Incidental Mutation 'R4735:2700049A03Rik'
ID |
356508 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
2700049A03Rik
|
Ensembl Gene |
ENSMUSG00000034601 |
Gene Name |
RIKEN cDNA 2700049A03 gene |
Synonyms |
talpid3, Ta3 |
MMRRC Submission |
041962-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R4735 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
12 |
Chromosomal Location |
71183622-71290077 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 71262897 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 1410
(I1410N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118956
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045907]
[ENSMUST00000149564]
|
AlphaFold |
E9PV87 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000045907
|
SMART Domains |
Protein: ENSMUSP00000044701 Gene: ENSMUSG00000034601
Domain | Start | End | E-Value | Type |
Pfam:TALPID3
|
116 |
1351 |
N/A |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000149564
AA Change: I1410N
PolyPhen 2
Score 0.876 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000118956 Gene: ENSMUSG00000034601 AA Change: I1410N
Domain | Start | End | E-Value | Type |
Pfam:TALPID3
|
116 |
1349 |
N/A |
PFAM |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.1%
- 20x: 95.0%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a conserved centrosomal protein that functions in ciliogenesis and responds to hedgehog signaling. Mutations in this gene causes Joubert syndrome 23. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Aug 2016] PHENOTYPE: Mice homozygous for a null allele die during organogenesis, lack cilia, and show randomized L-R patterning, face and neural tube defects, pericardial edema and hemorrhages. Mouse embryonic fibroblasts homozygous for a different null allele lack cilia and asymmetrical centriolar localization. [provided by MGI curators]
|
Allele List at MGI |
All alleles(12) : Targeted, other(2) Gene trapped(10) |
Other mutations in this stock |
Total: 133 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230106D20Rik |
T |
C |
10: 19,536,001 (GRCm39) |
|
noncoding transcript |
Het |
Acsf3 |
T |
A |
8: 123,508,218 (GRCm39) |
I238N |
probably damaging |
Het |
Ahctf1 |
T |
C |
1: 179,580,964 (GRCm39) |
N1746S |
probably benign |
Het |
Akap3 |
T |
C |
6: 126,842,601 (GRCm39) |
S407P |
probably damaging |
Het |
Ankfy1 |
T |
A |
11: 72,621,437 (GRCm39) |
M241K |
probably benign |
Het |
Ano7 |
C |
A |
1: 93,328,216 (GRCm39) |
T622K |
probably benign |
Het |
App |
T |
C |
16: 84,900,202 (GRCm39) |
T83A |
probably damaging |
Het |
Arhgef28 |
T |
A |
13: 98,036,237 (GRCm39) |
E1674V |
probably damaging |
Het |
Asb2 |
C |
A |
12: 103,291,317 (GRCm39) |
V489L |
probably benign |
Het |
Atrn |
T |
C |
2: 130,862,910 (GRCm39) |
V1330A |
probably benign |
Het |
Bltp1 |
T |
A |
3: 37,059,116 (GRCm39) |
N3267K |
possibly damaging |
Het |
Brca1 |
A |
G |
11: 101,383,001 (GRCm39) |
|
probably null |
Het |
Bspry |
G |
A |
4: 62,404,762 (GRCm39) |
R186Q |
probably damaging |
Het |
Ccdc168 |
A |
G |
1: 44,100,861 (GRCm39) |
I79T |
probably benign |
Het |
Cdkn2d |
C |
G |
9: 21,202,185 (GRCm39) |
V21L |
probably benign |
Het |
Celsr1 |
T |
A |
15: 85,790,230 (GRCm39) |
|
probably null |
Het |
Ckap4 |
A |
G |
10: 84,369,384 (GRCm39) |
V116A |
possibly damaging |
Het |
Crb3 |
A |
G |
17: 57,372,207 (GRCm39) |
T85A |
probably damaging |
Het |
Cyld |
T |
C |
8: 89,456,278 (GRCm39) |
S443P |
probably damaging |
Het |
Cyp27a1 |
T |
G |
1: 74,776,366 (GRCm39) |
V434G |
possibly damaging |
Het |
Cyp2b13 |
A |
G |
7: 25,787,720 (GRCm39) |
T339A |
probably benign |
Het |
Dars1 |
A |
T |
1: 128,303,971 (GRCm39) |
L252* |
probably null |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Ddx55 |
T |
C |
5: 124,704,539 (GRCm39) |
F382S |
probably damaging |
Het |
Dmtf1l |
T |
A |
X: 125,722,217 (GRCm39) |
K296M |
probably damaging |
Het |
Dnah7b |
G |
A |
1: 46,106,115 (GRCm39) |
R33Q |
unknown |
Het |
Dnm2 |
G |
T |
9: 21,385,883 (GRCm39) |
S302I |
probably damaging |
Het |
Dock4 |
T |
A |
12: 40,681,525 (GRCm39) |
F75I |
probably benign |
Het |
Dpp10 |
T |
C |
1: 123,326,356 (GRCm39) |
N365S |
probably benign |
Het |
Dpy19l3 |
G |
T |
7: 35,422,146 (GRCm39) |
Q236K |
probably benign |
Het |
Dsp |
T |
C |
13: 38,380,016 (GRCm39) |
S1655P |
probably damaging |
Het |
Ebpl |
A |
T |
14: 61,579,567 (GRCm39) |
I117N |
probably damaging |
Het |
Edc4 |
T |
A |
8: 106,613,818 (GRCm39) |
V386E |
probably damaging |
Het |
Eif2s2 |
T |
A |
2: 154,720,467 (GRCm39) |
|
probably null |
Het |
Elob |
A |
T |
17: 24,046,562 (GRCm39) |
|
probably null |
Het |
Enox2 |
T |
C |
X: 48,158,554 (GRCm39) |
I71V |
probably damaging |
Het |
Fez1 |
A |
T |
9: 36,772,141 (GRCm39) |
K149* |
probably null |
Het |
Fhip2a |
A |
G |
19: 57,359,661 (GRCm39) |
E67G |
probably damaging |
Het |
Fign |
A |
G |
2: 63,810,782 (GRCm39) |
Y163H |
probably damaging |
Het |
Flnc |
G |
A |
6: 29,455,812 (GRCm39) |
G2048S |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,736,022 (GRCm39) |
D539G |
probably benign |
Het |
Frmd4b |
T |
C |
6: 97,436,220 (GRCm39) |
|
probably benign |
Het |
Gan |
C |
T |
8: 117,920,970 (GRCm39) |
T402M |
probably damaging |
Het |
Ganc |
T |
A |
2: 120,267,104 (GRCm39) |
|
silent |
Het |
Ggt6 |
C |
A |
11: 72,327,425 (GRCm39) |
R103S |
probably benign |
Het |
Gli2 |
T |
C |
1: 118,768,052 (GRCm39) |
D725G |
probably damaging |
Het |
Gm15446 |
T |
A |
5: 110,090,818 (GRCm39) |
C357S |
probably damaging |
Het |
Gm44501 |
A |
G |
17: 40,889,810 (GRCm39) |
N108S |
probably benign |
Het |
Gm6309 |
A |
T |
5: 146,105,054 (GRCm39) |
D286E |
probably damaging |
Het |
Gm6358 |
G |
A |
16: 88,937,848 (GRCm39) |
G29E |
unknown |
Het |
Grik5 |
A |
G |
7: 24,757,713 (GRCm39) |
I422T |
probably damaging |
Het |
Grin2c |
A |
G |
11: 115,140,422 (GRCm39) |
I1232T |
possibly damaging |
Het |
Gsg1 |
C |
T |
6: 135,214,405 (GRCm39) |
R365H |
possibly damaging |
Het |
H2-M2 |
A |
G |
17: 37,794,135 (GRCm39) |
S30P |
possibly damaging |
Het |
Hcfc2 |
A |
G |
10: 82,547,914 (GRCm39) |
D302G |
probably damaging |
Het |
Hk2 |
T |
C |
6: 82,721,955 (GRCm39) |
D128G |
probably benign |
Het |
Hmcn2 |
C |
A |
2: 31,273,787 (GRCm39) |
Q1380K |
probably benign |
Het |
Hsp90b1 |
G |
T |
10: 86,529,819 (GRCm39) |
P617T |
probably damaging |
Het |
Htr1d |
A |
G |
4: 136,170,197 (GRCm39) |
E142G |
probably benign |
Het |
Hydin |
G |
A |
8: 111,282,264 (GRCm39) |
|
probably null |
Het |
Il1r1 |
T |
A |
1: 40,332,455 (GRCm39) |
N81K |
probably benign |
Het |
Inpp5b |
T |
C |
4: 124,677,760 (GRCm39) |
S407P |
probably damaging |
Het |
Itpkb |
T |
C |
1: 180,245,780 (GRCm39) |
Y766H |
probably damaging |
Het |
Lyrm2 |
T |
A |
4: 32,801,150 (GRCm39) |
I65N |
probably damaging |
Het |
Mink1 |
T |
A |
11: 70,500,086 (GRCm39) |
|
probably null |
Het |
Mkrn3 |
C |
T |
7: 62,069,452 (GRCm39) |
R113H |
probably damaging |
Het |
Msx3 |
G |
A |
7: 139,627,798 (GRCm39) |
A157V |
probably damaging |
Het |
Nrxn2 |
T |
G |
19: 6,548,484 (GRCm39) |
V59G |
possibly damaging |
Het |
Nt5c3b |
T |
C |
11: 100,331,732 (GRCm39) |
T12A |
probably benign |
Het |
Nwd2 |
G |
A |
5: 63,965,594 (GRCm39) |
R1726Q |
probably benign |
Het |
Nynrin |
A |
G |
14: 56,107,625 (GRCm39) |
T911A |
probably benign |
Het |
Or11i1 |
T |
A |
3: 106,728,996 (GRCm39) |
Y293F |
probably damaging |
Het |
Or4p18 |
T |
C |
2: 88,233,267 (GRCm39) |
T4A |
probably benign |
Het |
Or51aa5 |
A |
G |
7: 103,167,030 (GRCm39) |
I187T |
possibly damaging |
Het |
Or51af1 |
C |
T |
7: 103,141,267 (GRCm39) |
V273M |
possibly damaging |
Het |
Or52n20 |
C |
T |
7: 104,320,200 (GRCm39) |
T97I |
probably benign |
Het |
Or5p66 |
A |
G |
7: 107,885,520 (GRCm39) |
M271T |
probably benign |
Het |
Or6c212 |
A |
G |
10: 129,558,792 (GRCm39) |
I207T |
probably benign |
Het |
Patl1 |
G |
T |
19: 11,899,869 (GRCm39) |
M220I |
probably benign |
Het |
Pcnx2 |
A |
T |
8: 126,554,780 (GRCm39) |
|
probably null |
Het |
Pigr |
A |
T |
1: 130,774,291 (GRCm39) |
T424S |
probably damaging |
Het |
Pik3c2b |
T |
A |
1: 132,994,787 (GRCm39) |
D250E |
probably benign |
Het |
Ppa2 |
G |
A |
3: 133,076,186 (GRCm39) |
E272K |
probably benign |
Het |
Pramel7 |
G |
A |
2: 87,321,187 (GRCm39) |
Q283* |
probably null |
Het |
Prelid3b |
A |
G |
2: 174,307,683 (GRCm39) |
I81T |
probably benign |
Het |
Prpf38a |
T |
C |
4: 108,436,242 (GRCm39) |
I24V |
possibly damaging |
Het |
Ptger2 |
A |
G |
14: 45,239,295 (GRCm39) |
D311G |
possibly damaging |
Het |
Rab4b |
A |
T |
7: 26,872,191 (GRCm39) |
|
probably benign |
Het |
Rad17 |
A |
C |
13: 100,755,637 (GRCm39) |
D581E |
probably damaging |
Het |
Samd11 |
T |
C |
4: 156,333,230 (GRCm39) |
T333A |
probably benign |
Het |
Scaf4 |
C |
T |
16: 90,049,320 (GRCm39) |
D256N |
unknown |
Het |
Serinc2 |
A |
G |
4: 130,157,438 (GRCm39) |
F82L |
probably benign |
Het |
Serpina3g |
T |
A |
12: 104,205,372 (GRCm39) |
V37E |
probably damaging |
Het |
Serpinb9c |
T |
A |
13: 33,334,254 (GRCm39) |
M263L |
probably benign |
Het |
Shbg |
A |
G |
11: 69,508,326 (GRCm39) |
I67T |
possibly damaging |
Het |
Slc25a48 |
G |
A |
13: 56,596,887 (GRCm39) |
|
probably null |
Het |
Slc25a54 |
T |
C |
3: 109,005,923 (GRCm39) |
W144R |
probably damaging |
Het |
Slc34a1 |
A |
T |
13: 55,561,397 (GRCm39) |
T621S |
probably benign |
Het |
Slc6a18 |
A |
T |
13: 73,814,554 (GRCm39) |
C419S |
probably benign |
Het |
Smc5 |
A |
T |
19: 23,220,069 (GRCm39) |
D389E |
probably benign |
Het |
Smco3 |
T |
A |
6: 136,808,636 (GRCm39) |
E79D |
probably damaging |
Het |
Sox5 |
A |
G |
6: 143,906,561 (GRCm39) |
F298S |
probably damaging |
Het |
Sphkap |
A |
G |
1: 83,256,838 (GRCm39) |
S304P |
probably benign |
Het |
Tcea2 |
C |
T |
2: 181,328,514 (GRCm39) |
T211I |
probably damaging |
Het |
Tcf4 |
G |
T |
18: 69,697,226 (GRCm39) |
S34I |
possibly damaging |
Het |
Tlr4 |
C |
T |
4: 66,759,435 (GRCm39) |
R743C |
probably damaging |
Het |
Tmem183a |
T |
C |
1: 134,288,620 (GRCm39) |
E67G |
probably damaging |
Het |
Tpr |
C |
T |
1: 150,317,947 (GRCm39) |
R2152C |
possibly damaging |
Het |
Trbv15 |
T |
C |
6: 41,118,358 (GRCm39) |
I38T |
probably benign |
Het |
Treh |
G |
A |
9: 44,592,849 (GRCm39) |
A125T |
probably damaging |
Het |
Trio |
A |
T |
15: 27,752,875 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,782,293 (GRCm39) |
V981A |
probably damaging |
Het |
Uap1l1 |
A |
G |
2: 25,252,732 (GRCm39) |
L436P |
probably damaging |
Het |
Uba7 |
A |
T |
9: 107,854,115 (GRCm39) |
I182F |
possibly damaging |
Het |
Unc13c |
A |
T |
9: 73,600,620 (GRCm39) |
S1375T |
probably benign |
Het |
Usp48 |
C |
CT |
4: 137,360,680 (GRCm39) |
|
probably null |
Het |
Utp20 |
A |
C |
10: 88,652,780 (GRCm39) |
V378G |
possibly damaging |
Het |
Vmn1r69 |
A |
T |
7: 10,314,926 (GRCm39) |
|
probably benign |
Het |
Vmn1r86 |
A |
T |
7: 12,836,221 (GRCm39) |
H218Q |
probably damaging |
Het |
Vmn2r121 |
T |
A |
X: 123,038,335 (GRCm39) |
I562L |
probably benign |
Het |
Vmn2r45 |
A |
T |
7: 8,486,472 (GRCm39) |
I272N |
probably damaging |
Het |
Wdr90 |
A |
G |
17: 26,078,424 (GRCm39) |
V320A |
probably benign |
Het |
Wfikkn1 |
A |
G |
17: 26,097,367 (GRCm39) |
V319A |
possibly damaging |
Het |
Whamm |
A |
G |
7: 81,221,122 (GRCm39) |
D18G |
probably benign |
Het |
Wrn |
T |
A |
8: 33,775,250 (GRCm39) |
I605F |
probably damaging |
Het |
Zdhhc18 |
A |
G |
4: 133,341,178 (GRCm39) |
F232L |
probably damaging |
Het |
Zfp41 |
T |
C |
15: 75,490,609 (GRCm39) |
I187T |
probably benign |
Het |
Zfp418 |
A |
G |
7: 7,185,561 (GRCm39) |
Y508C |
probably damaging |
Het |
Zfp560 |
T |
G |
9: 20,260,347 (GRCm39) |
I172L |
probably benign |
Het |
Zfp943 |
A |
T |
17: 22,211,391 (GRCm39) |
D159V |
probably benign |
Het |
Zfp955a |
T |
C |
17: 33,460,696 (GRCm39) |
I479V |
probably benign |
Het |
Zfpm1 |
T |
A |
8: 123,062,219 (GRCm39) |
V426D |
probably benign |
Het |
Zic1 |
C |
T |
9: 91,246,558 (GRCm39) |
M171I |
possibly damaging |
Het |
|
Other mutations in 2700049A03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:2700049A03Rik
|
APN |
12 |
71,213,893 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01107:2700049A03Rik
|
APN |
12 |
71,241,242 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01404:2700049A03Rik
|
APN |
12 |
71,211,152 (GRCm39) |
splice site |
probably null |
|
IGL01835:2700049A03Rik
|
APN |
12 |
71,213,957 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01835:2700049A03Rik
|
APN |
12 |
71,213,955 (GRCm39) |
nonsense |
probably null |
|
IGL02122:2700049A03Rik
|
APN |
12 |
71,217,299 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02140:2700049A03Rik
|
APN |
12 |
71,195,034 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02385:2700049A03Rik
|
APN |
12 |
71,201,630 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03181:2700049A03Rik
|
APN |
12 |
71,240,147 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03253:2700049A03Rik
|
APN |
12 |
71,187,657 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03278:2700049A03Rik
|
APN |
12 |
71,205,599 (GRCm39) |
splice site |
probably benign |
|
G4846:2700049A03Rik
|
UTSW |
12 |
71,184,683 (GRCm39) |
missense |
probably benign |
|
PIT1430001:2700049A03Rik
|
UTSW |
12 |
71,207,160 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT4519001:2700049A03Rik
|
UTSW |
12 |
71,217,440 (GRCm39) |
missense |
probably benign |
0.05 |
R0108:2700049A03Rik
|
UTSW |
12 |
71,224,692 (GRCm39) |
missense |
probably benign |
0.14 |
R0165:2700049A03Rik
|
UTSW |
12 |
71,213,924 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0211:2700049A03Rik
|
UTSW |
12 |
71,262,870 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0211:2700049A03Rik
|
UTSW |
12 |
71,262,870 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0220:2700049A03Rik
|
UTSW |
12 |
71,195,194 (GRCm39) |
critical splice donor site |
probably null |
|
R0352:2700049A03Rik
|
UTSW |
12 |
71,184,804 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0468:2700049A03Rik
|
UTSW |
12 |
71,240,084 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0508:2700049A03Rik
|
UTSW |
12 |
71,211,162 (GRCm39) |
missense |
probably damaging |
0.98 |
R0673:2700049A03Rik
|
UTSW |
12 |
71,224,642 (GRCm39) |
missense |
probably damaging |
0.97 |
R0840:2700049A03Rik
|
UTSW |
12 |
71,205,657 (GRCm39) |
missense |
probably benign |
0.16 |
R0893:2700049A03Rik
|
UTSW |
12 |
71,266,082 (GRCm39) |
splice site |
probably benign |
|
R1244:2700049A03Rik
|
UTSW |
12 |
71,262,918 (GRCm39) |
missense |
probably benign |
0.25 |
R1432:2700049A03Rik
|
UTSW |
12 |
71,217,361 (GRCm39) |
splice site |
probably null |
|
R1599:2700049A03Rik
|
UTSW |
12 |
71,197,033 (GRCm39) |
missense |
probably damaging |
0.98 |
R1732:2700049A03Rik
|
UTSW |
12 |
71,265,995 (GRCm39) |
missense |
probably benign |
0.18 |
R1820:2700049A03Rik
|
UTSW |
12 |
71,197,018 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1939:2700049A03Rik
|
UTSW |
12 |
71,207,186 (GRCm39) |
splice site |
probably null |
|
R1998:2700049A03Rik
|
UTSW |
12 |
71,235,393 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2337:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2337:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2340:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2340:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2382:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2382:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2384:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2384:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2445:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2445:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2449:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2449:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R2512:2700049A03Rik
|
UTSW |
12 |
71,219,945 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2872:2700049A03Rik
|
UTSW |
12 |
71,201,530 (GRCm39) |
splice site |
probably benign |
|
