Busch Lab

ZMP

fam102ba

Ensembl ID:
ENSDARG00000053104
ZFIN ID:
ZDB-GENE-060616-312
Description:
hypothetical protein LOC724011 [Source:RefSeq peptide;Acc:NP_001038781]
Human Orthologue:
FAM102B
Human Description:
family with sequence similarity 102, member B [Source:HGNC Symbol;Acc:27637]
Mouse Orthologue:
Fam102b
Mouse Description:
family with sequence similarity 102, member B Gene [Source:MGI Symbol;Acc:MGI:3036259]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa17182 Essential Splice Site Available for shipment Available now
sa10391 Essential Splice Site Available for shipment Available now
sa19865 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17182
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125406 Essential Splice Site 189 366 None 11
ENSDART00000125406 Essential Splice Site 189 366 None 11

The following transcripts of ENSDARG00000053104 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 45731273)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45822935
GRCz11 2 45675933
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAAGACAGAAGAGGAGAGACACCAAAAACAACCAATTACTTTACAGG[T/A]ATAAAGCATAGAAAGTRTAGAACACTACCACCTAAATACAGTCCTCAGCA
Long Flanking Sequence:
AGTTTTAAAAATGTCAATTTCACGCTAACATTTGAGCGCTGTTGAGCGCGTTCTTAAACGGCGCTGATTAGCTGTTGTGTTCACGTGCTCAACAGAAATGACTGTGATTGGCTGTGAAGGTCATCAGTTCACCGAACTCATACAGATACAGGGACACTGGAGTGTTTCAGTCACATCAATCAGCTGGTTTGTTTTAGAACCTGACATACTAGCGATCCACTGATGAATCGCGGCTTTGAAATGCTCCAGTGTCCCTGTATCTGTAACCCTATTCTCAATACAAGAACTCATCCAAAAAATAATACAATGCTTAATGGATACTTCACACTGTGATGTATTGTTATCTTTTGTTTTCATATGTTTATATATTTTTAATGGTTATGCTTTTGTTCTAGGCCTCCATCCACTGCAATGACAATAGGATTTCCAGGAGACACAGAGACATGTCTGCATGAAGACAGAAGAGGAGAGACACCAAAAACAACCAATTACTTTACAGG[T/A]ATAAAGCATAGAAAGTATAGAACACTACCACCTAAATACAGTCCTCAGCATAAATAAGTACATCCTCTTTTAAAAATGAATATTCATATCCATTTCTCAGTGAATATAGCCAATATATTTAGGTGTGTTTAAACAACGCTGTTTTAATAAAAAGTTATATCCATTAAAATAAGAGTTTGGTCACCTGACATATTTAGTTATAGAAAGATAATATAATTACCTTCAGTTGAGTTATTGCAACAAAAACAAAATACAAACTACAAAATTATACATTTATATTTTAATGCATTTTTATATTACATTTAAATTTGTTTTGTTTCTCTTGATTTTTATTTCCTGTTTATTTTTTGTGTTTGATTAGTTCCAGTTTTGGCTTTTGTACAGACCAGTCTAATGTATATGCATAAATATATAATTGTAAAGCATCATATAGAAAAAAGAGGTGTGCGAGAGGTGCACTCATTTATGCTGAGCACTGTAGTTTATGGTAAAGCATTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10391
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125406 Essential Splice Site 189 366 None 11
ENSDART00000125406 Essential Splice Site 189 366 None 11

The following transcripts of ENSDARG00000053104 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 45731273)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45822935
GRCz11 2 45675933
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAAGACAGAAGAGGAGAGACACCAAAAACAACCAATTACTTTACAGG[T/C]ATAAAGCATAGAAAGTRTAGAACACTACCACCTAAATACAGTCCTCAGCA
Long Flanking Sequence:
AGTTTTAAAAATGTCAATTTCACGCTAACATTTGAGCGCTGTTGAGCGCGTTCTTAAACGGCGCTGATTAGCTGTTGTGTTCACGTGCTCAACAGAAATGACTGTGATTGGCTGTGAAGGTCATCAGTTCACCGAACTCATACAGATACAGGGACACTGGAGTGTTTCAGTCACATCAATCAGCTGGTTTGTTTTAGAACCTGACATACTAGCGATCCACTGATGAATCGCGGCTTTGAAATGCTCCAGTGTCCCTGTATCTGTAACCCTATTCTCAATACAAGAACTCATCCAAAAAATAATACAATGCTTAATGGATACTTCACACTGTGATGTATTGTTATCTTTTGTTTTCATATGTTTATATATTTTTAATGGTTATGCTTTTGTTCTAGGCCTCCATCCACTGCAATGACAATAGGATTTCCAGGAGACACAGAGACATGTCTGCATGAAGACAGAAGAGGAGAGACACCAAAAACAACCAATTACTTTACAGG[T/C]ATAAAGCATAGAAAGTATAGAACACTACCACCTAAATACAGTCCTCAGCATAAATAAGTACATCCTCTTTTAAAAATGAATATTCATATCCATTTCTCAGTGAATATAGCCAATATATTTAGGTGTGTTTAAACAACGCTGTTTTAATAAAAAGTTATATCCATTAAAATAAGAGTTTGGTCACCTGACATATTTAGTTATAGAAAGATAATATAATTACCTTCAGTTGAGTTATTGCAACAAAAACAAAATACAAACTACAAAATTATACATTTATATTTTAATGCATTTTTATATTACATTTAAATTTGTTTTGTTTCTCTTGATTTTTATTTCCTGTTTATTTTTTGTGTTTGATTAGTTCCAGTTTTGGCTTTTGTACAGACCAGTCTAATGTATATGCATAAATATATAATTGTAAAGCATCATATAGAAAAAAGAGGTGTGCGAGAGGTGCACTCATTTATGCTGAGCACTGTAGTTTATGGTAAAGCATTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19865
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125406 Nonsense 211 366 7 11

The following transcripts of ENSDARG00000053104 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 2 (position 45728661)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45820323
GRCz11 2 45673321
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTTTAGTCATGGTTCGGTTCCAGATGAACTGGGAAAGTGTGGCCACT[C/A]AAGAACCGCGAGCTACGCCAGCCAGCAGTCTAAGTTTTCAGGTGTGTTCA
Long Flanking Sequence:
GCTACCTTCCTGCAGATTTCAGTTGCTACCCATATCAAACACACCTAAACCAATTAATTAGGACCTGAACACCATGTGATAATTACAGGCAGGTGTGTTTAATATGGGTTGCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAACAGGATTGGCCACCCCTGTTCTACACTGTATGTTGTATACTGTAAACTTGCATACTTATTTGGTCACATCCATAATGCATGTTGATTTCCCTCAATTATACATTAAAAAATGTTTATTGATGAGATGAAATATTTTGCTGACCCCCCATAACTCTATGGTTGGTTGTTTTGAAAAAATATAAACAAATGTTTTAATATAATGTTAATATATACTTTCTCTGTTAATTAATATTTTAAGTTTGTACTGTTAATTGTCACATCTATAACACTGGAATTGCTCTTTTCTAGAAAACTTAGGAAAAAGTGGCTTTAGTCATGGTTCGGTTCCAGATGAACTGGGAAAGTGTGGCCACT[C/A]AAGAACCGCGAGCTACGCCAGCCAGCAGTCTAAGTTTTCAGGTGTGTTCATGAATATTTAATGGTTTTCCATTACATTTTATCATTTTATTCAATTGTATGTTTGCATAATATTACATAATAATATCAATCATTCTGGACATCCCCTCAGGTTACAGCACAGGTCACTCACGCTCCTCCAGCCTGACAGAGCTCTCTCATCGGAGGAACTTGTCTGTGGGCAGTGCCTCCACCGGGATAGGTAGCCTTCAAGAGCCCAGTGAGAACAGAGAGTCCCGCACACCTTTACCACAGCATTTACCCACACCGTCACACAGTGCATTCTCAGCCGGCAGGTAAACAATATGCAATGAATGATCAGTTTTCCGTGAAAACTTTAGATCAAGCAGTTAACAGAGTGTATGTTTGCATTTCAGACATCCAGTAAAGCAGGACTCGGTGGAGTGTCAGTTAAAGCGAGTAGATGCTACCAGAGTGGACGCTGATGACATCATTGAAACA
Associated Phenotype:
Not determined