ZMP
zgc:73336
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393767 [Source:RefSeq peptide;Acc:NP_957088]
Human Orthologue:
ROM1
Human Description:
retinal outer segment membrane protein 1 [Source:HGNC Symbol;Acc:10254]
Mouse Orthologue:
Rom1
Mouse Description:
rod outer segment membrane protein 1 Gene [Source:MGI Symbol;Acc:MGI:97998]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16839 | Nonsense | Available for shipment | Available now |
| sa33767 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16839
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011295 | Nonsense | 176 | 346 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 70133598)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66459756 |
| GRCz11 | 5 | 67138125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGATGGAGTTCCACTGCTGCGGAAACACAGACTACAGGGATTGGTTC[G/T]AGGTGCAGTGSATCAGCAACCGCTACCTGGATTTCAGCTCTAAGGAAGTT
Long Flanking Sequence:
CAATTGTCTAAATTAGTTTTTGCTATGCTATTTTGAAAGATAAAGTCTCAAAATGTCAACAACCTGATGTACACAATACATGCAAAATGCAGTCTGTCTGACATTAACATCCTGCTTTCCGTCAGGTAATGGACAACACAGACATCCATTGTGTGCCCAACACCTTGATGATTGTTGGTCTGGCTTCGATGGGCGGCAATTACTTTGCCAGTCGAATCTGCCAGGATGCCCTGGATGCCGGGCGTTTCCCACGGTGGAAGACCTACATGAAGCCTTTTTTTGGCTGCTCCATTTTCTTCACCACCCTCATGTTGATTTCAATCATCTTGAGTTACATCATGAAGGGCAGCCTGGAGACCTCGCTGAAAATCGGCCTGAAGAACGGCATCCGCTTCTACAAGGACACCGATATCCCTGGCCGCTGCTTCCAAAAGCAGACCATCGACCGGCTTCAGATGGAGTTCCACTGCTGCGGAAACACAGACTACAGGGATTGGTTC[G/T]AGGTGCAGTGGATCAGCAACCGCTACCTGGATTTCAGCTCTAAGGAAGTTAAGGAGTGAGTAAAACAGAATTTTAGTCAAAGAAATAGCTCATCCTAAAAATAAAAATTCTGCCATCCTGTACAGTGTTAAAAATTTCCTGCAGAATTTACGGTAACTTACTGTAGATCAATTACAGCAAAAGTACTGTATTTACATTTACAACACTATTTACCTTGCTCTATATGCATTTATAATATTGTATATCTTATTGTATTGTATATCTTTACCGTCATTTCCACTTTAATACTTTAAAATACAGTAATATACCGCATACCTGTCCAACAGCAAAATACAGTTCACATGAGACCAATTACAGCAAAAGTACTGCATTTATATTTACATCACTATTTATCTTATGTATGTATTTACAGTATTGCATATAATTACTGTAAAATATAGTAACTTTCACAATGCAACTTTAAAATACAATAAGATAGGGATAACTGTAAAATTTAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33767
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011295 | Essential Splice Site | 194 | 346 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 5 (position 70133541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 66459699 |
| GRCz11 | 5 | 67138068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGATCAGCAACCGCTACCTGGATTTCAGCTCTAAGGAAGTTAAGGAG[T/C]GAGTAAAACAGAATTTTAGTCAAAGAAATAGCTCATCCTAAAAATAAAAA
Long Flanking Sequence:
AACAACCTGATGTACACAATACATGCAAAATGCAGTCTGTCTGACATTAACATCCTGCTTTCCGTCAGGTAATGGACAACACAGACATCCATTGTGTGCCCAACACCTTGATGATTGTTGGTCTGGCTTCGATGGGCGGCAATTACTTTGCCAGTCGAATCTGCCAGGATGCCCTGGATGCCGGGCGTTTCCCACGGTGGAAGACCTACATGAAGCCTTTTTTTGGCTGCTCCATTTTCTTCACCACCCTCATGTTGATTTCAATCATCTTGAGTTACATCATGAAGGGCAGCCTGGAGACCTCGCTGAAAATCGGCCTGAAGAACGGCATCCGCTTCTACAAGGACACCGATATCCCTGGCCGCTGCTTCCAAAAGCAGACCATCGACCGGCTTCAGATGGAGTTCCACTGCTGCGGAAACACAGACTACAGGGATTGGTTCGAGGTGCAGTGGATCAGCAACCGCTACCTGGATTTCAGCTCTAAGGAAGTTAAGGAG[T/C]GAGTAAAACAGAATTTTAGTCAAAGAAATAGCTCATCCTAAAAATAAAAATTCTGCCATCCTGTACAGTGTTAAAAATTTCCTGCAGAATTTACGGTAACTTACTGTAGATCAATTACAGCAAAAGTACTGTATTTACATTTACAACACTATTTACCTTGCTCTATATGCATTTATAATATTGTATATCTTATTGTATTGTATATCTTTACCGTCATTTCCACTTTAATACTTTAAAATACAGTAATATACCGCATACCTGTCCAACAGCAAAATACAGTTCACATGAGACCAATTACAGCAAAAGTACTGCATTTATATTTACATCACTATTTATCTTATGTATGTATTTACAGTATTGCATATAATTACTGTAAAATATAGTAACTTTCACAATGCAACTTTAAAATACAATAAGATAGGGATAACTGTAAAATTTAGTTCATATTACAGTTCAATTCGCAAGTAAATTACAGTAAATCAATTACAGCAAAAGTACTG
Associated Phenotype:
Not determined