ZMP
si:ch211-196g2.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0R133]
Human Orthologues:
PRRT3, PRRT4
Human Descriptions:
proline-rich transmembrane protein 3 [Source:HGNC Symbol;Acc:26591]
proline-rich transmembrane protein 4 [Source:HGNC Symbol;Acc:37280]
proline-rich transmembrane protein 4 [Source:HGNC Symbol;Acc:37280]
Mouse Orthologues:
Prrt3, Prrt4
Mouse Descriptions:
proline-rich transmembrane protein 3 Gene [Source:MGI Symbol;Acc:MGI:2444810]
proline-rich transmembrane protein 4 Gene [Source:MGI Symbol;Acc:MGI:2141677]
proline-rich transmembrane protein 4 Gene [Source:MGI Symbol;Acc:MGI:2141677]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21375 | Nonsense | Available for shipment | Available now |
| sa41294 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21375
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109430 | Nonsense | 363 | 985 | 3 | 3 |
| ENSDART00000144285 | None | None | 322 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 48588964)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 46427222 |
| GRCz11 | 8 | 46435101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGTTTACCGAAAGAGACCAGTCAATATCTGTGGGAACAGTTCCATCTT[T/A]GAAGTCAAACCCTGGCTTTCCTACCCGTGCCCAACCCATTGATCCCTGTG
Long Flanking Sequence:
GCAGCTGTGCCGTCAGCCAATCGTTGCATTGCTGATCATGATTTCGAGGATCGACAGATCTGTCCTTCACAACACACGCAGCGATCTCAGATCTGTTTATACAGACATTCTAATCTGATTAGCGAACTTGTTTGAAGAACCAAATTAGCGAGAGATCAGTTATCAAGATTAAAAGATCCAGGATCTGCCAAATCATCTTAGATCATTTAAGCGAGGTACGAAGAACGGACCCCAGGAATGACATTTTAATTTAGTATTTAGAACTATTCAGTGTATGTCGTTGTTGCTTATATATTATTGAATGTAGTTATATGCTTTGTCATAGGATACATTTTCCACCTCAATAATATGTCCTCTGCCTCTTTTGATTTTCACAGGTAAGCCCACTTTTCAAAGGACTACCTCCCCTCTCCAAATTGGACATGGACATTTTGTGTTTGAAAATGACAGACGGTTTACCGAAAGAGACCAGTCAATATCTGTGGGAACAGTTCCATCTT[T/A]GAAGTCAAACCCTGGCTTTCCTACCCGTGCCCAACCCATTGATCCCTGTGATACTGGAGTGGGTCCCTGTGTTTCTTACAAAGACGAAGACAAAGCTAAAAATCATGAAACAACAAATGGCAGCTTTTTAGTGTGGGCAGATTTGAAACGCACATTATCATTTGCATGGGAACTGCATGTGTTTGGTTCTGCTGCCCTCTTCCTTCTACTTACTGCCGGTTCAATCCTCGGCTTAGTATTAGCTCCCAGCTTGAATTGCCCTCATTGTGGTGAGCTTATACTCACCAATAGTCTTTTGCTTTTTGTGGGTGTAATTAGAGCTGGGCACTTTTTGCTCGACCCATATGGGACACGGCTCCTCTTGCCACCTCCTGTAATAATAGCTTTATACACGCTACCATTGCCACTGTTAATTTTGGCACAAGCTGCACTAGTGATATTGGTACTAAAAGAAGCAGGAGTAACTTGGTTACCGCCAGCATTTCAGCGGCCCCCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41294
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 |
|---|---|---|---|---|---|
| ENSDART00000109430 | Nonsense | 758 | 985 | 3 | 3 |
| ENSDART00000144285 | None | None | 322 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 48590148)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 46428406 |
| GRCz11 | 8 | 46436285 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGGCTGGACAGGAGCGATCAGGAGCGGACATTAGCAAGAGCCTCATA[C/T]GAAATCGTGACCCACTCAAAGACAGCAATCACGGACGCAATCTGAAGAGC
Long Flanking Sequence:
GAAATAAGGGAACAGGCGAAGGAAAGATGCAGGTTTTGGCACGGGTTCTGGTAGTGTGCGCTCTCCTCGGGATATTGTGTTGTCTGTTGCACATTTATGCCTGCCTGTGGCTGTATGGACTACTAGGAGACTGGAGGCGCTTTCGTTGGGGATGGTGGCTCTGTCAGTTCTGGGTACGACTGCTGGAGCTTGCCTGGGCTTTTTGTCTACTTTTGGTGTCCTCCTGGGTCTTCTGGAGACCCAATGGAGGCCACATATGTGGAGCACAAAGACAGGAAGGAGAAGCCCCTGAAAGCTTGCCCTCACCGACTCAATCATCAAACTCTTCCAGCAGACATACATGCTGGGCAAAGATTGTGCAGAGCTTTAAGGTAAGGCAACAAAAAAAATCAGAAAGCAATGGGATTGGAGGATCTAACAGTGGGACAATGACTGGAGAGCTGCCCAATAACTGGGCTGGACAGGAGCGATCAGGAGCGGACATTAGCAAGAGCCTCATA[C/T]GAAATCGTGACCCACTCAAAGACAGCAATCACGGACGCAATCTGAAGAGCTTTGCAGGAGGCTCTGCAGGTTCACTGCTACGACTGCAGGCTCTTGCTCAGACACCTCGGTCTTTAAGCAACAGTCTGGACAGGGACAAGGAGTCAGCCCTTTCTCTCTTCGATTTTGACCTGCGCCCTCCAACCCCGATCGACCTTACCCGCAGTATTGACGCGGCACTTAATCGCGAGCATCTGTTTATGGGCGAAAGTTTGTTTCACCCATTGCGACCAGTATCGCCTCCTCCCTCTCCAGACCTGTGGATGCGACGGAATAGTGACCCCCAAATTACACTGTCACTTAGTAGTGATGAACACACTTTGCTCACAGAGTCCTCTGCAGGTCTAGATCGATCCATTCCCAGTGCTGTGCCAAGCCGCCAGGTCACAGCCCCTCCTACACCCACTCATCAAGGCTTCCGTTGGGTCTCTGAGATACCGGTGCCTTCTTCTTTGTCCTGC
Associated Phenotype:
Not determined