Incidental Mutation 'R5068:Erbb4'
ID |
388400 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Erbb4
|
Ensembl Gene |
ENSMUSG00000062209 |
Gene Name |
erb-b2 receptor tyrosine kinase 4 |
Synonyms |
Her4, ErbB4 |
MMRRC Submission |
042658-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R5068 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
68071345-69147218 bp(-) (GRCm39) |
Type of Mutation |
splice site (6 bp from exon) |
DNA Base Change (assembly) |
A to T
at 68083061 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000112713
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000119142]
[ENSMUST00000121473]
|
AlphaFold |
Q61527 |
Predicted Effect |
probably null
Transcript: ENSMUST00000119142
|
SMART Domains |
Protein: ENSMUSP00000112713 Gene: ENSMUSG00000062209
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Recep_L_domain
|
55 |
167 |
5e-34 |
PFAM |
FU
|
183 |
223 |
2.07e1 |
SMART |
FU
|
226 |
268 |
5.78e-10 |
SMART |
Pfam:Recep_L_domain
|
358 |
478 |
1e-29 |
PFAM |
FU
|
493 |
544 |
6.45e-8 |
SMART |
FU
|
549 |
599 |
3.51e-9 |
SMART |
FU
|
611 |
659 |
2.32e0 |
SMART |
TyrKc
|
718 |
974 |
7.53e-133 |
SMART |
low complexity region
|
1007 |
1023 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000121473
|
SMART Domains |
Protein: ENSMUSP00000114123 Gene: ENSMUSG00000062209
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
Pfam:Recep_L_domain
|
55 |
167 |
1.6e-34 |
PFAM |
FU
|
183 |
223 |
2.07e1 |
SMART |
FU
|
226 |
268 |
5.78e-10 |
SMART |
Pfam:Recep_L_domain
|
358 |
478 |
5.5e-29 |
PFAM |
FU
|
493 |
544 |
6.45e-8 |
SMART |
FU
|
549 |
599 |
3.51e-9 |
SMART |
FU
|
611 |
659 |
2.32e0 |
SMART |
TyrKc
|
718 |
974 |
7.53e-133 |
SMART |
low complexity region
|
1007 |
1023 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 96.8%
- 20x: 93.6%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a member of the Tyr protein kinase family and the epidermal growth factor receptor subfamily. It encodes a single-pass type I membrane protein with multiple cysteine rich domains, a transmembrane domain, a tyrosine kinase domain, a phosphotidylinositol-3 kinase binding site and a PDZ domain binding motif. The protein binds to and is activated by neuregulins and other factors and induces a variety of cellular responses including mitogenesis and differentiation. Multiple proteolytic events allow for the release of a cytoplasmic fragment and an extracellular fragment. Mutations in this gene have been associated with cancer. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008] PHENOTYPE: Homozygotes for a targeted null mutation exhibit cardiac defects, alterations in hindbrain development, and midgestational lethality. Heterozygotes show schizophrenia-like behavior. Genetically rescued females show mammary defects. [provided by MGI curators]
|
Allele List at MGI |
All alleles(7) : Targeted(6) Gene trapped(1)
|
Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,383,749 (GRCm39) |
S739P |
possibly damaging |
Het |
6030468B19Rik |
A |
G |
11: 117,693,701 (GRCm39) |
Y56C |
possibly damaging |
Het |
Actn2 |
A |
G |
13: 12,303,408 (GRCm39) |
I464T |
possibly damaging |
Het |
Add2 |
T |
A |
6: 86,084,440 (GRCm39) |
L496Q |
probably damaging |
Het |
Akt1s1 |
