Incidental Mutation 'R1656:Ehbp1'
| ID |
189127 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ehbp1
|
| Ensembl Gene |
ENSMUSG00000042302 |
| Gene Name |
EH domain binding protein 1 |
| Synonyms |
Flj21950, KIAA0903-like |
| MMRRC Submission |
039692-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.829)
|
| Stock # |
R1656 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
21955825-22237086 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 22096694 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 255
(I255T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118583
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045167]
[ENSMUST00000109563]
[ENSMUST00000134293]
[ENSMUST00000180360]
|
| AlphaFold |
Q69ZW3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000045167
|
| SMART Domains |
Protein: ENSMUSP00000037489
Gene: ENSMUSG00000042302
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NT-C2
|
12 |
165 |
3.8e-32 |
PFAM |
|
Blast:DUF3585
|
176 |
285 |
7e-6 |
BLAST |
|
low complexity region
|
332 |
343 |
N/A |
INTRINSIC |
|
low complexity region
|
374 |
392 |
N/A |
INTRINSIC |
|
low complexity region
|
411 |
422 |
N/A |
INTRINSIC |
|
CH
|
430 |
528 |
1.42e-15 |
SMART |
|
Blast:CH
|
757 |
826 |
3e-12 |
BLAST |
|
low complexity region
|
829 |
850 |
N/A |
INTRINSIC |
|
low complexity region
|
883 |
898 |
N/A |
INTRINSIC |
|
DUF3585
|
1043 |
1187 |
4.25e-61 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000109563
AA Change: I290T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000105191
Gene: ENSMUSG00000042302
AA Change: I290T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NT-C2
|
12 |
165 |
1.3e-29 |
PFAM |
|
Blast:DUF3585
|
176 |
285 |
7e-6 |
BLAST |
|
low complexity region
|
357 |
368 |
N/A |
INTRINSIC |
|
low complexity region
|
399 |
417 |
N/A |
INTRINSIC |
|
low complexity region
|
436 |
447 |
N/A |
INTRINSIC |
|
CH
|
455 |
553 |
1.42e-15 |
SMART |
|
Blast:CH
|
782 |
851 |
3e-12 |
BLAST |
|
low complexity region
|
854 |
875 |
N/A |
INTRINSIC |
|
low complexity region
|
908 |
923 |
N/A |
INTRINSIC |
|
DUF3585
|
1068 |
1212 |
4.25e-61 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000134293
AA Change: I255T
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000118583
Gene: ENSMUSG00000042302
AA Change: I255T
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NT-C2
|
12 |
165 |
3.5e-33 |
PFAM |
|
low complexity region
|
185 |
205 |
N/A |
INTRINSIC |
|
Blast:DUF3585
|
206 |
250 |
4e-18 |
BLAST |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152372
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000180360
|
| SMART Domains |
Protein: ENSMUSP00000136697
Gene: ENSMUSG00000042302
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:NT-C2
|
12 |
165 |
3.8e-32 |
PFAM |
|
Blast:DUF3585
|
176 |
285 |
7e-6 |
BLAST |
|
low complexity region
|
332 |
343 |
N/A |
INTRINSIC |
|
low complexity region
|
374 |
392 |
N/A |
INTRINSIC |
|
low complexity region
|
411 |
422 |
N/A |
INTRINSIC |
|
CH
|
430 |
528 |
1.42e-15 |
SMART |
|
Blast:CH
|
757 |
826 |
3e-12 |
BLAST |
|
low complexity region
|
829 |
850 |
N/A |
INTRINSIC |
|
low complexity region
|
883 |
898 |
N/A |
INTRINSIC |
|
DUF3585
|
1043 |
1187 |
4.25e-61 |
SMART |
|
| Meta Mutation Damage Score |
0.0589 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.6%
- 20x: 93.3%
|
| Validation Efficiency |
