ZMP
si:dkey-81j5.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate dipeptidyl-peptidase 4 (CD26, adenosine deaminase complexing pro
Human Orthologues:
DPP4, FAP
Human Descriptions:
dipeptidyl-peptidase 4 [Source:HGNC Symbol;Acc:3009]
fibroblast activation protein, alpha [Source:HGNC Symbol;Acc:3590]
fibroblast activation protein, alpha [Source:HGNC Symbol;Acc:3590]
Mouse Orthologues:
Dpp4, Fap
Mouse Descriptions:
dipeptidylpeptidase 4 Gene [Source:MGI Symbol;Acc:MGI:94919]
fibroblast activation protein Gene [Source:MGI Symbol;Acc:MGI:109608]
fibroblast activation protein Gene [Source:MGI Symbol;Acc:MGI:109608]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21604 | Essential Splice Site | Available for shipment | Available now |
sa15641 | Essential Splice Site | Available for shipment | Available now |
sa1475 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21604
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 |
---|---|---|---|---|---|
ENSDART00000109832 | Essential Splice Site | 255 | 753 | 8 | 25 |
ENSDART00000132896 | Essential Splice Site | 251 | 750 | 9 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 52584327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 51706639 |
GRCz11 | 9 | 51238062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATGGAAATGACCAGTACCCAGTCACAGTATTCGTCCCCTACCCGAAAG[T/C]AAGTAAACATCCCAGCATTTCAGAATGTCTAGTGTCACTACTGCCTGAGC
Long Flanking Sequence:
CAGCTTAAAGGCTTAACTAGGTAATTAGGCATGTCAGGGTAATTAGGCATGACATTATACAGCGATGGTTTGTTCTGTAGACAGCTGAAAAATAAATATTGCTTAAGAGGGCTAATACTATTGACCCTAAAATGGTTAAAATATTAAAAACAGCTTTAATTCTACCCAAAATAAAACAAAAAAGACTTTATCCAGAAGAAAAAAAACATAGGAAATACTGTGAAAAATCCCTTGCTCTGTTAAACATCATTTGGGAAATATTTGAAAGGGCTAATAATTCTGACTTCAACTGTACATTCATTCATACCTGCTAATCTATCTGTTTCTTTTCTCTCTCTCTCAAGAGGAAGTGTTTGCCTCCAATGAAGCCATCTGGTGGTCTCCGCAGGGCAAATATCTGGCTTACCTACAAGTTAATGACACTGGAGTTCACAGCATTGAATATTCATTGTATGGAAATGACCAGTACCCAGTCACAGTATTCGTCCCCTACCCGAAAG[T/C]AAGTAAACATCCCAGCATTTCAGAATGTCTAGTGTCACTACTGCCTGAGCGATACGTGACTGTCACACATCACAATAAGGCTTCAATAGTAAATGTATTTACTAAGTACTTGAACAGCATTTATGAACCATAGTTCAGCATTCACTAATTCCTAATTAACATCAAAATCCATGCTTGTAAATGCACCATGAGTTGACATGAACTAACAATGAAAAACTTTACATTCATTAACATGAACAAATACTGTAATAAATGTATTGTTTATTCATGTTATTAAATGACAATAAAAATTCTTCCTGAAATTAAATGACAATAAAACTGAACTTTTACTTATAGGTACACAATACACTTTAAATAAAATCACATAACTTTTCCATTCCCACAGAGGATTCTGTCATTATCTCCTCCCTTGAGGTTAAGAGTCTGGGGGTCATCTTCGACAGCACCCTTTTATTCACTGCACATGTTAATAATGTCACCCAGTCCTCCTATTTCCACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15641
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109832 | Essential Splice Site | 536 | 753 | 19 | 25 |
ENSDART00000132896 | Essential Splice Site | 532 | 750 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 52601168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 51723480 |
