Busch Lab

ZMP

si:ch211-93n23.6

Ensembl ID:
ENSDARG00000074760
ZFIN IDs:
ZDB-GENE-010319-27, ZDB-GENE-081028-67
Description:
Novel protein similar to vertebrate tetratricopeptide repeat domain 7 family [Source:UniProtKB/TrEMB
Human Orthologue:
TTC7A
Human Description:
tetratricopeptide repeat domain 7A [Source:HGNC Symbol;Acc:19750]
Mouse Orthologue:
Ttc7
Mouse Description:
tetratricopeptide repeat domain 7 Gene [Source:MGI Symbol;Acc:MGI:1920999]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa22223 Nonsense Available for shipment Available now
sa2679 Nonsense Available for shipment Available now
sa38921 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42138 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22223
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
ENSDART00000109059 Nonsense 96 885 3 21
ENSDART00000138448 Nonsense 96 877 3 21
Genomic Location (Zv9):
Chromosome 13 (position 8062347)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 8366867
GRCz11 13 8698890
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATGATTACAGGACGCTGCTGCTGGCCGAAGCGCTGCTGGAGGAATG[T/A]CTGCTGGAGAACATGACCCTACTGAAGAATTCTACTCCTCTGACCGAACA
Long Flanking Sequence:
ACTATAGACTTGTTACTGGTGTGAATTTAAGGGCACTTATGATGAAATTTATCTTTTGGAAGCTGTTCAGACAGAACTGTGTGCAGGTATAGTGTGCCCACAGTCAACTTTTTAAATATTTTGGAGCAGGAAACATGTCAGGGTAAATAATTCAAATGACTTCTGCTGTCTTCATTGGTTTCAAAAACACAGATTTCTTTACAGTTTAAAATGGCTTCTTTGAATATATTCTGCTGGAGATACTGTTGTAAAAATGACCAATCTTACACATATTATAGGAAATGTATAGCAAGAAATGTTGGCGGTTTTAAAACCTTGACTTTTCCAAACCGCGGTATACGTCGAAAATGGTTATTGTCGCATGCAAGAGAGATTACCATAATCAACCAGAATAAAAAAATGTTCCAGTCTTCCTTCTTCAGCCTTTACTCTATTTTTCTCTGATTGTCTGCAGATGATTACAGGACGCTGCTGCTGGCCGAAGCGCTGCTGGAGGAATG[T/A]CTGCTGGAGAACATGACCCTACTGAAGAATTCTACTCCTCTGACCGAACATTCACAGCTTAAACTGGCCCGAGCCAAAGCTCAACTCGACAGCATCCTTTGCAGGGGACACCTAGAGGTCTGGCCCTGTGTTAATTGGAGTCTCTTTATTTTTCTTTATTTCTTGAGAAGCTCGTTTGGAGCAAAGTTCAGTGATGTAACTTAAACTCCATCATTAAACTGAATTCAAACTGAATTTAAAAGGTTTGTTCACACAAAAAATTACAATAGTGTAATTAATCAATCTTATGTTGTTTCAATCCTCTGAGGTCTTTGTTCATCTTCAGAACACAAATATATAATAATAGGATATTTTAGATGAATCATGAGAGCTTCCTCATCCTTCATATAAAGCACGGGTGCTCAACCCTGTTCCTTAAGATCTACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACGCCTGCCTATAATTTTCAAGTGCTGTTCAGGTCCTAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2679
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109059 Nonsense 182 885 4 21
ENSDART00000138448 Nonsense 182 877 4 21
Genomic Location (Zv9):
Chromosome 13 (position 8064990)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 8369510
GRCz11 13 8701533
KASP Assay ID:
554-2520.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCGGGAGTCGATGAWTTCACCCACCAGGACCAGCCTGTCTACCAACTA[C/T]GAATGTTGGCAGAAGCTTTTGTCATCAAAGGTATGAACTAATGTATCAGT
Long Flanking Sequence:
CAGAAACTACAGACTACAATTTTTATTGAGGAATGCTCATTTGTTGTGTGGTTTAGATCATAGTAAGTTTTAACATTTGTTTAGCATTAAAAAACGAAGAAAGATTTTCAAATATTATTAAACATTAATTTTACTGCAACATTAAATCAATGGCAACATTTCTTATGCAGTTTTTAATTAAACCAACAATCTTAGTAATTATAACAGCAACACTGTTATATGGCTAAACTGTGCCACCAAACAAACAAGCTCAGCCAACCTGAATATGTTCAATTGTATTTTAAATCTGTTTTAATTTTATCAGAGGCATTGCCACTCGACTTTCTCAATTAATGGGAACCATTCTTACTCTTTCCCTGTAGCCTCACTACCTGAATGAAGCTCTGCTCCTGCTGGCTAAAGTGCACTATGTGCAGGGACGCTACAGGGATGCTCAAGGGATGTGCGCCAGAGCGGGAGTCGATGATTTCACCCACCAGGACCAGCCTGTCTACCAACTA[C/T]GAATGTTGGCAGAAGCTTTTGTCATCAAAGGTATGAACTAATGTATCAGTAATATCTCATTAATCCTCTCTTGTTGTAAAATTAAGTAATGGGAAGGTAATTAACATACAGTAACATGCAGTCTAAATATGTAGGATTTATGAAGAGTTGTACAATTTTATAAGCTCAGCAACTTTTTAAGTCTGCACTAATTGTGAAAAAAGGTTTATTTACAAAATAGTATTTACACAAAATCCATAAGTGACTTTCAGTCAATTATGTAGTACATGTAAAAGCAGATATTCCTTATATGGTTCTTGTACAGGCAAGACTATGCATGTATTTATAGAGTAATTAAGTCATTTCCACTGCTCCATTCCACTGAGCATTTACCTCAGGCATGCTTTTATTGGATTCATATCCAACTAAAGTGTACAGTGAAAGAAACTCTGCACTGAATTCAGCAAGTGTAATTTGGTCGCATTACAGTACTTAGAATATAACTATGGAAAAAGCCCAAA
Associated Phenotype:
Normal
Stage Entity Quality Tag
Larval:Day 5
ZFS:0000037		 whole organism
ZFA:0001094		 quality
PATO:0000001		 normal
PATO:0000461

