 |
PFAM |
low complexity region
|
1820 |
1839 |
N/A |
INTRINSIC |
low complexity region
|
1864 |
1880 |
N/A |
INTRINSIC |
Pfam:OTCace_N
|
1970 |
2004 |
4.6e-11 |
PFAM |
Pfam:OTCace
|
2010 |
2160 |
9.9e-37 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000202973
|
SMART Domains |
Protein: ENSMUSP00000144679 Gene: ENSMUSG00000013629
Domain | Start | End | E-Value | Type |
SCOP:d1gkra1
|
1 |
84 |
4e-28 |
SMART |
PDB:4C6N|A
|
1 |
119 |
4e-58 |
PDB |
low complexity region
|
156 |
170 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The de novo synthesis of pyrimidine nucleotides is required for mammalian cells to proliferate. This gene encodes a trifunctional protein which is associated with the enzymatic activities of the first 3 enzymes in the 6-step pathway of pyrimidine biosynthesis: carbamoylphosphate synthetase (CPS II), aspartate transcarbamoylase, and dihydroorotase. This protein is regulated by the mitogen-activated protein kinase (MAPK) cascade, which indicates a direct link between activation of the MAPK cascade and de novo biosynthesis of pyrimidine nucleotides. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,208,549 (GRCm39) |
S241P |
probably damaging |
Het |
Adam23 |
A |
T |
1: 63,576,102 (GRCm39) |
M295L |
probably benign |
Het |
Ano8 |
T |
A |
8: 71,933,726 (GRCm39) |
D522V |
unknown |
Het |
Asgr2 |
T |
C |
11: 69,988,667 (GRCm39) |
L120P |
probably damaging |
Het |
Atp5mc2 |
A |
G |
15: 102,573,580 (GRCm39) |
F79L |
probably damaging |
Het |
Baiap2 |
C |
T |
11: 119,847,958 (GRCm39) |
R29C |
probably damaging |
Het |
Bicdl2 |
A |
G |
17: 23,884,513 (GRCm39) |
E145G |
|
Het |
Dhrs7b |
A |
G |
11: 60,735,121 (GRCm39) |
R51G |
possibly damaging |
Het |
Dnah3 |
A |
T |
7: 119,670,236 (GRCm39) |
Y694N |
probably damaging |
Het |
Dnaja4 |
G |
A |
9: 54,616,644 (GRCm39) |
G216S |
probably null |
Het |
Dync1h1 |
T |
C |
12: 110,607,362 (GRCm39) |
V2651A |
probably benign |
Het |
Fbxw28 |
T |
C |
9: 109,167,515 (GRCm39) |
T81A |
probably benign |
Het |
Fga |
A |
T |
3: 82,940,064 (GRCm39) |
I573F |
probably damaging |
Het |
Fgd6 |
T |
A |
10: 93,879,674 (GRCm39) |
I176N |
probably damaging |
Het |
Fhl5 |
A |
T |
4: 25,214,653 (GRCm39) |
C41* |
probably null |
Het |
Fibcd1 |
A |
G |
2: 31,728,653 (GRCm39) |
V68A |
probably benign |
Het |
Fign |
T |
C |
2: 63,810,286 (GRCm39) |
D328G |
probably benign |
Het |
Gtpbp10 |
A |
C |
5: 5,607,396 (GRCm39) |
F15C |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,555,346 (GRCm39) |
V2475D |
probably damaging |
Het |
Iglv3 |
A |
G |
16: 19,060,221 (GRCm39) |
S36P |
probably damaging |
Het |
Igsf10 |
G |
T |
3: 59,226,869 (GRCm39) |
T2268N |
probably damaging |
Het |
Krt75 |
A |
G |
15: 101,474,677 (GRCm39) |
I473T |
probably benign |
Het |
Lcn3 |
A |
G |
2: 25,657,596 (GRCm39) |
E162G |
possibly damaging |
Het |
Lnpk |
A |
G |
2: 74,401,298 (GRCm39) |
V17A |
probably damaging |
Het |
Malrd1 |
A |
G |
2: 15,700,081 (GRCm39) |
S643G |
unknown |
Het |
Mcm5 |
C |
T |
8: 75,844,168 (GRCm39) |
S313F |
probably benign |
Het |
Mlip |
T |
A |
9: 77,045,797 (GRCm39) |
L894F |
possibly damaging |
Het |
Muc4 |
A |
T |
16: 32,577,234 (GRCm39) |
T175S |
|
Het |
Nkpd1 |
A |
C |
7: 19,257,462 (GRCm39) |
I414L |
possibly damaging |
Het |
Nrxn2 |
C |
A |
19: 6,540,203 (GRCm39) |
N834K |
probably damaging |
Het |
Oacyl |
A |
G |
18: 65,843,599 (GRCm39) |
T99A |
probably benign |
Het |
Patj |
T |
G |
4: 98,576,473 (GRCm39) |
F570L |
probably benign |
Het |
Piwil4 |
T |
C |
9: 14,614,443 (GRCm39) |
T107A |
|
Het |
Ppp1r12b |
G |
A |
1: 134,824,084 (GRCm39) |
Q180* |
probably null |
Het |
Prpf4b |
A |
G |
13: 35,068,032 (GRCm39) |
D287G |
unknown |
Het |
Rab17 |
T |
C |
1: 90,891,907 (GRCm39) |
Y39C |
probably damaging |
Het |
Rbsn |
T |
A |
6: 92,179,565 (GRCm39) |
I125F |
probably damaging |
Het |
Rnf207 |
C |
A |
4: 152,402,222 (GRCm39) |
G74C |
probably damaging |
Het |
Rrs1 |
T |
C |
1: 9,616,518 (GRCm39) |
L257P |
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,683,848 (GRCm39) |
