ZMP
si:ch211-173b16.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate neuronal ankyrin family [Source:UniProtKB/TrEMBL;Acc:B8JK14]
Mouse Orthologue:
Ank1
Mouse Description:
ankyrin 1, erythroid Gene [Source:MGI Symbol;Acc:MGI:88024]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20591 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38529 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20590 | Nonsense | Available for shipment | Available now |
sa10842 | Essential Splice Site | Available for shipment | Available now |
sa10265 | Nonsense | Available for shipment | Available now |
sa26632 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40606 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20591
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090092 | Essential Splice Site | 363 | 1929 | 9 | 49 |
ENSDART00000137443 | None | None | 1050 | None | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71913197)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68237715 |
GRCz11 | 5 | 69008382 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCCAAGGTGCTCCTGGATAAAGGAGCCAAACCAAACACCCGCGCTCTGG[T/G]CAGTGCACTTCCACAAAGAAGACTCCACACAATTAATGCATGTGATTATA
Long Flanking Sequence:
CAGCTTAAACCAGCCCAGGCTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTTTCCAGCCATTTCCAGCCTGGTCTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCTTGACCAGCCTAGCCAAGCTGGGAGTCCAGCCCAAACCAGCTATGCCCAGCTTAAACCAGGCTGGTCAAGCTGGTTTTAGCTGGATTTGGCTGGTCATTTTAAAGCAAATGTCACTGGCAGCTCTAAATGTCCTCATATGTTCACTGCACAGAATGGCCTGTCGCCGATCCACATGGCAGCCCAGGGCGATCACTTGGACTGTATCCGACAGCTCTTACAGTACAACGCAGAGATCGATGACATCACTCTGGACCACCTGACACCTCTGCATGTGGCGGCTCACTGCGGGCATCACCGCGTGGCCAAGGTGCTCCTGGATAAAGGAGCCAAACCAAACACCCGCGCTCTGG[T/G]CAGTGCACTTCCACAAAGAAGACTCCACACAATTAATGCATGTGATTATATTTACCCTGGTGTTCTTACTGTCGAATGTATTGGTCTTTGTGCGAAATTTTTATTCTAAAATGTCATATTTCCCAAGTGCTGTTTAACGGAGAGAGTATTTTTTTAAACATAAAATTTTTAATAACTAATTTCTAATTTATTTTGTCTTTGGCATGATGACAGTACGTAATATTTTACTGATTATTTCTCAAGATAGTAGTATTCAGCTTAAGGTTTAATTTAGGTTAATTTGATTAACTAGGCAGGTTTGGTTAATTAAACAAGTTATTAGATAACTGGTTTGTTCTGTAGACAATTAAAAATATGTTTTTTTTAGAATATTGACCTTAAAATTGTTATAAAACTGATTTTATTCCAGTCAAACTAAAAGAAAGAAGACATTTCTCAATTTTGCTCAATTCTCTTTTATTTCTCAATTTTTGCTCTGTTAAACATCACTTGGTGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38529
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 |
---|---|---|---|---|---|
ENSDART00000090092 | Essential Splice Site | 527 | 1929 | 14 | 49 |
ENSDART00000137443 | Essential Splice Site | 81 | 1050 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71906863)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68231481 |
GRCz11 | 5 | 69002148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCAGCATCCTCCTGGACATGAACGCCCAGCTCACCAAAATGACCAAG[G/A]TACTGTTCATATGCTTGTAATCAATAATTTAACATATTATGATAATGAAC
Long Flanking Sequence:
TTACAGTATTTCCTATAATATTTTTTCTTCTGAAGAAAGTTTTAATTGTTTTATTTCAGCTACAATAAAAGCAGTTTTTAAATTTTCAATATTGTTAACCCCCTTAAGCAATATTTTCTTTTCGAATGTCTCTAGTACAAACTATTATGATTAGAAATGTGTTGAAAAACATCTTTTTACTAAAAAAAAAAAAAAAAAAAAAATTAGGGAAAGAAATATACAGGGGTGCTAATAATTTGGATTTCAACTGTATATAAACTTTTTTTCCAATGACTGATCTCTTCCTTCACCTCCTGCATCAGGATGACCAGACGCCGCTACACTGTGCCTCCCGCATGGGCCACAACGAGATGGTGAAGTTGCTTCTGGAGCACAAGGCCAACTCAAACTCCACCACCACAGCAGGACACACACCGCTGCACATCGCGGCCCGCGAGGGACACACACAAACTGCCAGCATCCTCCTGGACATGAACGCCCAGCTCACCAAAATGACCAAG[G/A]TACTGTTCATATGCTTGTAATCAATAATTTAACATATTATGATAATGAACATGTACAAAAGGGATGTATACACTCACCAGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACACTCAGTTTTAATCAGCCAATCACATGGCAGCAACTCAATACATTTAGGCATGTAGACATGGTCAAGACGGTCTGCTCCAGTTCAAAGCGAGCATCAGATTGGAGAAGAAAGGGTATTTAAGTGACTTTGAACGTGGCATGGTTGTTGGTGCAAGACGGGCTGGTCTGAGTATTTCAGAAACTGCTGATCTGCTGGGTTTTTCACACACAACCATCTCTAGGGTTTACAGAATAAGAGAAAATATCCTGTGAGCGGCAGTTCTGTGGGCGCAAATGCCTTGTTGATGCCAGAGGTCAGAGGAAAATGGCCAGACTGGTTCCAGCTGACACAAGGCAAAAGTAACTCGTTACAACCGAGGTCTGCAGAAGAGCATCTCTGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20590
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 |
---|---|---|---|---|---|
ENSDART00000090092 | Nonsense | 780 | 1929 | 21 | 49 |
ENSDART00000137443 | Nonsense | 334 | 1050 | 9 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71899361)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68223979 |
GRCz11 | 5 | 68994646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTGCCATCGCCAAGCGGCTTGGATACATTTCAGTCATCGATGTGCTC[A/T]AACTGGTCACTGAAGAGACGGTCACTATGGTAAGAAAAATTGACATTAAA
Long Flanking Sequence:
TTTTTTGACCTGAGGCTATTGTTATAATGCATGAGAATTTAGTAAACATCTTTAATTAGAACGAAACTCGAGTCAATTTATTGCTCGACTGATTTCCTGAAAATTCTTATAGTACATAACATATGTACTACAACATGCATGCAGTGTTTTGAGGCCACCAGAGATCTTTCATAAGTCATCTTGTAAAAAGCAAGACCCTTAATAGAGATCTCAAAACATGCTTTTTCTTGCTTTCTTCATCCTCTTTTGTTAGATGAGCTACACGCCGCTACATCAGGCTGCTCAGCAGGGTCATACGGACATCGTGACGCTTCTGCTGAAACACGGAGCACAACCGAATGAAGTTACATCTGTAAGAGCCATGCCAATACTAAACGATCACCATCATTGCTTTTAAAAATGTGCTGGAGGTTTGACATGGTAATGTTTTTTGATAGAACGGCACCTCTGCTCTTGCCATCGCCAAGCGGCTTGGATACATTTCAGTCATCGATGTGCTC[A/T]AACTGGTCACTGAAGAGACGGTCACTATGGTAAGAAAAATTGACATTAAATCAATATATTTAGGTACAAACTGAACGTAATGCTTTCAGATGCTTAAATGCATGCTACACCTTAAAAATATCCGTAAATTAGCAGTTTTCAGGGTTTTGTGATCCATGTGTTTATCTTTTATTTATGAGACCTTGATTTTTTTTCTGACAACTTTTAACCTTAATAAGTTGGACTTTTATTAACATAAATTTTATTAAATTTATTAATTTAAATAATTTAATTTTTTTTTTACTTTTTTAAAACATTTTTAAAAGTTTGCTGTGCTATTTTGTCTTCTGTTGGTATTGGTTGGTGTTGTATATTACACTACAAAAACCTTGTAACAAGCTTCCAGTCCATTTTCTGTCATTTTACAGGTTTATTTTTCTCTATTTTAAAGGATTTAAATGAAAGTTTATTAAATCACAAAAATATTAAGTACATTAAATATTACATTCATATTCCCTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10842
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 |
---|---|---|---|---|---|
ENSDART00000090092 | Essential Splice Site | 813 | 1929 | 22 | 49 |
ENSDART00000137443 | Essential Splice Site | 367 | 1050 | 10 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71898489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68223107 |
