Incidental Mutation 'R4914:Glp2r'
| ID |
379841 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Glp2r
|
| Ensembl Gene |
ENSMUSG00000049928 |
| Gene Name |
glucagon-like peptide 2 receptor |
| Synonyms |
GLP-2, 9530092J08Rik |
| MMRRC Submission |
042516-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4914 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
67554877-67661979 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to T
at 67648419 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Stop codon
at position 94
(Y94*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000061560
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021289]
[ENSMUST00000051765]
|
| AlphaFold |
Q5IXF8 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000021289
|
| SMART Domains |
Protein: ENSMUSP00000021289
Gene: ENSMUSG00000049928
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:7tm_2
|
17 |
225 |
4.8e-54 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000051765
AA Change: Y94*
|
| SMART Domains |
Protein: ENSMUSP00000061560
Gene: ENSMUSG00000049928
AA Change: Y94*
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
26 |
N/A |
INTRINSIC |
|
Pfam:HRM
|
53 |
122 |
3.4e-16 |
PFAM |
|
Pfam:7tm_2
|
137 |
394 |
1.5e-79 |
PFAM |
|
| Meta Mutation Damage Score |
0.9717 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.4%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a G protein-coupled receptor that is closely related to the glucagon receptor and binds to glucagon-like peptide-2 (GLP2). Signalling through GLP2 stimulates intestinal growth and increases villus height in the small intestine, concomitant with increased crypt cell proliferation and decreased enterocyte apoptosis. [provided by RefSeq, Dec 2014]
PHENOTYPE: Mice homozygous for a null mutation display defects in Paneth cell physiology, increased small bowel bacterial loads, and increased susceptibility to small bowel injury. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 99 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Ace |
G |
A |
11: 105,870,423 (GRCm39) |
V281M |
probably damaging |
Het |
| Ap1b1 |
C |
T |
11: 4,974,400 (GRCm39) |
T363I |
possibly damaging |
Het |
| Apobec2 |
T |
C |
17: 48,730,153 (GRCm39) |
E171G |
probably benign |
Het |
| Arhgef1 |
T |
A |
7: 24,623,264 (GRCm39) |
L436Q |
probably damaging |
Het |
| Atxn2 |
T |
A |
5: 121,887,159 (GRCm39) |
D276E |
probably damaging |
Het |
| AU040320 |
A |
T |
4: 126,729,469 (GRCm39) |
K544* |
probably null |
Het |
| Baz2b |
T |
A |
2: 59,744,387 (GRCm39) |
T1373S |
possibly damaging |
Het |
| Bcas1 |
T |
C |
2: 170,220,806 (GRCm39) |
D324G |
probably damaging |
Het |
| Bdp1 |
A |
G |
13: 100,192,844 (GRCm39) |
V1330A |
probably benign |
Het |
| Bfsp1 |
C |
T |
2: 143,669,391 (GRCm39) |
R396Q |
probably benign |
Het |
| Bpifb9b |
T |
A |
2: 154,156,026 (GRCm39) |
|
probably null |
Het |
| Cabs1 |
T |
C |
5: 88,128,296 (GRCm39) |
Y316H |
probably damaging |
Het |
| Carmil2 |
A |
G |
8: 106,420,175 (GRCm39) |
K908E |
possibly damaging |
Het |
| Ccdc188 |
C |
A |
16: 18,036,083 (GRCm39) |
P86Q |
probably benign |
Het |
| Cdh26 |
T |
C |
2: 178,091,614 (GRCm39) |
S58P |
probably benign |
Het |
| Cemip2 |
G |
A |
19: 21,786,653 (GRCm39) |
V472I |
probably benign |
Het |
| Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
| Dclk2 |
A |
T |
3: 86,732,049 (GRCm39) |
|
probably null |
Het |
| Dennd5a |
A |
G |
7: 109,500,296 (GRCm39) |
F943S |
probably damaging |
Het |
| Disp2 |
A |
T |
2: 118,620,935 (GRCm39) |
S556C |
probably damaging |
Het |
| Dnai3 |
A |
G |
3: 145,772,582 (GRCm39) |
I488T |
probably damaging |
Het |
| Dpp4 |
A |
T |
2: 62,178,236 (GRCm39) |
M632K |
probably benign |
Het |
| E030030I06Rik |
G |
A |
10: 21,990,197 (GRCm39) |
T192M |
possibly damaging |
Het |
| Ece2 |
C |
T |
16: 20,462,820 (GRCm39) |
R582C |
probably damaging |
Het |
| Ehbp1 |
T |
C |
