ZMP
si:dkey-97a13.6
Ensembl ID:
ZFIN ID:
Human Orthologue:
RP4-697K14.7
Human Description:
Peroxisomal proliferator-activated receptor A-interacting complex 285 kDa protein [Source:UniProtKB/
Mouse Orthologue:
BC006779
Mouse Description:
cDNA sequence BC006779 Gene [Source:MGI Symbol;Acc:MGI:2385169]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32992 | Nonsense | Available for shipment | Available now |
sa16820 | Nonsense | Available for shipment | Available now |
sa32991 | Nonsense | Available for shipment | Available now |
sa14969 | Nonsense | Available for shipment | Available now |
sa32990 | Nonsense | Available for shipment | Available now |
sa7515 | Missense | Mutation detected in F1 DNA | Not yet available |
sa1075 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa32992
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 |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 184 | 2781 | 2 | 18 |
ENSDART00000131278 | None | None | 2190 | None | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42074658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42124122 |
GRCz11 | 2 | 41973540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTAGATGATGTGCGTGTTACACACGATGAGAATCTCAGTATGGACTG[T/A]TTACAAGAGGACAATGAAATCAGATGGAAATTCACAATCACCACTGAGGT
Long Flanking Sequence:
GGATCACATATGAAGATGCAGGTTAGATGTAGAATTTTACACACATCTGTTCTCTCAAACTTTGGAACCTAATTTTGTAAGCAAAGCTTGAGATATTTTAAATATGCAAAAGTGTTAGCCATTCATACCTGCGGGTGTGTGCTTTTGAGTCTGCAATCCTCCATGAATAGTCAAGAGGTGTGTTCAGACAAGGGTGGTCAGAACAGAAAATAGCATACTAATTCAAATTGTTTTGATGTACATATCATAATATTATAAATAGATGTGACATGTATCGTAGTATATTAAAAATTACACTGGGAGTGAATTTTATACAGTATAATGCGTCAGCTTATGAATTATGCCAGGGTTATCTATAAACACTACGTGGATTGTGAAATGTGATGAAACTTGACATAAGTTTTTTCCAAGTAAATCTTAGATACATGTGTGTATTTGCAGATCTCTGAGCATGTAGATGATGTGCGTGTTACACACGATGAGAATCTCAGTATGGACTG[T/A]TTACAAGAGGACAATGAAATCAGATGGAAATTCACAATCACCACTGAGGTCAGAAACACACGCTAACCTGCATCAGCTTACATTCAGCTAATATTAAACTTATTTTAATAACACACTAATAATAACCTAGTTTGTTTTGTGTGTGTGTGTGTGTATGTGCATGTCTAGAGATCCTTGGCTCACGTAGCTCTACTAAAAGTGGAAAATGGTGCTGTTTTCTCTTTGAGTGATAGTTTAAGAAACACCATCCCCCCAATCACACACATAGCAGGCCACGAGCTTCGTTCCTCTCAGTCCACCTACCAGCTGAGTGTGTCTTTCCTGTCTTTCCACCCTGGTGTGTACGAACAATGGCTGGTGTTTGATTTTGACATGCGACCAGTTCTGCTCAGGAAACTGAAGGTGAGGGTTGGACAGCAGTTCCTTGTCCAGCCTGAAGAGGCAGAAGAGAGTGAATGTGCTGAGATTCTTTCCAATGAGCGCTGGAACAGGGGAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16820
