Incidental Mutation 'R5121:Glp2r'
ID |
393050 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Glp2r
|
Ensembl Gene |
ENSMUSG00000049928 |
Gene Name |
glucagon-like peptide 2 receptor |
Synonyms |
GLP-2, 9530092J08Rik |
MMRRC Submission |
042709-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R5121 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
11 |
Chromosomal Location |
67554877-67661979 bp(-) (GRCm39) |
Type of Mutation |
splice site |
DNA Base Change (assembly) |
A to T
at 67612926 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000061560
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021289]
[ENSMUST00000051765]
|
AlphaFold |
Q5IXF8 |
Predicted Effect |
probably null
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
|
SMART Domains |
Protein: ENSMUSP00000061560 Gene: ENSMUSG00000049928
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 |
|
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.1%
- 20x: 91.7%
|
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: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1c |
A |
G |
2: 58,171,662 (GRCm39) |
I234T |
probably damaging |
Het |
Adam24 |
A |
G |
8: 41,132,550 (GRCm39) |
E6G |
probably damaging |
Het |
Amz1 |
A |
G |
5: 140,729,919 (GRCm39) |
D151G |
probably benign |
Het |
Arhgap24 |
T |
C |
5: 102,989,201 (GRCm39) |
L10P |
probably damaging |
Het |
Arhgap25 |
T |
G |
6: 87,509,846 (GRCm39) |
N8T |
probably benign |
Het |
Arsi |
T |
G |
18: 61,050,511 (GRCm39) |
F465V |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,326,024 (GRCm39) |
V293A |
probably damaging |
Het |
Bzw2 |
A |
G |
12: 36,154,350 (GRCm39) |
L340P |
probably damaging |
Het |
Camkmt |
C |
T |
17: 85,404,009 (GRCm39) |
T77I |
probably benign |
Het |
Camsap1 |
G |
T |
2: 25,825,562 (GRCm39) |
Q1375K |
probably benign |
Het |
Catsper2 |
G |
T |
2: 121,227,604 (GRCm39) |
|
probably null |
Het |
Cd163 |
T |
C |
6: 124,294,948 (GRCm39) |
C671R |
probably damaging |
Het |
Cdk7 |
T |
C |
13: 100,854,192 (GRCm39) |
|
probably null |
Het |
Cfi |
C |
T |
3: 129,666,726 (GRCm39) |
P483L |
probably damaging |
Het |
Chn2 |
C |
T |
6: 54,195,546 (GRCm39) |
L72F |
possibly damaging |
Het |
Cimip4 |
C |
T |
15: 78,270,373 (GRCm39) |
E132K |
probably benign |
Het |
Cntn2 |
C |
A |
1: 132,444,798 (GRCm39) |
E363* |
probably null |
Het |
Crebbp |
T |
C |
16: 3,911,375 (GRCm39) |
E999G |
probably damaging |
Het |
Cspp1 |
T |
A |
1: 10,196,688 (GRCm39) |
N900K |
probably damaging |
Het |
Cts3 |
A |
C |
13: 61,715,409 (GRCm39) |
I141M |
probably benign |
Het |
Cwc27 |
A |
T |
13: 104,940,861 (GRCm39) |
V166D |
probably damaging |
Het |
Defb26 |
T |
C |
2: 152,350,085 (GRCm39) |
E65G |
possibly damaging |
Het |
Dnah8 |
A |
G |
17: 31,029,327 (GRCm39) |
T4099A |
probably benign |
Het |
Eml6 |
A |
G |
11: 29,694,606 (GRCm39) |
F1953L |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,344,922 (GRCm39) |
|
probably null |
Het |
Fbln1 |
A |
G |
15: 85,121,872 (GRCm39) |