T |
C |
7: 44,499,432 (GRCm39) |
|
probably null |
Het |
Als2 |
G |
T |
1: 59,250,433 (GRCm39) |
P437Q |
probably benign |
Het |
Ankar |
T |
C |
1: 72,719,369 (GRCm39) |
|
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,402,667 (GRCm39) |
R1464G |
probably damaging |
Het |
Ankrd24 |
T |
C |
10: 81,475,699 (GRCm39) |
S121P |
possibly damaging |
Het |
Arvcf |
A |
G |
16: 18,217,736 (GRCm39) |
Y412C |
probably damaging |
Het |
Birc6 |
C |
T |
17: 74,872,967 (GRCm39) |
R409C |
probably damaging |
Het |
Bnip3l |
T |
C |
14: 67,237,081 (GRCm39) |
E57G |
possibly damaging |
Het |
Calcoco1 |
A |
G |
15: 102,619,527 (GRCm39) |
L354P |
probably damaging |
Het |
Cc2d1b |
T |
C |
4: 108,480,661 (GRCm39) |
V27A |
possibly damaging |
Het |
Cdc37 |
T |
C |
9: 21,061,099 (GRCm39) |
T19A |
probably damaging |
Het |
Cep152 |
T |
C |
2: 125,413,736 (GRCm39) |
I1199V |
probably benign |
Het |
Chd6 |
G |
T |
2: 160,808,289 (GRCm39) |
L1642I |
possibly damaging |
Het |
Chst13 |
T |
C |
6: 90,286,551 (GRCm39) |
E137G |
possibly damaging |
Het |
Cnrip1 |
A |
G |
11: 17,004,687 (GRCm39) |
D79G |
probably damaging |
Het |
Dars2 |
A |
T |
1: 160,869,483 (GRCm39) |
C589S |
probably benign |
Het |
Dhx15 |
T |
G |
5: 52,327,409 (GRCm39) |
I102L |
possibly damaging |
Het |
Dip2a |
A |
G |
10: 76,153,877 (GRCm39) |
L151P |
possibly damaging |
Het |
Dlc1 |
T |
C |
8: 37,405,184 (GRCm39) |
T202A |
probably benign |
Het |
Dlg1 |
G |
T |
16: 31,503,113 (GRCm39) |
|
probably null |
Het |
Dlgap4 |
T |
C |
2: 156,549,031 (GRCm39) |
F464L |
probably benign |
Het |
Dnah3 |
T |
C |
7: 119,632,013 (GRCm39) |
H1314R |
probably benign |
Het |
Dsp |
A |
C |
13: 38,381,099 (GRCm39) |
T2615P |
possibly damaging |
Het |
Dthd1 |
C |
A |
5: 62,976,059 (GRCm39) |
D244E |
probably benign |
Het |
Dtl |
A |
T |
1: 191,300,485 (GRCm39) |
D126E |
probably damaging |
Het |
Ell2 |
A |
G |
13: 75,911,737 (GRCm39) |
N341S |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,727,450 (GRCm39) |
Y513C |
probably damaging |
Het |
Erc2 |
A |
T |
14: 28,024,900 (GRCm39) |
H593L |
possibly damaging |
Het |
Ercc6 |
T |
C |
14: 32,292,020 (GRCm39) |
V1128A |
probably benign |
Het |
Fyn |
A |
G |
10: 39,402,839 (GRCm39) |
K204E |
probably damaging |
Het |
Gm4847 |
A |
T |
1: 166,465,953 (GRCm39) |
F212Y |
possibly damaging |
Het |
Gpc5 |
T |
C |
14: 115,654,676 (GRCm39) |
*499R |
probably null |
Het |
Hcn4 |
T |
C |
9: 58,767,304 (GRCm39) |
L955P |
unknown |
Het |
Hook2 |
C |
A |
8: 85,720,028 (GRCm39) |
L111I |
possibly damaging |
Het |
Hook3 |
C |
T |
8: 26,585,785 (GRCm39) |
|
probably null |
Het |
Hvcn1 |
T |
C |
5: 122,371,544 (GRCm39) |
F28S |
probably damaging |
Het |
Igkv6-32 |
A |
G |
6: 70,051,267 (GRCm39) |
F30L |
possibly damaging |
Het |
Inpp5b |
G |
A |
4: 124,636,442 (GRCm39) |
|
probably null |
Het |
Itgb2 |
G |
A |
10: 77,384,595 (GRCm39) |
A239T |
probably damaging |
Het |
Kcnrg |
T |
C |
14: 61,845,266 (GRCm39) |
L102P |
probably damaging |
Het |
Kif16b |
A |
T |
2: 142,553,627 (GRCm39) |
M1068K |
probably benign |
Het |
Kifc3 |
T |
C |
8: 95,836,844 (GRCm39) |
R109G |
possibly damaging |
Het |
Klhl28 |
A |
T |
12: 65,004,486 (GRCm39) |
M9K |
probably benign |
Het |
Kptn |
T |
C |
7: 15,857,027 (GRCm39) |
Y172H |
