ZMP
si:ch211-236l14.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B7ZCZ7]
Human Orthologue:
KIAA1161
Human Description:
KIAA1161 [Source:HGNC Symbol;Acc:19918]
Mouse Orthologue:
AI464131
Mouse Description:
expressed sequence AI464131 Gene [Source:MGI Symbol;Acc:MGI:2140300]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17442 | Nonsense | Available for shipment | Available now |
sa14522 | Nonsense | Available for shipment | Available now |
sa13364 | Nonsense | Available for shipment | Available now |
sa25227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44311 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8947 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12534 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17442
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 28 | 693 | 1 | 10 |
ENSDART00000136598 | None | None | 456 | None | 8 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 24468533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23647646 |
GRCz11 | 25 | 23745194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCCCAGAGGTGACATGGGACACGGGCTTGAAAGAGATGAACGAGACCT[G/A]GAAGGGCGCAATTGCTTGCTTGGGAGTCGCTGTGTTTTTTGTCATGACAA
Long Flanking Sequence:
TTGTACCTTTCTGAAGAAGCAGTATGACGTTACGTCACACCAGCGCAAAAGTGCAGGCCAAGCAAATAAGCCGCTGAGGAGCTATTTGTAGGCATTGCTGCCAAACCCGGGTAAGGCTGCTCACTCTTCTGCAATCAATGCTTTTAAACTTGCTATTGCACTAGAAGCAGCATGCATTACATTTTTTGTTCATTCTGGAATGGTTCTGTTTGGAGAACTTGACCTGGATCATTTGATGACCGGCGGCCAGTGCGCGCAACCGCGCAATTACTAAATCCAGCTCAAATATTAACATTCGCAGGGAAGAGAACGCGTTGGACCGTTACACGATGACCATTCTGCATTTTGAAGCAGAAAGATTGTTACTTCTTATCATTTTCGATTAGATATCATTTTTTTCTTTCTATCTGAAATCATCATGCCACATACTCGCAACAGGAACCCAAGTCCAATCCCAGAGGTGACATGGGACACGGGCTTGAAAGAGATGAACGAGACCT[G/A]GAAGGGCGCAATTGCTTGCTTGGGAGTCGCTGTGTTTTTTGTCATGACAATTGGGATCATTTATTGGCAAGTTGTGGATCAGCCCAACAAGAACTGGATCCTGAAGGGTAGCTTTAGTGGACTTATTTGGGAGAGACGGACGCAAACTCTGGTCATACAGACACTGACCGAGGACAAAACTTTTGCGGAGATAGACGTGGAGAACGTGGGGAACACAGACATCGAGGTTCCGTTCGTGAGGAACATGTGCTGGCTTAACAAAACCGAGTTCTGCTACACTTGGGATTCGGTCGCAGAGGTGAAGATATCTTTGGAATCCGAGGAGGACTCGGATACTGAGTGCTACAGTGTAACCTGGACTCCAATTCACTGTCATGTGGACCTGAAGGTAAAATGCTTTTAGAACTAAACTCTTATATTTAGAAAAAAATAAATAAATAGCTGTAAAGCATGCTAATACAAAGCGTTTAGAAAGTTCTGATCCACACGTATAAAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14522
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 |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 269 | 693 | 3 | 10 |
ENSDART00000136598 | Nonsense | 55 | 456 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24422178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23601291 |
GRCz11 | 25 | 23698839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGTGTGTGGGACACAACATTAAAGTTGTCYATCAAGAGTCAATGCGA[C/T]AGCTCTCCACAAYCAGACGAGAGCTGCCAAACATGGATGTCTWACGGTAC
Long Flanking Sequence:
CACATTCTGGGGACACAAAAGATTTATATTAAATATGAAAAAGGGGTAACCTATATGCCCTTTAAAACTGAGTGTGAAAGGGAAGGTTTTTTATTTTATTTTATTTGTTAGTACACTTGTTGTGTTAACCACTTATGTGTCTGATGATGTTGTTAATATTTGTTGGTTCTTTTTTAGAAAACACGGTGTAAATTGTATTCTATTTCATGAATACACTAATATATAGATGCTCTTACAGTTAGCAGACATGGATTACATCCCACAAAAAAAGTAAATTCTGAATTTCCAGATGAGCTGACAAATAGTGACTTGAAATTGTTTTGTTTTTTTCTTTTAAAGGTGTTTCAGTTCTAGTTGCCCCTAACATCCCACTACATGTAGGAATGGAAAGCCAGCAGCAGTTCTGTTTGCAGACGCCCCCCAGCATGGAGCGCATGCCTCTGCAGTACACTGTGTGTGTGGGACACAACATTAAAGTTGTCCATCAAGAGTCAATGCGA[C/T]AGCTCTCCACAATCAGACGAGAGCTGCCAAACATGGATGTCTTACGGTACAGCACCTTTGCAAACATTAATTTCACTGTATTTCAGTAATCTTTTTTTTTTTTACTTTGACTTTCTAGGGATGCAAAATATTGCTTGAAAATTTAAGATTTGTCAATGTTATGTCTACTGTTAGAACTGGAACAAGCTGCCCAACGAGTGGAAAAGAGATTCAACGATGTTACTGTATATTATGAAGTTTTGATTTCTGACCCATTTTGAATGATACACTTTATAATAAGGGTCTATCAGTTGATGTTAGTTAATGCATTAGTTAACATGATTTAACGGTGAACAAGACATCTGTTTAAGCATTACTTAATCGTGTTAATGTTATCTAAACCTGTAAGAATGTGTTAATCAACACATAATATACGAGTTAAGTCTGATTTAGTTTATGTTTACTTACACATAGACTAGGGCTGCACGATATTGGAAAAATCATTGCGTTATTTAATTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13364
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 |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 283 | 693 | 3 | 10 |
ENSDART00000136598 | Nonsense | 69 | 456 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24422135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23601248 |
GRCz11 | 25 | 23698796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGCGAYAGCTCTCCACAAYCAGACGAGAGCTGCCAAACATGGATGTCT[T/A]ACGGTACAGCACCTTTRCAAACATTWATTTCWCTGTATTTCAGTAATCTT
Long Flanking Sequence:
GGGTAACCTATATGCCCTTTAAAACTGAGTGTGAAAGGGAAGGTTTTTTATTTTATTTTATTTGTTAGTACACTTGTTGTGTTAACCACTTATGTGTCTGATGATGTTGTTAATATTTGTTGGTTCTTTTTTAGAAAACACGGTGTAAATTGTATTCTATTTCATGAATACACTAATATATAGATGCTCTTACAGTTAGCAGACATGGATTACATCCCACAAAAAAAGTAAATTCTGAATTTCCAGATGAGCTGACAAATAGTGACTTGAAATTGTTTTGTTTTTTTCTTTTAAAGGTGTTTCAGTTCTAGTTGCCCCTAACATCCCACTACATGTAGGAATGGAAAGCCAGCAGCAGTTCTGTTTGCAGACGCCCCCCAGCATGGAGCGCATGCCTCTGCAGTACACTGTGTGTGTGGGACACAACATTAAAGTTGTCCATCAAGAGTCAATGCGACAGCTCTCCACAATCAGACGAGAGCTGCCAAACATGGATGTCT[T/A]ACGGTACAGCACCTTTGCAAACATTAATTTCACTGTATTTCAGTAATCTTTTTTTTTTTTACTTTGACTTTCTAGGGATGCAAAATATTGCTTGAAAATTTAAGATTTGTCAATGTTATGTCTACTGTTAGAACTGGAACAAGCTGCCCAACGAGTGGAAAAGAGATTCAACGATGTTACTGTATATTATGAAGTTTTGATTTCTGACCCATTTTGAATGATACACTTTATAATAAGGGTCTATCAGTTGATGTTAGTTAATGCATTAGTTAACATGATTTAACGGTGAACAAGACATCTGTTTAAGCATTACTTAATCGTGTTAATGTTATCTAAACCTGTAAGAATGTGTTAATCAACACATAATATACGAGTTAAGTCTGATTTAGTTTATGTTTACTTACACATAGACTAGGGCTGCACGATATTGGAAAAATCATTGCGTTATTTAATTTTGCTGCAATTTATATTGCAATATGAATACAATTTCAGCAGATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25227
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 |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 436 | 693 | 6 | 10 |
ENSDART00000136598 | Nonsense | 199 | 456 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24400363)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23579476 |
GRCz11 | 25 | 23677024 |
KASP Assay ID:
554-7477.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGCCACGACTTGGTTTCTGGACAAAGTGGACAGCTTACATAGCCATT[T/A]GGGCATGGAGTATGTCATCCTGGAAGGCGGTGAGGGAAACCCTTTTGAGG
Long Flanking Sequence:
GTAGGAGATTTACAAAATTCTTTACATGATATTGTAATATTATAATTTTGACACATCGAATGTATTTTCATCTATTTTCACTAATATACTTAGCCAACATCTAGCGACACACTTTTTATACACAGTGCAGACTTCTATAGACTATTTCAATGTGGTCATGCCATTGGCACATGAGCAACTGTAACAAGGGGTAATTTAATCATAACTTAATGTTAAAACAACTATAATGACATTATTTCCAAATATGTGGACCTTTTTGGGTTGTTTGAATCTATAGAAATTAAAAATGTACAGCAGGAAATAAGTTGGGACCGTTGTTTTGTTTACATTCCTCGAAATACTCAATATATAGTTAGTTGACCCATGCATTACCATTATTGTTTCTCATAAGGTGCCTTTGTTGACTCGGTGGAAAGGAAAGTACAGTGTGAAGCTCAACATCACAAACCCTGAAGCCACGACTTGGTTTCTGGACAAAGTGGACAGCTTACATAGCCATT[T/A]GGGCATGGAGTATGTCATCCTGGAAGGCGGTGAGGGAAACCCTTTTGAGGAACAGGCCCTGCGCCCCCCTCTGGAATTGGTTGGGGATGAATATATCAGACTCTTGGCTGACTTGGCAGAGAGGATAGGGGACAATGCTATTGTGACCTCAGGAACAAGGTATTTGGTACAAATCAATTACTTTTATTTGGCCAACTAGAACACAAATCATTGTTGGAGTTATTTAAGCCTTTGCACTTTCGGTGGAATGCTACTATCTTGAGAAATATCTAGTAAACTATTATGTAATGTCATTATGTATAAAAGATATCAATTATTAGAAATAAGTTATTAAAGGTGCAGTAGGTGATCTGCCTAAATGCTAACTGGTTAGCATAATATCTATATATATATTTATATATATTTTTTTTTTGGTTGCAAAGGTCCAGCCACAAACCACTCTTCATCCGCATGAGTGCACTACAGTCAGACTGGAGTTATTCCGGCCTCAAGGGCATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44311
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089278 | Essential Splice Site | 489 | 693 | 6 | 10 |
ENSDART00000136598 | Essential Splice Site | 252 | 456 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24400202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23579315 |
GRCz11 | 25 | 23676863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGGCAGAGAGGATAGGGGACAATGCTATTGTGACCTCAGGAACAAGG[T/C]ATTTGGTACAAATCAATTACTTTTATTTGGCCAACTAGAACACAAATCAT
Long Flanking Sequence:
CATTGGCACATGAGCAACTGTAACAAGGGGTAATTTAATCATAACTTAATGTTAAAACAACTATAATGACATTATTTCCAAATATGTGGACCTTTTTGGGTTGTTTGAATCTATAGAAATTAAAAATGTACAGCAGGAAATAAGTTGGGACCGTTGTTTTGTTTACATTCCTCGAAATACTCAATATATAGTTAGTTGACCCATGCATTACCATTATTGTTTCTCATAAGGTGCCTTTGTTGACTCGGTGGAAAGGAAAGTACAGTGTGAAGCTCAACATCACAAACCCTGAAGCCACGACTTGGTTTCTGGACAAAGTGGACAGCTTACATAGCCATTTGGGCATGGAGTATGTCATCCTGGAAGGCGGTGAGGGAAACCCTTTTGAGGAACAGGCCCTGCGCCCCCCTCTGGAATTGGTTGGGGATGAATATATCAGACTCTTGGCTGACTTGGCAGAGAGGATAGGGGACAATGCTATTGTGACCTCAGGAACAAGG[T/C]ATTTGGTACAAATCAATTACTTTTATTTGGCCAACTAGAACACAAATCATTGTTGGAGTTATTTAAGCCTTTGCACTTTCGGTGGAATGCTACTATCTTGAGAAATATCTAGTAAACTATTATGTAATGTCATTATGTATAAAAGATATCAATTATTAGAAATAAGTTATTAAAGGTGCAGTAGGTGATCTGCCTAAATGCTAACTGGTTAGCATAATATCTATATATATATTTATATATATTTTTTTTTTGGTTGCAAAGGTCCAGCCACAAACCACTCTTCATCCGCATGAGTGCACTACAGTCAGACTGGAGTTATTCCGGCCTCAAGGGCATCATTCCATCCCTGCTGCATCACAGTCTTCTGGGATATAATTTCTTCATTCCTGATGCAGTAGGTAATACCTGCTCACACACACATAAATATACTTTTTCTTTTTTTGTGAAAAGGCATACCATAGATAAAGAAAACATAATCTTTCCACTAACTGCCACACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8947
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 583 | 693 | 9 | 10 |
ENSDART00000136598 | Nonsense | 346 | 456 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24389578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23568691 |
GRCz11 | 25 | 23666239 |
KASP Assay ID:
2261-9745.1 (used for ordering genotyping assays)
KASP Sequence:
TTATYAAGMATTCACTTTTCTGTCTAGGTTCTAAACCTCACCAGGTTCTA[C/A]ATAGCCAAGCATCATGACTTCGTAGTTCCTYTGATACTGAAATACGCAGA
Long Flanking Sequence:
CGTTACTGGACCATAAAATGGTTTTGATCTTGGATCATGGAAATTATCTTGACAATTTTAACCCTCTTAAATCCGTAGTCGTTAGTTTTAATTTTTAATATGCTGATTATACCAGACATTGTCTCTTGCTGTTATTTCAATTCTTGAGTTATTTCCCTCTGAACTCAGCGACTACACTTAGTATAAATAGGAGCAAAACGGGAAGCCACATGCCTGTTTTCTCTATTTAAAATTAGGCTGAGCGCAGGCAGTTATTCAAAATTCATCTCATGAAACTGTTTTCATCTAGAGGATACTTTTTTTATGAATGTGGTTTTGCTTAGTTTTCGTCACCAGAGACTGGCTATGTTAACTGATGGATGTGACCTCTTAAGGAATGTTAAAAACTAACCACAGCAGAACTAGACAAGAATGGTGTTAAGAAAAACTCACATCCTCTTTCATATAAGTTTATTAAGCATTCACTTTTCTGTCTAGGTTCTAAACCTCACCAGGTTCTA[C/A]ATAGCCAAGCATCATGACTTCGTAGTTCCTTTGATACTGAAATACGCAGACGAATGGCAAGAGACTGGAAACCCCATCTACAGACCACTGTGGTGGCTTAGTCCAAATGACCCAATCACTTTCAGCATTGATGATGAGTTTCTCATTGGAGATGAGGTAAGCAGCTTTTGGAAAAGTAAGATAATGGGCTCTATGGTTAGGTTTTTTCTTTGCCACTGCAGCCACTGATTGTCATTTACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGACCAGCTAGTGAAGTGCTGTGCAGGTAAGCCTCACTCCTCTGACCTCCTAAATGTGCTCTAGCGACAGAAACTAGAGGCAGGGGTCTTTAGCCCCTTTGTTAGAGCAACCGACTCCCATGTGAAAGATTGCCGGTTCAATCCCAGCATGGAGCTGGGGGGGTTACATATACTATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12534
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089278 | Nonsense | 614 | 693 | 9 | 10 |
ENSDART00000136598 | Nonsense | 377 | 456 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 25 (position 24389485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 23568598 |
GRCz11 | 25 | 23666146 |
KASP Assay ID:
2261-9744.1 (used for ordering genotyping assays)
KASP Sequence:
TACGCAGACGAATGGCAAGAGACWGGAAACCCCATCTACAGACCACTGTG[G/A]TGGCTTAGTCCAAATGACCYAATCACTTTCAGCATTGATGATGAGTTTCT
Long Flanking Sequence:
TTTAATATGCTGATTATACCAGACATTGTCTCTTGCTGTTATTTCAATTCTTGAGTTATTTCCCTCTGAACTCAGCGACTACACTTAGTATAAATAGGAGCAAAACGGGAAGCCACATGCCTGTTTTCTCTATTTAAAATTAGGCTGAGCGCAGGCAGTTATTCAAAATTCATCTCATGAAACTGTTTTCATCTAGAGGATACTTTTTTTATGAATGTGGTTTTGCTTAGTTTTCGTCACCAGAGACTGGCTATGTTAACTGATGGATGTGACCTCTTAAGGAATGTTAAAAACTAACCACAGCAGAACTAGACAAGAATGGTGTTAAGAAAAACTCACATCCTCTTTCATATAAGTTTATTAAGCATTCACTTTTCTGTCTAGGTTCTAAACCTCACCAGGTTCTACATAGCCAAGCATCATGACTTCGTAGTTCCTTTGATACTGAAATACGCAGACGAATGGCAAGAGACTGGAAACCCCATCTACAGACCACTGTG[G/A]TGGCTTAGTCCAAATGACCCAATCACTTTCAGCATTGATGATGAGTTTCTCATTGGAGATGAGGTAAGCAGCTTTTGGAAAAGTAAGATAATGGGCTCTATGGTTAGGTTTTTTCTTTGCCACTGCAGCCACTGATTGTCATTTACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGACCAGCTAGTGAAGTGCTGTGCAGGTAAGCCTCACTCCTCTGACCTCCTAAATGTGCTCTAGCGACAGAAACTAGAGGCAGGGGTCTTTAGCCCCTTTGTTAGAGCAACCGACTCCCATGTGAAAGATTGCCGGTTCAATCCCAGCATGGAGCTGGGGGGGTTACATATACTATATACCGTTTATAAATGCTTTGACATTTCTGAGTTAGTCTAAGGCTCAGCTGCTCAGATCAAGTTCTATGATTGATGATTCCACCAGCAGAAAACAG
Associated Phenotype:
Not determined