Incidental Mutation 'R0403:Itgae'
ID |
35722 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Itgae
|
Ensembl Gene |
ENSMUSG00000005947 |
Gene Name |
integrin alpha E, epithelial-associated |
Synonyms |
alpha-E1, CD103 |
MMRRC Submission |
038608-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R0403 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
11 |
Chromosomal Location |
72981409-73038272 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 73014009 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Aspartic acid to Alanine
at position 736
(D736A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000099596
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000006101]
[ENSMUST00000102537]
|
AlphaFold |
Q60677 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000006101
AA Change: D736A
PolyPhen 2
Score 0.741 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000006101 Gene: ENSMUSG00000005947 AA Change: D736A
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
Blast:Int_alpha
|
36 |
118 |
1e-24 |
BLAST |
VWA
|
193 |
380 |
1.13e-39 |
SMART |
Int_alpha
|
448 |
496 |
1.49e-3 |
SMART |
Int_alpha
|
502 |
559 |
6.83e-12 |
SMART |
Int_alpha
|
565 |
626 |
1.79e-15 |
SMART |
Int_alpha
|
633 |
685 |
6.29e0 |
SMART |
transmembrane domain
|
1115 |
1137 |
N/A |
INTRINSIC |
Pfam:Integrin_alpha
|
1138 |
1152 |
1.1e-6 |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000102537
AA Change: D736A
PolyPhen 2
Score 0.891 (Sensitivity: 0.82; Specificity: 0.94)
|
SMART Domains |
Protein: ENSMUSP00000099596 Gene: ENSMUSG00000005947 AA Change: D736A
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
19 |
N/A |
INTRINSIC |
Blast:Int_alpha
|
36 |
118 |
5e-25 |
BLAST |
VWA
|
193 |
380 |
1.13e-39 |
SMART |
Int_alpha
|
448 |
496 |
1.49e-3 |
SMART |
Int_alpha
|
502 |
559 |
6.83e-12 |
SMART |
Int_alpha
|
565 |
626 |
1.79e-15 |
SMART |
Int_alpha
|
633 |
685 |
6.29e0 |
SMART |
|
Meta Mutation Damage Score |
0.4108 |
Coding Region Coverage |
- 1x: 98.0%
- 3x: 96.8%
- 10x: 93.2%
- 20x: 83.7%
|
Validation Efficiency |
97% (110/113) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Integrins are heterodimeric integral membrane proteins composed of an alpha chain and a beta chain. This gene encodes an I-domain-containing alpha integrin that undergoes post-translational cleavage in the extracellular domain, yielding disulfide-linked heavy and light chains. In combination with the beta 7 integrin, this protein forms the E-cadherin binding integrin known as the human mucosal lymphocyte-1 antigen. This protein is preferentially expressed in human intestinal intraepithelial lymphocytes (IEL), and in addition to a role in adhesion, it may serve as an accessory molecule for IEL activation. [provided by RefSeq, Jul 2008] PHENOTYPE: Homozygotes for a targeted null mutation exhibit reductions in the numbers of intestinal and vaginal intraepithelial lymphocytes and of T lymphocytes of the lamina propria. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ace |
A |
G |
11: 105,864,706 (GRCm39) |
|
probably null |
Het |
Adgrg3 |
C |
T |
8: 95,763,550 (GRCm39) |
L284F |
probably benign |
Het |
Alkbh8 |
T |
A |
9: 3,385,469 (GRCm39) |
V587E |
probably damaging |
Het |
Ap4b1 |
T |
A |
3: 103,728,712 (GRCm39) |
M590K |
probably benign |
Het |
Ap4b1 |
T |
A |
3: 103,726,155 (GRCm39) |
C244S |
probably damaging |
Het |
Arhgap15 |
C |
T |
2: 43,953,778 (GRCm39) |
T168I |