11: 22,096,592 (GRCm39) |
D299G |
probably benign |
Het |
| Emc1 |
C |
T |
4: 139,102,476 (GRCm39) |
R924* |
probably null |
Het |
| Etaa1 |
A |
T |
11: 17,896,532 (GRCm39) |
S528R |
probably benign |
Het |
| Exoc2 |
A |
T |
13: 31,060,796 (GRCm39) |
N569K |
probably benign |
Het |
| Fasn |
T |
G |
11: 120,707,472 (GRCm39) |
N799T |
probably benign |
Het |
| Fbxo3 |
T |
G |
2: 103,885,311 (GRCm39) |
N388K |
probably damaging |
Het |
| Fbxw16 |
C |
T |
9: 109,267,245 (GRCm39) |
V329I |
probably benign |
Het |
| Fer1l4 |
T |
C |
2: 155,873,220 (GRCm39) |
K1287E |
probably benign |
Het |
| Fermt1 |
A |
G |
2: 132,748,760 (GRCm39) |
V621A |
probably damaging |
Het |
| Fnbp4 |
A |
G |
2: 90,581,513 (GRCm39) |
T189A |
probably benign |
Het |
| Fut8 |
G |
T |
12: 77,521,818 (GRCm39) |
A486S |
probably damaging |
Het |
| G6pd2 |
T |
A |
5: 61,967,672 (GRCm39) |
Y482* |
probably null |
Het |
| Gfra1 |
A |
T |
19: 58,255,522 (GRCm39) |
S308R |
probably damaging |
Het |
| Gper1 |
A |
G |
5: 139,412,623 (GRCm39) |
I323V |
probably benign |
Het |
| Grm5 |
C |
A |
7: 87,779,337 (GRCm39) |
R958S |
probably benign |
Het |
| H2-DMb2 |
A |
G |
17: 34,369,503 (GRCm39) |
T85A |
probably benign |
Het |
| Hgsnat |
A |
G |
8: 26,454,866 (GRCm39) |
S220P |
probably damaging |
Het |
| Hspa12a |
A |
T |
19: 58,787,884 (GRCm39) |
M646K |
probably damaging |
Het |
| Inpp5f |
A |
T |
7: 128,286,840 (GRCm39) |
D573V |
probably damaging |
Het |
| Jmjd1c |
A |
G |
10: 67,054,750 (GRCm39) |
N344D |
probably damaging |
Het |
| Kif1c |
A |
G |
11: 70,599,681 (GRCm39) |
E471G |
probably damaging |
Het |
| Lalba |
T |
A |
15: 98,380,061 (GRCm39) |
N63I |
probably benign |
Het |
| Mcoln1 |
T |
A |
8: 3,557,483 (GRCm39) |
L163* |
probably null |
Het |
| Mllt1 |
T |
C |
17: 57,206,813 (GRCm39) |
T344A |
probably benign |
Het |
| Mpzl2 |
T |
A |
9: 44,955,146 (GRCm39) |
D114E |
probably benign |
Het |
| Myef2 |
T |
A |
2: 124,951,659 (GRCm39) |
K259* |
probably null |
Het |
| Myh8 |
C |
A |
11: 67,183,510 (GRCm39) |
D740E |
probably damaging |
Het |
| Myo1b |
A |
T |
1: 51,863,367 (GRCm39) |
|
probably null |
Het |
| Nfix |
T |
C |
8: 85,498,458 (GRCm39) |
I172V |
probably benign |
Het |
| Or1b1 |
A |
T |
2: 36,995,170 (GRCm39) |
I164N |
possibly damaging |
Het |
| Or2h2 |
T |
C |
17: 37,396,883 (GRCm39) |
Y58C |
probably damaging |
Het |
| Or2w1b |
A |
T |
13: 21,300,567 (GRCm39) |
Q235L |
probably benign |
Het |
| Or3a1b |
A |
T |
11: 74,012,705 (GRCm39) |
I197F |
probably benign |
Het |
| Or5b106 |
T |
A |
19: 13,123,355 (GRCm39) |
I223L |
possibly damaging |
Het |
| Orc1 |
T |
C |
4: 108,461,755 (GRCm39) |
F584S |
probably damaging |
Het |
| Osgin1 |
C |
A |
8: 120,169,283 (GRCm39) |
A60D |
possibly damaging |
Het |
| Pde4dip |
C |
A |
3: 97,622,644 (GRCm39) |
V1522L |
probably benign |
Het |
| Phactr1 |
A |
G |
13: 43,287,439 (GRCm39) |
T556A |
possibly damaging |
Het |
| Ppfia2 |
G |
C |
10: 106,597,978 (GRCm39) |
L180F |
probably damaging |
Het |
| Ppm1k |
T |
A |
6: 57,487,762 (GRCm39) |
N354Y |
probably damaging |
Het |
| Ppp1r1a |
A |
G |
15: 103,446,265 (GRCm39) |
V14A |
probably damaging |
Het |
| Prkcd |
A |
T |
14: 30,327,395 (GRCm39) |
|
probably null |
Het |
| Ranbp17 |
T |
C |
11: 33,163,425 (GRCm39) |
S1082G |
probably benign |
Het |
| Rere |
T |
A |
4: 150,703,601 (GRCm39) |
W1528R |
probably damaging |
Het |
| Rnf103 |
T |
A |
6: 71,487,248 (GRCm39) |
F626L |
possibly damaging |
Het |
| Rsrc2 |
A |
G |
5: 123,877,613 (GRCm39) |
|
probably benign |
Het |
| Scin |
T |
A |
12: 40,119,373 (GRCm39) |
I552F |
possibly damaging |
Het |
| Scn3a |
T |
C |
2: 65,291,799 (GRCm39) |
N1649S |
probably damaging |
Het |
| Slain2 |
T |
A |
5: 73,115,609 (GRCm39) |
M448K |
probably benign |
Het |
| Slc25a54 |
T |
C |
3: 109,018,395 (GRCm39) |
F292L |
probably benign |
Het |
| Slc4a1 |
A |
G |
11: 102,243,279 (GRCm39) |
V784A |
probably damaging |
Het |
