ZMP
si:ch211-198c19.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA1009
Human Description:
KIAA1009 [Source:HGNC Symbol;Acc:21107]
Mouse Orthologue:
4922501C03Rik
Mouse Description:
RIKEN cDNA 4922501C03 gene Gene [Source:MGI Symbol;Acc:MGI:1925343]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22910 | Nonsense | Available for shipment | Available now |
| sa22911 | Essential Splice Site | Available for shipment | Available now |
| sa42783 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa22912 | Nonsense | Available for shipment | Available now |
| sa22913 | Nonsense | Available for shipment | Available now |
| sa12261 | Nonsense | Available for shipment | Available now |
| sa16595 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22910
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 266 | 1367 | 8 | 25 |
| ENSDART00000142104 | Nonsense | 266 | 1367 | 9 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40574016)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37958816 |
| GRCz11 | 16 | 37908848 |
KASP Assay ID:
2261-0098.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCAGTTCCAAGTTTGGCCGTTGCGAGAGAAAATCGTCCAGAAAGCAAA[C/T]AAACAGACATGCCAGCACTGGAACCCGCAGGTATGGCAAGCAGTTGGTTT
Long Flanking Sequence:
AGGCCTATCTAAAAGGTTAATGCTGCCAACTGATGATCAACAGTAAAAATTAAAAGTTTTACCTCTTCCCAACAGGGAAAACCACAAACAATCAAGAATGCATGGTTATATGCTGTCAAGGCTTTACAATCAAAAAATCTCGATATAATGGAAGTCAGTGGGGCAAAAACTGCCCCTAAAATAATGAAAGGGTAGTCAATATAAACAGTACACAAGGGTTAAAATGAATAATTTTTGTCATGAAATTTAATAGCTCCTAATTTTAAACCACAATATCTGCTTCTCTGTGATTTTTAGAAACCTGAAAGACTTGGGATGCTGGCCAAAGGTATACAACACTCCAAATGTCCACATATAATGCTGCAAATATTTTGAGGAAGCTGAAATGCTCTTCTTGTGTCCCAGTGTCATTACACGACTCTCTAAATTCCACGGATGGAGCATTGGCTCCGGCAGTTCCAAGTTTGGCCGTTGCGAGAGAAAATCGTCCAGAAAGCAAA[C/T]AAACAGACATGCCAGCACTGGAACCCGCAGGTATGGCAAGCAGTTGGTTTGTTTAAACCTACAGTATGTTGAGAAGGTAAACATCAGGCAGTTAATGTCACACCTTCTCTCCTCCGTATGTTTGAAGTGCAATCATATGGTCAGAGTGGAGGGAGTGAGATGGAGGCACTGCAGGAGGCGTACAGGCAGATCAGCGGCTCAGCAGGAGTGTGTGAAGATGGACAAGTCGAGGCTGGCAGGACTCCTCTTTCTCTCTCTACACTCCAGCCTGCGTCCACCGTGGAGTCAGGTCAGACTCGGCACATGGCTGGTTTCTGCCAGTCACTGTGGGCATGCCTGCACTACAGACCTTTTGATTTGCAGCTTTTTCTGTGCAAATGCTTCCAGTTAAACATTAAAGTGAAGAACGTGAGATGGCTAACAAGTTCTTTGTTTGCAGCAGAAGTCCTGTTAGCTGACTCTAAACAGCTCGATTTGGGACTGTCAAGTAACAGACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22911
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Essential Splice Site | 665 | 1367 | 15 | 25 |
| ENSDART00000142104 | Essential Splice Site | 665 | 1367 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40588410)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37973210 |
| GRCz11 | 16 | 37923242 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAAAGAGATGAAAGAACAAGAGACTCTGATTCAGGGTTACCATCAGG[T/C]AAGTCTTTCTCAAGGATAAAAATGGAGAGGAAAAAATGACCATTTCATCC
Long Flanking Sequence:
ATTTCATGGTGCCACAAAAGCAGTTGTTACACAAACACATTATTATTCATTATTCAAGGGAGTTTTTGTTTTGCTAGCATTTCATTATAAGAATCCATTTAAATGAGCTGCCTTAAAAAAGTGAACATACTAAAGCTATTCAAAATTGACTGAAGGAGGACAGCATGTCTCTGCCCACACTGTTGAAAGGCTTATGCAACGGTTACATAAAATATAACAACATGTCAACGTCAAAGAAAAGCTTTAAATACGCTATTATACAAAAAAAAAATATTTCCATGCTGCACTTTTTTGTTAATGCACCTAATAATGTTTGATCAGACAGTTCCCAGTCAATTACTGTTAATTGCTGTATTCGCAGTTGCACCGTGCCGAAGAGGCCAGTAACAAACGGAAGTGGAGTTTTGGTGAAGCTTCAGACCCTGTGACTGAAGAGAAACTCAAGCTCATAGAAAAAGAGATGAAAGAACAAGAGACTCTGATTCAGGGTTACCATCAGG[T/C]AAGTCTTTCTCAAGGATAAAAATGGAGAGGAAAAAATGACCATTTCATCCCATGACTGATCAGTCAAAAAGCCAAAATGTTCAGGTGATCTACAGTAGAGAATATTGCATTGTGTTAGCTACACATGTTTTTTTTACCCAAAATAAATCTAAAAGTCTTGCCCTCTCATAATTTTTGCAGCAGTCATGAAGTTTTTCATGTTTTTACTGAATGTTCAACATTGGTGCCACTTTTTAGATTGTTTAAATGCATTATTGAAGGATTGGGCTTTAGTTTCAACAACAACAAAAAATCTTTCTGGCTGTAAATATTCCAAGGAAAGAATGGAAAAATGTTAACTTTATAGTTGGCCAAGCAAAATTAGTTGCAGGATTAGTCTTAAGGTGTGGATAGTAAATGTTCTTAACTTGTTTACAGCTCTAGTGGAATTAAGAATAAGGGGAGAATATACTTTTTCCAACTATAAGGAACATGGATTTTTTTTTTTGCGCAGATGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42783
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 788 | 1367 | 19 | 25 |
| ENSDART00000142104 | Nonsense | 788 | 1367 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40599013)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37983813 |
| GRCz11 | 16 | 37933845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCAATAACCATTTTGCTTTTTCTGTCAGGCGATAAAGGTTTCGAATTG[A/T]AACTGCTCCATGACAAACATCGAGAGGAGGTCACAGAGCTGAAGAAAAGA
Long Flanking Sequence:
TAGGATCAAGTAAATTAGAAATTCCAAGAGTTCAGTCAAAAAAGGGTGAATCCACTATCAGCTACTATGCCCCCTGCTGCTGGAATCAGCTTTCAGAAATGATCAGATGTGCTCCAACATTAGGCACATTTAAATCAAGACTTCAATCCCATCTGTTTAGCTGTGTTTACTGAGTGAGCACTGTGTGATATGTGAACAGATCATGCTATTGTGTCTTTCTTTTCTTTTTTTCATTCCTTTAAAACCTGTTTTAACACTTTTTAATCAGTTTTTAATAATTTTTTTTCTTTGTTGTTTCTATTTTTGTAGACTTCCATTTAATGTTTCTTTTATTCTTGTTTATGTAAAGTGCTTTGAATTACCATTGTGTATGAAATGTGCTATATAAATACACTTGCCTTGTTTTGCCTACTAATTGAAAAACCCTGTTTTAGCCCATTCTAATCTTAGCAGCAATAACCATTTTGCTTTTTCTGTCAGGCGATAAAGGTTTCGAATTG[A/T]AACTGCTCCATGACAAACATCGAGAGGAGGTCACAGAGCTGAAGAAAAGACTGCAGTGGTACGCCAAGAACCAGGAACTACTGGACAAAGATGCAGCCAGACTCCACGCCGCCACCGCTGAGATTCAAAAGCTCACTGAGCAGGTAGAAAAGCTAAAAGCGGAGGTTAGCAGGAGGGCCAATGAGCAACAAAGAAAGGCAAAAGAAAAAGCAGGTGAAGCAAAAAGAATCCAAGACCTAGAGCGACAGGTCAGTCACTATGACATGCTCTCTCTCTCTTTCTCTCTCTCCAGATAGCATTGTTGCTGTGGGTACTGCTTATTTAAGCCACGTTCTTTTTTGGGCTCGATTTCCTGAGCGCCAGAATTATTCAGCCGTGTCCTTGAGCAGCTGGCCATCTGTCTGGATAGTCAGTTTTGCAAACTCCTCTTAATGTTATGCTTTTTTTATTCGACTGATATTCATCCATCATATCTGGATGAATAAATTTAATAGCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22912
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 869 | 1367 | 19 | 25 |
| ENSDART00000142104 | Nonsense | 869 | 1367 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40599256)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37984056 |
