ZMP
si:ch211-71k24.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate brefeldin A-inhibited guanine nucleotide-exchange protein 3 (KIA
Human Orthologue:
KIAA1244
Human Description:
KIAA1244 [Source:HGNC Symbol;Acc:21213]
Mouse Orthologue:
D10Bwg1379e
Mouse Description:
DNA segment, Chr 10, Brigham & Women's Genetics 1379 expressed Gene [Source:MGI Symbol;Acc:MGI:10638
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42119 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22200 | Nonsense | Available for shipment | Available now |
sa16643 | Essential Splice Site, Missense | Available for shipment | Available now |
sa44780 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13753 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42119
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114456 | Essential Splice Site | 141 | 1717 | None | 32 |
ENSDART00000137124 | None | None | 1352 | None | 23 |
ENSDART00000146355 | Essential Splice Site | 136 | 176 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 2233155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2200819 |
GRCz11 | 13 | 2453206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAAGATTTGTCATTAGGATTTGCTGAAAATCTGTGTTGTTGTTTCTCT[A/T]GGTATGTATAGAGACGTATATATCCAGTTGTCATCAGCGCAGTATCAACA
Long Flanking Sequence:
TTGGGTCAGTTTTCTGTGTGGAGTTTGCATGTTCTGCCCGTGTTTGTGTGGGTTTCTTCCTGGTGCTCTGGTTTCCCCCACAGTCCAAACACATGCGCTATAAGGGAATTGATTAAACTAAATTACCCGTTGTGTATGAATGCGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAATGAGTTGGAGGAGGAGTCTGTTGTAATAACTCTCTGCAAACACATTACCCCATATTTATGAAATGCCTACTTTACTACATCCAATCAGCTCGCAGCAGAAAAAACAAGCCACACCCACTGTTTTCTCATTTAATATTCCGTTTCTCTAGGAACTGCGTCTCAATATGGAAAAAAATAAACGGTCGCAGCTTCCGGTTCATGCAGACTATCTTCTCTGTACTCCACATACTCAATATAATCTCTGTACTCCACTGTAAATGAGGCTAACTTTTTAAGATTTGTCATTAGGATTTGCTGAAAATCTGTGTTGTTGTTTCTCT[A/T]GGTATGTATAGAGACGTATATATCCAGTTGTCATCAGCGCAGTATCAACACGGCGGTCAGAGCCACTCTCAGCCAGATTCTTGGAGACCTCACTCTACAGCTACGCCATAGACAAGAAAACACAGTGAGTCACGTGCTATAAGACTTCAACTGAGCTTCAATAAAAACAAACGCATGTCTATACAGAATGTCAGTGGTGGGATTCTGTGCACACATAATTTACAATAAGGTCTCATTTGTTTATTGAAACGGTTTAATCTGCAAAAACAACCCTCCTGAATATACTTTATCCGGTTTGTTACACTGCTACTTGCTACAAAACATAGACATTAGACACAAAACATTGTTCTGAGCCATAATAGTTTATGAATTCTTTAATTAAACACAAAACTGATAGAAACGTAACTGGCTGAATGGAGTATACACTAACCTGCGCATTTTTCAGACAGTCAAAAAAAGTCAAAACATGACAGACAAGCAGATACAAACTGTATGATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22200
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 |
---|---|---|---|---|---|
ENSDART00000114456 | Nonsense | 482 | 1717 | 12 | 32 |
ENSDART00000137124 | Nonsense | 254 | 1352 | 4 | 23 |
ENSDART00000146355 | None | None | 176 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 2240610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2193364 |
GRCz11 | 13 | 2460661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGAGTCAATGCGTGAGTCTGTGGAAGTCAACGAAGCGGACTTCCGCTG[G/A]CAGCGGCGAGTGCTCTCATCCGAAAACGCTGCATGGGAGGCGAGCATTAC