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 365 | 2781 | 3 | 18 |
ENSDART00000131278 | None | None | 2190 | None | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42073997)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42123461 |
GRCz11 | 2 | 41972879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTCATCGGGAAAACTACAGAGAGAGGGCTCACCACTTCCTGTTCAGG[G/T]AGGAAATTGCAGAGGAGGAGCTCATTAGCAGGTATAGACAGCTTGTAGAA
Long Flanking Sequence:
ATGTCTAGAGATCCTTGGCTCACGTAGCTCTACTAAAAGTGGAAAATGGTGCTGTTTTCTCTTTGAGTGATAGTTTAAGAAACACCATCCCCCCAATCACACACATAGCAGGCCACGAGCTTCGTTCCTCTCAGTCCACCTACCAGCTGAGTGTGTCTTTCCTGTCTTTCCACCCTGGTGTGTACGAACAATGGCTGGTGTTTGATTTTGACATGCGACCAGTTCTGCTCAGGAAACTGAAGGTGAGGGTTGGACAGCAGTTCCTTGTCCAGCCTGAAGAGGCAGAAGAGAGTGAATGTGCTGAGATTCTTTCCAATGAGCGCTGGAACAGGGGAAACAGGGTTATCGTGCCCTTCTTCGCCAGAAAGGAGGAGGACGAGCAGTTGCTCAGTAAATACAAACCACCTCAACTGAACCTGCAGTTCAATCCACATGCAGATCATAGTTTGCCACTTCATCGGGAAAACTACAGAGAGAGGGCTCACCACTTCCTGTTCAGG[G/T]AGGAAATTGCAGAGGAGGAGCTCATTAGCAGGTATAGACAGCTTGTAGAAATAGTGCACTTGAAATGTATGCTGTGGTGTAAATTTACTATATTTTCTTTATTTTTGTGGATGTATTCCCAAAACCAGTTAAACATAAATTGTGCATCAATGCTATGCTAAAGTTGAGGTGTGGGTTTAAGTTATGTTATAGGTTAATATTCGTGTTCAGTGTTCCAGTCAACAATTCTGAAACCAACAGAAGAACAATTAAATTAATTAGATGCAGGATTTACTGGTCTTCTGTTGGTTTTAGAATTTTCATTTTCAAAATCCCATAATAGGGGCTCTTTAATTAGTATGTTCTTTTACATTTAAATATATAATTTGGTACAATGCACTTATTGTGTACATACTGTACATTCTAATTTTACATAGTACTTATACTTTAAACATTATTCTAATGTAATTACACCTGTAATTATGTCTTAAATAACATTCAAAATTACATTGTTGATCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32991
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 |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 635 | 2781 | 5 | 18 |
ENSDART00000131278 | Nonsense | 44 | 2190 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42065393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42114857 |
GRCz11 | 2 | 41964275 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGGCAAACAAGGGAGGGTCCGCTATCATAGCAACTGATGACATCACT[C/T]GAAAATACTGTCTCTGCTCTCGAGATGGACAGTCGTTCATCCTCCCAGCA
Long Flanking Sequence:
ATGCAGCTGGGGACATGGAAACTAAGATGAATGTCCATGCTGTAGACAGCAGAACATACTGAGTATATATTGGTGGATTAATAAGACATGATGTATGAAATGTCAAACTATAAGGGAGGAGAAAAGTGTGTATAGGACTGTGTAAAACCAGTCAGACTAACAATCAGATCACCTCCGTTGTTGCATACTGCTTGTAACAATAAATGCTTCAGCCTGAGAAATTCAGAAGACTTCAGACTTCTTTTGATTCTTGACAATATATGCAATTATTAGTGAATGAGATCAAATGTTATCAGTATCAAGCTGTTTTGTGTAAAAAAAAACAGCTATTTAGAATGTATAATTAATAAATGTTGTGTTTTATTTCCTCTAGCTCTGCAGATTTATACGTAAGAGAGCACTTCCATCCATACATAATTAATGGACACCCAACTCTCAAACTACTCAGGATAAAGGCAAACAAGGGAGGGTCCGCTATCATAGCAACTGATGACATCACT[C/T]GAAAATACTGTCTCTGCTCTCGAGATGGACAGTCGTTCATCCTCCCAGCACGCTCTGACCTAGAGTCGCATCGCATCATTATAACCACCACATCAATAGCCCGACATCTCCATGAGCTGAAACTTCCCAAAGGTTTCTTCACTCATATCTTGATTGATGAGGCATCTCAAATGCTGGAAGGTGAAGCTCTAATGGCTCTGGGCTTAGCAGACAAACACACTCGAGTGGTTTTAGCAGGAGACCACATGCAGATGGCTCCAAAACTTTTCTCTGTAACCGATGACAAGAGATCAGAACACACCCTGCTCAATCGCCTCTTCCACTACTATCAGGATCAGAGCATCAACATCGCCAAGAAAAGCAGAATAATCTTTAACGAGAACTACCGCTCGACCACAGAAATTGTGGATTTTGTATCCACTTACTTCTATGTGAGTGATGGGATCAAGGCCAGAGGAGATGTGCATCCACACCCGAGGCTAAAACCCTTGATTTTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14969
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 |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 718 | 2781 | 5 | 18 |
ENSDART00000131278 | Nonsense | 127 | 2190 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42065144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42114608 |
GRCz11 | 2 | 41964026 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGCTTAGCAGACAARCACACTYGAGTGGTTTTAGCAGGAGACCACATG[C/T]MGATGGCTCCAAAACTTTTCTCTGTAACCGATGACAAGAGATCAGAACAC
Long Flanking Sequence:
CTTGACAATATATGCAATTATTAGTGAATGAGATCAAATGTTATCAGTATCAAGCTGTTTTGTGTAAAAAAAAACAGCTATTTAGAATGTATAATTAATAAATGTTGTGTTTTATTTCCTCTAGCTCTGCAGATTTATACGTAAGAGAGCACTTCCATCCATACATAATTAATGGACACCCAACTCTCAAACTACTCAGGATAAAGGCAAACAAGGGAGGGTCCGCTATCATAGCAACTGATGACATCACTCGAAAATACTGTCTCTGCTCTCGAGATGGACAGTCGTTCATCCTCCCAGCACGCTCTGACCTAGAGTCGCATCGCATCATTATAACCACCACATCAATAGCCCGACATCTCCATGAGCTGAAACTTCCCAAAGGTTTCTTCACTCATATCTTGATTGATGAGGCATCTCAAATGCTGGAAGGTGAAGCTCTAATGGCTCTGGGCTTAGCAGACAAACACACTCGAGTGGTTTTAGCAGGAGACCACATG[C/T]AGATGGCTCCAAAACTTTTCTCTGTAACCGATGACAAGAGATCAGAACACACCCTGCTCAATCGCCTCTTCCACTACTATCAGGATCAGAGCATCAACATCGCCAAGAAAAGCAGAATAATCTTTAACGAGAACTACCGCTCGACCACAGAAATTGTGGATTTTGTATCCACTTACTTCTATGTGAGTGATGGGATCAAGGCCAGAGGAGATGTGCATCCACACCCGAGGCTAAAACCCTTGATTTTTCATCATGTCAGAGGAGAATGCCATCTGAGTTCCACCATCACATCCACATCATGGTTAAATTATGCTGAGGTCAACAGTGTGGTAAACATGGTACAAGTGCTTCTGACTGACTGGCCAATGGAATGGGGTGATAAAGACCCAAAGCAGATTTGTGTTCTAAGTGAAGGCCAACAGGTACTTTTTATAGTGATAAAAACAAATATTTACATAAACATGAAGAAATATGTCATGATTCTAAATGATTACAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32990
