ZMP
col4a6
Ensembl ID:
ZFIN ID:
Description:
Type IV collagen alpha 6 chain [Source:UniProtKB/TrEMBL;Acc:Q4TZW7]
Human Orthologue:
COL4A6
Human Description:
collagen, type IV, alpha 6 [Source:HGNC Symbol;Acc:2208]
Mouse Orthologue:
Col4a6
Mouse Description:
collagen, type IV, alpha 6 Gene [Source:MGI Symbol;Acc:MGI:2152695]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34180 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7085 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41015 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41014 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34180
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121574 | Essential Splice Site | 4 | 1666 | 1 | 44 |
Genomic Location (Zv9):
Chromosome 7 (position 52557306)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50827056 |
GRCz11 | 7 | 51102126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCTACTTTACCTGCTGTTTCCTCAAAGCTTTGCAAAATGAGACTTTGG[T/C]AAGTTTATCATATCTTCAGATGTCATTTTTAGCTATTAGAAGTTGTTGGG
Long Flanking Sequence:
TTATGACAGATGCACTACATTAATGCTATTTTAGTTTACACTAGTAGCACGCTGTTTACTGATGAGATTGTGGTTATCTGTTTGTTTGAAGCCGACGCGTGAGTGTGGGTGATTGACGGCTGAAGCCCCGCCCTCTCTTCTCCTCTCAGAGCACAGCGCGCACTGGTGCTGCAGCGGTGCGTGAATCTATTCTGCCGCGAGGAGAGCGTTTTTCAGCACAGAAGTTTCTTGTGAGTCAGCTTCTCTTATTCTCAGAGGACAAACTGCAGCCAAAACTGCATAGAAAAAGTGTAGAATGTGCATTTATGTGTATTTAGCTCTCTAATTTGATTGTTTATGTTTATCCTTATCTCACTTCTTGTTCTCCGAAGTGGTCGAACCGCTCACCGGATTCTCAAATGAATAGGTCTGAAGCCATTAACCGAGGCTCACTGTGAAGACGAGGAGGATAGCCTACTTTACCTGCTGTTTCCTCAAAGCTTTGCAAAATGAGACTTTGG[T/C]AAGTTTATCATATCTTCAGATGTCATTTTTAGCTATTAGAAGTTGTTGGGAGTTCATACACATGAGCGTTAAACAATCAACTGTCATTTTAGTTAGCCGAGTCACACGAAGTGCTGTATTTTCAATCAGCACATGTGAGAAATTTGTTTATCTCTCCTTAGGAGTTTTGTGTTACCCTTTGTCTTGTATGCGGTGTCTGCACAGGGGGTAAGTAATCTATCTAATATTTAAAATACTAAACACTTGCCGATTATAACTTTTGCCTGTTTAATTATACATTGTATATGATAATTTGTTGGTTATTTAATCGCAACTCTTAGTAAAACAGGTTACACCTGGCGCATCATGTTTGTGTTCATTTATCAAAACACGTTTGGGTGTAATTTATCAGACACCTGTCTAATTTACAAACTGTGAAGTTCTGTTGACTATTTGTGGCAAAATATTTTGTCATCATTTTACAAGTTTTCGTTGAGAAGCTAATATTTAGCTTTACATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7085
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121574 | Essential Splice Site | 90 | 1666 | 4 | 44 |
Genomic Location (Zv9):
Chromosome 7 (position 52431370)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50701120 |
GRCz11 | 7 | 50976190 |
KASP Assay ID:
554-4354.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGGGCCATATAGGACGTAAAGGTCCTCCTGGACAAAATGGAGATAAG[G/A]TCAGCTTACTGTGGCACATGYGTGGACTTCTATTGCAGATTTMATTTTYT
Long Flanking Sequence:
AATAAAATAAACATTTAACTTTTTTTATAATTAATAAATGCCGCCTTGATGAAAATAATAATTTTATATAAATTATTAAAGAAAATTAATAAATAAAAAGACAAAATAAATATTACAGATTATGTAACTTTGTTTTTTTTCATGCATCAATTTAATCTGATTTTACCTAAGAACTCTCAAACTGAGTCAGATCAAGACAAATATCTGCAATGTTGGACAAGAAGTTTAAGATAAAATCTAATCTTTTTTTTTAAAGGATTTGTGCTTTATTTAGATTTTTGTGTTTTATTTCACAGATGCTGTTTTATAAACTGTATTAAAAAGTGACTCATTGATACCTTCTATCTATCTTTCTCACCATCTAGGGGCAACCAGGAGAACTTGGACCAGTGGGCAGCGGTGGTCCTGAGGGTTTCTATGGGGGCCCGGGACCAGTTGGGCCAAAAGCAGAGCAGGGCCATATAGGACGTAAAGGTCCTCCTGGACAAAATGGAGATAAG[G/A]TCAGCTTACTGTGGCACATGTGTGGACTTCTATTGCAGATTTCATTTTTTATTTACTGAAAAATGACAGAATGTAATGGAATGTTTACGTTTGCACATGCATGTTAGATCCAAATACAGGAATCAGTGTGATGCACATATAATACTAGAAAAGGCCTTTTCATGTGTTTTACATATTTTCTGACAGGGTCCAATGGGTGTTCCTGGTTATCCCGGTAATGATGGTGTTCCTGTAAGTATATAACTGTTTTATATACTGTTTTATATATATATATATATATATATATATATATATATATATATATATATATACAACTACATTAGTATAGAACTACATTAACTGTCTTAATGTAGTTTCACTCTTCTCTGAAAATTATTAATTAAGCTTTTTTTCAACGTGTTTTACAGGGACACCCTGGTCAGGAGGGGCCCAGGGGGCCTCCAGGTCTGGATGGGTGTAATGGCACACAAGGGGACACTGGTTACAGCGGCCTTGATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41015