Long Flanking Sequence:
ATAAACAGGTTAACTCTTCTAATAAGCATGTTGTTGTTTTCCCTCATTCTCCCAGATTGTGGGAAGCCCCCAGCGCTTGTTTGACCTCGCCGGTCCATGCGTGATTGAACACGAGACGAGAAAGAGGTCTTTCTCCAAAAGGAAATCACATCTCGATCTTCTCAAACTGTAAGATGTTTTGTATAAAATTCAGTGATGATCTAGTTACTATATTGGAGATCTTAAAAATCTGTTGTGTGTCTCCAATGAGTGATTCGTCTTTCCTAATTTCCCAGCGTAATGGATGGCATCACAGAAGCGTGTATGAAGGGTGGGATTGAGGCCTGTTACTCCTCCGTCTCCTGCGCCGGGGCCCTATTAGGTGCCTTGGATGAGCTCAGTCAGGGGCGTGGCCTGCAGCAGGACCAGACCCGCATGCTGCTGCGCCGATTGGAGGAGCTCAAGGAAGGGGCGGAGTCAATGCGTGAGTCTGTGGAAGTCAACGAAGCGGACTTCCGCTG[G/A]CAGCGGCGAGTGCTCTCATCCGAAAACGCTGCATGGGAGGCGAGCATTACCGAACGCAGCCCTGACATTAGCATTAGCGTCACCACCGACACAGGCCAGACCACTTTGGAAGGGGATGTAGGGCAGACTACGCTTGAAGGGGATATGGGGAGGACCACTCCTGAAGATTGCGGGGACGAACCGCGACTACCTTCGCCTACCTGTGGATCTCGTCAGGAGTGTGTCGCACCTGAAATCTCATCCTCTACGGCTCCTCCTGACGTAGTGCAACGCAGCCATGGCCTAGCCTATCCTGACATCACCAACTTCTTATCGGTGGAGTCCCGGACGCGTTCGCATGGCTCCCGATACAGCGAGAGTAACTTCAGTGCCGACGAGCAGGAGCTGTCCAGAACAGAGTTTGACTCCTGTGATCAGTACTCCATGGCTGCAGAAAAGGACTCCGGACGGTCTGATGTATCCGATATGGGCTCTGATAACTGCTCATTGGCTGATGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16643
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114456 | Missense | 509 | 1717 | 12 | 32 |
ENSDART00000137124 | Essential Splice Site | 280 | 1352 | 4 | 23 |
ENSDART00000146355 | None | None | 176 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 2240689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2193285 |
GRCz11 | 13 | 2460740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCATGGGAGGCGRGCATTACCGAACGCAGCCCTGAMATTAGCATTAGC[G/A]TCACCACCGACACAGGCCAGACCACTTTGGAAGGGGATGTAGGGCAGACT
Long Flanking Sequence:
TTTGACCTCGCCGGTCCATGCGTGATTGAACACGAGACGAGAAAGAGGTCTTTCTCCAAAAGGAAATCACATCTCGATCTTCTCAAACTGTAAGATGTTTTGTATAAAATTCAGTGATGATCTAGTTACTATATTGGAGATCTTAAAAATCTGTTGTGTGTCTCCAATGAGTGATTCGTCTTTCCTAATTTCCCAGCGTAATGGATGGCATCACAGAAGCGTGTATGAAGGGTGGGATTGAGGCCTGTTACTCCTCCGTCTCCTGCGCCGGGGCCCTATTAGGTGCCTTGGATGAGCTCAGTCAGGGGCGTGGCCTGCAGCAGGACCAGACCCGCATGCTGCTGCGCCGATTGGAGGAGCTCAAGGAAGGGGCGGAGTCAATGCGTGAGTCTGTGGAAGTCAACGAAGCGGACTTCCGCTGGCAGCGGCGAGTGCTCTCATCCGAAAACGCTGCATGGGAGGCGAGCATTACCGAACGCAGCCCTGACATTAGCATTAGC[G/A]TCACCACCGACACAGGCCAGACCACTTTGGAAGGGGATGTAGGGCAGACTACGCTTGAAGGGGATATGGGGAGGACCACTCCTGAAGATTGCGGGGACGAACCGCGACTACCTTCGCCTACCTGTGGATCTCGTCAGGAGTGTGTCGCACCTGAAATCTCATCCTCTACGGCTCCTCCTGACGTAGTGCAACGCAGCCATGGCCTAGCCTATCCTGACATCACCAACTTCTTATCGGTGGAGTCCCGGACGCGTTCGCATGGCTCCCGATACAGCGAGAGTAACTTCAGTGCCGACGAGCAGGAGCTGTCCAGAACAGAGTTTGACTCCTGTGATCAGTACTCCATGGCTGCAGAAAAGGACTCCGGACGGTCTGATGTATCCGATATGGGCTCTGATAACTGCTCATTGGCTGATGAGGAGCAGACGCCGCGGGACTGTCCCGGCCACCGTACACTGCGGACTGCAGCTTTGTCTTTAAAGCTGCTGAAGAACCAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44780
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114456 | Essential Splice Site | 977 | 1717 | 17 | 32 |
ENSDART00000137124 | Essential Splice Site | 700 | 1352 | 10 | 23 |
