ZMP
rasl11b
Ensembl ID:
ZFIN ID:
Description:
Ras-like protein family member 11B [Source:UniProtKB/Swiss-Prot;Acc:Q6P0U3]
Human Orthologue:
RASL11B
Human Description:
RAS-like, family 11, member B [Source:HGNC Symbol;Acc:23804]
Mouse Orthologue:
Rasl11b
Mouse Description:
RAS-like, family 11, member B Gene [Source:MGI Symbol;Acc:MGI:1916189]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23686 | Essential Splice Site | Available for shipment | Available now |
sa13617 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23686
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015755 | Essential Splice Site | 38 | 244 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23013338)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23126725 |
GRCz11 | 20 | 23025825 |
KASP Assay ID:
2261-4242.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTAATGTTCTGTGTGCTTTATCGTTAAAATTCTGGTCTTTTTCTTGC[A/T]GCATTGGTGGTTCGTTTCCTCACTAAGCGGTTTATCGGCGACTACGAGAG
Long Flanking Sequence:
TGTGGGCGGAGCTATGGAGCGTGAACGTAGTCTTGAGTAGCCAATCAGAGCCGAGCGCTTCTCTGGCTGTATAAATACATCCAAGCTCCAGTCTCGGCTCTCAGAAAACCAAGTAGAAGTCTTGGTGAGATCTAGGAGAAGGAATTTGGAAACATTCATATACTTTATCATTTAGAGAAAAACAGTGTCTTCGATTCTGACATTGCTTTTACGGCGTCTGTGGATATTTTGACTTAAGCCTTTTTATTCGTAAGCTTTGGATAGCATCTTCCTATCGCTCTTTTGCCAAAATGCGTCTGATCCAGAACATGTCAACTATTGCGGAGTACCCGAGCGCCGATTGCCCGTCCAGCCGGGTCATTAAGATCGCAGTCATCGGTGGCAGTGGGGTTGGCAAAACCGGTAAGTTTGTGGACAAGCTATGAGCAATTTTACATTCTCACAATACATCCTGTAATGTTCTGTGTGCTTTATCGTTAAAATTCTGGTCTTTTTCTTGC[A/T]GCATTGGTGGTTCGTTTCCTCACTAAGCGGTTTATCGGCGACTACGAGAGAAACGTTGGTAAGTTTGTCATCTTTCTAACAAGACAACCGATTTAGGAATCATTAAACCCATTTCTGCTGTTGTCAAATATATTAAACTATGCGCTTTCGCTTTACAGGCAACCTGTACTCCAGAGAGGTGCAGATAGACGGAGAACAAGTGGCCATTCAAGTTCAAGACACTCCTGGAGTTCAAGTGAGTACATATGAGCCATGCAGGAATACACTTGTTTTTTATGAGACATGTAACCGTTATAAGCGCTCGTAGAGCATCTTTCATTCATTCCCACGCTGCTACTTCACGGGTGAGAAGTGTAGAAAGAGCGCATACCTTCACCTATTGTCTTTCAGCGCTTCTTTTGTGTTTATCCGGGTTTCTGCTTAACACTTGGGGTTAATTGGCCAGCGGGGAGCCTGCTGTTGCACTCCTATATGGGGGAAGCTCGTTCATGTACAGCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13617
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015755 | Essential Splice Site | 57 | 244 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23013278)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 23126665 |
GRCz11 | 20 | 23025765 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTYGTTTCCTCACTAAGCGGTTTATCGGMGACTACGAGAGAAACGTTGG[T/G]AAGTTTGTCATCTTTCTAACAAGACAACCGATTTAGGAAKCATTAAACCC
Long Flanking Sequence:
CTCTGGCTGTATAAATACATCCAAGCTCCAGTCTCGGCTCTCAGAAAACCAAGTAGAAGTCTTGGTGAGATCTAGGAGAAGGAATTTGGAAACATTCATATACTTTATCATTTAGAGAAAAACAGTGTCTTCGATTCTGACATTGCTTTTACGGCGTCTGTGGATATTTTGACTTAAGCCTTTTTATTCGTAAGCTTTGGATAGCATCTTCCTATCGCTCTTTTGCCAAAATGCGTCTGATCCAGAACATGTCAACTATTGCGGAGTACCCGAGCGCCGATTGCCCGTCCAGCCGGGTCATTAAGATCGCAGTCATCGGTGGCAGTGGGGTTGGCAAAACCGGTAAGTTTGTGGACAAGCTATGAGCAATTTTACATTCTCACAATACATCCTGTAATGTTCTGTGTGCTTTATCGTTAAAATTCTGGTCTTTTTCTTGCAGCATTGGTGGTTCGTTTCCTCACTAAGCGGTTTATCGGCGACTACGAGAGAAACGTTGG[T/G]AAGTTTGTCATCTTTCTAACAAGACAACCGATTTAGGAATCATTAAACCCATTTCTGCTGTTGTCAAATATATTAAACTATGCGCTTTCGCTTTACAGGCAACCTGTACTCCAGAGAGGTGCAGATAGACGGAGAACAAGTGGCCATTCAAGTTCAAGACACTCCTGGAGTTCAAGTGAGTACATATGAGCCATGCAGGAATACACTTGTTTTTTATGAGACATGTAACCGTTATAAGCGCTCGTAGAGCATCTTTCATTCATTCCCACGCTGCTACTTCACGGGTGAGAAGTGTAGAAAGAGCGCATACCTTCACCTATTGTCTTTCAGCGCTTCTTTTGTGTTTATCCGGGTTTCTGCTTAACACTTGGGGTTAATTGGCCAGCGGGGAGCCTGCTGTTGCACTCCTATATGGGGGAAGCTCGTTCATGTACAGCAAAGTCTGCTTAATTCTGCGATTTGTATCAAAGAACTGGACACGAACGATTAAACTGAACTGA
Associated Phenotype:
Not determined