ZMP
tgfb3
Ensembl ID:
ZFIN ID:
Description:
transforming growth factor beta-3 [Source:RefSeq peptide;Acc:NP_919367]
Human Orthologue:
TGFB3
Human Description:
transforming growth factor, beta 3 [Source:HGNC Symbol;Acc:11769]
Mouse Orthologue:
Tgfb3
Mouse Description:
transforming growth factor, beta 3 Gene [Source:MGI Symbol;Acc:MGI:98727]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3526 | Nonsense | Available for shipment | Available now |
sa1467 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3526
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019766 | Nonsense | 181 | 410 | 3 | 7 |
ENSDART00000147600 | Nonsense | 66 | 295 | 2 | 6 |
The following transcripts of ENSDARG00000019367 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 52599463)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51999649 |
GRCz11 | 17 | 52070328 |
KASP Assay ID:
554-0143.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGTGTGTTTTTACGGCAGATTCTCCGTCCTGATGAGCACATCGGCAAG[C/T]AGCGCTACATCGGCAGAAAAAACGTGATGATTGGAGGGACGGATGAGTGG
Long Flanking Sequence:
AGTGTGCCATTTGGGACGACACTACATACATATACTATCCTGTTGAGTGTGTATGTGCATAGTGCATGATTGCATAGTGTATAGTGTGCAATTTGGGACGCAGCTCTAATTTTACATTTTATGATTCTGCAAGTGAATCTGGTGATGAAACAGAATAAATAGCGAGTTAATAAGAGCACAAAGCAAACAGTAAGCTTGCTATTGTCAACATTTCTAGTTTTACAATTCTGACTTTTGTCCACAAAATATTGAATTTACAGTACACGGTTTCCTCACGATTGTTTTTAATTTGTGCTCTAAAATGTAAAAAATATAAGCAGGGCTTGAAATTACCCTTTTTAAGTGCCCATGATGTCAATGTTGTGTTTATTACCACAATATATCGCATTATTGAATATCTCCACATGTCTAATCATGGATGTTGATTAATGGAGAGCAGAAATCAGCTTTTACGTGTGTTTTTACGGCAGATTCTCCGTCCTGATGAGCACATCGGCAAG[C/T]AGCGCTACATCGGCAGAAAAAACGTGATGATTGGAGGGACGGATGAGTGGGTTTCCTTCGACGTCACTGAGACCGTACGAGAGTGGCTGACAAACAGAGGTCAGTCCCATTTAACACTTTAAACTCATCGGAAAGACTCTGGTGTTTTTATTACAAGACTTTTGAACTGTTTTGAACTCTTATGCGATGATTAAAATGGATCCTTTTCACATTTCTGGGTTTCTCAGGAGCGGAAGTCAGCATAGTTGGTGAACTCAGAGCGCAGTGAATGGCAGAGTACAACAAATCGTTTGTTTACAATCCTATTTACTGAAATAATGAAAGAAAAACTCAGACAACAGTGTTGTCAAGACTATATTCAACAATCAAGACTAATATGAAATGTAAATTTTACCAGCATATAAAAATTCAGATTTATTAAATTACAATATTCAAATTCACACAGTTTCAGTTCAGGTTGTTTTGGCATATTATTAGCTCCATAGTGTTGTGATCTCAGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa1467
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019766 | Nonsense | 379 | 410 | 7 | 7 |
ENSDART00000147600 | Nonsense | 264 | 295 | 6 | 6 |
The following transcripts of ENSDARG00000019367 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 52588253)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51988439 |
GRCz11 | 17 | 52059118 |
KASP Assay ID:
554-1392.1 (used for ordering genotyping assays)
KASP Sequence:
TGTACAACACGCTGAACCCRGAGGCGTCTGCGTCCCCCTGCTGCGTTCCT[C/T]AAGACCTGGAGCCGCTCACCATCCTCTACTACGTGGGCCGGACGCCTAAA
Long Flanking Sequence:
TCAAGAATCAGATCTAGACTAACCATAGAGTATCCAAGACCTAGACAAAACCACACAAGACTCAAATTCTAAGACTAGACCATGAAGACCCATATCCAAACCAAGACTTGCCCCTTCAAGAACCAGATCTAGACTAACCAAGACCCAGATTAAGATTAGACGCCTCAAGACCCAGATGCAGACTAAGACTAAACAGACTACGGGCGTGTGTCCACTGAAGCACCTCTTTGCTGCAGCACAAAATGCTTCGGTGGTCGTGCATGCACCCTAAGACTAAACTCTGGAGAACCTCGAAGCTCTCCGCTTTCATCTAGAATATCTTGACTCATGTTCTGAAGATGAGCTTGGTCTCAGGGAGTTTGTGAAGCTGAATGTGTTTTGTTTGATGATGATGATGATGATGAAGATAATTTGACGTGGGCTCCTTCATGTGTGCACAGCTGCTGAGTCTGTACAACACGCTGAACCCAGAGGCGTCTGCGTCCCCCTGCTGCGTTCCT[C/T]AAGACCTGGAGCCGCTCACCATCCTCTACTACGTGGGCCGGACGCCTAAAGTGGAGCAGCTTTCCAACATGATCGTCAAATCCTGCAAGTGCAGCTGAGAGGTCCGTTTTCAACCCATCCACGAGCCAAAAGCTTCTGCGTTTTCAGACCAGCCAAAAGGCCACACGACCATCCCTCAGACTTCCAGACCTTTAAAGTGACCTGTAGCGTGTAATGTTCGGTCCGCTCTTTTAAACCTCATGGGCATTTCTGAACTCTGGAGCTCCATGGAAGATCTACAGACGGAGCTTTACTGAGATCCCACACATGCTGGAGCCACGGATGGGTTCAACCAGCGTTTCTGTACAACGTAATGATTCTTTTGTTCCTCCAGACTGTTTAAAGTGTGTACCACAGTAACTCGCACTGTCTAATGGGTTTTTTTTTTGTTAATACAAACATGCTGGAAAGAGAAAACATGGTGTTTGGCCTTGGTTATGTTTACCTCTGTCACACGGCAG
Associated Phenotype:
Not determined