ZMP
si:ch211-10e8.3
Ensembl ID:
ZFIN ID:
Description:
Novel Ras family member [Source:UniProtKB/TrEMBL;Acc:Q7T015]
Human Orthologue:
RAB44
Human Description:
RAB44, member RAS oncogene family [Source:HGNC Symbol;Acc:21068]
Mouse Orthologue:
Rab44
Mouse Description:
RAB44, member RAS oncogene family Gene [Source:MGI Symbol;Acc:MGI:3045302]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14499 | Nonsense | Available for shipment | Available now |
| sa13184 | Nonsense | Available for shipment | Available now |
| sa12366 | Nonsense | Available for shipment | Available now |
| sa45263 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33928 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31535 | Nonsense | Available for shipment | Available now |
| sa13349 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14499
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 |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 450 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40997125)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41068725 |
| GRCz11 | 6 | 41066261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTCCAGATGAATCTACATTACAAAACATGAAAGATGGAGCTGAAGAA[C/T]AGGAGAAGGAAATATGTCTGGAKAATGATGTTGGTCTTGTTGAAGAGTCT
Long Flanking Sequence:
ATGTAAATGTTTTAGTCAGAGAAGCTGAAGTTACTGGAGAATCAGTTATATTGGATAGTAATGTGACTGCAGAGTCAGATGTGATTCAAAAAGACACTTTAGCTGATGCAGAATTAGAAACATTGCAAGTTTCTGAAAATACAGAGGATGTTTCTGCTGTGACTGATACTGATTTTCTAGTGCAACATCATGGCACTGAACGAGCAGAAGGGACAGACACAATTTCTGTACAAAGTGGCATCAACATCATTCCTAGAGAGTCTCACGGAGAAGAGGCGAACTCAAAGTCGAGTCCAGTTGTTCAGAGGAGAAAAATGGGCTCAACTCGAAGACCTCTCAAAGGAAATAAAGGACAAAGAAAAGGACAAGAGCTTGATGATGAAAAGGAAACATTTCACTGTGAATTTTTGCTTGATGTAGAAAAAGAAACATTTAGTTTGGAGAATGAACCCTGTCCAGATGAATCTACATTACAAAACATGAAAGATGGAGCTGAAGAA[C/T]AGGAGAAGGAAATATGTCTGGAGAATGATGTTGGTCTTGTTGAAGAGTCTGAATCTGCTCTCATTCAGTCATATAGTTCAGATTTAGTGTCTGAAGAATCCACTGCATTGAGTGTCTGTAACATCACAGAATCACAAACCCTCACAAAAATTCAAGAAGAGTCCTGGGAAATAGTTGGAGATGTTGAAAGAGAATCAGTAGATGGAGATACAGACTTACAATTAGAAACAGAGTCACAAAACCAAACATGTGACTCAACCAGTAAAGCAGAACAAAACATCCATGATGTAAATGTATTAGTCAGAGAAGCTGAAGGTATTGGGGAATCAGTTAAAGTGGACAGCAATGTGATTGCAGAGTCAGATGTGCTTCAAAAAGCCACTTTAGCTGATCCAAAATTGGAAACATTGCACGTATCTGAAAATACTAAGGATGTTTCTGCTGTCACGGATTCTGATCTTCTAGTGCAACATGAACCAACTGTAGAAGCAGGAGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13184
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 |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 641 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40996551)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41068151 |
| GRCz11 | 6 | 41065687 |
KASP Assay ID:
2259-7945.1 (used for ordering genotyping assays)
KASP Sequence:
AATCAGCATCATTCCTGGAGATTCTCACAACGAAGAGGYAAACTCAAAGT[C/A]AAGTCCAGTTGTTCAGAGGAGAAAAATGGGCTCAACTCGAAGACCTCTCA
Long Flanking Sequence:
TAGTTCAGATTTAGTGTCTGAAGAATCCACTGCATTGAGTGTCTGTAACATCACAGAATCACAAACCCTCACAAAAATTCAAGAAGAGTCCTGGGAAATAGTTGGAGATGTTGAAAGAGAATCAGTAGATGGAGATACAGACTTACAATTAGAAACAGAGTCACAAAACCAAACATGTGACTCAACCAGTAAAGCAGAACAAAACATCCATGATGTAAATGTATTAGTCAGAGAAGCTGAAGGTATTGGGGAATCAGTTAAAGTGGACAGCAATGTGATTGCAGAGTCAGATGTGCTTCAAAAAGCCACTTTAGCTGATCCAAAATTGGAAACATTGCACGTATCTGAAAATACTAAGGATGTTTCTGCTGTCACGGATTCTGATCTTCTAGTGCAACATGAACCAACTGTAGAAGCAGGAGAAACAGACACGGTTCCTGAAAAAAGTGGAATCAGCATCATTCCTGGAGATTCTCACAACGAAGAGGCAAACTCAAAGT[C/A]AAGTCCAGTTGTTCAGAGGAGAAAAATGGGCTCAACTCGAAGACCTCTCAAAGGAAATAAAGGACAAAGAAAAGGACGAGAGCTTCAAGATGAAAATGAGACACTTAATAATGAAATTAGGTTTGATGTAGAGAAAGAAACATTTGGTTTGGAGAATGAACCCTGTCCAGATGAATCTGCATTACAAAACATAAAAGTTGGAGCTGAAGAACAGGAGAAGGAAATATGTGTGAAGAATGATGCTGGTGTTGTTGAAGAGTATGAATCTGATCTCATTCAGTCATTTTATGGTTCGGATTTAGTGTCTGAAGAATCCACTGCATTAAGTGTCTGCCACATCGAAGAAGCACAAACTCTCACAATTAGTCATGAACAATTTCAGAATAATCCTGGAGATGCAGAAAGAGCAGCAGTAGTTGAAGATGCTGCTGATACTGAAGATACTTCAGAAACTGAAGCTACAGTTACAATGAAGAGCACTACAAATACTGCATCACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12366
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 839 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40995958)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41067558 |
| GRCz11 | 6 | 41065094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCTACAAATGTCGAGGAAGATACTTCAGGAGACACAGACACAATTTTC[A/T]AGCAGAGTAACATCAACGTTGTTCATGAAGAWATTTATAGAGGGGAAGCT
Long Flanking Sequence:
AAAATGAGACACTTAATAATGAAATTAGGTTTGATGTAGAGAAAGAAACATTTGGTTTGGAGAATGAACCCTGTCCAGATGAATCTGCATTACAAAACATAAAAGTTGGAGCTGAAGAACAGGAGAAGGAAATATGTGTGAAGAATGATGCTGGTGTTGTTGAAGAGTATGAATCTGATCTCATTCAGTCATTTTATGGTTCGGATTTAGTGTCTGAAGAATCCACTGCATTAAGTGTCTGCCACATCGAAGAAGCACAAACTCTCACAATTAGTCATGAACAATTTCAGAATAATCCTGGAGATGCAGAAAGAGCAGCAGTAGTTGAAGATGCTGCTGATACTGAAGATACTTCAGAAACTGAAGCTACAGTTACAATGAAGAGCACTACAAATACTGCATCACATGTTTTTCAAACGTCTCCTAGTTCAAGCACAGATGCATTTAATATATCTACAAATGTCGAGGAAGATACTTCAGGAGACACAGACACAATTTTC[A/T]AGCAGAGTAACATCAACGTTGTTCATGAAGATATTTATAGAGGGGAAGCTCACCCAAAGTTAAGTCCAGTTGTTCAGAAGAGAAAAATGGGCTCAACTCGAAGACCTCTCAGGGGGAACAAAGGACAAAAAAAAGATAATGATGAAAAGGAAATCTCATTTCTGGAAAATGAACCCAATCCAGATGAGCTTATATACACTGCAATGGGTATCAGTGATATTTCAGAAGCTCAAACCCACGTAAAAGTTCACGAAGAGTCCCAGGACAACCATGAAGTTGTTGAAAAAGCAACAGTAGGGGAAAGCACACAATCACAAACAGAAAACAAAGTGAGTGTGTTAGTCAGAGAAGCTGAAGTTCCTGAAAATACAGTTGTGATTAATACAACTGAGGAGTCGTATTTGTTTCAATACGTCTCTGATTCAAAACTGACCATATCTGACTATGAACATGAGGCTCCAGTAATTCCAAACATAATTTCCAAACAAAGTGACTTCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45263
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 1059 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40995297)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41066897 |
| GRCz11 | 6 | 41064433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCAGAGAGAAGAATCCAAGGTAAAGAATAGAGATAATGAGGCAGGGT[C/A]AGAAGAGGAAAACACAGAAACACATTCAAAAGACCAGGAACAAAATGTGG
