ZMP
si:dkey-202m9.3
Ensembl ID:
ZFIN ID:
Human Orthologues:
COL6A5, COL6A6
Human Descriptions:
collagen, type VI, alpha 5 [Source:HGNC Symbol;Acc:26674]
collagen, type VI, alpha 6 [Source:HGNC Symbol;Acc:27023]
collagen, type VI, alpha 6 [Source:HGNC Symbol;Acc:27023]
Mouse Orthologues:
AC119951.1, Col6a4, Col6a6
Mouse Descriptions:
collagen alpha-5(VI) chain precursor [Source:RefSeq peptide;Acc:NP_001161395]
collagen, type VI, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:1915803]
collagen, type VI, alpha 6 Gene [Source:MGI Symbol;Acc:MGI:2444259]
collagen, type VI, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:1915803]
collagen, type VI, alpha 6 Gene [Source:MGI Symbol;Acc:MGI:2444259]
Alleles
There are 14 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17668 | Nonsense | Available for shipment | Available now |
sa22900 | Essential Splice Site | Available for shipment | Available now |
sa565 | Nonsense | Available for shipment | Available now |
sa14196 | Nonsense | Available for shipment | Available now |
sa12050 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17668
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 |
---|---|---|---|---|---|
ENSDART00000109703 | Nonsense | 219 | 2543 | 2 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 38081187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36721670 |
GRCz11 | 16 | 36675554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTACTGATGTAWTTGTGTTGGTGGACAGTACAGCTCAGGGGGAAAYA[C/T]AGCAAATAAGGGAACTTCTCAACCGACTGCTTGTGCAGCTCAATGTGGGY
Long Flanking Sequence:
ATTAATTGGAAGGCCTGGGGTTGGCTGACTGAAATTAAAAGTCAGTGTGCAAATACACCATTGCAAGGCAAACAACTTACTGTATGCATTGTTTTAATCAAGAATTAGACGCTCTTGTGGGCTGTTCGCACAAAACCCTTTTTTTGCTTTCCATTGCGCAGTTTTTTCCACATTTTGTTTCATAAACATGGACAGATGTGTTTAACCAGTTTCCTGCGTTTTGTTTGTGACTTTCTAAAAGCATGTTGCTTAAGTTAACAGATTGTCTGCCCTGAGTCTGGTGTTTTTAAAAGCACAAATGTGTTTTGTTTTATTTTTAAGGAACTTTGGTGATGAGGGTTCATTTGTAAGCAGTCATGGTATTAAAAATTGAACATCCATGTCTTTACAGTGCAGATGTATAAATGAATCGTAATTTCTTCTTTGTCTTTGTTTCAGCTCTGGCCCCGAAGTTTACTGATGTATTTGTGTTGGTGGACAGTACAGCTCAGGGGGAAACA[C/T]AGCAAATAAGGGAACTTCTCAACCGACTGCTTGTGCAGCTCAATGTGGGTGACGGATCTAATAAGATTGCGCTGGCTCAGTTTGGTGAGAACGTCGTCAAAGAGTTCCTGTTTAAAGACTACCAAACAGCGCAGAAAGCCAGAGAGTTCATAAATCGGTTCGAGCCCAGGCTTAATGGAGAGCGAAAATTGGGAAAAGCCATAGATTATGTTCGCACAAATTTTCTGAACACAGTATCTGGCAGCAGGATCGCGAAAGGCTACAAGCAGTATCTGCTGGTGCTGAGAACTGGAGACTCTTACGACTCTACTGTGAGGGCCATACGAACAATGAAGAATGAGGACGTGTCCGTCATTGATATCAGACTGGAACCAAATTTACAATCCTTGTTCCCCTCACTACGTGCCTTCCAGATCGACCAAAATGTTATTGATGTGGCTGCTGACGTCACAAAAAGAATTCAGGAGAAAGAGGTTTTCAATGTTACAGGAGGTTGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22900
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109703 | Essential Splice Site | 1672 | 2543 | 17 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 38106298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36746781 |