| GRCz11 | 16 | 37934088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGGCAAAAGAAAAAGCAGGTGAAGCAAAAAGAATCCAAGACCTAGAG[C/T]GACAGGTCAGTCACTATGACATGCTCTCTCTCTCTTTCTCTCTCTCCAGA
Long Flanking Sequence:
ACCTGTTTTAACACTTTTTAATCAGTTTTTAATAATTTTTTTTCTTTGTTGTTTCTATTTTTGTAGACTTCCATTTAATGTTTCTTTTATTCTTGTTTATGTAAAGTGCTTTGAATTACCATTGTGTATGAAATGTGCTATATAAATACACTTGCCTTGTTTTGCCTACTAATTGAAAAACCCTGTTTTAGCCCATTCTAATCTTAGCAGCAATAACCATTTTGCTTTTTCTGTCAGGCGATAAAGGTTTCGAATTGAAACTGCTCCATGACAAACATCGAGAGGAGGTCACAGAGCTGAAGAAAAGACTGCAGTGGTACGCCAAGAACCAGGAACTACTGGACAAAGATGCAGCCAGACTCCACGCCGCCACCGCTGAGATTCAAAAGCTCACTGAGCAGGTAGAAAAGCTAAAAGCGGAGGTTAGCAGGAGGGCCAATGAGCAACAAAGAAAGGCAAAAGAAAAAGCAGGTGAAGCAAAAAGAATCCAAGACCTAGAG[C/T]GACAGGTCAGTCACTATGACATGCTCTCTCTCTCTTTCTCTCTCTCCAGATAGCATTGTTGCTGTGGGTACTGCTTATTTAAGCCACGTTCTTTTTTGGGCTCGATTTCCTGAGCGCCAGAATTATTCAGCCGTGTCCTTGAGCAGCTGGCCATCTGTCTGGATAGTCAGTTTTGCAAACTCCTCTTAATGTTATGCTTTTTTTATTCGACTGATATTCATCCATCATATCTGGATGAATAAATTTAATAGCTTTCTCATACATTCTTTTGTATGAGTTTTGTTGTCAAAACTTTGTTTTGGTCAACTCTGGCTTGCAACATTTCACAAACCCTTCAGTTCACCAACACATATACATTTGTTGTGCCTTCTATGATTTTCTATTATCAGCATTTTAAAAAAATATATATAATTTTATTTACATTTAATTATACACGGTCAAAAGTTTGGGGTCAGTAGGATTTTTAAATGTTTTAAAATGAGCTTCTCCTGCTCACCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22913
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 946 | 1367 | 20 | 25 |
| ENSDART00000142104 | Nonsense | 946 | 1367 | 21 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40600979)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37985779 |
| GRCz11 | 16 | 37935811 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGGCCGAGATGAAGCAGCCAAACGCAGCCTCCGAGCAATGGAACAA[C/T]AGTATCACAGAATCAAAGTACTCTTTTCATATACAGATTACGTGTTCTTA
Long Flanking Sequence:
GGTGACATTTATTTTTTACTATTATCATCCTTTTACTTTTTTTTTGTATCCACCCAAGAGCCAAACATCTGCGATCCATTACCAGAAGACACTTTTCTCTTGCCCTACAGGTTTTTTTACTTGTTGTTTGTTGAACTTGTTGTTTCTACTTGTTGAACCCACTTCTTGATTTAAAGAATTTTCTGATATTTGGACTTGAAATGAGACAAAAAAAATCTTAAGTAAAGCATTTTTTGTAGTGCATCTATCACTCATGTTCTCATTTCCTCTCTCAGCTCAAACAGAAGGAAGAACTCTTGAAACGCAGGCATCCAAATTCTCTGCCAGCCCTGATTTTGGCAGCTGCGTCTACCGGGGCTGAAGAAGATCGACTGGATGTCCGTTCTCTAGCTCAGTCCTCTCAGACAGCGGCTTTGTTAGAGAGACGTGTTCATCGCCTGGAGGCAGAGCTGGAGGGCCGAGATGAAGCAGCCAAACGCAGCCTCCGAGCAATGGAACAA[C/T]AGTATCACAGAATCAAAGTACTCTTTTCATATACAGATTACGTGTTCTTAAATTTGCATATAAGGACTAAAAACACAATTATTAAACTGGTTTGTACTGCTGGAACATGATATAGCTGGTTTCACTGTTCACAGCATTTCTGTTTTTATTTAGTATGGGGACACGTAATTCAAAGTATTTGTCTGTTTTTTAAGCATGTTTTTTTTTTTACCAGAGCTCGCAGCTGGATCGATCTGTTTCCAGAAAATAAGTTTGCTGAGAAAATAAGGTTTCTATTTATAGTCTTAAGTGCACAGGGCTTATAATATGCCGTCTGAGTGGCATCATTTCATTCATTTCTAAACCCTGCTGTGTTCTACACGACTTGAATTTAGAAAGAGATGCTGATTCCAAGTAATGTTGGATAGTTACTCTATATTTGGTCAGTGTTTGAAAGTATTAATTTAACAGTAAATTCACCAAGGCCGAGTTTTCTTTGCTTAAAAACACACAAAAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12261
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 1288 | 1367 | 24 | 25 |
