Incidental Mutation 'R2029:Ecpas'
| ID |
220917 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Ecpas
|
| Ensembl Gene |
ENSMUSG00000050812 |
| Gene Name |
Ecm29 proteasome adaptor and scaffold |
| Synonyms |
AI314180 |
| MMRRC Submission |
040036-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.366)
|
| Stock # |
R2029 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
4 |
| Chromosomal Location |
58798911-58912749 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 58844165 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Stop codon
at position 534
(R534*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000117585
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000102889]
[ENSMUST00000107557]
[ENSMUST00000144512]
[ENSMUST00000149301]
|
| AlphaFold |
Q6PDI5 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000102889
AA Change: R534*
|
| SMART Domains |
Protein: ENSMUSP00000099953
Gene: ENSMUSG00000050812
AA Change: R534*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Ecm29
|
10 |
517 |
1.1e-155 |
PFAM |
|
low complexity region
|
627 |
642 |
N/A |
INTRINSIC |
|
low complexity region
|
653 |
665 |
N/A |
INTRINSIC |
|
SCOP:d1qbkb_
|
693 |
1491 |
3e-31 |
SMART |
|
low complexity region
|
1781 |
1797 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000107557
AA Change: R534*
|
| SMART Domains |
Protein: ENSMUSP00000103182
Gene: ENSMUSG00000050812
AA Change: R534*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Ecm29
|
10 |
517 |
7.6e-164 |
PFAM |
|
low complexity region
|
627 |
642 |
N/A |
INTRINSIC |
|
low complexity region
|
653 |
665 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000144512
AA Change: R534*
|
| SMART Domains |
Protein: ENSMUSP00000118103
Gene: ENSMUSG00000050812
AA Change: R534*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Ecm29
|
10 |
517 |
2.3e-164 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000149301
AA Change: R534*
|
| SMART Domains |
Protein: ENSMUSP00000117585
Gene: ENSMUSG00000050812
AA Change: R534*
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Ecm29
|
10 |
517 |
4e-163 |
PFAM |
|
low complexity region
|
627 |
642 |
N/A |
INTRINSIC |
|
low complexity region
|
653 |
665 |
N/A |
INTRINSIC |
|
SCOP:d1qbkb_
|
693 |
1490 |
8e-32 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151869
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.8%
|
| Validation Efficiency |
98% (97/99) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 100 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam18 |
C |
G |
8: 25,140,893 (GRCm39) |
G286A |
probably damaging |
Het |
| Adcy1 |
G |
A |
11: 7,089,142 (GRCm39) |
A519T |
probably benign |
Het |
| Anxa2 |
T |
A |
9: 69,371,762 (GRCm39) |
S2T |
possibly damaging |
Het |
| Ap3m1 |
G |
A |
14: 21,089,217 (GRCm39) |
S261L |
possibly damaging |
Het |
| Baz2b |
A |
T |
2: 59,743,067 (GRCm39) |
|
probably benign |
Het |
| Brdt |
T |
A |
5: 107,507,090 (GRCm39) |
S497T |
probably benign |
Het |
| Cdh11 |
A |
G |
8: 103,406,404 (GRCm39) |
F23S |
probably benign |
Het |
| Cdh16 |
A |
C |
8: 105,344,434 (GRCm39) |
L540R |
probably damaging |
Het |
| Ces5a |
A |
T |
8: 94,261,205 (GRCm39) |
L74Q |
probably damaging |
Het |
| Cfap69 |
A |
G |
5: 5,654,306 (GRCm39) |
S543P |
probably damaging |
Het |
| Cfap74 |
T |
C |
4: 155,526,538 (GRCm39) |
I763T |
possibly damaging |
Het |