probably damaging |
Het |
Atp8b1 |
A |
G |
18: 64,673,381 (GRCm39) |
V997A |
probably damaging |
Het |
Atrn |
G |
A |
2: 130,748,779 (GRCm39) |
C100Y |
probably damaging |
Het |
Baiap2l2 |
C |
A |
15: 79,155,416 (GRCm39) |
A151S |
probably benign |
Het |
Baz2b |
A |
T |
2: 59,799,721 (GRCm39) |
D199E |
possibly damaging |
Het |
Bmal2 |
T |
A |
6: 146,724,153 (GRCm39) |
H348Q |
probably damaging |
Het |
Cblb |
A |
G |
16: 51,972,989 (GRCm39) |
D440G |
probably benign |
Het |
Cdon |
T |
C |
9: 35,384,796 (GRCm39) |
V694A |
probably benign |
Het |
Cep250 |
A |
T |
2: 155,834,269 (GRCm39) |
R2065W |
probably damaging |
Het |
Ces2b |
G |
T |
8: 105,560,577 (GRCm39) |
A131S |
probably damaging |
Het |
Chrna9 |
A |
T |
5: 66,125,235 (GRCm39) |
T59S |
possibly damaging |
Het |
Cog3 |
T |
A |
14: 75,979,767 (GRCm39) |
|
probably benign |
Het |
Cpa1 |
G |
A |
6: 30,641,856 (GRCm39) |
V227I |
probably benign |
Het |
Cyp3a25 |
A |
T |
5: 145,935,323 (GRCm39) |
C98S |
probably damaging |
Het |
D8Ertd738e |
C |
T |
8: 84,976,230 (GRCm39) |
|
probably null |
Het |
Ddx60 |
A |
G |
8: 62,447,575 (GRCm39) |
|
probably benign |
Het |
Dhx16 |
T |
C |
17: 36,193,942 (GRCm39) |
|
probably null |
Het |
Dnah9 |
T |
A |
11: 65,975,615 (GRCm39) |
Q1478L |
possibly damaging |
Het |
Dock10 |
T |
C |
1: 80,501,787 (GRCm39) |
Y1434C |
possibly damaging |
Het |
Enpp3 |
T |
A |
10: 24,680,334 (GRCm39) |
D325V |
probably damaging |
Het |
Entpd6 |
C |
A |
2: 150,602,090 (GRCm39) |
T194K |
possibly damaging |
Het |
Fat2 |
A |
T |
11: 55,161,175 (GRCm39) |
V3185E |
probably benign |
Het |
Flrt1 |
A |
G |
19: 7,073,284 (GRCm39) |
L421P |
probably benign |
Het |
Fmn2 |
A |
T |
1: 174,521,844 (GRCm39) |
Q1292L |
probably damaging |
Het |
Fndc1 |
T |
C |
17: 7,972,555 (GRCm39) |
D1459G |
probably damaging |
Het |
Fndc1 |
T |
C |
17: 7,994,420 (GRCm39) |
|
probably null |
Het |
Fzr1 |
A |
G |
10: 81,205,202 (GRCm39) |
S265P |
possibly damaging |
Het |
Gpr142 |
G |
A |
11: 114,696,855 (GRCm39) |
V134M |
probably damaging |
Het |
Grid2ip |
G |
T |
5: 143,343,375 (GRCm39) |
V24L |
possibly damaging |
Het |
Herc2 |
G |
A |
7: 55,809,165 (GRCm39) |
R2555H |
probably damaging |
Het |
Hpdl |
A |
T |
4: 116,677,676 (GRCm39) |
Y262N |
possibly damaging |
Het |
Htr3a |
A |
G |
9: 48,819,959 (GRCm39) |
V57A |
probably damaging |
Het |
Igfbp7 |
T |
C |
5: 77,503,438 (GRCm39) |
I186V |
probably benign |
Het |
Itga2b |
C |
T |
11: 102,358,152 (GRCm39) |
|
probably null |
Het |
Itpkc |
T |
A |
7: 26,907,770 (GRCm39) |
M645L |
probably benign |
Het |
Jchain |
T |
C |
5: 88,669,237 (GRCm39) |
R139G |
probably benign |
Het |
Kif13a |
A |
G |
13: 46,944,877 (GRCm39) |
V908A |
probably damaging |
Het |
Kif1b |
T |
A |
4: 149,266,424 (GRCm39) |
K389* |
probably null |
Het |
Klhl12 |
T |
C |
1: 134,413,594 (GRCm39) |
Y360H |
possibly damaging |
Het |
Knop1 |
G |
A |
7: 118,452,276 (GRCm39) |
R148W |
probably damaging |
Het |
Lpar1 |
T |
A |
4: 58,487,191 (GRCm39) |
N27Y |
probably damaging |
Het |
Lpar2 |
T |
A |
8: 70,276,802 (GRCm39) |
V197D |
probably damaging |
Het |
Lrrc74a |
A |
G |
12: 86,787,753 (GRCm39) |
N128S |
probably damaging |
Het |
Lum |
G |
T |
10: 97,407,905 (GRCm39) |
V337F |
probably benign |
Het |
Mag |
T |
C |
7: 30,606,405 (GRCm39) |
D344G |
probably damaging |
Het |
Maip1 |
G |
A |
1: 57,446,355 (GRCm39) |
A142T |
probably benign |
Het |
Mlh3 |
A |
G |
12: 85,315,742 (GRCm39) |
V148A |
possibly damaging |
