ZMP
si:dkey-6e12.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A3KPL4]
Human Orthologue:
RLTPR
Human Description:
RGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing [Source:HGNC Symbol
Mouse Orthologue:
Rltpr
Mouse Description:
RGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing Gene [Source:MGI Sy
Alleles
There are 20 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36650 | Nonsense | Available for shipment | Available now |
sa23302 | Essential Splice Site | Available for shipment | Available now |
sa12493 | Nonsense | Available for shipment | Available now |
sa13235 | Essential Splice Site | Available for shipment | Available now |
sa23303 | Essential Splice Site | Available for shipment | Available now |
sa23304 | Nonsense | Available for shipment | Available now |
sa15203 | Nonsense | Available for shipment | Available now |
sa23305 | Nonsense | Available for shipment | Available now |
sa32208 | Essential Splice Site | Available for shipment | Available now |
sa13566 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36650
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Nonsense | 12 | 1338 | 1 | 39 |
ENSDART00000141051 | None | None | 594 | None | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22083466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22313689 |
GRCz11 | 18 | 22302755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGTGATCAACCATTATGGCGGCGCTGCCTGAGGTCCCGTTTTGCCTC[A/T]AAGGTAAGACTTTTATTTTAATCTCAGAATAAGCCACTGGAATATGAGAA
Long Flanking Sequence:
ACTTTCTTCAGTCAGCATTTATCTATTCGTATGTTTAAAAACGGTTTACGAAAATGCAACCTGACACATCTGTGAAGCACAAAGCCTCTGCCAAATGTCAATAGGTCAATAATTTGCCAAAAGGTGTCACACTAATCTCTGACTGAAGCGTCACACATTAACCTCATTTGCAAATATTAGTGTATTTGATTTACATCGGCCTATAAATGATTGTTGTATGTGTGAAATGGCACATTTCGAATCGACTGTAATGGATAGGATGCACTTCATGCAGTCAGGTGTCATATCCTGTCTTAGACCTGTACTCTCAAGCTGCGGTTTTCCCCTATGAGCATGAATCATAAAGTAGCAGGATGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTAGCAAGTGTCACACACTTGCACGAGAGCCAGGACTGTCGTCTTCACCGGGTTGTCACTGAATTTAGTGATCAACCATTATGGCGGCGCTGCCTGAGGTCCCGTTTTGCCTC[A/T]AAGGTAAGACTTTTATTTTAATCTCAGAATAAGCCACTGGAATATGAGAAAATCACGTATTGCTTTGGTTTGTTTATTATTTTTCCATGTTTGACATGTAATTGTTTGTGCAAGAGTTTGTGACCTTGCAACCTCAAGTTGCTCTAGGATTATATAACTGAACTGTACAGCATTTGATTTCTGCGTACAGTAGACTTTAAGTGGTTGTGTTTTTGAGTTGCAGAAGGTATAACCCAGTATTTGAAGCCACAAAGGGTTCAGTTTATGAGTTTGGTGCATCTCAACCAGGGCAAGGGACGCGCAGATAGCAGAGTTCTGGTATGTATACACAAACACATATATACACGTATATATAATAATGTACAGGATAAATTTATTAGACATTCCATATATTTCATTAGAGTGTTTGCATGCAAATGAGTTCCATTTATTATTTAAAACACAAAATACTGACTTTATTAAAGAATTATATAGTTTTAAAGTAAAATAAAAATGTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23302
