Busch Lab

ZMP

LOC100148564

Ensembl ID:
ENSDARG00000068719
Human Orthologue:
RP11-332P22.1
Human Description:
Geminin coiled-coil domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:A6NCL1]
Mouse Orthologue:
Gm606
Mouse Description:
predicted gene 606 Gene [Source:MGI Symbol;Acc:MGI:2685452]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa22699 Nonsense Available for shipment Available now
sa6391 Nonsense Mutation detected in F1 DNA Not yet available
sa470 Nonsense Confirmed mutation in F2 line Not yet available

Mutation Details

Allele Name:
sa22699
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099496 Nonsense 116 382 3 4
Genomic Location (Zv9):
Chromosome 15 (position 35578889)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 36453080
GRCz11 15 36311049
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAACAACAAGCTCAAAGAGTTTCTAAACTCGTCATATGTGAAGTCTT[T/A]GGAGGAAAAATCTAAGGTAAGAAACCTCTCAATTTGTCACAGATATTAAC
Long Flanking Sequence:
TTCTTCATGTTTTTGTTAGAGTAGCAATGGGCTGTGGAGTATCTGGCTACCTCCAAAGTGTTAGTTCTTTTGGGTACTTTCTTTTGTTTTTAAAGTAGCCTATTTTTTTAATTGATGTTTTGTTTTTATTTTCTTTTTTCCTTCACATTTCACATTGAAATTATCCCTAGACCATTACTAATGAGGATAATGACCTTTTTTCTTTCTTTCTTTAAATCGCCCATTTGTTTTAGATTCACTCCTTGAGAGTGGACTGGGACATCAGCCCACCTGGCATGACCAACTGTCACCTCAACTTCAACGGAACAAACAGGTATTGAAATTGTTGATCATATTTGAGTTACTCAGCCTAGCAGTTGAGACAGTGTTAATGATTGTGGTAACATTTTCCCTCGTGAAGCTCCAAGACACCTTAATGCAAAGAGAGGAAGAGCTGGCCCGACTGCAAGAAGAGAACAACAAGCTCAAAGAGTTTCTAAACTCGTCATATGTGAAGTCTT[T/A]GGAGGAAAAATCTAAGGTAAGAAACCTCTCAATTTGTCACAGATATTAACACTATATTTAGTGATGTGTGCAATTTTTTTCTATATTGAAATACTTAACATTACTTCAACTAAAGAAAAGCAAAAATAAAGTTAAAGGGGGGAATCGATGAATGGATATTCAACAAATACAACTGATAACTACTGCAATTAGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAGGAAGGTTGCTGGGTCTCTGGTTCAAACCTCGGCTCAATTGGCTTTTCTGTGTGGAGTTTGCATGTTCTCCATGCCTTCGCGTGCTCTGGTTTCCACCACACTCCAAATACATGTGGTACAGGTGAATTGGGTAAGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGAATGTGTGTGTGGACGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATGCTGGATAACTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6391
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099496 Nonsense 118 382 3 4
Genomic Location (Zv9):
Chromosome 15 (position 35578894)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 36453085
GRCz11 15 36311054
KASP Assay ID:
554-4231.1 (used for ordering genotyping assays)
KASP Sequence:
ACAACAAGCTCAAAGAGTTTYTAAACTCGTCWTATGTGAAGTCTTTGGAG[G/T]AAAAAWCTAAGGTRAGAAACCTCTCAATTTGTNNCAGATATTAAYACTAT
Long Flanking Sequence:
CATGTTTTTGTTAGAGTAGCAATGGGCTGTGGAGTATCTGGCTACCTCCAAAGTGTTAGTTCTTTTGGGTACTTTCTTTTGTTTTTAAAGTAGCCTATTTTTTTAATTGATGTTTTGTTTTTATTTTCTTTTTTCCTTCACATTTCACATTGAAATTATCCCTAGACCATTACTAATGAGGATAATGACCTTTTTTCTTTCTTTCTTTAAATCGCCCATTTGTTTTAGATTCACTCCTTGAGAGTGGACTGGGACATCAGCCCACCTGGCATGACCAACTGTCACCTCAACTTCAACGGAACAAACAGGTATTGAAATTGTTGATCATATTTGAGTTACTCAGCCTAGCAGTTGAGACAGTGTTAATGATTGTGGTAACATTTTCCCTCGTGAAGCTCCAAGACACCTTAATGCAAAGAGAGGAAGAGCTGGCCCGACTGCAAGAAGAGAACAACAAGCTCAAAGAGTTTCTAAACTCGTCATATGTGAAGTCTTTGGAG[G/T]AAAAATCTAAGGTAAGAAACCTCTCAATTTGTCACAGATATTAACACTATATTTAGTGATGTGTGCAATTTTTTTCTATATTGAAATACTTAACATTACTTCAACTAAAGAAAAGCAAAAATAAAGTTAAAGGGGGGAATCGATGAATGGATATTCAACAAATACAACTGATAACTACTGCAATTAGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAGGAAGGTTGCTGGGTCTCTGGTTCAAACCTCGGCTCAATTGGCTTTTCTGTGTGGAGTTTGCATGTTCTCCATGCCTTCGCGTGCTCTGGTTTCCACCACACTCCAAATACATGTGGTACAGGTGAATTGGGTAAGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGAATGTGTGTGTGGACGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATGCTGGATAACTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa470
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099496 Nonsense 349 382 4 4
Genomic Location (Zv9):
Chromosome 15 (position 35584309)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 36458500
GRCz11 15 36316469
KASP Assay ID:
554-0202.1 (used for ordering genotyping assays)
KASP Sequence:
GTATGTCCCGTAGCAAGACAGATTTAGCATTTAGCATGTCACTAAGTCCA[C/T]AAAACAGTGTGAAGACGCACAGTTTCCCTCAAGGACAAGCTTTCACACGC
Long Flanking Sequence:
TACTAGAGACTCTAGGTCTGCAAGACGAGAACACCATCAACCCAGAACGCAGTTTGAACACAACTACCTTCAGCCGTCCACTACCTACTGAAGATCGTTACAGTGTGGACAACACAACTGGCTTCAGTCCTAATGCTGGAACACATTGCGATTACAGCAGCATTGTAGACTCGAGCAGCAACTGCAGTCTTGACACATCCAGTGGCTACAGCACTTCTCAGAGCTTGGGTTCGGATTATTCAACTCTTGATCCCTCAGCTCTGTACACCATTACGTCTACAGGGTCACCGGTCAGCTCTCCACCAGCATTGACAACCGCTCAACACTTCACACCACCACGAGCTGCTTCTACCCCGTATCGACCTCAGGATGTAAGTCCATACTACAGCACACCAGGCTGTGGTTCCTCCACGTCACCAGGGGGCGACAAACAGCTGTTCTCCACACCTCGTATGTCCCGTAGCAAGACAGATTTAGCATTTAGCATGTCACTAAGTCCA[C/T]AAAACAGTGTGAAGACGCACAGTTTCCCTCAAGGACAAGCTTTCACACGCAGAGACGCGCAAGGTGGATGGAACTTCACCTGGGTGCCCAAACAATGTTCCTAGAGAGGATCGTTGGAGGAGAAAGCCCCTTTTTGGGAGTGATAACCCAAGGTGCCCCATACTTGCTAGAAACGCAACAACTTATGTATGATAGTACTTTATCATTGCATAGCTTTGTATATGATGTCATTGTAAATATGTATAGTGTTTTTATACATTGTGATCGAAAGGCTTTGTCTTTGATGTTAAATCATGACTGAATTCATTAAAATCACCAATTTCTTTCTGAATAAATGCTATTTTGTTGTTTCTTTTGAAAACATTTGACCCCTTACTTTCGATAATCACCGTCTTTAGTGTTACAATGTTAACAAATATACAAACAGAGCATATGTTACCTGCTCTCAGACACCTAGGTCAACATTGCCTCTTTAATTTTGAACTGACGCATCATAAGTA
Associated Phenotype:
Not determined