ZMP
slc25a13
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate solute carrier family 25, member 13 (Citrin) (SLC25A13) [Source:
Human Orthologue:
SLC25A13
Human Description:
solute carrier family 25, member 13 (citrin) [Source:HGNC Symbol;Acc:10983]
Mouse Orthologue:
Slc25a13
Mouse Description:
solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13 Gene [S
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43336 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36899 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43335 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43336
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102780 | Nonsense | 201 | 667 | 5 | 20 |
| ENSDART00000141163 | None | None | 103 | None | 3 |
The following transcripts of ENSDARG00000070172 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 42312031)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 41755354 |
| GRCz11 | 19 | 41340409 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGACATCATGGTGACCATCAGACCTCACATGCTCACTCGGTTTGTGGAG[G/T]AAAGTCTTGTCGCAGTGAGTTTTTCAGTCAGTGTTTTTACTGTATTCACA
Long Flanking Sequence:
ACATAAAATCTGAAAACCTTCAAAAATAAGATCATATTTTGCAATTAAACTCAGAAAAGAAACATGTCATAGGCACTTTATGTCTACAAATGCCTTAACGAATGCTAAAAAAATTATTTGAGCCTTATTGTAAAGAGTTACCATAATCTTCATATTGACATTTTTTCAGCAGTCTGAAGCTGAGTTTACTTTTTTTAAAGCAATGCATTTTTACATAATGAAAACCAGCTGTACAGCACGCACCTCACTTGGTTCTAAAATCACATGCATGTAATTAATCAAGTATTTGTTTTATTTTCTGCAGTACGAATCCCTCCAATCCAGCATTGGCAGCACTCAAACACTGACCGACCTTCACTGTGTTGCAGGAGATGCAGCTCGAACACGCTAGACAGGCTTTTGTGCAGCGGGACAAGGCCAAATCAGGCACCATCACCGCCCTGGACTTTAGGGACATCATGGTGACCATCAGACCTCACATGCTCACTCGGTTTGTGGAG[G/T]AAAGTCTTGTCGCAGTGAGTTTTTCAGTCAGTGTTTTTACTGTATTCACATGAAGTCAGAATTGTTAGCCCCCCTGTATATTTCTCCCATTTTCTGTTTAACGGAGCGAAGATTTTTTTCAACACATTTCTAAACATAATAGTTTTAATAACTCATATCTAATAACTGATTTATTTTATCTTCGCCATGATGACAGTAAATAACATTTGACTAGATATTTTTAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGTTAATTAGGTTAATAAGGCAAGTCTAAATTGTATAATGATGGTTTGCTCTGTAGACAATCGAATAAAAAATATTGCTGAAGAGGGCTAATAATATTGACCTTAAAAAGGGTTAAAAAATATTAAAAACTGCTTTTATTCTAGACGAAATAAAACAAATAAGACTTTCTCTAGAAGAAAAAATATTATTGGAAATACTGTGAAAAATTCCTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36899
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102780 | Nonsense | 307 | 667 | 8 | 20 |
| ENSDART00000141163 | None | None | 103 | None | 3 |
The following transcripts of ENSDARG00000070172 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 42295060)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGATGATTGCACCTCTGGAGGAGGGAGCGCTTCCTTACAACCTTGCT[G/T]AGATTCAAAGACAGGTATGTTTCAGATATAGACCTGGGAAAATGGATGGA
Long Flanking Sequence:
TTTCATGTACATTAACAAACCTTAAAATTCAGCAATTAGTAATTAATAGTGAAGTAAAAATACTAAGTTGATGGTACTGTATATACTGCAAAGCTCTTTTAAAGTAATGAGATTGAAAAAAAATATTCAGAAAATACCCATGAAGCTTTCAAAAAGCCAAAAACATCACATGAACATTCCGGAGAAGTCATGACCTTTGAACCGAATCATTACGCTACTGGGTGGGTCGTGATCAGGAATCATATTTTTTGATGTCATTATTTTTTTTCTTGCAATGCGATACTGTAATTACGCAACTCTCTTTGAGTCAGGATGGCGAGGGCACACTATACATCACTCTTTCTCAGAGATCTTAGAGATGTTGTGCTTTAAAAAAAGAGCTGGATAGAAAAATCTTTAATAATGCCTGCCTGTGTTTTGCTTTACACAGACGGCTTGGTTTAGTTGACATCGAGATGATTGCACCTCTGGAGGAGGGAGCGCTTCCTTACAACCTTGCT[G/T]AGATTCAAAGACAGGTATGTTTCAGATATAGACCTGGGAAAATGGATGGATTGTTTTGAAACTCTGTGAATATGTGATTTAATAAAAAAAAGTGGCTTTTATACACACTGGAATACAGTAGTGTGGAATACACCACCTGACAAAAGTCTTGTTGTCGATCCCAGTTGCAAAAGCAACAAATAATAACTTGACTTCTAGTTGAACATTTGGAAAAGTGGCAGAAGGTTGATTTTTCTGATGAATTATCTGTTGAACTGCATCCCGATCATCATAAATACTGCAGAAGACCTACTGGAACCCTCATATTCTCACAGAAATCAGTCAAGTTTGGTAAAGGAAAAATCATGGTTTTGGTTACATTCAGTATGGGGGTGTGCGAGAGATCTGCAGAGTGGATGGCAACATCAACAGCCTGAGGTATCAAGACATTTGTGCTGCCCATAACATTACAAACCACAGGGGAGGGCAAATTATTCAGCAGGATAGCGCTCCTTCTCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43335
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 |
|---|---|---|---|---|---|
| ENSDART00000102780 | Nonsense | 371 | 667 | 10 | 20 |
| ENSDART00000141163 | None | None | 103 | None | 3 |
The following transcripts of ENSDARG00000070172 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 42284893)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 41736836 |
| GRCz11 | 19 | 41321891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCATGCAGAACCAGCGCTCTTCAGGGTCCTTAGTGGAAGAGCTCATGTA[C/A]AAGAACAGCCTGGACTGCTTTAAGAAGGTCGTGCGCTACGAGGGCTTCTT
Long Flanking Sequence:
TGGCGAAATGGCGGCCGCGTGAAATCAGTCTATGTAGCGCTGAAAACAAAAACACAGTGCCGCGAACAAAGCAACAAACACACCTGGACGAGAGCAAGCTTCCCAAGCATATCCAAGACGGCGCTCGTACAAAGACGAAGACAGACAACGACAGAAAATGAGTGCTTGACCCAAGAAAACTCGAGCTGAGCACAACATACAAGACATGACAGGACTAGTGTCTGGAATCTGCCACCAAAACAGGAATTAACAAGATCGAAGTGGCAGAATCCTGACAAGGAGCTTGTGCAATATGTTCAGTGCAATGAAGTGAACTTCAGTGCAATATGTTACCAGACATAACATCTAGGAGGTTTACCAATATTACCATAGTTTTACACCCTTTTTCCCCCCCCTCATATATCAGCTGTAGGTGCGACGGCCGTGTACCCCATCGACCTGGTGAAGACCCGCATGCAGAACCAGCGCTCTTCAGGGTCCTTAGTGGAAGAGCTCATGTA[C/A]AAGAACAGCCTGGACTGCTTTAAGAAGGTCGTGCGCTACGAGGGCTTCTTCGGCCTCTACAGAGGTCAGTCAGGCAACAACAAAAAAAGCATTTTTCATGAAGCAGGGCCTGGGTCATCTTCCCTTTGACCTTTACCTGCTTTGAAGAGATTAAGTCTACCTTCAGTGCCGCAGGGGACAATGAGCAGAGCATGAAAGAGCGCATACCAGCACAGGGAACTCAACAATGAAGAACATGAATGCGCTACGCAGTCAATGGCACTCGGATAATGAGGATCTGCTCTGCTTTTAGAGTTTTTAAAGCACTGGGTGAGGTCACAGATTCAAATTGCGATTGCGAGGTGCAGTTGGCATGTGACCTCCATTGAGAAACACTAACTGCTGGTATTTGTCAATCATAAAGCCGACAAAAGACGGGCTGAGATCTTGATCACCCGCTGGATCATGAAACAGGGGTGGTTTTGAAAAATCCGCTGCTCGATTTAGCAGAGCGTATGGGT
Associated Phenotype:
Not determined