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Essential Splice Site | 407 | 1338 | 16 | 39 |
ENSDART00000141051 | Essential Splice Site | 346 | 594 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22108830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22339053 |
GRCz11 | 18 | 22328119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTTCTCTGCACAGACAGCATGTTTACACTGATCTGTTTGGCTCTGCT[A/G]GGAAAGTACGAGAGGTCACGCGCAGTGTGAGGGATTTCTTTAGCAAGAGC
Long Flanking Sequence:
AATCATCACCATAATTTACTCGAGTACATGCCTCAATGTCTTGCGGCCCCCACAGTTTGAAAAAGCCCTCCTTTAGACCATGTGCTTAGATCTGTAAAATAAAGCCCTCAGTGTTATATACTTCTGGGAGAGATAAACCCACTCATGTCTTAGAATCAACAGCAAAAAACTAAATGGGTTAAAATTATTTATTTATCTACGTACCTACCTTACTTTAAAATGCTTTTATACTGCATAAAATATCCATCCAGTATTTTCCCATGAGACTTGGAATGAGACACAGTTATTTGTTTAAAAGGGACTATATCGCTGACCTTTTCTTTTCTTTTGGTTTCTTATTAGCTGTTTGTGTCTCTTTCTTTGGGCTGCTGCACTACTCTGAACTACCTCAATCTCTCCAGGAACCCGTTCTCTCTTAGGTGAGCCATCAAAAGTGACATTATGAGTTATCAGCTTCTCTGCACAGACAGCATGTTTACACTGATCTGTTTGGCTCTGCT[A/G]GGAAAGTACGAGAGGTCACGCGCAGTGTGAGGGATTTCTTTAGCAAGAGCACTGTGTTGAAGTACGTGGGATTCTCTGGAACTAAACTACCTCCAGAAGCTCTCAGGTATGGGGCTTGTGCCGTTTTTATAACTAGCATGCCTTATTAGATTTTTTACATTGTACATTTACTCTAGCTTCTGTTTGTTAATTTTGTACACTGCCATTTAAGTTTTTTAGAAGTCTATTAGGCTCACCAGGTGAAGTTTATTTATAAATTAGTTTTGAGAGGATCACATGCTTACGATCGACCATGGCCCTCGCATTAGCTATCGTATGATTTACCAATCAGACTAATCCAAATGCACATAAATGAAAAGATTTCCTTATCTTATAGTCATCTTCATCTTGAAAATCCACCCCTACTCCCTTTCCTATTTCCTAGATTAATCCTGGGTAGCACTGCGTCATAGTGGTTAGCACTGTTGCCTCACAGCAAGAAGGTCACTGGTTCGAGGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12493
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 |
---|---|---|---|---|---|
ENSDART00000050311 | Nonsense | 536 | 1338 | 20 | 39 |
ENSDART00000141051 | Nonsense | 475 | 594 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22117470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22347693 |
GRCz11 | 18 | 22336759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGYATTCTTATTTTCAGGGCTCTAACAGATGTGTTGCACCGACTCGTA[C/T]AACTAATTCAAGAGGAGGAGTGTGTGAGTACATTATTTGTAATAAWACRA
Long Flanking Sequence:
CAATGAGATTACAGAGCACCTTAAAATAGTCCCCAGATAGGTAAGTAGGTAATAGTGGTGCATAATATCATTGCTCATATTAAGTTTTACACTGGAAAATTGTCAGAACTCTTGATTTTAAAATTTGTTGAGATACTAATGGTCTAATCCGATTCTATAAAATCCGATTCAATAATTTATGCTAAGCTAACAGTGCTACTCTCAGACCTGAATCAAATGAATGAATTAAAAATGGTGAAATTCAGCTCAATAAAAGTGGTATAAGTAAGGGCCAGGGACCACGTTGGAGGACCGCGCCTCTCTTTGATGCAAAAGTTAACTGTAGGGTTGTTAAAAAATGGGCCTATTAAAAAAAAGTGCAGTGTTCCTTTAAAATCCCTCCTTCTCAGTCCATTTTCCTCCTTGTAATTTCATTTACATGATGAATCATTCAAAAGCCTTCTTTCAAATGAAGTATTCTTATTTTCAGGGCTCTAACAGATGTGTTGCACCGACTCGTA[C/T]AACTAATTCAAGAGGAGGAGTGTGTGAGTACATTATTTGTAATAATACGAATCACTTGACTACACACATACACTACCCATTATTCCATTACACCCATGCCATAGTCATATTCACAGCAGGCTCTTTCAAATGATATGGTTATTACTGCAAAATAAGATCATGTCCATAAATAGACCACAGTGTCCACCTACAGTCGAAAGCTCTCGTATAACATTGCGAGAAAGAAGAGCCTGTCTTTGACTCGCTTAGTTGTAGAGATTGGTATGTGTGCTTCTGTGTGTATTTGCTTCTGTAATACTAGACCAATAAAGAGAGAAAGTCCACAGAGACACCCCCCCCCCATTCCTACACCAAGCCTTGAGTTTTAATTACCCAGAATGCCTCTCCATCAGGACACGGTCGGGCTCAGTAATTACACAAGCAGCTCTGACTCAAAGATAGGACTCATTAAAACACACTTTCAGCTTTATGTAACTTTATCCACTTTAATAGGAGCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13235
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 |
---|---|---|---|---|---|
ENSDART00000050311 | Essential Splice Site | 601 | 1338 | 21 | 39 |
ENSDART00000141051 | Essential Splice Site | 540 | 594 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22122084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22352307 |
GRCz11 | 18 | 22341373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGGAGCAAAGATGCTGGCAAAGGCCCTCATGATGAACACCAAGCTAAA[G/T]TAATTTGCCACTCACAGYGATTTRCAGCTTGWTTGACAGGTTTCTGGATC
Long Flanking Sequence:
TCGGTGAAGAATATTATGTAAAACCTTTGTTTATATACATCCATGATACATTTTTTTACACTATACACTTAAAATATGAAGGTTGCTGTTTGTTTAAACCACTTATTTAAAATGAGTTAGACAACAGAAATATTGTGTTTTTTAAAACAACTTAATTGTTTTATGTTCAATCCTTTTAAATTTGTAAAAACTGATAAGTTAACTTAATTCCTTCATGTTGTCTTAACATAAATTGATAGTGTGAAACCCAACATTTTTTGCAGTGTATGATTTGTGGATATTCCGTGGAATCTGATATCTTTTGCTTTTCTTTTCACACTTTTGTAGCCACTGGAGTCTCTCTCTGTTTGTGACTCCAAGTTGAAAACTGGTACCACCATCCTCATTAACAGCCTGGGCTGCAACGCTAGCCTGTCCAAGATTGATATCAGTGGAAACTGCATAGGTGACACAGGAGCAAAGATGCTGGCAAAGGCCCTCATGATGAACACCAAGCTAAA[G/T]TAATTTGCCACTCACAGTGATTTACAGCTTGTTTGACAGGTTTCTGGATCTTTGTTTCTGAGTGGTGAGGTTAAGTATCTTCTGTCTCACAGAAACAATCTTCCAGGAACAATAAAACAAATCAGATTTAGCATACTTACAATCGCTATCAATCTCATAAAAGGTGTGTTTATTTTTTGACAGAACACTGGTTTGGGACCGGAACAATGTGACTGCTGGAGGATTTATGGATGTGGCCAATGCCTTGGAAAAGTCAGAGTAACTCATAAAAGCCTACAGGCTATTGGTTTTCAGGGGGTTTGTTTTTGTAACAAAAAAAGTGTACTTATGTATGTTCAAACAGGAACTTGACACTACAAAACATTTCCATTCCAATGAGCGATGTTCTCCAAGCCCATCGAAGCGCCCCAGAGAAGACAGAGGAGGCTTTACAGAAAGTTAGTTCTAGTTCTGCACTAAAGAAAGCCTAGGAAAATACAATGACAAAATTTTTAATTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23303
