ZMP
zgc:85963
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC407981 [Source:RefSeq peptide;Acc:NP_999977]
Human Orthologue:
EPB41L3
Human Description:
erythrocyte membrane protein band 4.1-like 3 [Source:HGNC Symbol;Acc:3380]
Mouse Orthologue:
Epb4.1l3
Mouse Description:
erythrocyte protein band 4.1-like 3 Gene [Source:MGI Symbol;Acc:MGI:103008]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39960 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7313 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39960
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 |
|---|---|---|---|---|---|
| ENSDART00000004431 | Nonsense | 118 | 838 | 4 | 29 |
Genomic Location (Zv9):
Chromosome 2 (position 59027563)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 58085195 |
| GRCz11 | 2 | 58571168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTAATCTGCAATTGCCTCTCTGGATATACCACTAACTGTACTTAAAAA[A/T]AAATAAATAAATAAAAATTACTAATGTTTTGCTTCTTACACTTTACACAC
Long Flanking Sequence:
CCAGACTGGACTATTGCAACTCTCTACTAGTCGGGCTTCCAGCTAACTCAATCAAACCTCTTCAGCTCTTCAGAACGCAGCAGCACGAGTGGTCTTTAATGAACCTAAACGAGCACATGTCACTCCGCTGCTCATCCGTTTGCACTGGCTGCCAGTTGCTGCTCGCATCAAATTCAAAGCTCTGGTGTTTGCTTACAAAGCGACTTCTGGCTTTGCTCCTTCTTATCTGCTCTCACTTCTGCAGATGTATGTGTCCTCCAGAAACTTGCGTTCTGTGAATGAACGTCGCCTCGTGGTTCATCCCAAAGAGGGAAGAAATCACTTTCCCGAACTCTCGCATTCAATCTGCCTAGTTGGTGGAATGAACTCCCTAACTGCATCAGAACGGCAGAGTCACTCGCTGTCTTCAAGAAACCACTAAAAACTCAACTATTTAGTCTCCGCTTCCCTTCCTAATCTGCAATTGCCTCTCTGGATATACCACTAACTGTACTTAAAAA[A/T]AAATAAATAAATAAAAATTACTAATGTTTTGCTTCTTACACTTTACACACCTGAAACTTGCCTACAGCACTTCTTCATTGTTGCTCTTAGTTATGTAAATTGCTTCCTTGTCCTCATTTGTAAGTAGCTTTGGATAAAAGTGTCTGCTAAATGACGTGTTACTCTTTATTTTAATTTCACAGGAACTTTAAAAGTAAGCCAAGTCTGCGGGAAAACAGTGGACTTGGCAACCCTAGACTGTGATTCCTGACTGTGATTTTCATTAGTTTTTGTAATGCAACTCTTGATGTTTCTTTTCCTCCAGAACTGGCTGGACGCCTCCAAAGAGATCAAGAAGCAGATCAGCAGTAGGTTTTCCCTCAAACACAAGTGCTTTTGTCTTCTTTCTCATCCGCAGGATCTGACAGTAGCTCTTGTTTTTCAGCTTCTCCCTGGAGCTTCGCCTTCAACGTGAAGTTTTATCCTCCAGATCCAGCGCAGCTCTCGGAGGACATCACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7313
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 |
|---|---|---|---|---|---|
| ENSDART00000004431 | Essential Splice Site | 742 | 838 | 26 | 29 |
Genomic Location (Zv9):
Chromosome 2 (position 58975100)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 58032732 |
| GRCz11 | 2 | 58518705 |
KASP Assay ID:
554-4948.1 (used for ordering genotyping assays)
KASP Sequence:
GTGATTCTGCAGTGATGTGAAGTGTGCTGTGTTTGCCCCAGAGTTCAGAG[G/A]TAAAGACTCCCTCTGCTGGTGAAAAACTAAAGYACATGAAGGCTCTCAAT
Long Flanking Sequence:
TGGAGGTAGATTAGTGTCGTCTAGTGGGGAAGTATGTGTATATGTAAAGGTATGTGTGTTTTTTTCTCTGTTGTCATTTTTCACTTTAAAAAAATGAAGTGCTTCTTGTTTTTAAGACTACTTTTTAGGTCTATAATTTGTTTTATGTGTAAAATTGCTGCCAAATACTACAAAATGTCAATGATATGTGTTTTATAATGTAATAACCCTAAATGAATGGATGGAATGATTATTTCTTGTTGGTTTATTTCTCGACTCACAGCTCTTTGATATTATGGTTGATGCAGTGTCAATAACGAATGCTTTCCTTCTATTTCTCCTAAATAATATTTGAGAATAGATTTAGTGTGTCCCATGAAGATTGACAGGTGCTCGTATTGAGGAAATATTTGTCTTGAAGCTTGCACACTCAAAAATGGGCTTTTCAGGCTTAGTATACGTAGGAGAATTGTGATTCTGCAGTGATGTGAAGTGTGCTGTGTTTGCCCCAGAGTTCAGAG[G/A]TAAAGACTCCCTCTGCTGGTGAAAAACTAAAGTACATGAAGGCTCTCAATGAGGCCATCGCTAGGGGAAGACGCTCCGCATTCATTCATAATGGAGAAGAAGATGCATTAAACTGTGCAGGAGCTGCCAAAGATGATCAGTTTCCAGTACAAACCCGTGAACATATCCATGATGAAAGCCCAGACATGATGTGTCTGGAGAAAGATGAAGAAATGCTGCAAATCTGGGTTCCAGAAAAGCAAAATATTGAGGATAACAATAAAAACGAGGAAACTGCGTTTGAAACACAATCTGAAAAACACAAAATCACTTCAGAAACCAAACAGAGTACTTCAAGAATTGAAAAAGTGGTGTCTCATGAAGATGATTTTGGTGCAAAACACCAAAACAGTGCGTCTGAAATCAAGAAATCCTCAGGTGAAACTCAGTCTGAAGAAGGAGAAGAAACTGGACCAAAACACCATGAAATTTCTGCTGGAAACCAAGAAATGTTCCCAATA
Associated Phenotype:
Not determined