Busch Lab

ZMP

dpp4

Ensembl ID:
ENSDARG00000079420
ZFIN ID:
ZDB-GENE-081104-277
Description:
dipeptidyl-peptidase 4 [Source:RefSeq peptide;Acc:NP_001154809]
Human Orthologues:
DPP4, FAP
Human Descriptions:
dipeptidyl-peptidase 4 [Source:HGNC Symbol;Acc:3009]
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]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa24096 Nonsense Available for shipment Available now
sa43788 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43787 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24096
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109596 Nonsense 130 742 6 26
Genomic Location (Zv9):
Chromosome 22 (position 11755014)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 11615182
GRCz11 22 11644864
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTTAACAGCTATGGAGACACACATACACTGCATCATATTCCATCTA[T/G]GACCTGGAAAAAAGGTTTGTTTACTAATGTATTTGATTAGGAATTGGTGT
Long Flanking Sequence:
TAGAAGTGTCTTGAAAAATATCTGGTAAAATATTATCTACTGTCGTGATGGCAAAGATAAAATAAATCAGTTATTAGAAATGAGTTATATATAAATATATATATATATATATTTATATTTATATTTATATTTATATTTATATATATATATATATATATATAAAATAAATATATAAATATATATATATATATATATATTATATATATATATATATATATATATATATTTTATATATATATACACACACACACACACACACACACAGTAGTCTTTTTTTGATCTTTTCTTTTGTTATCAGGCCCGTGTGGCAGCGTTTGATTATCTGGTGTCAGCCGATCGAAAATACGTCTGCTTTCTGAGCAACTACACTAAGGTAATCAATAAAATGCTTTGATGCTTAATCAATCATTAATAATCTGATGCTGTCCTCTAAATGTTTAATGACGACTGTCTCTTTAACAGCTATGGAGACACACATACACTGCATCATATTCCATCTA[T/G]GACCTGGAAAAAAGGTTTGTTTACTAATGTATTTGATTAGGAATTGGTGTATTGAGCAAAAAGTTTATTCTAACAAACTATTTGCTATGAATCTCTGTGTTGTGACATAACTATGGGGCCGTTTTGTTCAATGATTCTGATTGGCTGACGTACATTCTAAAGGTGTGCCATTATTTTCTTATAAACGCACAGCTACAGTAGTTTCAGGCAGATTTTGAGCCTTGATTAGAAAAACCTAACAAATGTCTTAAAGTACAACATCTGCACAGTGTCTTAGGGCGTGATAACTGTAGTATCATGTAGTATGTGCATTATTTTCAAATAATTCAACAGCCCGTCATCAGTTATTTCTTATTTTATTATCACTTTGTTTTAATTAAAATTGTCTAACTTGCTTTATTTCAGGGATTTTATAAATACAGATATCCCGCACGATGTCCAGTACTTAGCATGGTCTCCAACTGGCCACAAACTGGTGAGTATCTTATCAGTACAATACG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43788
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109596 Essential Splice Site 158 742 7 26
Genomic Location (Zv9):
Chromosome 22 (position 11754537)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 11614705
GRCz11 22 11644387
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGCACGATGTCCAGTACTTAGCATGGTCTCCAACTGGCCACAAACTGG[T/G]GAGTATCTTATCAGTACAATACGGTATCATGTAAGACTCATAAAACCTTA
Long Flanking Sequence:
TACACTGCATCATATTCCATCTATGACCTGGAAAAAAGGTTTGTTTACTAATGTATTTGATTAGGAATTGGTGTATTGAGCAAAAAGTTTATTCTAACAAACTATTTGCTATGAATCTCTGTGTTGTGACATAACTATGGGGCCGTTTTGTTCAATGATTCTGATTGGCTGACGTACATTCTAAAGGTGTGCCATTATTTTCTTATAAACGCACAGCTACAGTAGTTTCAGGCAGATTTTGAGCCTTGATTAGAAAAACCTAACAAATGTCTTAAAGTACAACATCTGCACAGTGTCTTAGGGCGTGATAACTGTAGTATCATGTAGTATGTGCATTATTTTCAAATAATTCAACAGCCCGTCATCAGTTATTTCTTATTTTATTATCACTTTGTTTTAATTAAAATTGTCTAACTTGCTTTATTTCAGGGATTTTATAAATACAGATATCCCGCACGATGTCCAGTACTTAGCATGGTCTCCAACTGGCCACAAACTGG[T/G]GAGTATCTTATCAGTACAATACGGTATCATGTAAGACTCATAAAACCTTATCTGTGTTGTCTTCAGTTAGCCAGTTAATGTCACATCATTGTTCGATAAATGTTTGACTTTGTGTTGTTAAAGTTTATTCTTTCGGCTTGATAAGCTTGTTTTGCTGACGGTGCTAATATAAAACTGTTACAGCTAATTGTTCCAAACTCCTAGCATGACAAAATGCTAGGAGCCCCCTCCTAGCCCCTCTCTTCTTTCTGTTTTTGAGTTCTTTCAGTTATATGTTTAATTGATTTAGTCAGAGATAATAAATAAAAGGATCAATGATGCTAACTTGACTAGTAGTAAGTTATTCGCTATCTGTAAACAGCCTTTTCATTAACAAGCTAATTATTAGCAAGTAGCACTGTAGCATGATGATACTGTTTGATCATGGCTCTAGTGAAATAGAGGTTTATATTGATAATATTATTATGTTTTAGATTTATAGCAGTGATATATTTTTAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43787
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109596 Nonsense 285 742 11 26
Genomic Location (Zv9):
Chromosome 22 (position 11750798)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 11610966
GRCz11 22 11640648
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAATGATCTGACCGAACAGAAGGATCTGTTTTGTTCCAGAGAGCACTA[T/A]CTGAGCACTGTCACATGGGCGTCAGACCACCGAATCGCAGTGCAGTGGCA
Long Flanking Sequence:
TGTACATTTTGATTCATGCAGACTTTAAAGCTACAGAAATTACTCTAAAACATCATTTAAATGACTCTTCTTCCCTGTAGAGGAAATGTTCTCCACAAATTCTGCTTTATGGTGGTCACCAAATGGGAGGTTTGTGGCGTACGCCGAATTTAACGATTCAGAAGTCCACAATATTGAGTACACTTGGTTTGGAGAAGGGCAATATCCAGAAACGGTGTTTGTTCCATATCCCAAGGTAAAAACCATCAAGATTTGCAAAACTAATGTGATTGTATGCAGTTGTTGACATTGCCGTTCATCTTCTCCCAAGGCTGGAACCCCAAACCCAACTGTAAAACTGTTTGTTTTTGATACAAACACAAACACCATCAAGCAAGTCTCGGTTCCCAGTGATGTTGGTGCCGGGTAAGGGGTTTTAGTTTTTTTTCATAGATGTTTTCAGTCAGATATAATAATGATCTGACCGAACAGAAGGATCTGTTTTGTTCCAGAGAGCACTA[T/A]CTGAGCACTGTCACATGGGCGTCAGACCACCGAATCGCAGTGCAGTGGCAGAAAAGAACGCAGAATTATGTCGTTTTGGAAACGTATGACTTCAACGATGGAAACTGGACTGAAGGTTCATTGGTATGTCCTTTTAATTTATTATAGACTGTTTTAGTTTTAGAGTCAGTTGGATTTAATTTTGAGTGATAAATATTACAATAACAATAAAATGTGTAGATTTTCTAGTGGATATTTTAAGAAATCTAATGAAGCAAAATCTATTTTTTGTTGTGTTTTATTTCAGAATTTTCAGATTTTTAAAATTTTTTATCCTTAATATAATAATAATAATAATAATAATAATAATAATAATAATAATATTAAAAGTCCAGCTATAAACATGTAAATTAGGAATCCTTCAACAAATCTTAATACAATTGGGATTTTACTCCATTCACTCACTCATTCTGTCACTCATTTAATTATTCCCTCATTTATTTACACATCCATTCACTCAT
Associated Phenotype:
Not determined