| Cma1 |
T |
A |
14: 56,181,191 (GRCm39) |
R58S |
possibly damaging |
Het |
| Csmd3 |
C |
T |
15: 47,701,975 (GRCm39) |
D1599N |
probably damaging |
Het |
| Cyld |
A |
G |
8: 89,471,940 (GRCm39) |
K857R |
probably benign |
Het |
| Cyp3a16 |
T |
C |
5: 145,388,667 (GRCm39) |
D270G |
probably damaging |
Het |
| D1Pas1 |
T |
C |
1: 186,700,286 (GRCm39) |
S72P |
possibly damaging |
Het |
| Ddx3y |
T |
C |
Y: 1,266,389 (GRCm39) |
E331G |
probably benign |
Het |
| Degs1l |
T |
A |
1: 180,882,496 (GRCm39) |
I86K |
probably benign |
Het |
| Dis3l2 |
T |
C |
1: 86,782,189 (GRCm39) |
|
probably benign |
Het |
| Dop1a |
G |
T |
9: 86,403,418 (GRCm39) |
W1539C |
probably damaging |
Het |
| Dop1b |
A |
G |
16: 93,566,323 (GRCm39) |
K917E |
probably benign |
Het |
| Efcab3 |
T |
C |
11: 104,990,851 (GRCm39) |
I5462T |
probably damaging |
Het |
| Eif1ad15 |
A |
T |
12: 88,288,191 (GRCm39) |
S21T |
unknown |
Het |
| Epo |
A |
G |
5: 137,483,447 (GRCm39) |
|
probably benign |
Het |
| Figla |
T |
A |
6: 85,997,624 (GRCm39) |
|
probably benign |
Het |
| Flvcr1 |
T |
C |
1: 190,753,353 (GRCm39) |
D273G |
probably benign |
Het |
| Fryl |
T |
A |
5: 73,179,465 (GRCm39) |
R304* |
probably null |
Het |
| Gcm1 |
T |
G |
9: 77,972,326 (GRCm39) |
D422E |
possibly damaging |
Het |
| Get3 |
A |
T |
8: 85,746,403 (GRCm39) |
Y148* |
probably null |
Het |
| Ggt6 |
A |
G |
11: 72,328,367 (GRCm39) |
D251G |
possibly damaging |
Het |
| Git2 |
A |
G |
5: 114,904,511 (GRCm39) |
|
probably null |
Het |
| Gm18856 |
A |
T |
13: 14,139,376 (GRCm39) |
|
probably benign |
Het |
| Gm20939 |
T |
A |
17: 95,183,252 (GRCm39) |
|
probably benign |
Het |
| Gpr176 |
A |
G |
2: 118,109,913 (GRCm39) |
Y449H |
probably benign |
Het |
| H2-Eb1 |
A |
G |
17: 34,533,366 (GRCm39) |
E196G |
probably damaging |
Het |
| H2-M10.6 |
A |
G |
17: 37,124,799 (GRCm39) |
T239A |
possibly damaging |
Het |
| Haus5 |
T |
C |
7: 30,358,825 (GRCm39) |
N237S |
possibly damaging |
Het |
| Hectd3 |
T |
C |
4: 116,857,882 (GRCm39) |
M605T |
probably damaging |
Het |
| Hps3 |
T |
C |
3: 20,084,691 (GRCm39) |
I166V |
probably benign |
Het |
| Ighv5-21 |
A |
T |
12: 114,286,434 (GRCm39) |
|
probably benign |
Het |
| Kdm6b |
C |
T |
11: 69,294,418 (GRCm39) |
G1218D |
unknown |
Het |
| Klhl30 |
A |
G |
1: 91,285,636 (GRCm39) |
|
probably null |
Het |
| Kmt2a |
A |
T |
9: 44,729,747 (GRCm39) |
S3523R |
probably benign |
Het |
| Lnpep |
A |
T |
17: 17,788,661 (GRCm39) |
N481K |
probably damaging |
Het |
| Lrp1b |
T |
C |
2: 41,231,861 (GRCm39) |
H1203R |
probably benign |
Het |
| Lrrc8a |
C |
T |
2: 30,146,661 (GRCm39) |
R492W |
probably damaging |
Het |
| Magel2 |
T |
A |
7: 62,030,342 (GRCm39) |
V1082D |
unknown |
Het |
| Memo1 |
A |
C |
17: 74,552,049 (GRCm39) |
H82Q |
probably null |
Het |
| Myh13 |
A |
T |
11: 67,252,115 (GRCm39) |
T1408S |
probably benign |
Het |
| Myh2 |
A |
T |
11: 67,085,451 (GRCm39) |
N1792Y |
possibly damaging |
Het |
| Myo1e |
A |
T |
9: 70,275,969 (GRCm39) |
N728I |
possibly damaging |
Het |
| Myo1e |
T |
C |
9: 70,285,997 (GRCm39) |
|
probably benign |
Het |
| Myo5c |
T |
C |
9: 75,196,337 (GRCm39) |
|
probably benign |
Het |
| Or11l3 |
T |
A |
11: 58,516,319 (GRCm39) |
L184F |
probably damaging |
Het |
| Or1e19 |
A |
G |
11: 73,316,188 (GRCm39) |
V207A |
probably benign |
Het |
| Or2d2b |
T |
C |
7: 106,705,643 (GRCm39) |
I142V |
probably benign |
