ZMP
ctsf
Ensembl ID:
ZFIN ID:
Description:
cathepsin F [Source:RefSeq peptide;Acc:NP_001071036]
Human Orthologue:
CTSF
Human Description:
cathepsin F [Source:HGNC Symbol;Acc:2531]
Mouse Orthologue:
Ctsf
Mouse Description:
cathepsin F Gene [Source:MGI Symbol;Acc:MGI:1861434]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28260 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17667 | Essential Splice Site | Available for shipment | Available now |
sa35632 | Nonsense | Available for shipment | Available now |
sa22423 | Essential Splice Site | Available for shipment | Available now |
sa42345 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa28260
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129898 | Nonsense | 79 | 473 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 7164596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6834948 |
GRCz11 | 14 | 7141357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACGCGATGCATATACGTCGTGTCAGCAAAATCCTTTCGGCCAGCAAA[C/T]AGGTAACGTTAAATAAAAAATAATCCCTTAGAATTTCCGATTAACGTTAG
Long Flanking Sequence:
ATAAGATGAAGTACGTTTCAATAAATGAATGTTAAAGCTGCTAGTCGTTAAATATCAACACACAGCCTGAGGTGCATCAGTCCTCCATCTTTATGCGGGGCACCATCATCATAACTGCGTCTTTCAGGGCGTCCATCTTTATGCGGGGCGCCTCACACCGACTGACACTGTGCCGTGTGGAGCATCAAAACACTGCGAGTTTATAATCTGAACACAAACCTCTGCTGATCTGACGTCGCTGCTTTTTGTCCTGAAAGCTCGACAACATGTACTTCAACCGCGGTTACACCGTCATCGCCTGCTGGGTGTTGGTCGGGTTGGTTCTGGGTTTAGAAGATGGCCCGGACCGCCCGGTTATCGGAGCTCCAGGATCGCCGGTCCGTCTGTCGGATTCTGACCCGGGGGTTATGAAAGCAGTAAAGTTCGCCGAGGAACGATATAATATGGGCTCCAACGCGATGCATATACGTCGTGTCAGCAAAATCCTTTCGGCCAGCAAA[C/T]AGGTAACGTTAAATAAAAAATAATCCCTTAGAATTTCCGATTAACGTTAGTTTAATTGATATATAACCACATTTAGTATTTTGTCGATACGTTTAATTTGTATTTAATCTAATTATTCATTATACACAACAACGATTTGCATAATATTGGACATTAAGTTTATTATAAGGAGTTATTTTAACCGCTTTCACGTGATTAAACCAGACGTAAACAACCGCAGAGGCCTCACATACGTAACTGCTGAGCGGATTTAAGCAGCACAACACTGCGTGCCTTTTGCGCAGACGCGGAGTACATCTATTTATATAATAGCCTACTGTTATTTTTGCAGCTTGTGTGATTTAATCTGTTACAAATGTTTTTAGTTATATGAATTATTAGAAAGTGATCTAATGTATTAAGAGTCTTAAAGTATGACGTTTAACTCTTCTTTAAAAAGCCCAGAAAGATAAAGTGCTCTGATAAACAGTATCAGCTTTGCACATCAGTTTGCAGTTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17667
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129898 | Essential Splice Site | 79 | 473 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 7164593)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6834951 |
GRCz11 | 14 | 7141360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGCGATGCATATACGTCGTGTCAGCAAAATCCTTTCKGCCAGCAAAYAG[G/A]TAACGTTAAATAAAAAATAATCCCTTAGAATTTCYGATTAACGTKAGTTT
Long Flanking Sequence:
AGATGAAGTACGTTTCAATAAATGAATGTTAAAGCTGCTAGTCGTTAAATATCAACACACAGCCTGAGGTGCATCAGTCCTCCATCTTTATGCGGGGCACCATCATCATAACTGCGTCTTTCAGGGCGTCCATCTTTATGCGGGGCGCCTCACACCGACTGACACTGTGCCGTGTGGAGCATCAAAACACTGCGAGTTTATAATCTGAACACAAACCTCTGCTGATCTGACGTCGCTGCTTTTTGTCCTGAAAGCTCGACAACATGTACTTCAACCGCGGTTACACCGTCATCGCCTGCTGGGTGTTGGTCGGGTTGGTTCTGGGTTTAGAAGATGGCCCGGACCGCCCGGTTATCGGAGCTCCAGGATCGCCGGTCCGTCTGTCGGATTCTGACCCGGGGGTTATGAAAGCAGTAAAGTTCGCCGAGGAACGATATAATATGGGCTCCAACGCGATGCATATACGTCGTGTCAGCAAAATCCTTTCGGCCAGCAAACAG[G/A]TAACGTTAAATAAAAAATAATCCCTTAGAATTTCCGATTAACGTTAGTTTAATTGATATATAACCACATTTAGTATTTTGTCGATACGTTTAATTTGTATTTAATCTAATTATTCATTATACACAACAACGATTTGCATAATATTGGACATTAAGTTTATTATAAGGAGTTATTTTAACCGCTTTCACGTGATTAAACCAGACGTAAACAACCGCAGAGGCCTCACATACGTAACTGCTGAGCGGATTTAAGCAGCACAACACTGCGTGCCTTTTGCGCAGACGCGGAGTACATCTATTTATATAATAGCCTACTGTTATTTTTGCAGCTTGTGTGATTTAATCTGTTACAAATGTTTTTAGTTATATGAATTATTAGAAAGTGATCTAATGTATTAAGAGTCTTAAAGTATGACGTTTAACTCTTCTTTAAAAAGCCCAGAAAGATAAAGTGCTCTGATAAACAGTATCAGCTTTGCACATCAGTTTGCAGTTCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35632
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129898 | Nonsense | 284 | 473 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 7152279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6847265 |
GRCz11 | 14 | 7153674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTGCTTAATGTGTTACATGTTCTTTTACAGGGGATGTGTGGCTCTTG[C/A]TGGGCATTTTCTGTGACTGGAAACATCGAGGGACAGTGGTTTAAGAAAAC
Long Flanking Sequence:
GTAGTACACAGCATGTTACTGCAATGTTTACAGTGCTCGTCCTATACTTCCGGGTTTCTTCCCACCGCAGCCTCGCTTTGGTTCTTTAAAATGGCGGCCGCGTGAAATAAGTGTATAGCCTCATCCTAAATGACTGATAGCTCCGCCCTAAAGGTATTCCATGTGACCTGAAGTAAAGAAAATTGGTTTCGAGGGGGCAGGGAAGGTTATTGTGTTTGATAAAAGCCTGTGAGGGCAAATTAATTCATAACAAGCACTGTTTTATACATATAAAAATAAGGAGAGGCCAAAATAAAGGTACCAAAGAACAGAAATGGACTTTTATGATGTACACTTTGCAGCAGAACTTATCAAAATCTGAATAAGCTTGTATGTGATGATAAATTAAATGCTTATAAAATTAGTATCATGAAGAGCAATGTGTAAAGTGTGATATTTGTGATCAGTTTTGTTGTGCTTAATGTGTTACATGTTCTTTTACAGGGGATGTGTGGCTCTTG[C/A]TGGGCATTTTCTGTGACTGGAAACATCGAGGGACAGTGGTTTAAGAAAACTGGACAGCTGCTTTCTCTTTCTGAGCAGGGTATAAACAAAGTTTAGCTGCTAATGCACTTAAGAAGCTGAATGTGCTAGCTAAAGGCTAAACAAAAACATGAAACATGCTAATGGATGTTATCAGCAAGCTTTAACGTGCTATACTTGCTGGAAACATGCTAGTAACATTACAATTCATAATAGCCTTAGGTTGAAACAATGATGGAAATGTGCTAATTCATGTTAACAATTTGTTATCCAGGCTAAGAATCTGCTTGCAACATAGTGATTCAAGTTAACGATGTGTATGCTATATTGGAAACATTCTTAGAATGGGAACAAAATGGTAATCATGTTAGGAATGTGTTTGCAACATCAAATAATGGTAGCAGAATGCCATTTTATGCTAGCATATTGTTACATATGCAAAAACATTGCTAAATGCTAACAACATGTTCAATCTTGTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22423
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 |
---|---|---|---|---|---|
ENSDART00000129898 | Essential Splice Site | 378 | 473 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 7150001)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6849543 |