| ENSDART00000142104 | Nonsense | 1288 | 1367 | 25 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40607517)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37992317 |
| GRCz11 | 16 | 37942349 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACTAGCCTAGAGCAAAAAATTCAGWCCATGGARTTCAGATACAGTCAA[C/T]GAGAGAAACAACTTCAGCAGGTAAAACACCCACACATTCTTCTATATGTG
Long Flanking Sequence:
AAACTAATGAACTTCAACATGTCTGTTTATATGGCTGTGTGCAACAATTGGCACTGTACAGTATCTCACCTTGACACTAAAAACACCAAAGCCCTTGATTTGTTTCACTAGAAAAGAACTGATATAATTTGACTGCATCTTGAATCACTTTGAATCCTGAATCTTTGTTATTTTTACTACTCAGATCATAGTACAACATTTACAAGGGCAAGTAAAAGAGCTCCAGGGAACCAAAGAAGCTCTGGCTGTGACGAAGCTCAGAGAGGAGACCCTGCAGAATCAGGTAAAGTCTGACTTTACTGAGGTTTAGTGATTTCAGTTTCTGTAAACACAAGGTTTTTCATTTGCTTTCTGCTTTTTTGCTTTCTTTTTCTGTGCATCAATAGCTGTCTAAACTTCTAGAAGAGCTAAAAGAGGCCAAAGAAGCCCACAGTCCTGAACTAAAACACTTCACTAGCCTAGAGCAAAAAATTCAGTCCATGGAATTCAGATACAGTCAA[C/T]GAGAGAAACAACTTCAGCAGGTAAAACACCCACACATTCTTCTATATGTGCTATACTGTTCAAAAGTATTGAGTCAGAAAGATTTGTTTATAGTCATAAGGGGATAGGTCACCCAAAAATGAACATTTCCTCATTGTTTACTCGAATGGTTCTAAACTCGATGTTCTAAACTTTAGAACACTAGAGAGGTTCTAAACTTTTATGATGTTATTTCTACTGCAGATGCCTTTTACTGTTTCAAAACATAAAAAATGTGATCCATGTATACTGTATTAGTAACCAAACACCAACCAAAGTACACCCACCCTATCCCTGACAGAGCATAAAAACATATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATAATATAATATAATGAAAAGGGCAATTTGTAAAATACATTAAGAAAATGACAGTTCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16595
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 |
|---|---|---|---|---|---|
| ENSDART00000126898 | Nonsense | 1291 | 1367 | 24 | 25 |
| ENSDART00000142104 | Nonsense | 1291 | 1367 | 25 | 26 |
Genomic Location (Zv9):
Chromosome 16 (position 40607526)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 37992326 |
| GRCz11 | 16 | 37942358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAGCAAAAAATTCAGWCCATGGARTTCAGATACAGTCAAYGAGAGAAA[C/T]AACTTCAGCAGGTAAAACACCCACACATTCTTCTATATGTGCTATACTGT
Long Flanking Sequence:
AACTTCAACATGTCTGTTTATATGGCTGTGTGCAACAATTGGCACTGTACAGTATCTCACCTTGACACTAAAAACACCAAAGCCCTTGATTTGTTTCACTAGAAAAGAACTGATATAATTTGACTGCATCTTGAATCACTTTGAATCCTGAATCTTTGTTATTTTTACTACTCAGATCATAGTACAACATTTACAAGGGCAAGTAAAAGAGCTCCAGGGAACCAAAGAAGCTCTGGCTGTGACGAAGCTCAGAGAGGAGACCCTGCAGAATCAGGTAAAGTCTGACTTTACTGAGGTTTAGTGATTTCAGTTTCTGTAAACACAAGGTTTTTCATTTGCTTTCTGCTTTTTTGCTTTCTTTTTCTGTGCATCAATAGCTGTCTAAACTTCTAGAAGAGCTAAAAGAGGCCAAAGAAGCCCACAGTCCTGAACTAAAACACTTCACTAGCCTAGAGCAAAAAATTCAGTCCATGGAATTCAGATACAGTCAACGAGAGAAA[C/T]AACTTCAGCAGGTAAAACACCCACACATTCTTCTATATGTGCTATACTGTTCAAAAGTATTGAGTCAGAAAGATTTGTTTATAGTCATAAGGGGATAGGTCACCCAAAAATGAACATTTCCTCATTGTTTACTCGAATGGTTCTAAACTCGATGTTCTAAACTTTAGAACACTAGAGAGGTTCTAAACTTTTATGATGTTATTTCTACTGCAGATGCCTTTTACTGTTTCAAAACATAAAAAATGTGATCCATGTATACTGTATTAGTAACCAAACACCAACCAAAGTACACCCACCCTATCCCTGACAGAGCATAAAAACATATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATAATATAATATAATGAAAAGGGCAATTTGTAAAATACATTAAGAAAATGACAGTTCAACTTGTACACTG
Associated Phenotype:
Not determined