ZMP
si:ch1073-184j22.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to family with sequence similarity 132 [Source:UniProtKB/TrEMBL;Acc:B8JLI7]
Human Orthologue:
FAM132B
Human Description:
family with sequence similarity 132, member B [Source:HGNC Symbol;Acc:26727]
Mouse Orthologue:
Fam132b
Mouse Description:
family with sequence similarity 132, member B Gene [Source:MGI Symbol;Acc:MGI:3606476]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39756 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39756
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 |
---|---|---|---|---|---|
ENSDART00000077861 | Nonsense | 197 | 294 | 5 | 8 |
ENSDART00000139762 | Nonsense | 111 | 208 | 3 | 6 |
ENSDART00000146906 | Nonsense | 57 | 103 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 2 (position 5024247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5469975 |
GRCz11 | 2 | 5381857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTAACATCAGCAGCGGCCGCTATACGGCTCCAGTGTCTGGCTTCTAT[C/T]AGCTCTCAGCTAATCTGCTGCTAGGTATGGGTTTTTCTGGACGGCAGATT
Long Flanking Sequence:
CCATGATGACTGTAGATAATATTTGACTAGATATTCAGCTTAAAGTGACATTTAAAGGCTTAACTCGGCTAGTTAGGGTAATTAATCATTGTATAATGATGGTTTGCTCTGTAGACAATCGAAAATAAATACTGCTTAAGAGGGCTAGTGATATTGACCTTAAAATGATTGAACTAAATTAAAAGCTACTTTCATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCATTAAATATTGTAGGGAATACTGTGAAAGTTTCCTCTGTTAAATTCACCGGAGGACTAATGATTTTGACTTCAACTGTACGTTGGTTCAGCAGCAATGCTAGCTTCGGCTGACCACAGTGAAGAAGGGTTGGCAATGAAAGAGTTCGGCATATTCAATAATTCCATTTGTCTGTGTTTTCCACAGCCTTCGAACACAGAGCAGTTCCATCAGAGAGGACAGGGCTTTAACATCAGCAGCGGCCGCTATACGGCTCCAGTGTCTGGCTTCTAT[C/T]AGCTCTCAGCTAATCTGCTGCTAGGTATGGGTTTTTCTGGACGGCAGATTCTTACTTTTTTTTTCTGATTTTGAACAACTTTCTAATGCTGTGTTCACACCAGACATGGCATGCACGAATGAACCATACTATTCCTTCAGTAGGGTATCAAATTCACTTCATTCACATATGAGTTTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCTACCTTCTGTCTCCCTGTCTTTGTCTATCTATCTGTCCATCAGTCTGTCTGTCTGTCTGTCTGTCTGTCTATCTATCTATCCATCTATCTATCTATCTGTCACTGTCTACCTATCTAC
Associated Phenotype:
Not determined