ZMP
tnr
Ensembl ID:
ZFIN ID:
Description:
tenascin-R [Source:RefSeq peptide;Acc:NP_919364]
Human Orthologue:
TNR
Human Description:
tenascin R (restrictin, janusin) [Source:HGNC Symbol;Acc:11953]
Mouse Orthologue:
Tnr
Mouse Description:
tenascin R Gene [Source:MGI Symbol;Acc:MGI:99516]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44538 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30599 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6854 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31286 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44538
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015827 | Essential Splice Site | None | 1350 | 3 | 24 |
ENSDART00000143787 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 35079280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 35375990 |
GRCz11 | 2 | 35358447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCTTCTTTGTGGTGAGACAGGAGGAACATCAGCACTGGCACTTAAGG[T/A]AAGATAAGACTCCTTTAGCGAGAGCAGTTCTAATGTGTCTTTTCCAGCTA
Long Flanking Sequence:
CAGTGATTAATTCTGAGCTCACTTTGAGATTAAGTTTATGTATATTTGCTTAGCATATTGTATATAGCCGTGGTTGGAGTGTGAGAAACATTTGTATATGGGCCATGTTTTATTTGTGATAATGCAAAGGAACATGTCTATTGAGAAATGTGCACAAGAGAGGCTGCTAATTAAATTCAAGGGATGAACCAATAAAATAACACATATGTTAGTCAGTGTGTACTTTATTTCTGTCTGTTTGATGGTTAATTTAAAAAATCCATAGAATTCTGTCAGTCTAAATGCCAGTCAGTTTTAAACGGAGATGGTCCTCATATTTTGTCTGCGTATTTAAGCTTGCAGTGTCATTAAAACCAGATATTGTGCATATGTCCCCTCCAGACATCACTTTTGCCCACTTTTTTATGGCTCAATTCAGTGATGCACTTCCTCTTTTTTCTAGGCACTAGTTATCCTTCTTTGTGGTGAGACAGGAGGAACATCAGCACTGGCACTTAAGG[T/A]AAGATAAGACTCCTTTAGCGAGAGCAGTTCTAATGTGTCTTTTCCAGCTAGGGCTGCACAATTCTGGCTCAAATGAGATTCAAAATTTATTTAGCCTAAAATCAATATCACGGTTTTCTCCCGATTCTGTAGATGTAAAATAAAAGTTAATATGAGTAGCCTATTGTTATTGTTATTTCTCAAACATATGATAAAACAACAGTAATATTATTAGCCCTATATGTAGTACTTCTGTTGGATAAAAATGCTAAAAATTCTGTTCTCACTTGGAATAGTGGACTTGAACAGATTTTAAATATGTCCTAGCTGTTCATGACTCTGAAGTTGAATTATTGTGTTTGAGATGTTTGCTTGTCATTTGTCATTGAGAATATTGTTAGACAACTTTTTTCACTGGTAAAATGAGACATTTGTCATTATCAAATTCCATCTTGAATTATATTCAAAATTACATAGGCTACAGTAATTATACTGACCTAGTAAACATTTATTTTCATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30599
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015827 | Splice Site, Nonsense | 409 | 1350 | 7 | 24 |
ENSDART00000143787 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 35130544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 35427254 |
GRCz11 | 2 | 35409711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACGCACATAGGACGGAGGCCAATAATGCATCAATCTGTACCTTTCAGA[T/G]CTCTCAAATCCAGACGGTTTACTCTTCAAATCCATCATGGAGACATCCGT
Long Flanking Sequence:
ATTAAGAGGAACTGAGACTGTGAGAGCTATGGTAAAAATGATTGTATGACTGCACATTTATTACTTACACACTTTTGTATGCCATCATACACTTTCAATAATCCAAACACTCCCAGAGCAGAGATGGCGTGTTTTATTACTGTTTCCATGAAATTACCTTCAAATCCTCTTGAGGCTCATGCATTGTTGACAATGAAAAGGCTGGAGGTTTACTTGTATGTACTGTGAAATGACTGTAATAGTATTTTGTGACTTGTATTCTTTGGGATTCCCGACTGCATCTATTATACAACAAATGTAAACAGATAGAAGAGACGATGCATATTGAAAGTAACTCCAAAAAAATAAAATAAAATAAAATAAAATAAGCTGCTTAGTATCCACTGCTCTTTTTACAGAGCTAAAAGCAGAGTAAAGATCTGCCTTGGCTGAGAAAAATGCTGATTTATTGAACGCACATAGGACGGAGGCCAATAATGCATCAATCTGTACCTTTCAGA[T/G]CTCTCAAATCCAGACGGTTTACTCTTCAAATCCATCATGGAGACATCCGTGGAGGTTCAATGGCAACCCTTAGACTACTTGTTTGATGGTTGGGAAATAAGCTTCATTCCCAAGGTAAGGCTTTCCTTAGAAGGTCACACTTCATTTGATTCTGCCTCTGCTGTACCTTCTGGCGTAACAACACAGAGGTCCTGGAATCTTGTAGCATTTTCAGACTTTAGCGTCCACCGTGTTGTATTTGGACAACAATAAACAAGGAAAGAGCAATGTAAGGTTTTTACAGACATCTGGGCGCAGCTGATAATTTAATGCTTTTTGAAACGATGATTCGGTTTCTGACAGGTGCTTCTCAGCATGATAAATGTCAGTCTGTCTGTGTTTGAAAGAGAATTATTTTGCATCATGGCAGAAACACAATACATCCAGGCAGAGATGTTCACTAATCCCCTTTCAAATATTCCATCTGGAGAAAGGACAAAACATTTTCAGCATGTGCATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6854
