ZMP
fam49ba
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC337591 [Source:RefSeq peptide;Acc:NP_956364]
Human Orthologues:
FAM49A, FAM49B
Human Descriptions:
family with sequence similarity 49, member A [Source:HGNC Symbol;Acc:25373]
family with sequence similarity 49, member B [Source:HGNC Symbol;Acc:25216]
family with sequence similarity 49, member B [Source:HGNC Symbol;Acc:25216]
Mouse Orthologues:
Fam49a, Fam49b
Mouse Descriptions:
family with sequence similarity 49, member A Gene [Source:MGI Symbol;Acc:MGI:1261783]
family with sequence similarity 49, member B Gene [Source:MGI Symbol;Acc:MGI:1923520]
family with sequence similarity 49, member B Gene [Source:MGI Symbol;Acc:MGI:1923520]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19797 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19797
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000039717 | Essential Splice Site | 238 | 325 | 8 | 11 |
ENSDART00000056621 | None | None | 256 | None | 9 |
ENSDART00000141418 | None | None | 256 | None | 8 |
ENSDART00000146452 | None | None | 208 | None | 7 |
The following transcripts of ENSDARG00000020929 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 31938026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 32236933 |
GRCz11 | 2 | 32220151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTGTCTGAGCACGATGGCAAGTGTGTGTAAAGTCATGTTAGAGACACC[G/A]TGAGTTGACTTTTTTTGTGTTTAATCATTGTTTCTTCTGGAATGGGGTGT
Long Flanking Sequence:
TTCCATTTCCATGATTAACTACTTAAGTAAAAGCTGACCAAGTAAAAGAGCATCCGTAACCTCCCTCAACTGACCCCTTTAGTTTAAATCTTAAAAAGTATGGATTTTTATCTTCTCCTCCACATTTAGATACTATAAACCCCCCATGTGTGTTCTTTCTGCAGGCAGAGGAGCATAATGAGGTCGACAACGAATTGGCCAATCGCATGTCTCTCTTCTACGCCAATGCCACGCCCATGCTGAAAACGTTAAGCGATGCCACGACTAAATTTGTATCAAAGGTAGGTGTTTGGTCAACTCTACTGAGTGTGATATCCAATACGCAGCTCTGATCACTCAAATAGGTGTTAAGTAAACAAGTCCAGATGCTCATGAATACACGCTCCTGCAACATTCTGCTCTCTATGTCTATGTGATCAGCATGCAGAACTACCTGTAGAGAACACAACAGATTGTCTGAGCACGATGGCAAGTGTGTGTAAAGTCATGTTAGAGACACC[G/A]TGAGTTGACTTTTTTTGTGTTTAATCATTGTTTCTTCTGGAATGGGGTGTGTCTTTGTTGTTCATCCTCTCTCTTTGTTTCTCTGTATGTGTGTGTGTGTGTGTGTGTGTATTGATCAGGGAGTACCGCAGTCGTTTTGCCAGTGAGGACACAGTGTTATTCTGTCTGCGTGTGATGGTGGGAGTGATCATCCTTTACGACTATGTTCATCCGGCTGGAGCATTCGTCAAATCCTCCAAAATCGATGTATGCCTTATTCTGCTTTTTGAAAATTATTTACTGGCATCAACGAACAGATTATTTGATCAAATTGTGTTTTATAGTTAGGGCTGTCAATTTAAGACAAAACATTAAAAAGATAAAACAAGATTAAGCAAGCATTTAATTTAGTCTTTTTAGATTTAATGAAAAGAAGTGTTAAAGGGCACCTATGGTGAAAAATTTACTTTTCAAGCTGCTTGGACAGACATGTGTGTATATATAGTGTATAGACTATCATA
Associated Phenotype:
Not determined