ZMP
si:dkey-27p18.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to spectrin, beta, erythrocytic (Sptb) [Source:UniProtKB/TrEMBL;Acc:A2BGE8]
Human Orthologue:
SPTBN4
Human Description:
spectrin, beta, non-erythrocytic 4 [Source:HGNC Symbol;Acc:14896]
Mouse Orthologue:
Spnb4
Mouse Description:
spectrin beta 4 Gene [Source:MGI Symbol;Acc:MGI:1890574]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8680 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30614 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40405 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40404 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6970 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8680
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099325 | Nonsense | 283 | 652 | 5 | 10 |
| ENSDART00000133174 | Nonsense | 290 | 1412 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 24267464)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21980336 |
| GRCz11 | 5 | 22484136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCAGAGGTGGAGCTTGTGCGSGAGGGGGCGGGGCATGTGAGACAGCTGT[G/A]GGAGGTGCTTCAGGTGGAGATGGAACGCCGCACAGTGATGCTGGATGCTG
Long Flanking Sequence:
GTTTACGTGAGTTTTCTCTGGGTGATCCGGTTTCCCCTACAGTCCAAAGACATGAACTATAAGTGAATTGGGTAAACCAAACTGACTGTAGTGTTTGAGTTTGAGTGTGAGTGTTTGTGCGGCTATAAGGGCATTTGCTGTGTAAAACACATGCAGGAATAGCTGGCGGTTCATTCTGCTGTGGCAACCTCTGATTAAAAAGGGACTAAACCGTAAGAAAATGAATGAAGAGGCTTCTATTAGTATTAGTGTAGAAATTTAATGCAGCTTTTCTGGGTTTGATATTTCAAATTACATGGAGGGCAGTGATGAATTTTGATTGGCTTTGATGGACAGCTCATGCGTGTGTGTATGTTTGGACATGCAGGCACTGCAGATGGAGATGCAGGTTCGGAAGGGGAGACTCGAGGAGGTTCTGGAAAGGGCAGAGGCTGTTGCTGCCTTGCGGACCCCAGAGGTGGAGCTTGTGCGCGAGGGGGCGGGGCATGTGAGACAGCTGT[G/A]GGAGGTGCTTCAGGTGGAGATGGAACGCCGCACAGTGATGCTGGATGCTGTGAACCAAGCCCAGCAGTACTACAGCCAGGCAGCGAAGACAGAGTCCTGGCTCAGTGGACAGAAACTTCAGGTCCTCAATGAGGAGAAAGGAAACGTATGTAGTCTTCCATAAAACTCAATCTGTCTATTACTTTGAGTGGATTTTGAAATTTTTTATTGAATTTATAATGTTTTCATGGCCAATGTGTACACCACTTGTAACAAAACCTTTTCTGCATAAATATTGGTTTTGAAAGTCAAAGAATGTGATGTTTATCCATGCTTTAAAAACCTTTCATTCTATGACACTTGGAACAGATTTTTATTCAATGATCAGGATAATGATGAAAAAGCCATTCTGTCCAGTAATTTCAAATTTTCTAGCAAAGCAAGGGAATTCAATCAATATATAATCTCACAGCCAGATATGTAATGTCTATAATCTCAAATATATTTGAGGTGAAACACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30614
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 |
|---|---|---|---|---|---|
| ENSDART00000099325 | Essential Splice Site | 525 | 652 | 8 | 10 |
| ENSDART00000133174 | Essential Splice Site | 532 | 1412 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 24262721)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21975593 |
| GRCz11 | 5 | 22479393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGGCAGCATCCTACCAGCTGCACAAGTTCTTCACTGACTGTCAGGAG[G/A]TATACAGACTTGTACTATATACAGTTGTTATTTTAAATAATATTTCATTA
Long Flanking Sequence:
AAAACATCACATAATGTAAATAAGTTGTAATTTAAAAAGAATTTGTGAATAACTCAGTTTTGACAAAAATGTCAGATAGAACTGTATAATTCTAAGTTGATGTACTGTTGAATGAAAATGCAGCATCTAAATTTTTAATATGTAAGCACATTAAATTTTGCATGTGGATAAAATCAAGTCCTGTGCTAATGGATTTCCTGTTTTTCTGTGAGCTCATTTCTGACATACAATTTTTGTGCTGTTTAATTTCTCAGGTTCTTCAGAGCAGCTTCACGCAGTTTTCCTCTGAGACACGTGCAGTGGGCCAGAAACAGATGGATTCAGTCAATAAGATGGTGAATGAGATGATCGACTGCAGTCACTCTGATGCTGCCACCATTGCAGAGTGGAAAGACGGACTGAACGAGTCCTGGGCGGATCTACTGGAGCTCATGGAGACCAGAGCGCAGATGTTGGCAGCATCCTACCAGCTGCACAAGTTCTTCACTGACTGTCAGGAG[G/A]TATACAGACTTGTACTATATACAGTTGTTATTTTAAATAATATTTCATTAGAAGTGTTAAAAATCCTCTGTGTTTTGGCTATTTAGGTATTGGTACAGATAGAAGGAAAGATGAGACAGCTGCCAGAGGTGAGGTCCTGCCAGGTGAGCTCGGCCAACCCTGGCACACTACAGAGACTCCTGCACTCTTTCGAACACTCTCTGCAGCTGCTGGTCTCGCAGGTAAGACTCAATTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAAACACAACACACAACACCTGTTTTGAGCAGGTGCAGCAACCACGGGGAAGTGTTTAGGCTGGTTCATCTACCTGACCCAGCAAGAGGGGTTCCCATTTTAGTCCATGAGCACTAAAATACTGACAAAAAAACTGTTTCAAATATCACACACTAATACTGTGCAAACAATAAAGTTAATTGTATCGTTTTATCTATTTGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40405
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 |
|---|---|---|---|---|---|
| ENSDART00000099325 | Nonsense | 611 | 652 | 10 | 10 |
| ENSDART00000133174 | Nonsense | 614 | 1412 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 24259455)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21972327 |
| GRCz11 | 5 | 22476127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCGTGAGCAGGAAGTGATGCAGGCCTGGAAAGAGCTCCTCGTTGCATG[T/A]GAGGGCAGCCGTGTGCAGGTCACCACTGTAACCGATAAGATCCAGTTCTT
Long Flanking Sequence:
TATGTGTATATATATATATATTTGAGTGCTTATCTGGAGGTAACATCGAATCTGGACATGCCCACTTTACACAATACTCAACCACTGCCATTACCGTGTTAGATTAGGTCATAGCAACATTGTTGCTGCTATGCTAATTACTAATAATATTATAATTTTGTGGAGCATAAATATTATAATATTATACAACTTTATTGTAAAGCTGCTATAAAGTGGCTTCAAAACATCAATGAATTAGGTTGTAGATTAAATATATCTAAAATACATTTATGTGCTTACAATACAATTTTTCGTCCATCAGCCAATTCAAATCTAGCTTTGCAGCAGCTTCAAAATGCTTTTCAAGTATTGCAGCAGTTTTACCTTTTACCCCCTCAGGTACGCCAACTGCAAGAAAATGCAGTTCAGCTACGTGCAATCTATGCTGGGGAGAAGGCAGATGCCATTTTGAGCCGTGAGCAGGAAGTGATGCAGGCCTGGAAAGAGCTCCTCGTTGCATG[T/A]GAGGGCAGCCGTGTGCAGGTCACCACTGTAACCGATAAGATCCAGTTCTTTGCGGTGGTGCGGGAATTGAGCATGTGGATGGATGGAATCATGGGGCAGATTGGCCCAAATGACGATGCAAGGTACCAGATCATTTATAGAACTCTCTGAGTCATCCCAAATAGATGGTTAGATTAAAACCAATAACAGTAGACAATGTGCATCAGGGTAATGTGTCTGTGTGTTTCTTGTTTGCGTCTGGGCGTGGGCTTTGGTGTTGGGTGGGTCCTTGTGAACGTGTCAGGGACCTCTCAGTGCTAGAGGGCATGATGTCCCAACATCAGAATCTGAAGAGTAAGATGGAAAACAAGAGCAAGAACTTTGTGCACTGCGTGGAGATGGGAAAAATGCTGCTCGCTGCGCGCAACCCTGCAGCTGAAGAGGTGCACACATATTCTCATACTAAGATTTAAAGCATGCAAACAATGCATCCTTGATGAATAAATGCATTTGTTTCTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40404
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099325 | Nonsense | 644 | 652 | 10 | 10 |
| ENSDART00000133174 | Nonsense | 647 | 1412 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 24259358)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21972230 |
