ZMP
rhbdd3
Ensembl ID:
ZFIN ID:
Description:
rhomboid domain-containing protein 3 [Source:RefSeq peptide;Acc:NP_001121831]
Human Orthologue:
RHBDD3
Human Description:
rhomboid domain containing 3 [Source:HGNC Symbol;Acc:1308]
Mouse Orthologue:
Rhbdd3
Mouse Description:
rhomboid domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:2444684]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15827 | Nonsense | Available for shipment | Available now |
sa6975 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30616 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15827
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111302 | Nonsense | 137 | 348 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 26552304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 24379569 |
GRCz11 | 13 | 158462 |
GRCz11 | 5 | 24883369 |
KASP Assay ID:
554-4919.1 (used for ordering genotyping assays)
KASP Sequence:
GGGTCTCWGGATACGCAGCCATTCACCTCGCCCTKCTCACGGCTCAGWGY[C/T]KACAGGTCAAGCAGAGGAGAGTCCTGCGCTTTGTTCCTGTCTGGTTCTTA
Long Flanking Sequence:
GGTATGCGTTTGTCAGTTTACAATGCTTAATAATATCTTTCCGGCATGGATGTGGTCTGGATCAAACCGTCCAGGGTGTTGTAGTGGAACATTTTTAATCCTATCATTAATTGTGTCGACTTGGCTCTGTGGTATTCATGCCAGTCTAAGTTTAGGACCAGGTGGGGAATTTCCTGGATTTTATGGTAAGCAAAGTACTATTATATTATACTTAAAATAATGTCATCAACTTATTTACTTTCTTGTGTATTGCAGATTTCATCTTCTACGCCTTCAGTAATGAAGAGCTGACCTCATTTCTCCACAACATCTCCCTGCTGCTCTGGATTGGGCCCTGTCAGGAGAGAAGATGGGGGACTTTTACCTTCCTCACCCTCTCCTTCATCTCGGCTCTGCTCCTTCCTCCTATTTATGCCCTGTTTCTTTTTGTTACTGGAGATGAAGCCAGCAGGGTCTCTGGATACGCAGCCATTCACCTCGCCCTGCTCACGGCTCAGTGT[C/T]GACAGGTCAAGCAGAGGAGAGTCCTGCGCTTTGTTCCTGTCTGGTTCTTACCTTGGCTCTTGTTGATTTTTGACCTCTTCCTCCTTCCCAGTGCTCCAGGCCTGCTGCACTTCTATGCCATTTGCCTGGGACTCAACTGTATCCTTTACTACACCAATGGTTCACAGCCTTTTTGACTCCTTTTGTCTGAGACAATATTTTAAGATCACCATACTAGCTATTTCGTTTATTTTCCTGCAGTTTTGACAAATATTTTGTTTTAATTTCATTTAATCATCATTTTACTAATTTCAGACTGGTTTACACTTTTTAAATATATTATTATTAAATAGGCCTGTCACCATCATACATTTTGTGCTGATGATTAATTCTCAATTCATCATACAATTATGTTACAGTTTTTATATGCATAATTTTCTTTCTATTTTACCTAACGGCATTAAACTTGCCTGCAATATTTCCTGTCATGCTTTAAAAATAGTAAAAGTTCTATTTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6975
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 |
---|---|---|---|---|---|
ENSDART00000111302 | Nonsense | 137 | 348 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 26552304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 24379569 |
GRCz11 | 13 | 158462 |
GRCz11 | 5 | 24883369 |
KASP Assay ID:
554-4919.1 (used for ordering genotyping assays)
KASP Sequence:
GGGTCTCTGGATACGCAGCCATTCACCTCGCCCTKCTCACGGCTCAGWGT[C/T]GACAGGTCAAGCAGAGGAGAGTCCTGCGCTTTGTTCCTGTCTGGTTCTTA
