ZMP
zgc:110179
Ensembl ID:
ZFIN ID:
Description:
Ras-like protein family member 11A-like [Source:UniProtKB/Swiss-Prot;Acc:A1DZY4]
Human Orthologue:
RASL11A
Human Description:
RAS-like, family 11, member A [Source:HGNC Symbol;Acc:23802]
Mouse Orthologue:
Rasl11a
Mouse Description:
RAS-like, family 11, member A Gene [Source:MGI Symbol;Acc:MGI:1916145]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41019 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41019
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 |
---|---|---|---|---|---|
ENSDART00000067647 | Nonsense | 165 | 253 | 4 | 4 |
ENSDART00000098659 | None | 154 | 195 | 5 | 5 |
The following transcripts of ENSDARG00000046013 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 52771083)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 51040833 |
GRCz11 | 7 | 51315903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAACATCCCTGTCATCATCGTGGGAAACAAGAGCGACCTTCTGCGAGCC[C/T]GACAGGTCTCAGATCCCGAAGGGAAGGCGCTGGCGGATGAATTGGGAGGG
Long Flanking Sequence:
GTTTTTTTTTAGAATGAGCCTGGGTTGTGATTTTTAGACCTTAAAACTTCTCGGTATGCTGCTTCATGTTGCAAACAGATATTGTCTTATTATAGTTGTCTTCTTTTTATGTGTAGTCATGAACACACTTGTTTGTAGATCAGTTAGTTCGATCGTTTTCTGATGTATATTATCCCTAGTCATTTCTCCAATAGGCAACAGAATCAGAAGTACTAAAATAATCGCCAAAACTTCGAATAAGGTCAATATAAGATAAGTCGGACAGTGGACATACTGTAACAGCAGATTTCTCATTCCAGGATGATGCAGACGGCCTTTACTGTCAAGAGCAGATCAACCGTTCCATTTACTGGGCGGACGGTTATGTGCTCGTCTTCTCCATCACTGACCTCAACAGCTACCGCACCATCCAGCCTCTCTACCAACATGTGCGCCGAATCCACCCCAGCGGTAACATCCCTGTCATCATCGTGGGAAACAAGAGCGACCTTCTGCGAGCC[C/T]GACAGGTCTCAGATCCCGAAGGGAAGGCGCTGGCGGATGAATTGGGAGGGCTATACTTTGAGGCTTCGGCCAGGGAGAACCACGAGAGCGTCCAGGCAGCTTTTCTGCACTTATGTCAGGAGGTGAGCCGAGCGCTGGGAGGAGGAAACGGGGAAAAGAGAAAAGGTGGACTACACCTTGCCAGGCCAAAGAGCCCAAACATGCAGGAGTTGAAGAGAAGATTCCGGCAAGTGCTGTCATCCAAGGTCAAGTCGGCTACGGCGCTATGAGGATTTGATGAATGTGAGGATTGGGAAAGTGTTAAAGTGTTGCAGAAGTGATTGTGAAACACAAGGCAAAACAATGAGCTGTTTTAGCAAGCACTCATAGACGACAAGAGGTGAGATCACTGCTCTCTGGATGAACTCCTGGCACTAAACTTTAATGTTTTTAATGGTTTCAAGGCCATCAAGTCTGTTTTTGTTGGTTTGTTTTAGATGCTGTCAAGCAACGGTTTCCAG
Associated Phenotype:
Not determined