ZMP
TGFBR2 (2 of 2)
Ensembl ID:
Description:
transforming growth factor, beta receptor II (70/80kDa) [Source:HGNC Symbol;Acc:11773]
Human Orthologue:
TGFBR2
Human Description:
transforming growth factor, beta receptor II (70/80kDa) [Source:HGNC Symbol;Acc:11773]
Mouse Orthologue:
Tgfbr2
Mouse Description:
transforming growth factor, beta receptor II Gene [Source:MGI Symbol;Acc:MGI:98729]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23405 | Nonsense | Available for shipment | Available now |
sa12495 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23405
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082466 | Nonsense | 32 | 659 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 953757)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 1280309 |
GRCz11 | 19 | 917905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTCTGGTGTTTCTGCAGCTCTTCTCCGCACTGCTGATCTCCGCATCTG[C/A]AGCTCCTGTAAGCCTCATCCAGTCAACTGTGTGTCAAATCAGTGCTTCTC
Long Flanking Sequence:
TTTTAACACTTATTTTTAACACTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATGTATGTGTGTGTGTGTGTTTGTGTGTGTTTTTATGGGATGCTGACTGTTGTCTCATCTGATCGTGGTAATCTGGGGATCACATCAGTCTCTGCGGCTGCATGTGTTTGTGTTCATTTTCTGGCATGTCGAGCTGAATGTAGAGACACTGACATCATGCTTCATGTTGTAGAAATGTTTTTGCAAATTAAAACATCTGCTTGTGGTTAAAACCTCTGGCTTTGTGTTGATGTGTGAGTGAACATACAAACTGATGCTCTCTGGTAACGTAATAGTAATAACTAATAACAACAATAATAACATAATCATTATAACATAACTAATCGATCATCTGTGTGCGTGTGTGTGTGTGTTGTTGTTGATGAGTGAACGTATAAACTGATGTTCTCTGGTGTTTCTGCAGCTCTTCTCCGCACTGCTGATCTCCGCATCTG[C/A]AGCTCCTGTAAGCCTCATCCAGTCAACTGTGTGTCAAATCAGTGCTTCTCCAACTGCAGTGTGTCTACAGAGTGTGTGAATGAGCAGGACGTCTGTGCCGCCGTCTGGTATGAGCAACACTCCAGTCACACACACACATGTCTGAACTCGCTCATCCGCACATATACAGTACAATACCTAAGCTGTGTTCCAAATAACACACTATGCACTTATACACTATGTTTGTTTATGTTTGTTTTATACGCTCTGCACTTGTGCACTATGTATGTACACACAGACTATGCACTTATACACTATATAATACACTTTACATCATACAATATACACCATGCACTTCTGCACTACATAGCTATGCACTTATACACTATGCACTTATGCACTACATAGTTATGCACTTATACACTTATGCACTGCATAGTTATGCACTTATACACTATGCACTTATGCACTACATAGTTATGCACTTATACACTATGCACTACATAGTTATGCACTTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12495
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 |
---|---|---|---|---|---|
ENSDART00000082466 | Nonsense | 352 | 659 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 961047)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 1287599 |
GRCz11 | 19 | 925253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAACACTGAGCTGCTGCCCATCCAGCTGGACAGAGTTGTGGGAAAAGGA[C/T]GAWTCGCAGACGTTTATAAAGCCAAGCTGAAGCAGAGCGCAGACTCCTTC
Long Flanking Sequence:
TAATCATATATTTAATTTTTTTTAAATCCATATTTTTATATTATTTCTTTTATATTTTGTAGCATTTGGTTTAAATGCATTTTTTTGTTTAATTTACATTGAATAAAGATACTAAAACAATTAAATATGATCATTTATTAATTTATTTTTTATTAATCTTATATTAATTGTTTTTTTTATTGTTTTTCTCATGCTCAGATTTGAAACAATATCCAGGGGTTCAGTTCAATCCCCCCTCTGAGTCATCATGGTTCAGTCTGGCTCCAGTGCTGATCTCCGTCTTTGTCCTCATCCCAATCGTCCTGCTCTCCGTCTTCTACTGTTACCACATCAGTCAGCACAAACTGAAGCTCCCCAATAAGAAGAGTCTGGACAGCGAGAGATGCAACATTTTCATGAATCCAGAAGAGCATTCGGACAGCAGCTCCATCAACGCCAACAGCCTGAACCACAACACTGAGCTGCTGCCCATCCAGCTGGACAGAGTTGTGGGAAAAGGA[C/T]GATTCGCAGACGTTTATAAAGCCAAGCTGAAGCAGAGCGCAGACTCCTTCCAGACGGTGGCGGTAAAGATCTTCCCGTATGAGGAGTTTTCCTCGTGGAAGAGTGAATGGCAGATTTTCTCTGACGTCGAACTTCGGCATGAAAACGTCCTGCAGTTTCTGACAGCAGAAGAGCGGACGGCAGAGCGACAGTATTGGCTGATCACGGCCTATCACGAGCGAGGAAACCTGCAGGTGGGGACGACTGCCAAACTTTTATGACTCTTTGGTCTCAAATCAGTGATTTTAAGTGGATAAAAAATTGGGAAGTTCAGGTGATTTCAGTCATTACCGTTTCAAACTTTTTTAAAAACTAAAAAAAATTTCCACTAGGGGGCGATTTGTGTAAAGGCCGATTTGCAGACGAATGCAGTAGTGATGGCTGCTTACGAAGCATTGCTTCATGAAGCTTAAAAACTTTTATGAATCTTTGGTTTCGAATCAGTGATTTTAAGCATGTAT
Associated Phenotype:
Not determined