ZMP
si:ch73-215d9.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA0319
Human Description:
KIAA0319 [Source:HGNC Symbol;Acc:21580]
Mouse Orthologue:
D130043K22Rik
Mouse Description:
RIKEN cDNA D130043K22 gene Gene [Source:MGI Symbol;Acc:MGI:3036268]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18427 | Essential Splice Site | Available for shipment | Available now |
sa14911 | Nonsense | Available for shipment | Available now |
sa16403 | Nonsense | Available for shipment | Available now |
sa42778 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31007 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42779 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30691
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 194 | 1061 | 1 | 25 |
ENSDART00000143692 | Nonsense | 7 | 773 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38322369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36954897 |
GRCz11 | 16 | 36908781 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGGTAGAGCAAGAAGAGCAAACTGGGCTTTATGATTGGCCACCTGTT[C/T]AAAGAAAAGAGGAATTCAACCAATCAGAGACGGAGAGAGGCAGTAAAAGA
Long Flanking Sequence:
GGCAGGCCGCAACCTACTCTGAAAGCGTGGTGTCTCCGGAGCTGAGGAGCAGCAGTATTTTACGTGTCCCGGATGTGTCGTCCCTGGCTCAGTGTGCCGGGGCCTGCTGTGATCTCCCGGGCTGTGACCTGGCCTGGTTTTTTGAGCACCGATGCTATGTGCTCAGTTGTCAGCACACAGAAAACTGCCAGCCGAAGAAGAGACCTGGTACAGACTCTTACCTGGCCTTCCTGCAACGTGGGCCCCCACAAACACTTGTCCTGCAGTCCCTGGTTCGAGGAGAGTCTTTCCCAAACCATTGGCAGCCTCTGGCCAGACACCGGGGATCCGAGGATCCCATGAAGGATCTCGCTCTGCTTGAAGGGATTCAGGATTCGGACAACCCTGAGCCTGAGTATGCAGAGAGTTTTCGAAGTTTGGAAGACAAAAGAGCTGAAGACATAGACCTAAAAGCGGTAGAGCAAGAAGAGCAAACTGGGCTTTATGATTGGCCACCTGTT[C/T]AAAGAAAAGAGGAATTCAACCAATCAGAGACGGAGAGAGGCAGTAAAAGATTGACAACTGTTCAGGGCCCTGTTGAAAGTAGCACCATTACCCCAAGTCATCTTTCAGAAGAGAGAAATGAAAGCAGATCAACCATTATTGAAGCAGAATCTAATGTTACGGTACCATCAACCACTGTATTTGACATTAAGGTGAGATTTTTTTTAAGATAATGAAAACAGATAAAAGAAGTTAGTACTGCTTTTATTCAGCAAGGATGCATTTAAAGTTATTGAAAATTTTACCGTTGATAACTTTTTAAAAGCAAGCTTTTATGAAATAATTCTAAAAATAAATTGGATTTAACATTAAGAAATATGTTTTCTGTATTACAGCTATGAATATATATATATATATATATACACATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTATTTTTATTTATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18427
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Essential Splice Site | 306 | 1061 | None | 25 |
ENSDART00000143692 | Essential Splice Site | 123 | 773 | None | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38324926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36957454 |
GRCz11 | 16 | 36911338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCAGCCAACACTGAAGCTACACCGCAGATGACTTCAGAACAGCCAGG[T/G]ACTGTGCGCAATATTGGGGAAAGTTACTTTAAAAGCAAAAATGCTGTACT
Long Flanking Sequence:
ATTGTTTATAATTATAATAATTTAATTATAACATTAACTAATGAAACCTTATTGTAATCTGTGACTATTATAATTATTAATTTAAGTAAAATAATAACATTGAAGAATCCATTTGTAACCATGGCACAGTAATCAAGACCGGCATTGCTCTTACTGATAGCTGCCAGTTCATTATCATTGCTTGAAATGTCACGATTCTATTTTAATGCTGTGGCGTCATTAGGAAACATGGTGTCTTAAATGTTCTCCCACTCTGGCTAAGCGCTTAATCAGTCAGTTTTATGTCTCATCTGTTGTGTGAAATCTGTAGACATGAGTATGAAAACACTTTTATCATTAAAGGTTGAAGAAGAGCCACAGAACACATCGTCTGCAACTACTGCACCTAAAGTCGTGGAAGACCTCAGTACAGAGACCGCAAACTTTAGTGCAGTCAACGGTTCATTCATCACTCCAGCCAACACTGAAGCTACACCGCAGATGACTTCAGAACAGCCAGG[T/G]ACTGTGCGCAATATTGGGGAAAGTTACTTTAAAAGCAAAAATGCTGTACTAAGTAACTTTTTTTAATTAAAGTTATGTGTTACTTTTATGTTACTTTTTCATCTGGCCTGGGCCTGCTTTTAATAACACACACACAAAAAAAAAAAACATAAAAACCTGAATGTTTTTGTAAAACCCTTTTACTACAGTAGCTGAGAGAGCTCACAGTTAAACAAATGTAAATAAAGAAAACACTAACAAATTGAGAAAACATCTTAATCAATTTGACCACACATGTACATGCAAATTCTCACAACACATGCAAATACAGAAATGTGCTGCAAATAATGCACATTAAATAAATATTAAATGCTAATTGTGCAATTGTCAGGTTATTAGGGCTAAAAATACTCAAACTGAACGACCAGGGCATTAAAATTAACATAAAACTCACCTCAGATCTTCTCCAACACTGCTGACTTTAGTAACTGAAAGTAACTTAAAGTCATTGCCGGTCCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14911
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 501 | 1061 | 13 | 25 |
ENSDART00000143692 | Nonsense | 278 | 773 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38328749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36961277 |
GRCz11 | 16 | 36915161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGGAAAAAGGTGGACGGCCCGTTTTGGACACCTGAAGGTCCTGTTAAY[A/T]AAMCTGTACTGCAGCTGAAAAATCTTTTAYCTGGAGAATATACCTTCGAG
Long Flanking Sequence:
ATTATTTTCAATTTCTGAGAGCATTTCTGTATCCTTTATTCCAGCTGTCAGAGGGTGTTTACGCAGTCAGAGTGATTGTGAAAGCACATCAAGCATATGGAGAAGGTTCTGTGGACTTGACCGTACACCCTGGTACAACTATACCCTCTTTGCATCATCATTTATTCACCAAAAAAAAAAAAAAGTATGTGCATCATGTGCCTCACACAGTGGATGAATTGGCTTCCTTTTCATTCTACAGCAGAGAAAATAAACAAGCCTCCTAAAGCAGTCGTTCTTCCCAAGAGCCAAGATGTGCTGTTCAAAAAAGATTCTGTCTTAATCATTAACGGAAGTGGTATGTGGCCTGTTTCCTTTTTTCTGCTTTTTGCTATAGATCTATTAGGTCATGTGTTTTAACTAAATTTGCATTTCCAGAGAGTATGGATGATGCAGGGATTGTCAGTTATCTGTGGAAAAAGGTGGACGGCCCGTTTTGGACACCTGAAGGTCCTGTTAAC[A/T]AACCTGTACTGCAGCTGAAAAATCTTTTACCTGGAGAATATACCTTCGAGTAAGGACTTTTGTTTTACAAAAAATAAATAAGGCATTTGACACAGTAATAACACATTGATAAATTAAATATGGGCTGATTTGCATACATTTCTAACTAAAAAAAAAACTGATTAGAAATACTTATTATACTTATAATATATTTATTTAGGTTTAAAGGTTTTTCCAGGGGGGATTTTGGATTTTTTATTTATATCTCCTAATAATTTTGTTCTGTCATGACAACTCTATTACAACTAACTTGAGATATAGTATGGTAATAAATATGTATCTAGCAGTGTTGATGGGTTTGGTCTTGGTGGAATAAATGTGCTACGCTGCTGCTGCTGCTGCTTTGATTATTTTGGCAGAGCATATAAAGTTAACACACTGCTGTTCCAAACATAATATACAGTTAGGTCCATGAATATTTGGACATCGACACAATTCTAAAATTTTTGGCTCTGTACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16403
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 542 | 1061 | 14 | 25 |
ENSDART00000143692 | Nonsense | 319 | 773 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38331072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36963600 |
GRCz11 | 16 | 36917484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTGAGCGACTCCAGCACTGCCACCTTGAGGGTCAGCATCCCAAAAGAT[G/T]AGCCTCCTCTGGCCAGAGCGGGCACAGACCGGGTCATTACCCTGCCTCTC
Long Flanking Sequence:
AACCAAAAATATTTTATCATTTATTAATTTATTTTGTAGAAAAAAATGCTGTTCATAAGCAGACAAATTATCTATGAGCCCTCTAAATAAACCTTCAGAATTCATACTATATACATAAAACAAAGTTGTGTGTATGTCTGTACCGCTGAAGTGAATATTTATGGCTTAGTGCAGGAGAAAAAACTTATTTTGAGAAAATGTTTGATGTTCTAGAAATCCACAGACACAAATGACTAAAATGTGTTGAAATAAACTCTTTAAAGTGTTTATTTTCTATATGAAAACTATTATGCCGTGAAAAAGACCAAAACTGACATAGGCATGAGGCTGTTGAAATCTTTAGTGAATGATTCCTTTGGGTTTTCTTTTAATTAGTATTGACCTCATTAACTTCATCCTGACCTGATTTTTGCTTGGCCTACATTAGGCTGACAGTGTCTGATTCTGAGGGGCTGAGCGACTCCAGCACTGCCACCTTGAGGGTCAGCATCCCAAAAGAT[G/T]AGCCTCCTCTGGCCAGAGCGGGCACAGACCGGGTCATTACCCTGCCTCTCAACCACCTCACCCTGTGGGGAAACCAAAGCACAGATGACCAGGCCATTACAAGCTACCTCTGGACACTCCATCCCAGCAGCCCGACCCGAAAGGTCACCATGCAGGTAATTAGATCTTTACTTCACCCAGTGGAAAATGTAAGGTTGACCTTTTTTTTTAACTACAGTTGTTGACAGGAACGGTTTGTCTACTGCAATGTCACTTCTAAAACTCCTAAGGAGAAAGAAAATAAAATAAAATGGGTGTTCTGTTATTTTGTAACAATCTTTCTGTTTAGTTCATTCCCAAAACATTTGGGCATATACATTGTCAGTAAATAAACCAGATGGAAACCTACTGAAAAACGCCTTAGAATAACATTGAAATAAATTGCTATAACTTACTTAGGGAATGGTGGCAACATGCACGCTGGATGTATAAAACATCCTAGCATAACTTTCTAAAGAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42778
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 863 | 1061 | 20 | 25 |
ENSDART00000143692 | Nonsense | 639 | 773 | 14 | 18 |
ENSDART00000113025 | Nonsense | 863 | 1061 | 20 | 25 |
ENSDART00000143692 | Nonsense | 639 | 773 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38339149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36971677 |
GRCz11 | 16 | 36925561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAGAGAGACACAGTGATCAGACAGCTGGCCGCACTTCTGCATGTGT[T/A]GGACTCAGACATCGCACTAAAGGCTCTACATGGACAGTCTGACATCAGGT
Long Flanking Sequence:
GGTGAGAACATGCAAACTCCACACAGAAATGTCAACTGACCCAGCCGGGAGGCTGTAAAGTGATAGTGCTAACCACTGAGCCACTGTGTCGCCCATTTTGTAAATTTCCTTGAGAAAATCGTTTTTGGTTAGTAATATGCATTGCTTAGAACTTAATTTTGACATCTTTAAAGGTGATTTTCTTACTATTTAGATTTTCACCTTCAGATTTCAGTTGTTCAAATAGATGCATCTCGGCCAGATACTGTCCTTTCCTAACAAATCATACATCAATAGAAAGATTGTTTATTTTTTCATGCATACATCTCATTTACCAAAATTTAGCCTTATGGCTGATTTTGTGATCCTGGGTCACATATATTCTGCTTTTTGTTGATATTGATGTGCAGATCCGCGTGAGCGAGAGGAGGTGGAACTTGAGCTGCAGGTGAGCGTGGCTCAAGTCAGTCAGCAACAGAGAGACACAGTGATCAGACAGCTGGCCGCACTTCTGCATGTGT[T/A]GGACTCAGACATCGCACTAAAGGCTCTACATGGACAGTCTGACATCAGGTACAGTACATCTCACACATTAGCCAAACCACTCCAAATAAGGTCTTTTATTATAGAGGATCTGAAAGCATGAAGTCCAAAACTTCACTGAGTGCCTCAGACATTGTCTTGTTCAGTTTTAGATGCTTAAGTCTCAAGTCATTTAAAGAAATGGTCCACCCAAAAATGAAAATCCTGTTATTAACAACTCGCCCTCAAGTCGTTCTTAAAAGTCTTCATGCATCATCAGAACATAAATATTGATATTTTAGATGAAATCTGAAAGCTCTCTCATATTCCTCAGTAGACAGCAACAGTTCCAAGATGTTCAAAATCCAGAAATGGAAACATTCCATGTGACTTCAGTGCTTTAACTGTTATCATACAAAGCTCCAAAAACACTTTTGTCTTTACTCTCAGTTACACAATTACAAGAATTTATTAATTTTTCTCCCCCAAGCGACTGGTGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31007
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 863 | 1061 | 20 | 25 |
ENSDART00000143692 | Nonsense | 639 | 773 | 14 | 18 |
ENSDART00000113025 | Nonsense | 863 | 1061 | 20 | 25 |
ENSDART00000143692 | Nonsense | 639 | 773 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38339149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36971677 |