| Slco1b2 |
G |
A |
6: 141,615,096 (GRCm39) |
V334I |
probably benign |
Het |
| Slf2 |
T |
G |
19: 44,960,100 (GRCm39) |
D1022E |
probably damaging |
Het |
| Smg8 |
T |
C |
11: 86,971,536 (GRCm39) |
E745G |
probably damaging |
Het |
| Smyd1 |
T |
G |
6: 71,196,321 (GRCm39) |
I322L |
probably benign |
Het |
| Snx13 |
G |
A |
12: 35,182,032 (GRCm39) |
V694I |
possibly damaging |
Het |
| Sox6 |
T |
C |
7: 115,076,199 (GRCm39) |
D814G |
probably damaging |
Het |
| Spag6 |
A |
T |
2: 18,750,360 (GRCm39) |
I469F |
probably benign |
Het |
| Spsb2 |
A |
C |
6: 124,786,711 (GRCm39) |
E148A |
probably benign |
Het |
| Srprb |
C |
A |
9: 103,079,147 (GRCm39) |
V747L |
possibly damaging |
Het |
| Stam |
A |
G |
2: 14,107,227 (GRCm39) |
E16G |
probably damaging |
Het |
| Taar5 |
A |
T |
10: 23,847,468 (GRCm39) |
I289F |
possibly damaging |
Het |
| Tgif1 |
C |
T |
17: 71,152,242 (GRCm39) |
R70H |
probably damaging |
Het |
| Top2a |
A |
T |
11: 98,893,786 (GRCm39) |
L1036H |
probably damaging |
Het |
| Tph1 |
T |
A |
7: 46,303,283 (GRCm39) |
I232F |
probably damaging |
Het |
| Ttn |
T |
C |
2: 76,577,175 (GRCm39) |
T24573A |
probably damaging |
Het |
| Tub |
C |
T |
7: 108,620,161 (GRCm39) |
R102* |
probably null |
Het |
| Ube2n |
T |
A |
10: 95,377,607 (GRCm39) |
W129R |
possibly damaging |
Het |
| Usp8 |
A |
T |
2: 126,562,060 (GRCm39) |
K85* |
probably null |
Het |
| Vmn2r81 |
A |
T |
10: 79,106,357 (GRCm39) |
K445M |
probably null |
Het |
| Vps45 |
T |
C |
3: 95,926,943 (GRCm39) |
T535A |
probably damaging |
Het |
| Zfp1007 |
A |
G |
5: 109,826,396 (GRCm39) |
S59P |
probably damaging |
Het |
| Zfp157 |
T |
C |
5: 138,454,557 (GRCm39) |
S252P |
possibly damaging |
Het |
| Zfp605 |
T |
A |
5: 110,275,567 (GRCm39) |
C228* |
probably null |
Het |
| Zfp791 |
T |
A |
8: 85,837,580 (GRCm39) |
I95L |
probably benign |
Het |
|
| Other mutations in Glp2r |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01018:Glp2r
|
APN |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
IGL02244:Glp2r
|
APN |
11 |
67,612,817 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02484:Glp2r
|
APN |
11 |
67,630,992 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R0013:Glp2r
|
UTSW |
11 |
67,600,538 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R0013:Glp2r
|
UTSW |
11 |
67,600,538 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R0195:Glp2r
|
UTSW |
11 |
67,600,534 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1612:Glp2r
|
UTSW |
11 |
67,633,033 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R1699:Glp2r
|
UTSW |
11 |
67,648,367 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1944:Glp2r
|
UTSW |
11 |
67,637,618 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3971:Glp2r
|
UTSW |
11 |
67,637,641 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R4417:Glp2r
|
UTSW |
11 |
67,555,342 (GRCm39) |
intron |
probably benign |
|
|
R4681:Glp2r
|
UTSW |
11 |
67,621,453 (GRCm39) |
splice site |
probably null |
|
|
R4918:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
probably null |
|
|
R4938:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
probably null |
|
|
R4940:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
probably null |
|
|
R4941:Glp2r
|
UTSW |
11 |
67,637,529 (GRCm39) |
splice site |
probably null |
|
|
R4963:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
probably null |
|
|
R4966:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
probably null |
|
|
R5023:Glp2r
|
UTSW |
11 |
67,631,858 (GRCm39) |
missense |
possibly damaging |
0.82 |
|
R5121:Glp2r
|
UTSW |
11 |
67,612,926 (GRCm39) |
splice site |
probably null |
|
|
R5313:Glp2r
|
UTSW |
11 |
67,648,357 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5705:Glp2r
|
UTSW |
11 |
67,600,565 (GRCm39) |
missense |
probably benign |
0.30 |
|
R5790:Glp2r
|
UTSW |
11 |
67,655,625 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6074:Glp2r
