ZMP
impdh1a
Ensembl ID:
ZFIN ID:
Description:
inosine 5'-phosphate dehydrogenase 1a [Source:RefSeq peptide;Acc:NP_001002177]
Human Orthologue:
IMPDH1
Human Description:
IMP (inosine 5'-monophosphate) dehydrogenase 1 [Source:HGNC Symbol;Acc:6052]
Mouse Orthologue:
Impdh1
Mouse Description:
inosine 5'-phosphate dehydrogenase 1 Gene [Source:MGI Symbol;Acc:MGI:96567]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16224 | Essential Splice Site | Available for shipment | Available now |
sa23234 | Essential Splice Site | Available for shipment | Available now |
sa15860 | Nonsense | Available for shipment | Available now |
sa9932 | Nonsense | Available for shipment | Available now |
sa43048 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16224
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017619 | Essential Splice Site | None | 544 | 1 | 16 |
ENSDART00000101161 | None | None | 624 | None | 16 |
ENSDART00000137098 | None | None | 87 | None | 4 |
ENSDART00000143519 | None | None | 179 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 8277407)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8854785 |
GRCz11 | 18 | 8812804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTCAKCMGAAGGAAGTGTGTTCCGAAAGAGAAAGTAACTCGAGACTG[T/G]AAGTGGATTTATTTGTTTTTTCGACCTAASACGCTTTTAAAAYGAATGTT
Long Flanking Sequence:
TCTACTGCGACTTATAAAGACATTTTCCGTTTTCTCTCTCTTTTTAAATCGATTTATATCAGGTGAAACGATGCACGTTATATGCCTTCTAACACCAAAATACTAGTAAATATTTTACTTCGGTTTTTCACTCAGAATATATTCAAAAACTGGTCTCGAAAAAATGTTTAGAAACAGGTTTGAGGAGTTTTCAGTACCATCATACGATGATCATCTCTCCCTGAGATGCGAGCATGTATCATGTGACTTCAGTTCACGCTGTTGTCGGTCTGTAAACACACACAGACTGCGCGTCTCACCACGAGCCCGGAGACCCTTCATCCACAGCGGCTTTGCCCTTCAGAGCTCTGCTGCGCGGAAGGAGAGACTAGTGAACCCCGCGTTGATCCGTCACGCTCTTTAATATAAAAATGTAGCAGTCATCATGTGAGCTACTGTACATGGGGGCGAATATTCAGCAGAAGGAAGTGTGTTCCGAAAGAGAAAGTAACTCGAGACTG[T/G]AAGTGGATTTATTTGTTTTTTCGACCTAACACGCTTTTAAAATGAATGTTCTGTCATTAATGAAAGTTTTAGTACAACAGAAATTCCTAATTTTTGGTTTGAATGTATTTTAATTATATAATTGTGTCGTGTGTAATTTTGCTTTATTTTTCATCATTTAACTTACGTACAACGTCTGCCTGCCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTTACCTGTCTGTCTGTTTGTCTATCTATTATTTTTTTCAATTATACAAACCCTCATAGATTTCCTCAGCCCAAGTTTCTGTGTAGAGTTTGCATGTTCTCTCTGTTTTCGCGTGGATTTCCACCAGGTCTTGGAACTTGTGTGTATGTATGTTTCCCAGTGATGGGTTGCAGGTGGAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23234
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017619 | Essential Splice Site | 83 | 544 | 4 | 16 |
ENSDART00000101161 | Essential Splice Site | 163 | 624 | 4 | 16 |
ENSDART00000137098 | None | None | 87 | None | 4 |
ENSDART00000143519 | None | None | 179 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 8289935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8867313 |
GRCz11 | 18 | 8825332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTCCAATGGACACAGTCACAGAGTCCTCAATGGCCATTGCTATGGCT[G/T]TAAGTAACATTTACAAACACATATATAAAGTGTAAATTTTCCATTTCATT
Long Flanking Sequence:
CTCTTTATTGTTCAGTTGAGATTACATCAAACATCAAATACAAAAATGTAAAATTTAAAGCACTTCACAGGACCTTTAATTAAAAAATTCTAATATATGTCAAAAGTCAAGCAGGTTTGCAATGGATAGGATTACATTTCTGGCACTTTTCAATATCTATGGTGTCCTCAAACAGTGTTGACTGTCACAGCACTCAAGAAATCAGATCATGTTAAGGATGTGATTGCTTATCAAGGCACGTGATCCAAATCGGCCGTAACCTTTGTAGACCTATGTATATCTCAATAATATAATAATTGATCATACTATAGCATCATCTACATATAACATCTGCTGTATGCTAACACATGATACACTTTCGCCTCAGATTTTCATTGGAGTCTTGTTTTACATCATAGGATTTGACCTCTGCCCTGACCCGGAAAATAACCCTGAAGACGCCACTCATTTCCTCTCCAATGGACACAGTCACAGAGTCCTCAATGGCCATTGCTATGGCT[G/T]TAAGTAACATTTACAAACACATATATAAAGTGTAAATTTTCCATTTCATTACCAGTTATTTTTCCTCATAGCTCATGGGAGGAATTGGAATTATTCATCACAACTGCACGCCTGAGTTTCAGGCTAACGAGGTCCGGAAAGTTAAGGTTAGTGAAATTAAATGTAAGAGATATAACTTTGGAGGAAGTAAAAATGTGGTTAGATTTGTAGATTTATAACTCGCAGACTTTGATAATACAGATTTTTTTGAGTTCGCGATGATAAATACTATGTTTTGTGTCATATTGGCAGAAATTCGAGCAGGGCTTCATTACAGACCCTGTAGTGATGAGTCCACGACACACAGTAGGAGATGTGTTTGAAGCGAAGGTACGGCACGGTTTCTCTGGCATCCCAGTTACTGAAACTGGAAAGATGGGCAGCAAGCTGGTGGGCATTGTTACGTCACGAGACATCGACTTCCTGTCAGAAAAAGACTATGATAGGCCACTGGAGGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15860
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 |
---|---|---|---|---|---|
ENSDART00000017619 | Nonsense | 161 | 544 | 6 | 16 |
ENSDART00000101161 | Nonsense | 241 | 624 | 6 | 16 |
ENSDART00000137098 | None | None | 87 | None | 4 |
ENSDART00000143519 | None | None | 179 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 8290383)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8867761 |
GRCz11 | 18 | 8825780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACTGAAACTGGAAAGWTGGGCAGCAAGCTGGTGGGCATTGTTACGTCA[C/T]GAGACATCGACTTCCTGTCAGAAAAAGACTATGATAGGCCACTGGAGGAG
Long Flanking Sequence:
TTCCTCTCCAATGGACACAGTCACAGAGTCCTCAATGGCCATTGCTATGGCTGTAAGTAACATTTACAAACACATATATAAAGTGTAAATTTTCCATTTCATTACCAGTTATTTTTCCTCATAGCTCATGGGAGGAATTGGAATTATTCATCACAACTGCACGCCTGAGTTTCAGGCTAACGAGGTCCGGAAAGTTAAGGTTAGTGAAATTAAATGTAAGAGATATAACTTTGGAGGAAGTAAAAATGTGGTTAGATTTGTAGATTTATAACTCGCAGACTTTGATAATACAGATTTTTTTGAGTTCGCGATGATAAATACTATGTTTTGTGTCATATTGGCAGAAATTCGAGCAGGGCTTCATTACAGACCCTGTAGTGATGAGTCCACGACACACAGTAGGAGATGTGTTTGAAGCGAAGGTACGGCACGGTTTCTCTGGCATCCCAGTTACTGAAACTGGAAAGATGGGCAGCAAGCTGGTGGGCATTGTTACGTCA[C/T]GAGACATCGACTTCCTGTCAGAAAAAGACTATGATAGGCCACTGGAGGAGGTATGTGTTTGCACATTTTTTTTCAATTTCTAATTCAGCTTGAATCATTTTAATTTAGAATGCACAACTTATAAGTAAATTAGCACAACTTTTAAGTAATAGTAAATCCTCTGCAGCCTTGAAATTAGTTAATATTATTTATTGTGTTTAGATGGAGTGACAGAAAATACTGTACATTGGCCTAAATAGATTGAGGTGTTGTGAATTTGAAGAAGAGACAAAACCAGGAGGCTTTTTGGGCCTCTTTAAAGCAGAATTCTTTAATGAGGACTCACTGTCGCTGTGGCATGCATTGAAAAATCTCTGAAACTAGTGCAGCCAGGCACTCAGTTTAAATGCATTTTTATAGGCAGTAATACATAGGTGCAAATGAAGTGCAGGGGTCAGCAAGATAAATGGCATTTGCCTAGCCCTTATCTCATCAGTATAATAGTACCTATTCACATGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9932
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017619 | Nonsense | 233 | 544 | 8 | 16 |
ENSDART00000101161 | Nonsense | 313 | 624 | 8 | 16 |
ENSDART00000137098 | None | None | 87 | None | 4 |
ENSDART00000143519 | None | None | 179 | None | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 8291926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8869304 |
