ZMP
fam135a
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC566435 [Source:RefSeq peptide;Acc:NP_001139066]
Human Orthologue:
FAM135A
Human Description:
family with sequence similarity 135, member A [Source:HGNC Symbol;Acc:21084]
Mouse Orthologue:
Fam135a
Mouse Description:
family with sequence similarity 135, member A Gene [Source:MGI Symbol;Acc:MGI:1915437]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11265 | Essential Splice Site | Available for shipment | Available now |
sa14063 | Essential Splice Site | Available for shipment | Available now |
sa16461 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11265
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083641 | Essential Splice Site | 181 | 1338 | 5 | 20 |
ENSDART00000131434 | Essential Splice Site | 181 | 1338 | 7 | 22 |
ENSDART00000147971 | None | None | 160 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 39762036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 39076137 |
GRCz11 | 13 | 39202027 |
KASP Assay ID:
2260-6827.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCCACAATCCATGCTTCACTGGTGGCTCTGCATCAGCCTCTAATAAGG[T/G]CAGTGGTGCACTGAGAACTGGACCGACAGATTGTACTAGTCATTTTGAAT
Long Flanking Sequence:
TGTATTCAAAGTCATGATGCTGCTCGATGCAAAGAAGGTGAGTGAAATCTATAATTTAACTCATGGGTTAAGTAAATCTGCCTCTGCATCACTAGTTATGATGATTAGGGTGTTTTCCTTCTGCAGGTAGAAGAGTCTTTAAATGAAGTTGACTTTCAGCTGTGTTTGGACCTGTTCTTCACTGATGGAGACTACTCGTATGTAGAAAATTAGCTATTTTCAGATTGTACTTTTGCTCATATTTTGGGTTTTGTATTTAAAATAACAAAAATCATTACTTAAAACCAGTTGTTTCAGATTTAAGAGTGTTTTTGTCTGTATTCAGGCCTGAGGAGCCCAGTTCTCTGCAGAGCATCAGCAGCCGTACGCTGCGTTTGCACTTTAGCCTCCACAGAGGCATCCACCACCACGTCAACGTCATGTTTGACTACTTCCACCTGTCTGTCATCTCTGCCACAATCCATGCTTCACTGGTGGCTCTGCATCAGCCTCTAATAAGG[T/G]CAGTGGTGCACTGAGAACTGGACCGACAGATTGTACTAGTCATTTTGAATGTCATAAGTGATGACAGTACACTGACGGGTAAAATGACTTTAAACCAACAAAAAATAGCTAGGGAATTTTAATTCTGTTAACTTTTTAATTCTGTGAAAACAGGATCAAGATATACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCACTAATGCAAATGTCGAATCAGCCAATCACATGGCAGCAACTCAATGCATTTAGACATATGAACATGGTCAAGACGATCTGCTGCAGTTCAAACCTGGGGTTCAAACCCCAGGGCTTCCGGTTAATTGTCATCTCATACAAAATTGCAGAGTTTAAGATTTGATTTGTTTAAAAACCAGCGATCTTCATTGCCTGGCTAACATACGATATAAATTGGGTATCAGGCCAAACTGATCAGGTCTATTAGTCTCGATTTCTGCTGCAGAATTCAGATGGTAGGGTCAGAATTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14063
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083641 | Essential Splice Site | 181 | 1338 | 5 | 20 |
ENSDART00000131434 | Essential Splice Site | 181 | 1338 | 7 | 22 |
ENSDART00000147971 | None | None | 160 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 39762036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 39076137 |
GRCz11 | 13 | 39202027 |
KASP Assay ID:
2260-6827.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCCACAATCCATGCTTCACTGGTGGCTCTGCATCAGCCTCTAATAAGG[T/G]CAGTGGTGCACTGAGAACTGGACCGACAGATTGTACTAGTCATTTTGAAT
Long Flanking Sequence:
TGTATTCAAAGTCATGATGCTGCTCGATGCAAAGAAGGTGAGTGAAATCTATAATTTAACTCATGGGTTAAGTAAATCTGCCTCTGCATCACTAGTTATGATGATTAGGGTGTTTTCCTTCTGCAGGTAGAAGAGTCTTTAAATGAAGTTGACTTTCAGCTGTGTTTGGACCTGTTCTTCACTGATGGAGACTACTCGTATGTAGAAAATTAGCTATTTTCAGATTGTACTTTTGCTCATATTTTGGGTTTTGTATTTAAAATAACAAAAATCATTACTTAAAACCAGTTGTTTCAGATTTAAGAGTGTTTTTGTCTGTATTCAGGCCTGAGGAGCCCAGTTCTCTGCAGAGCATCAGCAGCCGTACGCTGCGTTTGCACTTTAGCCTCCACAGAGGCATCCACCACCACGTCAACGTCATGTTTGACTACTTCCACCTGTCTGTCATCTCTGCCACAATCCATGCTTCACTGGTGGCTCTGCATCAGCCTCTAATAAGG[T/G]CAGTGGTGCACTGAGAACTGGACCGACAGATTGTACTAGTCATTTTGAATGTCATAAGTGATGACAGTACACTGACGGGTAAAATGACTTTAAACCAACAAAAAATAGCTAGGGAATTTTAATTCTGTTAACTTTTTAATTCTGTGAAAACAGGATCAAGATATACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCACTAATGCAAATGTCGAATCAGCCAATCACATGGCAGCAACTCAATGCATTTAGACATATGAACATGGTCAAGACGATCTGCTGCAGTTCAAACCTGGGGTTCAAACCCCAGGGCTTCCGGTTAATTGTCATCTCATACAAAATTGCAGAGTTTAAGATTTGATTTGTTTAAAAACCAGCGATCTTCATTGCCTGGCTAACATACGATATAAATTGGGTATCAGGCCAAACTGATCAGGTCTATTAGTCTCGATTTCTGCTGCAGAATTCAGATGGTAGGGTCAGAATTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16461
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083641 | Essential Splice Site | 301 | 1338 | 8 | 20 |
ENSDART00000131434 | Essential Splice Site | 301 | 1338 | 10 | 22 |
ENSDART00000147971 | None | None | 160 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 39768393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 39082494 |
GRCz11 | 13 | 39208384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGTTCTCAGAAGACCTTACCCTCCAGGCCAAAGGCACGTCTAYATAGG[T/C]AYGTCCYTCCAAAACCGACCCTAAGCTCCACACGCCTCTTGCCTTTCATT
Long Flanking Sequence:
TCACTGAATTAATAACTTTCTTGACTCACTCACTAAACACTTAATTTCACTAATGCACTAATTTAGTAAAAATATATAGTATATAAATAAACATTCATGATTTAAAAGATCCTTAATGTCTCTAATAAGTCTTAATCTCTCACATGTCTGAAATTATATGCCTCTTTCTATTTATATGTATGTTTCAGCATGCAAATCCTTTTATCTCCTTATTTCTTTTACCTACTGACCTCTTTAATATGGGTTCCCCTCTCAGACTTTCACTATAATCCTTTACGCACTTAATAAAAACTAAACCACTCACCCCTTACTTTTTCTGACCAAGTGCATCGCTTGACTGAACTTAAGCATTCATTAAACTTAAGCAAAAAGGGGAGAGTGAAAATTTTAAACGTGCCTATATGTGCAATCCCACCACTAGCCAAGCCCAGCATGCAGGTCCTTTATGAACGAGTTCTCAGAAGACCTTACCCTCCAGGCCAAAGGCACGTCTACATAGG[T/C]ACGTCCCTCCAAAACCGACCCTAAGCTCCACACGCCTCTTGCCTTTCATTTGTGTTCACTTCTTTCTTCTATTGCCCCTAACTTGGACATTGGCCAATGGCAAGTGTCCTTGAGTGAGGGAGCTCTTAGTTCAGTTCAGTCCTTCTTCTGTCCTTTAGTAGTATCTCAGGCTGACTTGGGATCAGTTTTACTGCTTGAACGTAAGCTGTCCTCTGATTCCTACTTCCTGTGCTGTTCCTTCTAGCTTCCTCTCACGTGTTGTCATTTACAGGCTCTTCAGACTGACCCTTCTCTTTTATTCACTCCATACTAATGCTGTGTAGGAACATCATTTTCATGTTAGTGGTTTGTTTTGTTTTGTTTTTTCCTTTTGTTTCTTTAGAGGAACTTGATGTGGAGGTCCGACTTCATGAGCTTTGTGAACAAGTCAAGGTATGGAATGAATTTAAGACTAAAGTTAGACCGTGCATTGGTATTTATTTTTATATGTCTATATTGCA
Associated Phenotype:
Not determined