ZMP
dph1
Ensembl ID:
ZFIN ID:
Description:
Diphthamide biosynthesis protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q567W6]
Human Orthologue:
DPH1
Human Description:
DPH1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:3003]
Mouse Orthologue:
Dph1
Mouse Description:
DPH1 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2151233]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35893 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1222 | Essential Splice Site | Available for shipment | Available now |
sa16246 | Essential Splice Site | Available for shipment | Available now |
sa32037 | Missense, Nonsense | Available for shipment | Available now |
sa22651 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35893
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080740 | Nonsense | 128 | 381 | 4 | 11 |
ENSDART00000110408 | Nonsense | 143 | 439 | 4 | 12 |
ENSDART00000140214 | None | None | 51 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 25324719)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26054647 |
GRCz11 | 15 | 25989912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCCCGCGCTTTGGGAGCCGACTTCATGGTGCATTATGGGCACAGCTG[T/A]CTCAGTGAGTCAAACAGAAATGCGCAATCATTATTATGTGCATTTGCTTT
Long Flanking Sequence:
AGCACTTGCAAAATTTCAACCTCTAACCTTTCGGCCTCCAGCATACATTGTGCATTTGTTGGACAGACGGTATGCAACCATAGCTATTAACCTCAGCATGGAAAAAAGTGACCCTTTGCTACCATAAGTGAACATTTATGTTAATAGTAGCCCATTGCTCTGTTGTCTCTGAAGGTTATTGGAGATGTTTTGCCAGAGTGCATCAGTTTACGGCTAGCGGGAGCCCACTTAACTGGAGACATGGATGTCTGAGTGACATTTCTGCTGGAGAAGTGATTGATCTGCCAGCTGTGTGGACCTGTCATTTTACTTCCAGCCTGATTGATTTGAATGGCAATAGGGTGGTGATCAAGGTCATTGATTGGCTGTTTGTGTTTTGTCAGATTCACAGAGGCGGACACTCTGGTGATGGGAGATGTGACATACGGGGCCTGCTGCGTGGACGACTTCACTGCCCGCGCTTTGGGAGCCGACTTCATGGTGCATTATGGGCACAGCTG[T/A]CTCAGTGAGTCAAACAGAAATGCGCAATCATTATTATGTGCATTTGCTTTCCCTAATGTCATTTCAAAACATGTGTGGCTTTCTTCTGTGAAATGGATTTATATTATGAGTTATAATACATTTATAAAACTTCTTTTAATGTGTTTTTATTATTTTGGAGGTTAATTAACATCATTTGGAACATTGTATGTATGTATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAAGAGGAGGTAGATATCAGATCACAAGTATAATCAGGAGCAGAACTAGGGATGCTCATTTCGGTTAATTTTGCTAACCAACAACCGCCACTCATTAATCGGTTATTAACGGTTAACTGGTCAGATTACTATTAATTTTATATTAAACAAATTGATGTGTCTATTTTGTGTCTGACACATTAAATATTGCATTTTAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1222
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 |
---|---|---|---|---|---|
ENSDART00000080740 | Essential Splice Site | 245 | 381 | 7 | 11 |
ENSDART00000110408 | Essential Splice Site | 260 | 439 | 7 | 12 |
ENSDART00000140214 | None | None | 51 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 25300510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26030438 |
GRCz11 | 15 | 25965703 |
KASP Assay ID:
554-1131.1 (used for ordering genotyping assays)
KASP Sequence:
TTCATTTGGAATCCATCATGATTGCCAACCCAGACACACCTGCCTACAGG[T/C]AAACCAAACCAACGTTTACTACAGCAAGTATCATTATTATCATGGCTTGT
Long Flanking Sequence:
CTAATTGTGGCTACGTTCCTTTGGGTGTCCATCAGCTTTGCCAGGTTAATCTATACTCTCATTACCTATGGCAGGTCTTCTCCTGTCAGCACAGCAGAGGATAATCAGAATATTAAGTTCTGTTTGCATGCTGTCCGCGTTATGACCTAATCATATCATGGAGGGGTTTATTTGTGGAGTATTTGGATAATAGCCCAACAGCCTCCATGTCTATGACTGCTTTCCGGCTAGAGTGAGTAGGTCTTGCCCTGATCGCTTGTTCAATGTTAGGAGGGTGCTGATCCGGTTTACCCATCCTCTAGGCTGAGACCTGTTGGCCTTTATATTTTCAAACACAAATCCCAGAGAGAAGAAGGGGTTAGCGGAGTTTTACTGTTTGTGCACACTCAGATTGTCTTTCTCTCTGATAGAGTTGTGTTTCTGTCTATAGATATCTTGGGGATGGAAGATTTCATTTGGAATCCATCATGATTGCCAACCCAGACACACCTGCCTACAGG[T/C]AAACCAAACCAACGTTTACTACAGCAAGTATCATTATTATCATGGCTTGTAGTCTTCAACATTTTTCAGGGCTGTTTAAACTTTCGGAAAGCTCTTCTAAAAAATTCATATGTGGCCCGTTTCAACTGAGTGATTCGGTATGGTTTTAAATACACAGCAGAGACATTGCACCATAATAATTTATACATATAATAATGAGCCTTGGTCAGCCCGGGCTCAAAGAAACCTTGTCATCGTCTTGATGAACAGCCAGGAAGAACATAATCTGCTGGGCCCTGTTGTTGTTTTATGAGCCCATCTAAAATTGCGAGCGGTTTCACTTTGTCCACAGATTTTGCGATCTTGTCTGTATTTGAAATAACAAACTTTTTAAGCTCCTATTAGTATGCTCGTGATCAATGAATTGAAGCAATCTGATATCCGATCCTGTTAGAAAGGAACAAACGCGAGAATGAAGCGGGAAAAAACAAAGGAACTCAGAATGACAGAATTACTTTCTA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa16246
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 |
---|---|---|---|---|---|
ENSDART00000080740 | Essential Splice Site | 297 | 381 | 8 | 11 |
ENSDART00000110408 | Essential Splice Site | 312 | 439 | 8 | 12 |
ENSDART00000140214 | None | None | 51 | None | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 25296798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 26026726 |
GRCz11 | 15 | 25961991 |
KASP Assay ID:
2260-8552.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCATCCTAGGCACCCTTGGTCGTCAGGGCAACCCCAAAATTTTRGAGG[T/C]AAGACCATCTGCTACCTATTGTCCTACAGTATGTTTTTTTNATCAGAGTAA
Long Flanking Sequence:
AAACGGGAGATCTGCATCTTGTATGTGCAGTCGACAAATCTGCAACAACTGTGTGATGCTATCATGTCAATATGGAGCAAAATCTCCAGAATATTTCCAGTACCTTGTTGAATCTATGCCACGAAGGATTAAGGCAGTTCTGAAGGCAAAATTAGGTCCAATCCAGTACTAGTGAGGTGTACCTAACAAAGTGTGGATGTTCCAAGGTTGTACTTTGTGGGATTTATAACTTGGATCCAAGCAATCTAGACCAACAGCAAAACCCTGCTGTCACAGTGGAAAGTTTATTTTTGATTAGTATCTGTTTGATTAGTGTCTCATTGTTGTCCTCCATACCTGCAGGTATGACCCATACAGTAAAGTGTTTTCTCGAGAATATTATGACCATGATGCAATGCGGGCCACCAGACTGAAAGCCATCGAGAGTGCCCGCTCAGCACAGAGGTGGGGGCTCATCCTAGGCACCCTTGGTCGTCAGGGCAACCCCAAAATTTTGGAGG[T/C]AAGACCATCTGCTACCTATTGTCCTACAGTATGTTTTTTTATCAGAGTAAAGATTACACTGTCCTACATGTGCACCGAAACAGACACACACACCCTGCGGCATTTGGCCAGGAGGAAGGTTCAACAGGGGTGTTAATGGAATATTTTGTGAGGGGCAGGTCATCTCACTCTCTTCCTCTACTTCTCATTCAGATCCTTCTCTGTTTGTTCTCTGCCTGTTTTCATCTGTTCATTTGTATGTGTTTGGATTGGACTTTGTTTTGGCAGATTTCCTCTCTTTGCCGTTTCATCCTTTTTAACTGGTGTGCATAAACAAGACGAGTGAGATGAATTCAGCATCTAGATAAACAGACAGTGGATGGCGATTCTGAAGGAGATCTCTGTAGCTCTCCTCAGTGTTTTTTTTCTATCCCTGAATCTCATGACGCATTCCTGTTGGAGTGCCTTTTTGATCAGTGCTTCTCAACTGCTGGGCTGCATTCTAAAGTAGGCGTCTGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32037
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080740 | Missense | 345 | 381 | 10 | 11 |
ENSDART00000110408 | Nonsense | 386 | 439 | 11 | 12 |
