ZMP
im:7149048
Ensembl ID:
ZFIN ID:
Human Orthologue:
FAM38A
Human Description:
family with sequence similarity 38, member A [Source:HGNC Symbol;Acc:28993]
Mouse Orthologue:
Fam38a
Mouse Description:
family with sequence similarity 38, member A Gene [Source:MGI Symbol;Acc:MGI:3603204]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12608 | Essential Splice Site | Available for shipment | Available now |
sa17785 | Essential Splice Site | Available for shipment | Available now |
sa10147 | Essential Splice Site | Available for shipment | Available now |
sa21090 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12608
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 |
---|---|---|---|---|---|
ENSDART00000108646 | Essential Splice Site | 390 | 2538 | 9 | 51 |
Genomic Location (Zv9):
Chromosome 7 (position 56657533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55092859 |
GRCz11 | 7 | 55394270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTCAGATTGTGGGAGGCAAGGAGACAAAGCAGTGAAGAYGACACTAAG[G/A]TAAAGAATAAAACTTGACATTTTACATTTAYATATTATGGAACCTTAGAG
Long Flanking Sequence:
GTAATGTCTAAAGTGATTGCAAAACAGGTAATTTTACTAACTTTTTTTGCAAGATTATAAGGCTGAACCACATGAAATGCCATCAGTCTACAGAGATTTCCTAAAATTATTCTGCTGTAGAATTCTGGTAATTCTTGTGTTAGAAAAGGACAATAAAATAAGCATTAAAATTATGCATATCAACTGTGCATTTTATTCTCAAGCAATACATTGAATTTTAATACATTTATTTAGCTTACCTATTCCTTTGAGAGCCCTTTGTAAGGTCAAAAATCCAACATTTGTACAATCGTAAGCCAGTCAATCACATTGTTTGTGTATAATAAATTAGTTTGGGCTAGTGTCTGATTCACACAGTATATACACTGATGCGTAATGTCTTTATGTTTGTCTAGGCCCGTGAGGGTGAAGCTGTGAAAACAGTGCAGGGTGAAGCTGGAGAAGAAGTAGAGCTCAGATTGTGGGAGGCAAGGAGACAAAGCAGTGAAGATGACACTAAG[G/A]TAAAGAATAAAACTTGACATTTTACATTTATATATTATGGAACCTTAGAGAAAAAAATGTCTTTTGGGTTTTGAGGGGGTACAGAAGCACATATGCATGTCTGATGAAATATTTAAGGAGGTTTTATTAGTCTCTATGTTGTCATTGCTGTATCCACATGCTGTAATTAAAAAGTATTACATTTTAGTTGCTTTATGTGCATGCTGATGCCTCTATTATGATATATTAAATAATTTTATTAGGATCTCTTATGAAAAGTCTATTCAATATTTTAAAAAATAGAGCAAAAGCTTTTCTCCTTCTGTAACCGTTCATTCAAGGACTCAAGCTTCAAACAGCTATTTCACACTGCCTGAAAGATAAAATCTGTAAATGCAAAATAGGGGACGCCACTGGTAAACATTCCCTGCCTCTGGCATACAGCACCAAATGCACACATTTGTATCAGTATTTTAAAACCTGGCATCAGAAAAAGTATCACCATTGCATGTTTGTGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17785
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108646 | Essential Splice Site | 1065 | 2538 | 22 | 51 |
Genomic Location (Zv9):
Chromosome 7 (position 56631928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55067254 |
GRCz11 | 7 | 55368665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATAYCAGTATGTTCTGTGTGTGGGGATTCCTCCTGCCCTCTGTAYAGG[T/A]AAGTCAAACACTATAATYAATRMACTAGTTGTTGTTGTTGACATTATTCA
Long Flanking Sequence:
ACTTAATGTTCAATCTACCTAAGTTTGTTACATTAACTTAATTGGTTTGTGTTGGGAAAACATGAATGAATTGTGTGGAACCCTGCATTATTTCCCATGTGATCTATAGTGTTACCATCAGCTAGATGCAATGCTTTAAATATAAATTGCCTGGGAAGGTTTCCAAATTATCTTTTTTTTTTTTTTTTGAGCATGTTTTGAAGTTGATAATCAAAAGCACTTCCCAACATTGGTTTCTCAAATGTTAAATCTAATGATCATTTGTGGCTAATGATCATTTGGTCTTGCCTCTAGATCTGCTTTCTAATGACCGTGAATGTTATCGGTCAGCGCATGAATTTCCTGGTTATTATCCACGGCTGTTGGTTGGTGGCCATTATGGTGCGGCGGCGCAGAGCAAATATAGCCACGATTTGGTCAAAGTACTGCCTGTTTCTGGTTGTCTTCATGATATACCAGTATGTTCTGTGTGTGGGGATTCCTCCTGCCCTCTGTATAGG[T/A]AAGTCAAACACTATAATCAATGCACTAGTTGTTGTTGTTGACATTATTCAAGTCATTTGTTTTCACAACGTTATTTGTAGCATTAAAGAACACATTTTAATTACATTTAATGTACATTTATTTGTAAAAAAAATTTTATTTGTAAAACATTTTTACATGCTGCAAAAACCTTTTTCTAGTTTTCTTTCTAGTCCAAATGTAAAAAAAAAAAAAAACTTAAATCAAGAAGTATTTTCTAGACAAGTAAAATATTGTTTTGCTTTTAGAAATAATAAGTCAAAATTAACTGTTTTTTTTTTCCTTAAACAAGCAAAATAATCTGCTAATGTTATACGTATTATAATAATCTTATTTCAAACATAAAACACGGTTGTTTTATGTATCCCATTGGTAGATTAATTAGCTTTTTTTAATGGAAAAACAAACTTAATTTTGAGATTATTTCTGAAAACAAAATAAAATTTACTTGTCCATATAAAAAGCTTCTTTATGTAGGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10147