Het |
Nav3 |
A |
G |
10: 109,602,964 (GRCm39) |
V1195A |
probably damaging |
Het |
Ncor2 |
A |
G |
5: 125,110,401 (GRCm39) |
S868P |
possibly damaging |
Het |
Nek1 |
A |
G |
8: 61,559,889 (GRCm39) |
E907G |
probably damaging |
Het |
Nfam1 |
G |
A |
15: 82,900,580 (GRCm39) |
T134I |
probably benign |
Het |
Nr0b2 |
T |
C |
4: 133,281,070 (GRCm39) |
V112A |
probably damaging |
Het |
Nrp1 |
A |
G |
8: 129,184,450 (GRCm39) |
N365S |
probably damaging |
Het |
Nrsn2 |
T |
C |
2: 152,211,710 (GRCm39) |
Y107C |
probably damaging |
Het |
Ntng1 |
G |
A |
3: 109,841,927 (GRCm39) |
A282V |
probably damaging |
Het |
Nxf1 |
T |
C |
19: 8,742,392 (GRCm39) |
I337T |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,967,366 (GRCm39) |
G479D |
probably damaging |
Het |
Oprd1 |
T |
A |
4: 131,841,079 (GRCm39) |
D293V |
probably benign |
Het |
Or13a17 |
T |
C |
7: 140,271,222 (GRCm39) |
S135P |
possibly damaging |
Het |
P3h2 |
T |
G |
16: 25,788,700 (GRCm39) |
N586H |
possibly damaging |
Het |
Pcid2 |
T |
C |
8: 13,135,367 (GRCm39) |
Y214C |
probably damaging |
Het |
Pkd1l3 |
C |
G |
8: 110,350,281 (GRCm39) |
D375E |
possibly damaging |
Het |
Pkd1l3 |
G |
A |
8: 110,350,295 (GRCm39) |
S380N |
probably benign |
Het |
Ppic |
C |
A |
18: 53,544,143 (GRCm39) |
G81W |
probably damaging |
Het |
Ppp2r1a |
C |
A |
17: 21,177,303 (GRCm39) |
P246T |
probably damaging |
Het |
Ppp4r4 |
T |
G |
12: 103,550,361 (GRCm39) |
S46A |
probably benign |
Het |
Pramel31 |
A |
G |
4: 144,089,216 (GRCm39) |
N178S |
probably benign |
Het |
Prkce |
A |
G |
17: 86,476,081 (GRCm39) |
T21A |
probably damaging |
Het |
Prkg2 |
T |
C |
5: 99,142,504 (GRCm39) |
E210G |
possibly damaging |
Het |
Prss35 |
A |
G |
9: 86,638,090 (GRCm39) |
M287V |
probably damaging |
Het |
Psd |
G |
A |
19: 46,309,411 (GRCm39) |
|
probably benign |
Het |
Ptch2 |
A |
T |
4: 116,968,036 (GRCm39) |
K843* |
probably null |
Het |
Rab44 |
C |
A |
17: 29,364,235 (GRCm39) |
T603K |
probably damaging |
Het |
Rasal3 |
T |
A |
17: 32,611,764 (GRCm39) |
|
probably null |
Het |
Rbbp6 |
A |
G |
7: 122,591,519 (GRCm39) |
T526A |
probably damaging |
Het |
Ros1 |
A |
T |
10: 52,019,534 (GRCm39) |
|
probably benign |
Het |
Sec24b |
T |
A |
3: 129,783,325 (GRCm39) |
L1104F |
possibly damaging |
Het |
Sec24b |
A |
G |
3: 129,793,183 (GRCm39) |
S685P |
probably damaging |
Het |
Sema6a |
G |
A |
18: 47,423,112 (GRCm39) |
|
probably null |
Het |
Setmar |
A |
T |
6: 108,052,923 (GRCm39) |
H139L |
probably benign |
Het |
Slc28a2b |
T |
C |
2: 122,352,335 (GRCm39) |
L364S |
probably damaging |
Het |
Slc4a7 |
T |
C |
14: 14,766,808 (GRCm38) |
V710A |
probably benign |
Het |
Smarcc1 |
T |
A |
9: 110,066,876 (GRCm39) |
|
probably null |
Het |
Smchd1 |
G |
A |
17: 71,701,897 (GRCm39) |
L1032F |
probably damaging |
Het |
Speg |
T |
C |
1: 75,407,428 (GRCm39) |
|
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,632,052 (GRCm39) |
Y816* |
probably null |
Het |
Tcea1 |
C |
G |
1: 4,959,726 (GRCm39) |
R134G |
probably benign |
Het |
Tchhl1 |
C |
T |
3: 93,378,336 (GRCm39) |
Q347* |
probably null |
Het |
Tecrl |
A |
T |
5: 83,502,605 (GRCm39) |
|
probably benign |
Het |
Tepsin |
T |
C |
11: 119,984,508 (GRCm39) |
|
probably benign |
Het |
Tmem40 |
G |
A |
6: 115,710,946 (GRCm39) |
|
probably benign |
Het |
Tpr |
G |
A |
1: 150,283,165 (GRCm39) |
|
probably benign |
Het |
Ttll12 |
A |
T |
15: 83,464,859 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,739,952 (GRCm39) |
