ZMP
tnfsf10l
Ensembl ID:
ZFIN ID:
Description:
tumor necrosis factor (ligand) superfamily, member 10 like [Source:RefSeq peptide;Acc:NP_571918]
Human Orthologue:
TNFSF10
Human Description:
tumor necrosis factor (ligand) superfamily, member 10 [Source:HGNC Symbol;Acc:11925]
Mouse Orthologue:
Tnfsf10
Mouse Description:
tumor necrosis factor (ligand) superfamily, member 10 Gene [Source:MGI Symbol;Acc:MGI:107414]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40877 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34054 | Essential Splice Site | Available for shipment | Available now |
| sa34053 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40877
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101447 | Nonsense | 66 | 317 | 1 | 5 |
| ENSDART00000122113 | Nonsense | 56 | 264 | 1 | 5 |
The following transcripts of ENSDARG00000004196 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 24123643)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22685395 |
| GRCz11 | 7 | 22956552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATCGCGTCCACCACGGGGCTCTTTGTCTACTTAAACATGTCTTTATCG[C/T]AGGTGAGACAATGTTTGCACTCTTATTATATCTTTGGGTGAACTTTAAAA
Long Flanking Sequence:
GATATAATATAACAGGATATCAGTGGGATATCTTGCATGAGGAAAAGGATTAAGGAAGTCATGAAGACTTTGTAGCTCGTGTTGCCTTACCTTGAGAAACTCTTAAGACTCAACCCCTCAGCGTCTACACACACACACACACTTCAGTCTTCAAGCAGCACTAGTGGCTGCATGTGTGTGTGGGACAGACTCTACCCTCCCACGGCCGCGCGCTGAGCCAACAAGAAGGAGTTTATTCAGCGTCCCGTCGCTGATTTCAATTTGTTTGTCACTAACCGCGTATCTACCCACGTCTTAGGAATGCCATGGCCACTCAGAACAACCAGGATTACTACAGGTCGGTCAGCAGCGAGTCCACCACATACATGATGGTCCCGGCGAACAGCCGCGGGCGAGACTCGCCGTCAAAGTTATGGATCGCGATGGTCGTGATCGTGGTGGTCGTCCTGCAGATCGCGTCCACCACGGGGCTCTTTGTCTACTTAAACATGTCTTTATCG[C/T]AGGTGAGACAATGTTTGCACTCTTATTATATCTTTGGGTGAACTTTAAAAGTTTGTGAGTGAGTATTTTTGAGCACCACAGGCGCGTACGCTGATTAGACAGCAATGTTTACTCGCTAATATTCCCCTAAAATGATATCAGTGTAGGCAGCTCACTATGCTGTGGGATACAGTCCTGCCTGCAAACGAGGAGAACTTTTGCAAAGTTGCAGACTGGTGATAAATCAGTTAATATGACTAGATAAATTGCACCAGGATGAATTAAACACTGTAAGGGGAAGCGAAGTATGCATTGGAACTGGAAAATGGGTCATTTCTTGTCACTTAATGTGATTACTTGATTGTCTTTCTGTGAGGATTGATGCTTTAAATGGTTTTCATTTACAAATAACAAGCACAATGATTCACATCAGACTGTTTACAGTAACTGAATCACGTTTGAAATGTGCATTTAGCAATAATAATAATAATAATAATAATAATAATAATAACTTTTAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34054
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101447 | Essential Splice Site | 117 | 317 | 3 | 5 |
| ENSDART00000122113 | Essential Splice Site | 107 | 264 | 3 | 5 |
The following transcripts of ENSDARG00000004196 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 24089131)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22650883 |
| GRCz11 | 7 | 22922040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGTTTTCTCGACTGATGGAAGTGTTTTTGTTTGTTTTTTTGTCACA[G/T]GTTACGGACAGTATCATCTCTAAACAGACTTTACATGGTGAGTAGTCAGT