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108646 | Essential Splice Site | 1152 | 2538 | 24 | 51 |
Genomic Location (Zv9):
Chromosome 7 (position 56630207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55065533 |
GRCz11 | 7 | 55366944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGGAGAACATGCTTTTCAAWCCTGCCCCAAACTTCATCAACTGCAGG[T/A]ACGTACATCACRGTATTTGTACATGATGTAAGTTTCATTATCCCCACAGT
Long Flanking Sequence:
AAACATTCTTTGTTAATGATTCATTTTCCATTACTAATTTAAGTATTGCATTATTTACGAACCAGTTATTTAAAAATAATTGGTGTTTTTTTTTAAGATCATTCAGAATACGTAAGTAAATTATTAATTAACTATTCAAATTAACATTTATATAACTTATTATTCAGGCATATACTAATAGTTTCTTTGCATGTTAATAAATGCTTTTATAACTCAACTTCCTCCAGTTTTGTGACCTAATCTAAAGTGAGGGCTATTCATGCTTTGTAAATCTGCAATGATGACTGTCATCACACTTAAATTCTGAAACCTTGCCTAAATTTACAAACTGATCTTTTGCAGCGGACTTCCTTTTGCTGATGTGTGCCTCTCAGCAGTGGACGGTGTTTGACAATGAGAAAAAGGAAGAGTGGATGGTCATGGGAGGAGAAAACCGAGACAATCCAGACCCCATGGAGAACATGCTTTTCAATCCTGCCCCAAACTTCATCAACTGCAGG[T/A]ACGTACATCACGGTATTTGTACATGATGTAAGTTTCATTATCCCCACAGTAAATTCCTCTGAGTAAAATTTACTCAGTTTAAATAGTATTTGGTCCCTCTCTAAATTGAGTTTAAGTTATTCAAGTTTATTAGACAATGAAAGGAATAATTAGGTGATGATTAAGCATTGATATTGAACACCTGCTGTTAATAAACAGAAACACACAAGAGAAACACATAAGTCACTTCAGTCACAGCCTTAGATGAAATCAGCTGCAATATAATACATTTATTCTTTCAAAATCTCAGCAGAGGATCATTAAGCAACTCTACAAACAGCAGCTTTACTGATTACTAACCTTTTTGCCCTTGTTTAAAGAGGGACCAAATACTCTGTGAAGTAAGTCAATTTTACTCAGAGGAATTTGCTGTGTACATGCGTACCCCTGCAGCCTAACCTTTCTAAACTCAAATTCTTGAAATGTCTGAAGAAAAAATCAAAATAAGCAGCTCAGCTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21090
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108646 | Nonsense | 2134 | 2538 | 44 | 51 |
Genomic Location (Zv9):
Chromosome 7 (position 56603601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 55038927 |
GRCz11 | 7 | 55340338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTGTGTTTCTCCATAGATTCCGTCTGGTTCCATTTTTAGTGGAGCTT[C/T]GAGCTGTGATGGACTGGGTTTGGACAGACACCACACTCTCTCTCTCTAAC
Long Flanking Sequence:
AGTTCAGCACCATGATCATCGATCGAGCATTATACCTGCGGAAGAGCATCTTGGGAAAGCTCATCTTCCAGGTTATCCTGGTTTTTGGCATCCACCTTTGGATGTTTTTTATCCTTCCTGCTGTCACTGAAAGGTAAGAAAGACTCCAGGAGTGCATTTATTTATTATTATTATTTTTTTTTCAAAGAGTGAGTCATCTCCTTTTTTTTCACAGGATGTTCAATCATAACTCGGTGGCTCAGCTCTGGTATTTTTTCAAGTGCATCTACTTCACTTTGTCAGCGTATCAGATCCGCTGTGGATACCCTACAAGAATCCTTGGAAACTTCCTCACTAAAAAATTCAATCATCTTAACCTGTTCCTCTTCCAAGGGTGAGCACTTCTTGTCTCTTAATGTTCATCTTATTTTTTTTAAATACGATTGTTTGATAGCCACTATTTGTTCATTTACTGTGTGTTTCTCCATAGATTCCGTCTGGTTCCATTTTTAGTGGAGCTT[C/T]GAGCTGTGATGGACTGGGTTTGGACAGACACCACACTCTCTCTCTCTAACTGGATGTGTGTGGAGGACATCTATGCTAACATCTTCATCATCAAGTGTAGCCGGGAAACAGAAAAAGTAGGTCTTTAGCTTGTTTTTCAATTATACTTCTAAATAATAAATAAAACTGTTTATAATTTTTCATTCAGATTAAATTGAACTGTTGTGATATTTTACACACACCAATATACAGAGTTGGGTGTAATGTGTTCCACAGTAACGCGTTACTATATTCTAATGACATTTTTGGGGAACGCAGTAATGTATTGAATTACATTTTAAATTTGTGTAATTTGATTACAGTTACTAAAGTTAATGTAATTGCATTACTTATGTTACTAATATAGTTTTTAGAAGGAAAAATACTTCTTTCAAATCACGTTTTCTGCTGCAACGTCAGTTAATAAGCATGTGCTTTTAAATTCCTGGAGAACGCGAGCTGAAATGGCTGCTGACGAGAGT
Associated Phenotype:
Not determined