ZMP
si:dkey-94e7.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
RP1
Human Description:
retinitis pigmentosa 1 (autosomal dominant) [Source:HGNC Symbol;Acc:10263]
Mouse Orthologue:
Rp1
Mouse Description:
retinitis pigmentosa 1 (human) Gene [Source:MGI Symbol;Acc:MGI:1341105]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17309 | Nonsense | Available for shipment | Available now |
sa8750 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30596 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19789 | Nonsense | Available for shipment | Available now |
sa11691 | Nonsense | Available for shipment | Available now |
sa10620 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17309
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 |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 105 | 2130 | 1 | 3 |
ENSDART00000133769 | Nonsense | 94 | 259 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30448649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30750284 |
GRCz11 | 2 | 30733817 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAACACAYRCTGTCTGTTCCCTTGATGATGTGCAGGATGGGGGCTCTTA[T/A]CTGTGCTCGGATCAGAAGAAAGTCAAGCCTTTTAACTTGGACGAGGTCCA
Long Flanking Sequence:
CACAATGAATGTGGATGCAATTTCACTATGGCACTATAAACAAACCAAGTGGGACACTGTTTAGTAAAAACAGGACAATATTCTTGAATGATTTGCAGAATGTTATTAAGTACAAAATAAGACATGAAAATAAGACTGAAAATAAATGTTAACTGTTGTTTCTTTTTTTGTGTAGAATCTATTAATATGAGCACAACATCCCTGAATGATGGCCCCCATCCTGACCTGTCCCCAGGTAGCATGCAAACATTGGTCTCCAGGCCACTGCTCCCTCAGTCAGACCCCATTACCACTAAAAGGGTATGTTTCTACAAGAGCGGTGACCCTCAGTTTACTGGGCACCGGATGGTCATCAACAGTCGCACTTTTAAAACCTTTGATGCCCTACTAGATGCCCTCTCAAAGAAAGTGCCTCTGCCATTTGGAGTAAGGACCATCACAACACCCAGGGGAACACATGCTGTCTGTTCCCTTGATGATGTGCAGGATGGGGGCTCTTA[T/A]CTGTGCTCGGATCAGAAGAAAGTCAAGCCTTTTAACTTGGACGAGGTCCACAAGAGACAGGTCCCTTGGAACACTACCAGACCTGTCAGTGCGGGACGCCAAGCACGCAGAGAACTGGTCCGGCAACTAGCAAAGAGAAATCAAGTGTCCACAAGAACAATAAAAATGTCGGAAAACACTGTGGTGGTGCGGACACCAAAAAGACTGACAGTTTACAAAAACAGAGATCCAAGCATGAAGCGAGTAATTGTTCTTCATAGGAGAATAGCCCCTACGTTTGAAGCTCTTTTGGATTATCTTTCTCAAATGATGCAGTTTCCTGTTGTAAAGCTTTACACAGAAGATGGCAGAAGAGTAAGTATATCATTTATAAATATGTCTGTTTTCCTTGCTATGAGTGTCACTGAAGAATAATACCATAAGTAGGAATAAACTGCCTTTATGTGTTGATTTTGTTCAAAAGATTTTGGTAACTTCCTAAAATGTAGTTTTGCTGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8750
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 516 | 2130 | 3 | 3 |
ENSDART00000133769 | None | None | 259 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30446843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30748478 |