Het |
| Or4c11c |
T |
A |
2: 88,661,749 (GRCm39) |
M96K |
possibly damaging |
Het |
| Or51g1 |
T |
A |
7: 102,633,478 (GRCm39) |
T298S |
probably damaging |
Het |
| Or52e3 |
T |
C |
7: 102,868,967 (GRCm39) |
F14S |
probably damaging |
Het |
| Parp2 |
C |
T |
14: 51,047,543 (GRCm39) |
A18V |
probably benign |
Het |
| Peli1 |
T |
A |
11: 21,098,110 (GRCm39) |
C282S |
probably damaging |
Het |
| Phf8-ps |
G |
T |
17: 33,286,598 (GRCm39) |
S68* |
probably null |
Het |
| Piezo2 |
T |
C |
18: 63,252,006 (GRCm39) |
M404V |
possibly damaging |
Het |
| Pkn1 |
T |
A |
8: 84,404,592 (GRCm39) |
Q496L |
possibly damaging |
Het |
| Pla2r1 |
A |
T |
2: 60,262,317 (GRCm39) |
F1093L |
probably damaging |
Het |
| Ppp2r3d |
A |
G |
9: 101,022,680 (GRCm39) |
V323A |
probably damaging |
Het |
| Pramel16 |
T |
A |
4: 143,676,453 (GRCm39) |
Y217F |
probably benign |
Het |
| Prg2 |
C |
T |
2: 84,812,342 (GRCm39) |
|
probably benign |
Het |
| Ptprb |
G |
A |
10: 116,182,958 (GRCm39) |
G1545S |
probably benign |
Het |
| Rbm19 |
A |
G |
5: 120,258,307 (GRCm39) |
D174G |
possibly damaging |
Het |
| Rhbdf2 |
T |
A |
11: 116,491,974 (GRCm39) |
T526S |
probably damaging |
Het |
| Rpusd4 |
A |
G |
9: 35,179,310 (GRCm39) |
N42S |
probably benign |
Het |
| Ryr3 |
T |
A |
2: 112,477,361 (GRCm39) |
Q4455L |
possibly damaging |
Het |
| Sema4a |
G |
T |
3: 88,358,668 (GRCm39) |
H30Q |
probably damaging |
Het |
| Skint1 |
G |
A |
4: 111,878,653 (GRCm39) |
|
probably null |
Het |
| Slc1a3 |
A |
G |
15: 8,675,153 (GRCm39) |
V284A |
probably benign |
Het |
| Slc30a9 |
A |
T |
5: 67,497,318 (GRCm39) |
K288* |
probably null |
Het |
| Slc36a1 |
G |
T |
11: 55,119,164 (GRCm39) |
A380S |
probably benign |
Het |
| Slc47a1 |
G |
A |
11: 61,268,833 (GRCm39) |
|
probably benign |
Het |
| Snx19 |
A |
T |
9: 30,340,296 (GRCm39) |
E478V |
probably benign |
Het |
| Spag6 |
T |
C |
2: 18,738,916 (GRCm39) |
|
probably benign |
Het |
| Stag1 |
A |
T |
9: 100,668,740 (GRCm39) |
T223S |
probably damaging |
Het |
| Terb1 |
A |
T |
8: 105,224,732 (GRCm39) |
|
probably benign |
Het |
| Terf1 |
A |
G |
1: 15,876,170 (GRCm39) |
D90G |
possibly damaging |
Het |
| Tex15 |
A |
G |
8: 34,061,302 (GRCm39) |
D518G |
probably damaging |
Het |
| Tmem174 |
T |
A |
13: 98,773,546 (GRCm39) |
M95L |
possibly damaging |
Het |
| Tnnt3 |
GTCCAGGCATCTC |
GTC |
7: 142,066,364 (GRCm39) |
|
probably benign |
Het |
| Usp28 |
A |
G |
9: 48,896,803 (GRCm39) |
D8G |
probably benign |
Het |
| Vmn2r105 |
T |
C |
17: 20,444,840 (GRCm39) |
T551A |
probably damaging |
Het |
| Vmn2r107 |
A |
G |
17: 20,595,549 (GRCm39) |
I701V |
probably benign |
Het |
| Vmn2r13 |
A |
C |
5: 109,339,943 (GRCm39) |
F11V |
probably benign |
Het |
| Vmn2r85 |
G |
C |
10: 130,261,443 (GRCm39) |
S298* |
probably null |
Het |
| Wdr6 |
C |
G |
9: 108,452,554 (GRCm39) |
W443S |
probably damaging |
Het |
| Wipi1 |
A |
G |
11: 109,474,016 (GRCm39) |
V210A |
probably damaging |
Het |
| Zfp317 |
A |
G |
9: 19,556,532 (GRCm39) |
T47A |
probably benign |
Het |
| Zfp61 |
T |
C |
7: 23,991,714 (GRCm39) |
T146A |
probably benign |
Het |
| Zfp964 |
A |
G |
8: 70,116,567 (GRCm39) |
E389G |
unknown |
Het |
| Zfyve16 |
T |
C |
13: 92,640,985 (GRCm39) |
D1253G |
probably damaging |
Het |
| Zpld2 |
T |
C |
4: 133,929,669 (GRCm39) |
K212R |
possibly damaging |
Het |
| Zswim7 |
G |
A |
11: 62,158,299 (GRCm39) |
|
