ZMP
zgc:136903
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC562845 [Source:RefSeq peptide;Acc:NP_001103501]
Human Orthologue:
RHO
Human Description:
rhodopsin [Source:HGNC Symbol;Acc:10012]
Mouse Orthologue:
Rho
Mouse Description:
rhodopsin Gene [Source:MGI Symbol;Acc:MGI:97914]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21885 | Nonsense | Available for shipment | Available now |
sa45425 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21885
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103973 | Nonsense | 213 | 355 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 11 (position 19517434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18934748 |
GRCz11 | 11 | 19097090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGACTGAGAACGAGTCGTTTGTCATCTATATGTTCGTGGTTCATTTCT[C/A]AATCCCTCTCACCATCATTTCTTTCTGCTATGGGCGCCTGCTTTGCACTG
Long Flanking Sequence:
CCTCATCGTGACCTGCGTTCCTGTCAACGGTCTCACTTTGTACGTAACCATCGAAAACAAGAAGCTCCGGACGCCTCTGAACTATATCCTTCTGAATTTAGCGGTGGCTGACTTGTTTATGGTGTTCGGTGGATTTACAACGACCTTCTACACCTCCATGCATGGATACTTTGTCCTGGGACGGGCTGGTTGCAACTTAGAGGGTCTTTTTGCAACCGTTGGCGGTGAGATTGCACTTTGGTCTTTGGTTGTTCTGGCTGTTGAGAGATGGGTAGTCGTTTGCAAGCCTTTCACCAAATTTCGCTTCTCACAACTTCATGCTACCTTAGGAGTGGCTTTTTCTTGGTCGATGGCCTGTTCGTGTGCCATTCCTCCACTCCTAGGATGGTCCCGGTACATCCCCGAAGGCTTGCAGTGCTCTTGCGGAGTGGACTACTATACGCCGAATCCTGAGACTGAGAACGAGTCGTTTGTCATCTATATGTTCGTGGTTCATTTCT[C/A]AATCCCTCTCACCATCATTTCTTTCTGCTATGGGCGCCTGCTTTGCACTGTGAAGGTTGCAGCTGCCCAGCAGCAAGAATCAGAAACTACACAAAGGGCTGAGCGCGAAGTGACCCGAATGGTGATCCTCATGGTCATCGCATTTTTAATATGTTGGCTCCCCTATGCCAGCGTGGCCTGGTACATCTTCACCCACCAGGGGAGTCAATTCGGCCCTGTTTTTATGACGGTCCCGGCTTTTTTTGCCAAGAGCTCAGCTCTCTACAACCCGCTCATTTACGTCTTCATGAATAAGCAGTTTCGACACTCCATGATGATGACGGTGTGTTGTGGAAAGGATCCGTTCCAAGATGAGGAGGAAGGAAGCTCCAGCTCTAAGTCTAAGACTGAGACCTCGTCCGTCTCCTCTAGCTCAGCTTCTTCTGCCTGAGGCTCAGGCTCTGGGCTATTTGTGGAAAACACAACTCCACTGCCTGCAGATTATGACAGGACTTATGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45425
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103973 | Nonsense | 265 | 355 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 11 (position 19517277)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 18934591 |
GRCz11 | 11 | 19096933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGTGACCCGAATGGTGATCCTCATGGTCATCGCATTTTTAATATGTTG[G/A]CTCCCCTATGCCAGCGTGGCCTGGTACATCTTCACCCACCAGGGGAGTCA
Long Flanking Sequence:
ATGCATGGATACTTTGTCCTGGGACGGGCTGGTTGCAACTTAGAGGGTCTTTTTGCAACCGTTGGCGGTGAGATTGCACTTTGGTCTTTGGTTGTTCTGGCTGTTGAGAGATGGGTAGTCGTTTGCAAGCCTTTCACCAAATTTCGCTTCTCACAACTTCATGCTACCTTAGGAGTGGCTTTTTCTTGGTCGATGGCCTGTTCGTGTGCCATTCCTCCACTCCTAGGATGGTCCCGGTACATCCCCGAAGGCTTGCAGTGCTCTTGCGGAGTGGACTACTATACGCCGAATCCTGAGACTGAGAACGAGTCGTTTGTCATCTATATGTTCGTGGTTCATTTCTCAATCCCTCTCACCATCATTTCTTTCTGCTATGGGCGCCTGCTTTGCACTGTGAAGGTTGCAGCTGCCCAGCAGCAAGAATCAGAAACTACACAAAGGGCTGAGCGCGAAGTGACCCGAATGGTGATCCTCATGGTCATCGCATTTTTAATATGTTG[G/A]CTCCCCTATGCCAGCGTGGCCTGGTACATCTTCACCCACCAGGGGAGTCAATTCGGCCCTGTTTTTATGACGGTCCCGGCTTTTTTTGCCAAGAGCTCAGCTCTCTACAACCCGCTCATTTACGTCTTCATGAATAAGCAGTTTCGACACTCCATGATGATGACGGTGTGTTGTGGAAAGGATCCGTTCCAAGATGAGGAGGAAGGAAGCTCCAGCTCTAAGTCTAAGACTGAGACCTCGTCCGTCTCCTCTAGCTCAGCTTCTTCTGCCTGAGGCTCAGGCTCTGGGCTATTTGTGGAAAACACAACTCCACTGCCTGCAGATTATGACAGGACTTATGGAAGATTCTGAAATGAAAGATGGAGTTGTATAGATATGTTTCAAAAAATATTTTAAATATTATGTGCAATTACTATAATTGTTCTAATAATATATCAAGAATATTAGTTTATTATAAAAATGTGTGATTTTATATTTACATATTTTCTTTTACTTATGGT
Associated Phenotype:
Not determined