probably damaging |
Het |
Mib1 |
A |
G |
18: 10,793,002 (GRCm39) |
E646G |
probably damaging |
Het |
Mmp14 |
T |
A |
14: 54,676,570 (GRCm39) |
Y372N |
probably damaging |
Het |
Mrc1 |
T |
A |
2: 14,311,327 (GRCm39) |
M868K |
probably benign |
Het |
Mterf1a |
T |
C |
5: 3,941,854 (GRCm39) |
N5D |
probably benign |
Het |
Muc5b |
T |
C |
7: 141,412,345 (GRCm39) |
S1764P |
unknown |
Het |
Myo9b |
T |
C |
8: 71,801,699 (GRCm39) |
Y1275H |
probably damaging |
Het |
Nek1 |
T |
C |
8: 61,469,330 (GRCm39) |
I129T |
probably damaging |
Het |
Net1 |
G |
A |
13: 3,936,740 (GRCm39) |
A221V |
probably benign |
Het |
Nuak2 |
A |
T |
1: 132,259,509 (GRCm39) |
D429V |
probably benign |
Het |
Nup98 |
T |
C |
7: 101,794,862 (GRCm39) |
T882A |
probably benign |
Het |
Or11g2 |
T |
A |
14: 50,856,197 (GRCm39) |
C173S |
probably damaging |
Het |
Or11h4 |
C |
A |
14: 50,974,531 (GRCm39) |
L29F |
probably benign |
Het |
Or52ab4 |
A |
T |
7: 102,987,229 (GRCm39) |
|
probably null |
Het |
Or52h1 |
T |
A |
7: 103,829,448 (GRCm39) |
S56C |
probably damaging |
Het |
Or8b42 |
T |
C |
9: 38,341,760 (GRCm39) |
Y61H |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pcdh7 |
T |
C |
5: 57,879,508 (GRCm39) |
V1021A |
probably damaging |
Het |
Pclo |
G |
C |
5: 14,729,087 (GRCm39) |
|
probably benign |
Het |
Pds5a |
A |
C |
5: 65,772,615 (GRCm39) |
D1329E |
probably damaging |
Het |
Pex5 |
A |
G |
6: 124,390,555 (GRCm39) |
S97P |
probably benign |
Het |
Pias3 |
A |
G |
3: 96,611,171 (GRCm39) |
K431E |
probably damaging |
Het |
Piwil1 |
T |
C |
5: 128,818,678 (GRCm39) |
S158P |
probably damaging |
Het |
Plxnc1 |
A |
T |
10: 94,635,239 (GRCm39) |
I1329N |
possibly damaging |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Pnpla1 |
T |
A |
17: 29,098,397 (GRCm39) |
|
probably null |
Het |
Prdm10 |
T |
C |
9: 31,270,343 (GRCm39) |
Y827H |
probably damaging |
Het |
Prss3b |
A |
C |
6: 41,009,370 (GRCm39) |
Y155D |
probably benign |
Het |
Psma2 |
G |
A |
13: 14,790,613 (GRCm39) |
V20I |
probably benign |
Het |
Pwwp4a |
T |
C |
X: 72,171,577 (GRCm39) |
I323T |
probably damaging |
Het |
Rgl3 |
A |
G |
9: 21,899,340 (GRCm39) |
|
probably null |
Het |
Rnf17 |
T |
C |
14: 56,743,385 (GRCm39) |
V1317A |
probably damaging |
Het |
Rpp40 |
T |
C |
13: 36,082,681 (GRCm39) |
N254D |
probably benign |
Het |
Scin |
T |
A |
12: 40,174,699 (GRCm39) |
H128L |
probably damaging |
Het |
Sh3bp2 |
A |
T |
5: 34,714,311 (GRCm39) |
M225L |
probably benign |
Het |
Shisa9 |
C |
A |
16: 12,085,412 (GRCm39) |
H324Q |
possibly damaging |
Het |
Sipa1l1 |
A |
G |
12: 82,484,601 (GRCm39) |
D1585G |
probably damaging |
Het |
Slc11a1 |
G |
A |
1: 74,424,343 (GRCm39) |
A434T |
probably damaging |
Het |
Slc5a8 |
A |
T |
10: 88,722,460 (GRCm39) |
I98F |
possibly damaging |
Het |
Slc6a13 |
T |
C |
6: 121,310,301 (GRCm39) |
L320P |
probably damaging |
Het |
Spats2l |
A |
G |
1: 57,982,380 (GRCm39) |
T421A |
probably benign |
Het |
Spryd3 |
A |
T |
15: 102,037,046 (GRCm39) |
D207E |
probably benign |
Het |
Srrt |
T |
C |
5: 137,294,803 (GRCm39) |
N392S |
possibly damaging |
Het |
Stk36 |
G |
T |
1: 74,661,504 (GRCm39) |
R510S |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,288 (GRCm39) |
Y272C |
probably damaging |
Het |
Taar7b |
T |