E3072G |
probably damaging |
Het |
Scn8a |
A |
C |
15: 100,834,407 (GRCm39) |
I68L |
possibly damaging |
Het |
Slc14a1 |
C |
A |
18: 78,152,807 (GRCm39) |
A367S |
probably damaging |
Het |
Slc26a7 |
T |
A |
4: 14,532,636 (GRCm39) |
I413F |
probably damaging |
Het |
Slc4a11 |
T |
A |
2: 130,530,035 (GRCm39) |
T248S |
possibly damaging |
Het |
Spen |
A |
G |
4: 141,215,419 (GRCm39) |
I471T |
unknown |
Het |
Tbpl2 |
C |
T |
2: 23,977,197 (GRCm39) |
D274N |
probably damaging |
Het |
Timm23 |
A |
G |
14: 31,902,543 (GRCm39) |
M200T |
probably benign |
Het |
Tlr3 |
T |
C |
8: 45,850,117 (GRCm39) |
I851V |
probably benign |
Het |
Tnfrsf18 |
T |
A |
4: 156,113,208 (GRCm39) |
V298E |
possibly damaging |
Het |
Trav6-3 |
A |
G |
14: 53,667,618 (GRCm39) |
N41S |
possibly damaging |
Het |
Trim17 |
C |
A |
11: 58,855,964 (GRCm39) |
A7D |
probably damaging |
Het |
Ttbk1 |
T |
C |
17: 46,758,148 (GRCm39) |
T829A |
probably damaging |
Het |
Ugt3a1 |
A |
C |
15: 9,361,905 (GRCm39) |
E227A |
probably damaging |
Het |
Vmn1r218 |
C |
T |
13: 23,320,839 (GRCm39) |
T62I |
probably benign |
Het |
Vmn2r100 |
T |
C |
17: 19,743,732 (GRCm39) |
L465P |
probably damaging |
Het |
Vps13c |
A |
T |
9: 67,841,831 (GRCm39) |
Q1951L |
probably damaging |
Het |
Wdcp |
A |
G |
12: 4,900,258 (GRCm39) |
D38G |
probably damaging |
Het |
Xdh |
T |
A |
17: 74,231,990 (GRCm39) |
Q240L |
possibly damaging |
Het |
Zc3h4 |
T |
A |
7: 16,150,751 (GRCm39) |
V23D |
unknown |
Het |
Zkscan8 |
C |
A |
13: 21,709,434 (GRCm39) |
V155F |
possibly damaging |
Het |
|
Other mutations in Cad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00821:Cad
|
APN |
5 |
31,218,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00908:Cad
|
APN |
5 |
31,216,398 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01068:Cad
|
APN |
5 |
31,219,114 (GRCm39) |
splice site |
probably benign |
|
IGL01638:Cad
|
APN |
5 |
31,224,958 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02483:Cad
|
APN |
5 |
31,218,170 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02499:Cad
|
APN |
5 |
31,226,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02691:Cad
|
APN |
5 |
31,212,638 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03002:Cad
|
APN |
5 |
31,212,330 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4696001:Cad
|
UTSW |
5 |
31,229,438 (GRCm39) |
missense |
probably damaging |
0.99 |
R0212:Cad
|
UTSW |
5 |
31,235,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Cad
|
UTSW |
5 |
31,229,665 (GRCm39) |
missense |
probably benign |
0.01 |
R0335:Cad
|
UTSW |
5 |
31,231,329 (GRCm39) |
unclassified |
probably benign |
|
R0401:Cad
|
UTSW |
5 |
31,231,330 (GRCm39) |
unclassified |
probably benign |
|
R0445:Cad
|
UTSW |
5 |
31,230,053 (GRCm39) |
missense |
probably benign |
0.08 |
R0494:Cad
|
UTSW |
5 |
31,234,856 (GRCm39) |
unclassified |
probably benign |
|
R0532:Cad
|
UTSW |
5 |
31,219,531 (GRCm39) |
splice site |
probably benign |
|
R0539:Cad
|
UTSW |
5 |
31,232,801 (GRCm39) |
splice site |
probably benign |
|
R0578:Cad
|
UTSW |
5 |
31,216,120 (GRCm39) |
missense |
probably benign |
0.01 |
R0590:Cad
|
UTSW |
5 |
31,219,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R0638:Cad
|
UTSW |
5 |
31,235,032 (GRCm39) |
missense |
probably damaging |
0.98 |
R0831:Cad
|
UTSW |
5 |
31,224,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R1329:Cad
|
UTSW |
5 |
31,216,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Cad
|
UTSW |
5 |
31,226,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R1531:Cad
|
UTSW |
5 |
31,233,563 (GRCm39) |
missense |
probably benign |
0.14 |
R1763:Cad
|
UTSW |
5 |
31,218,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Cad
|
UTSW |
5 |
31,215,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2165:Cad
|
UTSW |
5 |
31,219,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R3103:Cad
|
UTSW |
5 |
31,219,018 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3113:Cad
|
UTSW |
5 |
31,231,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3762:Cad
|
UTSW |
5 |