D3529V |
probably benign |
Het |
Usp34 |
T |
A |
11: 23,283,838 (GRCm39) |
H177Q |
possibly damaging |
Het |
Vsig10 |
T |
A |
5: 117,476,526 (GRCm39) |
S327T |
probably benign |
Het |
Zbtb4 |
T |
A |
11: 69,668,465 (GRCm39) |
M396K |
probably damaging |
Het |
Zfp352 |
C |
T |
4: 90,113,246 (GRCm39) |
T462I |
possibly damaging |
Het |
Zfp385b |
T |
C |
2: 77,307,189 (GRCm39) |
M145V |
probably damaging |
Het |
Zfp780b |
C |
A |
7: 27,671,114 (GRCm39) |
V65F |
possibly damaging |
Het |
|
Other mutations in Itgae |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Itgae
|
APN |
11 |
73,036,461 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00472:Itgae
|
APN |
11 |
73,004,520 (GRCm39) |
missense |
probably benign |
0.06 |
IGL00821:Itgae
|
APN |
11 |
73,013,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01625:Itgae
|
APN |
11 |
73,010,263 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01639:Itgae
|
APN |
11 |
73,010,204 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Itgae
|
APN |
11 |
73,002,585 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01911:Itgae
|
APN |
11 |
73,006,963 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01949:Itgae
|
APN |
11 |
73,009,010 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02149:Itgae
|
APN |
11 |
72,994,720 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02179:Itgae
|
APN |
11 |
73,024,844 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02231:Itgae
|
APN |
11 |
72,981,448 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02292:Itgae
|
APN |
11 |
73,009,361 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02378:Itgae
|
APN |
11 |
73,008,947 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02525:Itgae
|
APN |
11 |
73,021,777 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02576:Itgae
|
APN |
11 |
73,009,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02729:Itgae
|
APN |
11 |
73,009,029 (GRCm39) |
splice site |
probably benign |
|
IGL02859:Itgae
|
APN |
11 |
73,005,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Itgae
|
APN |
11 |
73,016,136 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03107:Itgae
|
APN |
11 |
73,004,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03264:Itgae
|
APN |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03272:Itgae
|
APN |
11 |
73,024,680 (GRCm39) |
splice site |
probably null |
|
IGL03352:Itgae
|
APN |
11 |
73,022,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Itgae
|
UTSW |
11 |
73,002,168 (GRCm39) |
missense |
probably benign |
0.00 |
R0225:Itgae
|
UTSW |
11 |
73,002,168 (GRCm39) |
missense |
probably benign |
0.00 |
R0320:Itgae
|
UTSW |
11 |
73,021,825 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0344:Itgae
|
UTSW |
11 |
73,008,973 (GRCm39) |
missense |
probably benign |
0.13 |
R0631:Itgae
|
UTSW |
11 |
73,005,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Itgae
|
UTSW |
11 |
73,020,032 (GRCm39) |
missense |
probably benign |
0.02 |
R0836:Itgae
|
UTSW |
11 |
73,020,032 (GRCm39) |
missense |
probably benign |
0.02 |
R0973:Itgae
|
UTSW |
11 |
73,029,335 (GRCm39) |
nonsense |
probably null |
|
R1231:Itgae
|
UTSW |
11 |
73,010,205 (GRCm39) |
missense |
probably benign |
0.02 |
R1389:Itgae
|
UTSW |
11 |
73,016,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Itgae
|
UTSW |
11 |
73,006,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Itgae
|
UTSW |
11 |
