ZMP
epb41l5
Ensembl ID:
ZFIN ID:
Description:
erythrocyte membrane protein band 4.1 like 5 [Source:RefSeq peptide;Acc:NP_956383]
Human Orthologue:
EPB41L5
Human Description:
erythrocyte membrane protein band 4.1 like 5 [Source:HGNC Symbol;Acc:19819]
Mouse Orthologue:
Epb4.1l5
Mouse Description:
erythrocyte protein band 4.1-like 5 Gene [Source:MGI Symbol;Acc:MGI:103006]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2498 | Nonsense | F2 line generated | Not yet available |
| sa34663 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27410 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa7186 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9677 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2498
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000060315 | Nonsense | 349 | 445 | 13 | 17 |
| ENSDART00000101215 | None | None | 218 | 13 | 25 |
| ENSDART00000101269 | Nonsense | 353 | 776 | 13 | 26 |
| ENSDART00000101276 | Nonsense | 360 | 772 | 13 | 26 |
| ENSDART00000132878 | Nonsense | 353 | 776 | 12 | 25 |
| ENSDART00000135334 | Nonsense | 360 | 461 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 29935255)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29091201 |
| GRCz11 | 9 | 28901947 |
KASP Assay ID:
554-2890.1 (used for ordering genotyping assays)
KASP Sequence:
GACATAGATGTTTTTTNCCCTTTATTTGTGTAAAGTGGGAAGACAGAATA[T/A]CAGACAACAAAGGCAAACAAAGCTAGAAGGTCTGCCTCCTTTGAAAGAAG
Long Flanking Sequence:
ATAGCTGCTGTCAAGTTGTAAATTGTAGCATGTTTTACTCCAAGCACGGTGTGTGTTGGCTGTCTTTTCTTTGGAATTGCGTCTTATCTCCAGCTGCCAGCCCAAAGGCTTGACGATTTCCAGTTCAGCTCCCTACTGGTCAGGTTTTTTTTTTGTTTGCCTACACTTATTTTAGCACTTATCCTAGCTATCCAGAATAAGCCTATTTTTTGTTTACATCAATGAGTGTACTTTATCTTTGATTTCACCTGCATGTCTGATTGTCTCTTTGTTGTTGTGAGTTTGTTTGCCAATGCTGGTTTGTCCGCTTATCCTCTAATGAACAGTGGCATTATACTTTCTGATACTGTTTGACTTTCATTACTCTAAGCCTATAAAAGTAAATATCTGCAGTCTTTTCGAGTCAGCAGGGATTTATCATCAAGGTTTTAAAGGTAAATGTGTGTATCTGACATAGATGTTTTTTTCCCTTTATTTGTGTAAAGTGGGAAGACAGAATA[T/A]CAGACAACAAAGGCAAACAAAGCTAGAAGGTCTGCCTCCTTTGAAAGAAGACCAAGCCGTCGTTACTCTAGAAGGACCATGCTGAACAGAGGTGAGGAACTGACCTGCTCAGAGTTAGGAATATACATTTATATTGGTCTTAGAACTTTAGTATCTGTCTGTTTGTCTATTTGACATTGGCAGCTCATGCCAGCCAGTTTAAGATTGAGCCTCAACTCTCTTAACTCTCTATCTGTTTATCTGTCTATCTGTCTGTTTATCTATCTGTCTAGCCGTCTGTTGTTTTATTTGTCTCTCATTCTGTTCTTTTGTCTGCATGTCCTTCTATCATAAATAGCCTATAAAGATACATTATATTATGCATTTTATTTAGCTTTGGATATATTTGATTTTAATTCATTTAACAATTTTTGTTGGATTTTTAATTTTTTTTTAATTTGCTTAATTTTAATTTGACAATGCATTTTTGTACAAGCAATTAATAGTTAATTAATAAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34663