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Essential Splice Site | 601 | 1338 | 21 | 39 |
ENSDART00000141051 | Essential Splice Site | 540 | 594 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22122085)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22352308 |
GRCz11 | 18 | 22341374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAGCAAAGATGCTGGCAAAGGCCCTCATGATGAACACCAAGCTAAAG[T/A]AATTTGCCACTCACAGTGATTTACAGCTTGTTTGACAGGTTTCTGGATCT
Long Flanking Sequence:
CGGTGAAGAATATTATGTAAAACCTTTGTTTATATACATCCATGATACATTTTTTTACACTATACACTTAAAATATGAAGGTTGCTGTTTGTTTAAACCACTTATTTAAAATGAGTTAGACAACAGAAATATTGTGTTTTTTAAAACAACTTAATTGTTTTATGTTCAATCCTTTTAAATTTGTAAAAACTGATAAGTTAACTTAATTCCTTCATGTTGTCTTAACATAAATTGATAGTGTGAAACCCAACATTTTTTGCAGTGTATGATTTGTGGATATTCCGTGGAATCTGATATCTTTTGCTTTTCTTTTCACACTTTTGTAGCCACTGGAGTCTCTCTCTGTTTGTGACTCCAAGTTGAAAACTGGTACCACCATCCTCATTAACAGCCTGGGCTGCAACGCTAGCCTGTCCAAGATTGATATCAGTGGAAACTGCATAGGTGACACAGGAGCAAAGATGCTGGCAAAGGCCCTCATGATGAACACCAAGCTAAAG[T/A]AATTTGCCACTCACAGTGATTTACAGCTTGTTTGACAGGTTTCTGGATCTTTGTTTCTGAGTGGTGAGGTTAAGTATCTTCTGTCTCACAGAAACAATCTTCCAGGAACAATAAAACAAATCAGATTTAGCATACTTACAATCGCTATCAATCTCATAAAAGGTGTGTTTATTTTTTGACAGAACACTGGTTTGGGACCGGAACAATGTGACTGCTGGAGGATTTATGGATGTGGCCAATGCCTTGGAAAAGTCAGAGTAACTCATAAAAGCCTACAGGCTATTGGTTTTCAGGGGGTTTGTTTTTGTAACAAAAAAAGTGTACTTATGTATGTTCAAACAGGAACTTGACACTACAAAACATTTCCATTCCAATGAGCGATGTTCTCCAAGCCCATCGAAGCGCCCCAGAGAAGACAGAGGAGGCTTTACAGAAAGTTAGTTCTAGTTCTGCACTAAAGAAAGCCTAGGAAAATACAATGACAAAATTTTTAATTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23304
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Nonsense | 622 | 1338 | 22 | 39 |
ENSDART00000141051 | Nonsense | 561 | 594 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22122330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22352553 |
GRCz11 | 18 | 22341619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCGGAACAATGTGACTGCTGGAGGATTTATGGATGTGGCCAATGCCT[T/A]GGAAAAGTCAGAGTAACTCATAAAAGCCTACAGGCTATTGGTTTTCAGGG
Long Flanking Sequence:
CCCAACATTTTTTGCAGTGTATGATTTGTGGATATTCCGTGGAATCTGATATCTTTTGCTTTTCTTTTCACACTTTTGTAGCCACTGGAGTCTCTCTCTGTTTGTGACTCCAAGTTGAAAACTGGTACCACCATCCTCATTAACAGCCTGGGCTGCAACGCTAGCCTGTCCAAGATTGATATCAGTGGAAACTGCATAGGTGACACAGGAGCAAAGATGCTGGCAAAGGCCCTCATGATGAACACCAAGCTAAAGTAATTTGCCACTCACAGTGATTTACAGCTTGTTTGACAGGTTTCTGGATCTTTGTTTCTGAGTGGTGAGGTTAAGTATCTTCTGTCTCACAGAAACAATCTTCCAGGAACAATAAAACAAATCAGATTTAGCATACTTACAATCGCTATCAATCTCATAAAAGGTGTGTTTATTTTTTGACAGAACACTGGTTTGGGACCGGAACAATGTGACTGCTGGAGGATTTATGGATGTGGCCAATGCCT[T/A]GGAAAAGTCAGAGTAACTCATAAAAGCCTACAGGCTATTGGTTTTCAGGGGGTTTGTTTTTGTAACAAAAAAAGTGTACTTATGTATGTTCAAACAGGAACTTGACACTACAAAACATTTCCATTCCAATGAGCGATGTTCTCCAAGCCCATCGAAGCGCCCCAGAGAAGACAGAGGAGGCTTTACAGAAAGTTAGTTCTAGTTCTGCACTAAAGAAAGCCTAGGAAAATACAATGACAAAATTTTTAATTGAGACTTTTCGTATGCATATATGTAGATCCAGGATTTTTTACGCAGGAACAATCAGAGGCAGTGTGGAATGACTGAGGAAATGTGTCATTTACAACATGGACTAAAGACCACTCGCTCTGAGCAGGTTTGTTAGGATATTTCAGTTATCAACTGGTTATTTTATACCTTAAAGGTTTAGTTTACCCAAAACAGAAAATTTTAATTACTCATAATTACTCTTTTCATTCTAATTTCCTTATTAGTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15203
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Nonsense | 675 | 1338 | 24 | 39 |
ENSDART00000141051 | None | None | 594 | None | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 22122667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22352890 |
GRCz11 | 18 | 22341956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTACGCAGGAACAATCAGAGGCAGTGTGGAATGACTGAGGAAATGTG[T/A]CATTTACAACATGGACTAAAGACCACTYGCTCTGAGCAGGTTTGTYAGGA
Long Flanking Sequence:
TGTCTCACAGAAACAATCTTCCAGGAACAATAAAACAAATCAGATTTAGCATACTTACAATCGCTATCAATCTCATAAAAGGTGTGTTTATTTTTTGACAGAACACTGGTTTGGGACCGGAACAATGTGACTGCTGGAGGATTTATGGATGTGGCCAATGCCTTGGAAAAGTCAGAGTAACTCATAAAAGCCTACAGGCTATTGGTTTTCAGGGGGTTTGTTTTTGTAACAAAAAAAGTGTACTTATGTATGTTCAAACAGGAACTTGACACTACAAAACATTTCCATTCCAATGAGCGATGTTCTCCAAGCCCATCGAAGCGCCCCAGAGAAGACAGAGGAGGCTTTACAGAAAGTTAGTTCTAGTTCTGCACTAAAGAAAGCCTAGGAAAATACAATGACAAAATTTTTAATTGAGACTTTTCGTATGCATATATGTAGATCCAGGATTTTTTACGCAGGAACAATCAGAGGCAGTGTGGAATGACTGAGGAAATGTG[T/A]CATTTACAACATGGACTAAAGACCACTCGCTCTGAGCAGGTTTGTTAGGATATTTCAGTTATCAACTGGTTATTTTATACCTTAAAGGTTTAGTTTACCCAAAACAGAAAATTTTAATTACTCATAATTACTCTTTTCATTCTAATTTCCTTATTAGTTAATTTGCATTCAGAATACAACTAAAGATATTTAAGCTCAAATCTGAGAGCTCTTTTATCAATCAATAAACAACAATGACTTAATCAAAATCTTAATAAATACCAAAAAAATCCTCAAAACAGACCATATATTTGCCTTCAGTGGTTCAAATGAAATAATATTAAGATACAAGATTACATGTGTGGGCACGATTAAAACAGAAATTACCAAGTTTTCCTCAGTGTCAGTATATTGTGCAGGTTAACGAGATTGGTGTATTCTTTATGCAGGTCATGCTTAGTTTTGCTAGTGACATTTACCTCAGATTAATCTGTGCTGTGTTACAAACATAGAAATTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23305
