Incidental Mutation 'R7816:Cttnbp2'
ID |
601529 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Cttnbp2
|
Ensembl Gene |
ENSMUSG00000000416 |
Gene Name |
cortactin binding protein 2 |
Synonyms |
ORF4, Cortbp2, 4732477G22Rik, 9130022E09Rik, 3010022N24Rik |
MMRRC Submission |
045870-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R7816 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
6 |
Chromosomal Location |
18366477-18514842 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 18448413 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Glycine
at position 82
(D82G)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118432
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090601]
[ENSMUST00000129669]
[ENSMUST00000142963]
[ENSMUST00000148602]
|
AlphaFold |
B9EJA2 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000090601
AA Change: D82G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000088089 Gene: ENSMUSG00000000416 AA Change: D82G
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
30 |
N/A |
INTRINSIC |
Pfam:CortBP2
|
32 |
138 |
3.1e-34 |
PFAM |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
255 |
270 |
N/A |
INTRINSIC |
low complexity region
|
393 |
415 |
N/A |
INTRINSIC |
low complexity region
|
539 |
547 |
N/A |
INTRINSIC |
low complexity region
|
594 |
606 |
N/A |
INTRINSIC |
low complexity region
|
662 |
673 |
N/A |
INTRINSIC |
ANK
|
699 |
729 |
5.21e1 |
SMART |
ANK
|
733 |
762 |
7.02e-5 |
SMART |
ANK
|
766 |
795 |
6.55e-5 |
SMART |
ANK
|
799 |
828 |
4.1e-6 |
SMART |
ANK
|
832 |
861 |
1.09e-1 |
SMART |
ANK
|
901 |
931 |
4.43e-2 |
SMART |
Blast:AAA
|
1108 |
1285 |
1e-18 |
BLAST |
low complexity region
|
1609 |
1623 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000129669
AA Change: D40G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000116878 Gene: ENSMUSG00000000416 AA Change: D40G
Domain | Start | End | E-Value | Type |
Pfam:CortBP2
|
1 |
100 |
4.6e-44 |
PFAM |
Pfam:CortBP2
|
92 |
138 |
3.2e-13 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000142963
AA Change: D40G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000122590 Gene: ENSMUSG00000000416 AA Change: D40G
Domain | Start | End | E-Value | Type |
Pfam:CortBP2
|
1 |
94 |
1.8e-43 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000148602
AA Change: D82G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000118432 Gene: ENSMUSG00000000416 AA Change: D82G
Domain | Start | End | E-Value | Type |
Pfam:CortBP2
|
26 |
138 |
4.3e-50 |
PFAM |
Pfam:CortBP2
|
134 |
180 |
1.3e-12 |
PFAM |
low complexity region
|
197 |
213 |
N/A |
INTRINSIC |
low complexity region
|
255 |
270 |
N/A |
INTRINSIC |
low complexity region
|
393 |
415 |
N/A |
INTRINSIC |
low complexity region
|
539 |
547 |
N/A |
INTRINSIC |
low complexity region
|
594 |
606 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.6%
- 20x: 98.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with six ankyrin repeats and several proline-rich regions. A similar gene in rat interacts with a central regulator of the actin cytoskeleton. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
G |
1: 71,331,588 (GRCm39) |
S1321P |
probably benign |
Het |
Abcb1a |
T |
C |
5: 8,736,132 (GRCm39) |
V175A |
possibly damaging |
Het |
Adamts20 |
T |
A |
15: 94,220,725 (GRCm39) |
M1403L |
probably benign |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Amotl2 |
T |
A |
9: 102,608,853 (GRCm39) |
I789K |
probably benign |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bcar3 |
C |
T |
3: 122,220,343 (GRCm39) |
T80I |
probably benign |
Het |
Bcas1 |
G |
T |
2: 170,248,347 (GRCm39) |
F181L |
probably benign |
Het |
Cacnb1 |
T |
C |
11: 97,896,115 (GRCm39) |
E389G |
probably damaging |
Het |
Cd52 |
A |
T |
4: 133,821,199 (GRCm39) |
|
probably benign |
Het |
Cmtm1 |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
CGGCACGTACTGAAGGTCGCTGACTGGATGGTGTGGCACGTACTGAAGGTCGCTGACTGGATGGT |
8: 105,036,102 (GRCm39) |
|
probably benign |
Het |
Coro2a |
T |
C |
4: 46,546,809 (GRCm39) |
D182G |
probably benign |
Het |
Crp |
T |
C |
1: 172,526,277 (GRCm39) |
S121P |
possibly damaging |
Het |
Csnka2ip |
T |
C |
16: 64,299,852 (GRCm39) |
|
probably benign |
Het |
Cyp2b9 |
A |
G |
7: 25,900,517 (GRCm39) |
N385S |
probably benign |
Het |
Dppa1 |
A |
G |
11: 46,507,003 (GRCm39) |
S26P |
possibly damaging |
Het |
Eif4e3 |
T |
C |
6: 99,617,599 (GRCm39) |
R91G |
probably damaging |
Het |
F13a1 |
A |
T |
13: 37,209,745 (GRCm39) |
N73K |
probably benign |
Het |
Fbxl13 |
T |
C |
5: 21,748,785 (GRCm39) |
Y378C |
probably benign |
Het |
Glis2 |
G |
A |
16: 4,431,328 (GRCm39) |
R285H |
probably damaging |
Het |
Gm17174 |
T |
A |
14: 51,829,569 (GRCm39) |
|
probably benign |
Het |
Golga1 |
G |
A |
2: 38,942,110 (GRCm39) |
S102F |
probably damaging |
Het |
Hdac1 |
A |
T |
4: 129,411,888 (GRCm39) |
Y336N |
probably damaging |
Het |
Hfe |
G |
T |
13: 23,888,382 (GRCm39) |
T168K |
possibly damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv1-56 |
T |
C |
12: 115,206,846 (GRCm39) |
S4G |
probably benign |
Het |
Ino80d |
A |
G |
1: 63,125,556 (GRCm39) |
Y74H |
probably damaging |
Het |
Ints1 |
A |
T |
5: 139,757,134 (GRCm39) |
H427Q |
possibly damaging |
Het |
Itpkb |
T |
A |
1: 180,241,454 (GRCm39) |
V708E |
probably damaging |
Het |
Jmjd4 |
G |
T |
11: 59,341,162 (GRCm39) |
G31V |
probably benign |
Het |
Kcnh5 |
C |
T |
12: 75,023,457 (GRCm39) |
C537Y |
probably damaging |
Het |
Kcnj11 |
A |
T |
7: 45,749,281 (GRCm39) |
L14Q |
probably damaging |
Het |
Lipo4 |
A |
T |
19: 33,491,642 (GRCm39) |
W114R |
probably damaging |
Het |
Lrrc9 |
T |
A |
12: 72,542,466 (GRCm39) |
I1096N |
probably damaging |
Het |
Lyzl6 |
C |
T |
11: 103,527,680 (GRCm39) |
V15I |
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,053,368 (GRCm39) |
T856A |
possibly damaging |
Het |
Mks1 |
T |
A |
11: 87,751,542 (GRCm39) |
W346R |
probably damaging |
Het |
Mtmr14 |
T |
C |
6: 113,243,263 (GRCm39) |
Y32H |
probably damaging |
Het |
Muc13 |
A |
G |
16: 33,619,386 (GRCm39) |
S45G |
unknown |
Het |
Mx2 |
G |
A |
16: 97,346,812 (GRCm39) |
G93D |
probably damaging |
Het |
Noc4l |
A |
T |
5: 110,797,539 (GRCm39) |
V365E |
probably benign |
Het |
Odf2l |
T |
C |
3: 144,856,776 (GRCm39) |
I577T |
probably damaging |
Het |
Or4l1 |
T |
C |
14: 50,166,622 (GRCm39) |
I126M |
probably damaging |
Het |
Peg10 |
C |
CTCT |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pnoc |
A |
T |
14: 65,639,307 (GRCm39) |
I186N |
possibly damaging |
Het |
Pou4f3 |
A |
G |
18: 42,528,251 (GRCm39) |
I65V |
probably benign |
Het |
Pramel23 |
G |
T |
4: 143,424,764 (GRCm39) |
N226K |
probably benign |
Het |
Prss1l |
T |
C |
6: 41,371,707 (GRCm39) |
L51P |
probably damaging |
Het |
Ptpn21 |
G |
A |
12: 98,648,791 (GRCm39) |
A955V |
probably damaging |
Het |
Rabgap1 |
G |
T |
2: 37,453,476 (GRCm39) |
R968L |
probably benign |
Het |
Rarres1 |
T |
C |
3: 67,386,677 (GRCm39) |
N282S |
probably damaging |
Het |
Rgs17 |
T |
C |
10: 5,791,501 (GRCm39) |
N72S |
probably benign |
Het |
Rp1 |
T |
A |
1: 4,417,926 (GRCm39) |
N1062I |
probably damaging |
Het |
Rpn1 |
T |
A |
6: 88,080,378 (GRCm39) |
V559D |
possibly damaging |
Het |
Rrbp1 |
A |
T |
2: 143,830,855 (GRCm39) |
N437K |
probably damaging |
Het |
Rtn4r |
C |
A |
16: 17,969,399 (GRCm39) |
Q276K |
probably benign |
Het |
Rwdd4a |
T |
C |
8: 47,990,335 (GRCm39) |
S16P |
probably damaging |
Het |
S1pr1 |
A |
G |
3: 115,505,947 (GRCm39) |
