ZMP
LOC563403
Ensembl ID:
Human Orthologue:
RHBDF1
Human Description:
rhomboid 5 homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:20561]
Mouse Orthologue:
Rhbdf1
Mouse Description:
rhomboid family 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:104328]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17176 | Essential Splice Site | Available for shipment | Available now |
sa22083 | Essential Splice Site | Available for shipment | Available now |
sa42017 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42016 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35274 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9498 | Nonsense | Available for shipment | Available now |
sa35273 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17176
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Essential Splice Site | 155 | 856 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21603590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20129223 |
GRCz11 | 12 | 20251097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCCCTCCWCCTCTATATGTYCCACCGCCACATCATGGCATGCAGAGGG[T/C]AAGCTGAACACATAAAATCNTTTGCTTAAACTWTTCTATTGAAACCRTAG
Long Flanking Sequence:
TTGTGTTGATATGTTTGCATTTTCCCTGATTTCCTGAAACAAAAACAAAAAAAAAACAACTTCCTTGTGTGTACATCTGGCGAATAAAGCTCATTCTTATTCTAATCAAGTAGATTTATTGGAAAATCATCCTCAAATGTGTCTCAACTAGTTCTTTAGATTTATCTTCACTCTTCAGTGGATTTGATTATTTTTTCCATTGTCTTTTTAGACGTATACCTTTTGTATAATTGGTGTGATAAAAAGGTTGTATTTGTACTATAATAAATACTGATGTGACCACAGGGGCACAGCAGACTGGTTTGGGGTCAGCAATGATTTGGATGCCACCCAGAAATGGCAGCGGAAGAGTTTGCGTCACTGCACCCAGCGCTACGGCAAACTAAAGCCTCAGGTGATCCGAGAGATGGACCTGCCCAGCCAAGACAATCTCTCCATGACCAGCACCGAAACCCCTCCTCCTCTATATGTCCCACCGCCACATCATGGCATGCAGAGGG[T/C]AAGCTGAACACATAAAATCCTTTGCTTAAACTATTCTATTGAAACCATAGGCTATAAAAAAAAAAGATGGGTGTCATTTTTTCATTTGGGTGGCATTACCACTGGAAAAATGAAACCATGTCTCGGGTATGGTTGATGTCATGTTTTGAATGATGATAAAGGTGACATCATTTAGATCCTGAATCTTTATTGTGCTGAGCATGATCTACTCACAAGCACATAAAATGGACACCACACTTTGCTTTTATGGCGTTAGATAACAATAAAAGCAAACTTGATTAAGACCTACAATAGCGTTATACAATCAATATCAAAGTTATTCACACCCCATATTAAATATTTATGAATATTTATTTGAAGTTTAATAAGAAATTAGTTTTTTCATGTTTAAAGGTTTATGCTACAATTTGTTTGCTTGGATGACCGACACGGTGGCTCAGTGGTTAGCACTGTCGTCTCACAGCAAGAAGGTCCCGGTTAAGTCCCGGCTGGGTCATTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22083
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Essential Splice Site | 224 | 856 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21601440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20127073 |
GRCz11 | 12 | 20248947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGTCTGTCGCCAAGATGGGCTTCAGAGCTGCTGCTGCTCTGGTCAAG[G/A]TAATGTGAGGCCATTTGTTAAGCATGTTGCATTAGAACTGTGCATTGATC
Long Flanking Sequence:
AAAATAAAGTGTTACTTAAAATAATTTTATTTATAGTTGAACTATTCATTTAACATTAATATTTAATTCATAAAATATTAAATTTCTTGCTGTAAATTCAACAAGATATCCAAATTGTAAAAAAATTGTTTGTTTTTATAGAATACTGGAGTATTTATCCTTGCTCAATTTTATCATTTTTTTTTTTTGTAGTCCATGTGCCCTTGTAATGTTTATTTACCACAGCTGTTGGACTCAATGAGGAGCTAATGGTTAATAATGCAGAATATGACTCGCTGTTTATGATTTTGCAGATCGTAGACCCGCTGGCTCGAGGTCGAGCGTTCCGTAATGTGGATGAGGTGGATGGTGTGAATGTACCTCAGACCCCCATCACCCCCTGCGCCGCTTCCCTGTGCTCCTTCACCAGCTCCCGCTCCGGCTTCAACCGGCCTCCCCGCAGACGCAAGCGTGAGTCTGTCGCCAAGATGGGCTTCAGAGCTGCTGCTGCTCTGGTCAAG[G/A]TAATGTGAGGCCATTTGTTAAGCATGTTGCATTAGAACTGTGCATTGATCTACAGCAGGGATGCTATAGATTTTAAAGTGCTGTTTACCAAAGCAAAGACATTTTTCTCAGGGTTTATTTCAGGTATTTTCTGTAACATATTTCTTCTGGAGAAAGTTTTATTGCTTTTACTTTGGCTGTAATTACAACAGAACTGAAAACTCAAATTGCTTTAAAACTAGTCAAGTGTGAGTTAACTATGACATAATTTTCTTTTTTTGTGTGTGAGCTATACCCTTAATTAAAATTTGAGACACAGCTACTTTTTTAATTACAAGTGTAGAAGAGGCCATACAGTGAAAAGCTGTGAAGGTTGTTAGAGCAACCGACTCCCATGCAGAAGGTTGCTGGTTCGATCCAAGCTTAGAGTTGGTTGCGTGGTGTAGGACCGGAGTGGGACTCCTTTTCAACTCTGGAACCCATATTAAAACAACGTCATTTCCAATTCAGTACTTTAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42017
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Essential Splice Site | 224 | 856 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21601439)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20127072 |
GRCz11 | 12 | 20248946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTCTGTCGCCAAGATGGGCTTCAGAGCTGCTGCTGCTCTGGTCAAGG[T/G]AATGTGAGGCCATTTGTTAAGCATGTTGCATTAGAACTGTGCATTGATCT
Long Flanking Sequence:
AAATAAAGTGTTACTTAAAATAATTTTATTTATAGTTGAACTATTCATTTAACATTAATATTTAATTCATAAAATATTAAATTTCTTGCTGTAAATTCAACAAGATATCCAAATTGTAAAAAAATTGTTTGTTTTTATAGAATACTGGAGTATTTATCCTTGCTCAATTTTATCATTTTTTTTTTTTGTAGTCCATGTGCCCTTGTAATGTTTATTTACCACAGCTGTTGGACTCAATGAGGAGCTAATGGTTAATAATGCAGAATATGACTCGCTGTTTATGATTTTGCAGATCGTAGACCCGCTGGCTCGAGGTCGAGCGTTCCGTAATGTGGATGAGGTGGATGGTGTGAATGTACCTCAGACCCCCATCACCCCCTGCGCCGCTTCCCTGTGCTCCTTCACCAGCTCCCGCTCCGGCTTCAACCGGCCTCCCCGCAGACGCAAGCGTGAGTCTGTCGCCAAGATGGGCTTCAGAGCTGCTGCTGCTCTGGTCAAGG[T/G]AATGTGAGGCCATTTGTTAAGCATGTTGCATTAGAACTGTGCATTGATCTACAGCAGGGATGCTATAGATTTTAAAGTGCTGTTTACCAAAGCAAAGACATTTTTCTCAGGGTTTATTTCAGGTATTTTCTGTAACATATTTCTTCTGGAGAAAGTTTTATTGCTTTTACTTTGGCTGTAATTACAACAGAACTGAAAACTCAAATTGCTTTAAAACTAGTCAAGTGTGAGTTAACTATGACATAATTTTCTTTTTTTGTGTGTGAGCTATACCCTTAATTAAAATTTGAGACACAGCTACTTTTTTAATTACAAGTGTAGAAGAGGCCATACAGTGAAAAGCTGTGAAGGTTGTTAGAGCAACCGACTCCCATGCAGAAGGTTGCTGGTTCGATCCAAGCTTAGAGTTGGTTGCGTGGTGTAGGACCGGAGTGGGACTCCTTTTCAACTCTGGAACCCATATTAAAACAACGTCATTTCCAATTCAGTACTTTAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42016
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Nonsense | 372 | 856 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21594252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20119885 |
GRCz11 | 12 | 20241759 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCATTACTGTGCCTGTTAAAAAACTCTTTGCTAAGGAAAAACGTCCTTA[T/A]GGGCTTGGCATGGTGGGGAAACTGACCAACCGCACCTATCGCAAACGCAT
