MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012] PHENOTYPE: Homozygotes exhibit double outlet right ventricle {SDD}, pulmonary atresia/hypolastic pulmonary artery, atrioventricular septal defect, and right aortic arch. Non-cardiovascular defects include cleft palate, polydactyly, transparent chest wall (sternal bone hypoplasia) and hypoplastic lungs. [provided by MGI curators]
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Other mutations in this stock |
Total: 19 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahctf1 |
C |
T |
1: 179,793,811 |
E130K |
probably damaging |
Het |
Atf7ip |
C |
A |
6: 136,560,688 |
S306R |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,785,203 |
V1208A |
probably benign |
Het |
Ctsl |
C |
T |
13: 64,366,512 |
A195T |
probably damaging |
Het |
Dennd2c |
T |
C |
3: 103,137,203 |
Y367H |
possibly damaging |
Het |
Endod1 |
T |
A |
9: 14,356,870 |
T440S |
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,723,949 |
R526G |
probably damaging |
Het |
Ighv1-39 |
T |
C |
12: 114,914,682 |
T90A |
probably damaging |
Het |
Kdm2a |
G |
A |
19: 4,362,902 |
R19C |
probably damaging |
Het |
Klra1 |
C |
T |
6: 130,375,240 |
E180K |
possibly damaging |
Het |
Odam |
A |
G |
5: 87,885,864 |
Q21R |
probably benign |
Het |
Olfr1205 |
A |
G |
2: 88,831,642 |
Y175C |
probably damaging |
Het |
Olfr145 |
G |
A |
9: 37,897,982 |
V193I |
probably benign |
Het |
Plk1 |
A |
G |
7: 122,169,166 |
E504G |
possibly damaging |
Het |
Rtl3 |
T |
C |
X: 106,839,544 |
I37M |
possibly damaging |
Het |
Srebf2 |
A |
G |
15: 82,147,467 |
E22G |
possibly damaging |
Het |
Tmem74b |
A |
G |
2: 151,706,391 |
S13G |
probably benign |
Het |
Utp14b |
T |
C |
1: 78,664,607 |
V74A |
possibly damaging |
Het |
Znrf3 |
T |
C |
11: 5,289,085 |
M93V |
probably damaging |
Het |
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