ZMP
insm1a
Ensembl ID:
ZFIN ID:
Description:
insulinoma-associated 1a [Source:RefSeq peptide;Acc:NP_991207]
Human Orthologue:
INSM1
Human Description:
insulinoma-associated 1 [Source:HGNC Symbol;Acc:6090]
Mouse Orthologue:
Insm1
Mouse Description:
insulinoma-associated 1 Gene [Source:MGI Symbol;Acc:MGI:1859980]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa195 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa43534 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa195
Status:
Confirmed mutation in F2 line
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124040 | Nonsense | 141 | 383 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 48788645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 48677291 |
GRCz11 | 20 | 48484863 |
KASP Assay ID:
554-0148.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAGAGCGCAAAGGCAAACCGGCATCCAAGAAAGCCAAAGCCATGCGG[A/T]AGCTGCAGTTCGAGGATGAGATGACCACCTCTCCAGTGCTCGGACTGAAG
Long Flanking Sequence:
AGATCACCGCGCGCGTCCAAATATAGTACCAGGTGTGCCTCTGATTTCAACCCGACTGAAGTGCCTTTCAGCTGGCGAAGATGCCCAGAGGATTTTTAGTCAAGCGAAATAAGAAAGCGACACCTGTTTCGTACCGGGTCCGCTCGGAGGAGGACGAGCAGGGCGCGTTTGTCGCGCAGGATGTTCCGTGCGCGCGCCGCCCGGTGTCACCCGTGCAGTTCGGGAACCCCGAGACAGTCTACCGGGCTATGTACAGCCCGACGCGTCCCGTCAGCAGAGAGCACGAGAGGGCGTGTTTGGAGCGGCGCTTTAATCTCGGCTCGCCCATCTCAGCGGAGTCTTTCCCGGCGGCGCCAAACTGCTCCGACCAAGCGCCGGTGGATCTTAAAATCGGCACCAGCAACAGCAACCGAACCGGCACCACAGTAACCACCAAAAGACCCGCGTCCGACACAGAGCGCAAAGGCAAACCGGCATCCAAGAAAGCCAAAGCCATGCGG[A/T]AGCTGCAGTTCGAGGATGAGATGACCACCTCTCCAGTGCTCGGACTGAAGATCAAAGAAGGTCCGGTGGAGCAGAAGCCCAGATCGCAGTGCGCAAGCGGAGACAAGCCGCTCGGAGAGTTCGTCTGTCAGCTGTGCAGAGAGGCATACGCGGACCCCTTCTCTCTAGCCCAGCACAAATGCTCCAGGATCGTCAGGATCGAGTACAGATGTCCCGAATGCGACAAGCTCTTCAGCTGCCCGGCGAACCTCGCCTCGCACCGGCGGTGGCACAAACCCAAGCAGAGCGCGGAAAGCAATAAAACACCCGCGCCCGAGAAAGAGGAGACTTCCAGCGACAGGGACACTCCTAGTCCCGGACTTTCCGAAAGCGGCTCTGAGGACGGCCTGTACGACTGCCAGCACTGCGGGAAGAAGTTCAAGCGTCAGGCGTACCTGAAGAAGCATGTGACTGCGCACCACGACGCGCCAGAAAAACCCCAAAGCCACGCGCCTCTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43534
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 |
---|---|---|---|---|---|
ENSDART00000124040 | Nonsense | 143 | 383 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 48788639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 48677285 |
GRCz11 | 20 | 48484857 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGCAAAGGCAAACCGGCATCCAAGAAAGCCAAAGCCATGCGGAAGCTG[C/T]AGTTCGAGGATGAGATGACCACCTCTCCAGTGCTCGGACTGAAGATCAAA
Long Flanking Sequence:
CCGCGCGCGTCCAAATATAGTACCAGGTGTGCCTCTGATTTCAACCCGACTGAAGTGCCTTTCAGCTGGCGAAGATGCCCAGAGGATTTTTAGTCAAGCGAAATAAGAAAGCGACACCTGTTTCGTACCGGGTCCGCTCGGAGGAGGACGAGCAGGGCGCGTTTGTCGCGCAGGATGTTCCGTGCGCGCGCCGCCCGGTGTCACCCGTGCAGTTCGGGAACCCCGAGACAGTCTACCGGGCTATGTACAGCCCGACGCGTCCCGTCAGCAGAGAGCACGAGAGGGCGTGTTTGGAGCGGCGCTTTAATCTCGGCTCGCCCATCTCAGCGGAGTCTTTCCCGGCGGCGCCAAACTGCTCCGACCAAGCGCCGGTGGATCTTAAAATCGGCACCAGCAACAGCAACCGAACCGGCACCACAGTAACCACCAAAAGACCCGCGTCCGACACAGAGCGCAAAGGCAAACCGGCATCCAAGAAAGCCAAAGCCATGCGGAAGCTG[C/T]AGTTCGAGGATGAGATGACCACCTCTCCAGTGCTCGGACTGAAGATCAAAGAAGGTCCGGTGGAGCAGAAGCCCAGATCGCAGTGCGCAAGCGGAGACAAGCCGCTCGGAGAGTTCGTCTGTCAGCTGTGCAGAGAGGCATACGCGGACCCCTTCTCTCTAGCCCAGCACAAATGCTCCAGGATCGTCAGGATCGAGTACAGATGTCCCGAATGCGACAAGCTCTTCAGCTGCCCGGCGAACCTCGCCTCGCACCGGCGGTGGCACAAACCCAAGCAGAGCGCGGAAAGCAATAAAACACCCGCGCCCGAGAAAGAGGAGACTTCCAGCGACAGGGACACTCCTAGTCCCGGACTTTCCGAAAGCGGCTCTGAGGACGGCCTGTACGACTGCCAGCACTGCGGGAAGAAGTTCAAGCGTCAGGCGTACCTGAAGAAGCATGTGACTGCGCACCACGACGCGCCAGAAAAACCCCAAAGCCACGCGCCTCTGAATCTCAGC
Associated Phenotype:
Not determined