probably benign |
Het |
|
| Other mutations in Ecpas |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00799:Ecpas
|
APN |
4 |
58,828,047 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01145:Ecpas
|
APN |
4 |
58,811,501 (GRCm39) |
missense |
probably null |
0.08 |
|
IGL01371:Ecpas
|
APN |
4 |
58,809,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01445:Ecpas
|
APN |
4 |
58,833,988 (GRCm39) |
missense |
probably benign |
0.08 |
|
IGL01452:Ecpas
|
APN |
4 |
58,836,181 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01626:Ecpas
|
APN |
4 |
58,832,814 (GRCm39) |
splice site |
probably benign |
|
|
IGL01672:Ecpas
|
APN |
4 |
58,814,041 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL01943:Ecpas
|
APN |
4 |
58,849,937 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL01944:Ecpas
|
APN |
4 |
58,861,544 (GRCm39) |
missense |
probably benign |
0.42 |
|
IGL02190:Ecpas
|
APN |
4 |
58,800,190 (GRCm39) |
missense |
probably benign |
0.12 |
|
IGL02272:Ecpas
|
APN |
4 |
58,811,731 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL02435:Ecpas
|
APN |
4 |
58,830,325 (GRCm39) |
splice site |
probably benign |
|
|
IGL02516:Ecpas
|
APN |
4 |
58,877,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02540:Ecpas
|
APN |
4 |
58,805,534 (GRCm39) |
splice site |
probably benign |
|
|
IGL02709:Ecpas
|
APN |
4 |
58,872,699 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL02742:Ecpas
|
APN |
4 |
58,840,757 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02812:Ecpas
|
APN |
4 |
58,864,343 (GRCm39) |
splice site |
probably benign |
|
|
IGL02828:Ecpas
|
APN |
4 |
58,875,512 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
IGL03130:Ecpas
|
APN |
4 |
58,800,288 (GRCm39) |
missense |
probably benign |
|
|
IGL03179:Ecpas
|
APN |
4 |
58,832,777 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03237:Ecpas
|
APN |
4 |
58,810,668 (GRCm39) |
missense |
probably benign |
0.40 |
|
IGL03344:Ecpas
|
APN |
4 |
58,828,538 (GRCm39) |
missense |
probably damaging |
1.00 |
|
boone
|
UTSW |
4 |
58,877,157 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Crockett
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
frontiersman
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
|
BB006:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB016:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0051:Ecpas
|
UTSW |
4 |
58,832,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0051:Ecpas
|
UTSW |
4 |
58,832,729 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0313:Ecpas
|
UTSW |
4 |
58,811,892 (GRCm39) |
missense |
probably benign |
0.11 |
|
R0399:Ecpas
|
UTSW |
4 |
58,827,047 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R0487:Ecpas
|
UTSW |
4 |
58,819,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0492:Ecpas
|
UTSW |
4 |
58,864,418 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0705:Ecpas
|
UTSW |
4 |
58,885,366 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0847:Ecpas
|
UTSW |
4 |
58,841,439 (GRCm39) |
missense |
probably benign |
0.14 |
|
R1467:Ecpas
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
|
R1467:Ecpas
|
UTSW |
4 |
58,832,753 (GRCm39) |
missense |
probably benign |
|
|
R1482:Ecpas
|
UTSW |
4 |
58,820,163 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R1529:Ecpas
|
UTSW |
4 |
58,832,701 (GRCm39) |
splice site |
probably null |
|
|
