ZMP
gli1
Ensembl ID:
ZFIN IDs:
Description:
zinc finger protein GLI1 [Source:RefSeq peptide;Acc:NP_840081]
Human Orthologue:
GLI1
Human Description:
GLI family zinc finger 1 [Source:HGNC Symbol;Acc:4317]
Mouse Orthologue:
Gli1
Mouse Description:
GLI-Kruppel family member GLI1 Gene [Source:MGI Symbol;Acc:MGI:95727]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8554 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38271 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31210 | Nonsense | Available for shipment | Available now |
sa32697 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8554
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049151 | Nonsense | 106 | 1404 | 4 | 13 |
ENSDART00000123101 | Nonsense | 106 | 1404 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 30733084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59444779 |
GRCz11 | 6 | 59439991 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTCAGGTATGAGCGGCGCCCCCTACTGTAACCAGAACATGATGACAT[C/A]SCATCATAATCTCCCTCATAACCAGCACACATCTGAACTCATGGCATCAG
Long Flanking Sequence:
ACAGAGAATAAAGGCTCTTGCTTTTGCCCTCCTTTATTTCGGACACCGTGAGAATGAGCTTCTCCCCCGTGGTGCACAACAACACTGAAAACACTGTGCGGCTGCCACAAGGGGGCGTATTCCGACGGTCGTGTCCAAATGTCGTGTGCAGTGGAAAGGCGGCTTAAACGTGTTTGACCACTACTCTCGAGTCTCACGTCTTTTGAAGTGCAGCGCATGAGAGAGGAAAATGCATTCTGTGTGAACGGCCCCAACAGTCAAACTCATTCAATCAGCGCGTTTACATTGAAAAACATCAGAAAAGTAGTGTGTTGGAAAGGAAAAATGCATTCTGTGTGAACGGCCCCTAAGCAGCATGCAAAATACTCAAGGAAAAAAGCGCGTCCTGTGTGAACGACCCCTGAATGATAAGGAAATGTGTGAACTAATCCCTTATGAAAACGGTGCTGTTGTTTCAGGTATGAGCGGCGCCCCCTACTGTAACCAGAACATGATGACAT[C/A]GCATCATAATCTCCCTCATAACCAGCACACATCTGAACTCATGGCATCAGGAGACGGTGAGACCACAAACCTACACGCATAAAACATCTGAACGACATTCAGCAAATGTATTAACGCGCAGTAATGCAAAACGGTTGAAAACATTTGATTCTGTTAGTAATTGTTGTTCAAGTTATTGTTAAACGTTTTAGGCCAAAACATTTTACACAAACTAATGAGAGGAATAACGAAGCTTCAATGCCTTTCAGAGTTTCCTGCCACAGGAAGAGACATCCCTTGGAGCAAGTCACTTGCTTTCTCTATCAGCGATTTACAGATTGATCTGCCTTTTTAAAACCAAAAGAGTTTTGCAAAGTCAAACCTAAATTGCAAATAATACAATAAATATTCATGCAAATGTGTATTTAAGTTGGTAGAGTTAAGAAAAATGTATATGAGCCTTAATTATTCCATGATATTTAAAGCTGAATGTATTATTCAACAGTCTAAGACATGCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38271
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049151 | Nonsense | 344 | 1404 | 9 | 13 |
ENSDART00000123101 | Nonsense | 344 | 1404 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 30740275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59437588 |
GRCz11 | 6 | 59432800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATCCACGGAGAGAAGAAGGAGTTCGTTTGCCACTGGAAGGACTGTTCC[C/T]GAGAGCAGCGTCCGTTTAAAGCGCAGTACATGCTGGTGGTGCACATGCGC
Long Flanking Sequence:
AAGCATACAAAAAAAACCGGTGTCATAAGTACAATACTGTAAATCCATGCATTTTTCACGCCAGCTGTTAAAATGTATAAAATTAGGTGAATAAAATTATTCCGGAGTTGAACCAGTGAAAAAGAGTGAATGAACACGTGCATCAACCAAAGTTTTCGAGGCTTAAACCTGTTCATAAAAAATTAAGTGTTGCTAGTCTTCCACTAAAGCGGGGTGTCAAACTCAAACTTAGTTCCTGGAGGGCCGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAACTGCGGCCCTCCAGGAACTGAGTTTGACACCTGTGTTCTAAACTCTGCTTCTATTTGTGCAGCACATCAATAATGAGCACATCCACGGAGAGAAGAAGGAGTTCGTTTGCCACTGGAAGGACTGTTCC[C/T]GAGAGCAGCGTCCGTTTAAAGCGCAGTACATGCTGGTGGTGCACATGCGCAGACACACCGGAGAAAAACCACACAAGTGCACTGTGAGTACTGACACTTTCCATTCATTTCCTTCTAATGATCTGCAATGATTAACAACATATGTACACTTCACACTTGTATGTTCATGTGCATCAGTTTGAAGGCTGTAATAAAGCATACTCGCGGCTGGAGAACCTGAAGACGCATCTGCGCTCACACACCGGAGAGAAACCCTACGTTTGTGAACACGAGGGCTGTAACAAGGCTTTCTCTAATGCTTCAGATCGAGCAAAGCACCAGAACAGAACACACTCCAATGAGGTAATATCACACACATTAATGCATGCACTGATATACACTTGTGTCTTAATAAACTCAGTATCAATGCATGCACTGATATACACTTGTTGACAAAATTTGCAGAATGTTTTTTTATGTGTAATAAATCTGTTTATTTTTATAATATAATCCTCACCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31210
