Busch Lab

ZMP

hhipl1

Ensembl ID:
ENSDARG00000062501
ZFIN ID:
ZDB-GENE-090306-3
Description:
LOC100002738 protein [Source:UniProtKB/TrEMBL;Acc:A4IG31]
Human Orthologue:
HHIPL1
Human Description:
HHIP-like 1 [Source:HGNC Symbol;Acc:19710]
Mouse Orthologue:
Hhipl1
Mouse Description:
hedgehog interacting protein-like 1 Gene [Source:MGI Symbol;Acc:MGI:1919265]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa17970 Nonsense Available for shipment Available now
sa23038 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17970
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090447 Nonsense 174 820 2 9
Genomic Location (Zv9):
Chromosome 17 (position 17776782)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 17926793
GRCz11 17 17946629
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTATTGTCTGACGATCCACGTCTTGCAGAACTTGAGCATGACCAACGC[A/T]AGCTTTGTCAGTATTTAGAACTGGACGACCCAGATTACTGCTATCCTCAT
Long Flanking Sequence:
CAATGTGAGCGATATCTTAGGGAATATTGTTTATGTTAATGTCTTGAATTCATTACTTGAGTCATTTGTCTTTTTAAAAGACAGTCTTAACATAGAGTCTATGTTTTGCAACTGGTAGCTTACGTAATTAAGCTATAGGGGGTCAAATAGGGACTTCTGGGGTTACTTCTACCCCAATGCAGAGTGGTTTGCTGTAAACACTACCTTGAGGTTTAAGTGGTTGTGGTCTTTCAGAGTGTTGCATGTGGAAAGGCAGACATGACTAGTCAAGTACATTGTTTAAGAGTGGCACAATTCAGTTCCATCCCCCCTCTGTTTGTCTTCAGGAATGTTCTCCATATGCTGCTCACTTGTTTGATGCCGAAGACCCCAGTACGCCTTTACGGACAATACCTGGACTCTGTCCAGACTACTGCGCTCAATTCCATTCCAAGTGCAGGTCTTTTCTTACCTTATTGTCTGACGATCCACGTCTTGCAGAACTTGAGCATGACCAACGC[A/T]AGCTTTGTCAGTATTTAGAACTGGACGACCCAGATTACTGCTATCCTCATTTGCTGAGTAATGAACATTTGAACAAAAATCTGGGCCGCACTGCAGCAGACTCTGAGGGCTGTTTACAGTTATGTTTGGAAGAGGTAGCTAATGGACTCAGAAATCCTCTTGCCATGGTTCATGCCAATGATGGCACACACAGGTTTTTTGTTGCCGAACAAGTTGGCCTGGTCTGGGTGTACCTTCCAGATCAATCAAAGCTTGAAAAGCCCTTTCTAAACATCACAAAAGCCGTGTTGACATCTCCATGGGAAGGTGATGAACGAGGATTTTTGGGGCTCACCTTTCACCCCCGCTTTAAATACAATGGGAAACTGTATGTCTACTACTCTGTCGAAGTGGGCTTTGATGAGAGAATCCGTATCAGTGAGTTCCGTATCTCTTCTACGGATATGAATGTGGTGGATCACACTTCAGAGAGGTGAGCAGCTGTTTTTTTTTTTTTTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23038
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090447 Nonsense 251 820 2 9
Genomic Location (Zv9):
Chromosome 17 (position 17776549)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 17926560
GRCz11 17 17946396
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCACACACAGGTTTTTTGTTGCCGAACAAGTTGGCCTGGTCTGGGTGTA[C/G]CTTCCAGATCAATCAAAGCTTGAAAAGCCCTTTCTAAACATCACAAAAGC
Long Flanking Sequence:
GAGTGTTGCATGTGGAAAGGCAGACATGACTAGTCAAGTACATTGTTTAAGAGTGGCACAATTCAGTTCCATCCCCCCTCTGTTTGTCTTCAGGAATGTTCTCCATATGCTGCTCACTTGTTTGATGCCGAAGACCCCAGTACGCCTTTACGGACAATACCTGGACTCTGTCCAGACTACTGCGCTCAATTCCATTCCAAGTGCAGGTCTTTTCTTACCTTATTGTCTGACGATCCACGTCTTGCAGAACTTGAGCATGACCAACGCAAGCTTTGTCAGTATTTAGAACTGGACGACCCAGATTACTGCTATCCTCATTTGCTGAGTAATGAACATTTGAACAAAAATCTGGGCCGCACTGCAGCAGACTCTGAGGGCTGTTTACAGTTATGTTTGGAAGAGGTAGCTAATGGACTCAGAAATCCTCTTGCCATGGTTCATGCCAATGATGGCACACACAGGTTTTTTGTTGCCGAACAAGTTGGCCTGGTCTGGGTGTA[C/G]CTTCCAGATCAATCAAAGCTTGAAAAGCCCTTTCTAAACATCACAAAAGCCGTGTTGACATCTCCATGGGAAGGTGATGAACGAGGATTTTTGGGGCTCACCTTTCACCCCCGCTTTAAATACAATGGGAAACTGTATGTCTACTACTCTGTCGAAGTGGGCTTTGATGAGAGAATCCGTATCAGTGAGTTCCGTATCTCTTCTACGGATATGAATGTGGTGGATCACACTTCAGAGAGGTGAGCAGCTGTTTTTTTTTTTTTTTTGGCAACACATTCCTAAAAATAAAGGTGCTAAAATATGACTTTGATTTCAGTGCAGTAGAACAATTCTGGGTTGCCAAAAGAAAAAAATCTTAAAGTTCTTAATGTGAGAAATATTTTAAAGGGGTCACATTATGTTTTTCTACAATTGATAAAGCACAAGTTCCATTTCAAATTGAGTAATCTAAATCAGATTCAGGGAGCACTGTTTATGAGCTCCCACAAATGCCTTAATGT
Associated Phenotype:
Not determined