E331G |
probably damaging |
Het |
Gabra4 |
G |
A |
5: 71,729,546 (GRCm39) |
H76Y |
probably benign |
Het |
Gcat |
T |
C |
15: 78,919,482 (GRCm39) |
V149A |
probably damaging |
Het |
Gm572 |
T |
C |
4: 148,751,302 (GRCm39) |
|
probably null |
Het |
Golgb1 |
T |
C |
16: 36,739,620 (GRCm39) |
V2653A |
probably damaging |
Het |
Grap2 |
G |
A |
15: 80,530,345 (GRCm39) |
R155Q |
possibly damaging |
Het |
Gspt1 |
T |
A |
16: 11,041,165 (GRCm39) |
I533L |
probably damaging |
Het |
Gypa |
A |
T |
8: 81,222,977 (GRCm39) |
Y27F |
unknown |
Het |
Hipk4 |
G |
A |
7: 27,228,917 (GRCm39) |
V456I |
probably benign |
Het |
Homer2 |
A |
T |
7: 81,299,311 (GRCm39) |
D51E |
probably benign |
Het |
Hspa1b |
A |
T |
17: 35,176,980 (GRCm39) |
V335E |
possibly damaging |
Het |
Ift122 |
A |
G |
6: 115,889,495 (GRCm39) |
T827A |
probably benign |
Het |
Igkv1-35 |
T |
C |
6: 69,988,119 (GRCm39) |
N58S |
probably benign |
Het |
Kat6b |
A |
T |
14: 21,669,326 (GRCm39) |
H297L |
probably damaging |
Het |
Kirrel3 |
G |
T |
9: 34,924,601 (GRCm39) |
G296W |
probably damaging |
Het |
Klhl17 |
A |
G |
4: 156,315,082 (GRCm39) |
V525A |
probably benign |
Het |
Lrrn1 |
G |
T |
6: 107,546,168 (GRCm39) |
R655S |
possibly damaging |
Het |
Ltk |
T |
C |
2: 119,583,708 (GRCm39) |
N256D |
probably damaging |
Het |
Mill2 |
G |
A |
7: 18,590,591 (GRCm39) |
G209S |
probably benign |
Het |
Mmp27 |
A |
T |
9: 7,581,369 (GRCm39) |
H544L |
probably benign |
Het |
Mphosph10 |
A |
G |
7: 64,039,344 (GRCm39) |
S209P |
probably damaging |
Het |
Mphosph8 |
A |
T |
14: 56,914,003 (GRCm39) |
K415* |
probably null |
Het |
Myb |
T |
A |
10: 21,002,137 (GRCm39) |
M616L |
probably benign |
Het |
Myo15b |
C |
T |
11: 115,776,880 (GRCm39) |
R867W |
probably damaging |
Het |
Myo18b |
A |
T |
5: 113,022,346 (GRCm39) |
|
probably benign |
Het |
Nip7 |
A |
G |
8: 107,783,589 (GRCm39) |
E8G |
possibly damaging |
Het |
Optn |
T |
A |
2: 5,050,917 (GRCm39) |
I155F |
probably benign |
Het |
Or2f1b |
T |
A |
6: 42,739,931 (GRCm39) |
L315* |
probably null |
Het |
Or4f62 |
A |
T |
2: 111,986,631 (GRCm39) |
M112L |
possibly damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,689 (GRCm39) |
T79A |
possibly damaging |
Het |
Or5c1 |
T |
G |
2: 37,222,601 (GRCm39) |
F281V |
probably damaging |
Het |
Or6b6 |
T |
C |
7: 106,571,438 (GRCm39) |
I38V |
probably benign |
Het |
Papolb |
A |
T |
5: 142,514,592 (GRCm39) |
H350Q |
probably benign |
Het |
Pappa2 |
T |
A |
1: 158,666,197 (GRCm39) |
M1128L |
probably benign |
Het |
Pcdhb5 |
T |
A |
18: 37,454,170 (GRCm39) |
N183K |
probably benign |
Het |
Pde12 |
G |
T |
14: 26,390,577 (GRCm39) |
S44* |
probably null |
Het |
Peg3 |
T |
C |
7: 6,713,288 (GRCm39) |
K645E |
probably benign |
Het |
Pkd1 |
C |
T |
17: 24,792,437 (GRCm39) |
R1375C |
probably benign |
Het |
Plekha5 |
G |
A |
6: 140,525,200 (GRCm39) |
E21K |
probably damaging |
Het |
Plk2 |
C |
T |
13: 110,535,958 (GRCm39) |
P554L |
probably benign |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Polg |