96% (79/82) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes an Eps15 homology domain binding protein. The encoded protein may play a role in endocytic trafficking. A single nucleotide polymorphism in this gene is associated with an aggressive form of prostate cancer. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 77 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700024G13Rik |
A |
T |
14: 32,099,901 (GRCm39) |
I42N |
possibly damaging |
Het |
| Adarb2 |
T |
A |
13: 8,253,287 (GRCm39) |
S11T |
unknown |
Het |
| Adgrg1 |
C |
T |
8: 95,738,438 (GRCm39) |
Q644* |
probably null |
Het |
| Akr1c18 |
T |
G |
13: 4,195,252 (GRCm39) |
I69L |
probably benign |
Het |
| Anxa9 |
C |
T |
3: 95,207,884 (GRCm39) |
V219I |
probably benign |
Het |
| Aqp9 |
T |
C |
9: 71,045,385 (GRCm39) |
T101A |
probably benign |
Het |
| Arhgef1 |
C |
T |
7: 24,613,057 (GRCm39) |
R251W |
probably damaging |
Het |
| Arl13b |
T |
A |
16: 62,627,007 (GRCm39) |
E231D |
possibly damaging |
Het |
| Atosa |
C |
T |
9: 74,916,241 (GRCm39) |
A280V |
probably benign |
Het |
| Bcl2l11 |
C |
T |
2: 128,000,176 (GRCm39) |
A173V |
probably benign |
Het |
| Ccni |
A |
T |
5: 93,335,933 (GRCm39) |
|
probably null |
Het |
| Cdh18 |
A |
G |
15: 23,474,485 (GRCm39) |
E785G |
probably benign |
Het |
| Cdk4 |
A |
G |
10: 126,900,849 (GRCm39) |
Y167C |
probably benign |
Het |
| Clip1 |
A |
C |
5: 123,768,466 (GRCm39) |
V757G |
possibly damaging |
Het |
| Ctsc |
T |
C |
7: 87,930,616 (GRCm39) |
V65A |
possibly damaging |
Het |
| Cuedc2 |
G |
A |
19: 46,320,427 (GRCm39) |
S48L |
probably damaging |
Het |
| Cyp39a1 |
T |
A |
17: 43,978,510 (GRCm39) |
M4K |
possibly damaging |
Het |
| Dgcr8 |
T |
C |
16: 18,074,577 (GRCm39) |
S733G |
probably benign |
Het |
| Dnhd1 |
T |
C |
7: 105,363,488 (GRCm39) |
S4017P |
probably damaging |
Het |
| Fam83e |
T |
C |
7: 45,371,687 (GRCm39) |
V28A |
probably benign |
Het |
| Fanci |
A |
G |
7: 79,054,936 (GRCm39) |
|
probably benign |
Het |
| Fat1 |
C |
T |
8: 45,478,567 (GRCm39) |
Q2538* |
probably null |
Het |
| Fshr |
A |
G |
17: 89,508,009 (GRCm39) |
F11S |
unknown |
Het |
| Gab1 |
G |
T |
8: 81,515,388 (GRCm39) |
P310Q |
probably damaging |
Het |
| Galnt18 |
A |
G |
7: 111,215,699 (GRCm39) |
|
probably benign |
Het |
| Gm28042 |
C |
A |
2: 119,869,370 (GRCm39) |
P355Q |
probably damaging |
Het |
| H2-DMa |
A |
G |
17: 34,357,116 (GRCm39) |
T205A |
possibly damaging |
Het |
| Hnf4g |
A |
T |
3: 3,718,011 (GRCm39) |
D420V |
probably benign |
Het |
| Ift70b |
T |
C |
2: 75,767,760 (GRCm39) |
K331R |
probably benign |
Het |
| Il1b |
A |
G |
2: 129,207,989 (GRCm39) |
V164A |
probably damaging |
Het |
| Irf4 |
C |
A |
13: 30,941,485 (GRCm39) |
H279Q |
probably benign |
Het |
| Loxhd1 |
A |
G |
18: 77,409,364 (GRCm39) |
T203A |
possibly damaging |
Het |
| Lsamp |
C |
T |
16: 41,775,682 (GRCm39) |
P178S |
probably damaging |
Het |
| Mcm6 |
T |
C |
1: 128,277,155 (GRCm39) |
S223G |
possibly damaging |
Het |
| Misp |
G |
T |
10: 79,661,777 (GRCm39) |
V65L |
possibly damaging |
Het |
| Mov10 |
A |
G |
3: 104,706,912 (GRCm39) |
V666A |
probably benign |
Het |
| Mycbp2 |
A |
T |
14: 103,485,194 (GRCm39) |
D1102E |
probably damaging |
Het |
| Myef2 |
G |
T |
2: 124,939,860 (GRCm39) |
|
probably null |
Het |
| Myo1e |
T |
A |
9: 70,303,216 (GRCm39) |
I1079N |
probably damaging |
Het |
| Nisch |
G |
T |
14: 30,899,228 (GRCm39) |
|
probably benign |
Het |
| Obox7 |
T |
C |
7: 14,399,346 (GRCm39) |
S191P |
probably benign |
Het |
| Or11h7 |
T |
C |
14: 50,891,465 (GRCm39) |
V257A |
probably benign |
Het |
| Or13p10 |
A |
G |
4: 118,523,385 (GRCm39) |
I224V |
probably damaging |
Het |
| Or14c40 |
C |
T |
7: 86,313,331 (GRCm39) |
L154F |
probably benign |
Het |
| Or1j11 |
G |
A |
2: 36,311,658 (GRCm39) |
V83M |
probably benign |
Het |
| Or5w14 |
A |
T |
2: 87,541,422 (GRCm39) |
V276D |
possibly damaging |
Het |
| Or7d9 |
A |
G |
9: 20,197,873 (GRCm39) |
R301G |
probably damaging |
Het |
| Phf1 |
T |
C |
17: 27,156,333 (GRCm39) |
S492P |
possibly damaging |
Het |
| Phyh |
A |
T |
2: 4,943,164 (GRCm39) |
N337I |
probably damaging |
Het |
| Poteg |
A |
T |
8: 27,985,060 (GRCm39) |
|
probably benign |
Het |
| Prag1 |
G |
T |
8: 36,571,500 (GRCm39) |
K694N |
probably damaging |
Het |
| Proser2 |
C |
T |
2: 6,107,870 (GRCm39) |
E49K |
probably damaging |
Het |
| Pskh1 |
T |
C |
8: 106,656,389 (GRCm39) |
V355A |
possibly damaging |
Het |
| Psmc2 |
T |
C |
5: 22,004,549 (GRCm39) |
V182A |
possibly damaging |
Het |
| Rbfox1 |
A |
G |
16: 7,124,333 (GRCm39) |
|
probably benign |
Het |
| Slc26a7 |
A |
T |
4: 14,621,221 (GRCm39) |
I55K |
possibly damaging |
Het |
| Slc5a8 |
G |
A |
10: 88,761,648 (GRCm39) |
|
probably null |
Het |
| Slitrk3 |
T |
C |
3: 72,957,672 (GRCm39) |
R367G |
probably damaging |
Het |
| Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
| Spata31 |
A |
G |
13: 65,068,953 (GRCm39) |
E367G |
probably benign |
Het |
| Srrm3 |
A |
T |
5: 135,863,892 (GRCm39) |
|
probably null |
Het |
| Ssmem1 |
T |
C |
6: 30,517,507 (GRCm39) |
S6P |
probably damaging |
Het |
| Swap70 |
A |
G |
7: 109,821,034 (GRCm39) |
D6G |
probably benign |
Het |
| Syt1 |
T |
C |
10: 108,419,776 (GRCm39) |
E295G |
probably damaging |
Het |
| Tap2 |
A |
T |
17: 34,424,927 (GRCm39) |
I192F |
possibly damaging |
Het |
| Tgoln1 |
C |
T |
6: 72,591,068 (GRCm39) |
R348H |
probably damaging |
Het |
| Tln2 |
C |
T |
9: 67,134,389 (GRCm39) |
V1373I |
possibly damaging |
Het |
| Tmc2 |
A |
G |
2: 130,089,854 (GRCm39) |
D613G |
possibly damaging |
Het |
| Tmem62 |
T |
A |
2: 120,837,483 (GRCm39) |
Y597N |
probably benign |
Het |
| Trhr2 |
T |
A |
8: 123,084,185 (GRCm39) |
T272S |
probably damaging |
Het |
| Vmn2r92 |
T |
C |
17: 18,372,198 (GRCm39) |
S3P |
probably benign |
Het |
| Wdfy3 |
A |
T |
5: 102,089,313 (GRCm39) |
I627N |
probably damaging |
Het |
| Zfhx4 |
T |
C |
3: 5,478,076 (GRCm39) |
S3564P |
probably damaging |
Het |
| Zfp467 |
T |
G |
6: 48,416,013 (GRCm39) |
E213A |
possibly damaging |
Het |
| Zfp746 |
T |
G |
6: 48,041,411 (GRCm39) |
K437N |
probably damaging |
Het |
| Zfp853 |
A |
G |
5: 143,274,840 (GRCm39) |
|
probably benign |
Het |
| Zranb1 |
T |
A |
7: 132,551,496 (GRCm39) |
V49D |
probably benign |
Het |
|
| Other mutations in Ehbp1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00754:Ehbp1
|
APN |
11 |
22,197,967 (GRCm39) |
splice site |
probably benign |
|
|
IGL00786:Ehbp1
|
APN |
11 |
22,050,460 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
IGL01308:Ehbp1
|
APN |
11 |
22,088,022 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01322:Ehbp1
|
APN |
11 |
22,039,636 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01590:Ehbp1
|
APN |
11 |
22,045,611 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL01611:Ehbp1
|
APN |
11 |
22,122,883 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL01636:Ehbp1
|
APN |
11 |
22,039,584 (GRCm39) |
missense |
probably benign |
0.03 |
|
IGL01728:Ehbp1
|
APN |
11 |
22,051,115 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02012:Ehbp1
|
APN |
11 |
22,051,218 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02034:Ehbp1
|
APN |
11 |
22,235,486 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02324:Ehbp1
|
APN |
11 |
22,046,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02511:Ehbp1
|
APN |
11 |
22,039,653 (GRCm39) |
missense |
probably damaging |
1.00 |
|
trajan
|
UTSW |
11 |
22,101,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
K7894:Ehbp1
|
UTSW |
11 |
22,039,683 (GRCm39) |
splice site |
probably benign |
|
|
PIT4418001:Ehbp1
|
UTSW |
11 |
22,003,494 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0218:Ehbp1
|
UTSW |
11 |
22,181,992 (GRCm39) |
splice site |
probably benign |
|
|
R0294:Ehbp1
|
UTSW |
11 |
22,045,427 (GRCm39) |
missense |
probably benign |
0.27 |
|
R0398:Ehbp1
|
UTSW |
11 |
22,045,886 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0420:Ehbp1
|
UTSW |
11 |
22,101,836 (GRCm39) |
missense |
probably benign |
|
|
R0468:Ehbp1
|
UTSW |
11 |
22,119,184 (GRCm39) |
splice site |
probably benign |
|
|
R0943:Ehbp1
|
UTSW |
11 |
22,045,883 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1181:Ehbp1
|
UTSW |
11 |
22,012,831 (GRCm39) |
missense |
probably benign |
0.25 |
|
R1481:Ehbp1
|
UTSW |
11 |
21,956,782 (GRCm39) |
makesense |
probably null |
|
|
R1493:Ehbp1
|
UTSW |
11 |
21,956,866 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1563:Ehbp1
|
UTSW |
11 |
22,009,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1648:Ehbp1
|
UTSW |
11 |
22,046,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1696:Ehbp1
|
UTSW |
11 |
22,003,441 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1923:Ehbp1
|
UTSW |
11 |
22,101,850 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1950:Ehbp1
|
UTSW |
11 |
22,009,228 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2263:Ehbp1
|
UTSW |
11 |
22,045,462 (GRCm39) |
missense |
probably benign |
|
|
R2436:Ehbp1
|
UTSW |
11 |
22,039,524 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3148:Ehbp1
|
UTSW |
11 |
22,050,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3973:Ehbp1
|
UTSW |
11 |
22,087,867 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3974:Ehbp1
|
UTSW |
11 |
22,087,867 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4030:Ehbp1
|
UTSW |
11 |
22,235,498 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4085:Ehbp1
|
UTSW |
11 |
22,045,898 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4089:Ehbp1
|
UTSW |
11 |
22,045,898 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4524:Ehbp1
|
UTSW |
11 |
22,101,843 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4641:Ehbp1
|
UTSW |
11 |
22,045,892 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4873:Ehbp1
|
UTSW |
11 |
22,051,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4875:Ehbp1
|
UTSW |
11 |
22,051,164 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4914:Ehbp1
|
UTSW |
11 |
22,096,592 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4915:Ehbp1
|
UTSW |
11 |
22,096,592 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4916:Ehbp1
|
UTSW |
11 |
22,096,592 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4917:Ehbp1
|
UTSW |
11 |
22,096,592 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4918:Ehbp1
|
UTSW |
11 |
22,096,592 (GRCm39) |
missense |
probably benign |
0.20 |
|
R4929:Ehbp1
|
UTSW |
11 |
22,189,169 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R4995:Ehbp1
|
UTSW |
11 |
22,051,073 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5325:Ehbp1
|
UTSW |
11 |