Long Flanking Sequence:
GACTGTTATTATAAGTTATTGTGTTAAATAAGCTCCAGATTTGGCTTACACTAATCTAATGTATATTATGCACAAATATAATAGCTTCCTATAGAAAATATTCATTTAAAAGAGAGATTTGTTAGGGGTGTACTTATATATGCTAAACACTGTAAAAGTTCTTCTGGCATACCTGGATATTGACTGAATGGTTGTGAAAACTGAAGTTTAGTGTTCCTTTAAAAACAATTTTTAGTCATTTAATATCATGGCTGGACCTAAACATTTCATTAATTAAAAACTTTTATAGCGAAACCTTTCAGTATAAAACAGATGGTTAACTTGCTGTTTGTAACTTGAGGTAAACTTTAACCACAGTCATACGCCTGAGCAAAACAAAAAAAAGAGGAAAGACTTGATGAATCTGAATCATCCAGTTTCACGTTTTCAAATTTGAAGAGTCATCAGATTGTTCAGTTTTCTCGACTGATGGAAGTGTTTTTGTTTGTTTTTTTGTCACA[G/T]GTTACGGACAGTATCATCTCTAAACAGACTTTACATGGTGAGTAGTCAGTCAGTCATTGTTATTTTTAACAATTGCTTTTATCACTACGACTGCAGAATGTACCGTGCTGGAAATACCCGGAACCATCAGACAGAAAAACATAATTCAACACAGTTCAAAGAAGTCATTAAAATCTCTTGTGCAATAGCAATTCATTTTTTATGGTGTATTTTGAATGTGCTGACTGTTTTCTGTCTGTCTGTCCTTCAGCAGCAAGAACACAAACTCATTCATATAATACAACAGGGTCAAAGTTTATGACCACAGTGATGCAGCGGCCATCAGCCCACCTGACCCTCAGCAGTGAGTCTGTTTGTATGTATGGCCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCCTGTTTATGTCTGTTTTTATGTTTTATCAATATATCAAGTTTACTGTCATTAACTTTTTCAGCAAACATTAGCATGAGTAAATTTGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34053
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:
T > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101447 | Nonsense | 137 | 317 | 4 | 5 |
| ENSDART00000122113 | Nonsense | 127 | 264 | 4 | 5 |
The following transcripts of ENSDARG00000004196 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 24088855)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22650607 |
| GRCz11 | 7 | 22921764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTCTGTCTGTCTGTCCTTCAGCAGCAAGAACACAAACTCATTCATA[T/G]AATACAACAGGGTCAAAGTTTATGACCACAGTGATGCAGCGGCCATCAGC
Long Flanking Sequence:
AAAACTTTTATAGCGAAACCTTTCAGTATAAAACAGATGGTTAACTTGCTGTTTGTAACTTGAGGTAAACTTTAACCACAGTCATACGCCTGAGCAAAACAAAAAAAAGAGGAAAGACTTGATGAATCTGAATCATCCAGTTTCACGTTTTCAAATTTGAAGAGTCATCAGATTGTTCAGTTTTCTCGACTGATGGAAGTGTTTTTGTTTGTTTTTTTGTCACAGGTTACGGACAGTATCATCTCTAAACAGACTTTACATGGTGAGTAGTCAGTCAGTCATTGTTATTTTTAACAATTGCTTTTATCACTACGACTGCAGAATGTACCGTGCTGGAAATACCCGGAACCATCAGACAGAAAAACATAATTCAACACAGTTCAAAGAAGTCATTAAAATCTCTTGTGCAATAGCAATTCATTTTTTATGGTGTATTTTGAATGTGCTGACTGTTTTCTGTCTGTCTGTCCTTCAGCAGCAAGAACACAAACTCATTCATA[T/G]AATACAACAGGGTCAAAGTTTATGACCACAGTGATGCAGCGGCCATCAGCCCACCTGACCCTCAGCAGTGAGTCTGTTTGTATGTATGGCCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCCTGTTTATGTCTGTTTTTATGTTTTATCAATATATCAAGTTTACTGTCATTAACTTTTTCAGCAAACATTAGCATGAGTAAATTTGGCAAGAAATGTTGATAACAAATAGCAATGATAATGATAATAATAATAATAATAATCATAATAATAATAAATGACAACAGTAATTTTATATATATATATATATATATATATATATATATATATATATATATATATATAATGATGATGATTATGATGATGATAATGATAATTACAATAATAATACAAATAAGTTGTATTATTTATTATTATTATTGGCTGTGGTGTTATTTCAAAACTCAGTGCTTTATATTTTTATTTGCTGAAATAATAATAATAATAA
Associated Phenotype:
Not determined