ZMP
btr26
Ensembl ID:
ZFIN IDs:
Description:
bloodthirsty [Source:RefSeq peptide;Acc:NP_001018311]
Human Orthologues:
CTD-2611O12.2, CTD-2611O12.3, ERMAP, RFPL1, RFPL2, RFPL3, RFPL4A, RFPL4B
Human Descriptions:
erythroblast membrane-associated protein (Scianna blood group) [Source:HGNC Symbol;Acc:15743]
ret finger protein-like 1 [Source:HGNC Symbol;Acc:9977]
ret finger protein-like 2 [Source:HGNC Symbol;Acc:9979]
ret finger protein-like 3 [Source:HGNC Symbol;Acc:9980]
ret finger protein-like 4A [Source:HGNC Symbol;Acc:16449]
ret finger protein-like 4B [Source:HGNC Symbol;Acc:33264]
ret finger protein-like 1 [Source:HGNC Symbol;Acc:9977]
ret finger protein-like 2 [Source:HGNC Symbol;Acc:9979]
ret finger protein-like 3 [Source:HGNC Symbol;Acc:9980]
ret finger protein-like 4A [Source:HGNC Symbol;Acc:16449]
ret finger protein-like 4B [Source:HGNC Symbol;Acc:33264]
Mouse Orthologues:
Ermap, Rfpl4
Mouse Descriptions:
erythroblast membrane-associated protein Gene [Source:MGI Symbol;Acc:MGI:1349816]
ret finger protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2149590]
ret finger protein-like 4 Gene [Source:MGI Symbol;Acc:MGI:2149590]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29134 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29134
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 |
|---|---|---|---|---|---|
| ENSDART00000007454 | None | None | 559 | None | 7 |
| ENSDART00000059894 | None | None | 532 | None | 6 |
| ENSDART00000092911 | Essential Splice Site | 365 | 557 | 6 | 8 |
| ENSDART00000105111 | Essential Splice Site | 134 | 326 | 3 | 5 |
| ENSDART00000147590 | None | None | 532 | None | 7 |
The following transcripts of ENSDARG00000040860 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 4859534)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 4133095 |
| GRCz11 | 19 | 4063921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTCAGTAAACTGAAGGACACTCTAAATGAGAAACTCAGTCAAACTGG[T/A]ATGTCAATATCAAATAAAATTTTATTTAAGTACTGGAGAATGAGTCTTAG
Long Flanking Sequence:
TAGCAAACTCCACTAATAATTTTCTGTCTGACCTGTTTGAGCAGATATACTCAGAAAAGGAGAAAGCAGCTCATGTGGAGATCTTCACTGATCTGATCCGCTCCATTGAGAGATGTCAGACTGAACTGCTGGAGATGATGGAGGAGCAGCAGAAAGCAGCAGAGAAACAGGAGGAAGAGCTGATTAAAGAGCTGGAGCAGGAGATCACTGAGCTGAAGATGAGAAACACTGAGCTGGAGCAGCTCTCACACACTGAAGATCACCTCCACCTCCTACAGGTCAGTCAACATCTCTCTGAGCAATGACACACCAGAACACTCCCCATGCTGAAGGCTTTCTCGTCTCTCTCTCCTGCTGTAGATTTACTCATCCCTGCACAGACCTACAGACACCAGGAACTGGCCTGAGATCAGTCTGAAGACTCAGGAGAATCTGGAGACTCTGAGAAGAGCTTTCAGTAAACTGAAGGACACTCTAAATGAGAAACTCAGTCAAACTGG[T/A]ATGTCAATATCAAATAAAATTTTATTTAAGTACTGGAGAATGAGTCTTAGCTGAAATAAGAGTATATGACAGTGTTTGATCATGTATTTGTCATTATCAGTAATATTATCCCTGTATTCCTAGTATTTTGAAGTGTTTACAATATAAATAATGTCTGTGTTCATTGCCACAATATATGAATTATTGAATATCTGCATATGTTGAGTCATTCACTAAATTACATCTGATGCATAAACAGAAAGCTGCCCGATTCTCTATAAATCATACATTGATCAGATGTAAATGTGATGTTGCACAATATTCCTAAAATATAACCTTAAGTTTTGTGTAATTTCACACATGAAAACATCTCAAAGATCTCCTCATGTTTTATTGTCATCAGTGTCTGCAGAGCTGAAGTGGATGCAGCAGTATGCAGGTACAGTGTGCTGAACTACACTAGTCTACACTCAGATTCAGTTCAATTTAATACAATTCATTTCAGTATTATTTGTATAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39224
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 |
|---|---|---|---|---|---|
| ENSDART00000007454 | None | None | 559 | None | 7 |
| ENSDART00000059894 | Nonsense | 195 | 532 | 2 | 6 |
| ENSDART00000092911 | None | None | 557 | None | 8 |
| ENSDART00000105111 | None | None | 326 | None | 5 |
| ENSDART00000147590 | Nonsense | 195 | 532 | 3 | 7 |
The following transcripts of ENSDARG00000040860 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 4864039)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 4137600 |
| GRCz11 | 19 | 4068426 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCTGTTCTCTGTCTCTAGACTGAACTGATGAAGACACAGAAAGACGTG[C/T]AGCAGATGATCGAGGACAGAATCAAGAAGATTCAAGACATCAAACACTCA
Long Flanking Sequence:
CTGATCTCAAGATTAACACCACACTCAGAGAGATCTCTGAGCACTATAAGGAGAAAAATCCTGCAAAAAAGCCAAGAATTATGTGTGAAATCTGTGAGGGCAGAAAGCTGAAAGCCCTGAAGTCGTGTCTGGTGTGTCAGAGCTCTTACTGTCAAACTCACCTGGAGCCTCATTTGAGAGTGGCAGGATTAAAGAAACACAAACTGATGGATCCTGTGAGGAATCTGGAGGACTATATATGTCAGAAACACGACAGACCTCTGGAGCTCTTCTGTAGAGATGATCAGACGTGTGTGTGTTCATTCTGTACTGTGAAAGATCACAAAAACCACAACACTGTTCCTCTAGAAGAGGATATTGAAGAGAAGAAGGTAGACAAGGCTGAGGCTCATATTATGGGGAATCAAAGTCTGAATGCAGATTGATTTTCTTCAGTAAATCTGCTAAAAATACCTGTTCTCTGTCTCTAGACTGAACTGATGAAGACACAGAAAGACGTG[C/T]AGCAGATGATCGAGGACAGAATCAAGAAGATTCAAGACATCAAACACTCAGCAGAAGTCAGAAAAGTGAGTTCATAAAAGATTAATATAAATGATACATGATTCACTCTAGTTCAGCAAGAGTCCAACAGTACTGAGAGTTTCAGTGTCCTCCACTGGTCTGTTTATTTCAGACAGTTCGGACCATCAGTTTATGTATGCGATGGGTTTGGAGAGTCACTCTTTCTATAAGTTACTTTGTTAGATCTGTTACTAGTAAATAAAAAAGGACGTAAACTAGTGAGTGGGTATGCAGCAACTGTCCAGACTGTAATCAGGGTATATGGAGAATACTCACAGACAGAATTCCAGGCTTTGTACAGGACAAACAGCTTACAGTCAAAAACGATGGTAAAGGCTTTGGCCAGGGCAGGCAGCATACAATCAAAAACAAGGAATCAGGCAGTAGGAAAAAGAAAAGCAGTCAGAATACACAAGAAATGCTCAGAAATGTAAGCAAAA
Associated Phenotype:
Not determined