GRCz11 | 2 | 30732011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTACAGTKGGTGCGTACTCATACATGGAGCGGACTGCACAGGGAGAGT[T/A]GATGGAAGGCTACTGTGTGGTCAGTCGCAGCAGTAGCAGCAGCACAAGAA
Long Flanking Sequence:
TTGCCCCACAATGCCTAACGAAGACGACATTGAAAAATCATTTCGGGTTAATGAGGATGGAAGCATGACAGTAGAGATGAAGGTGCATCTTACTATAAAACAAGAGGAAATGATCCACTGGACGACTACATTGAGCCGCACCTCAGTTAATAGCCAGCAGAGGGCAGTGTGCAATTCCAAACCAGAATCGGGGGCAAACTCAGTAGATATAACCAATGACTCAGGCAAAGAGTCGAATGGACCTCATAGCCTAGATTCAAAAGAAATCAATACTGTACCTAATAAAACTGTAGGATTCATCAAGGAAGAAAGAGAAAATTATGGCAGTGATACATCTTCTGAAAAGCCTATGCCCATCTATAGAAGGCTGCCCACTCCAGCCCCTAGACAACGTCGAAAAGAGGTCTCAGTTGAAAACATTAAAACTGTTTCAGAGACTGAAGTTCAGGAGAGTACAGTTGGTGCGTACTCATACATGGAGCGGACTGCACAGGGAGAGT[T/A]GATGGAAGGCTACTGTGTGGTCAGTCGCAGCAGTAGCAGCAGCACAAGAACTGTGTCAAAACCCGGGAAGAGTGAATCAGGAGAGATTAAACAGAAGAAGTCTCATTCTTCCTTTAGATCCTCAGGGGTGGCAGAGGTACTTCAGCTACAAAACAATGGGACGATGGGAATAACAGAGACTGTGGTGCATATATATGAATCACAGGGTACATGTGACAATTACTATGCAAATACACAGATGGATACGGACAACAAGCCTGGATACTGCACAAAAGCTTTGCCTCAAAGTAAGCCAGGCTCAACAGACTCAGGACCCTGTTCATCAAGTAACGATTGTGATGTTGATCTCACAAGGCAGTCCACAAGCTCCAACTCCCTGGATGGTGGAAAAAGTAATATGCTGTCATTATCTTCTGACCGTTCAACACCTCCAAAAAAGATAAATAGCAATCTTTCCATCCTTACCGATGACGAAAAACAATCCTTGGTTGAGTGCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30596
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 620 | 2130 | 3 | 3 |
ENSDART00000133769 | None | None | 259 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30446532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30748167 |
GRCz11 | 2 | 30731700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATACTGCACAAAAGCTTTGCCTCAAAGTAAGCCAGGCTCAACAGACTCA[G/T]GACCCTGTTCATCAAGTAACGATTGTGATGTTGATCTCACAAGGCAGTCC
Long Flanking Sequence:
GAGAAAATTATGGCAGTGATACATCTTCTGAAAAGCCTATGCCCATCTATAGAAGGCTGCCCACTCCAGCCCCTAGACAACGTCGAAAAGAGGTCTCAGTTGAAAACATTAAAACTGTTTCAGAGACTGAAGTTCAGGAGAGTACAGTTGGTGCGTACTCATACATGGAGCGGACTGCACAGGGAGAGTTGATGGAAGGCTACTGTGTGGTCAGTCGCAGCAGTAGCAGCAGCACAAGAACTGTGTCAAAACCCGGGAAGAGTGAATCAGGAGAGATTAAACAGAAGAAGTCTCATTCTTCCTTTAGATCCTCAGGGGTGGCAGAGGTACTTCAGCTACAAAACAATGGGACGATGGGAATAACAGAGACTGTGGTGCATATATATGAATCACAGGGTACATGTGACAATTACTATGCAAATACACAGATGGATACGGACAACAAGCCTGGATACTGCACAAAAGCTTTGCCTCAAAGTAAGCCAGGCTCAACAGACTCA[G/T]GACCCTGTTCATCAAGTAACGATTGTGATGTTGATCTCACAAGGCAGTCCACAAGCTCCAACTCCCTGGATGGTGGAAAAAGTAATATGCTGTCATTATCTTCTGACCGTTCAACACCTCCAAAAAAGATAAATAGCAATCTTTCCATCCTTACCGATGACGAAAAACAATCCTTGGTTGAGTGCACATCTGAAACAATACAAAAGAAGATTATGCATCCAGCAAAAGAAACAAATTCCAGTAATAAAAGCACTGCTGTTAATAAAAATAATTCACCAAAGTCCAAAAAATCAAAGCAAAGCACTTCTTCTGGATCATCTAGGCTTGGGAAAAACATAAAAGGCAGTGCTCCAGGCTCTTCAAAAGACCTCCGAGTGACTTCAGACACAACGAGCCACACAGGATCAGAGAAAAAGACTAGCTCAGCAGAAAGTGATAAACATGAGCACAAAGCAGTGAGAGACAAAAATAAGAAGACAAAGACATTTGAAAGTTCTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19789
