Busch Lab

ZMP

gli2b

Ensembl ID:
ENSDARG00000020884
ZFIN ID:
ZDB-GENE-050523-1
Description:
GLI-Kruppel family member GLI2b [Source:RefSeq peptide;Acc:NP_001015069]
Human Orthologue:
GLI2
Human Description:
GLI family zinc finger 2 [Source:HGNC Symbol;Acc:4318]
Mouse Orthologue:
Gli2
Mouse Description:
GLI-Kruppel family member GLI2 Gene [Source:MGI Symbol;Acc:MGI:95728]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa6221 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38862 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38861 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa18473 Nonsense Available for shipment Available now
sa27835 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7354 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6221
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Essential Splice Site 229 1225 5 10
Genomic Location (Zv9):
Chromosome 11 (position 45030778)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43609022
GRCz11 11 43684396
KASP Assay ID:
554-4025.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTGCACGATTACGTGTGTGTTCAGTARAGTGTGTATGYCGTTCCCTGC[A/T]GGAGCACCTGAGCAGTGCACAGGACCTGAAGGAGGACATGGACGACTGTA
Long Flanking Sequence:
GGCCACTATTAATACTGTTAAGTAATTAAATTGTGTTAAGTTAATTAAAAAGCACCGCTCACTCATCCAGTGGGCCTACAGTGGCATGAACCGTTGGCATTTGGTTGATTATTGGTTCTGATGGCAACCTTTAATGCCATCAAGTAAAATAAAAGGTGTTAAGTTAGTAAAATAGCATGTATAATCTAAATGCTGTTCAATATTGGATTTTGACATCAGCTTGATTTTTATTTCTCTTTAAAATATATAACAGCAGGACATTTCCTCTGAGGGATTTAAGTCTACACAGGAAAGCCCTTATATGGAAATAGTTGGGGGAGTGTTTATGCAAATCAATAGACTCATTTGGAATGCTCCCAAATTTAATTATTATTAGAGCAATTAATCAATTAATGAATTAATATGCATACACACACACACACACACACAGTGTGCATGTAAATATCAATAATGTGCACGATTACGTGTGTGTTCAGTAGAGTGTGTATGCCGTTCCCTGC[A/T]GGAGCACCTGAGCAGTGCACAGGACCTGAAGGAGGACATGGACGACTGTAAGCAGGAGGCGGAGCTTGTGTACGAGACCAACTGCCACTGGGAGGGCTGCAGCAAAGAGTACGACACGCAGGAGCAGCTGGTGCATGTAAGTGTGTGTGTGTGCGTGAGAGTGTGTGTTTGTGTGATTGTGTTAAAGTGTGTGTGTGCATTTATGTGACTGTGTTTAAGTGTGCGTCGGTGTGTGATATTCAGACAGACCTGCTGTGTTTGGACACAGATGAGCAGCAGCAGCGCAGCACAGATGCGTCATCACAAATCACACACTTTCAGCAGCAAATGCATGACAGTGTGTTTTATTCTGAGCCTCTAAACAAGCTTTTGTTTGCTTGCAACTTTATTGAGGACAAGAAGCACCGAGCCGTCAGTCACAGCGCAGCCTGCTGATCTCAGAAAGCTCCTGCTGTTCTTGTGTTTTTTTTCTGTTCTGTGTATTTGGCTCTTAACCGCAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38862
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Essential Splice Site 273 1225 5 10
Genomic Location (Zv9):