ENSDART00000146355 | None | None | 176 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 2249129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2184845 |
GRCz11 | 13 | 2469180 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACAAAGAGGAGAAAGAATTAGGAGACACTGGAGATGCCATTACTCAAG[G/A]TACACTCACACATTTCACATAAACCGCGATCACAGTCATGCATAGGGATG
Long Flanking Sequence:
ATACCTGTTTTATCTGACCCCATGCTCAATAATGTTCATGTATGGTGACTGGGCTGGCCAATCCTGGAGCAGCTTGACCTTCTTTGCTTTCAGGAGCTTTGATGTGGAGGCTGAATCTTCCACTTTGCAGATCTTGCACGTACTGAATGAAACCCCAAACCATGATTTCTCCTTCACCAAACTTGACTGATTTCTGTAAGAATCTTCAGTCCATGCTGGTTCCAGTAGGTCTTCATCGAAAAAAATCGACCTTCTGCCACTTTTCCAGATGATCCGCTAGAAGTCAAGTTATTATTGGTTGCTCTTACAACTGAGATCCATGACAAGGCTTTTGTCAGGTAGTGCAGGACATTAATGTGTCTGCTGGGCCTTCATTCTCTGTTATCCAGGGGTGGCAGCCAACTGTGCTTCAGCACTGGCGCAGATGGCAGCGGCTTCATGTGTTCAGGAGGACAAAGAGGAGAAAGAATTAGGAGACACTGGAGATGCCATTACTCAAG[G/A]TACACTCACACATTTCACATAAACCGCGATCACAGTCATGCATAGGGATGACATATTGGCAGAGCCAGACAGAATCTGCATTTTGTTTACCCCATCTGTGCAGAATTGTCTGAAAAGTGAAGTTTATGTATAAACTAATTTCGAGAGGATCACGTGCTTATGATTGCTAGCGGCTGGATCCCATTATCCAATTCACTACGCTCTAATCAGATGACTCCTAAACTACTATAAATACCCTGGGTTTCATTCCACTGCTATCTTCGTTTTGAAGAGTCCCCCCTTCCACCCCTAATCCTCCTTCTTAGATGGGTGACACGGTGGCCCAGTGCGTAGCACTGTCGCCTCACAGCAAGAATGTCTCTGGTTCCAGGCTTTACCAAACCAGCTGACATTTCTGTGTGGAGTTTGCACTTCTCCCCGTGCTCACGTGGGTTTCTTCCGGGTTCCCCGGTTTCCTCCCACCGTCTAAAAACATGCAATTAAGTTAATTGACTAATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13753
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 |
---|---|---|---|---|---|
ENSDART00000114456 | Nonsense | 1251 | 1717 | 22 | 32 |
ENSDART00000137124 | Nonsense | 974 | 1352 | 15 | 23 |
ENSDART00000146355 | None | None | 176 | None | 6 |
Genomic Location (Zv9):
Chromosome 13 (position 2258289)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2175685 |
GRCz11 | 13 | 2478340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCCGTGTCCTTCATCCATGATGTCCTGATGGAGGTTTTGAGCAGCTG[G/A]CCGGAGCTGCCGCATTTTCACTTCAATGAGGCTCTTTTCAGRCCGTTTGA
Long Flanking Sequence:
GTGAAGAACAAGAGCAGGCCGCTGCTGCACATGATGAGAGCCTGGAGCGTTGTAGCACCACACCTGGTGGAGGTTTGTGCCCCTTTTTACAAGACGTAAAATAAGTCTCTGATGTCCCTTAGAGTGTGTTTGTGAAGTTTCAGCTCATAATACCACACAAATAATGTCTGATAACTGCCTCCTGTAGGCTTTGATCCTAATTGTGTCGTTTTGGTGACTGTCGCTTTAAATTCAAATGAGATTGTGCTCTTTTTAAAAGTGGGCGGAGTGTAAGCATAGTGGCAGACTCAAAAACAAGACAGAACTTGGGGGGAAAATATAATAATTCAGGAGGGCAAATAACTCTGACTTAACTGTTAATGCACATCTATATTATTGAGGTTTTCAGATTCCAACTCTTTGACCTGTTCCCCACAGGCGGCCTGTCACAAGGAGCGCCACGTGTCCCAGAAGGCCGTGTCCTTCATCCATGATGTCCTGATGGAGGTTTTGAGCAGCTG[G/A]CCGGAGCTGCCGCATTTTCACTTCAATGAGGCTCTTTTCAGACCGTTTGAGCACATCATGCAGCTGGAGCTCTGCGATGAAGACGTCCAGGATCAGGTCAGGATCCACGCACTGAATTAGACTTATAATGCATTCAGCAAAAACCCTGCAGTCACTCGTCAGACAAAATCTGTAGATATTATTAGCTATTTCTGTGCAGGATCTGAAGATTTGATTTTTTAGAGTTTAGTAAATACAAACAACACATAAAAAAAATAATAATAATAAATAAATAAATAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACATATATGTGTATATAGTTGAAAATTTATTTAATATTTTTTAATAATATGTCAAAATTATTTAATTTTTTTTTTTTCTTTTTCAAATATTTCCCAA
Associated Phenotype:
Not determined