73,036,431 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1833:Itgae
|
UTSW |
11 |
73,007,988 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1914:Itgae
|
UTSW |
11 |
73,009,469 (GRCm39) |
splice site |
probably benign |
|
R1915:Itgae
|
UTSW |
11 |
73,009,469 (GRCm39) |
splice site |
probably benign |
|
R2061:Itgae
|
UTSW |
11 |
73,009,448 (GRCm39) |
missense |
probably benign |
0.00 |
R2380:Itgae
|
UTSW |
11 |
73,036,395 (GRCm39) |
missense |
probably benign |
0.00 |
R2435:Itgae
|
UTSW |
11 |
73,012,763 (GRCm39) |
nonsense |
probably null |
|
R2680:Itgae
|
UTSW |
11 |
73,005,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R2886:Itgae
|
UTSW |
11 |
73,031,513 (GRCm39) |
missense |
probably benign |
0.04 |
R3873:Itgae
|
UTSW |
11 |
73,004,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Itgae
|
UTSW |
11 |
73,006,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R4010:Itgae
|
UTSW |
11 |
73,002,165 (GRCm39) |
missense |
probably benign |
0.00 |
R4059:Itgae
|
UTSW |
11 |
73,002,960 (GRCm39) |
missense |
probably benign |
|
R4212:Itgae
|
UTSW |
11 |
73,010,178 (GRCm39) |
missense |
probably benign |
|
R4213:Itgae
|
UTSW |
11 |
73,010,178 (GRCm39) |
missense |
probably benign |
|
R4691:Itgae
|
UTSW |
11 |
73,010,345 (GRCm39) |
nonsense |
probably null |
|
R4736:Itgae
|
UTSW |
11 |
73,005,706 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5152:Itgae
|
UTSW |
11 |
73,021,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R5201:Itgae
|
UTSW |
11 |
73,001,382 (GRCm39) |
missense |
probably benign |
0.00 |
R5307:Itgae
|
UTSW |
11 |
73,036,464 (GRCm39) |
missense |
probably benign |
0.00 |
R5362:Itgae
|
UTSW |
11 |
73,002,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R5448:Itgae
|
UTSW |
11 |
73,024,734 (GRCm39) |
critical splice donor site |
probably null |
|
R5645:Itgae
|
UTSW |
11 |
73,020,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R5672:Itgae
|
UTSW |
11 |
73,036,377 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6079:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6138:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6226:Itgae
|
UTSW |
11 |
73,031,583 (GRCm39) |
missense |
probably benign |
0.11 |
R6244:Itgae
|
UTSW |
11 |
73,036,427 (GRCm39) |
missense |
probably damaging |
0.96 |
R6326:Itgae
|
UTSW |
11 |
73,022,519 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6332:Itgae
|
UTSW |
11 |
73,002,228 (GRCm39) |
splice site |
probably null |
|
R6502:Itgae
|
UTSW |
11 |
73,036,418 (GRCm39) |
missense |
probably benign |
0.10 |
R6825:Itgae
|
UTSW |
11 |
73,009,322 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7016:Itgae
|
UTSW |
11 |
73,010,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R7020:Itgae
|
UTSW |
11 |
73,002,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R7069:Itgae
|
UTSW |
11 |
73,006,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R7132:Itgae
|
UTSW |
11 |
73,002,184 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7473:Itgae
|
UTSW |
11 |
73,031,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7599:Itgae
|
UTSW |
11 |
73,012,786 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7637:Itgae
|
UTSW |
11 |
73,004,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Itgae
|
UTSW |
11 |
73,014,095 (GRCm39) |
critical splice donor site |
probably null |
|
R7829:Itgae
|
UTSW |
11 |
73,029,618 (GRCm39) |
missense |
probably benign |
|
R7860:Itgae
|
UTSW |
11 |