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 |
---|---|---|---|---|---|
ENSDART00000049151 | Nonsense | 1182 | 1404 | 13 | 13 |
ENSDART00000123101 | Nonsense | 1182 | 1404 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 30743456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59434407 |
GRCz11 | 6 | 59429619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTTACCAAGGCTACCCAAATCAGAACTTGATGAGCCCACAGCAAAAT[C/T]GAGTTCCTGGATCTGTCAAAGAGCAAATGCAAAGCTCCTGCTATGGGCCA
Long Flanking Sequence:
AAAGAGTTACTGTAAAACCAGAGCAATTCCATCCATCAATGGGAGGATCTAGTTCTTGCCAAAACACTAAAGCTCTGCACCAGAATAGGCATAATGCAAATATGCAAACATATCCACTACAAGGCCAAGGTATTATGAATAGGTCCTCCAGTGCAAGTTGTGACTTCCATCATTCCCAAATGGGAACACAACCAAACCAGGGGGGATCATTCCAGAGTGGTACTGGTATAAACCTTGCCCTGGCAGAAAGCCGCAGATCACAAACACCAATGCATCAAATGAAGGAAATGATGGTCAGGAACTATGTGCAATCCCAGCAAGCTCTCCTATGGGAACAGCAGCAAGAGCAGAGTGTGTCCGAAAAACCTGATGGCATGGACATGGGACAAACACAGATGATGCAGCACAGTCCGCAGCATCAACAAGCCAACCAGAATCTTTATCCTGGTAACACTTACCAAGGCTACCCAAATCAGAACTTGATGAGCCCACAGCAAAAT[C/T]GAGTTCCTGGATCTGTCAAAGAGCAAATGCAAAGCTCCTGCTATGGGCCAGACATGATTCCAAGGCCACCCCAAGTGCGAAAATCTTTAAGTCGCCAAAACAGCCTTTCCCAACAAGCAGGTGGAGCTTACCTGGGAAGCCCACCTCACCTCAGCCCGGTCCACTCTACAGCTAGTCCCAGAAGAGGAGTTAGACTCCCGCCAGTTCAACAACAACAACAACAGCAGCAGCAGCATTCAGAAAACTTCAACAACAACAACAACCCAATGTACTACTCAGGCCAGATACACATGCACCACGACCTAGAGAAGACTCCAGAGGGTCCATGCCTTGCTCAGCAGCACCTAACAAGCTCAGACCCCACTACAAAACCAACATCAATCTCTTATCCAGACCCTGCCCCCATGTCCAATGCCTTAGAACACCTAGACTTGGAGAACGCTCAGATTGACTTTACCTCCATCATTGATGACCAAGAACCTTCATCTTACAGTCCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32697
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049151 | Nonsense | 1273 | 1404 | 13 | 13 |
ENSDART00000123101 | Nonsense | 1273 | 1404 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 1 (position 30743731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 59434132 |
GRCz11 | 6 | 59429344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCAGCAGCATTCAGAAAACTTCAACAACAACAACAACCCAATGTACTA[C/A]TCAGGCCAGATACACATGCACCACGACCTAGAGAAGACTCCAGAGGGTCC
Long Flanking Sequence:
CAAATGAAGGAAATGATGGTCAGGAACTATGTGCAATCCCAGCAAGCTCTCCTATGGGAACAGCAGCAAGAGCAGAGTGTGTCCGAAAAACCTGATGGCATGGACATGGGACAAACACAGATGATGCAGCACAGTCCGCAGCATCAACAAGCCAACCAGAATCTTTATCCTGGTAACACTTACCAAGGCTACCCAAATCAGAACTTGATGAGCCCACAGCAAAATCGAGTTCCTGGATCTGTCAAAGAGCAAATGCAAAGCTCCTGCTATGGGCCAGACATGATTCCAAGGCCACCCCAAGTGCGAAAATCTTTAAGTCGCCAAAACAGCCTTTCCCAACAAGCAGGTGGAGCTTACCTGGGAAGCCCACCTCACCTCAGCCCGGTCCACTCTACAGCTAGTCCCAGAAGAGGAGTTAGACTCCCGCCAGTTCAACAACAACAACAACAGCAGCAGCAGCATTCAGAAAACTTCAACAACAACAACAACCCAATGTACTA[C/A]TCAGGCCAGATACACATGCACCACGACCTAGAGAAGACTCCAGAGGGTCCATGCCTTGCTCAGCAGCACCTAACAAGCTCAGACCCCACTACAAAACCAACATCAATCTCTTATCCAGACCCTGCCCCCATGTCCAATGCCTTAGAACACCTAGACTTGGAGAACGCTCAGATTGACTTTACCTCCATCATTGATGACCAAGAACCTTCATCTTACAGTCCAATCAATGCACCTATAGGACACAATCAATGCTCCTCTCAGACGTCCTCTCGCCTTACAACACCCCAAAACTCCATCACACTTCCCAGTGGCCTTTCTAATATGGCAATCGGAGACATGAGCTCAATGTTGACATCCCTTGCTGGGGAAAACAAGTATCTAAACACGTTATCTTAAGGTGCTTCGGCTTATAATCGGGCTAAAGTGAACTTGTAGAAGGTGATGTATCAGGACCTTGTGGGACAAGCCAATACTAGGGTGCAGAAATGCAAGGACAGCGC
Associated Phenotype:
Not determined