R1771:Ecpas
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1776:Ecpas
|
UTSW |
4 |
58,879,100 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1822:Ecpas
|
UTSW |
4 |
58,805,539 (GRCm39) |
critical splice donor site |
probably null |
|
|
R1864:Ecpas
|
UTSW |
4 |
58,849,942 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R2061:Ecpas
|
UTSW |
4 |
58,824,270 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2125:Ecpas
|
UTSW |
4 |
58,833,978 (GRCm39) |
missense |
probably benign |
|
|
R2266:Ecpas
|
UTSW |
4 |
58,830,332 (GRCm39) |
critical splice donor site |
probably null |
|
|
R2889:Ecpas
|
UTSW |
4 |
58,836,165 (GRCm39) |
missense |
probably benign |
|
|
R2902:Ecpas
|
UTSW |
4 |
58,809,691 (GRCm39) |
missense |
probably benign |
0.31 |
|
R2903:Ecpas
|
UTSW |
4 |
58,828,622 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R2925:Ecpas
|
UTSW |
4 |
58,833,928 (GRCm39) |
nonsense |
probably null |
|
|
R4151:Ecpas
|
UTSW |
4 |
58,836,254 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R4225:Ecpas
|
UTSW |
4 |
58,847,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4486:Ecpas
|
UTSW |
4 |
58,820,086 (GRCm39) |
intron |
probably benign |
|
|
R4576:Ecpas
|
UTSW |
4 |
58,834,708 (GRCm39) |
intron |
probably benign |
|
|
R4580:Ecpas
|
UTSW |
4 |
58,840,751 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4654:Ecpas
|
UTSW |
4 |
58,834,523 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R4688:Ecpas
|
UTSW |
4 |
58,840,757 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R4726:Ecpas
|
UTSW |
4 |
58,844,191 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4825:Ecpas
|
UTSW |
4 |
58,850,911 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4928:Ecpas
|
UTSW |
4 |
58,827,073 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5098:Ecpas
|
UTSW |
4 |
58,877,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5284:Ecpas
|
UTSW |
4 |
58,836,172 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5375:Ecpas
|
UTSW |
4 |
58,809,401 (GRCm39) |
nonsense |
probably null |
|
|
R5382:Ecpas
|
UTSW |
4 |
58,850,934 (GRCm39) |
missense |
probably benign |
0.38 |
|
R5487:Ecpas
|
UTSW |
4 |
58,809,421 (GRCm39) |
missense |
probably benign |
0.22 |
|
R5703:Ecpas
|
UTSW |
4 |
58,877,171 (GRCm39) |
splice site |
probably null |
|
|
R5761:Ecpas
|
UTSW |
4 |
58,853,131 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5791:Ecpas
|
UTSW |
4 |
58,822,111 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5791:Ecpas
|
UTSW |
4 |
58,814,027 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5928:Ecpas
|
UTSW |
4 |
58,849,948 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R6062:Ecpas
|
UTSW |
4 |
58,826,453 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R6246:Ecpas
|
UTSW |
4 |
58,811,365 (GRCm39) |
splice site |
probably null |
|
|
R6298:Ecpas
|
UTSW |
4 |
58,877,157 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6326:Ecpas
|
UTSW |
4 |
58,827,068 (GRCm39) |
missense |
probably benign |
0.34 |
|
R6478:Ecpas
|
UTSW |
4 |
58,810,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6707:Ecpas
|
UTSW |
4 |
58,879,101 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R6846:Ecpas
|
UTSW |
4 |
58,814,081 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R6857:Ecpas
|
UTSW |
4 |
58,814,065 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6951:Ecpas
|