22,045,370 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R5579:Ehbp1
|
UTSW |
11 |
22,087,846 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5979:Ehbp1
|
UTSW |
11 |
22,101,887 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6025:Ehbp1
|
UTSW |
11 |
22,189,156 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6259:Ehbp1
|
UTSW |
11 |
22,235,684 (GRCm39) |
start gained |
probably benign |
|
|
R6685:Ehbp1
|
UTSW |
11 |
22,096,641 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6893:Ehbp1
|
UTSW |
11 |
21,964,945 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7127:Ehbp1
|
UTSW |
11 |
22,003,529 (GRCm39) |
nonsense |
probably null |
|
|
R7465:Ehbp1
|
UTSW |
11 |
22,088,001 (GRCm39) |
missense |
probably benign |
|
|
R7722:Ehbp1
|
UTSW |
11 |
22,039,572 (GRCm39) |
missense |
probably null |
|
|
R7724:Ehbp1
|
UTSW |
11 |
22,039,572 (GRCm39) |
missense |
probably null |
|
|
R7797:Ehbp1
|
UTSW |
11 |
22,046,109 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7868:Ehbp1
|
UTSW |
11 |
22,096,542 (GRCm39) |
nonsense |
probably null |
|
|
R8088:Ehbp1
|
UTSW |
11 |
22,039,572 (GRCm39) |
missense |
probably null |
|
|
R8218:Ehbp1
|
UTSW |
11 |
22,046,096 (GRCm39) |
missense |
possibly damaging |
0.77 |
|
R8235:Ehbp1
|
UTSW |
11 |
22,189,153 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8267:Ehbp1
|
UTSW |
11 |
22,096,562 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8318:Ehbp1
|
UTSW |
11 |
22,087,980 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8334:Ehbp1
|
UTSW |
11 |
21,957,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8425:Ehbp1
|
UTSW |
11 |
21,963,495 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8439:Ehbp1
|
UTSW |
11 |
22,046,109 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R8493:Ehbp1
|
UTSW |
11 |
22,235,842 (GRCm39) |
start gained |
probably benign |
|
|
R8745:Ehbp1
|
UTSW |
11 |
22,119,064 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R8824:Ehbp1
|
UTSW |
11 |
22,182,053 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8964:Ehbp1
|
UTSW |
11 |
22,101,154 (GRCm39) |
nonsense |
probably null |
|
|
R8987:Ehbp1
|
UTSW |
11 |
22,003,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9144:Ehbp1
|
UTSW |
11 |
22,018,463 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9187:Ehbp1
|
UTSW |
11 |
22,101,184 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9448:Ehbp1
|
UTSW |
11 |
22,087,881 (GRCm39) |
missense |
probably benign |
|
|
R9549:Ehbp1
|
UTSW |
11 |
22,012,788 (GRCm39) |
missense |
probably benign |
0.44 |
|
R9612:Ehbp1
|
UTSW |
11 |
22,119,124 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9645:Ehbp1
|
UTSW |
11 |
22,051,052 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9678:Ehbp1
|
UTSW |
11 |
22,101,108 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R9745:Ehbp1
|
UTSW |
11 |
22,096,692 (GRCm39) |
missense |
probably benign |
0.19 |
|
RF016:Ehbp1
|
UTSW |
11 |
22,096,646 (GRCm39) |
missense |
probably benign |
|
|
RF037:Ehbp1
|
UTSW |
11 |
21,956,783 (GRCm39) |
small deletion |
probably benign |
|
|
X0018:Ehbp1
|
UTSW |
11 |
22,051,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Ehbp1
|
UTSW |
11 |
22,045,590 (GRCm39) |
missense |
probably benign |
0.03 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACTACATGGGCTACGCTGTGATGG -3'
(R):5'- TCCAGGAGATGAGAGGTGGCATTC -3'
Sequencing Primer
(F):5'- AGCAGATGTACTTACTCATCCAG -3'
(R):5'- TTCTCTAACGAAGGAGGCAAAAATC -3'
|
| Posted On |
2014-05-09 |
Incidental Mutation