GRCz11 | 16 | 36700665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGGAAGCTCAGGAAGCCCAGGACAACGAGGCCTGAGAGGAGATCCGG[T/G]TAGTAGAATTCAGCTGCAAATAAATCTCTTAAAGGGATAGTTCACCCAAA
Long Flanking Sequence:
AACTCTACAGTTTAACAAAGTGACTTTTATTAGCATTTAGTAGCTTAAAATAATATAATGTATAAAAAATATTATATAGAGAAGTAAGTCTGTAAAATAAAAAGGTTTTGCAAGGTTTATGCAGGATTTTTGTGTTATATACAACACCAACCCAGAAACTATGTCACTTTAAATTATTAAAGATGTTAAAAAACGTCACTTTTTTAACTTTTCAAGGATAAAAATTTTTGGAAGAAAGATCATGCCTTGCATTTTACTTTTTGAAATTTTCAGGGTAAAACTGGAGCACCGGGAAGTCCAGGAGAGCGAGGAGATCCAGGCAATCCGGTAAAATACACCACTTATGTTCCTCTCAACTATGATCCAGTCTCGCTGTAGTGCTCCATCTTCTCTGATTTATACATATGTATCGTCTTTGTTTGTTACTTTTGTGAAGGGTCCAACAGGTATTTCAGGAAGCTCAGGAAGCCCAGGACAACGAGGCCTGAGAGGAGATCCGG[T/G]TAGTAGAATTCAGCTGCAAATAAATCTCTTAAAGGGATAGTTCACCCAAAACATTTGTTTATTCACTTTCCTTCGGCTTAGTCCCTTTATTCATCAGGGGTTGGCACAGGGGAATGAACCATCAACTTATCCCGTATATGTTTTACACAGTGGATGCCCTTCCAGCTGCAACTCAGTACTGGGAAACATCCATACACACTCATTCACTCTTATTTAGTTTATTCAATTCACCTGTACCGCCTGTCTTTTGGACTGTGGGGGAAGCCATAGCACCCAGAGACAACCCACGCCAACACAAAGAGAACTTGCAAACTCCAAACAGAAATGCCAACTGACCCAGCCAGGACTCGAACCAGCGACTTTCTTGCTGAGGCGACAGTGCTTATCACTGAGCCATTGTGTCCCCCCTCACCCAAAACAACAACAACAAAATTCTTTTATTATTTACTCAGCATTCACTTGTTCCAAACCTGTTTTTTTTCCGTTTTTTTAACACACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa565
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109703 | Nonsense | 2034 | 2543 | 32 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 38113026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36753509 |
GRCz11 | 16 | 36707393 |
KASP Assay ID:
554-0475.1 (used for ordering genotyping assays)
KASP Sequence:
GAGTGCGAAAAGGCRTCCTGATGAGGAAGGTTGCCATTTTCCTYACTGCT[G/T]GAGAATCTCAAGATTCGATATCTCTCACCACTGCCATTCTAGAGTACAAA
Long Flanking Sequence:
TTTGTATAAGGCTAAAGGGCTTCTTCATCATCCTTACAAATAAATATTATATTTAATTTGTGAATTATCTGTCATGTGTACACAATTAAATATGAAACTCTTCTACTGAATGTGTTCTTCTAGACAACATAAAATGTCCGGCATACCCCACTGATCTTGTGATTGGCATGGACATGTCTGAAGATGTGACCCCTCAAGGCTTTGAGCGCATGCGTTCTGTGGTCCTCAGACTGCTGGACAACATGAAAATTGCAGAGAGTAGCTGCCCGACAGGGGCTCGAGTGGCTCTGGTGTCCTACAGCTCATTCACCAAATACCTGATCCGCTTTAACGACTACCACCGCAAGAAGCAGCTTATCGATGCCGTCAACAACATCGCCCTGGAACGCACTTCAAATCGCCGCAACATTGGCGCTGCCATGCGGTTTGTGGGCAGAAATGTTCTGAAGCGAGTGCGAAAAGGCATCCTGATGAGGAAGGTTGCCATTTTCCTCACTGCT[G/T]GAGAATCTCAAGATTCGATATCTCTCACCACTGCCATTCTAGAGTACAAAGCCCTGAATATTAAACTTGGGGTCATTGCTCTGAGGAATGTCCCTGCTATCAGGAGAGCTTTTGAGGTAAAGATGAGTGCCTCATAAACAAAATGTTTAAAAATAGCTGATTGATTTAAAAGTGGTTAACTCTTTAAATTGGTTAACTTTGTATGCGTTTTTAACTCCAAGGTGACCAGTTGTTTGAACTACTATAATTCACTAGTATTATTCAAACTAAAAACATCTCATCCACAATGACCTGAGCACTTAAAAAAACACTCCCCCCCCTCCTTAGCTCTCCCTGAGCACTAACTGTTACTTTTTATAATTAGCACTTCTTGCGTGTATTGCCTCTTCTTGTTAAATCACTGAATGTCTCCTCATTTGAAAGTCGCCTTGGATAAAAGCATCTGTTAAATGCAACATAGGCTCATTGTGAAAACATAGCCCTGTATACATTTCTGGAGA
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:
sa14196