Long Flanking Sequence:
TCTGGAAAATGAACCCAATCCAGATGAGCTTATATACACTGCAATGGGTATCAGTGATATTTCAGAAGCTCAAACCCACGTAAAAGTTCACGAAGAGTCCCAGGACAACCATGAAGTTGTTGAAAAAGCAACAGTAGGGGAAAGCACACAATCACAAACAGAAAACAAAGTGAGTGTGTTAGTCAGAGAAGCTGAAGTTCCTGAAAATACAGTTGTGATTAATACAACTGAGGAGTCGTATTTGTTTCAATACGTCTCTGATTCAAAACTGACCATATCTGACTATGAACATGAGGCTCCAGTAATTCCAAACATAATTTCCAAACAAAGTGACTTCAGCATTCCTGGAGATTCTCACAAAGAAGAGGAAAACTCACAATTAAGTCCAGTTGTTCAAAAGAGAAAAATGGGCTCAACTCGAAGACCTCTCAAAGGGAATAAGGGACAAGGAAAGCAGAGAGAAGAATCCAAGGTAAAGAATAGAGATAATGAGGCAGGGT[C/A]AGAAGAGGAAAACACAGAAACACATTCAAAAGACCAGGAACAAAATGTGGCAAAAGACAATATGAATATAATAGATAATGTCAATGAAGAAAAAAAGGCAACAAAGGCATTGGATACATCCATGCAGGAACTATGTGAACAAGAGCAAAGATCAGATGTATCACAAACACATGCTGATACATCACAGGATGAAACCAGCTCACATTTATTGGACATCCCAGAAAGAACTGTAGATTTTGTTAGGGAGTCTACGAGTCAGCCTGATCTTGTTCTGTCTGATGTGTTGCTTATGACAGAAGCTCAAACGTATTTGTCATCAGAAGATAATGTCATGGGTAACAGTTCAATATCTATAACAGAGGTACATGAAATGCATGCAGACTCCAATACATCCAAGAGAAAAATGGGGTCAACTAGAAAGAGAGGAAAGAGGATGGTGAATGAAGAGGAAGAGGAAGCTGAAAATACAATTGGTTCTGGAGCCACAAGTTCCAAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33928
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 |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 1073 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40995256)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41066856 |
| GRCz11 | 6 | 41064392 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCAGGGTCAGAAGAGGAAAACACAGAAACACATTCAAAAGACCAGGAA[C/T]AAAATGTGGCAAAAGACAATATGAATATAATAGATAATGTCAATGAAGAA
Long Flanking Sequence:
CAATGGGTATCAGTGATATTTCAGAAGCTCAAACCCACGTAAAAGTTCACGAAGAGTCCCAGGACAACCATGAAGTTGTTGAAAAAGCAACAGTAGGGGAAAGCACACAATCACAAACAGAAAACAAAGTGAGTGTGTTAGTCAGAGAAGCTGAAGTTCCTGAAAATACAGTTGTGATTAATACAACTGAGGAGTCGTATTTGTTTCAATACGTCTCTGATTCAAAACTGACCATATCTGACTATGAACATGAGGCTCCAGTAATTCCAAACATAATTTCCAAACAAAGTGACTTCAGCATTCCTGGAGATTCTCACAAAGAAGAGGAAAACTCACAATTAAGTCCAGTTGTTCAAAAGAGAAAAATGGGCTCAACTCGAAGACCTCTCAAAGGGAATAAGGGACAAGGAAAGCAGAGAGAAGAATCCAAGGTAAAGAATAGAGATAATGAGGCAGGGTCAGAAGAGGAAAACACAGAAACACATTCAAAAGACCAGGAA[C/T]AAAATGTGGCAAAAGACAATATGAATATAATAGATAATGTCAATGAAGAAAAAAAGGCAACAAAGGCATTGGATACATCCATGCAGGAACTATGTGAACAAGAGCAAAGATCAGATGTATCACAAACACATGCTGATACATCACAGGATGAAACCAGCTCACATTTATTGGACATCCCAGAAAGAACTGTAGATTTTGTTAGGGAGTCTACGAGTCAGCCTGATCTTGTTCTGTCTGATGTGTTGCTTATGACAGAAGCTCAAACGTATTTGTCATCAGAAGATAATGTCATGGGTAACAGTTCAATATCTATAACAGAGGTACATGAAATGCATGCAGACTCCAATACATCCAAGAGAAAAATGGGGTCAACTAGAAAGAGAGGAAAGAGGATGGTGAATGAAGAGGAAGAGGAAGCTGAAAATACAATTGGTTCTGGAGCCACAAGTTCCAAGGAGACATTAACTCCTAAAAAATTAATTGCAGAATCTTCTGTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31535
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 |
|---|---|---|---|---|---|
| ENSDART00000028292 | Nonsense | 1621 | 1952 | 1 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40993612)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41065212 |