S216P |
possibly damaging |
Het |
Scn8a |
C |
A |
15: 100,908,917 (GRCm39) |
T795K |
possibly damaging |
Het |
Spryd3 |
A |
C |
15: 102,026,141 (GRCm39) |
F401C |
probably damaging |
Het |
Stk36 |
G |
T |
1: 74,650,328 (GRCm39) |
E287* |
probably null |
Het |
Tbc1d1 |
G |
T |
5: 64,507,095 (GRCm39) |
S1104I |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,071,683 (GRCm39) |
D2410G |
probably benign |
Het |
Tmem92 |
T |
A |
11: 94,669,784 (GRCm39) |
I116F |
possibly damaging |
Het |
Trp53bp2 |
A |
G |
1: 182,276,260 (GRCm39) |
E747G |
probably damaging |
Het |
Trp63 |
A |
T |
16: 25,707,990 (GRCm39) |
D562V |
probably damaging |
Het |
Ttc21b |
A |
G |
2: 66,077,705 (GRCm39) |
Y167H |
possibly damaging |
Het |
Ubr5 |
G |
A |
15: 37,980,076 (GRCm39) |
A2434V |
probably null |
Het |
Uggt1 |
G |
A |
1: 36,202,396 (GRCm39) |
S1067F |
possibly damaging |
Het |
Vmn2r103 |
T |
A |
17: 20,014,476 (GRCm39) |
Y423N |
probably benign |
Het |
Vmn2r111 |
A |
G |
17: 22,792,083 (GRCm39) |
Y58H |
probably damaging |
Het |
Ypel3 |
T |
A |
7: 126,377,013 (GRCm39) |
V2E |
probably damaging |
Het |
Ythdf3 |
T |
C |
3: 16,243,681 (GRCm39) |
V34A |
probably damaging |
Het |
Zfp180 |
A |
T |
7: 23,804,570 (GRCm39) |
S330C |
probably damaging |
Het |
Zfp292 |
G |
A |
4: 34,809,865 (GRCm39) |
P1060S |
probably benign |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp981 |
C |
T |
4: 146,622,100 (GRCm39) |
R342C |
probably benign |
Het |
|
Other mutations in Cttnbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00954:Cttnbp2
|
APN |
6 |
18,381,061 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01014:Cttnbp2
|
APN |
6 |
18,423,894 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01148:Cttnbp2
|
APN |
6 |
18,382,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01903:Cttnbp2
|
APN |
6 |
18,501,964 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01906:Cttnbp2
|
APN |
6 |
18,378,375 (GRCm39) |
nonsense |
probably null |
|
IGL01994:Cttnbp2
|
APN |
6 |
18,420,814 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02212:Cttnbp2
|
APN |
6 |
18,382,748 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02696:Cttnbp2
|
APN |
6 |
18,434,128 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02813:Cttnbp2
|
APN |
6 |
18,367,537 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02864:Cttnbp2
|
APN |
6 |
18,374,548 (GRCm39) |
missense |
probably benign |
0.21 |
IGL03309:Cttnbp2
|
APN |
6 |
18,381,035 (GRCm39) |
missense |
probably damaging |
0.98 |
Feelers
|
UTSW |
6 |
18,405,278 (GRCm39) |
splice site |
probably null |
|
warning
|
UTSW |
6 |
18,375,952 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
BB019:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4304:Cttnbp2
|
UTSW |
6 |
18,367,457 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4449:Cttnbp2
|
UTSW |
6 |
18,367,461 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4548:Cttnbp2
|
UTSW |
6 |
18,367,462 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4589:Cttnbp2
|
UTSW |
6 |
18,367,457 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cttnbp2
|
UTSW |
6 |
18,367,466 (GRCm39) |
utr 3 prime |
probably benign |
|
FR4976:Cttnbp2
|
UTSW |
6 |
18,367,460 (GRCm39) |
utr 3 prime |
probably benign |
|
R0165:Cttnbp2
|
UTSW |
6 |
18,435,409 (GRCm39) |
nonsense |
probably null |
|
R0382:Cttnbp2
|
UTSW |
6 |
18,435,342 (GRCm39) |
missense |
probably benign |
0.39 |
R0464:Cttnbp2
|
UTSW |
6 |
18,408,690 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0550:Cttnbp2
|
UTSW |
6 |
18,435,308 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0571:Cttnbp2
|
UTSW |
6 |
18,381,102 (GRCm39) |
missense |
probably benign |
|
R0627:Cttnbp2
|
UTSW |
6 |