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 |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 718 | 2130 | 3 | 3 |
ENSDART00000133769 | None | None | 259 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30446238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30747873 |
GRCz11 | 2 | 30731406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAAAGCACTGCTGTTAATAAAAATAATTCACCAAAGTCCAAAAAATCA[A/T]AGCAAAGCACTTCTTCTGGATCATCTAGGCTTGGGAAAAACATAAAAGGC
Long Flanking Sequence:
ATTCTTCCTTTAGATCCTCAGGGGTGGCAGAGGTACTTCAGCTACAAAACAATGGGACGATGGGAATAACAGAGACTGTGGTGCATATATATGAATCACAGGGTACATGTGACAATTACTATGCAAATACACAGATGGATACGGACAACAAGCCTGGATACTGCACAAAAGCTTTGCCTCAAAGTAAGCCAGGCTCAACAGACTCAGGACCCTGTTCATCAAGTAACGATTGTGATGTTGATCTCACAAGGCAGTCCACAAGCTCCAACTCCCTGGATGGTGGAAAAAGTAATATGCTGTCATTATCTTCTGACCGTTCAACACCTCCAAAAAAGATAAATAGCAATCTTTCCATCCTTACCGATGACGAAAAACAATCCTTGGTTGAGTGCACATCTGAAACAATACAAAAGAAGATTATGCATCCAGCAAAAGAAACAAATTCCAGTAATAAAAGCACTGCTGTTAATAAAAATAATTCACCAAAGTCCAAAAAATCA[A/T]AGCAAAGCACTTCTTCTGGATCATCTAGGCTTGGGAAAAACATAAAAGGCAGTGCTCCAGGCTCTTCAAAAGACCTCCGAGTGACTTCAGACACAACGAGCCACACAGGATCAGAGAAAAAGACTAGCTCAGCAGAAAGTGATAAACATGAGCACAAAGCAGTGAGAGACAAAAATAAGAAGACAAAGACATTTGAAAGTTCTTCAAAAAGTAAAAACTTGAATCTTGATAATGGGAATCAAAGACCATCAGATAAAGATGTTAAGTTAAAAGATAAAACCATAAAAGACACTTCCCACAAGATAAACACAAACAGCCATGACTCTCAAGGGCCAAAATTGAAAAAGAGTAGTTTAGACATTGAATCACCAGCCCATCCAGCAAAACTAATAAAGAGGCTTCCGAAACAAAGATCCATGAATGGTGTAAAACCAAAATCCTCTAAACCAAGACAGGAACTGAGTGAAAGCGTGTCATTGCCTGTGTTACAGTCATCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11691
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 |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 854 | 2130 | 3 | 3 |
ENSDART00000133769 | None | None | 259 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30445830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30747465 |
GRCz11 | 2 | 30730998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATTGAATCACCAGCCCATCCAGCAAAACTAATAAAGAGGCTTCCGAAA[C/T]AAAGATCCATGAATGGTGTAAAACCAAAATCCTCTAAACCAAGACAGGAA
Long Flanking Sequence:
AAAAGAAGATTATGCATCCAGCAAAAGAAACAAATTCCAGTAATAAAAGCACTGCTGTTAATAAAAATAATTCACCAAAGTCCAAAAAATCAAAGCAAAGCACTTCTTCTGGATCATCTAGGCTTGGGAAAAACATAAAAGGCAGTGCTCCAGGCTCTTCAAAAGACCTCCGAGTGACTTCAGACACAACGAGCCACACAGGATCAGAGAAAAAGACTAGCTCAGCAGAAAGTGATAAACATGAGCACAAAGCAGTGAGAGACAAAAATAAGAAGACAAAGACATTTGAAAGTTCTTCAAAAAGTAAAAACTTGAATCTTGATAATGGGAATCAAAGACCATCAGATAAAGATGTTAAGTTAAAAGATAAAACCATAAAAGACACTTCCCACAAGATAAACACAAACAGCCATGACTCTCAAGGGCCAAAATTGAAAAAGAGTAGTTTAGACATTGAATCACCAGCCCATCCAGCAAAACTAATAAAGAGGCTTCCGAAA[C/T]AAAGATCCATGAATGGTGTAAAACCAAAATCCTCTAAACCAAGACAGGAACTGAGTGAAAGCGTGTCATTGCCTGTGTTACAGTCATCTTCCACCAGTGTAAATCAGTATGTTGAAAACTGGCTGAAAAGACTTGAACCAGAGTCTCTGCCCTATGAAGATGAGACAGACCCTCCCGAGATTGTGCCAAGGGCTGTATTCCAGATAGGGGCTGACTCCACTGAAGACTCTGAGATTAAAAGCAACCCTGATGGAGATAGCATAGAGGAAAAAGAACAATTACTAGAAGATCATGTTGACGAAAGCCCAATGTGTCACCCACCAGTGCAAATAAGGTGTGAGGGAGAGCCAATTGAGCCACAGAAGACAATGGGCTTTTGTAAATCAATGCCAATTTTGAGGGTGCCTTCTGAACAAGAAGGTATTGTAAGAATGCACAAGTCATCCGAGCACTTGTTTCCCCCAGAACCCTCTGGGAAATCACAAAGTACAGAGGTCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10620
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 |
---|---|---|---|---|---|
ENSDART00000110515 | Nonsense | 1187 | 2130 | 3 | 3 |
ENSDART00000133769 | None | None | 259 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 30444831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 30746466 |
GRCz11 | 2 | 30729999 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTGCTCTAGAAGTGGACTTGGAAGGAGAAACGGATGATCAGGACAAA[C/T]AGCACAGTTTTAGTATTGCACAGTTACTGGATGAACTGAACATGCCTGAA
Long Flanking Sequence:
GTGTTAGATCAGGCATGAAACCAGTTTTGCAACAGTTGTGTTTGTCTGTTCAGTCCATCAAGCGTGCTTTGAGTCAGACCTGCTTAACATCTGGGGAAAGGGAAAAGTCCAGTAGCCTCCCAGACTTTTCATCTCAGGTGGCCTCTGCCTTTGGTTCTCCATCCAGAGCTCTTCTTTCTTTCTTGTCAGTCATGACTCTGAGAGATGGGCTTTCAGTCCTTTATAAAAACGAATCAGAAACTGGCAACTCAAATGACTGCCCAGAGGCCCTGCAGGTAATGCAGTCTTTGGAAAAATTATCTAACATTAAAGATGAAGATGAGCTAAGGGCCAGCTTGACCAGTCTTCGAAGTTCAACTTCGTCCAAATTAAATCAAAGCTGGAAAGATTTCCAAGAGCAAAATATCTATGACGATAGTCCCCCACTGTCACCAAGACTATCGGAACAGGAGTTTGCTCTAGAAGTGGACTTGGAAGGAGAAACGGATGATCAGGACAAA[C/T]AGCACAGTTTTAGTATTGCACAGTTACTGGATGAACTGAACATGCCTGAAGATGTTCAAAGAGAAATATCCTCTCTTGTTGAAGGAGAACTTAATTATTTTACTCAGTCAGACTCAATCAAAGATGCTGAGAACATCAGTGACATTTTAGGTAAAAAGGAGGAAAACGATGATGGCTCCTTAGGTGGTAGTTTAGAGAAAGCTGCAGAAATGGAAGAAGAAAGGGATAATATTGGCCAAGACAATGATGTAGCCAATGATGACATAACCAATGATCCAAAAGACCCAGAACCTTTAGAGATGCATTTAAATCAGTCTCATTCCCCTGACTCGGAAACTGTAGATAAGGACTTTTGTAATGAAGATTCTGGTATAGCAGTGCCTAATCAGTCACCTGAAGGTAATGGTAGTGATTCAAGTAAAGCAGAGGCTTTAAAAATCTGTAATAACAACCAAGTAAATGCAGAATGCTTGCAAGAAAAGGTGATGAATAAAGACTTA
Associated Phenotype:
Not determined