Incidental Mutation 'R1528:Erbb4'
ID |
166320 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Erbb4
|
Ensembl Gene |
ENSMUSG00000062209 |
Gene Name |
erb-b2 receptor tyrosine kinase 4 |
Synonyms |
Her4, ErbB4 |
MMRRC Submission |
039568-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R1528 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
68071345-69147218 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
A to T
at 68117741 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Stop codon
at position 891
(C891*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000114123
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000119142]
[ENSMUST00000121473]
|
AlphaFold |
Q61527 |
Predicted Effect |
probably null
Transcript: ENSMUST00000119142
AA Change: C891*
|
SMART Domains |
Protein: ENSMUSP00000112713 Gene: ENSMUSG00000062209 AA Change: C891*
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 null
Transcript: ENSMUST00000121473
AA Change: C891*
|
SMART Domains |
Protein: ENSMUSP00000114123 Gene: ENSMUSG00000062209 AA Change: C891*
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: 99.4%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.4%
|
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: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
A |
10: 78,903,530 (GRCm39) |
Q262L |
possibly damaging |
Het |
Abcg4 |
T |
C |
9: 44,186,020 (GRCm39) |
Y617C |
probably damaging |
Het |
Amph |
G |
A |
13: 19,326,198 (GRCm39) |
V643M |
probably damaging |
Het |
Ano1 |
T |
G |
7: 144,149,303 (GRCm39) |
S853R |
probably damaging |
Het |
Ap4e1 |
T |
A |
2: 126,853,743 (GRCm39) |
S60R |
possibly damaging |
Het |
Atp4b |
C |
A |
8: 13,439,693 (GRCm39) |
K176N |
possibly damaging |
Het |
Atxn2 |
A |
T |
5: 121,940,171 (GRCm39) |
D982V |
probably damaging |
Het |
Atxn2 |
T |
C |
5: 121,951,593 (GRCm39) |
F646S |
probably damaging |
Het |
Bcl2l13 |
T |
C |
6: 120,847,755 (GRCm39) |
C136R |
possibly damaging |
Het |
Bltp1 |
C |
T |
3: 37,106,684 (GRCm39) |
H5005Y |
unknown |
Het |
Cacna1i |
A |
G |
15: 80,275,975 (GRCm39) |
|
probably null |
Het |
Ccdc122 |
T |
A |
14: 77,305,379 (GRCm39) |
V11D |
possibly damaging |
Het |
Cdnf |
A |
G |
2: 3,522,078 (GRCm39) |
D90G |
probably damaging |
Het |
Cep104 |
T |
G |
4: 154,078,965 (GRCm39) |
V323G |
probably benign |
Het |
Chmp6 |
A |
G |
11: 119,807,541 (GRCm39) |
D128G |
probably benign |
Het |
Clec18a |
A |
T |
8: 111,805,498 (GRCm39) |
M201K |
probably benign |
Het |
Col11a1 |
A |
T |
3: 114,010,644 (GRCm39) |
|
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,952,419 (GRCm39) |
M493K |
probably damaging |
Het |
Crygd |
A |
C |
1: 65,102,216 (GRCm39) |
|
probably null |
Het |
Dennd1c |
T |
C |
17: 57,373,935 (GRCm39) |
T543A |
probably benign |
Het |
Ercc5 |
A |
T |
1: 44,217,401 (GRCm39) |
K915* |
probably null |
Het |
Ercc6 |
A |
T |
14: 32,240,979 (GRCm39) |
N168Y |
probably damaging |
Het |
Esrp2 |
G |
T |
8: 106,863,384 (GRCm39) |
P6T |
unknown |
Het |
Exoc1 |
A |
G |
5: 76,697,411 (GRCm39) |
K396R |
possibly damaging |
Het |
Fat3 |
T |
A |
9: 15,836,387 (GRCm39) |
Y4039F |
probably benign |
Het |
Fcsk |
A |
T |
8: 111,609,873 (GRCm39) |
L1047Q |
probably damaging |
Het |
Fgf7 |
T |
A |
2: 125,877,738 (GRCm39) |
M35K |
probably damaging |
Het |
Fras1 |
G |
A |
5: 96,784,678 (GRCm39) |
G887D |
probably damaging |
Het |
Gbp4 |
A |
T |
5: 105,269,658 (GRCm39) |
|
probably null |
Het |
Homez |
A |
T |
14: 55,095,162 (GRCm39) |
M182K |
probably benign |
Het |
Hrnr |
G |
A |
3: 93,230,101 (GRCm39) |
S113N |
possibly damaging |
Het |
Ifit3b |
T |
G |
19: 34,589,072 (GRCm39) |
S83A |
probably benign |
Het |
Ildr2 |
A |
G |
1: 166,098,064 (GRCm39) |
|
probably null |
Het |
Klhdc1 |
A |
T |
12: 69,309,972 (GRCm39) |
R291S |
probably benign |
Het |
Krt77 |
T |
A |
15: 101,769,523 (GRCm39) |
I413F |
probably damaging |
Het |
Lipn |
A |
G |
19: 34,046,070 (GRCm39) |
I14M |
probably damaging |
Het |
Macf1 |
T |