ENSDART00000140214 | Missense | 15 | 51 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 25248963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25978891 |
GRCz11 | 15 | 25914156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTTCAGGCAGCAGTGGCGCTACAGCAGGTTGGATGGCAGGATGTGTA[T/A]CCCATGGATTTCTATTCCAATCAGAGTCTGGGGGCCTGGACTCCTAATCA
Long Flanking Sequence:
TCATACACCAGTCTGAACTATGTTTTATTTTATTTTATTAATCACATTGACATCGGGTAATTACAATGTAAATGCAACAGACAATAGTACAAACAATGCTTTTTGCAATAAGGAAGATATAACAGTTTTAAAGAAGTGTAACAGTGGTATAGCAGCAAGCAAGCAAGAAAAAGGTCACAATGTAACCACAGAAGAAGCTTTAAATAGAAAATTAGCAAAAATATTTTTTGAAGGAAGATGCTAATAGTCTAATCCAATTCCATGACCTAAGCTAAGCTAAAATTGTTCCTGCCAGATCTGGAGATCACAACTAGAACTCCCTTGATATTGGACTGGATTCTGTGGCTGATGTGTGTATGAAGCCCATTGTCCTGTTGTTAATCCTACAGTAAGTCAGCATGCTGATGTGTTTAATAAACTCACACAATGTGTGTATGTGTGTGTGTGTGTGTGTTTCAGGCAGCAGTGGCGCTACAGCAGGTTGGATGGCAGGATGTGTA[T/A]CCCATGGATTTCTATTCCAATCAGAGTCTGGGGGCCTGGACTCCTAATCATCCGGATAACCAACCTAAACGGCCTGCACGCAAAACCGCACAGGTGTGTATGCTGAAAGGGTTTTTAGAAAAAAAAAGCTTTAAATATTATTTCATTATCGTGTTCAAAGTATAATGTTTATTCCCATATTTCATTATTAATTAGGTAACAATTTACAATAAAGTTTTATTAGTTGATGGTAATGCATTTACTAACATGAACAATACATTTATTACAGTATTTGTTCATGTTAGTTAACATTAGTTAATGAAAATACAGTTGTTCATCGTTAATGTTAACTGACTGTGCATTAACTAATGTTGTTAATAACATTAGTGTTAATAATAGATGTTAATAATGCATTAGTAAATGTTGAACTAATAAATGGCGGTCCAGTATTATTCATAATAAGTTCAAGTTAGTAATCAAATTCACCAAAGAAAGCTGTTGTGACCAATAATTTATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22651
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000080740 | None | None | 381 | 11 | 11 |
ENSDART00000110408 | Nonsense | 437 | 439 | 12 | 12 |
ENSDART00000140214 | None | None | 51 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 25245766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25975694 |
GRCz11 | 15 | 25910959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGCAGGTGATCAGCTGTGGTCAGGAACAGAGCGCCTCCTGTGGTTGT[C/T]AACCAAAATAACATACAGCCTCATGAACATCTGCCGGAGACAAGCGGACC
Long Flanking Sequence:
ATTTTTTGTGAAACCCATCATACTCTTTACAAGATTTTTGCTTGATGATTATTTCATTCATTGACTGACTGACTGAAAAAGTTTTCAATTAGTAGCAGATAAATAGACAATGTATTTTAATTTCCAGTTCTGTGAAAATCAGCGGAAAAATAACAAAAATTCAGATTTTGTCGTTTCTCATGACCAACTTAAAAGCACCTGGGGATTTTAGGACCAGTACTTTAAACAGAAATGATTTTTTAATCCCTTAATTACTCTTCTAAGTGTATGATTAATCCACCAATATAACAGACACAATCTGCGAGTCTCTAAATCCACACAGGATGTCTGTCCTGTGTTTTATTCCTTATTGTATCTCTCTCCTTTTATCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTTATCAGAAGGCTGGTCAGCAGGTGATCAGCTGTGGTCAGGAACAGAGCGCCTCCTGTGGTTGT[C/T]AACCAAAATAACATACAGCCTCATGAACATCTGCCGGAGACAAGCGGACCAATCACACTTCATCACATCAGCCTTCTGTTCACACGCACCGTCAGTCAGTCAGTCAGTGAGTGAGTGTGTGTGTGTGTATGTGTGTATGAGATAAAAGCTCCCCCTTGAATGAACAAAGTGTGGTTTCGCTTTAGTCAAACGTAAGCATGTTGTCCCTCACCTACAAAAAGAAAGGGGCTGGCAGACATGTTTTCATGGTTGACCTTCATCCCTTCAGAATTACAGCAGGAAAGAGTGGATTCTTTCTGTGTGTATGAAGAGAAAATACTCATTCTGTACTCTACATCCAGCTTTTTATTTGCCTTAATGCTAAGCTTCTCCGACAGAAGCACTTTGAATGTTTTGTACAGGATATCTTTTAATTATGGGCAAAAATAAAATGAAATCTTTACAGTTTTCTGTCGGACTTGATTGAGTCTGAGTGCTGGTGTTATCATTATCAAAAAGCC
Associated Phenotype:
Not determined