ZMP
si:ch211-261p9.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens C3orf38, chromosome 3 open reading frame 38 (C3orf38) [Source:Uni
Human Orthologue:
C3orf38
Human Description:
chromosome 3 open reading frame 38 [Source:HGNC Symbol;Acc:28384]
Mouse Orthologue:
4930453N24Rik
Mouse Description:
RIKEN cDNA 4930453N24 gene Gene [Source:MGI Symbol;Acc:MGI:1914859]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9465 | Nonsense | Available for shipment | Available now |
sa41381 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9465
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113349 | Nonsense | 135 | 320 | 6 | 8 |
ENSDART00000136493 | None | None | 89 | None | 2 |
ENSDART00000143122 | None | None | 165 | None | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 16333243)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 16310388 |
GRCz11 | 9 | 16247654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTTTTTTNAANCCAGATATCAAAGCCTGAGAGGAATACARACAATTCCTA[T/A]GAGGTTGGAGATGGTCTATCAGACCTTGCAGCATTGGGAAAACAGTTTTG
Long Flanking Sequence:
TTCTAATTACTAATTTATTTTGTCTTTGCCATGGTAACATGGTAAGACATTTTTTAACTTATTTGGCAAGATACTGGTATTCAGCTTAAAGTGCAATTTAAAGCTAGATTATTATGTTACCTGGGGAAGTTAGGTTAATTAGGCAAGTTATTGGATAACAGTGGTTTGTTCTGTAGACACTGTAGACCTTTAAATTGTTTTAATCATTCCAGCCAAACTAAAATAAGCTAAAATAACCTAAAGAAAAAAAGTCTTATAGGAAATACTGTGAAAACATATATGGTCTTTTAGGCTTCACATAGGAAATATCTATAATAGAATACAAATTTCACAGGAAGGCTAATAATTTTGACTTAAACTGTATGTAGGCTAGACACACATGCACAGACACACCTGTGTTGATTTTGATTTATAAAATGTACATTTTCTGGGTTATATTTTTGACATTGCATTTTTTTTAACCAGATATCAAAGCCTGAGAGGAATACAAACAATTCCTA[T/A]GAGGTTGGAGATGGTCTATCAGACCTTGCAGCATTGGGAAAACAGTTTTGCCAGTGGTTCTTCTGCCTTTTGAACTCTCAGAACCCCAGTCAAGGACATCCGGTGCAGGACTGGGGACCTCAACATTTCTGGGAGAATGTGAGCCTTCGGCTTCTCTTGTGCACCGGAGAGCAGCGTGTTGATGAGTTCAGTGGGGCAGAACTTGTCAGCAAGCGGCTTCAAGCTCTTGCAGAAGAAGAACGTCTATTATTCTGTCCAAACCTGGAAGGTCATGGGTTAAAGTGTATGTCCTCCCCTCATGGACTGGTATTAGTGGCCGTAGCAGGGACTATCCACCGTGACAATACCTGCCTTGGGATTTTTGAGCAAGTGTTTGGGCTCATTCGCTCACCAATGGACAATAATTTCTGGAAAATTAAGCTAGTAAATATAAAAATTGAAGCACAAAGTGCTGTTGCAGACAGACAGTTACCAGTTGTCACATATGACATGAAAGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41381
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113349 | Nonsense | 197 | 320 | 6 | 8 |
ENSDART00000136493 | None | None | 89 | None | 2 |
ENSDART00000143122 | Nonsense | 55 | 165 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 16333059)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 16310572 |
GRCz11 | 9 | 16247838 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATGTGAGCCTTCGGCTTCTCTTGTGCACCGGAGAGCAGCGTGTTGAT[G/T]AGTTCAGTGGGGCAGAACTTGTCAGCAAGCGGCTTCAAGCTCTTGCAGAA
Long Flanking Sequence:
GACCTTTAAATTGTTTTAATCATTCCAGCCAAACTAAAATAAGCTAAAATAACCTAAAGAAAAAAAGTCTTATAGGAAATACTGTGAAAACATATATGGTCTTTTAGGCTTCACATAGGAAATATCTATAATAGAATACAAATTTCACAGGAAGGCTAATAATTTTGACTTAAACTGTATGTAGGCTAGACACACATGCACAGACACACCTGTGTTGATTTTGATTTATAAAATGTACATTTTCTGGGTTATATTTTTGACATTGCATTTTTTTTAACCAGATATCAAAGCCTGAGAGGAATACAAACAATTCCTATGAGGTTGGAGATGGTCTATCAGACCTTGCAGCATTGGGAAAACAGTTTTGCCAGTGGTTCTTCTGCCTTTTGAACTCTCAGAACCCCAGTCAAGGACATCCGGTGCAGGACTGGGGACCTCAACATTTCTGGGAGAATGTGAGCCTTCGGCTTCTCTTGTGCACCGGAGAGCAGCGTGTTGAT[G/T]AGTTCAGTGGGGCAGAACTTGTCAGCAAGCGGCTTCAAGCTCTTGCAGAAGAAGAACGTCTATTATTCTGTCCAAACCTGGAAGGTCATGGGTTAAAGTGTATGTCCTCCCCTCATGGACTGGTATTAGTGGCCGTAGCAGGGACTATCCACCGTGACAATACCTGCCTTGGGATTTTTGAGCAAGTGTTTGGGCTCATTCGCTCACCAATGGACAATAATTTCTGGAAAATTAAGCTAGTAAATATAAAAATTGAAGCACAAAGTGCTGTTGCAGACAGACAGTTACCAGTTGTCACATATGACATGAAAGAATTGCTGAGTCTTTGCAATTAAGAGTCAGAAATCTACAATTAGTCCATTATGTAAGATTTGATTTTCAGAAACAAGGATGATTTACTGTTCCATGAAAAGGGCTTTGTTGTGGGATATATATATATATATATATATATATATATATATATATATATGTGTGTGTCTATAAAACGTTTATCTAGTTAT
Associated Phenotype:
Not determined