Busch Lab

ZMP

dnttip2

Ensembl ID:
ENSDARG00000057648
ZFIN ID:
ZDB-GENE-080513-5
Description:
deoxynucleotidyltransferase, terminal, interacting protein 2 [Source:RefSeq peptide;Acc:NP_00113925
Human Orthologue:
DNTTIP2
Human Description:
deoxynucleotidyltransferase, terminal, interacting protein 2 [Source:HGNC Symbol;Acc:24013]
Mouse Orthologue:
Dnttip2
Mouse Description:
deoxynucleotidyltransferase, terminal, interacting protein 2 Gene [Source:MGI Symbol;Acc:MGI:1923173

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa8878 Nonsense Mutation detected in F1 DNA Not yet available
sa27156 Nonsense Mutation detected in F1 DNA Not yet available
sa15115 Nonsense Available for shipment Available now
sa38678 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa8878
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050651 Nonsense 148 941 2 7
ENSDART00000146965 Nonsense 165 958 2 7
Genomic Location (Zv9):
Chromosome 8 (position 15797824)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 15243168
GRCz11 8 15280873
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAATCTTGCTCCTCGGCAGCATCAGCGACCCATTCCCRCACTGCCCCA[C/T]GAAGCCTCAGGAAACGAGTTTTGACTTCAGCTTCCGCAAAAGAYGCAGAT
Long Flanking Sequence:
GTATTGTCAGATTTTCATATTAAAGGTTAAGAAAACAAATGTTATGCTACACATTATGTACAAAAAAGGCATTTAAGTCACAAAGGTATGTAAATGAATTTAATACTAATGTAAGGCAAATGTTCTTGTTCTTACAGAAGCCTACTCCTTCGACTAGAAGAACTCGACGCAAGACACTGACGGAGGAAAATCAGTCCCAGTCGGATTCCCAGCCAGATGAGCCGAAGGATGACAGTACTGCCTCTTCCCTAGCAAGTCCACCTAAGAAAGACACTAGAAGATCCACACGTCTCACTGTTAACAAAAAGCAGCCAGACTCTACTCATGAAGCGGATGTTTCTGAATCAGAATCCTGCTGCTCTGTAGCTTCCGGTGTACAACCCACACCTAGAACCCGCCGAAGAACTGCAGTCAGAGACAAGCGCACCATTGAAGAGGAGGCATCCGAAGCTGAATCTTGCTCCTCGGCAGCATCAGCGACCCATTCCCGCACTGCCCCA[C/T]GAAGCCTCAGGAAACGAGTTTTGACTTCAGCTTCCGCAAAAGATGCAGATGCCTCTGGGGCTGAGTCTTGCAGTTCTGCGGTGTCACTCACCAAAGGTACGGACACTCAACGGATGACTAGGAGTCATCAAAAAACTGCTGTTCCCACCAGAGATGCAGATCAGTCTGAACCAGAATCATGTTCCTCCAGTGTTTCTGGCCTTCGTGGATCTGTGGTGCGCAGATCTACACGAAACCAGAAGGTGACAGTGACCGAGCCGATCCCTTTGAACTTAGAAGAAACTACAGACGCCCCTTCTTCTCCAGTGTCCAGGAAGCCTAGAGGGCGTAGGCGAAAAACAGAAGGTAATGATGATGAGTCTGATGGATGCAAGTCTGGTCCCAGCATGAGTCCCTGGAGATCCCTTAGGCGCCAGCCAAAAGGTGACACCATAGTTGGTGAATCTGATTCAGAATCGGTAGCTACTGACGTCTGCACCTCTCATGGGAGTCCAAGCCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27156
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050651 Nonsense 355 941 2 7
ENSDART00000146965 Nonsense 372 958 2 7
Genomic Location (Zv9):
Chromosome 8 (position 15798445)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 15243789
GRCz11 8 15281494
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGACGAGAAGTAAAGCTAAAGTGATTACTTCTGCCATGTCTGAGGAA[C/T]AAAGTGAAGATGAGCAACTTGTAACTCATCATGAAGGTATTCAAGCACCT
Long Flanking Sequence:
GGAGTCATCAAAAAACTGCTGTTCCCACCAGAGATGCAGATCAGTCTGAACCAGAATCATGTTCCTCCAGTGTTTCTGGCCTTCGTGGATCTGTGGTGCGCAGATCTACACGAAACCAGAAGGTGACAGTGACCGAGCCGATCCCTTTGAACTTAGAAGAAACTACAGACGCCCCTTCTTCTCCAGTGTCCAGGAAGCCTAGAGGGCGTAGGCGAAAAACAGAAGGTAATGATGATGAGTCTGATGGATGCAAGTCTGGTCCCAGCATGAGTCCCTGGAGATCCCTTAGGCGCCAGCCAAAAGGTGACACCATAGTTGGTGAATCTGATTCAGAATCGGTAGCTACTGACGTCTGCACCTCTCATGGGAGTCCAAGCCCTCAAAGAGGAAGAGGAACACCTTGTAGTAGCCGAACTGGGTCTGCAAGCAGCAACCGTGCTGTTCCTGCAAGCAGGACGAGAAGTAAAGCTAAAGTGATTACTTCTGCCATGTCTGAGGAA[C/T]AAAGTGAAGATGAGCAACTTGTAACTCATCATGAAGGTATTCAAGCACCTGAAGAACAACTGGATCAAACCATGACCATGGAAACCAGTGAAGCTCAAGAGAGCACCATGATTGAGGAGGGAGCTGAAGATACTACTATAGTTGAGGATGAGCCTGTTGAGATGCTAGAAGTTCAAAGCAGCTCAAAAGAAGTCAAGAAGATAGAGGATCATGGAATTATCATGAAAGAAACAGGAACTGAAACTTCATTAAAGGAAGCCGAGTTTATGGAAACACTTTCAGAGTCCGTAGTAGAAGCCACCTCAAAAGTCCCAGAGAAGGTTGACGAGGCCATTGAGGATCAAACATGTGCTGAGCCTGTAAAAGAGGATGCCATTCATGAAGATGCAGTCATGGTTGAGGATGCTTCTGAGCCTGAAAAAGCAGGATCCAACCAAAAAGATACAGAGATGATTGAAGTTCAAACATGTCCTGAACCTGCAAAAGAGGAAACAACTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15115
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050651 Nonsense 691 941 2 7
ENSDART00000146965 Nonsense 708 958 2 7
Genomic Location (Zv9):
Chromosome 8 (position 15799453)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 15244797
GRCz11 8 15282502
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGGCTCATGGTAATGGACTGTTTGTCATAGACACTAGACCTGGGCTA[C/T]GACCTGAAGACCAGTACTATGTGGATGCCAAGCAAACTGAGGAAGAGGAT
Long Flanking Sequence:
CAGTCATGGTTAAAGAGGATGCAGAGTTTCAAACATCATTAGAGCCCTCAAAAGAGGAAACCATCCAAACAAATGTAGCCCTGATTGAGGAGGCTCAAACATCAGCTGAACCAGCGGAAAAGGTAAAAGTCACTTCAGACGATCCAGAACCAGCCGTGATCGAGGAGAAGAAAGGTGTGACGGTTACAGAGGAATCAAATGAATTGATTAAGACAACTGATGATGACTCTGATGCTGGCCCTTCTACAAGCTCAAATACTCGAGTAGATTTGAGCACCGCAGAAGAATCATCCAAGGAGCACCCTGCTCAAAAAGAAATGATCAGTTTACTGGACAGCAGTGATGAAGAAGATAGTGGTGACGAAGGTCTGTCTGCAGAAGAAGAGGGCGGTTCACAGGAAGATGAAGATGATTTAATTTGTCCTGATGATGAACCGATGCCAGAAGAAGCAGAGGCTCATGGTAATGGACTGTTTGTCATAGACACTAGACCTGGGCTA[C/T]GACCTGAAGACCAGTACTATGTGGATGCCAAGCAAACTGAGGAAGAGGATGAGGAGGAGGACTATGTTGACGAGGAAGGAGATGATGAGGATGATGAAGATTCAAAGGTGCTTTTTGCTCCCAAAAAGCCTCTGTAAGTTATCGCCACTATATAAATCACAATATATGAAAAAAAAAGATATTTGAAATGTGATTTTGTAAATTATGATTTGTGAGCGATGATTTAAATTTAGTATCAAAACTAATTTTTTTCTCTCCTTCTCAGGATGCAACTCTCTACTTCCATTGACACGGGTTTGAAATTGAAGGAGCTTGGTGGTTTGTACGTCAGTTTTGATGGCAACAAACCAAAGACTCTTTCCAGGGTCTTGAAGGCCCAGAAGGACGTGGGCGGTCAGGATGAGGTAAATAAGTTGCGCATTTTTCTGGATGAGACATTTGATTGTATATAATTTCAAAGAGTTTTGTGCAGCTAATAATAAATTAAAACGCTGAATGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38678
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000050651 Essential Splice Site 905 941 6 7
ENSDART00000146965 Essential Splice Site 922 958 6 7
Genomic Location (Zv9):
Chromosome 8 (position 15802717)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 15248061
GRCz11 8 15285766
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAACGTACCATTGTGGAGGAGCTTCTTGCTGATGCTGAGTTTAGAAG[G/A]TATGTTGGAGAAACTGTGGCTGATTAGCTTTATGTGGAGGAAAATGTGAT
Long Flanking Sequence:
TTTTATATATTGTATCCAGGCGGAAAGAGAAAAGACGACTGGCGATGGCTGGTTCAACATGAGAGCTCCTGAATTAACAGAGGAGCTGAAAAATGACCTGAAGGCACTGAAGATGCGTGCAGCCATGGACCCCAAGCGCTTCTACAAGAAGAATGATAGAGAAGGCTTTCCAAAGTACTTTCAGGTAGGTTACTTTTTTTTTTATCATCAGCAACAGACTGTTCTTCTTTCCTCAAACAACTTTTTGATAAGCCATTGTTTCTAAGACAAAAAACAAAGAATGGTAGCATCAAAATACCCCAATTAACCGCAGCCTTATGTGTTTAAAGGTAGCAGACAATGACACATTATTCGGTTCTTTCTATTAAAGTTTGGCTGTTTTTGTTTCAGGTTGGCACAGTGGTTGACAGCCCTGTAGACTTTTATAATTCACGAATGGCTAAGAAACAAAGGAAACGTACCATTGTGGAGGAGCTTCTTGCTGATGCTGAGTTTAGAAG[G/A]TATGTTGGAGAAACTGTGGCTGATTAGCTTTATGTGGAGGAAAATGTGATAAATTATTTGTATTCCTGACAGCGGGCTTTTTTTATCGATTGTTCTCGCTATTGTTTTAAATGAACTGTCATGTTCTAAAATGCATCTTTTCTTCTCTTTTTAGCTCTAATAAAAGGAGATATCAGGAGATCATGGCAGAAAAAGCAGCACAGGCCGCTGGAAAGCAGCACAGAAAGAAGCACACAAAGTTCTCTAAAAAGAAAACAAATAAATAATTTCATGAGGCAAATCAGATTATTTTTCCCTCTTATGTTTTTTTATTTTTAATAAAAAAAAAAACATTTCAAGAGATTGTCAAGCTTTTGTAAATAGAAGCCCACCATATTTTGTTTTAGTAAATTTCTGAGAAGGTTATTTTGGTATTAATGTGCAACTTGTACAGAGAAAGTAAAGAAGATTTTATACTTTTTAAAGGTTGACTTTCACTTGGCTTAAGATTACGTCGAGAA
Associated Phenotype:
Not determined