UTSW |
4 |
58,853,114 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7088:Ecpas
|
UTSW |
4 |
58,849,766 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R7302:Ecpas
|
UTSW |
4 |
58,834,593 (GRCm39) |
missense |
probably benign |
0.43 |
|
R7337:Ecpas
|
UTSW |
4 |
58,827,047 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R7341:Ecpas
|
UTSW |
4 |
58,809,415 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7344:Ecpas
|
UTSW |
4 |
58,824,770 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7525:Ecpas
|
UTSW |
4 |
58,847,038 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R7530:Ecpas
|
UTSW |
4 |
58,815,317 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7533:Ecpas
|
UTSW |
4 |
58,809,411 (GRCm39) |
missense |
probably benign |
0.12 |
|
R7557:Ecpas
|
UTSW |
4 |
58,849,691 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R7698:Ecpas
|
UTSW |
4 |
58,832,660 (GRCm39) |
missense |
unknown |
|
|
R7793:Ecpas
|
UTSW |
4 |
58,853,150 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7892:Ecpas
|
UTSW |
4 |
58,828,593 (GRCm39) |
missense |
probably benign |
|
|
R7894:Ecpas
|
UTSW |
4 |
58,853,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7929:Ecpas
|
UTSW |
4 |
58,869,554 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8010:Ecpas
|
UTSW |
4 |
58,832,681 (GRCm39) |
missense |
unknown |
|
|
R8082:Ecpas
|
UTSW |
4 |
58,807,852 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8175:Ecpas
|
UTSW |
4 |
58,872,756 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8191:Ecpas
|
UTSW |
4 |
58,872,587 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8326:Ecpas
|
UTSW |
4 |
58,847,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8459:Ecpas
|
UTSW |
4 |
58,821,379 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8683:Ecpas
|
UTSW |
4 |
58,834,515 (GRCm39) |
missense |
probably benign |
0.31 |
|
R8747:Ecpas
|
UTSW |
4 |
58,828,632 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8981:Ecpas
|
UTSW |
4 |
58,801,796 (GRCm39) |
missense |
probably benign |
|
|
R9206:Ecpas
|
UTSW |
4 |
58,875,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9208:Ecpas
|
UTSW |
4 |
58,875,444 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9231:Ecpas
|
UTSW |
4 |
58,875,533 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9249:Ecpas
|
UTSW |
4 |
58,869,427 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9355:Ecpas
|
UTSW |
4 |
58,844,114 (GRCm39) |
missense |
probably benign |
0.23 |
|
R9534:Ecpas
|
UTSW |
4 |
58,807,867 (GRCm39) |
missense |
probably benign |
|
|
R9555:Ecpas
|
UTSW |
4 |
58,879,083 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9570:Ecpas
|
UTSW |
4 |
58,832,796 (GRCm39) |
nonsense |
probably null |
|
|
R9673:Ecpas
|
UTSW |
4 |
58,822,060 (GRCm39) |
missense |
probably benign |
|
|
R9707:Ecpas
|
UTSW |
4 |
58,824,816 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
R9721:Ecpas
|
UTSW |
4 |
58,850,938 (GRCm39) |
missense |
probably benign |
0.39 |
|
X0060:Ecpas
|
UTSW |
4 |
58,840,752 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
Z1177:Ecpas
|
UTSW |
4 |
58,861,614 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGACACCTGGTACCCTTAAGAAC -3'
(R):5'- CAAGCCAAGTGACTCAGCAG -3'
Sequencing Primer
(F):5'- CTTTGGAAAAGCAAATTAACTGCATG -3'
(R):5'- AGTGACTCAGCAGATATCACTG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation