ZMP
si:dkey-13f9.5
Ensembl ID:
ZFIN ID:
Human Orthologue:
FAM114A2
Human Description:
family with sequence similarity 114, member A2 [Source:HGNC Symbol;Acc:1333]
Mouse Orthologue:
Fam114a2
Mouse Description:
family with sequence similarity 114, member A2 Gene [Source:MGI Symbol;Acc:MGI:1917629]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37359 | Nonsense | Available for shipment | Available now |
sa24007 | Nonsense | Available for shipment | Available now |
sa39342 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12732 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37359
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 |
---|---|---|---|---|---|
ENSDART00000110220 | Nonsense | 193 | 520 | 5 | 13 |
ENSDART00000133585 | Nonsense | 193 | 572 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 36756226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37745575 |
GRCz11 | 21 | 37430762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTTTGATGACTAGAGTAAAACAGTAATAAGCGGTGGCCTTGATGCAT[T/A]GGAGTTTATCGGGAAGAAAACCATGGATGTGATTGCAGAGGGAGACCCCG
Long Flanking Sequence:
GCTAAGCAGTTAATTAATTATTTTGGTTATATTTTATTTTAAAGTACAATTCTTGCTATTATTAAACCATTAACTTTGGCTTTTGCCTCATTAAACTCCTAATTTGCTGTTTATCAATAGTTATTAAGATAATAGTTGGATTTAGTTACTGGCTTAGGGATGCAGAATATGTACTTTATGTACTAAAAGGCCAATATCATCATCATAATAATAGGCATGCCAATAAGGAACTAGTTACACTGAAGTGTTATCATTATTTATGTATTTATTATTTAATAATTTTAAAATAATTTTTCCACGGCTTGGTATGCTGGTTGAACATTTCTGAATTTTCATTGCCAATTTTAGCCAATGGTTATTCAGTTAAAAGCCAATGGTCGTAATAGTTTGTTTTGGGCCAATTTCCACATTTTCTTTGTTTTATTGTATGTATGTTTTTACACTTCTTCTCATGTTTGATGACTAGAGTAAAACAGTAATAAGCGGTGGCCTTGATGCAT[T/A]GGAGTTTATCGGGAAGAAAACCATGGATGTGATTGCAGAGGGAGACCCCGGCTTTAAGAAAACCAAAGGACTGATGAACAGAAACTCCACACTATCACAGGTACAGGAGAGAATAAGATTAAAGAATATATTCATAGCAACTTCAGCTGCCCTCCTGACACAAATATATTACTCAATCCTATCTGATTTTGTTTGCATTAAACTGATCTGATTTTTGTTTCCTTAAAGGTCTTGAGAGAAGCCAAAGAATGCGAGGAGCAGCAAAAAGCTGAAAATGCCACTTCAGAACCAAACAAAAAGGCTCATTATGGGATGCTGTTCGACGAGTTTCAAGGCTTGTCTCATTTGGAGGCTTTGGAGATCCTGTCTAGAGAGAGCGAAGCCAAGGTCAGTTCTTGACTGATTTAACACACTGAGATAGAATATGAAATGGTGAAAGATTTAAACATGTTGTGATTTGGTGCAGGTGAAATCTGTTCTGACAACGCTGTCTGGCGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24007
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110220 | Nonsense | 249 | 520 | 6 | 13 |
ENSDART00000133585 | Nonsense | 249 | 572 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 36755931)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37745280 |
GRCz11 | 21 | 37430467 |
KASP Assay ID:
2261-5936.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAATGCGAGGAGCAGCAAAAAGCTGAAAATGCCACTTCAGAACCAAAC[A/T]AAAAGGCTCATTATGGGATGCTGTTCGACGAGTTTCAAGGCTTGTCTCAT
Long Flanking Sequence:
CCACGGCTTGGTATGCTGGTTGAACATTTCTGAATTTTCATTGCCAATTTTAGCCAATGGTTATTCAGTTAAAAGCCAATGGTCGTAATAGTTTGTTTTGGGCCAATTTCCACATTTTCTTTGTTTTATTGTATGTATGTTTTTACACTTCTTCTCATGTTTGATGACTAGAGTAAAACAGTAATAAGCGGTGGCCTTGATGCATTGGAGTTTATCGGGAAGAAAACCATGGATGTGATTGCAGAGGGAGACCCCGGCTTTAAGAAAACCAAAGGACTGATGAACAGAAACTCCACACTATCACAGGTACAGGAGAGAATAAGATTAAAGAATATATTCATAGCAACTTCAGCTGCCCTCCTGACACAAATATATTACTCAATCCTATCTGATTTTGTTTGCATTAAACTGATCTGATTTTTGTTTCCTTAAAGGTCTTGAGAGAAGCCAAAGAATGCGAGGAGCAGCAAAAAGCTGAAAATGCCACTTCAGAACCAAAC[A/T]AAAAGGCTCATTATGGGATGCTGTTCGACGAGTTTCAAGGCTTGTCTCATTTGGAGGCTTTGGAGATCCTGTCTAGAGAGAGCGAAGCCAAGGTCAGTTCTTGACTGATTTAACACACTGAGATAGAATATGAAATGGTGAAAGATTTAAACATGTTGTGATTTGGTGCAGGTGAAATCTGTTCTGACAACGCTGTCTGGCGAGGAGCTGACAAAACTTAGAGAAGATCTGCAGAATATTAAAGAGCCTTTTTCACTCATGGAGTTTGACGATGAGCTGGAGGATGATACGAAATGTAAGAAACTACAATTAATACAAGGCTAAAATTTACAAAATTAAACATTAAATTCTTAGTTCAAGCACAAATTAAGATATTTTAAATCAAATCTTAGAAATGCATGTCCCTTAATTGAAAGTCTATTCTCCTAAAACTCTTCAAAATGTTTATAAAGAGATTTTTAAAACTCCATATGGATTGAGCAGTTTAATCTAAGCCTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39342
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110220 | Essential Splice Site | 349 | 520 | 8 | 13 |
ENSDART00000133585 | Essential Splice Site | 349 | 572 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 36751602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37740951 |
GRCz11 | 21 | 37426138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCTTAAAGGACTACAGATTTCCACATCAGCAGACAAACTCAGCAAG[G/A]TTTCACTTGAAGATTAGTTACAAATAAATGCTCAGGTATTTTGCTTGTGA
Long Flanking Sequence:
AAATATATTCAATATATTTTATCGGATTGTATTGTATTGTATTTTATTGTGACAAGATGTTCAGTTTACACCCCTACTCAGTTTTAGTCATAGAACTCATACATGCTTTCTCAATGTGTGAGTACCAACGAGGTTTATTCTTGCATCACATGACAGATGTTTGAGCTTCTGCAAGGACCAATAAGCTTTGCTGATGTGTGTCAATATGTAAATAAAACATCCAATGAAACACATTCCTTATGTAGAGAAACAATTTGAATCTAATCAGTTTGGAAGCATGAGAGTTTCAGAGTGAAAAGACTTTAAAAGGACGGACCGAAATTTCTCCCATTTTATTAAAAATATCTTCCATGTGCTCCAAATGATGAACAAAAGTCACAGGTTTGCTCATATTATTATTTTTTTAATCCTCAGGTGATGATGGAGAGGACTTTGTGAAGGAACTAACAGATGTTCTTAAAGGACTACAGATTTCCACATCAGCAGACAAACTCAGCAAG[G/A]TTTCACTTGAAGATTAGTTACAAATAAATGCTCAGGTATTTTGCTTGTGAGATTATTTACACTTTCTTATATTAACTTAGGCCAGAAAAAATGCATTCAACCATATCACAAACATGAAACTACGAAGTGAAAACATTGAGAAAGAAAAAGAGGACAAAGAAGAAGGAGAAGGAGAGAAAGAAGAAAGACAGAAGGAGAAGAACACAGAAACCGCAGAGACCGAATACACAGTTGAGGTCTGCATTAACATTATTTAGCCGTAAATAATGTAAATGTTATACACATGCACATATTTTACATTAAATAATCTGTTTTTATTAAGTTTTCATTGCATTGACTAAAGCTCTTTTTATAGGATGCCCATTTGTCTGCCATCACGAGTTTGGCCGAGTTCACAGCGAGGTCCATCGAGCAGTTCCACAAAACAGCTGAAATGTTGCTTTACTCTAACACTGAAGGGGCCGCGGCCCCAGAACAAGCAAAAATCCTATCACAGTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12732
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 |
---|---|---|---|---|---|
ENSDART00000110220 | Nonsense | 454 | 520 | 11 | 13 |
ENSDART00000133585 | Nonsense | 454 | 572 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 36751013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37740362 |
GRCz11 | 21 | 37425549 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAATTWAAAKCAYSTGTGTTTCTCTTGCAGAGTCACCATTGTTATTTG[T/A]AAGGAGGTCTCACTGCTATCCAAAAAGTTTACAWCATGTTTGACTACCAT
Long Flanking Sequence:
AAATGCATTCAACCATATCACAAACATGAAACTACGAAGTGAAAACATTGAGAAAGAAAAAGAGGACAAAGAAGAAGGAGAAGGAGAGAAAGAAGAAAGACAGAAGGAGAAGAACACAGAAACCGCAGAGACCGAATACACAGTTGAGGTCTGCATTAACATTATTTAGCCGTAAATAATGTAAATGTTATACACATGCACATATTTTACATTAAATAATCTGTTTTTATTAAGTTTTCATTGCATTGACTAAAGCTCTTTTTATAGGATGCCCATTTGTCTGCCATCACGAGTTTGGCCGAGTTCACAGCGAGGTCCATCGAGCAGTTCCACAAAACAGCTGAAATGTTGCTTTACTCTAACACTGAAGGGGCCGCGGCCCCAGAACAAGCAAAAATCCTATCACAGTGAGTTATCCTGTTGAAGAAACTGCCTAACATTGTCCTTTTGAGAAATTTAAATCACCTGTGTTTCTCTTGCAGAGTCACCATTGTTATTTG[T/A]AAGGAGGTCTCACTGCTATCCAAAAAGTTTACATCATGTTTGACTACCATTGGGGTAGGATGCTTATCTTGCTTAAAAGACAGTCTGGAGATCTTTAATATTGTTTGTAAACATTAACTCTTGTGCATCTGTGTGAACATTTTACCTTTATCCATTTTATTGTTAGATTTGTTAATGCAGACAGCTCACATTTTGGCAAAAAAGGTTGCATTTTTATTGAAATTTACCTTCATAAATATTTTTCACTCGGTACAAAAATGTCCCAATTGAAACCCATTAAATCGGCAATATTTCATCACAGTGGCATATAAACAAAAATCAAGCCATTTTTGTTAACAGGCATTCATTTGTTTGGCTTCAACGATTTTACAAATGGTAAAATTTGGAATATTTTGTCAGCTTTGGTCTGTGGATTTGATTTTTACTGTTTCGGGCCAAATTGCAGGCCAAATTAAATATCTTATGTAGTTATGAATAATTAATTTTGCTGTTATGAAGAT
Associated Phenotype:
Not determined