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
sa10391 Essential Splice Site Available for shipment Available now
sa17182 Essential Splice Site Available for shipment Available now
sa19865 Nonsense Available for shipment Available now
sa44548 Nonsense Mutation detected in F1 DNA Not yet available

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:
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
Order Allele From EZRC
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:
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

Mutation Details

Allele Name:
sa44548
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125406 Nonsense 296 366 9 11

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

Genomic Location (Zv9):
Chromosome 2 (position 45728215)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 45819877
GRCz11 2 45672875
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGTATGTTTGCATTTCAGACATCCAGTAAAGCAGGACTCGGTGGAGTG[T/A]CAGTTAAAGCGAGTAGATGCTACCAGAGTGGACGCTGATGACATCATTGA
Long Flanking Sequence:
AAAGTGGCTTTAGTCATGGTTCGGTTCCAGATGAACTGGGAAAGTGTGGCCACTCAAGAACCGCGAGCTACGCCAGCCAGCAGTCTAAGTTTTCAGGTGTGTTCATGAATATTTAATGGTTTTCCATTACATTTTATCATTTTATTCAATTGTATGTTTGCATAATATTACATAATAATATCAATCATTCTGGACATCCCCTCAGGTTACAGCACAGGTCACTCACGCTCCTCCAGCCTGACAGAGCTCTCTCATCGGAGGAACTTGTCTGTGGGCAGTGCCTCCACCGGGATAGGTAGCCTTCAAGAGCCCAGTGAGAACAGAGAGTCCCGCACACCTTTACCACAGCATTTACCCACACCGTCACACAGTGCATTCTCAGCCGGCAGGTAAACAATATGCAATGAATGATCAGTTTTCCGTGAAAACTTTAGATCAAGCAGTTAACAGAGTGTATGTTTGCATTTCAGACATCCAGTAAAGCAGGACTCGGTGGAGTG[T/A]CAGTTAAAGCGAGTAGATGCTACCAGAGTGGACGCTGATGACATCATTGAAACAATCCTACAGGGTCAAGACTTCAGCCACAGCATTCTGGACTCCAGTAATGAAGGTACTGTTCATTTTTAATAACAATCTTTCCTGATTTCTACAGGACACTTTCATAATTGCAGAATTTGTAGTTCAGATGTTATGTAGTTTATGGAATAATTATGTAAAAAAATGATTGTAATAGCTCACTTAAAATAGCAGTTTGGTTCATTATGAAGACATGCAATGCTATTTGAAAATGTATGGTTCTTGTACACTTTTGATATGCTGCTTTCCAAGCCTGTACAATAAGTATTGAATATGTCACCATTTTTCTTAGAAAACATATTTCTAAAAGTGCTGTTGACTTGAAATTTTCCCTGGATGTTGGTAACATCCAAATAAATCCATATATGCAAAGACAATAAATCTAATTAGTTTACAAATTAAGCTATGCATAATAAAATGAAGTGACG
Associated Phenotype:
Not determined