Long Flanking Sequence:
TAAGAGTGGGAAAAACTGGCCATTGACTTCCATAGTATTTTTTTGTTTGTACATGTCAATGACTGCTTTTTTCCCAACACTCTTCAGAATGTCTTGTTTAGTGTTTAACAGAAAGAAGAAATTCATTAACATTTAGAAACTGTTGAGTGAGGAAATTGGAAGGAAATGTTCATTTTTGGGAGAATTTGCCCTTTAATTCAATCTTATTGTGTATTTTTCAATTTTAAGTTTTAAAACATGAGTGTGAGTAAGTAATGAGGATTTTTATTTTACATATCGGTGTTGAGCTATCCCTTTAAGACCTTTTGTGAATACTAATTTCTGTATCTCTGCCTCTGTCTCAGGCCTCTGGAGAGGGGTTGGCGTAAAGCAAAGGATGGTGCTCTGGTTCAGCCTAAAGTGCGCTTACGGCAAGAGGTGGTGAGTGTGACTGGGCAGCGGCGTGGTCAGCGCATTACTGTGCCTGTTAAAAAACTCTTTGCTAAGGAAAAACGTCCTTA[T/A]GGGCTTGGCATGGTGGGGAAACTGACCAACCGCACCTATCGCAAACGCATTGACAGCTATGTGAAGAAACAGATCGAAGACATGAACGACCACAGGTATTTACCACAGTGTTGCTGGAGCTCTTGCAGATGTTGACCATTGTGATAACGTCATATTTTTGGGCGCAATTGTACAATTTGCGATTGAATTAAAGGGATAGTTCACTCAAAAATTGAAAATGACGAAAGGAAATGATGTTTACTCAAATTTTAGTGGTTCAAAACTTTTAAGATTTTCTATTGTCTGTTGAACACAAAACAACATATTCTGAAGAGTGTTGGAAAAAAGCATCCAATGACATCCATTATAGGAACAAAATATGCTATGAAAGTCAATGGCTGTTTTTTTTTTTAACAGAAGAAGAAACTCAAACAGGTTTGGAACAAGTAGAGAATGAGTACATTTTATTTTTGGGTGACCATTCCCTTTAATTCTAGATGTCTGTACAGTGTGATGAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35274
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Essential Splice Site | 521 | 856 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21590981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20116614 |
GRCz11 | 12 | 20238488 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATATCCACTCCAGCTATATTTAACCAAACGTCCTTGTAATTTTCTCA[G/A]AGCACTCTGGCATTATGGGTAAAGTGGCCTCAGCACCCAAGTGCTCCAGT
Long Flanking Sequence:
AAAATATAATAATATTATATAATAATATAATAAATAATTATATATTATATTAATTTGTAAACTAATTTATGTATTATAACAATATCAATATGATAATATATAATAGAATTTTATATAATAATATAATATGATATATATTTTATAACAAAAAAATAAAATAAATACAATTTGAAATATCAATAAATAGTACAATAGTATACAGTAACTCTACAAATGACAAAATCTAACAGTTAGTTGTTTTTTGTGTCCTGCAGGAGGCGCTGATTCACTTGGGGGCGAAGTTTTCCCCCTGTATGCGACAGGATGAAGAGGTTCACCAGCTCATCCAGCAGAAAAAGGCCAGCGAAAAACACTCGGCCTGCTGCGTCCGCAATGACCAGTCCGGCTGCGTTCAGACCTCTCAGGAGGAGTGTTCAGTCAGTTCCTCCTTTCACATCACGTATGCACTTTATTATATCCACTCCAGCTATATTTAACCAAACGTCCTTGTAATTTTCTCA[G/A]AGCACTCTGGCATTATGGGTAAAGTGGCCTCAGCACCCAAGTGCTCCAGTTCTAGGGGATAAAGTGCGTCAGTACGGCTCCGTGTGCCATCAAGACCCCAGGTACATTTATAATCCTCTTTATTTTCTTTTTTTAAGCTATCCTCATCTTCTATTGGATGACTATTTATTTTGTGTATTAATAATGTTAGGATTTGTCTGGAGCCTGCCTCTGTTTCTCCTCATGTGTGGCCTGATGACATCAGCAAGTGGCCGGTGAGTGTGAAACGGTGATCAGTATGACCATGCATTATGTACAGTGCCCAACAAGCAGTTTTTGCAAACATTTGTGCACCCCTCCTTGGTTGCATAATAATGTGCTCTTATGTTATAAGAGAAGATCGCAGTGAAATGCCATTCTGTTTCTAGAGAAAGCTAGATAATGTCATGTTTTTCAGACAGAAATACATAGTGTAGCAGTATTGAGATGTGTGAAACTAAATTGAAACTGAAAAAATAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9498
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040909 | Nonsense | 690 | 856 | 16 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21584081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20109714 |
