ZMP
zgc:175140
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC324863 [Source:RefSeq peptide;Acc:NP_001120937]
Human Orthologue:
FNIP1
Human Description:
folliculin interacting protein 1 [Source:HGNC Symbol;Acc:29418]
Mouse Orthologue:
Fnip1
Mouse Description:
folliculin interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:2444668]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32363 | Nonsense | Available for shipment | Available now |
sa9714 | Essential Splice Site | Available for shipment | Available now |
sa43727 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32362 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32363
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 |
---|---|---|---|---|---|
ENSDART00000099448 | Nonsense | 54 | 1077 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 43682297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45479437 |
GRCz11 | 21 | 45521774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCAGTCAGATCCGGCTGATCGTCTACCAGGACTGCGAGCGGCGTGGA[C/T]GAAATGTCCTCTTTGACTCGGATGCCAGAAAGAGAAGCACAGAAGATGGC
Long Flanking Sequence:
GGGATTAAAGAGTTGTGATTGGCCCTTTGTTTGGGGTTTAAAGAGTTGTGATTGGCCCTGTGTTTAGGGTTTAAAGAGCTGTGATTGGCCCTGTGTTTGTAGTGTTAAGAGCTGTGATTGGCCCTGTGTTTGGGGTTTAAAGAGCTGTGATTGGCCCTGTGTTTGGGGTTTAAAGAGCTGTGATTGGCCCTGTGTTTGAGGTTTAAAGAGCTGTGATTGGCCCTGTCTGCGTTTGGGATAAAAAGAGTTGTGATTGGCCCTGTCTGTGTTTGGGGTTTAAGAGTTGTGATTGTCCCTGTGTTTGGGGTGTAAAGAGTTGTGATTGGCTCTGTGTTTGGGGTGTAAAGAGTTGTGATTGGCTCTGTGTTTGGGGTGTAAAGAGCTGTGATGTTATAGGTGTTTTACTCTTGTGCATGTGTGTTTTCCTCAGCTGGTCGTCCCCAGAGCTGGAGCCCAGTCAGATCCGGCTGATCGTCTACCAGGACTGCGAGCGGCGTGGA[C/T]GAAATGTCCTCTTTGACTCGGATGCCAGAAAGAGAAGCACAGAAGATGGCCCGGCTACAGTGAGTGTTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGGGTGTGAATGTATGTATGTTAGGGCTTTTGAGACTCATCAGGAGTCGGGACATGCCTGTATAACCACATGGCTATGATTCGGGTATTACAGAAGGTGGTGAATTATCATCACACTGCTGATGTCCTTATTTCTCAAAATCTCACAGAACTGTTTTCTAGTATGTTGGGGTAGGTTCTTAGAAAATACAGTTTGTACAGTTTAAAAATTATGGACAATGTCTAATTCACAAAAAATAACATGTATGAGAGAGCCAGAGACCTTATTTATTAATTAATTAATTTATTTGTTTATTTATTTTATCCTATCATTGAATCTAATTATTATGTAAATGTCTAAACTTTATATTTTATTAGTTTTACAATAATTATTATTTAGTATTAATATCAATATTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9714
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 |
---|---|---|---|---|---|
ENSDART00000099448 | Essential Splice Site | 152 | 1077 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 43674929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45486211 |
GRCz11 | 21 | 45528548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGGCCATGAGCTACAAGGGTTCAACGCTGAAGATCCACCAGATAAGG[T/A]GAGACTRAAGGCACAGCRGTCAGAATTAACCATGCAAAAATCTGAAAGAG
Long Flanking Sequence:
GAAGGCAATCCTGACACGAAGTGAACGCGCGGTGGCGTTTGAAGGTGTCAGACATGGAGCACAGACGCTCTTGATCCATAGGTCATTAATGGTATAGCACTAATACTGAAACAGTTAGGCATTTTAGAATGACCAAAACAACATTTCAGATGGTTTACAGTGTGCTCAGCCTGCTGGTTTATCCATCCGCACATATTTTCATCATCACATGATCATCACATGACTATATCATATAGAAATGGAAAACAAAAACACTGAGCCCTGCATTTGTGTTTCCGCTGAGTGAGCGACACTGGAAAATGATTCCAGACTGCCATTTCTGCACATTTATGATGCTTTTATGTGTGTGTGTCTCTGTCTGTCTGTCTGTGTGTGTGTGTGTGTGTCCTCCACAGGCCTCATCGCGGTGCTCGTCAGATGCTAACATGCTTGGAGAAATGATGTTCGGCTCTGTGGCCATGAGCTACAAGGGTTCAACGCTGAAGATCCACCAGATAAGG[T/A]GAGACTGAAGGCACAGCGGTCAGAATTAACCATGCAAAAATCTGAAAGAGCCACAAAGAAATGGACATATGATAAAGTATAGTTAACTCTATGCTATAACAATATAAAAGATCTAATAATACAATAATGAATGAAACGTGAACATAATAAAAGTCTCCATGATTTGAGATGAAAGTCAGCCACAGAGGTGCTGCAGGATTCAGCATAAGCAGTCGCTGATGTAAATGCAGTATTACTTTTACTCTTTTAATCTAAGGATTTTACACTCAGAAGAACAACATTTCAGATCTTGTAAAGCTGCAATCCAACATTAATGTGAAGCCCTGAATCACACATGTATATCTGTGAAATCATCGGTCAAACTAAACCACATCATGCAGACGATTTTACTCTAAAAAGTGCATTAAAATATGGGGATGGAAATATGGCTATTGAAGCGCCTGTTCTGATAATGTGTGTGTTTCAGATCTCCTCCTCAGATGATGCTCAGTAAGGTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43727