GRCz11 | 18 | 8827323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGCTTGTTGCAATAAKCGCTCGTACCGATTTGAAGAAGAACMGAGATTA[T/A]CCTCTGGCCTCCAAAGACTCCCGCAAACAGCTCCTGTGCGGCGCCGCCAT
Long Flanking Sequence:
GCACATTTTTTTCTTAATTAAGTACTGTCTAGAGTACGATATTTAAAAAAAAAAGATGTGCACATGTAATCAAAACTATAGCTGAAATTATTAAAATAACCAGCTGAAAAAGTTTAGATTTTTTGTTTCCTGATGATCTCCTGATGATTTTTTTTGCTTTGTGACATTTTGAGATTATGTTTTCTTTGATAAGACTCCCGAATTTCAATAATAAGCCTGAACTTTTTGAATGCTAAATCTTCTATCCTCCAGTCAATGACAAAACGAGAAGATTTAGTGGTTGCTCCAGCTGGTGTAACATTAAAAGAGGCAAATGACATCTTACAGCGCAGTAAAAAAGGTAGACGCAATAACTTCAGTCCTGTTTATGTTGTGATGTTTACCGCAAATATTTTCATCACATCATTTTTTTCTCTCTCAGGTAAACTGCCTATAGTGAATGACAGTGATGAGCTTGTTGCAATAATCGCTCGTACCGATTTGAAGAAGAACCGAGATTA[T/A]CCTCTGGCCTCCAAAGACTCCCGCAAACAGCTCCTGTGCGGCGCCGCCATCGGCACCCGAGAGGACGACAAGTACCGGCTAGATCTGCTCATGCAGGCTGGAGTGGACGTGATCGTTCTGGTGGGTACAAAAGGGAGTAGGGGGACATAAATCTTATTCTGCCTTGATATTAGAGAGCCCCTGGGATCCATTCAGCTTGATTCATGAAACAGGGGACTTATTACAGAGAGATCATAATCCTGTCTGTTTGGTAAATTCAATTAGGACCATATTTAGGACAAAAGCTTTTACAGAACAGCATGTGTGTTATCTTAACTACAAATAGGAAAAACGAATTAGATGGTATTAGAGCACATGTGTCAAACTCAGTTCCTGGAGGGCCACATCTCTGCACAGTTTAGTTCCAACCCTAATTACACCTGATCCAACTATTTGAGTCCTCTAGACTTGTTTGATACCAAAGGTAAGCGTGTTGGAGCCGGGTTGGAACTAAACTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43048
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 |
---|---|---|---|---|---|
ENSDART00000017619 | Essential Splice Site | 514 | 544 | 16 | 16 |
ENSDART00000101161 | Essential Splice Site | 594 | 624 | 16 | 16 |
ENSDART00000137098 | None | None | 87 | None | 4 |
ENSDART00000143519 | Essential Splice Site | 173 | 179 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 8306525)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 8883903 |
GRCz11 | 18 | 8841922 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATGTAGAGAAAAAAGGCTCATGTTTAATGCTCTGTTTGTCTTCCGGCA[G/A]TTACGAGAAACGGTTATATTGAGCCTGGCAGCAGAGGGCACCCAAGAGCT
Long Flanking Sequence:
TCTCTTCATTTATTAGGTTTTACTGTGCTCAAATTGCTTTGTCTACCCAAATTGATTAAGTTCACAGTACTCATTAGGATTAGAGTCAAACGGTTTGTTGCAGTTGTTTGAGTTACCTTAAATTTTTGGGTTTTATAGTGAAAGTCTATGAGGGGGTGCATTTCTCGGCACAACACCGGCTTGATTGCAATGGAAATCTACAGACACGTATTTTAAAAAACGCAACTAAAGGTGCATTTAGCCATGTATTTTAGATTTTTTTTCACATAAAGCTGTAAAAAATGATCAAAAGCCAAGAGTAAATAAAAATGAACAGTAAACAACTTAAAATGGACAAGTGCATGAAAAAACAAAGACTTACTTCCATGGTGCTTTTTATATTTTCACTTTTGGGTGAACTGTTTTTTTATATGGGTAATATATTTGTAAAAAAAAAAAACTCTTAATTGTATATGTAGAGAAAAAAGGCTCATGTTTAATGCTCTGTTTGTCTTCCGGCA[G/A]TTACGAGAAACGGTTATATTGAGCCTGGCAGCAGAGGGCACCCAAGAGCTGGACCTAATGTCCCGTCACCGGCCGTCACTAAACACAGCAGCTAAAAAAAAAGCCATTTCTACACAACCCTCAATCCTTTGTCCTTCTTCCTGATGGCTCTCAAATCCTTGGTAAACTTAAAAAACACTTTATTGCAAGCCATCATTGGGACTAAATAACCTATGGAGCTTTTGTTTCATAGCTGCATTTTTGTTTTGTTCGGGCTTCCCTAAAAAAATGTAGACTATGAATGTACTCTGAAATATGAAGATCCTATACGTGTGTGTATGTGAAACAGAGTGTATCTTATATATTTGTGGTATACAGGGTATGTTTAGTCTGTCTTGTTCCAAAGATCCTAATTAAAAACGTCTGTTGGTTTAATAGCAATAATATATGTTGAGGTGAATCATGTGCACCACATGTGTAAGTGTTATGAGTTCAGTTCTATTGAAATCTATTATGAAATG
Associated Phenotype:
Not determined