Incidental Mutation 'R4780:Erbb4'
| ID |
366369 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Erbb4
|
| Ensembl Gene |
ENSMUSG00000062209 |
| Gene Name |
erb-b2 receptor tyrosine kinase 4 |
| Synonyms |
Her4, ErbB4 |
| MMRRC Submission |
041993-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4780 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
68071345-69147218 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 68337473 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Arginine
at position 615
(H615R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000114123
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000119142]
[ENSMUST00000121473]
[ENSMUST00000153432]
|
| AlphaFold |
Q61527 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000117740
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000119142
AA Change: H615R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000112713
Gene: ENSMUSG00000062209
AA Change: H615R
| 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 damaging
Transcript: ENSMUST00000121473
AA Change: H615R
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000114123
Gene: ENSMUSG00000062209
AA Change: H615R
| 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 |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000126682
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131148
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000153432
AA Change: H615R
PolyPhen 2
Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
|
| SMART Domains |
Protein: ENSMUSP00000115373
Gene: ENSMUSG00000062209
AA Change: H615R
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
25 |
N/A |
INTRINSIC |
|
Pfam:Recep_L_domain
|
55 |
167 |
1.7e-34 |
PFAM |
|
FU
|
183 |
223 |
2.07e1 |
SMART |
|
FU
|
226 |
268 |
5.78e-10 |
SMART |
|
Pfam:Recep_L_domain
|
358 |
478 |
5.7e-29 |
PFAM |
|
FU
|
493 |
544 |
6.45e-8 |
SMART |
|
FU
|
549 |
599 |
3.51e-9 |
SMART |
|
FU
|
611 |
649 |
2.98e0 |
SMART |
|
PDB:2R4B|B
|
680 |
732 |
1e-25 |
PDB |
|
| Meta Mutation Damage Score |
0.0948 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.6%
|
| Validation Efficiency |
98% (107/109) |
| 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: 105 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110002E22Rik |
A |
G |
3: 137,771,131 (GRCm39) |
N107D |
probably benign |
Het |
| 4833413E03Rik |
A |
C |
17: 31,777,738 (GRCm39) |
|
noncoding transcript |
Het |
| 4931429L15Rik |
G |
T |
9: 46,220,144 (GRCm39) |
H129Q |
possibly damaging |
Het |
| A730018C14Rik |
A |
G |
12: 112,382,069 (GRCm39) |
|
noncoding transcript |
Het |
| Abcc6 |
T |
A |
7: 45,646,115 (GRCm39) |
K791N |
probably benign |
Het |
| Adcy4 |
T |
G |
14: 56,012,493 (GRCm39) |
Q550P |
probably benign |
Het |
| Add3 |
C |
A |
19: 53,223,223 (GRCm39) |
A325E |
possibly damaging |
Het |
| Agbl4 |
T |
A |
4: 111,514,528 (GRCm39) |
I513N |
possibly damaging |
Het |
| Agfg1 |
C |
A |
1: 82,864,108 (GRCm39) |
T392K |
probably damaging |
Het |
| Akna |
C |
A |
4: 63,297,491 (GRCm39) |
M854I |
probably benign |
Het |
| Ankrd44 |
T |
C |
1: 54,802,916 (GRCm39) |
N194S |
probably benign |
Het |
| Anks1b |
A |
G |
10: 89,709,594 (GRCm39) |
K21E |
probably damaging |
Het |
| Ap1s3 |
A |
G |
1: 79,586,889 (GRCm39) |
F154L |
probably benign |
Het |
| Apbb2 |
T |
A |
5: 66,520,160 (GRCm39) |
N477I |
probably damaging |
Het |
| Apobec3 |
T |
C |
15: 79,783,225 (GRCm39) |
C101R |
possibly damaging |
Het |
| Arnt |
G |
T |
3: 95,395,696 (GRCm39) |
V410F |
probably damaging |
Het |
| Arsg |
G |
A |
11: 109,424,839 (GRCm39) |