A |
T |
7: 79,114,353 (GRCm39) |
W203R |
probably damaging |
Het |
Ppcdc |
A |
G |
9: 57,328,446 (GRCm39) |
V65A |
possibly damaging |
Het |
Ppm1m |
T |
A |
9: 106,073,004 (GRCm39) |
Q353L |
probably benign |
Het |
Ppp1r13l |
G |
C |
7: 19,104,020 (GRCm39) |
R167P |
probably damaging |
Het |
Ppp1r9b |
T |
A |
11: 94,887,479 (GRCm39) |
V497E |
probably damaging |
Het |
Prpf6 |
T |
A |
2: 181,277,836 (GRCm39) |
H399Q |
probably benign |
Het |
Psg25 |
T |
A |
7: 18,260,461 (GRCm39) |
I146F |
possibly damaging |
Het |
Rasgef1c |
A |
T |
11: 49,851,256 (GRCm39) |
Q116L |
probably damaging |
Het |
Rbbp9 |
A |
G |
2: 144,392,676 (GRCm39) |
V8A |
possibly damaging |
Het |
Rfk |
T |
C |
19: 17,376,930 (GRCm39) |
F144S |
probably damaging |
Het |
Rfwd3 |
A |
C |
8: 112,009,385 (GRCm39) |
|
probably null |
Het |
Rhpn1 |
T |
C |
15: 75,581,109 (GRCm39) |
I117T |
probably damaging |
Het |
Sars2 |
A |
T |
7: 28,447,333 (GRCm39) |
N244Y |
probably damaging |
Het |
Scnn1b |
A |
T |
7: 121,502,110 (GRCm39) |
H256L |
probably benign |
Het |
Sgcz |
G |
A |
8: 38,006,821 (GRCm39) |
T195I |
probably damaging |
Het |
Sh3gl2 |
T |
A |
4: 85,297,494 (GRCm39) |
H157Q |
probably benign |
Het |
Spen |
T |
A |
4: 141,203,410 (GRCm39) |
Q1739L |
probably benign |
Het |
Susd1 |
G |
T |
4: 59,379,657 (GRCm39) |
S323R |
possibly damaging |
Het |
Szt2 |
T |
C |
4: 118,242,641 (GRCm39) |
E1482G |
possibly damaging |
Het |
Tex15 |
A |
T |
8: 34,061,794 (GRCm39) |
K408I |
probably damaging |
Het |
Trem1 |
T |
A |
17: 48,539,864 (GRCm39) |
F14L |
probably null |
Het |
Trim26 |
G |
T |
17: 37,161,958 (GRCm39) |
E126* |
probably null |
Het |
Trpv3 |
T |
C |
11: 73,168,660 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,746,835 (GRCm39) |
|
probably null |
Het |
Ubap1 |
C |
T |
4: 41,379,688 (GRCm39) |
L301F |
probably benign |
Het |
Uchl1 |
T |
C |
5: 66,833,780 (GRCm39) |
M12T |
probably benign |
Het |
Vill |
C |
T |
9: 118,899,093 (GRCm39) |
T253I |
possibly damaging |
Het |
Vmn2r107 |
C |
T |
17: 20,576,015 (GRCm39) |
T115I |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,273,815 (GRCm39) |
S21P |
probably benign |
Het |
Wapl |
A |
G |
14: 34,399,119 (GRCm39) |
K63E |
probably benign |
Het |
Wnt2 |
T |
C |
6: 18,023,125 (GRCm39) |
K175E |
possibly damaging |
Het |
Zfp592 |
T |
C |
7: 80,673,309 (GRCm39) |
L91P |
probably damaging |
Het |
Zfp74 |
T |
C |
7: 29,631,932 (GRCm39) |
|
probably null |
Het |
Zglp1 |
A |
T |
9: 20,973,957 (GRCm39) |
I243N |
probably benign |
Het |
Zranb1 |
A |
G |
7: 132,551,916 (GRCm39) |
E215G |
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 |
|
R4914:Glp2r
|
UTSW |
11 |
67,648,419 (GRCm39) |
nonsense |
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 |
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'- AAGAGTGTGTTGGTCCCCAG -3'
(R):5'- TCATTCCATAAATGCTCCCTGAG -3'
Sequencing Primer
(F):5'- CTTTCTTCTCTGAGCCAAGGTATGAG -3'
(R):5'- GCTCCCTGAGTATTTGTTACATACAG -3'
|
Posted On |
2016-06-15 |