18,367,372 (GRCm39) |
makesense |
probably null |
|
R0788:Cttnbp2
|
UTSW |
6 |
18,423,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Cttnbp2
|
UTSW |
6 |
18,405,177 (GRCm39) |
splice site |
probably benign |
|
R1319:Cttnbp2
|
UTSW |
6 |
18,434,629 (GRCm39) |
missense |
probably benign |
0.00 |
R1476:Cttnbp2
|
UTSW |
6 |
18,434,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R1572:Cttnbp2
|
UTSW |
6 |
18,375,974 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1596:Cttnbp2
|
UTSW |
6 |
18,408,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1607:Cttnbp2
|
UTSW |
6 |
18,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Cttnbp2
|
UTSW |
6 |
18,435,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Cttnbp2
|
UTSW |
6 |
18,408,656 (GRCm39) |
missense |
probably benign |
0.39 |
R1661:Cttnbp2
|
UTSW |
6 |
18,434,982 (GRCm39) |
missense |
probably benign |
0.20 |
R1665:Cttnbp2
|
UTSW |
6 |
18,434,982 (GRCm39) |
missense |
probably benign |
0.20 |
R1834:Cttnbp2
|
UTSW |
6 |
18,501,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1853:Cttnbp2
|
UTSW |
6 |
18,408,601 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Cttnbp2
|
UTSW |
6 |
18,378,412 (GRCm39) |
missense |
probably benign |
|
R2018:Cttnbp2
|
UTSW |
6 |
18,434,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2169:Cttnbp2
|
UTSW |
6 |
18,426,096 (GRCm39) |
missense |
probably benign |
0.00 |
R2175:Cttnbp2
|
UTSW |
6 |
18,434,828 (GRCm39) |
splice site |
probably null |
|
R2202:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2203:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2204:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2205:Cttnbp2
|
UTSW |
6 |
18,408,693 (GRCm39) |
missense |
probably benign |
0.12 |
R2371:Cttnbp2
|
UTSW |
6 |
18,380,603 (GRCm39) |
missense |
possibly damaging |
0.69 |
R2416:Cttnbp2
|
UTSW |
6 |
18,448,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R3414:Cttnbp2
|
UTSW |
6 |
18,389,204 (GRCm39) |
missense |
probably benign |
|
R3617:Cttnbp2
|
UTSW |
6 |
18,414,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R3861:Cttnbp2
|
UTSW |
6 |
18,423,832 (GRCm39) |
missense |
probably benign |
0.11 |
R3862:Cttnbp2
|
UTSW |
6 |
18,434,905 (GRCm39) |
missense |
probably benign |
0.02 |
R3940:Cttnbp2
|
UTSW |
6 |
18,420,974 (GRCm39) |
missense |
probably benign |
0.34 |
R3941:Cttnbp2
|
UTSW |
6 |
18,427,452 (GRCm39) |
missense |
probably benign |
0.11 |
R4097:Cttnbp2
|
UTSW |
6 |
18,420,871 (GRCm39) |
missense |
probably benign |
|
R4211:Cttnbp2
|
UTSW |
6 |
18,427,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Cttnbp2
|
UTSW |
6 |
18,514,703 (GRCm39) |
missense |
probably benign |
0.00 |
R4367:Cttnbp2
|
UTSW |
6 |
18,405,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4652:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4660:Cttnbp2
|
UTSW |
6 |
18,406,536 (GRCm39) |
missense |
probably benign |
0.05 |
R4975:Cttnbp2
|
UTSW |
6 |
18,406,525 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5064:Cttnbp2
|
UTSW |
6 |
18,448,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5205:Cttnbp2
|
UTSW |
6 |
18,427,432 (GRCm39) |
splice site |
probably benign |
|
R5305:Cttnbp2
|
UTSW |
6 |
18,381,097 (GRCm39) |
missense |
probably benign |
|
R5484:Cttnbp2
|
UTSW |
6 |
18,427,689 (GRCm39) |
intron |
probably benign |
|
R5629:Cttnbp2
|
UTSW |
6 |
18,405,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Cttnbp2
|
UTSW |
6 |
18,414,298 (GRCm39) |
missense |
probably benign |
0.00 |
R5766:Cttnbp2
|
UTSW |
6 |
18,381,032 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5942:Cttnbp2
|
UTSW |
6 |
18,448,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6073:Cttnbp2
|
UTSW |
6 |
18,448,368 (GRCm39) |