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 1188 | 2781 | 7 | 18 |
ENSDART00000131278 | Nonsense | 597 | 2190 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42061917)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42111381 |
GRCz11 | 2 | 41960799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGGCAATTGGACAATAACAGGAAGAGTTCCTATTAATGAACAAACA[A/T]AACAGAACTATGTTTTTGTCGTGCAGATATTGGGCTGGAAAGAACACTGT
Long Flanking Sequence:
ATGAACAAAAGAGGCGGATATTCACTTCCGCTGAAAAAGAAAACCTTTTGGAGATGGTCAGGAATCAGCCTGCTCTCTACAAACGTGGAGAATTGGTGATGGAAGGATATCAGTCAGGTTATATAATACCATATGACAACCCATCTGAACGCATTGATATTAAAGGGAGGAAAAACATTGGCATGTCTTTCCCTGGTGATGAAGTTGTGGTTGAGATTAGACGACATGATGAAGGGCATCTCACTGGAAGAGTTTTAGGGCTCACAAATAGATCACCAACATCCTCTGAATGTGTGTGTTCATTAGAAGATGAAAATTACAATAGAAAAAAACTGAATCCTGACCAAAACCTGGTGCCAAAAATGATGATACCCCTCGACCACACAACCACCAAAATACGCATTTTGGTAAAGAAAGAGGCTCGCAAATTAATTCCTCTGTGGAAATGTGTCAGTGGCAATTGGACAATAACAGGAAGAGTTCCTATTAATGAACAAACA[A/T]AACAGAACTATGTTTTTGTCGTGCAGATATTGGGCTGGAAAGAACACTGTTCCTTTCCACTTGGTAGAGTTACAGATATTCTACCAGTTGGGACATCTTTAGAGGAGGGTCTTAAGATTTTAAAATCAGAATTCAAACTAATGTCTCCTCCTCTGATGCAAGAGAACACGCTTTTAGAAATCAGAATTGATGACAAGAGAAGAAAGGATTTTACAGGTTTAAAAACCTTTACTGTTGATCCACCTAACGCTGAAGTCTTAGATGATGCCATCAGCATCAATGATCTTGGAAGCTGCTATGAAATAGGAGTTCATGTTGCAGATGTAGCTAGTTTTGTGTCTAAGGACAGTTCCATTGATGCATTCGCAAAGGATATGGGAGCAACCTTTTATGCACCTGGAAAAGAACCAGCATTTATGTTCCCCAAACATCTCTCCACCACCTGTTGGAGTCTTCTCCCAGGCAAAGATCGGAAAGCAATTTCTTTAATTGTTGAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7515
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:
C > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017829 | Missense | 1438 | 2781 | 7 | 18 |
ENSDART00000131278 | Missense | 847 | 2190 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42061167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42110631 |
GRCz11 | 2 | 41960049 |
KASP Assay ID:
554-4246.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGCTATGCCCAGCYTAATAAACACCAGAAGCCAGGGGAGAGAGAAGCA[C/T]ATCGAATGATTGAAGAGTTAAACATCATGTTTAACCATGAAGTGTCAAAA
Long Flanking Sequence:
CTGAAGTCTTAGATGATGCCATCAGCATCAATGATCTTGGAAGCTGCTATGAAATAGGAGTTCATGTTGCAGATGTAGCTAGTTTTGTGTCTAAGGACAGTTCCATTGATGCATTCGCAAAGGATATGGGAGCAACCTTTTATGCACCTGGAAAAGAACCAGCATTTATGTTCCCCAAACATCTCTCCACCACCTGTTGGAGTCTTCTCCCAGGCAAAGATCGGAAAGCAATTTCTTTAATTGTTGAAGTGGAAAAGCAGTCAGGGGTCATCACAAAAAAGACCTTTGATCTCTCTATGGTCAAATCTAAAAGGCAGCTGACCTACAATGAGGCTGAGGATATAATATGTCAGTGTGATGGTGAACTAAGATTTGATACATTGGAGGACTGTGTCCGAGTGGCTTACCATTTTGCCAGAAGCCAGCGCAAAACACGACTTAAAGAAGACTGGAGCTATGCCCAGCTTAATAAACACCAGAAGCCAGGGGAGAGAGAAGCA[C/T]ATCGAATGATTGAAGAGTTAAACATCATGTTTAACCATGAAGTGTCAAAATTTCTGTCAGAGTACACAGACACCAAATCCTGCACTCCTCTGAGGTGCCAGGATTCTCCTAATGCAGAAGCTTTAGAGAAGATTAGTAATCAACACATGGAACTCATTCCTTTTTCATCCCACCTGACATTTCATTTAGAGAGACAGCGAATGGACCTGAATAATGCAGTTACCTTCACTGTGTATTCTTTAGGGTCTAGATATGTTCACCCAAACAATAATCCTAACCCTGAAGCTAACTCCAGCCCTTTATCAAGCCAACTACGAGATGCCATCTCTGTCAGCGAGTCTGAATTTCATTTTGAAATTGGAATTCACAAGGCAGATTTTTTAAACTATGTGTCTGAGGACAATATTCAGAACTTGGGAGCACAATCAGACATGTGGAATTTGGCACCAGGCAAAAAACGCTGTGCCATCTCTTTGATGCTGAAAGTAGAAAAGAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1075
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000017829 | Nonsense | 1872 | 2781 | 7 | 18 |
ENSDART00000131278 | Nonsense | 1281 | 2190 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 2 (position 42059863)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42109327 |
GRCz11 | 2 | 41958745 |
KASP Assay ID:
554-0977.1 (used for ordering genotyping assays)
KASP Sequence:
GATCTGCTGTGTGAAAAGTGTAAAAGAGGAGAAAAGAGGGCACAGGAGTA[T/A]GAGAGCAAAGTTGAGGCACTTCAAATAGCAGTCAATCTACAGAAACAAAG
Long Flanking Sequence:
CAAACCCAATTTCCAAACACCTCTCCTGGACTGGTGAATAGACTTAAGAAATACAATGAGAAGTTTGAGTCTCTCCAAGTACTAGAGAAATGTCTGGATCCAAACAACGGGCAGAACTGTGGAAGTTTCATCATTCTGACATCTGTGTGGAAAAAGATCAAATCAGCAGCTTTGACATGTGATTTCTACAAAATGGCTGACCTCATTTCTACAGATGACATTCATCCTCAATTGGTTCCGGCAATTGTTCAATTAAGTGCCAGCATCAACAAAGCCTTCTTCATTCGTTCTCTCTCCTGCAGAGAAGCTTTAGTTGGGCACTATTCATTACATCTAGACTCTTACACACATGCATCTTCACCCATTCGGCGGTACATTGATGTGGTTCTTCAGAGGCTCATGCATGCAGTTCTCGGTAATCGTCCTGTAGAGTACTCTCAGACAGACATTGATCTGCTGTGTGAAAAGTGTAAAAGAGGAGAAAAGAGGGCACAGGAGTA[T/A]GAGAGCAAAGTTGAGGCACTTCAAATAGCAGTCAATCTACAGAAACAAAGCACATACAAAGTGGCTTTTGTCACCGTTGTTAAACGGGACAGTGAAAGCTTTAAACTGTCATTTCCATTTGACAAAGGAACTTTCCCGGAAAAGCTTCCTGTTCAGTACAGAAATTTACAGCTTGAAGATCAACCACTATTTATCAAAAAGCCAAAACATGTGAAGCTAACGTGGAAAAAGCGTATATACGGATTGAGCATGACCCAGAGCCCCCTCCAGAACATGAAAATCTCTTCAGAGATTCAGCAGAGCACTTGGCAAGCTATTGTTGAGGCTGTGAGAGACGAAAAGTGGGATGAGGCAAAGTCTCTCGTATTGGCAGCACATGTGAAAGATAACAGCAGGAACAGTGAATTGTCTGATACATCTCGATGGGATCCTGATCGCACATTTACTTCTGAAGAGGATCATTACACTGACTTCCAAATTAATCTGAAAGTTGGAGACAC
Associated Phenotype:
Not determined