ZMP
tnfrsf1a
Ensembl ID:
ZFIN ID:
Description:
tumor necrosis factor receptor superfamily member 1A [Source:RefSeq peptide;Acc:NP_998355]
Human Orthologue:
TNFRSF1A
Human Description:
tumor necrosis factor receptor superfamily, member 1A [Source:HGNC Symbol;Acc:11916]
Mouse Orthologue:
Tnfrsf1a
Mouse Description:
tumor necrosis factor receptor superfamily, member 1a Gene [Source:MGI Symbol;Acc:MGI:1314884]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8496 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15813 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8496
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002493 | Essential Splice Site | 53 | 389 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 19132987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17163310 |
GRCz11 | 16 | 17071287 |
KASP Assay ID:
2260-9465.1 (used for ordering genotyping assays)
KASP Sequence:
AATGAATACTGGAATAAGGAAGGATTCWGCTGTGATAAATGCCATCAAGG[T/G]AAAGAAAATTAATTCAGTCCTTTATGAAACTGAACTTTCAGTTGGCATTT
Long Flanking Sequence:
GCAAGTTATTACTTAAAATACTTCCGTGAGTATTTAATCTTCTTGTATGGCTTCAACATTGACTGACATCACGAGGTGTTTTGATTGGCTGATAACATAATTCTCTAAAACTTTTACCACACAGACAAAAAATATATAACAAAGGTAACATTAGACATTTAAAATTTATATAAAGTTTTAAAGTAGATCAAAACTTTACATTAATATATGATGTAAGGAATGACTTCTCAGAATGTTTGTATATTGTCAAGTAAATAGAGATAAAGTAGCTATTGTACAGACAGGGCACAGCATACATTCCAATTGTATTCTATTCAAAGCATAGCCACTGTGACTTTTCTTGTAATTTTAGCCAAATTCAATTTCTGTTCCCCACAGGTTCTAACCAGCCAGTTATATACAATATCAGGACTTGGTGGAAACAAGACTATGAAGGGAAATTGTCTTGAAAATGAATACTGGAATAAGGAAGGATTCTGCTGTGATAAATGCCATCAAGG[T/G]AAAGAAAATTAATTCAGTCCTTTATGAAACTGAACTTTCAGTTGGCATTTTGGTGTTGAGTTCAGATGTTCTCCCCATGTTTCCTCCGCATGCTCCGGTTTCCCCCCACAGTCAAAAGACATGCGATAATGGCCGAAGTGTATGTTTGAATGAGTGCGTATGAATTTCCCAGTACTGGGTTGCAGCTGCATGGGCATCCATTGCGTAAAATATATGCTAGTTTGGTGGTTCATTCCGCTGTGGCGATCACTGATAATCAGAGACTTAGCTGAAGGAAAATGAATGAATGAGACTGAATTTTTGGTTAGAATGTTTAATAAAAGCCAAAACACTGTTGACATTTATCCCTTATCCAGAAAGAACAGTGTGCGTTTTCCAAAGAAATGTTTTGTTCAGCTTTCTGCCTCTTTCTCTTCCTTTCTACAATTCATTTTTAGGGTATAAGTTAAAACAGGAATGCAGTGCAGAAAACATGAGGTCAAAATGTGAGAAATGTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15813
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002493 | Essential Splice Site | 201 | 389 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 19128559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 17158882 |
GRCz11 | 16 | 17066859 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAMTGCTGAGGTCTATTTAATGTTGCTTAAACTCTTCRWGTTAAWGTTTC[A/T]GACACGGTACCTAAAATAGTAGTTCCTGTTTGTGCAAGTATCATGGTTCT
Long Flanking Sequence:
TATTCACTACTGGACATGGTGAACAAAATAATGAACATATTTAATAATGTGTTTTTAATTCCCTATAGATGTCAGCCAGGATGTGATCACCTATGCAAAACCAGCATTCCCCCAGTCTTTTTTACATCTACTAAGTCAAATAGTCCTGAAGGTGAGTACTGTGTACCCAACAACATCCATTAGCATGAGATCTATCCCACATTTGGGTCTATCACAGGTGAACCAAAAAGCAGTCAGTTGTAGATGTCAGTTTTCTTTTTTTCTTGTTTTGGATGCCAGACAGATGACTCCTTTTCTTCTCAAGTTTTGTCGAATTGAACTATTACTAAAATCAAAAACATGAGTCATTTGGAAAGTCCCTCTAGCGTTTATATTCTGTTGAATTTGCCTTGCCATGACTAAGCAAGTCTCTCTTTGGGTTAAAAACAACATGTGTCTTCAGGCAAGAGATAATGCTGAGGTCTATTTAATGTTGCTTAAACTCTTCGTGTTAATGTTTC[A/T]GACACGGTACCTAAAATAGTAGTTCCTGTTTGTGCAAGTATCATGGTTCTATCGTTAGCCATTTTTATGGCATACGAAGGCATCAGACATTGGCGGAAGAGGGCACAAGCTTCGTCATCTCAGTCATCGTCACCTGCTACAGAAGAAGAGGTAAAAGGCTTACCATTTGACAAATGCTGACAAAGAACTCGCATTTTCTTCTTAGTGTGAATGATTCACATCTGATGCTAAACGCATAATTGCTGTAATGATGTTTTCACAGAAGATGATTCACTTTAATGATAAATACTAATTTATATGCTATTGCGTTATTAGCAAATCCAAGGACCCCTAATTTAAAAAAAAAAGAAAAGACAATTATAATATCATAAGAGCTAAACTATTCTGCATGTATAAAAACTGCCATCGTAATTCTCAAATTGTTTTCGTAATTATCACCAAAACTGTATTATCTACACCAGGCATGTCCAAACTTGGTCGTGGAGGGCCGGTGTCCTGCT
Associated Phenotype:
Not determined