Busch Lab

ZMP

ENSDARG00000075905

Ensembl ID:
ENSDARG00000075905
Human Orthologue:
TGFBRAP1
Human Description:
transforming growth factor, beta receptor associated protein 1 [Source:HGNC Symbol;Acc:16836]
Mouse Orthologue:
Tgfbrap1
Mouse Description:
transforming growth factor, beta receptor associated protein 1 Gene [Source:MGI Symbol;Acc:MGI:24474

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9094 Nonsense Mutation detected in F1 DNA Not yet available
sa14167 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9094
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110272 Nonsense 317 456 6 7
Genomic Location (Zv9):
Chromosome 17 (position 15425227)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15576055
GRCz11 17 15583988
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAAGACCAGCAGGCTGCTGAATGCTACTGTTGGAGGACCTCTGCTGGA[C/T]GAGACAAGAAGTTCACGCAGACCATATTTCTCACTYTACTACAAATCTAC
Long Flanking Sequence:
GAAAAAAAGACAATTTAAAAAAATCTAAACTGAGAAAAAATATATAAAAGCAATAACCTTTTTTTGTGACAGACTTACATAAAAATTCTTAATTTCTAAATGAATCAGGTGATTTTACAGAACCAATTATTAAGACAGAGATCTGCCTCCAACTACTGGTGTTTTAAGTGCCATGACAGATCTAAGCCACCCAAAATACCAGGAAAAAAACACTCAGATTAGTGCTTTAATCTTAACTTTATATAAAAAAGGCAACAAATAAAAAGATACGAGATGTTTTTTCAGTCAATATTACACACCCCTAGTTTGATATTTCAGGTCCATGAAATAAACCAACTTCTACACCTTTTACAGACCAAATAGCATCCTCATCTCTTCATGTGGAGCAAGCAATTTCGCTTGGAAAGAATGGAAAACACAAAAAGGCCCTGCAGGTTTTAGTCAATGAGGAGAAAGACCAGCAGGCTGCTGAATGCTACTGTTGGAGGACCTCTGCTGGA[C/T]GAGACAAGAAGTTCACGCAGACCATATTTCTCACTCTACTACAAATCTACCTGGAGTCCAGCCATCACGTCATCGCAGCAGTGGACCTGCTGAACAAAAACCCAGAGTCTTTTGATTTATCCAGCGTGTTGATGGTGCTTCCGGAGTCCTGGTCTCTAAAAGTGGTCCTGCGGTTCCTGTGTGAATCACTGAGAGGAACGGTGCATGACAAAAGAATGAGAGGTCTGGAGATGAGCCTAGCCAAAGTGGAAACTCTACGGCACAGACATGCATTGGTGAGACATGCTATGAATTAAGTCAATTGACATGCAAAAACACTCACTGACCCAAATCGCAATGACTAATGTTTTTCTTTATGCTCTGAAAGTTTAACTTTGCAGTGACATTAATGGACATTTTTGGTAGTTTTAAACAATATATAATGTTGGAATAAATCAAGTACTGGCAGTTCATAGACTGCTTTTTGGACTGTAATTTGCATGACAATATATGGTTTTAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14167
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000110272 Nonsense 435 456 7 7
Genomic Location (Zv9):
Chromosome 17 (position 15422353)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15573181
GRCz11 17 15581114
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGACAGAGGATGTGTTTGCCATTYATGCCAGAAACGTCTTACTGGAGCC[G/T]AGTTCCTGCGCAGGCCGACAGGAGAGCTGACACACATAACCTGTCATAAT
Long Flanking Sequence:
GAAAATCCCTATAGATCAGTTGTTTCTGAAATACTCCGACCAGCCCATCTGGCACCAACAACCATGCCACATTCAAAGTCACCTAAACACATTTCTTACCCGTTCTGATGCTCGGTTTAAACTGCAGCAGATCGTCTTGACCATGTCTACATGCCTAAATGCATTGAGTTGCTGCCATGTGATTGGCCGATTAGAAATTTGCACTGACAAGAAGTTGGACAGATGTACCTAATAAAGTGGCCGGTGACTATATAAATATCTAAGGAAATTATGTGCAAAGGAATAATGTGATTTATTGTATATTTTAACACTATATGAATATATATCCTGGTTGAGACAGGCTATAAATAAAGCCATTTTAACATCCAAAAATACCCACTAAGCCAAACAGCAATGCTTAATATTATTCTTTATGCACCCAGATGGCAGCAACGCATGAAAAAATCCAAGTTGACAGAGGATGTGTTTGCCATTCATGCCAGAAACGTCTTACTGGAGCC[G/T]AGTTCCTGCGCAGGCCGACAGGAGAGCTGACACACATAACCTGTCATAATGGTGAAAGCAGCCACTGAACACCAGAGACACTATTATTCACACCTGTTCACATTTACTCCGCCGCTGTTTACAATAAAGACAGTAATTACAAGGACAGTTAGGGCAATTACTATGACAAATTGCTAAGAGTATGTGACACATGCTAAGCTGAGCCACAAACACCAGAAGGAAACCCACAACAACTGCACACAGCACAGGCTGACAGTACACTTATCCACAATATAGCTGCGATGATACTCTACATGTTACTCTGTATGTTAGAGAGGCATTTTAGAGAGGCACAAGGCATTTTTAGTGCAGAAATACTTTTTTTTTTTTAAATATGAACTAGTTTAATGGCTAAAGTAAAGTAAAAAATTGTGAAATATTTATCTTTTTCAAATATTTCTCAAGTAATATTTAATGGATCAAAAAAAAATTATAACAGTATTTCCGACAATATTTTTTTT
Associated Phenotype:
Not determined