G |
10: 23,876,359 (GRCm39) |
S175A |
probably benign |
Het |
Tmem131 |
A |
G |
1: 36,893,986 (GRCm39) |
I139T |
probably damaging |
Het |
Tph2 |
T |
A |
10: 114,987,079 (GRCm39) |
Y237F |
probably benign |
Het |
Trim35 |
C |
T |
14: 66,546,421 (GRCm39) |
|
probably benign |
Het |
Tsc22d1 |
T |
C |
14: 76,655,750 (GRCm39) |
I661T |
probably benign |
Het |
Ttc27 |
T |
A |
17: 75,106,337 (GRCm39) |
H541Q |
probably damaging |
Het |
Uap1 |
G |
T |
1: 169,989,032 (GRCm39) |
P130Q |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,806,352 (GRCm39) |
|
probably null |
Het |
Umad1 |
A |
T |
6: 8,401,157 (GRCm39) |
|
probably null |
Het |
Usp34 |
T |
C |
11: 23,410,665 (GRCm39) |
V2705A |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,723,422 (GRCm39) |
S259G |
probably benign |
Het |
Vwa7 |
G |
A |
17: 35,243,166 (GRCm39) |
V615I |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 102,042,803 (GRCm39) |
T1983A |
probably benign |
Het |
Wdr24 |
T |
G |
17: 26,044,753 (GRCm39) |
F203V |
possibly damaging |
Het |
Xlr4c |
T |
A |
X: 72,282,290 (GRCm39) |
K121M |
probably damaging |
Het |
Zfc3h1 |
T |
A |
10: 115,254,688 (GRCm39) |
C1427* |
probably null |
Het |
Zfp282 |
A |
C |
6: 47,854,637 (GRCm39) |
Q11P |
probably benign |
Het |
Zfp750 |
T |
A |
11: 121,403,021 (GRCm39) |
T576S |
probably benign |
Het |
|
Other mutations in Erbb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00965:Erbb4
|
APN |
1 |
68,110,789 (GRCm39) |
nonsense |
probably null |
|
IGL01020:Erbb4
|
APN |
1 |
68,337,608 (GRCm39) |
splice site |
probably benign |
|
IGL01349:Erbb4
|
APN |
1 |
68,385,752 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01386:Erbb4
|
APN |
1 |
68,383,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Erbb4
|
APN |
1 |
68,367,404 (GRCm39) |
nonsense |
probably null |
|
IGL01536:Erbb4
|
APN |
1 |
68,329,441 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01721:Erbb4
|
APN |
1 |
68,293,722 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01832:Erbb4
|
APN |
1 |
68,293,725 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02002:Erbb4
|
APN |
1 |
68,119,885 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02040:Erbb4
|
APN |
1 |
68,081,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02371:Erbb4
|
APN |
1 |
68,329,453 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02399:Erbb4
|
APN |
1 |
68,081,596 (GRCm39) |
splice site |
probably benign |
|
IGL02553:Erbb4
|
APN |
1 |
68,345,023 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03118:Erbb4
|
APN |
1 |
68,081,878 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03329:Erbb4
|
APN |
1 |
68,367,281 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03405:Erbb4
|
APN |
1 |
68,369,397 (GRCm39) |
missense |
probably benign |
0.02 |
earthworm
|
UTSW |
1 |
68,289,739 (GRCm39) |
missense |
possibly damaging |
0.67 |
excrescence
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
Mole
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
P0018:Erbb4
|
UTSW |
1 |
68,110,835 (GRCm39) |
missense |
probably benign |
0.05 |
PIT4480001:Erbb4
|
UTSW |
1 |
68,114,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0193:Erbb4
|
UTSW |
1 |
68,083,119 (GRCm39) |
intron |
probably benign |
|
