ZMP
si:ch211-42i9.8
Ensembl ID:
ZFIN ID:
Description:
folliculin interacting protein 2 [Source:RefSeq peptide;Acc:NP_001139090]
Human Orthologues:
FNIP1, FNIP2
Human Descriptions:
folliculin interacting protein 1 [Source:HGNC Symbol;Acc:29418]
folliculin interacting protein 2 [Source:HGNC Symbol;Acc:29280]
folliculin interacting protein 2 [Source:HGNC Symbol;Acc:29280]
Mouse Orthologues:
Fnip1, Fnip2
Mouse Descriptions:
folliculin interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:2444668]
folliculin interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:2683054]
folliculin interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:2683054]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10994 | Essential Splice Site | Available for shipment | Available now |
sa15502 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10994
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 |
---|---|---|---|---|---|
ENSDART00000112490 | Essential Splice Site | 352 | 1083 | 13 | 30 |
ENSDART00000138276 | Essential Splice Site | 348 | 897 | 11 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 18530186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19095354 |
GRCz11 | 1 | 19788291 |
KASP Assay ID:
2259-0449.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTCTTTTCGAGTCTCACATGAACAAACTCAAGACTGCCATCGAGAGGG[T/C]GAGTKTGAAAGCGCAGGACAGTGATTTATTATAGCAGCCTTTGTAGGAGC
Long Flanking Sequence:
ATTACAGCTATTGAAAAAAGAAAAAGAGAGGTATTATAATGTAAATATACAGTTAATCAAATTCCACTTCTCCATTGTGTAGCATCTCTGAGCAGTTTGCTGGCCACCCCGCAGCCTTCACCTGGCTCTTCCTTCAGCAGTGGCTGTGCCAGCAGCTACCAGCGCCGGTGGCTCCGCAGCCAGGCCACCAGTCTACAGCATGGCCCCATGCCCCGCTGGTGAGTTCAGTGATACACAAGAAACCAGTAAGAAATGGAGAAGCCAGATTAGATGTAGTTGTGTATGTCCGTTCATCAGGAACGCAGAGGAAATGTTCAACCTGTCTGACGAGAGCTGCAGCTCCAACCCTGCCATGATCCGGAGGAAGAAGATTGCCATCAGCATCATCATCAGCCTGCCGGAGCGAGAAGAGGAAAATCACAACTTTCAGGAGTTTTTCTTCTCCCACTTTCCTCTTTTCGAGTCTCACATGAACAAACTCAAGACTGCCATCGAGAGGG[T/C]GAGTGTGAAAGCGCAGGACAGTGATTTATTATAGCAGCCTTTGTAGGAGCAAGTGTTGTAGGGTTTCATCAGAATTCATAATCAGAATTTAAAATTTATTATTGATTTGTAAAGGTAGGTATAGGCAAAACGTGACAGAAAAAGGCAAAAAGTGTTGTGAACAGTCATTATGTTGTTATTTGCAGGCTGAAAAAAACAAGCAACTAGGCTGATATTAGACTGAGACACCATCTTTAGAATGACTTCTTTTAAAATGACTGAATTCGCCAGCAATGCAGCATTGTTGCTTTAAAACTGAAATGCCTTCAATATGTTCTGAATAAGATTTTGACTCACTAAAAATGCAAGTAGGTTTGCAAGCATCAGAACAGTGTGTCAAACTAACTGTCGTTTTGTGTTTTTTTTTAACATACAATAGAATTTTCCTGATTATATTTTTAAATGTATACTTTTAATTACATTTATACTATGGTTTACTAAACACAAGCACTAATTACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15502
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 |
---|---|---|---|---|---|
ENSDART00000112490 | Nonsense | 609 | 1083 | 17 | 30 |
ENSDART00000138276 | Nonsense | 605 | 897 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 18538124)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19103292 |
GRCz11 | 1 | 19796229 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACCAATACACCYACYGGTCTAGAAGCGAGCAYGGTCAGGCCTGAATG[T/A]ACTGAAATGGGACCGGAATGTTTTGGAGAACACGTCGACTCTGTTGGAGG
Long Flanking Sequence:
AAAAAGGACAGAATAGGTTCCCTTACAAAAATGAAAAGTACAGTACTGTACAAATAAAAAAGACAAATTCAGAGAGTTACCCTGTTTGTGTTAACCAGTCTCATTATTGTATGCTGTTGTTTGTTGTCTTGTTTAGGTGACCTGTACGGAGCTTTGGGCTCTCCGGTGAGAGTGTGTCGAACGGTGGTCGTGGGCCGCAGAAGGGAGCTGGTACAGAGGGTCTTGTATATTCTCTCCTACTTCATTCGCTGCTCGGACCTGCAGGAACATGTGCAACCACAAGGACAAAAGGACAATCCAGCCAATCCCTGCACCTCTCCAACCACTGACCCCAACCCTGCCAGTGAGAGAATCTGCGAAAAAACATTTCCCCCTCCACCAGACACAATAAAGCCCATTCCAGGCACCTTTATGGAGCAAAATGACGAGACTGTTTCAGCAGATACACACTCAACCAATACACCCACTGGTCTAGAAGCGAGCATGGTCAGGCCTGAATG[T/A]ACTGAAATGGGACCGGAATGTTTTGGAGAACACGTCGACTCTGTTGGAGGTGGATTAGAGCATATTTTGGCAAATCAGAGTCCTCTTCCACAAAGGGTGCAGTTTCACATTGGCAGCCCCAGAGAGGTGGAGAATGTGGGACAGGCTGGGGGTTTGATGTGTGGAGGGCAAGGGTTGGACAGGAAGTTGCATCAAAGGCTTTTGACGGACATAAGGAGGAACGAAAGTTCGGATAGTGCTCTAGGTGACAGTGATGATGAGGAAACATCATCGAGAGAAATGTACATGGCCGCTGAACAAACAGAGTACGAGTTACCACTACCAAGGTAAGCTAAACTCATTTTATTATGAACCCTCTCTTAATATAAACACGTATTTGCCATCTCCAAAAACAGCATTGAACTTGAAACATGGTTTCCACAAATATATGTTGTCAAACAAACAAATGCATTTGAAACCTGACTGTGCACATCTACAGGACAGCGCTGCCTATTTGGTGT
Associated Phenotype:
Not determined