ZMP
si:dkey-24n17.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA1967
Human Description:
KIAA1967 [Source:HGNC Symbol;Acc:23360]
Mouse Orthologue:
2610301G19Rik
Mouse Description:
RIKEN cDNA 2610301G19 gene Gene [Source:MGI Symbol;Acc:MGI:2444228]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa735 | Missense, Nonsense | Available for shipment | Available now |
sa34811 | Nonsense | Available for shipment | Available now |
sa13417 | Essential Splice Site | Available for shipment | Available now |
sa21636 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa735
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:
Missense, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075709 | Nonsense | 161 | 860 | 5 | 20 |
ENSDART00000133128 | Missense | 180 | 233 | 7 | 8 |
ENSDART00000136618 | None | None | 112 | None | 4 |
ENSDART00000140803 | Missense | 180 | 792 | 7 | 19 |
ENSDART00000141505 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 2907749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2853386 |
GRCz11 | 10 | 2880557 |
KASP Assay ID:
554-0642.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGGGAGGAGACCTCATGCACCAGAAACGRAAGAGATGGAGGGCCACAT[C/T]AGAAGAGGAAGCGCCCAAAAAGASCAGCTCTGCAGCCACACACAGCGTGC
Long Flanking Sequence:
ACACTTTGCGCATGGATTGTTTAAATAGAACCCTAAGTTTACCAACTATGACGACTTTCACTACTGAGAAACCTGGAAATGTGAATAGGCTCCATTAGGGGTGCTGCATAATCCTGTGGTAGTCATCTAAATCTGTCTGATACTTCCCAGGTGGGATGATCCAGCTGTCCCATCACCAGCAGATGGGCTGGAATGGGCCATTTGATGGATGGGGTGGAGGACGGAAGAGGCACTCGGAGGGGATGGGAGGGCGCAGAGCTGGACGCTGGTAAGTGGATGAAAATTGATCAGGCTGTCTGTAAATTAAACGTCAGAGTGTATATAGCCTAATAAAATATCGGTTTCTTTTAGAATATTTAATATATTTTCTTTAAACAGTCTGATTAATTCAGTTTATTTCGTGAATAACGTGTGTGAACTGTGTTTTAGGGAGGACGGTGGTGGAGGGCTGTGGGGAGGAGACCTCATGCACCAGAAACGAAAGAGATGGAGGGCCACAT[C/T]AGAAGAGGAAGCGCCCAAAAAGACCAGCTCTGCAGCCACACACAGCGTGCCTCTGTTCTCCTGCTTCTCCAGGGACACGTAAGGGCTCGTTCACACACAACACATCTTTGCTTCTGAATTGCAAGACACAACACTTTGGAATAGTGTGAAAAAAGAACAGGATAAAGCACGAGCAGGGTTTATACGGTCTGTGTGCACAGAGGATAACGAAAGTGTAAATCAGCCTTAATAGGGAGTGATATGATCATAATAGGGAGTGATATGATCAAGGCACTCTTAAAGCTGCATTTTAATCACCTAAGTTTGTTAATCAGACAGCCATGTACATGGCAACCATCTAGTAACGCATTACAGTAATCTAACCTAGAGGTCATAAAAGCATGAGTGTGTTTTTCCACATTAGACATTGATTTCATATGTTGTAGTTTGTCAAAAGTACTGGACCTGTTCTGTTAACCTCATTAATTACTAAATGTATCAAAACTACATAGAAATGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34811
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 |
---|---|---|---|---|---|
ENSDART00000075709 | Nonsense | 239 | 860 | 6 | 20 |
