Symbol Name ID |
Tbc1d32
TBC1 domain family, member 32 MGI:2442827 |
Caption: Mutant 2596-005-1 (E15.5) exhibits hydrops, excencephaly, polydactyly, anopthalmia, short snout, and micrognathia
(details)
Represented Alleles:
Tbc1d32b2b2596Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2596 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 3260-003-2 (E17.5) shows abnormal outflow tracts which is diagnosed as pulmonary atresia, AVSD, right aortic arch, aberrant right subclavian artery forming an incomplete vascular ring, and a tracheoesophageal fistula by episcopic confocal histopathology
(details)
Represented Alleles:
b2b3260Clo,
Mutant line 3260 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 3260 Cecilia Lo
Tbc1d32b2b3260.1Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 3260, subline 1 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 2284-002-3 (E15.5) presents with facial cleft and anophthalmia, preaxial digit duplication on all four limbs, and hydrops
(details)
Represented Alleles:
Tbc1d32b2b2284Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2284 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Kidneys of 2596-005-1 (E15.5) presents with bilateral glomerular cysts. Left kidney is duplex
(details)
Represented Alleles:
Tbc1d32b2b2596Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2596 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 3260-003-2 (E17.5) presents with hydrops, petechiae, bilateral anopthalmia, short snout, and micrognathia.
(details)
Represented Alleles:
b2b3260Clo,
Mutant line 3260 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 3260 Cecilia Lo
Tbc1d32b2b3260.1Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 3260, subline 1 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 2284-002-3 (E15.5) has anophthalmia and a cleft lip
(details)
Represented Alleles:
Tbc1d32b2b2284Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2284 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 2596-006-2 (E15.5) exhibits excencephaly, omphalocele, cleft lip, micrognathia, and microphthalmia
(details)
Represented Alleles:
Tbc1d32b2b2596Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2596 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 3260-003-2 (E17.5) exhibits preaxial digit duplication and syndactyly
(details)
Represented Alleles:
b2b3260Clo,
Mutant line 3260 Cecilia Lo; Bench to Bassinet Program (B2B/CVDC), mutation 3260 Cecilia Lo
Tbc1d32b2b3260.1Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 3260, subline 1 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 2284-002-3 (E15.5) presents with persistent truncus arteriosus (PTA) and heterotaxy comprising of levocardia and dextrogastria
(details)
Represented Alleles:
Tbc1d32b2b2284Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2284 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Caption: Mutant 2596-006-2 (E15.5) has a cleft lip and cleft palate
(details)
Represented Alleles:
Tbc1d32b2b2596Clo,
TBC1 domain family, member 32; Bench to Bassinet Program (B2B/CVDC), mutation 2596 Cecilia Lo
Copyright: This image is from the Laboratory of Dr. Cecilia Lo, a member of the Cardiovascular Development Consortium (CvDC), Bench to Bassinet (B2B) program of the National Heart Lung and Blood Institute (NHLBI), and is displayed with the permission of the authors.
J:175213
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 11/12/2024 MGI 6.24 |
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