G |
4: 123,369,807 (GRCm39) |
R86S |
probably benign |
Het |
Mroh8 |
C |
A |
2: 157,071,975 (GRCm39) |
G510V |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,470,033 (GRCm39) |
D1255E |
possibly damaging |
Het |
Nckap5 |
C |
T |
1: 125,952,659 (GRCm39) |
V1234I |
possibly damaging |
Het |
Nlrp9c |
T |
C |
7: 26,081,723 (GRCm39) |
K668E |
probably damaging |
Het |
Nod2 |
T |
C |
8: 89,391,217 (GRCm39) |
M508T |
possibly damaging |
Het |
Npffr1 |
A |
G |
10: 61,450,016 (GRCm39) |
M97V |
possibly damaging |
Het |
Nsd3 |
G |
A |
8: 26,188,795 (GRCm39) |
V43M |
probably damaging |
Het |
Nubp2 |
A |
G |
17: 25,103,388 (GRCm39) |
V163A |
probably damaging |
Het |
Oas1e |
A |
T |
5: 120,926,054 (GRCm39) |
F338Y |
probably damaging |
Het |
Oat |
C |
A |
7: 132,165,998 (GRCm39) |
G196C |
probably damaging |
Het |
Or4a69 |
C |
T |
2: 89,312,897 (GRCm39) |
G194D |
probably damaging |
Het |
Or52e8b |
A |
T |
7: 104,673,971 (GRCm39) |
L72Q |
probably damaging |
Het |
Or7a41 |
T |
C |
10: 78,871,398 (GRCm39) |
L256P |
probably damaging |
Het |
P2ry13 |
T |
C |
3: 59,117,710 (GRCm39) |
T23A |
probably benign |
Het |
Phf8-ps |
A |
G |
17: 33,286,215 (GRCm39) |
S196P |
probably damaging |
Het |
Pja2 |
C |
A |
17: 64,616,217 (GRCm39) |
S226I |
possibly damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,390,120 (GRCm39) |
V1412A |
probably damaging |
Het |
Plekhs1 |
T |
C |
19: 56,468,427 (GRCm39) |
S332P |
probably damaging |
Het |
Polr3e |
T |
A |
7: 120,539,820 (GRCm39) |
N522K |
probably damaging |
Het |
Prdm10 |
A |
G |
9: 31,268,582 (GRCm39) |
T844A |
probably damaging |
Het |
Ripk1 |
C |
T |
13: 34,212,130 (GRCm39) |
P480L |
probably benign |
Het |
Rnf139 |
T |
C |
15: 58,771,064 (GRCm39) |
V363A |
probably damaging |
Het |
Rnf19a |
A |
T |
15: 36,265,801 (GRCm39) |
S99T |
possibly damaging |
Het |
Rnf224 |
G |
A |
2: 25,126,110 (GRCm39) |
T81I |
probably benign |
Het |
Rpgrip1 |
T |
C |
14: 52,349,681 (GRCm39) |
L23S |
probably benign |
Het |
Setd5 |
T |
A |
6: 113,098,699 (GRCm39) |
F758L |
probably damaging |
Het |
Smlr1 |
C |
A |
10: 25,411,976 (GRCm39) |
V4L |
possibly damaging |
Het |
Snx1 |
T |
C |
9: 66,016,825 (GRCm39) |
D34G |
probably damaging |
Het |
Spaca5 |
A |
T |
X: 20,942,892 (GRCm39) |
T92S |
probably benign |
Het |
Speer4f2 |
A |
G |
5: 17,581,540 (GRCm39) |
T161A |
|
Het |
Swi5 |
C |
A |
2: 32,170,716 (GRCm39) |
|
probably null |
Het |
Syne2 |
T |
A |
12: 76,012,874 (GRCm39) |
D2689E |
probably benign |
Het |
Tcof1 |
T |
A |
18: 60,948,071 (GRCm39) |
K1299* |
probably null |
Het |
Tmprss11e |
G |
A |
5: 86,872,069 (GRCm39) |
T49I |
probably damaging |
Het |
Tmx3 |
T |
A |
18: 90,555,210 (GRCm39) |
V309D |
possibly damaging |
Het |
Trim30b |
C |
G |
7: 104,006,506 (GRCm39) |
V117L |
possibly damaging |
Het |
Tsen2 |
C |
A |
6: 115,536,989 (GRCm39) |
H248Q |
probably benign |
Het |
Ttn |
T |
C |
2: 76,567,412 (GRCm39) |
Y19500C |
probably damaging |
Het |
Tubgcp2 |
A |
G |
7: 139,613,696 (GRCm39) |
|
probably benign |
Het |
Vwf |
A |
C |
6: 125,585,254 (GRCm39) |
D712A |
possibly damaging |
Het |
Wfdc2 |
A |
G |
2: 164,407,828 (GRCm39) |
K166E |
probably damaging |
Het |
Xrcc2 |
T |
C |
5: 25,897,292 (GRCm39) |
D219G |
probably benign |
Het |
Zc3h6 |
C |
T |
2: 128,858,989 (GRCm39) |
P1007S |
probably benign |
Het |
Zdhhc17 |
A |
T |
10: 110,784,050 (GRCm39) |
|
probably null |
Het |
Zfp369 |
T |
A |
13: 65,439,979 (GRCm39) |
I221N |
probably damaging |
Het |
Zfp655 |
A |
T |
5: 145,181,411 (GRCm39) |
N423I |
probably damaging |
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 |
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 |
R5068:Erbb4
|
UTSW |
1 |
68,083,061 (GRCm39) |
splice site |
probably null |
|
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'- ccaccctGCCAGTAAATTTTCTACCAT -3'
(R):5'- GCCAGGCTTAACGTCAGGTCAA -3'
Sequencing Primer
(F):5'- gtgtgtgtgtgtAAGAATCAATAGAC -3'
(R):5'- GGCTTAACGTCAGGTCAAAATTTAG -3'
|
Posted On |
2014-04-13 |