ENSDART00000133128 | None | None | 233 | None | 8 |
ENSDART00000136618 | None | None | 112 | None | 4 |
ENSDART00000140803 | Nonsense | 258 | 792 | 8 | 19 |
ENSDART00000141505 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 2909438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2855075 |
GRCz11 | 10 | 2882246 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGCCACTACCTCTAAGAGGACCCTGTCTCTTCCACATAGGACCAAAC[C/T]AGCCGGAGACTGAAGCGGACGTTTGCGAGTCCACCGATGATGCTTTTGCT
Long Flanking Sequence:
AACAGTACAACAGCGAGTGTGTCAAGTATAAAAGCCTTCACAACTTCAGCAGAGGTTCAAGAAAAGTATAAATCAGCCTTATTAGAGAGCCACTATAAGTACCGGAGTACTATAATCATAGTTCTTAGTTGTAGAAAGCACTCTAGCAGCTGCATTTTGAACCAGCTTGGTTTGCTAATTAGGCCTACAGGGCAACCATCTAGTAATGCATTACAGTAATCTAACCTAGAGGTCATAAAATCATGAAGTCTTTCCGTATAGGACATTGATAGCATATGTCTTAGCTTGTCAGCAATTTTTAGATGGAAAAAAAATGTTTGCTAACATTTGCTCTTGGTTTTTCCAGCCAGGCCTGTGATTACCTGGAGCTTCAGCGCCGGTATCCACACCTGCACATCCCATCCAGCCTCTTCCACCTCCAGCTGTCCTGGACGGAAAGTTTCCCTCTGGACCAGCCACTACCTCTAAGAGGACCCTGTCTCTTCCACATAGGACCAAAC[C/T]AGCCGGAGACTGAAGCGGACGTTTGCGAGTCCACCGATGATGCTTTTGCTGTTAGGGTACGAGTACAGATCATGTGGTCGCGTCAGGCTCACGTTCTCCTGCATTGGTTCACGAATAGCTCTTGTTCTCCACGCAGGTCCTGTTGTTTTCTATGCCGTGTCTTGAGGACGTGTATTCACAGTGTTGTAACCTCTCGAATGACGGTCAGACGCAGAAGGAGGCCGTTCATCCCTCCACACTTCTCAAAGTAAAAACATCTACTTAAGCCATGCAATTTATGAACAGACCTGACTGTTTTGCTTTTGTTTTCTATGCTAAACAGCATCAATGTTTTTACAGTTTTGCATTTTTAAATTAGATTTTATATTGAGACCAGTAAATTTCAGTTTGTTTTTAGTTGGCTTTATTATCGGTTGGCTTCATTGTTATCGATTTTTATAAATGTAAAAGATGTTTTATGATGAAGCATGATGAGTTTAATGTGTGATTGTGTGCTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13417
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075709 | Essential Splice Site | 295 | 860 | 8 | 20 |
ENSDART00000133128 | None | None | 233 | None | 8 |
ENSDART00000136618 | None | None | 112 | None | 4 |
ENSDART00000140803 | Essential Splice Site | 314 | 792 | 10 | 19 |
ENSDART00000141505 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 2909949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2855586 |
GRCz11 | 10 | 2882757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAAGCRTGATGAGTTTAATGTGTGATTGTGTGSTCTTCTTCCCTAATA[G/A]TTTCTGATAGTGGACAGTGGAGGTGAMCAGCGTCTTCCAGRAGGCCAYTG
Long Flanking Sequence:
TGAAGCGGACGTTTGCGAGTCCACCGATGATGCTTTTGCTGTTAGGGTACGAGTACAGATCATGTGGTCGCGTCAGGCTCACGTTCTCCTGCATTGGTTCACGAATAGCTCTTGTTCTCCACGCAGGTCCTGTTGTTTTCTATGCCGTGTCTTGAGGACGTGTATTCACAGTGTTGTAACCTCTCGAATGACGGTCAGACGCAGAAGGAGGCCGTTCATCCCTCCACACTTCTCAAAGTAAAAACATCTACTTAAGCCATGCAATTTATGAACAGACCTGACTGTTTTGCTTTTGTTTTCTATGCTAAACAGCATCAATGTTTTTACAGTTTTGCATTTTTAAATTAGATTTTATATTGAGACCAGTAAATTTCAGTTTGTTTTTAGTTGGCTTTATTATCGGTTGGCTTCATTGTTATCGATTTTTATAAATGTAAAAGATGTTTTATGATGAAGCATGATGAGTTTAATGTGTGATTGTGTGCTCTTCTTCCCTAATA[G/A]TTTCTGATAGTGGACAGTGGAGGTGAACAGCGTCTTCCAGGAGGCCACTGGTCCCCGGAAGCAGACGGAGCCAATCCAGCGAAGGACAGTTTGACGCTGGTCAACACGGCGGTCCGATGCTTGAAGGAGCAAGCTGGACTGGACCTCTCAGCCTGCACACAGTGGTCCGTATATTTCATTTATCATTTTAATTTAATAGTCAAGTTATGTTGTTTAACTATTGTCTACTACTCTGGAACTGTTTACACCTGATCACTTTATGCGTTTTATTTCTGATTGCATTACTATCTGGCTTGTGAAAATGCTTCCATTTATAGTTAAAGTCAATTTCCAAATATTTCCCAAATGAAAATGACATTTTTCACAGTATTTCCTATAATATGTTGTCTTCTGGAGAAAATCAAAGATAACAAAACAAACATCTCAAATTGTCACCTGTGGCCTTCTGTTGCTTATGGTTTTGCGCTTGTATATCTGACAGCCATATAGGCCACCACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21636
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 |
---|---|---|---|---|---|
ENSDART00000075709 | Nonsense | 505 | 860 | 14 | 20 |
ENSDART00000133128 | None | None | 233 | None | 8 |
ENSDART00000136618 | None | None | 112 | None | 4 |
ENSDART00000140803 | Nonsense | 471 | 792 | 13 | 19 |
ENSDART00000141505 | None | None | 140 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 2915286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 2860923 |
GRCz11 | 10 | 2888094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGAGATGTTCAGCGAGATGCTCCAGAGGGATTTTGGGCTTCAGCTGTA[T/A]CGGTGTCTCTGCAGTCTGCCTCAAAACATCAGCGACCCACAGACTGAAGC
Long Flanking Sequence:
TCGGACGCAGCCACAATCTTACAATCACTCCATATCTCCAAAAAAAAAAAAAAAATGTGCATTTATGAAGTGAGCTTCACAGAAGTGAGTGGGCTTGACAAACCACCTGTAGAAACGCTCTTCATTCTATATATCTAAAAAATATCATTACTTTAGCATTACTTTATCAATTCAAGTAAATATCATTACTCTATCAACTCTTTGAGCACTAACAGTTCCTTTGTATAATTCACACTTCTTGTGTGTGTTGCCTCTTCTTGTTGAATCGCTGAATGCCTCCTCAATTGTAAGTCGTTTTGGGCGAAAGCGTCTGATAAATGACTAAAAACAGCCCCTTTCACACATACAGAGGTTTCCGGAAAATTGTGGGTGTACTCATTTATGCTGAGCTCTGTATTTTAGGATCATCTTCTGACCTCTGTCATGTGCTGCCGTCAGGTGAGCTTGATTGCGGAGATGTTCAGCGAGATGCTCCAGAGGGATTTTGGGCTTCAGCTGTA[T/A]CGGTGTCTCTGCAGTCTGCCTCAAAACATCAGCGACCCACAGACTGAAGCCAAACAGGACAACAACACCGCCAAGGTACACTAGTTCAGTATGTTTTTATTACATGTATAGTTCAAGCCAGAATTATTCAACCTCCTTTAAATCCGTTTTCTTTTTTTTTTTTTCAAATATTTCACAAATGATGTTTAACAGAGCAAGGGATTTTTCACAGTATTTCCTATAATATTTTATATTCTTATTTGTTTTATTTCGGCTGGAATAAAAGCAGTTTTTTATTTTTTAAAACTATTTTAAGGTCAACATTATTAGGCTTCTAAGTCAGGAAAGTGGGTGAGTCCAGTTCTGTTTAGGTGGGAGTGTCGGGGGAGGGAAAGAGGGAAGGTTTTGCATAAAAATGAGAGTTTCCGTTCGGGCACACACTGATTTTCACAGACAAAACAAACACAGAGACAGGGGAGATAGACAGTGACGGTGTTTACATGGACATCAGTCATCCAATT
Associated Phenotype:
Not determined