Mutation Details

Allele Name:
sa38921
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109059 Essential Splice Site 455 885 11 21
ENSDART00000138448 Essential Splice Site 455 877 11 21
Genomic Location (Zv9):
Chromosome 13 (position 8084877)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 8389397
GRCz11 13 8721420
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCATCTTTGGTATCAGCTTGGCTTGTCATTAATGGCAAGTGGGAAGG[T/C]GAGATTGCTGACATCATTATGCTTCTATTGATTTATTAGTCATTTGTTGC
Long Flanking Sequence:
TTTCAGTAGTTGAGCCATTGTGTGATGGTGAGCGTTTACTCAGAGACGTTCTCAGGTGAATCTGATCTCAGTGCTTTTAGTAGGTTCGTTTCAACTGATTCCATGTCATTTCACTGGTAACCCACATTACACTGCTTTTACTCAGTATTTCCAAGTCATGTCTGCTTGCATGTCGAATGTAAATCCCTTTCTCATTAAATTTAAGCGCACTTTGTCATGCATGTGCCATGAGGGTATGTGTACAGGATACACACAATCCCGTATCAGGGCTGAAACAAGATCCTTCCTAGAAAAACTGAGTAATGCTGAACAACGCATTATCATTTAGCTCTGTTTCTTCTGATGTGCTTCTTGGAAAGCTGAATCCCTGATTCAGAGTTTCTTTCTGACTGCGATGTGTATTTTTTGTCATCAGTGTTTGGAGCGGGCCATGAAGTTCTCCTATAATGAGTTTCATCTTTGGTATCAGCTTGGCTTGTCATTAATGGCAAGTGGGAAGG[T/C]GAGATTGCTGACATCATTATGCTTCTATTGATTTATTAGTCATTTGTTGCTATGACTGGCTGTGTTTTTGATTCTGTTAAATAAGATCTGACGTTTAATAAAATGTAAGTATTCAAGGTCAAAATCAAATTTATTATCGTTCTAAAGCAGCTTTAAGACAAATCATGATAACTAAATGGTAATGCTTTTAGTCACATGTAGCAGATTAGAGATGCTATTATATGTACTTATACAGTAAATGCACACCGTACACACATATACAGTAGAAATCAAACATACAGAATCACTTCTAAATGTTTTTTTTTCATAAATAAAATCTTTACCATTTCACGTTTAAACCAGTTAAACTCAGCGGACGCGGTAACCGTGACGTCATCGACATTCGCTTTAAGATTTAAAGGGCTAGCATTGCACCAGACCCCCTTAAGTGGTTTCGTTTGAAAGCGCAGAATCTATATTGTATGCACATATGCATCACTTTGGTTTTTATTCTACTGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42138
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
ENSDART00000109059 Essential Splice Site 666 885 18 21
ENSDART00000138448 Essential Splice Site 666 877 18 21
Genomic Location (Zv9):
Chromosome 13 (position 8102340)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 8406860
GRCz11 13 8738883
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTGTATTAGATGAAGTGAATTCATATTTTCTTCTCTTTTTC[A/G]GTGAAGAAGATGACTCTAATAGCATACCTCCTGAACCAGGCCCACTGAGC
Long Flanking Sequence:
GATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATACTGCAGACAGAGATAGATAGACAGACGGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGGTACTACAGACAGAGAGACAGACAGATGGATGGATGGATGGATGGAAGGATGGATGGATATGACAGACAGACAGACTGACCCATTTATTCATTCATTCATTGTTGTTTTAGTCTTCTCTTTACCAAAGTGAAGCTGGAGCAGGTTTTGTTTGGTCCGGGTGCAGCTTTACAGACCTGTGCAGAAATGCTGCAGCTGTGGCAAAGTCGCTATGATTTTACCCGACCCAGGTAATATGCTACATCTCTCTCAGGTGTGTATGTGTGTGTGTGTATTAGATGAAGTGAATTCATATTTTCTTCTCTTTTTC[A/G]GTGAAGAAGATGACTCTAATAGCATACCTCCTGAACCAGGCCCACTGAGCAGAAAACCCAGCGGCCTCCATCTCACCCTTCCAGACTTCCAGGAGACAGAGACTGGTGTGCATAATCAGTATATGTGTGCATGTATGAGCAGGCATGCGTGTGTTCCTTGTACAGTATTTGTTACATAATGTGGACACAATGTCCCCACAAGTATAGCAATACCGTTAAATTTTGACCTTGTGGGGACATTTTTGTGTCCCCATGAGGAAAACGGCTCATAAATCACATAGAATGACGTATTTTGAAAATAAAAAAAGCACATTGTTTCCTGTGAGACTAGGGTTTAGGGTAAGTGTATTAAAGCATTACTTCTATAGGAAGTCACTTTAAACTTAGGTGTGTGTGCGTGTTTGTTTGTGTGTGTATGTGAGATTGCATGCATGTTAATGTAAATGTGTATCATGTCACCAGGGTCTCAGAGTGCTCCATCTCTAGCTGTGTCTCGTCTG
Associated Phenotype:
Not determined