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099448 | Essential Splice Site | 237 | 1077 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 43669809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45491377 |
GRCz11 | 21 | 45533714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCGGGTGTGTGTAAACTCTCTCTTACAGTGTTTCTCTGCCTCCGCTC[A/C]GGACACAGTAACCCAATGGACATGCCTGGACGAGGCCTGTATGACGAGCG
Long Flanking Sequence:
AAACAGAATCTGTGTTTTTCAGTGGAATCTGACAGTATTGGGGTGCAGAAGTCAACTCTAATATAACACTGTGTAGTTTTATTGTATAAATAATTGAACAGAAGTAATGTTTGTTAAATTACCAGCTTTATAATTTTTTGTGCTCACTTGAAATCTTGCAGTCACTGGAATTTAAAACACATCCAGATAAAAATCACACTGTTGGATTAAACTTTACAGTGACTATTCGGATCATGTGTTCAGAACTGTGCTCCTGGTTATGATAATCCCAATGTGACATTGCAGATTGTAGACCATTGCAGAAGCGCATGTTACGATATCGGTGCTGAAACCATATATTGTGCAGCCCTAATGTGAAGCATGCCATCTGGTAGGACGTGTAGTGGTGAGTGTGAGTGTGTGTTTGCTGGCGTAGGTAGATCACAGTGGAGATGCTGGGCTGGTGGTGGTTCTGCGGGTGTGTGTAAACTCTCTCTTACAGTGTTTCTCTGCCTCCGCTC[A/C]GGACACAGTAACCCAATGGACATGCCTGGACGAGGCCTGTATGACGAGCGGGACAGCGGCATCGCACGCTCAGGTCAGCTACTGCACATTTACACACACTGACACATACTGCAGGTCAGCACTGTGATTGCCACCTTAAAGTCCATTAGATTTATTTTGTTTTTGTGAGTTTTATTTTAATCAAATTTGCAGAAAATGAGTGCTGGACAAACATTACTCACAACTAATCGCATCCAAAATAAAGTGTGCGTGCGTGCGCTGTCATTATTTACTATGATCATATAAATTAACAAATGCATGCATCATGCAGTGTAATGTAATGCAGTGCTGCTTGTCTGGTGTGAAGCCCACTTTATATCGAGTCTCAATCAGGCAGTGAAGATCATCGATTTAAAACAAACCAGATCCTAAATGTGGTGAGTTTATAATGGCATGACAGTTCACCGGAAACACCTGAGAGAACTTAATGAAACAAAACTACAGTCCCTGTGCATGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32362
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 |
---|---|---|---|---|---|
ENSDART00000099448 | Nonsense | 850 | 1077 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 43658612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45502573 |
GRCz11 | 21 | 45544910 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTGTAGAGCAGAAGAAAGCAGCTCCTCTGAATGACTGGGAGATCCCT[C/T]GAAACGAGAGCTCGGACAGCGCTCTGGGGGACAGCGAGAGCGAGGACGCA
Long Flanking Sequence:
AGAGCTTTCCAGACATCGAACCCTCAGCCAAAGTCACATTCCTCATCGGCGACTCCATGTCTCCTGAATCTGACCTGGAGAGCCGGCAGCAGAAGGTGGAGCAGGAGATACGGAGACACAAGCAGAAGCTCCTCAGAGACGCTCAGCAGACTAACACTGAGAATAAACTCCAAGTGGACCAAATCAAGAGTAAATCCAGAGAATTAATGACTGGAAGGACGCCTCGGTGGAGTGCGAGTGCGCAGGAGGACTGTGTGGACATGTTTGAGGAGTACTTCAGTGAGGACAACCCTGTGCAGACCTTGACTATTGATGATGTCTACGGGAAACATGCACCGAAAGACAAGTCCGATGTGCAGCTGGAGTGTGTGCGTGTGGACGCCGGCTGCTGTAAAAGCTGCAGTTCTGCTGATCTGGATAAAGGCATTGAGATCTCTCTGAGTGTCCCTTCAGCTGTAGAGCAGAAGAAAGCAGCTCCTCTGAATGACTGGGAGATCCCT[C/T]GAAACGAGAGCTCGGACAGCGCTCTGGGGGACAGCGAGAGCGAGGACGCAGGCCCCGATCTGCCCAGAGCGGACCCCGATGGAGCCTTCGACAGCGACTTCCAGGACGAGCTGGAGCTGCCGCTGCCCGGGTGAGTCTGATATTAAACTCTACATCATTTGCTGTATTGCAGTGCACACACACACACAAATATAAACATGTTGTGTCATATGACCCCTAAAGTACACACATGATCTTTGCAGAAGTGTGTGAAAGTGCTGATAATAAACATGATTGGATGTTTTGCAGGGCGAAGCTGGTGGAGAACTACTCTAAACCCAGCATCGCTAACTTCGGCAGGTCGTTGTTTGGAGGTTACTGCCCCTCATACGTTCCAGACTTCGTTCTGCAAGGAGTCCCCAACGATGAGAAGCTGAAGCAGAACCTGGTGTCCGACCTGGCTCACGCTGTGCAGGTAACCACTAAATGCACATTTCATCTGCTGTTGCCAGCCAGCTTAT
Associated Phenotype:
Not determined