ZMP
si:ch73-173k21.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
FRMPD1
Human Description:
FERM and PDZ domain containing 1 [Source:HGNC Symbol;Acc:29159]
Mouse Orthologue:
Frmpd1
Mouse Description:
FERM and PDZ domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2446274]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19485 | Nonsense | Available for shipment | Available now |
| sa15183 | Nonsense | Available for shipment | Available now |
| sa39603 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa32657 | Nonsense | Available for shipment | Available now |
| sa19484 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19485
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 |
|---|---|---|---|---|---|
| ENSDART00000114719 | Nonsense | 187 | 1757 | 6 | 15 |
| ENSDART00000139937 | None | None | 122 | None | 3 |
| ENSDART00000140553 | Nonsense | 49 | 267 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 20734977)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21207073 |
| GRCz11 | 1 | 21900010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTCCAGGGCAATTCTCTGCTGTTCCTGCCTAATGTTCTGAAGGTCTA[T/A]CTGGAGAACGGCCAAACGAAGGCTTTCAAGTTTGAATCTAAAACCACTGT
Long Flanking Sequence:
ATGCATTTGCGCTGTTTTCGGGTGTTCATATAGCCAAAAAAACGTGGGCTATTGATACAGTTTTGGGAGAAGCAAAATTTCCATATGTGGTTTCAGTAGCCTGATGCATTTAGACCTGTCCAGTTTCCTCTGGAATGCATCCCAGACGACCTCCTGAAGTGGTTTGAGTGATCGGATTTAAAATCTGTCTCAAATGTGTTTTGGAGGGCATTTACCTCTGTCCCTTTCACGATCTAATAACTATCCCATCAGAAAAAAACACATGTAGTGACAAGGTGTAGCTTAAGTAGCTCCCATATGACTAATTAAACAATAGTTTCAACACTTTGTTGAAAGAGACTGCTGTTTAATAATTTAGCATATATGCTAACATTGCTATTAATATTATCTATTTTACATATTATATTTATAAATGCGTGTCTATTGACCTTGGTTCATATATTGATCTTTGACCTCCAGGGCAATTCTCTGCTGTTCCTGCCTAATGTTCTGAAGGTCTA[T/A]CTGGAGAACGGCCAAACGAAGGCTTTCAAGTTTGAATCTAAAACCACTGTTAAGGTAATGTAGACACATTCACTATAATGTCACTAATGTAATGAGTTATGATGGATTTTTCGGTCAGCATGAAATATGGTTTTAAAGTACAATGGTAAATACATATAACAACATATATATGTATATTAAAAAACATACATATGTTACATAGCCTTGCGTGAAAATGTAATTTTTCCAAAAATAATAAGCAGTATATATTTTTTACTGTAATTAAAATAATAATGTATCAGTTCAGTACTTACAATGGCTGCTGAAAATTCAGCTTCAACACAGGAGCAAAAAACATTTTTAAATTACATTTAAAAGAGTATATTATGTAAAAAGGGAAATTTGTTTTGCATATTATGCAAAAATCACTTCTATAAGGGACTTAAACACAATTGTGTGGCAACAGTATGTGAAAATACAGCCAGCCTCTAAAACAATTATTCAATTTTTTTACAATCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15183
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 |
|---|---|---|---|---|---|
| ENSDART00000114719 | Nonsense | 230 | 1757 | 7 | 15 |
| ENSDART00000139937 | None | None | 122 | None | 3 |
| ENSDART00000140553 | Nonsense | 92 | 267 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 20731945)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21204041 |
| GRCz11 | 1 | 21896978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAACTGTCAATAACCCGTATAGAACACTTCTCYCTAGTACTGGAACAA[C/T]AATACAGCATMAGCAAACTCTATCTACTGCATGAGGAAGAGATTATTCAA
Long Flanking Sequence:
AGGGTCAGCTTCAAAGATTTATCAAAAAATTATATATGTGTGGTATTTTGAGCTGAAACTTCACATACACACTAGGGACATCAGAGACTTATTTTACATCTAGCAAAAAGGGGCATAGTAGGTCACCTTTAAATTTGTTACAAAATAAATTATTGCAATTATATTGAAAACGACAAGCTTTTTTTTTTTTTTTTTTTTTTAAATGTGTATAAAACTACTATCATTTTAATTTGCTGTTTTGTTATTAAATAAAATATAATTGGTGAAGTGCTCTTTCTGACCAAACTGAATGACTACAAATGTGAATGGCAGAGCAAGTACTCTAAACAGGACAATGATATTCATTCAGTATAACATTATTTATCCTGTTCTGTGTACTAATGTCCTCAAACTAAACGTTTAATATAACCTCTTTGTGTTTTCTCTAGGACATAGTGATGACTCTGAAGGAGAAACTGTCAATAACCCGTATAGAACACTTCTCCCTAGTACTGGAACAA[C/T]AATACAGCATCAGCAAACTCTATCTACTGCATGAGGAAGAGATTATTCAAAAGGTACACACAAACACCATACAAGATCAAACAGAAATACACATTAGTACGTTAGGGCTTATTCATCCTCATGTTGTTGCAAAACTGTTCTTTTGTTCATAAACAAATATATTATTATATAAAATTATTATTATATATATAATTATTTAAAAAATATTATTAAGATTATCCTAAAAACTCGTGGAGTTATAAAAGTGACAATGTAAGAATATTGGCTCTTAAAATCATAAAATTCGTCCAAAAGATTTTCAGTACTTATTATTATTATGTACTCCAGAAAAAATACTGCACATGGGCGAACAAATTCTTTTGCTCATTCACTTGTCCTACGTAGGTTAAAGTATATGTGGAGACCATCTATAGGACATACCATAATAGTTTTATACATTTCAATGCTTTCATTTTTAAAAAATGTGGCATGTTTGTGTGCTGCTATGCGTCCTGTGTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39603
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114719 | Essential Splice Site | 287 | 1757 | 8 | 15 |
| ENSDART00000139937 | None | None | 122 | None | 3 |
| ENSDART00000140553 | Essential Splice Site | 149 | 267 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 20730343)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21202439 |
| GRCz11 | 1 | 21895376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCATGCTTACAGAAGATCCTGTGGGCTTTGAGTATCTGTACTTACAG[G/A]TGAGTGTTTCTTTCATGTTAGTTTCCTGCTATAACCACTAGTAAATGATT
Long Flanking Sequence:
CAATTTACAATGTTGTTTTTCTGTAAATGTATCTTTTATTCATAACATTTCAATTACTTTAATTTGATATAATTGACAGAAAACACACATAATGCTATAAAAGTTTCTATTTAAAAATAATTTTTGAACATTCTATTCATAAAACAATGTTAAACCAAAATATATTATGATTTTTCCATAAATATTAAGGAGCATAACTTTTGAACACTCTTCATATCCCTGTTTGTTTTCTACATGGAACACCATATTGAAGAGTAAACAGTGTTGTAAGAGAGCATTCTTTAAAAGATTTGTTACTTCTTCTTTACACACGTTTGTAATTGTTAATTGGCTGACGTTCAGTGTAATTTTTAATTTAATATACTTTGTATGTGTGACAGGTGGTTGAAAAAAAGGAGACACATGACTACAGGTGTCTGTTCCGTGTCTGTTTTCTACCCAGAGACTTTAAAAGCATGCTTACAGAAGATCCTGTGGGCTTTGAGTATCTGTACTTACAG[G/A]TGAGTGTTTCTTTCATGTTAGTTTCCTGCTATAACCACTAGTAAATGATTGTACTCCTGTAAGGAAATATCTAACCCTAATGCACATCCATCTATATTTTATAAACAGCATTACAAATGATTGGCATTAGATTGTTTTCTGATTATATGAATATTCTTTGGTGTATTACAAAGACTACGCTTGTTTGCATTCTTAGTGTATACACTAGGACACACACAGGTTTAAACTTAAAGTCAGCATGAAATGGAAGTTAAGTTCAAGGAAGTTTCCTTTATCATGATATATATTTGACTGAAATGGTTTTTAAAGTGGGGGAAAAAATGAAGGGCAGTGCATGATTTCATCCTTTGGGAATCTATATCATTGCTGTTGCTAAAAGAAAGAGGAAGATTTGAATGTCAGTTTTACTAAGTTGTAGAGGATTACCAACAGTGAATTTAGGCATGGACTCAGGCAGGGCGGCATCTTCCCGGGGGAGGCACGGGAAGTCAGTTTTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32657
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 |
|---|---|---|---|---|---|
| ENSDART00000114719 | Nonsense | 755 | 1757 | 14 | 15 |
| ENSDART00000139937 | None | None | 122 | None | 3 |
| ENSDART00000140553 | None | None | 267 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 20721664)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21193760 |