GRCz11 | 9 | 51254903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTACANATTATTTCTCTGCTATAGCTGTGTTTTTCCACTGTCACATTAA[A/G]GGTATGGTGGTCCAGCCAGCCAGAACATAGACTATGTGTTTCGCTTGGAG
Long Flanking Sequence:
CAAATACAAATACCGGCTGCTCCGCACATCCCTAATATATATATATATATATATATATATATATATATATATTCGACCTTTATGTGTTAATTTTAAGTCTTAATTTGGCAACAACCTTCTCTGTGTTTCAGCAAATGGAATGATTTTTGATGTTAAACCTTATTTTGACACGTATTTTGGGAAATTGCTTTGAAAATGTTCACTAATTCAAAACACTCTGGACAAATTTACTACACTTTCATCATGTTGTTAACAGTTTATGCCCTATTTTCTTCCATTATAAATGACATAAGCCCACCTCATTCCCAACACAATCAAGAATGCATTATTATATGCTGTCTTAGCTTTTCAATAAAAAAAAAAATAGTTGTAATGCAAGTCAAAAACATAATGAAAGGGTAGTCAATTTGAACAGTACACAAGGCTTAATAAATGATATATGCATGCAGTTATTACAATTATTTCTCTGCTATAGCTGTGTTTTTCCACTGTCACATTAA[A/G]GGTATGGTGGTCCAGCCAGCCAGAACATAGACTATGTGTTTCGCTTGGAGTGGGCGACGTACCTGTGCAGCACCGAGAGGATCATCGTGGCCAGTTTTGACGGCAGGGGAAGTGGTTTCCAGGGGGATGAAATAATGCACGCCATCTACGAGCGGCTGGGGACGTACGAGGTGGAAGATCAGATCACGGCCGTGAGGTGAGGCGGAGGGAACGATGTGCACACGCTCATGCTGATCCACAACCATTTAACCTGACGTAACATTTACAGACAGATCAGAGATACCAGTCCTGTCCGCTTCCTGAAAGAGAAAAAAAAGAGAAAGTGTCATGGGGAATCTGTCAAAAAGAGGTTGATGAAGGACAAATGCTAGACAAGCTGACAGATTTTCATGACAAATCATCATCTACAAAAGATGTTTGGTTTATAAGAGTTGTTTTGTAATTGCTTTGTGCGTTTCATTTCAGAAAGTTCATTGAAATGGGTTTCATTGACAAGGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1475
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 |
---|---|---|---|---|---|
ENSDART00000109832 | Essential Splice Site | 696 | 753 | 23 | 25 |
ENSDART00000132896 | Essential Splice Site | 692 | 750 | 24 | 26 |
Genomic Location (Zv9):
Chromosome 9 (position 52604954)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 51727266 |
GRCz11 | 9 | 51258689 |
KASP Assay ID:
554-1400.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAAAYTTCAAGTCGGTGCAGTACTTGCTGGTGCACGGCACTGCAGACG[G/A]TAACTAATTAAATACACATCTGAGAGCAGACAAAACAGCAATGTACAGTA
Long Flanking Sequence:
TGGACTATATTTTGTGGGATTTGATTGGATATTCATGTGTTGACAGATGTGAGTGATAGATTGATCCCGCCCCTCACACCAATGAACACCAATCAGTAAAGAGATGCTGTGGGAGGGGAAGTTATATAAAGATCATGAGGACATGAACTAAAATAAAAGCACACAAATGAATCCCTTATAATAAACACTGCCATATTCTGTTAAAATAGTTATTGAGGCCATGATTTCATTGTGATTTACCAGAAATGGTTGTGCAGTCTTAACTCAATCCAACTACATTTTCACAGATGCCGTTTACACAGAGAGATACATGCATCGCCCTCAAGACAACTTTGAAAGTTATAAAGTAAGTTGACCTGTAAGAAAGCACATGCCTGATTTCAGAACAGTGCTTATTATAGCACTTCATATATTTGTTTGTTTCCAGAATTCGACAGTGACCGACAGGGCAAAAAATTTCAAGTCGGTGCAGTACTTGCTGGTGCACGGCACTGCAGACG[G/A]TAACTAATTAAATACACATCTGAGAGCAGACAAAACAGCAATGTACAGTATCATTTTTTTTTTATTAGAATATGCAAAAAGGTACATAAATTGGGATCATACAAATACAAAAAACATCAACAAAAAACCATAACAAAACAATTAAAAAAAAAAACAAAAAAAACAATATAGTCAGGTACAGTAAATGAATCTAGTCTCGCAGATATAAGTAAAACAGATACAGAAGAAACCAGTCAGAGTTAGGGAGTAACAACTATGTTTAGTAATGTATAATAGAAATAATGACAGTAAAAAGAAAGAAAGGACAACAGTAATAATAAATGACAATGATAATAAATCACAAGTACTACCCTAACTACTACTACTGCAGAAAGTTACTTATATTACTATATAATTATTAACTACTATTGCTGCTACTACAATCACAACCACAACTATTACTATAATGTCTACTACTGCTGATACTACCACAACAATGACTACCACTACTGATACTACAG
Associated Phenotype:
Not determined