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060315 | Essential Splice Site | 400 | 445 | None | 17 |
| ENSDART00000101215 | Essential Splice Site | None | 218 | None | 25 |
| ENSDART00000101269 | Essential Splice Site | 403 | 776 | None | 26 |
| ENSDART00000101276 | Essential Splice Site | 410 | 772 | None | 26 |
| ENSDART00000132878 | Essential Splice Site | 403 | 776 | None | 25 |
| ENSDART00000135334 | Essential Splice Site | 410 | 461 | None | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 29933325)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29089271 |
| GRCz11 | 9 | 28900017 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCACAGTAACCACAATAACGGTGTGAGCCCAAGTATAGAAAAAAAGG[T/A]ATGACATTCTTAAAGATGTCTTGCAAGTATACTTTTTATTACATTTCAGA
Long Flanking Sequence:
CTTTTTCAATTCATTGTTATTCTACAGGCTAAATGCATGACTGGTCTGTCAGCTTAAGGATATGCTGTTACACTGAGTGTTCTGCTTTAGTCTTCTAAGTACCCCTACTTAGACTGTGATTCAGCTGGTGTTAAAGGCACAAACGTGAACATCATGTGCTGCTGCTTTTGTAGTGCTGATTTACAGGGATTTTTTAAGACTCATGCTGTGACTAAGCATTAATGCTTAGCAAGTGTGATTATTTGACTAATTTCTCTTTTAAAGATTTGGTCACAAGCTAAAAATGTCATCAGGAATGTCTTGGCTGACTCTGATCCTTTGAGTCACCATGTCTGTTCACCTGCATGAAGGAGCACTTTTTTTTTTTTTTTTGCTTCCATTGTGCATTTCAAGTCAGTCAACAGAAGCCCATAAATCAAGACCGGTTCTAATCTTGCTTGCATTTTTTTCTGTCCACAGTAACCACAATAACGGTGTGAGCCCAAGTATAGAAAAAAAGG[T/A]ATGACATTCTTAAAGATGTCTTGCAAGTATACTTTTTATTACATTTCAGATTAAATCTAATGTTGTTAAATTGTTTGGTTTAATCTTACAAAAGAATGTCAGGTTATATTTTACTTGTAAGTAAACTTATCATTTGAAGAAAATATGCTTTGCTAAAATTATATATTAAATTGTATATTAATAATTATTACAGTTAATAATAATAATAATAGTACCAAATAAAGATATTAGGACAATTTCTTGAAGAATGAATTGACACTGAGGGCTGGGGTAATAGTAGTTAAAAATGTAATTTTATTACAGGTAAACTCATTTAAAATATTGTGTATAATATTTTAGATTATAATAATAATATAATATAATATAAAAATATGTATTAAATTGGAAAACGGTTAATGAATTGTAAATTGTATTTATAAAATATTCATATTTACAATATATGAATGCCAAAATATGTTAAAATTGTGTTATATTATTATAAATGTATGAATATAATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27410
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 |
|---|---|---|---|---|---|
| ENSDART00000060315 | None | None | 445 | None | 17 |
| ENSDART00000101215 | Essential Splice Site | 137 | 218 | 22 | 25 |
| ENSDART00000101269 | Essential Splice Site | 668 | 776 | 22 | 26 |
| ENSDART00000101276 | Essential Splice Site | 664 | 772 | 22 | 26 |
| ENSDART00000132878 | Essential Splice Site | 668 | 776 | 21 | 25 |
| ENSDART00000135334 | None | None | 461 | None | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 29912587)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29068533 |