73,011,099 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7978:Itgae
|
UTSW |
11 |
73,024,913 (GRCm39) |
missense |
probably damaging |
0.98 |
R8197:Itgae
|
UTSW |
11 |
73,011,210 (GRCm39) |
missense |
probably benign |
|
R8911:Itgae
|
UTSW |
11 |
73,004,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R9155:Itgae
|
UTSW |
11 |
73,016,089 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9284:Itgae
|
UTSW |
11 |
73,012,752 (GRCm39) |
missense |
probably benign |
0.25 |
R9355:Itgae
|
UTSW |
11 |
73,006,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R9414:Itgae
|
UTSW |
11 |
73,002,629 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9595:Itgae
|
UTSW |
11 |
73,016,182 (GRCm39) |
missense |
probably damaging |
0.99 |
R9618:Itgae
|
UTSW |
11 |
73,011,171 (GRCm39) |
missense |
possibly damaging |
0.78 |
U15987:Itgae
|
UTSW |
11 |
73,006,400 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0024:Itgae
|
UTSW |
11 |
73,002,202 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1186:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1186:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1186:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1186:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1187:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1187:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1187:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1187:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1187:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1188:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1188:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1188:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1188:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1188:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1188:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1189:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1189:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1189:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1189:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1189:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1190:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1190:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1190:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1191:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
Z1191:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1191:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1191:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1191:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1192:Itgae
|
UTSW |
11 |
73,012,783 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Itgae
|
UTSW |
11 |
73,012,757 (GRCm39) |
missense |
probably benign |
0.00 |
Z1192:Itgae
|
UTSW |
11 |
73,008,913 (GRCm39) |
missense |
probably benign |
0.01 |
Z1192:Itgae
|
UTSW |
11 |
73,006,466 (GRCm39) |
missense |
probably benign |
|
Z1192:Itgae
|
UTSW |
11 |
72,994,786 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Itgae
|
UTSW |
11 |
72,994,713 (GRCm39) |
missense |
possibly damaging |
0.74 |
Z1192:Itgae
|
UTSW |
11 |
73,024,953 (GRCm39) |
missense |
probably benign |
0.36 |
|
Predicted Primers |
PCR Primer
(F):5'- ATGTTCAGCTCAGCACACAGCC -3'
(R):5'- TGGTGTCTGAGATCCACCTCTGGTAG -3'
Sequencing Primer
(F):5'- ACAGCCTCAGCAGGCAG -3'
(R):5'- GAGATCCACCTCTGGTAGATACTTTC -3'
|
Posted On |
2013-05-09 |