GRCz11 | 14 | 7155952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCCGCCTACATTAACAGCTCAGTGGAGCTGCCCAAAGACGAGAAGGG[T/C]GAGTGAAAACACGATATGTGTCAATAAACTTAATTAATTGAAGAACACAT
Long Flanking Sequence:
AACAATTTTGAACAATAGTGTGTTTCTTTCTTAGAAACAACTGATAAAGTGTGAGAAAACAAGCTAAGTTTTGTTCACACTGCATCATTTGAGATTTATTCATGTCCTTCATGAATAATATCAGATGAAGGCTGTGCTGTAGCATACACATGAAGTATTCTGAACCTAATTGATCAAAAATGTATATTCATTAGTTTGTACTCCTTCTCATCACAGAATTGGTGGACTGTGATAAGCTGGACCAGGCATGTGGAGGTGGGCTGCCATCTAACGCTTATGAAGCCATCGAAAACCTTGGTAAGGCATTTTTAAGCTATGTGGAATCTGTGAGACTGAATAAACGTGCCATTTAAATGTGCTTTCTTTCTTGCCTATGAAGGAGGTTTGGAGACTGAAACAGACTACAGCTACACTGGACACAAGCAGAGCTGTGATTTCTCCACAGGGAAAGTGGCCGCCTACATTAACAGCTCAGTGGAGCTGCCCAAAGACGAGAAGGG[T/C]GAGTGAAAACACGATATGTGTCAATAAACTTAATTAATTGAAGAACACATTAAATCAACACTGATAATGGGAATACCTGCACTAGAGAAAATGAACGCAGGAAATTGAAAATATCAAATATTTATATCAGAACGTCTGGAGAGAAATGTGAGCGATAAGTTAATCTTTCTTTAATGGGAATGTAGATTAATACTGCACACCAAGTGTTATAGAAATAAATATTATACCCATCAAATTTTGGGGATGGTATTATTTTCTATGGTATTCACTAAGGCTTTTATTTTAATAACAAATTAAAGCTAAATAATATATATATTATTATAATTTAATCATTTAGAATATCATTTATTTCTGTGATTTTAAGTTGAATTTTCAGCATTATTACTCCAGTCACATAATATCCTATGCCGTTTAGAATCTTACTGACCTTATACTTTTAAATAGTAGTGTATTTTTTAAATCTGTATTTTAATTCTTGTATTTTTATTTCTCCTTACCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42345
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 |
---|---|---|---|---|---|
ENSDART00000129898 | Essential Splice Site | 429 | 473 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 14 (position 7147676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 6851868 |
GRCz11 | 14 | 7158277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACCCGAGGATGATTGATCACGCTGTGCTGCTTGTGGGATTCGGACAAC[G/A]TGAGTTACATTCACTTAGGCCCCGTTTACACTAGTTCGTTTTAGTTTTAA
Long Flanking Sequence:
ACCATGACTTTATTTTCTATACTGTACATTATTTCTGTTTAGTGACAAGACTTTTGTCTAAGCAAAGTCAGACCTTACTGTCTTAATTAAACAATAAAAAATCAAGGCCTGATCATATTTTATTTAGGTAAAATTAGCATAATCTAGAGGCCTTTGCCTTTCATATAAGCCACTTCTGATACCAAATGATCAACTAGAAGTCAAATTATTATTTGTTGTTCATAAAACTTGAATAGGTGACAAGACATTTGTCAGGTGGTGTAATAACGAATAAAATAAACAAGTTTAAAAGCAGCAGCACAAGTTTGCGATGCAAAAAAAAAAAAGTCTCAAATCTTTAAAAAAAGTCTCAATCATATAAGTTGTGCAAAATACATTCTAAAGTCTCTTTTGTTGCATTGCTGTTTAGTTCTACAGAAAAGGAGTTTCTCATCCTCTGAAGATCTTTTGCAACCCGAGGATGATTGATCACGCTGTGCTGCTTGTGGGATTCGGACAAC[G/A]TGAGTTACATTCACTTAGGCCCCGTTTACACTAGTTCGTTTTAGTTTTAAAACGGCGTTTTAGAATGAAAACGATCCGCGTCCACACTAGCGTTTTACCCAGCGTTTCTGAACAGCTCTCTGTCCACACCGAAACACGCACTCTGGCATGCGCTGCAGCCTATCTACCCAGATGAGAGCTGTGTTTGTAGGATCTACCGCTGGATCTAATCTCACTATATTTGTTAAACGTGATATTTTAATCATCTTTATTTCTATATCTAACAACATTTACCCCGACTTTGGCTTTTTTAATCTATTACTTGTTCTCAGGTAACGTGTTTTGGCTGAGCGCAAAGATAAGTTAATAATTAATGTAACCACGTACATTCTGTATATCGAGTAATTGCTTGCCTTTATTTCCTATAATGTATAAACTTATTGTACGTTACACTTTTATAAAGGCCATTATCGAATATTAAAACTGATATTCAGCAAAAGAGAGGGTATGTTTCGGATTTT
Associated Phenotype:
Not determined