GRCz11 | 5 | 68993774 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTTTYCCTGAAACCGTTGATGAGATCCTGGAWGTGTCTGAAGATGAAG[G/A]TAAAAACAACTCTNNATTCACCATCACAATCTGTTTTTRMGTTATTAGCA
Long Flanking Sequence:
TAACAAGCTTCCAGTCCATTTTCTGTCATTTTACAGGTTTATTTTTCTCTATTTTAAAGGATTTAAATGAAAGTTTATTAAATCACAAAAATATTAAGTACATTAAATATTACATTCATATTCCCTAAGTGTCTAATCAATAAATTATTATTTATTTTTAGGTCGTTCAATGTTTTTTAAGTAATTTAATAGGTTTTTATAAAAATAAATACAAATATTTAAGCATTTTTGTCCATCTAATATATGCAAACGCGTTTAAATAATGGTAGTTTGTTTTGTTTTTTTAATCTAAAGTCCCTATTTAGGCTATTTCCAAACAACCCCACCTAACAAACAATATATTAAAACACTCAATACAATGGGTATGCCTACTGTAAAATGTCACTAATATAAAAAAAAAAAACAATATTTATTTATTCTATTTCAGACCACCACTGAAAAACATCGCATGAGTTTCCCTGAAACCGTTGATGAGATCCTGGATGTGTCTGAAGATGAAG[G/A]TAAAAACAACTCTGTATTCACCATCACAATCTGTTTTTGAGTTATTAGCATTTACTTATTTGAATACAAGACAATGATCGGCCATTTAAAGAGCATCCTGAAGTAGATTCCTCTTGGTTTTTCTAGGAATTGCACAGCTAACATTAGGTATGAACTTCCCTTTCTTCTGTGTGCGGTGGTCATTGTCAGTGACTTCATTTCAAACACACACACACACACATACACACAAACACACATTGTCATTGTCTGGTGCACTTATGATGAATTACGATGGATGTGACATTAGCATGTGTGCGATGATAAGCCTGCTTTTATTCCTCAAGGTTGCTAACTGTGGCAGAATGCTTACAGTAACTATTCCTGAATCCTCTCCCACTAACCTGCTTCATCTCCTTTTTCATTTTTGTACTGAAGCAGAACAGATTTTCTTGAATTTAGTTCAGTAGAACTTGTGGAAAAGCAGCTGTGGTGTCAACATGAACTTGTGACTAAGATTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10265
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 |
---|---|---|---|---|---|
ENSDART00000090092 | Nonsense | 1026 | 1929 | 28 | 49 |
ENSDART00000137443 | Nonsense | 573 | 1050 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71885762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68210380 |
GRCz11 | 5 | 68981047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTGCGGCTCTCGGTCGGGGAGATCGGGAACTCGTGGTCTTGAGGAGT[G/T]AGAACGGATCKGTCTGGAAGGARCATCGTAACCGATAYGGAGATGAAGTG
Long Flanking Sequence:
TACAGAGCGCCCTCTAGTAGATTTAAGGTGGAAAAACCTAGCAAGGAGACGGAGCCCAAAGTACGTATTTCTCGGTTCTCAAGAATGTAGCCCTGGGTACATTTTCACAATCAGCCTGGGCAAACGCCTTATCTTTCAACTCTCGTAATAATGATGCTAATAATAATAATAATAATAATAGTCTAGGGCTTGTTGAATGTAAATAAATGTCATTTTGCAAGTTCAGAAATTTTTTAATTTAGTAAAATTAGTTTTTCTGAATTTTTGAAAATTTTAAATCTTCTTTTTGGCCTTTTGTCCTGCATTTTCAGTGCATTCAGAGTTTAAGTTGTCAGCACAATTTAAATTTCGGTGCCTGCCTAATTTATTTTATTTATTTTTTAAATTTTTAAGCAAACTAACACTTTAACTCTTCTTATTGGTGAAGGCCTGTGATTGTGGAGATTCCTCATTTTGCGGCTCTCGGTCGGGGAGATCGGGAACTCGTGGTCTTGAGGAGT[G/T]AGAACGGATCGGTCTGGAAGGAACATCGTAACCGATATGGAGATGAAGTGCTAGAGACCATCCTCAACGGCATGGATGAAGGTGTGCTGTATTTATATATTTAGAAACAATCAAAAATGTTCATTTCTGTACAATATAATATCTTAAATGTCCATACGAAAATTATAATGTACAGTTGAAGTCTCTGCCTAAATTATTAGCCCCCCTGTATATTTCTGTTTAATTAAGAGAAGATTTTTTCAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTGATAACTGATTTCTTTTAACTTTGCCATGATGACAGTAAGAGAATATATATTCTTCAAGGTACCAGTATTCAGCTTAAAGTGACATTTAAAAACTTAACTAGGTTAATTAGGGAGTAGTTAGGATAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTAGACAATCAAAAAAATATAGCTTAAGTGGGCGAATGATTTTGACCTTAAAATGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26632
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090092 | Essential Splice Site | 1344 | 1929 | 34 | 49 |