GRCz11 | 12 | 20231588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGCTTCCAGATGACCATTCTAAGGGATTTGGAGAAGCTGGCAGGCTG[G/A]CTGAGAATCTCTATCAKCTATATCCTCAGCGGGATTACGGGCAACCTCGC
Long Flanking Sequence:
TCTTATTTTTATTCGATTTTCTGCTGGTTTATAATGAGTGTCACTACAATGTGCAATCATGTAAAACACCAGCAGGGGGTGTAGAGATCTACATTTGTCCCAGTATCCATAATGTCAGTGTACAGACAAACCTTTAGCCATGAATTGTAATTTGTGTAATTACGGATAAAACTGATGATCTGTTCTCAGGTTCATTGCATGGATGATGTTTGTGGCCTCCTGCCTTTTCTGAACCCAGAGATCCCAGACCAGTTCTATCGACTCTGGCTATCTCTGTTTCTTCACGCCGGGTGAGTAGGAGGAAGCGTGATCCGTCACAGGGGGGCCTATTGTGAATTTCCCAATAAATTAAATGCAGTGTCAGATTACTGTCCTGACAAAGGTAAAGCCGTGTTTGATTGATAGAGAAAGTCTCTGTGTCTCTGCAGGATCCTGCACTGCCTGGTGTCTGTGTGCTTCCAGATGACCATTCTAAGGGATTTGGAGAAGCTGGCAGGCTG[G/A]CTGAGAATCTCTATCATCTATATCCTCAGCGGGATTACGGGCAACCTCGCCAGTGCCATCTTCTTACCGTACAGAGCAGAGGTACAGAAAAACCTAATGAGTCTAAATCAGGGATCATTGAGTTTCTTTGTTCAGTAATGAGATCATGTAACTAATTTGGACCCAAAAATTTTTAAAAGTTTAGTTCAGCCTTTCATAGGTCTTTAGGATATTGGCTGGATAATTCTTATAGACCACTTATTCTAAAACACCTCAATTATTATTAATCACTAAAAATGTTTTTTTTTTTTATTAAAAAATAAAAAATAGCACCAATGGATTAAGGGAAGTTTATTTATAAACTAAATTCGAGAGGATCACAGGCTTATGATTGCTTGTAGCTGGTCCCGCATTATTTAATTTATGATTCACCAATCAGATGATTCCTAATAAATACTCTAAGTTCCATATTACAGCCATCTTCGTTTTGAAGAATCCCCCATTCCACCCCTACTCCTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35273
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 |
---|---|---|---|---|---|
ENSDART00000040909 | Nonsense | 849 | 856 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 12 (position 21579947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20105580 |
GRCz11 | 12 | 20227454 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAGTTTCTCACCTGCATCCCGCTGACGGACAAGTTTTGTGAGAAATA[C/A]GACCTCAATGCTCACCTCCACTGAGGCCTTGCAGAAATAGGGCTGCGCTT
Long Flanking Sequence:
AATCATCATTGAATGTTTTTTTCAGTGCAGTTTATTTGAGGAGGTTCAGTGCAGAAATGTCTCTCTCAAGCCATAAAACGTTATTCCCTCTGCTTCTGATGCCAGGTGGGTCCGGCTGGCTCTCAGTTTGGCATCTTGGCCTGTCTGTTCGTGGAGCTGTTCCAGAGCTGGCAGATCTTGGCACGGCCGTGGAGGGCCTTCACCAAGCTCTCATGTGTAGTGCTGTTCCTTTTCGCCTTTGGCCTGCTGCCCTGGATAGATAATTTCGCTCACATCTGTGGCTTCGTCTCGGGCTTCTTCCTGTCCTTCGCCTTCCTGCCCTACATCAGCTTCGGCCGCATGGACATGTACCGCAAACGTCTACAGATCCTCGTGGCACTTACCCTTTTTGTGGGCATCTTCTCCAGCTTCGTGGTACTCTTCTATGTTTATCCAGTTAAATGCGAGTGGTGTGAGTTTCTCACCTGCATCCCGCTGACGGACAAGTTTTGTGAGAAATA[C/A]GACCTCAATGCTCACCTCCACTGAGGCCTTGCAGAAATAGGGCTGCGCTTGAAGGCATCTGGATGCCAACTCTTGACTCTTAAGCTTATATAAAATACACTCTTTTTATACAATGTTGTTTCATACGGAAAGTTTTATTGTTTTTAATATTTCTCCGGCTCAGAGAGTCCACCCCAGGAGGGAAGAATAGCCAGTTGTGCCTTTTCATTGACTACCAGCTACTGCCATATCCGAGTCCTGTTAGATCAGAGCACTTTTGGAGCAAACCTGTGATGCATGTAGTGCTACTACTACAAAGGTTAAATTCGGTAGCGTTTTAGCTACCTGTTCAAAAGTAAGAGAACAAAATAAATTGTGACAAAATCACAAAGTTTGCTGTCATGTTTGGCTGTTTTTCCACTTTGGTCCCACTTTATCTTAAGTGTCACTTATAACTGTGAACTTACAAGGTAGATGTGTAAATAGTATATAACTACAGTGTATGTACACATTGGTACATA
Associated Phenotype:
Not determined