R0329:Erbb4
|
UTSW |
1 |
68,337,439 (GRCm39) |
splice site |
probably benign |
|
R0335:Erbb4
|
UTSW |
1 |
68,298,418 (GRCm39) |
missense |
probably benign |
|
R0362:Erbb4
|
UTSW |
1 |
68,369,429 (GRCm39) |
missense |
probably damaging |
0.99 |
R0579:Erbb4
|
UTSW |
1 |
68,081,621 (GRCm39) |
missense |
probably benign |
0.17 |
R0730:Erbb4
|
UTSW |
1 |
68,298,449 (GRCm39) |
missense |
probably damaging |
0.98 |
R1029:Erbb4
|
UTSW |
1 |
68,348,773 (GRCm39) |
missense |
probably damaging |
0.96 |
R1444:Erbb4
|
UTSW |
1 |
68,293,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Erbb4
|
UTSW |
1 |
68,599,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Erbb4
|
UTSW |
1 |
68,599,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1503:Erbb4
|
UTSW |
1 |
68,385,705 (GRCm39) |
missense |
probably benign |
0.00 |
R1523:Erbb4
|
UTSW |
1 |
68,435,411 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1528:Erbb4
|
UTSW |
1 |
68,117,741 (GRCm39) |
nonsense |
probably null |
|
R1604:Erbb4
|
UTSW |
1 |
68,385,728 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1611:Erbb4
|
UTSW |
1 |
68,079,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Erbb4
|
UTSW |
1 |
68,370,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Erbb4
|
UTSW |
1 |
68,114,569 (GRCm39) |
splice site |
probably benign |
|
R1929:Erbb4
|
UTSW |
1 |
68,238,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R2046:Erbb4
|
UTSW |
1 |
68,337,482 (GRCm39) |
missense |
probably benign |
0.02 |
R2139:Erbb4
|
UTSW |
1 |
68,385,788 (GRCm39) |
missense |
probably damaging |
0.96 |
R2271:Erbb4
|
UTSW |
1 |
68,238,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R2298:Erbb4
|
UTSW |
1 |
68,081,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Erbb4
|
UTSW |
1 |
68,117,755 (GRCm39) |
missense |
probably benign |
0.00 |
R3821:Erbb4
|
UTSW |
1 |
68,345,072 (GRCm39) |
missense |
probably damaging |
0.97 |
R4007:Erbb4
|
UTSW |
1 |
68,779,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R4012:Erbb4
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Erbb4
|
UTSW |
1 |
68,079,496 (GRCm39) |
missense |
probably benign |
0.07 |
R4196:Erbb4
|
UTSW |
1 |
68,383,014 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4536:Erbb4
|
UTSW |
1 |
68,385,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Erbb4
|
UTSW |
1 |
68,383,080 (GRCm39) |
nonsense |
probably null |
|
R4642:Erbb4
|
UTSW |
1 |
68,289,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R4737:Erbb4
|
UTSW |
1 |
68,383,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4739:Erbb4
|
UTSW |
1 |
68,383,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4780:Erbb4
|
UTSW |
1 |
68,337,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Erbb4
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Erbb4
|
UTSW |
1 |
68,369,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Erbb4
|
UTSW |
1 |
68,293,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Erbb4
|
UTSW |
1 |
68,369,397 (GRCm39) |
missense |
probably benign |
0.02 |
R5546:Erbb4
|
UTSW |
1 |
68,337,452 (GRCm39) |
missense |
probably damaging |
0.99 |
R5755:Erbb4
|
UTSW |
1 |
68,599,678 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6189:Erbb4
|
UTSW |
1 |
68,083,075 (GRCm39) |
missense |
