Incidental Mutation 'PIT1430001:2700049A03Rik'
ID |
499906 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
2700049A03Rik
|
Ensembl Gene |
ENSMUSG00000034601 |
Gene Name |
RIKEN cDNA 2700049A03 gene |
Synonyms |
talpid3, Ta3 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
PIT1430001 (G1)
|
Quality Score |
100 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
71183622-71290077 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 71207160 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Phenylalanine
at position 524
(I524F)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000118956
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000045907]
[ENSMUST00000149564]
|
AlphaFold |
E9PV87 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000045907
AA Change: I524F
PolyPhen 2
Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000044701 Gene: ENSMUSG00000034601 AA Change: I524F
Domain | Start | End | E-Value | Type |
Pfam:TALPID3
|
116 |
1351 |
N/A |
PFAM |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000149564
AA Change: I524F
PolyPhen 2
Score 0.711 (Sensitivity: 0.86; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000118956 Gene: ENSMUSG00000034601 AA Change: I524F
Domain | Start | End | E-Value | Type |
Pfam:TALPID3
|
116 |
1349 |
N/A |
PFAM |
|
Meta Mutation Damage Score |
0.2558 |
Coding Region Coverage |
- 1x: 0.0%
- 3x: 0.0%
- 10x: 0.0%
- 20x: 0.0%
|
Validation Efficiency |
99% (136/137) |
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: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930511M06Rik |
T |
C |
18: 57,517,241 (GRCm39) |
|
probably benign |
Het |
9330159F19Rik |
T |
A |
10: 29,100,711 (GRCm39) |
N361K |
probably damaging |
Het |
Adgra2 |
A |
G |
8: 27,604,216 (GRCm39) |
M469V |
possibly damaging |
Het |
Akap9 |
A |
G |
5: 4,079,849 (GRCm39) |
D1867G |
probably damaging |
Het |
Ankrd17 |
T |
C |
5: 90,400,832 (GRCm39) |
T1687A |
possibly damaging |
Het |
Ap1m2 |
G |
A |
9: 21,209,548 (GRCm39) |
P376L |
probably damaging |
Het |
Bicc1 |
A |
G |
10: 70,793,511 (GRCm39) |
S196P |
possibly damaging |
Het |
Cacnb2 |
C |
T |
2: 14,976,412 (GRCm39) |
R228* |
probably null |
Het |
Ccdc43 |
A |
G |
11: 102,582,976 (GRCm39) |
S83P |
probably damaging |
Het |
Cdc42bpg |
T |
A |
19: 6,372,582 (GRCm39) |
|
probably null |
Het |
Cdh16 |
C |
A |
8: 105,344,271 (GRCm39) |
M89I |
probably benign |
Het |
Cecr2 |
A |
C |
6: 120,735,440 (GRCm39) |
H892P |
probably benign |
Het |
Chd5 |
T |
A |
4: 152,455,094 (GRCm39) |
S859T |
probably damaging |
Het |
Chrd |
G |
A |
16: 20,557,748 (GRCm39) |
|
probably null |
Het |
Chrna2 |
T |
A |
14: 66,387,186 (GRCm39) |
L444Q |
probably benign |
Het |
Ckap4 |
A |
G |
10: 84,363,630 (GRCm39) |
S478P |
probably damaging |
Het |
Cldn4 |
A |
T |
5: 134,975,514 (GRCm39) |
M29K |
possibly damaging |
Het |
Clpb |
T |
C |
7: 101,435,926 (GRCm39) |
V615A |
possibly damaging |
Het |
Cyb5r4 |
G |
A |
9: 86,920,791 (GRCm39) |
G142E |
probably benign |
Het |
Cyp1a1 |
A |
G |
9: 57,608,194 (GRCm39) |
Y274C |
probably benign |
Het |
D2hgdh |
T |
C |
1: 93,754,001 (GRCm39) |
|
probably benign |
Het |
Dgkh |
T |
A |
14: 78,818,953 (GRCm39) |
E919V |
probably damaging |
Het |
Dnah1 |
A |
G |
14: 30,984,537 (GRCm39) |
Y3916H |
probably damaging |
Het |
Dpp10 |
A |
G |
1: 123,268,911 (GRCm39) |
|
probably benign |
Het |
Dync2i2 |
T |
C |
2: 29,922,147 (GRCm39) |
Y438C |
probably damaging |
Het |
Egfr |
A |
G |
11: 16,860,214 (GRCm39) |
T1043A |
probably benign |
Het |
Elp5 |
T |
G |
11: 69,857,935 (GRCm39) |
|
probably null |
Het |
Emilin3 |
A |
T |
2: 160,750,402 (GRCm39) |
M449K |
possibly damaging |
Het |
Epb41l4a |
T |
G |
18: 33,930,400 (GRCm39) |
T686P |
probably damaging |
Het |
Eppk1 |
A |
G |
15: 76,105,236 (GRCm38) |
C2482R |
probably benign |
Het |
Eps8l3 |
T |
C |
3: 107,792,183 (GRCm39) |
L370P |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,996,017 (GRCm39) |
S228R |
probably damaging |
Het |
Fam149a |
C |
T |
8: 45,804,743 (GRCm39) |
E280K |
probably benign |
Het |
Fam78b |
T |
C |
1: 166,829,313 (GRCm39) |
I60T |
probably benign |
Het |
Fank1 |
A |
T |
7: 133,478,529 (GRCm39) |
R197* |
probably null |
Het |
Fbxo21 |
C |
T |
5: 118,115,931 (GRCm39) |
S83F |
possibly damaging |
Het |
Fbxo4 |
G |
C |
15: 4,008,782 (GRCm39) |
T42R |
probably benign |
Het |
Fhad1 |
C |
G |
4: 141,637,060 (GRCm39) |
E1135D |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,657,622 (GRCm39) |
E506D |
probably benign |
Het |
Glipr1l2 |
A |
T |
10: 111,942,745 (GRCm39) |
T231S |
probably benign |
Het |
Gm11651 |
C |
G |
11: 105,863,917 (GRCm39) |
|
probably benign |
Het |
Gm16043 |
A |
G |
6: 8,426,969 (GRCm39) |
|
probably null |
Het |
Gm572 |
T |
G |
4: 148,755,850 (GRCm39) |
W389G |
unknown |
Het |
Gpc6 |
G |
A |
14: 118,188,594 (GRCm39) |
W409* |
probably null |
Het |
Gpr155 |
T |
C |
2: 73,200,482 (GRCm39) |
T342A |
probably benign |
Het |
Hcn4 |
A |
C |
9: 58,766,833 (GRCm39) |
H798P |
unknown |
Het |
Herc2 |
T |
C |
7: 55,876,702 (GRCm39) |
S4513P |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,684,488 (GRCm39) |
R361C |
probably benign |
Het |
Hoxa4 |
G |
T |
6: 52,168,199 (GRCm39) |
P157Q |
possibly damaging |
Het |
Ift122 |
A |
C |
6: 115,902,705 (GRCm39) |
|
probably benign |
Het |
Igfbpl1 |
G |
A |
4: 45,826,756 (GRCm39) |
S13L |
unknown |
Het |
Igsf10 |
T |
C |
3: 59,235,579 (GRCm39) |
D1534G |
probably benign |
Het |
Il1rap |
T |
G |
16: 26,529,343 (GRCm39) |
L339V |
possibly damaging |
Het |
Irf2bpl |
C |
T |
12: 86,930,229 (GRCm39) |
R148H |
possibly damaging |
Het |
Ivns1abp |
A |
T |
1: 151,237,356 (GRCm39) |
R58W |
probably damaging |
Het |
Kcnq5 |
C |
T |
1: 21,605,405 (GRCm39) |
V167M |
probably damaging |
Het |
Lrrcc1 |
G |
A |
3: 14,610,656 (GRCm39) |
C337Y |
probably damaging |
Het |
Lrriq3 |
A |
G |
3: 154,804,507 (GRCm39) |
I56V |
probably benign |
Het |
Masp1 |
C |
A |
16: 23,332,694 (GRCm39) |
S47I |
probably damaging |
Het |
Mcm7 |
A |
T |
5: 138,165,708 (GRCm39) |
|
probably benign |
Het |
Mdm2 |
G |
T |
10: 117,530,840 (GRCm39) |
S210R |
probably damaging |
Het |
Mical1 |
A |
G |
10: 41,359,492 (GRCm39) |
R500G |
possibly damaging |
Het |
Mtarc1 |
T |
G |
1: 184,539,246 (GRCm39) |
T37P |
probably benign |
Het |
Myc |
A |
C |
15: 61,859,542 (GRCm39) |
T73P |
probably damaging |
Het |
Myh15 |
G |
A |
16: 49,017,254 (GRCm39) |
|
probably null |
Het |
Myh4 |
A |
G |
11: 67,149,658 (GRCm39) |
M1768V |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,322,597 (GRCm39) |
Y66H |
probably damaging |
Het |
Ncoa1 |
C |
T |
12: 4,373,005 (GRCm39) |
R132K |
probably benign |
Het |
Nfatc3 |
C |
T |
8: 106,786,605 (GRCm39) |
S28F |
possibly damaging |
Het |
Nhlrc3 |
T |
A |
3: 53,361,050 (GRCm39) |
K235M |
probably damaging |
Het |
Nrk |
G |
A |
X: 137,879,463 (GRCm39) |
E757K |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,482,811 (GRCm39) |
P20S |
probably damaging |
Het |
P2rx7 |
C |
T |
5: 122,819,279 (GRCm39) |
A567V |
probably damaging |
Het |
Pate9 |
A |
T |
9: 36,446,295 (GRCm39) |
L39* |
probably null |
Het |
Pcdhb15 |
G |
A |
18: 37,608,724 (GRCm39) |
R652H |
probably benign |
Het |
Pcdhga4 |
T |
C |
18: 37,819,267 (GRCm39) |
V272A |
probably benign |
Het |
Pcdhgb1 |
T |
G |
18: 37,814,472 (GRCm39) |
V321G |
probably damaging |
Het |
Pde2a |
C |
G |
7: 101,100,684 (GRCm39) |
|
probably benign |
Het |
Pdhb |
C |
T |
14: 8,170,425 (GRCm38) |
E109K |
probably damaging |
Het |
Pkd1 |
C |
A |
17: 24,788,485 (GRCm39) |
L748M |
probably damaging |
Het |
Pkd2 |
A |
T |
5: 104,607,654 (GRCm39) |
E51V |
probably damaging |
Het |
Pkdrej |
A |
G |
15: 85,705,493 (GRCm39) |
Y148H |
probably damaging |
Het |
Polr3gl |
C |
G |
3: 96,488,228 (GRCm39) |
|
probably benign |
Het |
Ppfia1 |
A |
T |
7: 144,052,073 (GRCm39) |
L882Q |
probably damaging |
Het |
Ppp4r3b |
G |
T |
11: 29,159,434 (GRCm39) |
R596L |
probably benign |
Het |
Ppp6r3 |
G |
A |
19: 3,521,059 (GRCm39) |
Q85* |
probably null |
Het |
Prss8 |
A |
G |
7: 127,521,424 (GRCm39) |
|
probably benign |
Het |
Qng1 |
T |
A |
13: 58,532,827 (GRCm39) |
K48* |
probably null |
Het |
Rab22a |
A |
G |
2: 173,536,963 (GRCm39) |
I87V |
probably benign |
Het |
Rev1 |
A |
C |
1: 38,095,337 (GRCm39) |
|
probably benign |
Het |
Rnase13 |
A |
G |
14: 52,159,987 (GRCm39) |
Y51H |
probably damaging |
Het |
Rnf26 |
T |
C |
9: 44,023,942 (GRCm39) |
H102R |
probably damaging |
Het |
Rnf5 |
T |
C |
17: 34,822,341 (GRCm39) |
E36G |
probably damaging |
Het |
Rplp1 |
T |
G |
9: 61,821,658 (GRCm39) |
D18A |
probably benign |
Het |
Rrs1 |
C |
A |
1: 9,616,150 (GRCm39) |
D134E |
probably damaging |
Het |
Sec14l1 |
A |
G |
11: 117,034,629 (GRCm39) |
Y166C |
probably damaging |
Het |
Sec14l2 |
A |
T |
11: 4,059,209 (GRCm39) |
Y153* |
probably null |
Het |
Senp1 |
A |
G |
15: 97,982,870 (GRCm39) |
L39P |
probably damaging |
Het |
Senp2 |
T |
A |
16: 21,832,864 (GRCm39) |
|
probably benign |
Het |
Sh3bp1 |
G |
A |
15: 78,798,224 (GRCm39) |
A19T |
probably benign |
Het |
Sis |
G |
A |
3: 72,830,162 (GRCm39) |
P1130S |
probably damaging |
Het |
Slc16a12 |
C |
T |
19: 34,654,759 (GRCm39) |
A95T |
possibly damaging |
Het |
Slc22a4 |
A |
G |
11: 53,918,783 (GRCm39) |
V7A |
probably benign |
Het |
Slc35c2 |
C |
T |
2: 165,119,452 (GRCm39) |
S296N |
probably benign |
Het |
Slf1 |
A |
G |
13: 77,198,169 (GRCm39) |
|
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,859 (GRCm39) |
V616E |
possibly damaging |
Het |
Smarca2 |
T |
A |
19: 26,626,493 (GRCm39) |
M439K |
probably benign |
Het |
Snx29 |
G |
A |
16: 11,221,488 (GRCm39) |
A305T |
probably benign |
Het |
Socs5 |
C |
T |
17: 87,441,044 (GRCm39) |
|
probably benign |
Het |
Spata31d1a |
G |
T |
13: 59,849,010 (GRCm39) |
H1039Q |
probably benign |
Het |
Srgap1 |
G |
A |
10: 121,732,658 (GRCm39) |
|
probably benign |
Het |
Synj1 |
A |
T |
16: 90,761,396 (GRCm39) |
I650N |
probably damaging |
Het |
Tac4 |
A |
C |
11: 95,158,190 (GRCm39) |
|
probably benign |
Het |
Tbck |
A |
C |
3: 132,428,487 (GRCm39) |
T281P |
probably benign |
Het |
Tbx22 |
T |
C |
X: 106,720,611 (GRCm39) |
L62P |
probably damaging |
Het |
Terf2 |
G |
C |
8: 107,822,934 (GRCm39) |
R70G |
probably damaging |
Het |
Tfdp1 |
C |
T |
8: 13,422,526 (GRCm39) |
P138S |
probably benign |
Het |
Tigd2 |
T |
C |
6: 59,188,233 (GRCm39) |
Y367H |
probably damaging |
Het |
Tmprss15 |
A |
T |
16: 78,821,640 (GRCm39) |
|
probably null |
Het |
Tmprss6 |
C |
T |
15: 78,324,827 (GRCm39) |
G741D |
probably damaging |
Het |
Tnrc6b |
A |
C |
15: 80,813,387 (GRCm39) |
T1715P |
probably damaging |
Het |
Tpcn1 |
T |
C |
5: 120,686,388 (GRCm39) |
|
probably benign |
Het |
Trappc2l |
T |
C |
8: 123,339,874 (GRCm39) |
S35P |
probably damaging |
Het |
Trim63 |
T |
C |
4: 134,048,484 (GRCm39) |
|
probably benign |
Het |
Trim66 |
G |
T |
7: 109,074,454 (GRCm39) |
D602E |
probably damaging |
Het |
Trp53bp1 |
G |
A |
2: 121,101,756 (GRCm39) |
P2S |
probably damaging |
Het |
Tspan14 |
A |
G |
14: 40,637,488 (GRCm39) |
L100P |
probably damaging |
Het |
Tspan15 |
C |
T |
10: 62,023,899 (GRCm39) |
E260K |
probably damaging |
Het |
Ubxn10 |
T |
C |
4: 138,448,199 (GRCm39) |
D159G |
probably benign |
Het |
Unc5a |
T |
G |
13: 55,151,709 (GRCm39) |
V713G |
probably damaging |
Het |
Usp16 |
C |
T |
16: 87,270,020 (GRCm39) |
A324V |
probably damaging |
Het |
Uvssa |
G |
A |
5: 33,559,914 (GRCm39) |
R422Q |
possibly damaging |
Het |
Wipf1 |
A |
C |
2: 73,267,946 (GRCm39) |
F151V |
probably damaging |
Het |
Xpo1 |
A |
T |
11: 23,226,437 (GRCm39) |
K104N |
possibly damaging |
Het |
Ybx3 |
T |
C |
6: 131,356,422 (GRCm39) |
T150A |
probably damaging |
Het |
Yju2 |
C |
T |
17: 56,271,479 (GRCm39) |
|
probably benign |
Het |
Zap70 |
T |
A |
1: 36,818,250 (GRCm39) |
S312R |
possibly damaging |
Het |
Zfp534 |
T |
G |
4: 147,759,880 (GRCm39) |
K263T |
probably benign |
Het |
Zfp534 |
T |
G |
4: 147,759,917 (GRCm39) |
N251H |
probably benign |
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 |
|
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 |
|
R4735:2700049A03Rik
|
UTSW |
12 |
71,262,897 (GRCm39) |
missense |
possibly damaging |
0.88 |
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 |
|
Posted On |
2017-11-21 |