| GRCz11 | 5 | 22476030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTGCGGTGGTGCGGGAATTGAGCATGTGGATGGATGGAATCATGGGG[C/T]AGATTGGCCCAAATGACGATGCAAGGTACCAGATCATTTATAGAACTCTC
Long Flanking Sequence:
GTTAGATTAGGTCATAGCAACATTGTTGCTGCTATGCTAATTACTAATAATATTATAATTTTGTGGAGCATAAATATTATAATATTATACAACTTTATTGTAAAGCTGCTATAAAGTGGCTTCAAAACATCAATGAATTAGGTTGTAGATTAAATATATCTAAAATACATTTATGTGCTTACAATACAATTTTTCGTCCATCAGCCAATTCAAATCTAGCTTTGCAGCAGCTTCAAAATGCTTTTCAAGTATTGCAGCAGTTTTACCTTTTACCCCCTCAGGTACGCCAACTGCAAGAAAATGCAGTTCAGCTACGTGCAATCTATGCTGGGGAGAAGGCAGATGCCATTTTGAGCCGTGAGCAGGAAGTGATGCAGGCCTGGAAAGAGCTCCTCGTTGCATGTGAGGGCAGCCGTGTGCAGGTCACCACTGTAACCGATAAGATCCAGTTCTTTGCGGTGGTGCGGGAATTGAGCATGTGGATGGATGGAATCATGGGG[C/T]AGATTGGCCCAAATGACGATGCAAGGTACCAGATCATTTATAGAACTCTCTGAGTCATCCCAAATAGATGGTTAGATTAAAACCAATAACAGTAGACAATGTGCATCAGGGTAATGTGTCTGTGTGTTTCTTGTTTGCGTCTGGGCGTGGGCTTTGGTGTTGGGTGGGTCCTTGTGAACGTGTCAGGGACCTCTCAGTGCTAGAGGGCATGATGTCCCAACATCAGAATCTGAAGAGTAAGATGGAAAACAAGAGCAAGAACTTTGTGCACTGCGTGGAGATGGGAAAAATGCTGCTCGCTGCGCGCAACCCTGCAGCTGAAGAGGTGCACACATATTCTCATACTAAGATTTAAAGCATGCAAACAATGCATCCTTGATGAATAAATGCATTTGTTTCTTTCTAAAATAACAAACGTCTATTAAACTGTTAAAATCTAAGGATCTCAGTTTTTTTATTTGCTATTTGATTGTAATATTAAATACGTCTTAAAAGACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6970
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099325 | None | None | 652 | None | 10 |
| ENSDART00000133174 | Nonsense | 900 | 1412 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 5 (position 24257428)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21970300 |
| GRCz11 | 5 | 22474100 |
KASP Assay ID:
554-5238.1 (used for ordering genotyping assays)
KASP Sequence:
TACCATGGGCTACAGCAGCCATCGGGGGTCGTCAATGAAAGTCCTTTATA[T/G]CAATCGATAAAACAACAGGGTGTTTCAAGTTTGGATAATTCCAGCTATMA
Long Flanking Sequence:
AAAATAAAAAAAGAAATCCACCACTATTTGTTTTACTTTTATTCTGTTGAGGAGCTTTGTGCACCCACTGTCAGGTAAAAGGCTGACATTTTGTACAATATTGGCAAAGCACGTTAAATATGAATAAAATATGTAATTAACATCAAATTAATATATATATCTGTCTGTCTCCATTTACAGGCAGAAAAGATGAAGGAGGAACTGAACAAACCACCTTCTACCTCCTCTCTTCTCAGCAGGCAGATGTTCCCTCTCTCCTGTCTTGTGCCCAGCTCTTCTTCCTCCTCTTCATCATCATCTCTTTTCCGTAACCCCCTTCAGGACTCACTCCTCGAGTCTAAGCCTGGACCAGACCACATGCACTCCATAGAACACACAGTGACTCACACTCTCCCTCAGCGGCTTGGGTCCAGCCTGAACCCCTACACACCTGTTATGAATGGCTCCTCCTACCATGGGCTACAGCAGCCATCGGGGGTCGTCAATGAAAGTCCTTTATA[T/G]CAATCGATAAAACAACAGGGTGTTTCAAGTTTGGATAATTCCAGCTATCAGGGGCTTAACCAACAAGTTGGTGTCTTTGGGGGGAACAGCTCCAGCTATACTGGACTAAATCAACAGGGTGCTTTAGCAGAGGACGGCTCCAGTTACCATAGCCTGAACCATTTAGGTGCCGTAGGGGTTGTGGAACCCAAAATTGGATATGCTTGGCAGCATCTGAAAGCTGACTGCTTTCAGCCCAAAATCAACCACATTCACAAAGCGGTTTCACCTTTACTGGAGGCCCACCGAGCTCAGCTTGCTAGCGCAGGAGCAAACATGCCGGCTCCTCCAGTGGGCATGGACCCCTCGCTGGAGATGATCCACAGTCGTTTACAAAGAGACCCCCGGGGGAGCCGCTCTGACCCACAGATGGATCACCTGCGGCGGGAGAGGGAGTACAGGCTAGGCAGACAGACTTCCAGCGAGCAGGAGATCCAGGCTCGACTCAACGAGCTGCCGTT
Associated Phenotype:
Not determined