probably benign |
|
R6257:Erbb4
|
UTSW |
1 |
68,435,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Erbb4
|
UTSW |
1 |
68,599,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Erbb4
|
UTSW |
1 |
68,081,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R6602:Erbb4
|
UTSW |
1 |
68,409,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R6808:Erbb4
|
UTSW |
1 |
68,079,462 (GRCm39) |
missense |
probably benign |
0.00 |
R7087:Erbb4
|
UTSW |
1 |
68,779,650 (GRCm39) |
missense |
probably null |
1.00 |
R7215:Erbb4
|
UTSW |
1 |
68,378,619 (GRCm39) |
missense |
probably benign |
|
R7356:Erbb4
|
UTSW |
1 |
68,378,514 (GRCm39) |
critical splice donor site |
probably null |
|
R7509:Erbb4
|
UTSW |
1 |
68,289,739 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7593:Erbb4
|
UTSW |
1 |
68,293,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R7743:Erbb4
|
UTSW |
1 |
68,367,278 (GRCm39) |
missense |
probably benign |
0.00 |
R7784:Erbb4
|
UTSW |
1 |
68,114,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Erbb4
|
UTSW |
1 |
68,081,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R7923:Erbb4
|
UTSW |
1 |
68,298,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Erbb4
|
UTSW |
1 |
68,435,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R8288:Erbb4
|
UTSW |
1 |
68,337,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R8356:Erbb4
|
UTSW |
1 |
68,110,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8456:Erbb4
|
UTSW |
1 |
68,110,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Erbb4
|
UTSW |
1 |
68,348,785 (GRCm39) |
missense |
probably benign |
|
R8783:Erbb4
|
UTSW |
1 |
68,079,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8830:Erbb4
|
UTSW |
1 |
68,114,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Erbb4
|
UTSW |
1 |
68,382,997 (GRCm39) |
critical splice donor site |
probably null |
|
R9053:Erbb4
|
UTSW |
1 |
68,289,779 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9142:Erbb4
|
UTSW |
1 |
68,388,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:Erbb4
|
UTSW |
1 |
68,081,601 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9350:Erbb4
|
UTSW |
1 |
68,329,638 (GRCm39) |
missense |
probably benign |
0.00 |
R9374:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9434:Erbb4
|
UTSW |
1 |
68,081,773 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9499:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9551:Erbb4
|
UTSW |
1 |
68,779,642 (GRCm39) |
nonsense |
probably null |
|
R9753:Erbb4
|
UTSW |
1 |
68,238,062 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Erbb4
|
UTSW |
1 |
68,112,304 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Erbb4
|
UTSW |
1 |
68,367,418 (GRCm39) |
nonsense |
probably null |
|
Z1176:Erbb4
|
UTSW |
1 |
68,337,561 (GRCm39) |
frame shift |
probably null |
|
Z1177:Erbb4
|
UTSW |
1 |
68,348,802 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Erbb4
|
UTSW |
1 |
68,329,635 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Erbb4
|
UTSW |
1 |
68,298,342 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- CAATAACTACTGAAAGTGCCTGTTG -3'
(R):5'- AAATCACTGTTGCGCCTTTC -3'
Sequencing Primer
(F):5'- TTCAGTTATCACCCAAGTTACAGAC -3'
(R):5'- CCCCTTTGGCTCATGCAAATCG -3'
|
Posted On |
2016-06-06 |