ENSDART00000137443 | Essential Splice Site | 891 | 1050 | 22 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 71867387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68192005 |
GRCz11 | 5 | 68962672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATACCTGTATCATAATCACTCGTTTGTGCTTAATTTATCTCTATCTC[A/C]GGTGAGGGACAGCAGTAAAGACCCCTCTGGGTTTTTGTCTTTCTTGCGCA
Long Flanking Sequence:
GTGTGTTTCCCAGTACCGGGTTGTGGCTAGAAAGGCTGCGTAAAACGTGCTGGAATAATTGGCATTTCATTCTGCTTTGGCTACCCCTGATAAATAAGGGACTAAGCTGAATGAATGAATGAATGAATGAATGAATGAATGAATAAGTGAGCCTGGCTTTAAGAGACTTTAAATGTCTCAGCCATCGCTAGGGTTTACAGAAAATGGACCATAAAAGATACTAGTTTAGAGAATTAGTTGTGTGGGTGAAACTGGCTTGAGGTCAGAGGAGAAACCCCAGACTGGTTTAAGCAGATGGAAGAATCAATAGAACTCAAAAGAAATTTTTCGCACAATGTCTAGTTCTGTCTTCTAAGCTAAATATATGTTCACAGAGACACATTGGTTGTTGACCTCCATAGAGCATTTGTGTGGAATAAGGCATTTGCCATTTAGTATTTTTTTAAATATTAAATACCTGTATCATAATCACTCGTTTGTGCTTAATTTATCTCTATCTC[A/C]GGTGAGGGACAGCAGTAAAGACCCCTCTGGGTTTTTGTCTTTCTTGCGCAAGTCAACCAAATATGAAGACAGCCAACACGTGCTGTGCAACCTCAACGTGACCATGCCGCCGTGCATTAAGGTACTATGATCACTGTGTCCATACACATCCCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGATGTGCTAGTAAGCTCTTTGTGAACCTAAAAAGTCTGCAGAATTTCAAATAATCAGAGTATCTAGAGCATCTGACTCATCAGAACAGAGTAGAGCAATCTGACCAGTCAGAGCAGAGCAGAACCCTTTGACCAATCAGAGCAGAGTACAGCAATCTGACCCAACAGAGCAGAGTAGAATAATCTAACCAATCAAAGCAGAGTAGTGCAATCTGACCAATCAGAGCAGAAGAGAGCATCTGACGCACCAGAGCAGAGTAGAGTCATCTGACCAATAAGAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40606
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 |
---|---|---|---|---|---|
ENSDART00000090092 | Nonsense | 1862 | 1929 | 48 | 49 |
ENSDART00000137443 | None | None | 1050 | None | 26 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 71811967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 68136585 |
GRCz11 | 5 | 68907252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCCATCTGTACACGTGGCTGATGTAGATTGTGAGGAAAGTGGTCCGG[A/T]GAGGAAAAGGGGAGGAAGGGGGTCAGGAGCTGATCATTGAAGGTCTGCAG
Long Flanking Sequence:
AAAGCACCCTTAATAAATGGGTCATCGTTTACTCACCCTGGCCTTGTATTAAACCTTTATGAGTTTCTTTATTCTGTTGAACACGAAAGAAGATCATTTGAAGAATGCTGAATACCTGACTTCCATTGCTTTTCCTTCTATGGAAGTCAATGGTTACAGGTTTCCAGTTTTCTTCAAATGATCTTCTTTAGTGTTCAACAGAAGAAAGAAACTCATATGTGTTTGGAAACACTTGGGGGTGAGTAAACAGTGACGTTTTTTGGTGAACTATGCCTTCAACTCAAGATTACAGTATAGAAAATAGGTCAGATAGATGCATTGGGATGTTTCATGTTGACTTTAAATGCAACTTTTAATCACACTATTATTTTTGCATGTTGTTTTTCCCCATCTGTCACCCTGATTATCTGTTTTCATGTCTCCTCCTCGTCTGCTCATCCACCGATTCTCTCATCCATCTGTACACGTGGCTGATGTAGATTGTGAGGAAAGTGGTCCGG[A/T]GAGGAAAAGGGGAGGAAGGGGGTCAGGAGCTGATCATTGAAGGTCTGCAGCAGGATATCAGTGAGCCTGACTTTGATGGAGAACAGTTCATGAGCTATGCCGTCCTGGGACGTGACAGCAAGGTGGGCTTTTGAGTTAGATGAGGTGGTTTAAAAAGGGAAATGCAAAGATGCTTGTATAGTGAAAGTTTAGTAGATCAGGGAAACTGCAAAACACAAAGCGTTATTGGTGACATTACGATAAGGTTTCATTTGTGAAAAGGACATGGACTAAGAATAAACTAAAGCATTTATTAAATTCCCAAGTGTGATTTGTTTTTTGTTTTTGCATGCAGCTATGCAGAACAATTAGTGTTGTATTGCGACCAAGAGAGCTTAACTTGCTGCAATTACAAAAAACAATATAAATAGACTTGAAAACACTGCAGTATTTACTATAGTATCCATATATAATGAAATCCAAATGCATAAATGGTGCAGAATATAAAATATAATGCTAAT
Associated Phenotype:
Not determined