Long Flanking Sequence:
GGTATGCGTTTGTCAGTTTACAATGCTTAATAATATCTTTCCGGCATGGATGTGGTCTGGATCAAACCGTCCAGGGTGTTGTAGTGGAACATTTTTAATCCTATCATTAATTGTGTCGACTTGGCTCTGTGGTATTCATGCCAGTCTAAGTTTAGGACCAGGTGGGGAATTTCCTGGATTTTATGGTAAGCAAAGTACTATTATATTATACTTAAAATAATGTCATCAACTTATTTACTTTCTTGTGTATTGCAGATTTCATCTTCTACGCCTTCAGTAATGAAGAGCTGACCTCATTTCTCCACAACATCTCCCTGCTGCTCTGGATTGGGCCCTGTCAGGAGAGAAGATGGGGGACTTTTACCTTCCTCACCCTCTCCTTCATCTCGGCTCTGCTCCTTCCTCCTATTTATGCCCTGTTTCTTTTTGTTACTGGAGATGAAGCCAGCAGGGTCTCTGGATACGCAGCCATTCACCTCGCCCTGCTCACGGCTCAGTGT[C/T]GACAGGTCAAGCAGAGGAGAGTCCTGCGCTTTGTTCCTGTCTGGTTCTTACCTTGGCTCTTGTTGATTTTTGACCTCTTCCTCCTTCCCAGTGCTCCAGGCCTGCTGCACTTCTATGCCATTTGCCTGGGACTCAACTGTATCCTTTACTACACCAATGGTTCACAGCCTTTTTGACTCCTTTTGTCTGAGACAATATTTTAAGATCACCATACTAGCTATTTCGTTTATTTTCCTGCAGTTTTGACAAATATTTTGTTTTAATTTCATTTAATCATCATTTTACTAATTTCAGACTGGTTTACACTTTTTAAATATATTATTATTAAATAGGCCTGTCACCATCATACATTTTGTGCTGATGATTAATTCTCAATTCATCATACAATTATGTTACAGTTTTTATATGCATAATTTTCTTTCTATTTTACCTAACGGCATTAAACTTGCCTGCAATATTTCCTGTCATGCTTTAAAAATAGTAAAAGTTCTATTTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30616
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 |
---|---|---|---|---|---|
ENSDART00000111302 | Nonsense | 216 | 348 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 26554557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 24381822 |
GRCz11 | 5 | 24885622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTGCCTGCTTGCCAAAATGGGCCTACATCCCAGTCACCTCTCGTTCG[C/T]AGCTACCAGTTTACAACAACACCTCAACAAGGTCAGTTCAATCTCTTTGC
Long Flanking Sequence:
TGTTTTAAATCTTAACATTCCATATCTTCATATGGTTATGATTCGGCCGAATATTGTTCAATGCTAACAAAGTGTACATCAAAGGAAACCTTATTTATTCACCTTTCAGATTTGAAAATTGACAGTTCTGACTTGTTTTGTTGTCTAGCATCACAAAAGTTATCGTAAAGTAAATGAAGAACTAATGTCTTGAGGGATACACAAAGTGTTTTTTTTCTCATTTTACATTTACATTGTACAGTTATCTTACCTTATTACAAACATACCAAATAAACCTGATCAGATGATTAATTAGTAACTGTGGCAGGCCTAACTGATCTTCAATTAAAACTAATTTAAAGGTATGAAATGATATCTCTTTTTAACCACATTATAAAGTGATGCCCTTAATATACGCTACAGACAATAATGAGTTAATCGAAATGCTGGAGCAGATAGAGAGACTGGGTGCATGTGCCTGCTTGCCAAAATGGGCCTACATCCCAGTCACCTCTCGTTCG[C/T]AGCTACCAGTTTACAACAACACCTCAACAAGGTCAGTTCAATCTCTTTGCTAATATTACCCAAAAATTGTTTTCTCAGATCACATCAAATAACTAGAATTAACAAGCTTAATTACTGTTGTTGTGCAATAGACCGGAGCCATTTAGCAGTGCATTCCAGTCTGAGAATTATTCAACATGGCAGCAGTCTGTGTCAGAGTGGCCCCAGGAATCTCCGTTGGCAACAGATTCACAGTTATTAGAGGAGCAGATGCTGAGAGCAGGAATATTAGCATCTCTCCACGACGCACCTGAGGGTACAGCCGACAAAGTGGAAGTACCAAAGTCCTCAGTATCCTCATTACGGTTAGTGCATACCGCAATTATAAGTAATCATAAGTTGAGCGCTTGGTTTTTATCAATCTTTTTCACCTCCAGTTTGCAGCAGCTGGAGAAGATGGGCTTTCCCACAGAGAAAGCTGTAGTGGCTCTGGCAGCTACAGGGCAGCTGGATGGAGCCAT
Associated Phenotype:
Not determined