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121574 | Nonsense | 122 | 1666 | 6 | 44 |
Genomic Location (Zv9):
Chromosome 7 (position 52430912)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50700662 |
GRCz11 | 7 | 50975732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACACCCTGGTCAGGAGGGGCCCAGGGGGCCTCCAGGTCTGGATGGGTG[T/A]AATGGCACACAAGGGGACACTGGTTACAGCGGCCTTGATGGGTATTCTGG
Long Flanking Sequence:
CATATAGGACGTAAAGGTCCTCCTGGACAAAATGGAGATAAGGTCAGCTTACTGTGGCACATGTGTGGACTTCTATTGCAGATTTCATTTTTTATTTACTGAAAAATGACAGAATGTAATGGAATGTTTACGTTTGCACATGCATGTTAGATCCAAATACAGGAATCAGTGTGATGCACATATAATACTAGAAAAGGCCTTTTCATGTGTTTTACATATTTTCTGACAGGGTCCAATGGGTGTTCCTGGTTATCCCGGTAATGATGGTGTTCCTGTAAGTATATAACTGTTTTATATACTGTTTTATATATATATATATATATATATATATATATATATATATATATATATATACAACTACATTAGTATAGAACTACATTAACTGTCTTAATGTAGTTTCACTCTTCTCTGAAAATTATTAATTAAGCTTTTTTTCAACGTGTTTTACAGGGACACCCTGGTCAGGAGGGGCCCAGGGGGCCTCCAGGTCTGGATGGGTG[T/A]AATGGCACACAAGGGGACACTGGTTACAGCGGCCTTGATGGGTATTCTGGTATTCCTGGTTCTCCTGTAAGTTATAGGCTATGTTTGCATTTGAAGAACATTTCTGAATAATCAATATTAATAATAGTTGCAGGTTCAAATGATAAAATAGAAATTAACTTCTCTGTTTTTATAGCAAAAATGGAAAATACGTTTTCGGATCACATGTGTTTTTATTTAAAGAGGCCCTATTATGCATTAAAAAGATCATACTTTGGTTTTGGGGGTCTCCAACAACAGGCTGATATGCATGCAAGGTCAAAAACACTTTCATTGTCTTATAATATGCATTTATTTTTACCTAATTACCACAACAACTCCCATATGACTCAGCGATTCATTTGCTCCCAAAGCCCTCCTCAGCACAATGCTATGCGCTGGTTGGTGTGATGAACCAGTCTGTTGCGATTAGCTAACTGCTTTCAGCATGAGACAGAGAAAAATGCCCAGCAAGAAGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41014
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000121574 | Essential Splice Site | 1024 | 1666 | 31 | 44 |
Genomic Location (Zv9):
Chromosome 7 (position 52388683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 50658433 |
GRCz11 | 7 | 50933503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGGATCTTGTTTGTTGTATTTTTATATTTTATGTTGTTCTTATCTGT[A/G]GGGTGATAATGGTGTCCCTGGGGTTCCTGGGTTCCCGGGTGCTCAAGGAC
Long Flanking Sequence:
CTCCTGGACGTCCAGGATTTCCAGGACCACCTGGCTTTGCAGACCAGGCAAAGGGTTTACCTGGCCAGCCTGGAATCCCAGGTGTTCCTGGTTCATCTGGCTTCCCTGGACCCAAAGGCTTTCCTGGAGTTATGGGCTTCCCTGGCTTTTCAGGTGTGAAGGTAAGCATTCTGTATTCAGACACAGCACAGTATACTATGGATTCATCACATCTGATACTGGTATCATCATCAGGTTCAATCTAGTTGTCATAATTTGTACTTACGTGCTATGTATATAGGGACACTGTTTAGAAATAATAACATTTTGTATACGATATGCCTGATTGTCATAGAAATAATGTTAGAAACCTTTAATTTCCTTTAAATATCTAAATATTTGTTGTTATTATTATTATTTGTTTGATTGATATGTAATCTGGACAAGTTCTTGACCGAGTGTGAAGTTAGCACATGGATCTTGTTTGTTGTATTTTTATATTTTATGTTGTTCTTATCTGT[A/G]GGGTGATAATGGTGTCCCTGGGGTTCCTGGGTTCCCGGGTGCTCAAGGACCACCTGGTGCCAAAGGTGAGATTTCTGTAAATCTGTGTTTATTTCTGACCTCAACTGTATGGCAAAAGATTTCAATAGAAGGCTAAAGGCAGCTATAACTGGTCTCACGGTTCGGTACGGATTATCATGCCATCGATTTGGTTCAATTCGATATCGCGGTGCATCGCGGTACATAAACGATGCTTTCCATACACAGTGTTGTACTTTAGGGGGAGGCTTTAACAAGCTGTCGCTATAAACACACACACACATACACACAGCACCACACTGTTTCTCATTCACACACATACACAAACATAGACAGCACCAAACAAATACACGCACACACACACACACACGAAATGCACGCTTGCTTGCTTGCTCGCTCGCTTGGGAGCGATATTGTGTGGGGCCGCCCACTCCTGTTAAAATTACACCAGAGTTACTGACCGCTCTCACACTTTATTCGGA
Associated Phenotype:
Not determined