|
UTSW |
11 |
67,637,640 (GRCm39) |
missense |
unknown |
|
|
R6595:Glp2r
|
UTSW |
11 |
67,655,603 (GRCm39) |
missense |
probably benign |
0.10 |
|
R6910:Glp2r
|
UTSW |
11 |
67,621,497 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7511:Glp2r
|
UTSW |
11 |
67,648,417 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7627:Glp2r
|
UTSW |
11 |
67,637,589 (GRCm39) |
missense |
unknown |
|
|
R7681:Glp2r
|
UTSW |
11 |
67,600,505 (GRCm39) |
missense |
probably benign |
0.45 |
|
R7779:Glp2r
|
UTSW |
11 |
67,600,609 (GRCm39) |
nonsense |
probably null |
|
|
R8743:Glp2r
|
UTSW |
11 |
67,612,901 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8841:Glp2r
|
UTSW |
11 |
67,653,555 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9093:Glp2r
|
UTSW |
11 |
67,621,459 (GRCm39) |
nonsense |
probably null |
|
|
R9380:Glp2r
|
UTSW |
11 |
67,637,572 (GRCm39) |
missense |
possibly damaging |
0.67 |
|
R9576:Glp2r
|
UTSW |
11 |
67,655,622 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9733:Glp2r
|
UTSW |
11 |
67,648,367 (GRCm39) |
missense |
probably benign |
0.09 |
|
Z1186:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1186:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1186:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Glp2r
|
UTSW |
11 |
67,630,949 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1186:Glp2r
|
UTSW |
11 |
67,630,993 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1186:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1186:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1187:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,630,993 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1187:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1187:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1188:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1188:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,630,993 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1188:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1188:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1189:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1189:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1189:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1189:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1190:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,630,993 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,630,949 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1190:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1190:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1190:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1190:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1191:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,630,993 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1191:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1191:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1192:Glp2r
|
UTSW |
11 |
67,661,662 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1192:Glp2r
|
UTSW |
11 |
67,635,773 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Glp2r
|
UTSW |
11 |
67,633,129 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Glp2r
|
UTSW |
11 |
67,631,885 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1192:Glp2r
|
UTSW |
11 |
67,631,878 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Glp2r
|
UTSW |
11 |
67,600,472 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Glp2r
|
UTSW |
11 |
67,600,470 (GRCm39) |
missense |
probably benign |
|
|
Z1192:Glp2r
|
UTSW |
11 |
67,600,394 (GRCm39) |
missense |
probably damaging |
0.98 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAGTGCTGGTGGAAGGTCTC -3'
(R):5'- GTTTCTTCCCATCCCAAATAAACAG -3'
Sequencing Primer
(F):5'- AAGGTCTCGTGTCCCCCTAAAG -3'
(R):5'- TCCCAAATAAACAGTAGGGATGC -3'
|
| Posted On |
2016-04-15 |
Incidental Mutation