| GRCz11 | 1 | 21886697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCTGAATGTCTACCTAGTCCCCCTGCAGCCAGCGAAGAGGAAGACTG[T/A]GAGGAGTCAGGAATAGAGAATGAAAACCATAAAAAGGAGTCACCTGCAAA
Long Flanking Sequence:
GAAAGAGAAGAGGACCAAGAACCCATCAATGAATCTATAAATGATAATAATGAAAAGACAACAGATATAAATGATGAGAGACTGGGCACAGAAAAGGAAGGCAAATCTCAAGAGAATAAGCCTGAACACCCTCCCTGTATCATTATTGTAGATGACCCTTCATCTGAAGCATCTGATTCATACCAAACGGAGTCACATTTCATGACCAGCATGTCCAGTGACTCTATAGATGCTTTGGAGGAGGATGATCTTATGACCTATTTTTCTACCAGACACCCATGGCATTTACCAGTGAAAGACTCTTACCACTGTGAAGACCGCTTTTCACCATCACTGTCTCCACAGCAACAGCTTTGCAAAGACTCTCAGTCCCAGAGTGACCTGTGCTCTGCTGATTCCCATTGTGAGCCAGATATTGACCAATTCTTTTGCTTTGCTGCACTCTCAAACATTGCTGAATGTCTACCTAGTCCCCCTGCAGCCAGCGAAGAGGAAGACTG[T/A]GAGGAGTCAGGAATAGAGAATGAAAACCATAAAAAGGAGTCACCTGCAAAATGTCCTGAAAGCAACCTACCCCTTCCTGCAGATTATGTGTTCACATTTGAACAAGGAGACACTAGACATTACTACAATATCTGCTCCAATGTTACTCCTGACAGTGCTCGCAGCCTTCCAAAACCTTTCTCTTCTCCAGATTCTACAGAAACACGCCAGGATCAGGAAGGAGTGGCAAGGAATGGGAAAGAAGCAGTGCCAATTTTTCATCCCCCACCAGGGTTTGGAGACAGCAGTTCAGATGATGAGTTCTTTGACGCTCAGGAAAGATTCACATCCCCGGAAGAACCTTTATCTACTGCTATGACTAGGGGTATGACAAGGAAAAATCTCTCTAATTATATGTATAGCTAATAATATAGAATTTAAAGTTATTCACATGTAAAGTTTTGTATATGATTGATGTAAATTTTTGCTGACAAGCACTTAACATTTGTCTTTGCTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19484
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 |
|---|---|---|---|---|---|
| ENSDART00000114719 | Nonsense | 790 | 1757 | 14 | 15 |
| ENSDART00000139937 | None | None | 122 | None | 3 |
| ENSDART00000140553 | None | None | 267 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 20721561)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 21193657 |
| GRCz11 | 1 | 21886594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCTGAAAGCAACCTACCCCTTCCTGCAGATTATGTGTTCACATTTGAA[C/T]AAGGAGACACTAGACATTACTACAATATCTGCTCCAATGTTACTCCTGAC
Long Flanking Sequence:
AATCTCAAGAGAATAAGCCTGAACACCCTCCCTGTATCATTATTGTAGATGACCCTTCATCTGAAGCATCTGATTCATACCAAACGGAGTCACATTTCATGACCAGCATGTCCAGTGACTCTATAGATGCTTTGGAGGAGGATGATCTTATGACCTATTTTTCTACCAGACACCCATGGCATTTACCAGTGAAAGACTCTTACCACTGTGAAGACCGCTTTTCACCATCACTGTCTCCACAGCAACAGCTTTGCAAAGACTCTCAGTCCCAGAGTGACCTGTGCTCTGCTGATTCCCATTGTGAGCCAGATATTGACCAATTCTTTTGCTTTGCTGCACTCTCAAACATTGCTGAATGTCTACCTAGTCCCCCTGCAGCCAGCGAAGAGGAAGACTGTGAGGAGTCAGGAATAGAGAATGAAAACCATAAAAAGGAGTCACCTGCAAAATGTCCTGAAAGCAACCTACCCCTTCCTGCAGATTATGTGTTCACATTTGAA[C/T]AAGGAGACACTAGACATTACTACAATATCTGCTCCAATGTTACTCCTGACAGTGCTCGCAGCCTTCCAAAACCTTTCTCTTCTCCAGATTCTACAGAAACACGCCAGGATCAGGAAGGAGTGGCAAGGAATGGGAAAGAAGCAGTGCCAATTTTTCATCCCCCACCAGGGTTTGGAGACAGCAGTTCAGATGATGAGTTCTTTGACGCTCAGGAAAGATTCACATCCCCGGAAGAACCTTTATCTACTGCTATGACTAGGGGTATGACAAGGAAAAATCTCTCTAATTATATGTATAGCTAATAATATAGAATTTAAAGTTATTCACATGTAAAGTTTTGTATATGATTGATGTAAATTTTTGCTGACAAGCACTTAACATTTGTCTTTGCTGTTTACAGAAAATTCTGCAGAATCCAGCACCATATTAAACACACTACGCCTGGGACAGATTGGCATCTGTGTCAGTGAACAAGAGGCAAAGGATTCAGAGAGGAAACA
Associated Phenotype:
Not determined