R270H |
possibly damaging |
Het |
| B3gnt7 |
T |
A |
1: 86,232,992 (GRCm39) |
D79E |
probably damaging |
Het |
| Cd44 |
G |
T |
2: 102,691,910 (GRCm39) |
A126D |
probably damaging |
Het |
| Cd69 |
A |
G |
6: 129,248,318 (GRCm39) |
I56T |
probably damaging |
Het |
| Cep120 |
G |
A |
18: 53,857,608 (GRCm39) |
P286S |
probably benign |
Het |
| Ces2a |
T |
C |
8: 105,463,840 (GRCm39) |
F184S |
probably damaging |
Het |
| Chrng |
A |
G |
1: 87,135,246 (GRCm39) |
N185S |
probably damaging |
Het |
| Cldn6 |
A |
T |
17: 23,900,221 (GRCm39) |
M62L |
probably benign |
Het |
| Cntn6 |
T |
A |
6: 104,822,745 (GRCm39) |
N765K |
probably damaging |
Het |
| Cspg4b |
A |
G |
13: 113,454,392 (GRCm39) |
Y146C |
probably damaging |
Het |
| Ctnnal1 |
T |
C |
4: 56,847,857 (GRCm39) |
D94G |
probably damaging |
Het |
| Cyp2c69 |
T |
C |
19: 39,866,038 (GRCm39) |
N185S |
probably benign |
Het |
| Depdc1a |
A |
G |
3: 159,232,343 (GRCm39) |
N698S |
probably benign |
Het |
| Dnah2 |
A |
T |
11: 69,364,697 (GRCm39) |
I1986N |
probably damaging |
Het |
| Dnah7b |
A |
G |
1: 46,392,174 (GRCm39) |
E3845G |
probably benign |
Het |
| Dpysl3 |
C |
T |
18: 43,487,867 (GRCm39) |
V159I |
probably benign |
Het |
| Dync1h1 |
T |
C |
12: 110,627,630 (GRCm39) |
Y4047H |
probably damaging |
Het |
| E130308A19Rik |
C |
T |
4: 59,691,057 (GRCm39) |
P297L |
probably benign |
Het |
| E2f5 |
A |
G |
3: 14,652,379 (GRCm39) |
T72A |
probably benign |
Het |
| Ephb6 |
G |
T |
6: 41,593,073 (GRCm39) |
R437L |
probably damaging |
Het |
| Erbin |
T |
C |
13: 104,020,714 (GRCm39) |
T82A |
probably damaging |
Het |
| Eri2 |
T |
C |
7: 119,384,903 (GRCm39) |
N533D |
probably benign |
Het |
| Fkbp9 |
A |
G |
6: 56,827,701 (GRCm39) |
N174S |
probably damaging |
Het |
| Fsbp |
C |
T |
4: 11,583,709 (GRCm39) |
T136I |
possibly damaging |
Het |
| Fubp3 |
C |
A |
2: 31,473,223 (GRCm39) |
D47E |
probably damaging |
Het |
| Gm21850 |
G |
A |
2: 153,898,419 (GRCm39) |
|
noncoding transcript |
Het |
| Gm5141 |
T |
A |
13: 62,922,764 (GRCm39) |
Y135F |
unknown |
Het |
| Gm7353 |
T |
A |
7: 3,160,725 (GRCm39) |
|
noncoding transcript |
Het |
| Gm9925 |
T |
C |
18: 74,198,344 (GRCm39) |
|
probably benign |
Het |
| Greb1l |
T |
C |
18: 10,541,792 (GRCm39) |
S1180P |
probably benign |
Het |
| H2ac11 |
G |
A |
13: 22,227,079 (GRCm39) |
Q7* |
probably null |
Het |
| Ift70a2 |
A |
C |
2: 75,807,920 (GRCm39) |
C197W |
probably benign |
Het |
| Kiz |
A |
G |
2: 146,731,166 (GRCm39) |
T192A |
possibly damaging |
Het |
| Klhl24 |
T |
A |
16: 19,925,708 (GRCm39) |
C79S |
probably damaging |
Het |
| Map3k11 |
A |
G |
19: 5,740,966 (GRCm39) |
H231R |
probably damaging |
Het |
| Mbd4 |
C |
A |
6: 115,826,345 (GRCm39) |
R194S |
probably benign |
Het |
| Mettl21e |
A |
C |
1: 44,250,303 (GRCm39) |
S34R |
probably benign |
Het |
| Mrps5 |
T |
C |
2: 127,440,161 (GRCm39) |
V245A |
probably benign |
Het |
| Mtrf1 |
T |
C |
14: 79,639,128 (GRCm39) |
Y87H |
probably benign |
Het |
| Myh15 |
T |
C |
16: 48,940,420 (GRCm39) |
I790T |
probably benign |
Het |
| Necab1 |
T |
G |
4: 14,989,248 (GRCm39) |
I176L |
probably benign |
Het |
| Nfkb2 |
T |
A |
19: 46,298,361 (GRCm39) |
L555Q |
probably damaging |
Het |
| Nhlrc3 |
T |
A |
3: 53,365,988 (GRCm39) |
E168D |
probably benign |
Het |
| Nlrp5 |
T |
A |
7: 23,135,203 (GRCm39) |
C949S |
probably damaging |
Het |
| Nup155 |
C |
A |
15: 8,187,187 (GRCm39) |
A1372E |
probably benign |
Het |
| Nynrin |
G |
T |
14: 56,100,720 (GRCm39) |
R170L |
probably damaging |
Het |
| Ogfrl1 |
T |
A |
1: 23,409,402 (GRCm39) |
N275Y |
probably damaging |
Het |