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015827 | Nonsense | 475 | 1350 | 8 | 24 |
ENSDART00000143787 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 35134486)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 35431196 |
GRCz11 | 2 | 35413653 |
KASP Assay ID:
554-5300.1 (used for ordering genotyping assays)
KASP Sequence:
AGTACCATCACATCTTTCCACCAAACGGGACTGAAGCCTGGAGAAGAATA[C/A]ACTGTCAACCTGGTGGCCCTGAAAGACCAAGGCAGGAGCCTGCCTGYTAC
Long Flanking Sequence:
GACAAGTGTGCATTCACCAAGTCAATGGCAAAGAACAAAAGGGAAAAGGCTTTTTAGAACAGTCACATCTTCTGAAACTCTCACACACTTTGATATTGCTTGATTTCGTAAGCTTTCCAGGGAGGTTAGTCGATGTCTTGTGGGGTGTGATGCATCAAACTTACAAAGTGCTCTGCTAAGCGATTTGGGGAAAAAACAAGACTTGATTCAATACATCAAACATCTGGCGAAACCAATCTAAACAGAAATTCTAGCAGCTTGTTCTTTTTTTTTTTTTAAACAGCTGACTGGCTTCTGAAAACAGTTTCTGTTGATTTGAGCGGTAGACTGTTGTTTCTGCATGCCTGCCTGCACTCTGATGCCAGAATTTTGAAATGTGATCTATTTGCATGTGTTTGTGTCTTGTGCATATCAAAGGACAATGATGGAGGGATGACAGCACAGCTACCCAGTACCATCACATCTTTCCACCAAACGGGACTGAAGCCTGGAGAAGAATA[C/A]ACTGTCAACCTGGTGGCCCTGAAAGACCAAGGCAGGAGCCTGCCTGTTACCGCAACTGTTACCACACGTATGCCTCTCACTCATTTACATCACTTTTATGCAGTTGGCAGACTTTTATTCCAAGCGATTTAAAGTGCATTTAAGTACTATGCTTATGAGGACATGCTGTATGTGTATGTGTGTTTCCCTGAAAATCAAATCTGCGACCTTGGTCATTGTTAGCGCCATGCTCCACCAGCCAATCTATAGAACACCCACGCCTCACTGTTTCGTTCTCCAATAACTGCGCTGCGTTTTTCTTGAGCTTTCTGTATATAGCTTTGATTTTTAATGACCTACAGTACCACAATTGTTCGGTTCATGCATTTACCCTACACTTTCACTATATTTTAAGTCAATAAGTTTTGTGTAAGAATCCATACTGTGGCTTAAGCACTTTGTAGTTGTTTGTTAATTGTTTTTAAGGAACTTTCATCTCTGCTTCATGGAGATAAAACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31286
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 |
---|---|---|---|---|---|
ENSDART00000015827 | Nonsense | 1287 | 1350 | 23 | 24 |
ENSDART00000143787 | None | None | 156 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 35189747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 35486457 |
GRCz11 | 2 | 35468914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAGGACAAAGACAATGACATTGCTGTCACCAACTGTGCACTGTCTTA[C/A]AAGGGAGCCTGGTGGTACAAAAACTGTCATCGGGCAAACCTTAACGGCAA
Long Flanking Sequence:
GAATGAACCTCATGATCGCTCAAAGTTCATAGTTATGAAACATAAACCTTAATGTGTTTATTTTATTTACAATAACTTTCACTTTCAAATGAAAACCGTATATATATTTTTTTTCATAGTCCCATGATTTTTTAAAAGACAAACATATGTTTATCAGCAAAATTCGACCTCAATATGTTGATGCTGATATAATTCTAGGTTTTTCTAGAAGCTTAACCATTTGTTAAAATGTGAACAAAATAATCTACATTCTGAGAGTCTTAAAGCGAAAATTTACTTTAAAACAGAAAAAAAATATGCTTTAAAATACAATAATATGCTTTAAAAAATATTTATGTTCTTGGTGAAACCTGACTTGAAAGAGTTGTAAGGGTTAAGCTTGTTTTTTATGTGTGGTCTCTTTTTGTTCCAGGAGATTCTTTGAGCTACCACCAGAGCCGACCTTTCTCTACCAAGGACAAAGACAATGACATTGCTGTCACCAACTGTGCACTGTCTTA[C/A]AAGGGAGCCTGGTGGTACAAAAACTGTCATCGGGCAAACCTTAACGGCAAATACGGAGAGTCTAGACATAGTCAGGTAAGCCTGATAGTACATACTGTAGCACTGGACTAAAATATCTACTATAGAGTATACTCCTATGAAGTTTCAGTTTATTTCATGTTCTGCAATATTTGTTAGCAAACATTTTACAAACAGTGCAATCTGGAATTTTAAATGAGGATGAAAGATTCCTCAGTTATCTTGCCAAATCTGAAACAATTCTGAAATTATTAGTAAATTTCACAAACATACAAAGTTAACCAACTTAATTGGTTTTAGTTCGCATTCAGCTAGAAGCAGTAACAAAACAACAGCATCCCATTTATTTCAGTAAAGTTCTGCGGATTTCTGGTAGCAAGAGTGACAGTAACTGGTGGCAAAATGGCATCCTGGTAGTGATATAAAAATTACAAATGGTTTTGGCAGTATGAATGGATTTAAATAGTATTTTTTAAAGGTTG
Associated Phenotype:
Not determined