R3236:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3236:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3237:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3237:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3734:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3734:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3808:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3808:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3809:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3809:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3944:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3944:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3959:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3959:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3960:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R3960:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4593:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4593:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4595:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4595:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4596:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4596:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4600:2700049A03Rik
|
UTSW |
12 |
71,195,037 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4649:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4649:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4651:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4651:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4652:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4652:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4714:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4714:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4810:2700049A03Rik
|
UTSW |
12 |
71,236,216 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4852:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4852:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4854:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4854:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4855:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4855:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4884:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4884:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4893:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4893:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4905:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4905:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4915:2700049A03Rik
|
UTSW |
12 |
71,236,420 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4919:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4919:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4959:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4959:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4989:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R4989:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5011:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5011:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5012:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5012:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5118:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5118:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5146:2700049A03Rik
|
UTSW |
12 |
71,289,799 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5163:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5163:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5188:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5188:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5189:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5189:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5189:2700049A03Rik
|
UTSW |
12 |
71,240,123 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5190:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5190:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5290:2700049A03Rik
|
UTSW |
12 |
71,235,565 (GRCm39) |
missense |
probably benign |
0.00 |
R5344:2700049A03Rik
|
UTSW |
12 |
71,289,801 (GRCm39) |
missense |
probably benign |
|
R5502:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5502:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5503:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5503:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5619:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5619:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5667:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5667:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5669:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5669:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5671:2700049A03Rik
|
UTSW |
12 |
71,211,321 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5671:2700049A03Rik
|
UTSW |
12 |
71,211,320 (GRCm39) |
nonsense |
probably null |
|
R5725:2700049A03Rik
|
UTSW |
12 |
71,240,093 (GRCm39) |
missense |
probably benign |
0.05 |
R5956:2700049A03Rik
|
UTSW |
12 |
71,203,893 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6051:2700049A03Rik
|
UTSW |
12 |
71,231,304 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6148:2700049A03Rik
|
UTSW |
12 |
71,234,200 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6158:2700049A03Rik
|
UTSW |
12 |
71,217,410 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6916:2700049A03Rik
|
UTSW |
12 |
71,211,318 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7129:2700049A03Rik
|
UTSW |
12 |
71,263,004 (GRCm39) |
splice site |
probably null |
|
R7168:2700049A03Rik
|
UTSW |
12 |
71,262,831 (GRCm39) |
missense |
probably damaging |
0.98 |
R7193:2700049A03Rik
|
UTSW |
12 |
71,265,963 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7200:2700049A03Rik
|
UTSW |
12 |
71,187,680 (GRCm39) |
missense |
probably damaging |
0.96 |
R7359:2700049A03Rik
|
UTSW |
12 |
71,236,348 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7488:2700049A03Rik
|
UTSW |
12 |
71,197,179 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7755:2700049A03Rik
|
UTSW |
12 |
71,236,187 (GRCm39) |
missense |
probably benign |
0.02 |
R7757:2700049A03Rik
|
UTSW |
12 |
71,236,187 (GRCm39) |
missense |
probably benign |
0.02 |
R7922:2700049A03Rik
|
UTSW |
12 |
71,211,180 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7966:2700049A03Rik
|
UTSW |
12 |
71,219,903 (GRCm39) |
missense |
probably benign |
0.00 |
R8082:2700049A03Rik
|
UTSW |
12 |
71,188,895 (GRCm39) |
critical splice donor site |
probably null |
|
R8311:2700049A03Rik
|
UTSW |
12 |
71,184,815 (GRCm39) |
unclassified |
probably benign |
|
R8408:2700049A03Rik
|
UTSW |
12 |
71,236,356 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8852:2700049A03Rik
|
UTSW |
12 |
71,231,197 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8860:2700049A03Rik
|
UTSW |
12 |
71,231,197 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9039:2700049A03Rik
|
UTSW |
12 |
71,213,849 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9281:2700049A03Rik
|
UTSW |
12 |
71,205,687 (GRCm39) |
missense |
possibly damaging |
0.51 |
R9308:2700049A03Rik
|
UTSW |
12 |
71,231,233 (GRCm39) |
missense |
probably benign |
0.23 |
R9385:2700049A03Rik
|
UTSW |
12 |
71,207,966 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9412:2700049A03Rik
|
UTSW |
12 |
71,235,457 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9643:2700049A03Rik
|
UTSW |
12 |
71,211,189 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9676:2700049A03Rik
|
UTSW |
12 |
71,207,905 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9776:2700049A03Rik
|
UTSW |
12 |
71,235,448 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9789:2700049A03Rik
|
UTSW |
12 |
71,231,357 (GRCm39) |
missense |
probably benign |
|
Z1177:2700049A03Rik
|
UTSW |
12 |
71,211,258 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- TGCTTAGGAATGCTGGGAAG -3'
(R):5'- CCCGGCCCCTAAAATGTTTTAG -3'
Sequencing Primer
(F):5'- CTTAGGAATGCTGGGAAGTGTAGTC -3'
(R):5'- AGGGATTGAAATCAAGTCTGTTTTTG -3'
|
Posted On |
2015-11-11 |