| GRCz11 | 6 | 41062748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAGAAGATGAAGACAAAGTAGATCAGAAGACAGAGTCAAACAAAGAA[G/T]AAATAACGGAGGGGTCGCTAGTGCATAATATCACAGAAGACCCTCCAAAT
Long Flanking Sequence:
AAAGTCTACAGTCGGAATCTGTTCCCATTGAGAGGAGAAGGAAGATGGGCTCGACCCGGAAAAATATTGGAAGAGAAGGAAGAATGCAAAGAAAGCGAGATGGATATGAGGACACAGAAATCATAGACACAAATCTGCAGATGTCTCACGACCCTGAAATGAGCTCATCAGGTATAACTGCAGAAGAACAAACAACTGAAGATTACTCCAATCAGTCAGAGGATTCACTTCTTGGTGAAATACAGCGAATGCTAAAAACAACTTCTCAAAGTGCATCCAATTTTGAATTGATTATTGATGAGCCGAAATCAAATTCACCAGAAGGCTCAGAAATCAGATCTCTTTCACCATCACAGAGCTTGACAACTCTAAATGATCCAAACTCTCCAGAAAGACGACGGCGAAAAATGGGTTCAACTCGCAAGAACCCTAAACGGCAGTTCAAAGCAGAAAGAGAAGATGAAGACAAAGTAGATCAGAAGACAGAGTCAAACAAAGAA[G/T]AAATAACGGAGGGGTCGCTAGTGCATAATATCACAGAAGACCCTCCAAATAAAGAGTATCTTGATGTTCCCAGTGCACACACAAGCAGCCAGCAAGAAGAGAGCGATAGCCCTGTTGTTCAAGAAAGTGCGTCACCATCAACTAAAAGGAAGTTTGGGTCCAGACGAGCTAATAAGGGCAAACTTGGTAGGCTTGAGGCATCTGATGGTATGACTGAATCAGAAGATGGAGATCATAAACCAGATGGCTCTGCTGTTGAGGACAGACAGCACAGGGATGGTTCAATGGTATGTACGTCTTTGTTTATAAAATGTCCTTTAATTTTATATTTTAATAGAAAAAAGCTTTGCTTTAAAACTAGGGTAACATTCTGTATTTATTAGAGCAAAAAACAGTTTCGCATAATATGAGTGTTTGCATTAAATGAAACCAACAAAAAAAATGTGTAGTTAAACCAAAGTAAACACAAATTTACCATGGTTTTGCTACACTAACCATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13349
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000028292 | Essential Splice Site | 1925 | 1952 | 9 | 9 |
| ENSDART00000137283 | None | None | 166 | None | 5 |
Genomic Location (Zv9):
Chromosome 6 (position 40989407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 41061007 |
| GRCz11 | 6 | 41058543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAAAATGTGYCGTCTCTGCTTGCATAATGTGTAATTTGYCTTTGCTGYT[A/C]GGTTGTTAGTGCAGCGCAAGAGAAAAAGGGAGGAACACACAACGCTGAGA
Long Flanking Sequence:
GGATCTCTCAAGCCCGGGTAGCTATCATATCTTCATATAGCCAAAATAAAACTATTCCACTAACATAATAACATGATAGAATAAAAATGATTTTGCTGAGAGACTCTATCTGTTTCCTTCCCTAAATTGTACAATTACAATGTCACACAGGAAAGGGCTCAAGATGATGTCGTCATGATGTTGCTCGGAAACAAGAATGATTCAGTTAATCGTGAAGTCCAGATTCAGGAAGGAGCAGATCTGGCCAGAGTAAGAGTTTATTATGTTTTGATGAAGTCTATTTGTACTGAAAAGTAAAATTAATAATAATGGATTGTTGTGTTTTTCCACTCGTAAGGAGTATAACATACATTTCATGGAGTGCAGTGCTGCAAACGGGGCTAATGTGTCAGAATCTATGAGGACTCTTGCTGAGTAAGACTATAATAGATTATACCAGTTATTGCTTGCATAAAATGTGCCGTCTCTGCTTGCATAATGTGTAATTTGTCTTTGCTGCT[A/C]GGTTGTTAGTGCAGCGCAAGAGAAAAAGGGAGGAACACACAACGCTGAGAAGAGAACCACAACAGAAGAAATCTGGATGCTGTTAAAAAAAAACTCCCAACACATATAAACACAACACTGTTCAAATGTTTGGGTTGGTAAGAATGCGTTAAAATCGATTACTGTTTTTTTTCATAAAATATAATTCACATTATTTTATATACACTCACAGGTCACTTTATTAGGTACACCTTACTAGTACCAGGTTAGACAGACTTTTGCCTTCAGAACGCCCTTAATCCTTCATGGCATAGATTCAACAAGGTACTGGAAATATTTCTCTGAGATTTTGGTCCATTTTGACATGATAGCTTTACACAGTTGCTGCAGATTATTTGGCTGCACATCCATGATTTGAAATTCCACCACATCCCAAAGGTTCTCTATTGGATTGAAGTGGTGGCTGTGGAGGCCATTTGAGTACAGTGAACTCATTGTCATGTTCAAGAAACTCATCTGAG
Associated Phenotype:
Not determined