| Olr1 |
A |
T |
6: 129,465,839 (GRCm39) |
S56T |
probably damaging |
Het |
| Or4k52 |
A |
G |
2: 111,611,190 (GRCm39) |
D175G |
probably damaging |
Het |
| Or5aq1 |
C |
T |
2: 86,966,221 (GRCm39) |
S148N |
probably damaging |
Het |
| Or5b121 |
A |
G |
19: 13,507,319 (GRCm39) |
N138S |
probably benign |
Het |
| Or8b48 |
A |
G |
9: 38,493,265 (GRCm39) |
T231A |
possibly damaging |
Het |
| Ovol2 |
A |
T |
2: 144,173,203 (GRCm39) |
|
probably benign |
Het |
| Pcdha6 |
A |
T |
18: 37,102,906 (GRCm39) |
I700F |
probably damaging |
Het |
| Prkcz |
C |
T |
4: 155,374,159 (GRCm39) |
V86M |
probably damaging |
Het |
| Ptpn13 |
A |
G |
5: 103,734,639 (GRCm39) |
T2124A |
probably benign |
Het |
| Ranbp3 |
G |
T |
17: 56,980,346 (GRCm39) |
|
probably benign |
Het |
| Rapgef2 |
A |
G |
3: 79,077,076 (GRCm39) |
|
probably benign |
Het |
| Rbl1 |
A |
G |
2: 157,016,724 (GRCm39) |
V625A |
probably benign |
Het |
| Rbm38 |
G |
T |
2: 172,863,944 (GRCm39) |
G38C |
probably damaging |
Het |
| Reg1 |
T |
G |
6: 78,403,333 (GRCm39) |
F7C |
possibly damaging |
Het |
| Retnlg |
A |
T |
16: 48,694,697 (GRCm39) |
Q115L |
possibly damaging |
Het |
| Rhobtb1 |
G |
A |
10: 69,105,983 (GRCm39) |
V183I |
probably benign |
Het |
| Rims1 |
T |
C |
1: 22,361,329 (GRCm39) |
Q1186R |
probably damaging |
Het |
| Ryr1 |
A |
G |
7: 28,794,522 (GRCm39) |
F1246L |
possibly damaging |
Het |
| Samm50 |
A |
G |
15: 84,094,811 (GRCm39) |
N401S |
possibly damaging |
Het |
| Scn3a |
T |
A |
2: 65,336,537 (GRCm39) |
I690F |
probably damaging |
Het |
| Sdk1 |
A |
G |
5: 141,944,993 (GRCm39) |
D304G |
probably damaging |
Het |
| Skint6 |
T |
C |
4: 113,093,594 (GRCm39) |
Y183C |
probably damaging |
Het |
| Slamf1 |
A |
T |
1: 171,604,829 (GRCm39) |
T200S |
probably benign |
Het |
| Slc34a2 |
C |
T |
5: 53,226,793 (GRCm39) |
R639C |
probably damaging |
Het |
| Smap1 |
A |
T |
1: 23,892,517 (GRCm39) |
M149K |
probably benign |
Het |
| Sorcs1 |
T |
C |
19: 50,132,419 (GRCm39) |
|
probably benign |
Het |
| Sp140 |
T |
A |
1: 85,538,549 (GRCm39) |
D95E |
possibly damaging |
Het |
| Spata13 |
G |
A |
14: 60,991,356 (GRCm39) |
W366* |
probably null |
Het |
| Spata31e4 |
C |
A |
13: 50,855,116 (GRCm39) |
S251R |
probably damaging |
Het |
| Strip1 |
G |
A |
3: 107,534,314 (GRCm39) |
T136I |
probably benign |
Het |
| Tacr1 |
A |
T |
6: 82,534,053 (GRCm39) |
T360S |
probably benign |
Het |
| Tbc1d14 |
T |
A |
5: 36,728,600 (GRCm39) |
|
probably benign |
Het |
| Tcaf2 |
T |
C |
6: 42,604,996 (GRCm39) |
Y596C |
probably damaging |
Het |
| Tspoap1 |
C |
T |
11: 87,669,269 (GRCm39) |
T1454I |
possibly damaging |
Het |
| Ttn |
A |
T |
2: 76,744,927 (GRCm39) |
M5374K |
probably benign |
Het |
| Uts2r |
G |
A |
11: 121,051,705 (GRCm39) |
V190I |
possibly damaging |
Het |
| Vmn1r181 |
A |
G |
7: 23,684,008 (GRCm39) |
T158A |
possibly damaging |
Het |
| Wdr35 |
A |
T |
12: 9,068,150 (GRCm39) |
T778S |
probably benign |
Het |
| Xrn1 |
A |
T |
9: 95,856,797 (GRCm39) |
|
probably benign |
Het |
| Zfp35 |
A |
T |
18: 24,136,326 (GRCm39) |
K223N |
probably damaging |
Het |
| Zfp764 |
T |
C |
7: 127,003,943 (GRCm39) |
Q396R |
probably benign |
Het |
| Zfyve1 |
T |
C |
12: 83,605,421 (GRCm39) |
Y11C |
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 |
|
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 |
|
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'- AGCAGAGATATTTTAGAGGTCCACC -3'
(R):5'- GGGAATTGAACCCAGTTTTCTTTC -3'
Sequencing Primer
(F):5'- CATAGATGGCATCGTGGA -3'
(R):5'- AACCCAGTTTTCTTTCTCCATATTTG -3'
|
| Posted On |
2015-12-21 |
Incidental Mutation