Chromosome 11 (position 45030641)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43608885
GRCz11 11 43684533
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGGGAGGGCTGCAGCAAAGAGTACGACACGCAGGAGCAGCTGGTGCAT[G/A]TAAGTGTGTGTGTGTGCGTGAGAGTGTGTGTTTGTGTGATTGTGTTAAAG
Long Flanking Sequence:
CATCAAGTAAAATAAAAGGTGTTAAGTTAGTAAAATAGCATGTATAATCTAAATGCTGTTCAATATTGGATTTTGACATCAGCTTGATTTTTATTTCTCTTTAAAATATATAACAGCAGGACATTTCCTCTGAGGGATTTAAGTCTACACAGGAAAGCCCTTATATGGAAATAGTTGGGGGAGTGTTTATGCAAATCAATAGACTCATTTGGAATGCTCCCAAATTTAATTATTATTAGAGCAATTAATCAATTAATGAATTAATATGCATACACACACACACACACACACAGTGTGCATGTAAATATCAATAATGTGCACGATTACGTGTGTGTTCAGTAGAGTGTGTATGCCGTTCCCTGCAGGAGCACCTGAGCAGTGCACAGGACCTGAAGGAGGACATGGACGACTGTAAGCAGGAGGCGGAGCTTGTGTACGAGACCAACTGCCACTGGGAGGGCTGCAGCAAAGAGTACGACACGCAGGAGCAGCTGGTGCAT[G/A]TAAGTGTGTGTGTGTGCGTGAGAGTGTGTGTTTGTGTGATTGTGTTAAAGTGTGTGTGTGCATTTATGTGACTGTGTTTAAGTGTGCGTCGGTGTGTGATATTCAGACAGACCTGCTGTGTTTGGACACAGATGAGCAGCAGCAGCGCAGCACAGATGCGTCATCACAAATCACACACTTTCAGCAGCAAATGCATGACAGTGTGTTTTATTCTGAGCCTCTAAACAAGCTTTTGTTTGCTTGCAACTTTATTGAGGACAAGAAGCACCGAGCCGTCAGTCACAGCGCAGCCTGCTGATCTCAGAAAGCTCCTGCTGTTCTTGTGTTTTTTTTCTGTTCTGTGTATTTGGCTCTTAACCGCACTATTTTGAGGAGACTTCTTGACGTTAGCAAGTCAGAGCAGCTGAGTGGCTTAAAGGGTCACGAAACACCAGAACACATGTGTTGAGCTGTTGACAGTCATATAAGTGTCCCACACTGCTAAAAACACTATCAGGACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38861
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Essential Splice Site 274 1225 6 10
Genomic Location (Zv9):
Chromosome 11 (position 45023393)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43601637
GRCz11 11 43691781
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTATGTCTCCTGCATTGACGTGTTGCATGTGTGTGTGTGTGTTTGC[A/G]GCACATCAACAATGAGCACATCCACGGGGAGAAGAAGGAGTTTGTGTGCC
Long Flanking Sequence:
TGACTTTTACTTTCTGAAAGCATATATACACAGCGCGGGAAATAAGTATTGAACACGTCACCGTTTTTCTCAGCTAACATCTTTCTAAAGGTGCTGTTGACTTAATCTTTCCACCAGATGTTGATAACAGCAAAAGAAATCTATAAATGCAAAGAAAACAAATCGAATTAGTTTAGAAAGGAAGTTCTGTGTAATCAAATGAAATGACACATGGATTGAACACATGAAGAAAGCAAGGTGTAGTTGGGCAGTGAAAGCCCAGACAGCAGCTGAAATCTCTCAGTTTTCTTCAGCAAGCCTCTGCCCTTCCTCAGTGTAAATGAATATCAGCTGCTCCAGTCCAACATCCACATTAGCAGGAGGATGAAGATGAACGCATTTCAGTAAGAGAATGATCCAGAACACAGCGTGTGTGTTTGTGTGCATGTGTGTGTGCATTTGCCTGTTTGTGTGTGTATGTCTCCTGCATTGACGTGTTGCATGTGTGTGTGTGTGTTTGC[A/G]GCACATCAACAATGAGCACATCCACGGGGAGAAGAAGGAGTTTGTGTGCCGCTGGGACGAGTGCTCACGCGAGCAGAAGCCCTTCAAAGCGCAGTACATGCTGGTGGTCCACATGCGCAGACACACCGGGGAGAAACCGCACAAATGCACGGTAAGTCTCACACACACACTATTTTTTTTTTAAACTGCAGTTTAAAAAATTTATTAAAAATTGTGCTGAAAAAAATGAACAAATGAATATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTTATTTATTTATTTATTTATTTTTTATTTATTTATTTATTTATTTATATATTTATTTATCCATTTATTTATTTATTTATTTATTTATATATTTATTTATCCATTTATTTATTTATTTATTTATTTAATAATAAATTAATTAATTAATTTAATTTAATAATTATATAAAATAATATTTATTTATTTATTTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18473
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Nonsense 392 1225 8 10
Genomic Location (Zv9):
Chromosome 11 (position 45018846)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43597090
GRCz11 11 43696328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCGCAGAAACCCTAYGTGTGTAAGATCCCGGGCTGTACCAAGCGCTA[T/A]ACTGATCCCAGTTCGCTTCGGAAACACGTTAAAACCGTGCACGGGCCCGA
Long Flanking Sequence:
TTCCAGCACACGCTAACAAATTTAGGCCAAAATTAGATTTGTTTACGCATTCCCTCATCATCTGTAGTGATTGCTCCAGGACGCCCAATGCTGTCCCATTAACCAGCAAGTGTGCGCAATGTGTGTGTGTGTGTGCGTGAATAATGAGCTGTGATGCTAATGAGTCCGGCATCCCATAATGCATTAGTGGGAATAAAGCTCAGAGGAACAGACCACCTGCAGACGGAAATGAAGCCTTCCCGCGCCGATCCATCACTAGCATAAAAGATCAACTCAACTTTATTAGCAAACAGCCATGCATCACGATAGCATTCGTAGCATCAGTACGTCAGCGCATTTGTAATTCATTCCCATAATCGTGCGTTCATTTGTTCTTTGAGGATAATCTGACTTAAAGGGAAGAGATAAAACTCTAATTCAGAGTTGTATATTTGAGCGGTGTGATATTTATCTTCGCAGAAACCCTACGTGTGTAAGATCCCGGGCTGTACCAAGCGCTA[T/A]ACTGATCCCAGTTCGCTTCGGAAACACGTTAAAACCGTGCACGGGCCCGAAGCACACGTCACCAAGAAACAACGCGGAGATCTGCCGTCCAGACCACATCCGCCGAAGGAGAACGGAGAAAATGAAGCCGGAGCCAAGATGGCGGAGGAGAAAATTGAAGCCAACAGCACTACTAGAGGAGTGGAGGACTACCTGCAGGTCAAGTCTATCAAGACTGAGAACTCAATGGTAAGATCTTGTATGAAACTTGATCAAGTGTTTATAAAATATATAAGTAGGCTCAGTTTATAGTTGATTGCAGTTATGCAGTATAGATACACGAGTAATTCATTTCTAACTCACGTAAAGCTCTCGTGAAGTGCTTTAAAATTAGCATTTTTATTGGATGTTTTGACGTAATCTCAACTGAAACGGTAAAGTCTAGAAAAGTCTAGATCGGATATATAGTCGGCCGGATGTGCGATATGCACATTAATATAGCAGCATTTTTTATGACACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27835
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Essential Splice Site 577 1225 10 10
Genomic Location (Zv9):
Chromosome 11 (position 45003684)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43581928
GRCz11 11 43711490
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTGATTAACCCGCCTAGTCCTAACAGATGTCATTTCTACTTTATGGC[A/T]GGTTCTTTATTGGACGGTCTGTGTGATCCAGGGCTTTCCATCTCCAGCCC
Long Flanking Sequence:
TAAACCTTAAAGATATAGCAACAAAATCTAACGCATCTAAATACAGCTTTTGGCCAAATTTGGGGCTTGTATAATTTTTTTATATGCTCGGATTATAAAAATTTAATATTTAACATTTTTTATTAAAAAAAAACAAAAAGTCTTACAGGCATGAGGAGATATAGCAACAATCTTGAATGCAGAAGGCATATTTTGACCACATTTGAGCCTTGTGGCATGAACGGCCTAGGAGGAGATACGTTTGTTTTCAAGGACAGAGTAGCATGACAGTATGTTGGCTTTCTCAAGCCAACATAAATATGGAGTAGTGTAATATGAAGCTGTGATATCACCCTAACCTACCTAATCCCTAACCCCAACCAAATACAAATATAGTGCTGGTTGCGTAATCTGATGAGTGGGATAAAATGTCAGGACAACGGCTTTACTGATTAACTTTGCATGAAATTCGTCTTGATTAACCCGCCTAGTCCTAACAGATGTCATTTCTACTTTATGGC[A/T]GGTTCTTTATTGGACGGTCTGTGTGATCCAGGGCTTTCCATCTCCAGCCCGCGTCTGGGCGACCTCTGTCCTGGCGAGACTACAGTGTTAAGTCAGTTGGTGGAGCGTCGGGACAGCCTGGCCAGCACTGTGAGCTCTGCGTACACCTTCAGCCGGCGCTCATCCGGAATATCACCATGTTATTCGAGCCGTCGGTCCAGCCAAACATCCCAACCTGGCGGCCGTCACAACAACATCAGCTCTGCTGACTCCTATGACCCCATTTCAACCGATCTGTCTCGAAGGTCCAGCGAGGCCAGCCTATATGGGGGAATCTTCAGCTTGACTCCTGCACAACACTACCGACTTAAAGCCAAATATGCTGCGGCCACAGGCGGAGCACCACCCACGCCTCTGCCTAACATAGACTGCAAGACTCTGTTAGGAGATTCGCATGAAATCCCCATACATCCCCCTTTGGTTCCCAGAAGGTGCAGTGACACCGGCTATGCCAACCGTAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7354
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 > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000017912 Missense 633 1225 10 10
Genomic Location (Zv9):
Chromosome 11 (position 45003514)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 43581758
GRCz11 11 43711660
KASP Assay ID:
554-4170.1 (used for ordering genotyping assays)
KASP Sequence:
RGCCAGCACTGTGAGCTCTGCGTACACCTTCAGCCGGCGCTCATCYGGAA[T/G]ATCACCATGTTATTCGAGCCGTCGGTCCAGCCAAACATCMCAACCTGGCG
Long Flanking Sequence:
TCTTGAATGCAGAAGGCATATTTTGACCACATTTGAGCCTTGTGGCATGAACGGCCTAGGAGGAGATACGTTTGTTTTCAAGGACAGAGTAGCATGACAGTATGTTGGCTTTCTCAAGCCAACATAAATATGGAGTAGTGTAATATGAAGCTGTGATATCACCCTAACCTACCTAATCCCTAACCCCAACCAAATACAAATATAGTGCTGGTTGCGTAATCTGATGAGTGGGATAAAATGTCAGGACAACGGCTTTACTGATTAACTTTGCATGAAATTCGTCTTGATTAACCCGCCTAGTCCTAACAGATGTCATTTCTACTTTATGGCAGGTTCTTTATTGGACGGTCTGTGTGATCCAGGGCTTTCCATCTCCAGCCCGCGTCTGGGCGACCTCTGTCCTGGCGAGACTACAGTGTTAAGTCAGTTGGTGGAGCGTCGGGACAGCCTGGCCAGCACTGTGAGCTCTGCGTACACCTTCAGCCGGCGCTCATCCGGAA[T/G]ATCACCATGTTATTCGAGCCGTCGGTCCAGCCAAACATCCCAACCTGGCGGCCGTCACAACAACATCAGCTCTGCTGACTCCTATGACCCCATTTCAACCGATCTGTCTCGAAGGTCCAGCGAGGCCAGCCTATATGGGGGAATCTTCAGCTTGACTCCTGCACAACACTACCGACTTAAAGCCAAATATGCTGCGGCCACAGGCGGAGCACCACCCACGCCTCTGCCTAACATAGACTGCAAGACTCTGTTAGGAGATTCGCATGAAATCCCCATACATCCCCCTTTGGTTCCCAGAAGGTGCAGTGACACCGGCTATGCCAACCGTAGCGTTTTACCCCATGAGGTGACAGCAAACATTACTCGAAGAGCAAGCGACCCAGTTAGACGAATAGCTGCTGAGCAGCATTCGCTCTACAACAGTGTAAACCCGTATCCAACATTACACCCTCTTGCGTCAAGCCGACACTTTTACAGCACGTCTGAGAGTAACGTCAACC
Associated Phenotype:
Not determined