missense |
probably benign |
0.01 |
R6073:Cttnbp2
|
UTSW |
6 |
18,434,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R6163:Cttnbp2
|
UTSW |
6 |
18,434,950 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6545:Cttnbp2
|
UTSW |
6 |
18,405,278 (GRCm39) |
splice site |
probably null |
|
R6858:Cttnbp2
|
UTSW |
6 |
18,448,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Cttnbp2
|
UTSW |
6 |
18,435,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Cttnbp2
|
UTSW |
6 |
18,448,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7141:Cttnbp2
|
UTSW |
6 |
18,380,467 (GRCm39) |
missense |
probably benign |
0.00 |
R7353:Cttnbp2
|
UTSW |
6 |
18,375,943 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7465:Cttnbp2
|
UTSW |
6 |
18,501,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7500:Cttnbp2
|
UTSW |
6 |
18,378,419 (GRCm39) |
missense |
probably benign |
0.00 |
R7534:Cttnbp2
|
UTSW |
6 |
18,420,764 (GRCm39) |
critical splice donor site |
probably null |
|
R7646:Cttnbp2
|
UTSW |
6 |
18,375,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Cttnbp2
|
UTSW |
6 |
18,382,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Cttnbp2
|
UTSW |
6 |
18,514,734 (GRCm39) |
start codon destroyed |
possibly damaging |
0.82 |
R7809:Cttnbp2
|
UTSW |
6 |
18,434,289 (GRCm39) |
missense |
probably damaging |
0.99 |
R7817:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7932:Cttnbp2
|
UTSW |
6 |
18,427,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8011:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8014:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8015:Cttnbp2
|
UTSW |
6 |
18,426,092 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8095:Cttnbp2
|
UTSW |
6 |
18,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R8754:Cttnbp2
|
UTSW |
6 |
18,434,037 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8769:Cttnbp2
|
UTSW |
6 |
18,376,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R8836:Cttnbp2
|
UTSW |
6 |
18,375,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8886:Cttnbp2
|
UTSW |
6 |
18,414,298 (GRCm39) |
missense |
probably benign |
0.00 |
R8921:Cttnbp2
|
UTSW |
6 |
18,434,877 (GRCm39) |
missense |
probably benign |
0.10 |
R8931:Cttnbp2
|
UTSW |
6 |
18,434,808 (GRCm39) |
missense |
probably benign |
0.00 |
R8956:Cttnbp2
|
UTSW |
6 |
18,434,165 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9005:Cttnbp2
|
UTSW |
6 |
18,434,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R9141:Cttnbp2
|
UTSW |
6 |
18,429,138 (GRCm39) |
nonsense |
probably null |
|
R9194:Cttnbp2
|
UTSW |
6 |
18,434,850 (GRCm39) |
missense |
probably benign |
0.00 |
R9425:Cttnbp2
|
UTSW |
6 |
18,423,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Cttnbp2
|
UTSW |
6 |
18,427,467 (GRCm39) |
nonsense |
probably null |
|
R9563:Cttnbp2
|
UTSW |
6 |
18,367,382 (GRCm39) |
missense |
probably benign |
0.03 |
R9661:Cttnbp2
|
UTSW |
6 |
18,429,151 (GRCm39) |
missense |
|
|
R9763:Cttnbp2
|
UTSW |
6 |
18,435,240 (GRCm39) |
missense |
probably benign |
|
R9790:Cttnbp2
|
UTSW |
6 |
18,376,027 (GRCm39) |
missense |
probably benign |
0.03 |
R9791:Cttnbp2
|
UTSW |
6 |
18,376,027 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,408,724 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,408,708 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cttnbp2
|
UTSW |
6 |
18,501,959 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cttnbp2
|
UTSW |
6 |
18,420,835 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
Predicted Primers |
PCR Primer
(F):5'- CATGTGAGCCAGTTCTGCTG -3'
(R):5'- TGACAACACTGTTCTTTATAGCAGC -3'
Sequencing Primer
(F):5'- TTATGGGAAAAACAGATGACGTCTC -3'
(R):5'- ATAGCAGCTTTGAGTATCGCATG -3'
|
Posted On |
2019-12-03 |