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Nonsense | 1052 | 1338 | 32 | 39 |
ENSDART00000141051 | None | None | 594 | None | 20 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 22157305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22387528 |
GRCz11 | 18 | 22376594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGACCTTGTATTCGTTTGTGTCTGTAAAGGAGCAGGCCGCAGAGATC[G/T]AGAATGAGGCCAATGAGAACATGGGGAGGGTTGATGAAGGTGTAGAAGAG
Long Flanking Sequence:
TGGTAAGCATGAAAAGGAACGTTGTCATAGCACTCTGTAGCGCTCATTTTAAAGATGAAATGCAGCCATACGTACTTCTGACTACATAATTTGCGATCTCCAGAAATGAAATATAGGGCTCCGTTTTCCGAATGAGCATGTTGCACAATCACTGAACGTGTCATGAATGGATGTTGCAAACTGAGATCTCACTATGTTACATGGCATATAGCTGGGAACAGCTTTGTTTTTAGGTTTGACAAGCAGCAAACATAAAGAACTCTTATAAATGGTCTAATATACACCTTGCTTTAGCTGCTGAGTGAAAGGATTGTGGGCGATCTGTGGGTGTATCATCTGAGGTTAAGGTTGTTGATCAAGGGTCAAATCTCACGTCAATCTTTTGATTCTGTTTGGTTAAGATGCAGTTTTTCATGTTCTGATGAAATATTCAGTAGATTTTAATTGGTTGGCTGACCTTGTATTCGTTTGTGTCTGTAAAGGAGCAGGCCGCAGAGATC[G/T]AGAATGAGGCCAATGAGAACATGGGGAGGGTTGATGAAGGTGTAGAAGAGTTCTTCACCAAAAAAATCATCCCCGATGACCCCCTGTGAGTACATCACACATGCAAATGCACTCATCTATGCAGATCACTGTTAATCAACATGTATTTAACTGGAATTAATCACAGCATATCATTAAATCATGATCTCTAACAAAGAAATATCCTTACCGGTTGTCAAAAGACATTTCCCATCATGCCTCTCCTCTCCTCGTGTTCAGAAAGCACCAGAGGGAGGAGCCCCTCATTAAAGCACAACCTGCAGAGCCCACGTGTGTCACAACTGCCCCTCCTACCACCTCCACTACAACCCCCATCCCCACCACAGCCCCCTCCAAAAACATTAAGAAGAAGTTTGGTGATTTTTTTGCCTTTAAGAAAGTGCGTGCAGGTCGAGGGGCCAAGGGCGACGGCGTTCCTGAAGGCAAGGTCAAAAAGACTTCAATAGCCGATCTCATCCGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32208
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Essential Splice Site | None | 1338 | None | 39 |
ENSDART00000141051 | None | None | 594 | None | 20 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 22201336)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22431559 |
GRCz11 | 18 | 22420625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAATCACAATTACTAAGGTGTTCGATTTTGCTGGAGAAGAGGTTCGG[T/C]AAGTACAAGTCGTTTGTGTGGCCACTAGATGGCAGCATCTAATCATGAAA
Long Flanking Sequence:
CATCTTTTAGAATAGAAAGTAAATAAATTTAAATTATAGTTCATTATTATCATTATTAAACACTTTATTGGAGAAAAAAATGACAAATTACAACATTTCAACTAAATGTTACATTTTTGTTATTTAGTTGTTATTATATGTTATTTTTAAAAAAAAAATTTAATTGAATAATTCTTTCCAATTTTTTACATTTTAATTTGCGTGTACTTCTTTTGGACTAGACAGATTATATATTATTATTTAAAAAAGAGAGATCTGTGAGCGGTATACACATTTATGGTGAGCACTGTTATATTTAAATAGCATTTTCTGTGATTTTGCTTTTTTAATTTTAAACTAATAAGCATTTTTTTTTCCATCTCATATAGTTCACATCCGCAGCTGCTACAGATGAACCCAGTAAACTCTCTACAGCGTCTTCCCAGAAGGAGGACAAACCCAAAGATTCCTCCAAAATCACAATTACTAAGGTGTTCGATTTTGCTGGAGAAGAGGTTCGG[T/C]AAGTACAAGTCGTTTGTGTGGCCACTAGATGGCAGCATCTAATCATGAAAAAGCTGTGCAAACGATTGCTTTTGAGGTGAAAGCGGCAGTAATATTTTTTATTGCTTATTGCCAAACTCAAACAGCAACAAGGAGATGAGACAAAGTCTCATCACTTGCATGTGAAATATAATACAGGAAAAAACATTGTTATTGTGCCTAAATCAAGCTATGATATCATCAATAGCATAAAAAAAGACTTCAACTCAAAAAGGTTGTCATAATGCATCAGAAATGTAGCACTTTAATTTTTATTTATTCCTCTAAAAGAGTAAGAGAGTTAAGTTCAGTATGAAAGGGGAATGTATAAAGGAGATTTAAGTTCTTTTTGATTATTAATAAAGAATTTAGCATTCTATAGACCATTTTGAGGAATGTAAACAACAGTCCCAACTTATTTTTGGTTTTACATTTTAAATTTCTATAGCTTCTGATAATCCAAAAAGAGACGCATATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13566
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050311 | Essential Splice Site | None | 1338 | None | 39 |
ENSDART00000141051 | None | None | 594 | None | 20 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 18 (position 22251713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 22481936 |
GRCz11 | 18 | 22471002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGGGCATCACAGATGAGCTGGCAATCCATAATMGAGGCAAAGAAGGG[T/A]AWGTTTAAGCCTCATTAGTGACCCAGACAAACACATCATCTCGTATTATC
Long Flanking Sequence:
TCTACACACCTAAATGCATTGAGCTGCTGCCATTTAATTGACTGATTAGACATTTGCGTTAACGAGCAATTGGAAAAGTGTACCCAATAAAGTGGCTGGTGAGTGTATTTACATTTTAATAAAATGTCATTAGTTGTTTACATTAACCAACTGTAATGCAAAGCAACAATTGTTTTGCTAAATATTAATAGCTATATTATACACACATTTTCCTCCTTCCATTTATGCCAATATTTTGATGATGAAAAAAACACACCTCTTTTTGCTTGGAAACTGGCATCTATAATGCATAAAAACAATTATGGTCTAAAATATTTCTGTATGTTTATCCTCTCTCTAGTGCGAAGAGACCAGCAGGCATGGGGAGCATCCTGAATCGCATTGGGGCCAAAAAGCAGAAGATGAGCACTCTGGAGAAGTCGAAGATGGACTGGGATGCCTTTAAATCAGAGGAGGGCATCACAGATGAGCTGGCAATCCATAATCGAGGCAAAGAAGGG[T/A]ATGTTTAAGCCTCATTAGTGACCCAGACAAACACATCATCTCGTATTATCTCCCATTAGAGTCTCACACTAGCCTCTGAGATTTTCATCAGAGCTGAATAAATATCATTAAGTGTCTTAAGTGCTTAAAGCAACAGCACACTGAAATGTTGCATTTCAGGCCGTTTTTGTGATACATTGCGATTTATTAATTATTCACAAGTTAACTGGACAGTGAAATGAATGTATTTGGGAAAAAACCTTATGCTGCGCACGCATTAGATTAATATGTTGACCTTTGTGGTTGCTGTTAGAATTGAGGATGAGCATTTGGAGTACAAAAAATGTACTTGGATTCTGTTCTGGCCACATTATGAGATGATTGTGTACTATTTGTTTTGGGTTTCTGTCTTTAAATTGTTTTCTGCATATGCATGTAAGATCACACTTTACTTTAAAGTAATTCTCACTACTTGATGCTGCTTAATAGTTATTAAAGTAGTAGTTAGTATTAGGTATTGG
Associated Phenotype:
Not determined