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109703 | Nonsense | 2294 | 2543 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 38115224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36755707 |
GRCz11 | 16 | 36709591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGTGGGAGACTCCATCGCCTCTAGTCAGGTGGAGGAGCTTGCCAGCTA[T/A]CCTTTAGWACAGCACATCATTCACCTGGGCCACTTGAAACATGGAGAACA
Long Flanking Sequence:
GACTTTGTGATGGTTGTGGACGGGTCCCGTAGCATCCTGGCTGACGAGTTCAAGGGTGTCAAGGAGGTGCTCGGCGGTGTGCTCGATCAAATTGTTGTGAGCAGTCAACCCACCAGGGCTGACAGACAGGCCAGAGTGGCTCTCTACCAGCAGACGTCTACCTATAGTGACCCCCAGCCTGCACACGAGATATTCAGCTTACGTGAGTTCTCTGATCGCAATCTAATGAAGACAAGCATCATCCAAAAACTAAAGCAAACCGGAGGATCTCATGAACTGGGTTCTACTTTGGAGTTTGCTTTCAAGAAGTGTTTCAACGCAGTTCCAGAAAGTCGCAAGAACAAGATGCTGCTGGCCATCATTGGGGAGGAGACAGCGTTACAGGAGAAAAAACGTCTGGACTCTTTCTCCAGGTTGGCGAAGTGTAGCGGCATTGTTCTTTTCACCTTGACAGTGGGAGACTCCATCGCCTCTAGTCAGGTGGAGGAGCTTGCCAGCTA[T/A]CCTTTAGAACAGCACATCATTCACCTGGGCCACTTGAAACATGGAGAACAGGAGTACACACAACGCTTCATGAGGACTTTCTTCCATATACTGAGCAGTAAGGAGTGTTTCATGTTAATGCTGATTTGATTTGGGTCAAAAGAATTGCAGTAGTTATTCTGGTGGCTATCTTGCCTCTCTAATGTTGCTCAGAAAATGCAACAAACATCATAAAAGGTATCATTGTGAGCCTTATAGCTTTACAATAGCTTTATGTGAGGAACAAGTCTAATTTCAGTTTATACCATGCTTTTTGGTAAACCAGGGCAATGTCAACAGAACCTGACTAAAATGTAACCCTGGACCACAAATGTTGCGCAGGTATACACATTTTATTGGTCAAAATGTGGCCAAAATGATCAAAAATATGACTAAAAATCAATGTTTCATGAAGATTTCTTTGTAAATTTTCTACTGTAAATATTAAATCTTATTTTTTATAATAATATTAATAATTCCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12050
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109703 | Essential Splice Site | 2327 | 2543 | 34 | 39 |
Genomic Location (Zv9):
Chromosome 16 (position 38115323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 36755806 |
GRCz11 | 16 | 36709690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAGTACACACAACGCTTCATGAGGACTTTCTTCCATATACTGAGCAG[T/C]AAGGAGTKTTTCATGTTAATGCTGATTTGAWTTGGGTCAAAAGAATTGCA
Long Flanking Sequence:
AGCAGTCAACCCACCAGGGCTGACAGACAGGCCAGAGTGGCTCTCTACCAGCAGACGTCTACCTATAGTGACCCCCAGCCTGCACACGAGATATTCAGCTTACGTGAGTTCTCTGATCGCAATCTAATGAAGACAAGCATCATCCAAAAACTAAAGCAAACCGGAGGATCTCATGAACTGGGTTCTACTTTGGAGTTTGCTTTCAAGAAGTGTTTCAACGCAGTTCCAGAAAGTCGCAAGAACAAGATGCTGCTGGCCATCATTGGGGAGGAGACAGCGTTACAGGAGAAAAAACGTCTGGACTCTTTCTCCAGGTTGGCGAAGTGTAGCGGCATTGTTCTTTTCACCTTGACAGTGGGAGACTCCATCGCCTCTAGTCAGGTGGAGGAGCTTGCCAGCTATCCTTTAGAACAGCACATCATTCACCTGGGCCACTTGAAACATGGAGAACAGGAGTACACACAACGCTTCATGAGGACTTTCTTCCATATACTGAGCAG[T/C]AAGGAGTGTTTCATGTTAATGCTGATTTGATTTGGGTCAAAAGAATTGCAGTAGTTATTCTGGTGGCTATCTTGCCTCTCTAATGTTGCTCAGAAAATGCAACAAACATCATAAAAGGTATCATTGTGAGCCTTATAGCTTTACAATAGCTTTATGTGAGGAACAAGTCTAATTTCAGTTTATACCATGCTTTTTGGTAAACCAGGGCAATGTCAACAGAACCTGACTAAAATGTAACCCTGGACCACAAATGTTGCGCAGGTATACACATTTTATTGGTCAAAATGTGGCCAAAATGATCAAAAATATGACTAAAAATCAATGTTTCATGAAGATTTCTTTGTAAATTTTCTACTGTAAATATTAAATCTTATTTTTTATAATAATATTAATAATTCCTTACATTTATACAGTTCTTTTCTAGACACTTACAGTGCTTTTCACATTGGGGGGAACCTCCGCATCCACCACCAGTGTGCAGCATCTACCTGGATGATGAG
Associated Phenotype:
Not determined