| GRCz11 | 9 | 28879279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGCCGCCTCTATCATCAGATCCAGTGAATGAAGCTCACTCATCCAAG[G/A]TAACAGAAGTGGCTTAATGTTATTCCAGCTGCTGGCACGCAGTAGAGAGA
Long Flanking Sequence:
GTGAAAGGGGCTATTAAGACATCTGGTTAAATTGTATTCATCTCACAATATATATTGCAAAATAAAGAAATATCACAATTTTAAGTTTTTCATACTTACAGTATATTGTCTTGAAACCAACCAACATTTGTTTAGTACAGCATTTATGCAGCATGTTCAAGATTGACTCGCAAAGAAAGTGTATTTGTTCATGAATTAGCTGAAACTCTCCATTGTGTGTTCTCAGCCTGAAAGAGAACACTGATGAATTCATCATCAATTCACAGAAAATATATTTCACTCTTTCTTTTCTTGCCAACTGTACTATGTTTGCTTGTTTGGCTAAATGCAGTGTAGTTTCTTCTCTAACTGAAAACCGCATTTTCACGATTGACTCATAGCGCATTTGTTCACACAACTCTTCATTGTCTGTCCTCAGCCTGGAAGAGAAGGCCGATGACTTCATCTCTTCAGTGCCGCCTCTATCATCAGATCCAGTGAATGAAGCTCACTCATCCAAG[G/A]TAACAGAAGTGGCTTAATGTTATTCCAGCTGCTGGCACGCAGTAGAGAGAGTCCACAGCAGCTGTCAGGACACACACACCATCATTAACTTACTGACACACGCTCTAACAGTAAACTGAGTCCAGCGAAAAGCTGCACTTATTCTCTTCGGCTTTCTTACAGTTTTTTGAAGTTTTGCCATTTACTCACTGCTTCATGCTAAATTCTGTGGGGATGATGTGCTGTTTTCGGCTATATTGAAAGTTAGCCTCACTTTTGTTCCAAAAAGCTTCTTTTTCATTAGTTTTATTTATTGCAGAACATGAGCTTTCTGAGCACTTAAAGTGTGTGAACCTCACACAAATCATGATAATCACAATTATTATGTGTTCATCCGTTCATTCATTCATTCTTTCATTTTCTTTTCGGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGTGGAATGAACCGCCAATTTATCCAGCACATGTTTTATGCAGCAGATTCCTTTCCAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7186
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060315 | None | None | 445 | None | 17 |
| ENSDART00000101215 | Nonsense | 178 | 218 | 24 | 25 |
| ENSDART00000101269 | Nonsense | 736 | 776 | 25 | 26 |
| ENSDART00000101276 | Nonsense | 732 | 772 | 25 | 26 |
| ENSDART00000132878 | Nonsense | 736 | 776 | 24 | 25 |
| ENSDART00000135334 | None | None | 461 | None | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 29908636)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29064582 |
| GRCz11 | 9 | 28875328 |
KASP Assay ID:
554-5330.1 (used for ordering genotyping assays)
KASP Sequence:
TTACTAACGGCCTCCTCGACTGTCCCACAAAGGTGTCATCTCACCATCCT[G/T]AGGGCTCTRTTTCCCCTCTTCCTCAGCTCTCTCAAACTCACAATGTCATT
Long Flanking Sequence:
AATATTGTGCAGCTCTAGTCTGAACTTGCAGTTGAGCAGACTTTCCTAATTCTTGAAAAAAATTAAGAAACAAAAATTATTAAAATTCAATGTTAAATGATAAATTAAATTGATTAGAATTTGATTAGTGACATATTGGATAAACCTAGACTTGTTTTTACAATTGCGGGGTGTAAAAATGACAATTGCAAAAAATGAAATACACATAAAACTGGTGTCCATGAATCCTTATTGAACAATGCCTGTGTTTCTTTACACAGATGCTCTATGTAGATTTATACATTTAGCTTTTCATATTGCAGCTAATAATTATAACTTCCAAGCCACGCATTCAATAGAGTGTACGATTTCACTATCCTTTCTTCTTCTCCCATTTGTAGCAGTTGATGTAGTGACTGACTATCCCCCTGCTTCCTCTCTCTCTTTCTCTCCTCTAGCAGTCTGGCACCTTTACTAACGGCCTCCTCGACTGTCCCACAAAGGTGTCATCTCACCATCCT[G/T]AGGGCTCTGTTTCCCCTCTTCCTCAGCTCTCTCAAACTCACAATGTCATTGCCACCAGGTTTGTTTCATCCCTGCTACCCTTTTCTGCTCTCTTGAGAACAATTGTTGCTTTTCAGTCACTCTGATTAACTGTTTTTAGCTTGGTGGTCAATAAAACCTAGAGGAGTCATGCTTTATTACACTATTATCTGGGTGCATCTGTTTCAGCCGTTCAAAAGTAGAAGTCTATGAAAAAAAAATGTTTTTCTTTTAAAGGTTTGGAGAAGTTGCATTGCTTTTTTAAATTGTCCTTGTTACTGCACATGTTACATGTACTTACTATATTAACCCTTTAACTGCCCCACCAATATTTTTTTTCTGGATATGTCACTAGTTAACACAATCGATGCATTTTTTTAACACATGCCATAATTTCTAAAATATCAACCTCCCCCAAATAGTTGATACGTATGTGGGTTTATGATAAAAGTATTGAAATTAATATATAAACTATGAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9677
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 |
|---|---|---|---|---|---|
| ENSDART00000060315 | None | None | 445 | None | 17 |
| ENSDART00000101215 | Nonsense | 211 | 218 | 25 | 25 |
| ENSDART00000101269 | Nonsense | 769 | 776 | 26 | 26 |
| ENSDART00000101276 | Nonsense | 765 | 772 | 26 | 26 |
| ENSDART00000132878 | Nonsense | 769 | 776 | 25 | 25 |
| ENSDART00000135334 | None | None | 461 | None | 17 |
Genomic Location (Zv9):
Chromosome 9 (position 29905621)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 29061567 |
| GRCz11 | 9 | 28872313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTTGACAGCATTGTGGCTCAYTCGACCAAGGACAACAACCACAAGCCC[A/T]AAGGTCTACTGACCACTGAACTCTGAAAGCGATGCCTCAAGCACATGCCC
Long Flanking Sequence:
TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTAATTTTTTTATGCTGTTACTGTCCTCACTTCCTCACTTCAGACAGTAAAAAGCATTCATTACATTCAGGAACACTAGTTTTGTACATGCATGTTGTTAATTAAATGTTTTTAATGCTTTAATGTACAGTAGCATACACTGAAAAAATTATTCATGGGATTTAATAAATTGTTTTATGTTAAGTGGTTGCAAACAATTTAAATGGGCTGAATTTAAACAAACGAATAAATTTAGTCATGTTCAACTTGATTTGTTTAAATTCAGCTTGTATAAATTATTTGCAACAATTTGCAATGACACATTTTTTTTCAGTGTAGCATACTATAACTTTAAAATTTCTTTAAAATGTAATCTGCATTTACTAGTTAATAAACAATTTGATTGATTCTTTGACAGCATTGTGGCTCACTCGACCAAGGACAACAACCACAAGCCC[A/T]AAGGTCTACTGACCACTGAACTCTGAAAGCGATGCCTCAAGCACATGCCCAGCACCTGTACCTTGGACCATCAAAACATTTCTTTTGAGCACGACATTCCAGTCAAACACATTCCAGTGCCCTTGCAGTGCAGGAACAGACAACTGTGCTGGGCTAACATAGAGAACAGATGGCATCCACGAGCCCAGATCTCACCACAAATAAGAGAACTTGAAGGGCTAGCAGCACGTTCTCAGTGTTTGACGACCACCTTTCCTTTTATAACTCTTATACCTCTTTTGATTGACTCTATACAGCTCTTTGTTGTAGCAGCAGCAGCAGCAGCACATAGATGACCCGCTCCTGTTGTGAATGGATGTTTGATCATCTAGAATGTTTGATCTACTTGCTGTCCACTTCTTGTTCAGATCTTCTGATTGGACGACTGAGCGCATCACTGACTGTTTTTCTTCATGCAGAAGTTCTATTTTTATCTTTGCCTTTCTTTTATGTTCTTATGA
Associated Phenotype:
Not determined