31,232,890 (GRCm39) |
splice site |
probably null |
|
R3847:Cad
|
UTSW |
5 |
31,218,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R3898:Cad
|
UTSW |
5 |
31,231,366 (GRCm39) |
missense |
probably benign |
0.06 |
R3943:Cad
|
UTSW |
5 |
31,229,729 (GRCm39) |
critical splice donor site |
probably null |
|
R4213:Cad
|
UTSW |
5 |
31,229,688 (GRCm39) |
missense |
probably benign |
0.01 |
R4458:Cad
|
UTSW |
5 |
31,218,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4562:Cad
|
UTSW |
5 |
31,215,477 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4629:Cad
|
UTSW |
5 |
31,227,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Cad
|
UTSW |
5 |
31,224,030 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4811:Cad
|
UTSW |
5 |
31,232,034 (GRCm39) |
missense |
probably benign |
0.02 |
R5044:Cad
|
UTSW |
5 |
31,212,365 (GRCm39) |
missense |
probably benign |
0.00 |
R5630:Cad
|
UTSW |
5 |
31,217,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5660:Cad
|
UTSW |
5 |
31,234,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Cad
|
UTSW |
5 |
31,226,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R6029:Cad
|
UTSW |
5 |
31,212,327 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6073:Cad
|
UTSW |
5 |
31,219,906 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6240:Cad
|
UTSW |
5 |
31,230,322 (GRCm39) |
missense |
probably benign |
0.00 |
R6260:Cad
|
UTSW |
5 |
31,224,144 (GRCm39) |
missense |
probably null |
|
R7145:Cad
|
UTSW |
5 |
31,224,956 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7303:Cad
|
UTSW |
5 |
31,217,557 (GRCm39) |
critical splice donor site |
probably null |
|
R7352:Cad
|
UTSW |
5 |
31,215,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Cad
|
UTSW |
5 |
31,233,173 (GRCm39) |
missense |
probably benign |
|
R7387:Cad
|
UTSW |
5 |
31,219,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R7455:Cad
|
UTSW |
5 |
31,231,506 (GRCm39) |
missense |
probably damaging |
0.99 |
R7596:Cad
|
UTSW |
5 |
31,226,392 (GRCm39) |
missense |
probably benign |
|
R7627:Cad
|
UTSW |
5 |
31,217,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R7898:Cad
|
UTSW |
5 |
31,218,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8022:Cad
|
UTSW |
5 |
31,226,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Cad
|
UTSW |
5 |
31,218,271 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8511:Cad
|
UTSW |
5 |
31,233,165 (GRCm39) |
missense |
probably benign |
0.00 |
R8523:Cad
|
UTSW |
5 |
31,215,450 (GRCm39) |
missense |
probably damaging |
0.98 |
R8690:Cad
|
UTSW |
5 |
31,232,500 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8697:Cad
|
UTSW |
5 |
31,231,945 (GRCm39) |
missense |
probably benign |
0.06 |
R8698:Cad
|
UTSW |
5 |
31,234,819 (GRCm39) |
missense |
probably benign |
|
R8699:Cad
|
UTSW |
5 |
31,233,605 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8803:Cad
|
UTSW |
5 |
31,226,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Cad
|
UTSW |
5 |
31,225,009 (GRCm39) |
missense |
probably null |
|
R9272:Cad
|
UTSW |
5 |
31,218,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9287:Cad
|
UTSW |
5 |
31,230,000 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9314:Cad
|
UTSW |
5 |
31,234,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Cad
|
UTSW |
5 |
31,229,703 (GRCm39) |
missense |
probably benign |
0.28 |
RF001:Cad
|
UTSW |
5 |
31,217,556 (GRCm39) |
critical splice donor site |
probably benign |
|
RF012:Cad
|
UTSW |
5 |
31,217,556 (GRCm39) |
critical splice donor site |
probably benign |
|
X0021:Cad
|
UTSW |
5 |
31,225,475 (GRCm39) |
missense |
probably null |
1.00 |
X0022:Cad
|
UTSW |
5 |
31,229,661 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Cad
|
UTSW |
5 |
31,232,472 (GRCm39) |
missense |
probably benign |
0.25 |
Z1177:Cad
|
UTSW |
5 |
31,225,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGGCAGCTACAAGGTACCAG -3'
(R):5'- TCTCCCTTGTGAGCGGAGTTAG -3'
Sequencing Primer
(F):5'- GCTACAAGGTACCAGGGCCAC -3'
(R):5'- GGTCATTAATAGCAGTACGAACC -3'
|
Posted On |
2022-09-12 |