GRCz11 | 16 | 36925561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAGAGAGACACAGTGATCAGACAGCTGGCCGCACTTCTGCATGTGT[T/A]GGACTCAGACATCGCACTAAAGGCTCTACATGGACAGTCTGACATCAGGT
Long Flanking Sequence:
GGTGAGAACATGCAAACTCCACACAGAAATGTCAACTGACCCAGCCGGGAGGCTGTAAAGTGATAGTGCTAACCACTGAGCCACTGTGTCGCCCATTTTGTAAATTTCCTTGAGAAAATCGTTTTTGGTTAGTAATATGCATTGCTTAGAACTTAATTTTGACATCTTTAAAGGTGATTTTCTTACTATTTAGATTTTCACCTTCAGATTTCAGTTGTTCAAATAGATGCATCTCGGCCAGATACTGTCCTTTCCTAACAAATCATACATCAATAGAAAGATTGTTTATTTTTTCATGCATACATCTCATTTACCAAAATTTAGCCTTATGGCTGATTTTGTGATCCTGGGTCACATATATTCTGCTTTTTGTTGATATTGATGTGCAGATCCGCGTGAGCGAGAGGAGGTGGAACTTGAGCTGCAGGTGAGCGTGGCTCAAGTCAGTCAGCAACAGAGAGACACAGTGATCAGACAGCTGGCCGCACTTCTGCATGTGT[T/A]GGACTCAGACATCGCACTAAAGGCTCTACATGGACAGTCTGACATCAGGTACAGTACATCTCACACATTAGCCAAACCACTCCAAATAAGGTCTTTTATTATAGAGGATCTGAAAGCATGAAGTCCAAAACTTCACTGAGTGCCTCAGACATTGTCTTGTTCAGTTTTAGATGCTTAAGTCTCAAGTCATTTAAAGAAATGGTCCACCCAAAAATGAAAATCCTGTTATTAACAACTCGCCCTCAAGTCGTTCTTAAAAGTCTTCATGCATCATCAGAACATAAATATTGATATTTTAGATGAAATCTGAAAGCTCTCTCATATTCCTCAGTAGACAGCAACAGTTCCAAGATGTTCAAAATCCAGAAATGGAAACATTCCATGTGACTTCAGTGCTTTAACTGTTATCATACAAAGCTCCAAAAACACTTTTGTCTTTACTCTCAGTTACACAATTACAAGAATTTATTAATTTTTCTCCCCCAAGCGACTGGTGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42779
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 |
---|---|---|---|---|---|
ENSDART00000113025 | Nonsense | 907 | 1061 | 21 | 25 |
ENSDART00000143692 | Nonsense | 683 | 773 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 38340089)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36972617 |
GRCz11 | 16 | 36926501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTTGATCCCTGGCCCTAAACTTGCCCGCCTGCTGAGAAACCAGCTGT[T/A]GAGAGAGAAAAGCGACTTCTTGCTCTTTAGGGTCTTAAGAGTGGACACAG
Long Flanking Sequence:
ACTCTCAGTTACACAATTACAAGAATTTATTAATTTTTCTCCCCCAAGCGACTGGTGTTATACTCAGAAACTATATACATATTATATATACAAAATAAGATAAACTTTAGAATGTTGGGCAAAAAGAAGCAAATTACTTCAATTGTATTTTTTGTTCCGGCTATGGGTGTCAATAGCTGCTTTTTCCAACATTCTTTAAAATAATATTGTTTTGTTTTCAACAGAAGAAATTCATTAAAAGTTTAGAACCCCTTGAGTGTGAGTAAATGCTATGGAAATTTTCATTTTTGAGTGAACTATCCCTTTAACTGACTAAACATGTAATTAATAATCCTAGTTTAATTAGGATTATTAAAATCCTATATTTTATACAATTATACAATTATATACAATTATAAATGTGCCTCCTGTGTTTAGCACAGTATTCAGGTTCTCGGTGCAGGGTCCTGATGGTTTGATCCCTGGCCCTAAACTTGCCCGCCTGCTGAGAAACCAGCTGT[T/A]GAGAGAGAAAAGCGACTTCTTGCTCTTTAGGGTCTTAAGAGTGGACACAGTCAGTGAGTGACTTGAATCCTTTACTAAATAATTTCACTAATGTTTTACAACAAAGGAGAATTAATTTATTGTTTAATTGACTTCATTTGAATGCAATCTTTCTTATATTATCTTAATGAACACTGCAGTGTGTTTGCTGCTGTGTTCTGGGCGTGGTCAGTGTGACCCCATTACAAAAAGCTGTTCCTGTGACCCTCTGTGGATGGAGAACCCCATCCGCCTCTTCATAGACGATGGAGAGAGCAATTGTGGTTAGTATGACCTTTCCTATTTAAATTAGCAATTTCAAATAGTGGTTAAAAAAAGAGGTAAGCAAACTAAGAAGGTGTGGTCACATTTGATGAAAACCTGTGTAGGTTCAGTAACTTTTATGGTGATGAATAGGTTATTTACATTCCGTTTTTTTTTGCTTCTCAACTCTTCATTTACTATTATGTGAAAGTTCACAT
Associated Phenotype:
Not determined